Sandbox: Ventricular Arrhythmias ACC -2017: Difference between revisions
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{| class="wikitable" style="width:80%" | {| class="wikitable" style="width:80%" | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' Patients presenting with syncope for which VA is documented, or thought to be a likely cause, should be hospitalized for evaluation, monitoring, and management. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' Patients presenting with syncope for which VA is documented, or thought to be a likely cause, should be hospitalized for evaluation, monitoring, and management. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
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{| class="wikitable" style="width:80%" | {| class="wikitable" style="width:80%" | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with sustained, hemodynamically stable, wide complex tachycardia, a 12-lead ECG during tachycardia should be obtained. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with sustained, hemodynamically stable, wide complex tachycardia, a 12-lead ECG during tachycardia should be obtained. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''2.''' In patients with VA symptoms associated with exertion, suspected ischemic heart disease, or catecholaminergic polymorphic ventricular tachycardia, exercise treadmill testing is useful to assess for exercise-induced VA. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''2.''' In patients with VA symptoms associated with exertion, suspected ischemic heart disease, or catecholaminergic polymorphic ventricular tachycardia, exercise treadmill testing is useful to assess for exercise-induced VA. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''3.''' In patients with suspected or documented VA, a 12-lead ECG should be obtained in sinus rhythm to look for evidence of heart disease. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''3.''' In patients with suspected or documented VA, a 12-lead ECG should be obtained in sinus rhythm to look for evidence of heart disease. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| Ambulatory Electrocardiography | | Ambulatory Electrocardiography | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' Ambulatory electrocardiographic monitoring is useful to evaluate whether symptoms, including palpitations, presyncope, or syncope, are caused by VA. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' Ambulatory electrocardiographic monitoring is useful to evaluate whether symptoms, including palpitations, presyncope, or syncope, are caused by VA. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| Implanted Cardiac Monitors | | Implanted Cardiac Monitors | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with sporadic symptoms (including syncope) suspected to be related to VA, implanted cardiac monitors can be useful. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with sporadic symptoms (including syncope) suspected to be related to VA, implanted cardiac monitors can be useful. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-R]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| Noninvasive Cardiac Imaging | | Noninvasive Cardiac Imaging | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with known or suspected VA that may be associated with underlying structural heart disease or a risk of SCA, echocardiography is recommended for evaluation of cardiac structure and function. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with known or suspected VA that may be associated with underlying structural heart disease or a risk of SCA, echocardiography is recommended for evaluation of cardiac structure and function. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients presenting with VA who are suspected of having structural heart disease, cardiac magnetic resonance imaging (MRI) or computed tomography (CT) can be useful to detect and characterize underlying structural heart disease. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients presenting with VA who are suspected of having structural heart disease, cardiac magnetic resonance imaging (MRI) or computed tomography (CT) can be useful to detect and characterize underlying structural heart disease. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-EO]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| Biomarkers | | Biomarkers | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients presenting with VA who are suspected of having structural heart disease, cardiac magnetic resonance imaging (MRI) or computed tomography (CT) can be useful to detect and characterize underlying structural heart disease. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients presenting with VA who are suspected of having structural heart disease, cardiac magnetic resonance imaging (MRI) or computed tomography (CT) can be useful to detect and characterize underlying structural heart disease. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| Genetic Considerations in Arrhythmia Syndromes | | Genetic Considerations in Arrhythmia Syndromes | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients and family members in whom genetic testing for risk stratification for SCA or SCD is recommended, genetic counselling in beneficial. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients and family members in whom genetic testing for risk stratification for SCA or SCD is recommended, genetic counselling in beneficial. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-EO]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| Invasive Cardiac Imaging: Cardiac Catheterization or CT Angiography | | Invasive Cardiac Imaging: Cardiac Catheterization or CT Angiography | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients who have recovered from unexplained SCA, CT or invasive coronary angiography is useful to confirm the presence or absence of ischemic heart disease and guide decisions for myocardial revascularization. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients who have recovered from unexplained SCA, CT or invasive coronary angiography is useful to confirm the presence or absence of ischemic heart disease and guide decisions for myocardial revascularization. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-EO]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| Electrophysiological Study for VA | | Electrophysiological Study for VA | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with ischemic cardiomyopathy, NICM, or adult congenital heart disease who have syncope or other VA symptoms and who do not meet indications for a primary prevention ICD, an electrophysiological study can be useful for assessing the risk of sustained VT. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with ischemic cardiomyopathy, NICM, or adult congenital heart disease who have syncope or other VA symptoms and who do not meet indications for a primary prevention ICD, an electrophysiological study can be useful for assessing the risk of sustained VT. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-R]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightCoral" | [[ | | colspan="1" style="text-align:center; background:LightCoral" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class III - No Benefit]] | ||
|- | |- | ||
| bgcolor="LightCoral" |<nowiki>"</nowiki>'''1.''' In patients who meet criteria for ICD implantation, an electrophysiological study for the sole reason of inducing VA is not indicated for risk stratification. ''([[ | | bgcolor="LightCoral" |<nowiki>"</nowiki>'''1.''' In patients who meet criteria for ICD implantation, an electrophysiological study for the sole reason of inducing VA is not indicated for risk stratification. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-R]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightCoral" |<nowiki>"</nowiki>'''1.''' In patients who meet criteria for ICD implantation, an electrophysiological study for the sole reason of inducing VA is not indicated for risk stratification. ''([[ | | bgcolor="LightCoral" |<nowiki>"</nowiki>'''1.''' In patients who meet criteria for ICD implantation, an electrophysiological study for the sole reason of inducing VA is not indicated for risk stratification. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| Preventing SCD With HF Medications | | Preventing SCD With HF Medications | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with HFrEF (LVEF ≤40%), treatment with a beta blocker, a mineralocorticoid receptor antagonist and either an angiotensin-converting enzyme inhibitor, an angiotensin-receptor blocker, or an angiotensin receptor- neprilysin inhibitor is recommended to reduce SCD and all-cause mortality. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with HFrEF (LVEF ≤40%), treatment with a beta blocker, a mineralocorticoid receptor antagonist and either an angiotensin-converting enzyme inhibitor, an angiotensin-receptor blocker, or an angiotensin receptor- neprilysin inhibitor is recommended to reduce SCD and all-cause mortality. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: A]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| Surgery and Revascularization Procedures in Patients With Ischemic Heart Disease | | Surgery and Revascularization Procedures in Patients With Ischemic Heart Disease | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' Patients with sustained VA and survivors of SCA should be evaluated for ischemic heart disease, and should be revascularized as appropriate. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' Patients with sustained VA and survivors of SCA should be evaluated for ischemic heart disease, and should be revascularized as appropriate. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with anomalous origin of a coronary artery suspected to be the cause of SCA, repair or revascularization is recommended. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with anomalous origin of a coronary artery suspected to be the cause of SCA, repair or revascularization is recommended. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-EO]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| Surgery for Arrhythmia Management | | Surgery for Arrhythmia Management | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIb]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with monomorphic VT refractory to antiarrhythmic medications and attempts at catheter ablation, surgical ablation may be reasonable. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with monomorphic VT refractory to antiarrhythmic medications and attempts at catheter ablation, surgical ablation may be reasonable. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-LD]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| Autonomic Modulation | | Autonomic Modulation | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with symptomatic, non–life-threatening VA, treatment with a beta blocker is reasonable. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with symptomatic, non–life-threatening VA, treatment with a beta blocker is reasonable. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-LD]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIb]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with VT/VF storm in whom a beta blocker, other antiarrhythmic medications, and catheter ablation are ineffective, not tolerated, or not possible, cardiac sympathetic denervation may be reasonable. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with VT/VF storm in whom a beta blocker, other antiarrhythmic medications, and catheter ablation are ineffective, not tolerated, or not possible, cardiac sympathetic denervation may be reasonable. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-LD]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
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| Recommendations for Management of Cardiac Arrest | | Recommendations for Management of Cardiac Arrest | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' CPR should be performed in patients in cardiac arrest. according to published basic and advanced cardiovascular life support algorithms. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' CPR should be performed in patients in cardiac arrest. according to published basic and advanced cardiovascular life support algorithms. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: A]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''2.''' In patients with hemodynamically unstable VA that persist or recur after a maximal energy shock, intravenous amiodarone should be administered to attempt to achieve a stable rhythm after further defibrillation. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''2.''' In patients with hemodynamically unstable VA that persist or recur after a maximal energy shock, intravenous amiodarone should be administered to attempt to achieve a stable rhythm after further defibrillation. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: A]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''3.''' Patients presenting with VA with hemodynamic instability should undergo direct current cardioversion. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''3.''' Patients presenting with VA with hemodynamic instability should undergo direct current cardioversion. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: A]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''4.''' In patients with polymorphic VT or VF with ST-elevation MI, angiography with emergency revascularization is recommended. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''4.''' In patients with polymorphic VT or VF with ST-elevation MI, angiography with emergency revascularization is recommended. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''5.''' Patients with a wide-QRS tachycardia should be presumed to have VT if the diagnosis is unclear. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''5.''' Patients with a wide-QRS tachycardia should be presumed to have VT if the diagnosis is unclear. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-EO]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with hemodynamically stable VT, administration of intravenous procainamide can be useful to attempt to terminate VT. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with hemodynamically stable VT, administration of intravenous procainamide can be useful to attempt to terminate VT. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: A]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''2.''' In patients with a witnessed cardiac arrest due to VF or polymorphic VT that is unresponsive to CPR, defibrillation, and vasopressor therapy, intravenous lidocaine can be beneficia. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''2.''' In patients with a witnessed cardiac arrest due to VF or polymorphic VT that is unresponsive to CPR, defibrillation, and vasopressor therapy, intravenous lidocaine can be beneficia. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-R]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''3.''' In patients with polymorphic VT due to myocardial ischemia, intravenous beta blockers can be useful. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''3.''' In patients with polymorphic VT due to myocardial ischemia, intravenous beta blockers can be useful. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-R]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''4.''' In patients with a recent MI who have VT/VF that repeatedly recurs despite direct current cardioversion and antiarrhythmic medications (VT/VF storm), an intravenous beta blocker can be useful. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''4.''' In patients with a recent MI who have VT/VF that repeatedly recurs despite direct current cardioversion and antiarrhythmic medications (VT/VF storm), an intravenous beta blocker can be useful. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIb]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients in cardiac arrest, administration of epinephrine (1 mg every 3 to 5 minutes) during CPR may be reasonable. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients in cardiac arrest, administration of epinephrine (1 mg every 3 to 5 minutes) during CPR may be reasonable. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: A]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''2.''' In patients with hemodynamically stable VT, administration of intravenous amiodarone or sotalol may be considered to attempt to terminate VT. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''2.''' In patients with hemodynamically stable VT, administration of intravenous amiodarone or sotalol may be considered to attempt to terminate VT. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-R]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightCoral" | [[ | | colspan="1" style="text-align:center; background:LightCoral" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class III - No Benefit]] | ||
|- | |- | ||
| bgcolor="LightCoral" |<nowiki>"</nowiki>'''1.''' In patients with cardiac arrest,administration of high-dose epinephrine (>1mg boluses) compared with standard doses is not beneficial. ''([[ | | bgcolor="LightCoral" |<nowiki>"</nowiki>'''1.''' In patients with cardiac arrest,administration of high-dose epinephrine (>1mg boluses) compared with standard doses is not beneficial. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: A]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightCoral" |<nowiki>"</nowiki>'''2.''' In patients with cardiac arrest,administration of high-dose epinephrine (>1mg boluses) compared with standard doses is not beneficial. ''([[ | | bgcolor="LightCoral" |<nowiki>"</nowiki>'''2.''' In patients with cardiac arrest,administration of high-dose epinephrine (>1mg boluses) compared with standard doses is not beneficial. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: A]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightCoral" | [[ | | colspan="1" style="text-align:center; background:LightCoral" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class III - Harm]] | ||
|- | |- | ||
| bgcolor="LightCoral" |<nowiki>"</nowiki>'''3.''' In patients with suspected AMI, prophylactic administration of lidocaine or high dose amiodarone for the prevention of VT is potentially harmful. ''([[ | | bgcolor="LightCoral" |<nowiki>"</nowiki>'''3.''' In patients with suspected AMI, prophylactic administration of lidocaine or high dose amiodarone for the prevention of VT is potentially harmful. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-R]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightCoral" |<nowiki>"</nowiki>'''4.''' In patients with a wide QRS complex tachycardia of unknown origin, calcium channel blockers (e.g., verapamil and diltiazem) are potentially harmful . ''([[ | | bgcolor="LightCoral" |<nowiki>"</nowiki>'''4.''' In patients with a wide QRS complex tachycardia of unknown origin, calcium channel blockers (e.g., verapamil and diltiazem) are potentially harmful . ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-LD]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
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| '''Recommendations for Secondary Prevention of SCD in Patients With Ischemic Heart Disease''' | | '''Recommendations for Secondary Prevention of SCD in Patients With Ischemic Heart Disease''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with ischemic heart disease, who either survive SCA due to VT/VF or experience hemodynamically unstable VT (LOE: B-R) or stable VT (LOE: B- NR) not due to reversible causes, an ICD is recommended if meaningful survival greater than 1 year is expected. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with ischemic heart disease, who either survive SCA due to VT/VF or experience hemodynamically unstable VT (LOE: B-R) or stable VT (LOE: B- NR) not due to reversible causes, an ICD is recommended if meaningful survival greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-R / B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| '''"2. Value Statement: Intermediate Value''' (LOE: B-R) | | '''"2. Value Statement: Intermediate Value''' (LOE: B-R) | ||
A transvenous ICD provides intermediate value in the secondary prevention of SCD particularly when the patient’s risk of death due to a VA is deemed high and the risk of nonarrhythmic death (either cardiac or noncardiac) is deemed low based on the patient’s burden of comorbidities and functional status. | A transvenous ICD provides intermediate value in the secondary prevention of SCD particularly when the patient’s risk of death due to a VA is deemed high and the risk of nonarrhythmic death (either cardiac or noncardiac) is deemed low based on the patient’s burden of comorbidities and functional status. | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |'''"3.''' In patients with ischemic heart disease and unexplained syncope who have inducible sustained monomorphic VT on electrophysiological study, an ICD is recommended if meaningful survival of greater than 1 year is expected. ''([[ | | bgcolor="LightGreen" |'''"3.''' In patients with ischemic heart disease and unexplained syncope who have inducible sustained monomorphic VT on electrophysiological study, an ICD is recommended if meaningful survival of greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
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| '''Recommendations for Patients With Coronary Artery Spasm''' | | '''Recommendations for Patients With Coronary Artery Spasm''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with VA due to coronary artery spasm, treatment with maximally tolerated doses of a calcium channel blocker and smoking cessation are indicated to reduce recurrent ischemia and VA. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with VA due to coronary artery spasm, treatment with maximally tolerated doses of a calcium channel blocker and smoking cessation are indicated to reduce recurrent ischemia and VA. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients resuscitated from SCA due to coronary artery spasm in whom medical therapy is ineffective or not tolerated, an ICD is reasonable if meaningful survival of greater than 1 year is expected. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients resuscitated from SCA due to coronary artery spasm in whom medical therapy is ineffective or not tolerated, an ICD is reasonable if meaningful survival of greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIb]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients resuscitated from SCA due to coronary artery spasm, an ICD in addition to medical therapy may be reasonable if meaningful survival of greater than 1 year is expected. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients resuscitated from SCA due to coronary artery spasm, an ICD in addition to medical therapy may be reasonable if meaningful survival of greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 202: | Line 202: | ||
| '''Recommendations for Primary Prevention of SCD in Patients With Ischemic Heart Disease''' | | '''Recommendations for Primary Prevention of SCD in Patients With Ischemic Heart Disease''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with LVEF of 35% or less that is due to ischemic heart disease who are at least 40 days’ post-MI and at least 90 days postrevascularization, and with NYHA class II or III HF despite GDMT, an ICD is recommended if meaningful survival of greater than 1 year is expected. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with LVEF of 35% or less that is due to ischemic heart disease who are at least 40 days’ post-MI and at least 90 days postrevascularization, and with NYHA class II or III HF despite GDMT, an ICD is recommended if meaningful survival of greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: A]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |'''"2.''' In patients with LVEF of 30% or less that is due to ischemic heart disease who are at least 40 days’ post-MI and at least 90 days postrevascularization, and with NYHA class I HF despite GDMT, an ICD is recommended if meaningful survival of greater than 1 year is expected. ''([[ | | bgcolor="LightGreen" |'''"2.''' In patients with LVEF of 30% or less that is due to ischemic heart disease who are at least 40 days’ post-MI and at least 90 days postrevascularization, and with NYHA class I HF despite GDMT, an ICD is recommended if meaningful survival of greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: A]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| '''"3.Value Statement: High Value''' (LOE: B-R) | | '''"3.Value Statement: High Value''' (LOE: B-R) | ||
A transvenous ICD provides high value in the primary prevention of SCD particularly when the patient’s risk of death due to a VA is deemed high and the risk of nonarrhythmic death (either cardiac or noncardiac) is deemed low based on the patient’s burden of comorbidities and functional status. | A transvenous ICD provides high value in the primary prevention of SCD particularly when the patient’s risk of death due to a VA is deemed high and the risk of nonarrhythmic death (either cardiac or noncardiac) is deemed low based on the patient’s burden of comorbidities and functional status. | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with NSVT due to prior MI, LVEF of 40% or less and inducible sustained VT or VF at electrophysiological study, an ICD is recommended if meaningful survival of greater than 1 year is expected. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with NSVT due to prior MI, LVEF of 40% or less and inducible sustained VT or VF at electrophysiological study, an ICD is recommended if meaningful survival of greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-R]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In nonhospitalized patients with NYHA class IV symptoms who are candidates for cardiac transplantation or an LVAD, an ICD is reasonable if meaningful survival of greater than 1 year is expected. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In nonhospitalized patients with NYHA class IV symptoms who are candidates for cardiac transplantation or an LVAD, an ICD is reasonable if meaningful survival of greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightCoral" | [[ | | colspan="1" style="text-align:center; background:LightCoral" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class III - No Benefit]] | ||
|- | |- | ||
| bgcolor="LightCoral" |<nowiki>"</nowiki>'''1.''' An ICD is not indicated for NYHA class IV patients with medication-refractory HF who are not also candidates for cardiac transplantation, an LVAD, or a CRT defibrillator that incorporates both pacing and defibrillation capabilities. ''([[ | | bgcolor="LightCoral" |<nowiki>"</nowiki>'''1.''' An ICD is not indicated for NYHA class IV patients with medication-refractory HF who are not also candidates for cardiac transplantation, an LVAD, or a CRT defibrillator that incorporates both pacing and defibrillation capabilities. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-EO]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 230: | Line 230: | ||
| '''Recommendations for Treatment of Recurrent VA in Patients With Ischemic Heart Disease''' | | '''Recommendations for Treatment of Recurrent VA in Patients With Ischemic Heart Disease''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with ischemic heart disease and recurrent VA, with significant symptoms or ICD shocks despite optimal device programming and ongoing treatment with a beta blocker, amiodarone or sotalol is useful to suppress recurrent VA. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with ischemic heart disease and recurrent VA, with significant symptoms or ICD shocks despite optimal device programming and ongoing treatment with a beta blocker, amiodarone or sotalol is useful to suppress recurrent VA. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-R]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''2.''' In patients with prior MI and recurrent episodes of symptomatic sustained VT, or who present with VT or VF storm and have failed or are intolerant of amiodarone (LOE: B-R) or other antiarrhythmic medications (LOE: B-NR) catheter ablation is recommended . ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''2.''' In patients with prior MI and recurrent episodes of symptomatic sustained VT, or who present with VT or VF storm and have failed or are intolerant of amiodarone (LOE: B-R) or other antiarrhythmic medications (LOE: B-NR) catheter ablation is recommended . ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-R / B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIb]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with ischemic heart disease and ICD shocks for sustained monomorphic VT or symptomatic sustained monomorphic VT that is recurrent, or hemodynamically tolerated, catheter ablation as first-line therapy may be considered to reduce recurrent VA. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with ischemic heart disease and ICD shocks for sustained monomorphic VT or symptomatic sustained monomorphic VT that is recurrent, or hemodynamically tolerated, catheter ablation as first-line therapy may be considered to reduce recurrent VA. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-LD]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightCoral" | [[ | | colspan="1" style="text-align:center; background:LightCoral" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class III - Harm]] | ||
|- | |- | ||
| bgcolor="LightCoral" |<nowiki>"</nowiki>'''1.''' In patients with prior MI, class IC antiarrhythmic medications (e.g., flecainide and propafenone) should not be used. ''([[ | | bgcolor="LightCoral" |<nowiki>"</nowiki>'''1.''' In patients with prior MI, class IC antiarrhythmic medications (e.g., flecainide and propafenone) should not be used. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-R]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightCoral" |'''"2.''' In patients with incessant VT or VF, an ICD should not be implanted until sufficient control of the VA is achieved to prevent repeated ICD shocks. ''([[ | | bgcolor="LightCoral" |'''"2.''' In patients with incessant VT or VF, an ICD should not be implanted until sufficient control of the VA is achieved to prevent repeated ICD shocks. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-LD]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightCoral" | [[ | | colspan="1" style="text-align:center; background:LightCoral" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class III - No benefit]] | ||
|- | |- | ||
| bgcolor="LightCoral" |'''"3.''' In patients with ischemic heart disease and sustained monomorphic VT, coronary revascularization alone is an ineffective therapy to prevent recurrent VT. ''([[ | | bgcolor="LightCoral" |'''"3.''' In patients with ischemic heart disease and sustained monomorphic VT, coronary revascularization alone is an ineffective therapy to prevent recurrent VT. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-LD]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 257: | Line 257: | ||
| '''Recommendations for Patients With NICM''' | | '''Recommendations for Patients With NICM''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with suspected NICM from myocardial infiltrative processes, cardiac MRI with late gadolinium enhancement is useful for diagnosis. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with suspected NICM from myocardial infiltrative processes, cardiac MRI with late gadolinium enhancement is useful for diagnosis. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with suspected NICM, cardiac MRI with late gadolinium enhancement can be useful for assessing risk of SCA/SCD. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with suspected NICM, cardiac MRI with late gadolinium enhancement can be useful for assessing risk of SCA/SCD. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with NICM who develop conduction disease or LV dysfunction at less than 40 years of age, or who have a family history of NICM or SCD in a first-degree relative (<50 years of age), genetic counseling and genetic testing are reasonable to detect a heritable disease that may clarify prognosis and facilitate cascade screening of relatives. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with NICM who develop conduction disease or LV dysfunction at less than 40 years of age, or who have a family history of NICM or SCD in a first-degree relative (<50 years of age), genetic counseling and genetic testing are reasonable to detect a heritable disease that may clarify prognosis and facilitate cascade screening of relatives. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-EO]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 274: | Line 274: | ||
| '''Recommendations for Secondary Prevention of SCD in Patients With NICM''' | | '''Recommendations for Secondary Prevention of SCD in Patients With NICM''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with NICM who either survive SCA due to VT/VF or experience hemodynamically unstable VT (LOE: B-R) or stable VT (LOE: B-NR) not due to reversible causes, an ICD is recommended if meaningful survival greater than 1 year is expected. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with NICM who either survive SCA due to VT/VF or experience hemodynamically unstable VT (LOE: B-R) or stable VT (LOE: B-NR) not due to reversible causes, an ICD is recommended if meaningful survival greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-R / B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with NICM who experience syncope presumed to be due to VA and who do not meet indications for a primary prevention ICD, an ICD or an electrophysiological study for risk stratification for SCD can be beneficial if meaningful survival greater than 1 year is expected. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with NICM who experience syncope presumed to be due to VA and who do not meet indications for a primary prevention ICD, an ICD or an electrophysiological study for risk stratification for SCD can be beneficial if meaningful survival greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIb]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with NICM who survive a cardiac arrest, have sustained VT, or have symptomatic VA who are ineligible for an ICD (due to a limited life-expectancy and/or functional status or lack of access to an ICD), amiodarone may be considered for prevention of SCD. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with NICM who survive a cardiac arrest, have sustained VT, or have symptomatic VA who are ineligible for an ICD (due to a limited life-expectancy and/or functional status or lack of access to an ICD), amiodarone may be considered for prevention of SCD. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-R]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 293: | Line 293: | ||
| '''Recommendations for Primary Prevention of SCD in Patients With NICM''' | | '''Recommendations for Primary Prevention of SCD in Patients With NICM''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with NICM, HF with NYHA class II–III symptoms and an LVEF of 35% or less, despite GDMT, an ICD is recommended if meaningful survival of greater than 1 year is expected. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with NICM, HF with NYHA class II–III symptoms and an LVEF of 35% or less, despite GDMT, an ICD is recommended if meaningful survival of greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: A]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with NICM due to a Lamin A/C mutation who have 2 or more risk factors (NSVT, LVEF <45%, nonmissense mutation, and male sex), an ICD can be beneficial if meaningful survival of greater than 1 year is expected. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with NICM due to a Lamin A/C mutation who have 2 or more risk factors (NSVT, LVEF <45%, nonmissense mutation, and male sex), an ICD can be beneficial if meaningful survival of greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIb]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with NICM, HF with NYHA class I symptoms and an LVEF of 35% or less, despite GDMT, an ICD may be considered if meaningful survival of greater than 1 year is expected. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with NICM, HF with NYHA class I symptoms and an LVEF of 35% or less, despite GDMT, an ICD may be considered if meaningful survival of greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-R]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightCoral" | [[ | | colspan="1" style="text-align:center; background:LightCoral" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class III - No benefit]] | ||
|- | |- | ||
| bgcolor="LightCoral" |'''"1.''' In patients with medication-refractory NYHA class IV HF who are not also candidates for cardiac transplantation, an LVAD, or a CRT defibrillator that incorporates both pacing and defibrillation capabilities, an ICD should not be implanted. ''([[ | | bgcolor="LightCoral" |'''"1.''' In patients with medication-refractory NYHA class IV HF who are not also candidates for cardiac transplantation, an LVAD, or a CRT defibrillator that incorporates both pacing and defibrillation capabilities, an ICD should not be implanted. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-EO]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 316: | Line 316: | ||
| '''Recommendations for Treatment of Recurrent VA in Patients With NICM''' | | '''Recommendations for Treatment of Recurrent VA in Patients With NICM''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with NICM and an ICD who experience spontaneous VA or recurrent appropriate shocks despite optimal device programming and treatment with a beta blocker, amiodarone or sotalol can be beneficial. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with NICM and an ICD who experience spontaneous VA or recurrent appropriate shocks despite optimal device programming and treatment with a beta blocker, amiodarone or sotalol can be beneficial. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-R]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''2.''' In patients with NICM and recurrent sustained monomorphic VT who fail or are intolerant of antiarrhythmic medications, catheter ablation can be useful for reducing recurrent VT and ICD shocks. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''2.''' In patients with NICM and recurrent sustained monomorphic VT who fail or are intolerant of antiarrhythmic medications, catheter ablation can be useful for reducing recurrent VT and ICD shocks. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 329: | Line 329: | ||
| '''Recommendations for Arrhythmogenic Right Ventricular Cardiomyopathy''' | | '''Recommendations for Arrhythmogenic Right Ventricular Cardiomyopathy''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In selected first-degree relatives of patients with arrhythmogenic right ventricular cardiomyopathy, clinical screening for the disease is recommended along with genetic counseling and genetic testing, if the proband has a disease causing mutation. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In selected first-degree relatives of patients with arrhythmogenic right ventricular cardiomyopathy, clinical screening for the disease is recommended along with genetic counseling and genetic testing, if the proband has a disease causing mutation. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''2.''' In patients with suspected arrhythmogenic right ventricular cardiomyopathy and VA or electrocardiographic abnormalities, cardiac MRI is useful for establishing a diagnosis and for risk stratification. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''2.''' In patients with suspected arrhythmogenic right ventricular cardiomyopathy and VA or electrocardiographic abnormalities, cardiac MRI is useful for establishing a diagnosis and for risk stratification. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''3.''' In patients with arrhythmogenic right ventricular cardiomyopathy and an additional marker of increased risk of SCD (resuscitated SCA, sustained VT, significant ventricular dysfunction with RVEF or LVEF ≤35%), an ICD is recommended if meaningful survival greater than 1 year is expected. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''3.''' In patients with arrhythmogenic right ventricular cardiomyopathy and an additional marker of increased risk of SCD (resuscitated SCA, sustained VT, significant ventricular dysfunction with RVEF or LVEF ≤35%), an ICD is recommended if meaningful survival greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''4.''' In patients with arrhythmogenic right ventricular cardiomyopathy and VA, a beta blocker is recommended.''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''4.''' In patients with arrhythmogenic right ventricular cardiomyopathy and VA, a beta blocker is recommended.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''4.''' In patients with a clinical diagnosis of arrhythmogenic right ventricular cardiomyopathy , avoiding intensive exercise is recommended.''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''4.''' In patients with a clinical diagnosis of arrhythmogenic right ventricular cardiomyopathy , avoiding intensive exercise is recommended.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with clinically diagnosed or suspected arrhythmogenic right ventricular cardiomyopathy , genetic counseling and genetic testing can be useful for diagnosis and for gene-specific targeted family screening. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with clinically diagnosed or suspected arrhythmogenic right ventricular cardiomyopathy , genetic counseling and genetic testing can be useful for diagnosis and for gene-specific targeted family screening. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''2.''' In patients with arrhythmogenic right ventricular cardiomyopathy and syncope presumed due to VA, an ICD can be useful if meaningful survival greater than 1 year is expected. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''2.''' In patients with arrhythmogenic right ventricular cardiomyopathy and syncope presumed due to VA, an ICD can be useful if meaningful survival greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''3.''' In patients with clinical evidence of arrhythmogenic right ventricular cardiomyopathy but not VA, a beta blocker can be useful. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''3.''' In patients with clinical evidence of arrhythmogenic right ventricular cardiomyopathy but not VA, a beta blocker can be useful. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''4.''' In patients with arrhythmogenic right ventricular cardiomyopathy and recurrent symptomatic sustained VT in whom a beta blocker is ineffective or not tolerated, catheter ablation with availability of a combined endocardial/epicardial approach can be beneficial . ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''4.''' In patients with arrhythmogenic right ventricular cardiomyopathy and recurrent symptomatic sustained VT in whom a beta blocker is ineffective or not tolerated, catheter ablation with availability of a combined endocardial/epicardial approach can be beneficial . ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''5.''' Inpatientswithsuspectedarrhythmogenicrightventricularcardiomyopathy, a signal averaged ECG can be useful for diagnosis and risk stratification . ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''5.''' Inpatientswithsuspectedarrhythmogenicrightventricularcardiomyopathy, a signal averaged ECG can be useful for diagnosis and risk stratification . ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIb]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In asymptomatic patients with clinical evidence of arrhythmogenic right ventricular cardiomyopathy , an electrophysiological study may be considered for risk stratification. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In asymptomatic patients with clinical evidence of arrhythmogenic right ventricular cardiomyopathy , an electrophysiological study may be considered for risk stratification. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 364: | Line 364: | ||
| '''Recommendations for Hypertrophic Cardiomyopathy ''' | | '''Recommendations for Hypertrophic Cardiomyopathy ''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with HCM, SCD risk stratification should be performed at the time of initial evaluation and periodically thereafter. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with HCM, SCD risk stratification should be performed at the time of initial evaluation and periodically thereafter. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''2.''' In patients with HCM who have survived an SCA due to VT or VF, or have spontaneous sustained VT causing syncope or hemodynamic compromise, an ICD is recommended if meaningful survival greater than 1 year is expected. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''2.''' In patients with HCM who have survived an SCA due to VT or VF, or have spontaneous sustained VT causing syncope or hemodynamic compromise, an ICD is recommended if meaningful survival greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''3.''' In first-degree relatives of patients with HCM, an ECG and echocardiogram shouldbeperformed. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''3.''' In first-degree relatives of patients with HCM, an ECG and echocardiogram shouldbeperformed. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''4.''' In first-degree relatives of patients with HCM due to a known causative mutation, genetic counseling and mutation-specific genetic testing are recommended. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''4.''' In first-degree relatives of patients with HCM due to a known causative mutation, genetic counseling and mutation-specific genetic testing are recommended. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with clinically suspected or diagnosed HCM, genetic counseling and genetic testing are reasonable. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with clinically suspected or diagnosed HCM, genetic counseling and genetic testing are reasonable. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''2.''' In patients with HCM and 1 or more of the following risk factors, an ICD is reasonable if meaningful survival of greater than 1 year is expected: | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''2.''' In patients with HCM and 1 or more of the following risk factors, an ICD is reasonable if meaningful survival of greater than 1 year is expected: | ||
Line 383: | Line 383: | ||
'''b.''' SCD in 1 or more first-degree relatives presumably caused by HCM (LOE: C-LD) | '''b.''' SCD in 1 or more first-degree relatives presumably caused by HCM (LOE: C-LD) | ||
'''c.''' 1 or more episodes of unexplained syncope within the preceding 6 months (LOE: C-LD). ''([[ | '''c.''' 1 or more episodes of unexplained syncope within the preceding 6 months (LOE: C-LD). ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR / C-LD]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''3.''' In patients with HCM who have spontaneous NSVT (LOE: C-LD) or an abnormal blood pressure response with exercise (LOE: B-NR), who also have additional SCD risk modifiers or high risk features, an ICD is reasonable if meaningful survival greater than 1 year is expected. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''3.''' In patients with HCM who have spontaneous NSVT (LOE: C-LD) or an abnormal blood pressure response with exercise (LOE: B-NR), who also have additional SCD risk modifiers or high risk features, an ICD is reasonable if meaningful survival greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR / C-LD]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIb]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with HCM who have NSVT (LOE: B-NR) or an abnormal blood pressure response with exercise (LOE: B-NR) but do not have any other SCD risk modifiers, an ICD may be considered, but its benefit is uncertain. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with HCM who have NSVT (LOE: B-NR) or an abnormal blood pressure response with exercise (LOE: B-NR) but do not have any other SCD risk modifiers, an ICD may be considered, but its benefit is uncertain. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''2.''' In patients with HCM and a history of sustained VT or VF, amiodarone may be considered when an ICD is not feasible or not preferred by the patient. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''2.''' In patients with HCM and a history of sustained VT or VF, amiodarone may be considered when an ICD is not feasible or not preferred by the patient. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-LD]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightCoral" | [[ | | colspan="1" style="text-align:center; background:LightCoral" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class III - No benefit]] | ||
|- | |- | ||
| bgcolor="LightCoral" |'''"1.''' In patients with HCM, an invasive electrophysiological study with programmed ventricular stimulation should not be performed for risk stratification. ''([[ | | bgcolor="LightCoral" |'''"1.''' In patients with HCM, an invasive electrophysiological study with programmed ventricular stimulation should not be performed for risk stratification. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightCoral" |'''"2.''' In patients with an identified HCM genotype in the absence of SCD risk factors, an ICD should not be implanted. ''([[ | | bgcolor="LightCoral" |'''"2.''' In patients with an identified HCM genotype in the absence of SCD risk factors, an ICD should not be implanted. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 406: | Line 406: | ||
| '''Recommendations for Myocarditis ''' | | '''Recommendations for Myocarditis ''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with life-threatening VT or VF associated with confirmed or clinically suspected myocarditis, referral to centers with mechanical hemodynamic support and advanced arrhythmia management is recommended. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with life-threatening VT or VF associated with confirmed or clinically suspected myocarditis, referral to centers with mechanical hemodynamic support and advanced arrhythmia management is recommended. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-LD]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIb]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with giant cell myocarditis with VF or hemodynamically unstable VT treated according to GDMT, an ICD and/or an anti arrhythmic medication may be considered if meaningful survival of greater than 1 year is expected. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with giant cell myocarditis with VF or hemodynamically unstable VT treated according to GDMT, an ICD and/or an anti arrhythmic medication may be considered if meaningful survival of greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-LD]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 421: | Line 421: | ||
| ''' Recommendations for Cardiac Sarcoidosis ''' | | ''' Recommendations for Cardiac Sarcoidosis ''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with cardiac sarcoidosis who have sustained VT or are survivors of sudden cardiac arrest (SCA) or have an LVEF of 35% or less, an ICD is recommended, if meaningful survival of greater than 1 year is expected. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with cardiac sarcoidosis who have sustained VT or are survivors of sudden cardiac arrest (SCA) or have an LVEF of 35% or less, an ICD is recommended, if meaningful survival of greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with cardiac sarcoidosis and LVEF greater than 35% who have syncope and/or evidence of myocardial scar by cardiac MRI or positron emission tomographic (PET) scan, and/or have an indication for permanent pacing implantation of an ICD is reasonable, provided that meaningful survival of greater than 1 year is expected. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with cardiac sarcoidosis and LVEF greater than 35% who have syncope and/or evidence of myocardial scar by cardiac MRI or positron emission tomographic (PET) scan, and/or have an indication for permanent pacing implantation of an ICD is reasonable, provided that meaningful survival of greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''2.''' In patients with cardiac sarcoidosis and LVEF greater than 35%, it is reasonable to perform an electrophysiological study and to impant an ICD, if sustained VA is inducible, provided that meaningful survival of greater than 1 year is expected. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''2.''' In patients with cardiac sarcoidosis and LVEF greater than 35%, it is reasonable to perform an electrophysiological study and to impant an ICD, if sustained VA is inducible, provided that meaningful survival of greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-LD]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''3.''' In patients with cardiac sarcoidosis who have an indication for permanent pacing, implantation of an ICD can be beneficial. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''3.''' In patients with cardiac sarcoidosis who have an indication for permanent pacing, implantation of an ICD can be beneficial. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-LD]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''4.''' In patients with cardiac sarcoidosis with frequent symptomatic VA and evidence of myocardial inflammation, immunosuppression in combination with antiarrhythmic medication therapy can be useful to reduce VA burden. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''4.''' In patients with cardiac sarcoidosis with frequent symptomatic VA and evidence of myocardial inflammation, immunosuppression in combination with antiarrhythmic medication therapy can be useful to reduce VA burden. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-LD]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 442: | Line 442: | ||
| '''Recommendation for Heart Failure With Reduced Ejection Fraction ''' | | '''Recommendation for Heart Failure With Reduced Ejection Fraction ''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with HFrEF who are awaiting heart transplant and who otherwise would not qualify for an ICD (e.g., NYHA class IV and/or use of inotropes) with a plan to discharge home, an ICD is reasonable. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with HFrEF who are awaiting heart transplant and who otherwise would not qualify for an ICD (e.g., NYHA class IV and/or use of inotropes) with a plan to discharge home, an ICD is reasonable. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 453: | Line 453: | ||
| '''Recommendation for Patients With an LVAD ''' | | '''Recommendation for Patients With an LVAD ''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with an LVAD and sustained VA, an ICD can be beneficial. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with an LVAD and sustained VA, an ICD can be beneficial. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-LD]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 464: | Line 464: | ||
| ''' Recommendation for ICD Use After Heart Transplantation ''' | | ''' Recommendation for ICD Use After Heart Transplantation ''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIb]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with a heart transplant and severe allograft vasculopathy with LV dysfunction, an ICD may be reasonable if meaningful survival of greater than 1 year is expected. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with a heart transplant and severe allograft vasculopathy with LV dysfunction, an ICD may be reasonable if meaningful survival of greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 475: | Line 475: | ||
| ''' Recommendations for Neuromuscular Disorders ''' | | ''' Recommendations for Neuromuscular Disorders ''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with neuromuscular disorders, primary and secondary prevention ICDs are recommended for the same indications as for patients with NICM if meaningful survival of greater than 1 year is expected. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with neuromuscular disorders, primary and secondary prevention ICDs are recommended for the same indications as for patients with NICM if meaningful survival of greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with Emery-Dreifuss and limb-girdle type IB muscular dystrophies with progressive cardiac involvement, an ICD is reasonable if a meaningful survival of greater than 1 year is expected. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with Emery-Dreifuss and limb-girdle type IB muscular dystrophies with progressive cardiac involvement, an ICD is reasonable if a meaningful survival of greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''2.''' In patients with muscular dystrophy, follow-up for development of cardiac involvement is reasonable, even if the patient is asymptomatic at presentation. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''2.''' In patients with muscular dystrophy, follow-up for development of cardiac involvement is reasonable, even if the patient is asymptomatic at presentation. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIb]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with myotonic dystrophy type 1 with an indication for a permanent pacemaker, an ICD may be considered to minimize the risk of SCA from VT if meaningful survival of greater than 1 year is expected. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with myotonic dystrophy type 1 with an indication for a permanent pacemaker, an ICD may be considered to minimize the risk of SCA from VT if meaningful survival of greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 496: | Line 496: | ||
| ''' Recommendations for Cardiac Channelopathies ''' | | ''' Recommendations for Cardiac Channelopathies ''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In first-degree relatives of patients who have a causative mutation for long QT syndrome, catecholaminergic polymorphic ventricular tachycardia, short QT syndrome, or Brugada syndrome, genetic counseling and mutation-specific genetic testing are recommended. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In first-degree relatives of patients who have a causative mutation for long QT syndrome, catecholaminergic polymorphic ventricular tachycardia, short QT syndrome, or Brugada syndrome, genetic counseling and mutation-specific genetic testing are recommended. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with a cardiac channelopathy and SCA, an ICD is recommended if meaningful survival of greater than 1 year is expected. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with a cardiac channelopathy and SCA, an ICD is recommended if meaningful survival of greater than 1 year is expected. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 509: | Line 509: | ||
| ''' Recommendations for Long QT Syndrome ''' | | ''' Recommendations for Long QT Syndrome ''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with long QT syndrome with a resting QTc greater than 470 ms, a beta blocker is recommended. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with long QT syndrome with a resting QTc greater than 470 ms, a beta blocker is recommended. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''2.''' In high-risk patients with symptomatic long QT syndrome in whom a beta blocker is ineffective or not tolerated, intensification of therapy with additional medications (guided by consideration of the particular long QT syndrome type), left cardiac sympathetic denervation, and/or an ICD is recommended. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''2.''' In high-risk patients with symptomatic long QT syndrome in whom a beta blocker is ineffective or not tolerated, intensification of therapy with additional medications (guided by consideration of the particular long QT syndrome type), left cardiac sympathetic denervation, and/or an ICD is recommended. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''3.''' In patients with long QT syndrome and recurrent appropriate ICD shocks despite maximum tolerated doses of a beta blocker, intensification of medical therapy with additional medications (guided by consideration of according to the particular long QT syndrome type) or left cardiac sympathetic denervation, is recommended. ''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''3.''' In patients with long QT syndrome and recurrent appropriate ICD shocks despite maximum tolerated doses of a beta blocker, intensification of medical therapy with additional medications (guided by consideration of according to the particular long QT syndrome type) or left cardiac sympathetic denervation, is recommended. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |'''"4.''' In patients with clinically diagnosed long QT syndrome, genetic counseling and genetic testing are recommended. ''([[ | | bgcolor="LightGreen" |'''"4.''' In patients with clinically diagnosed long QT syndrome, genetic counseling and genetic testing are recommended. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with suspected long QT syndrome, ambulatory electrocardiographic monitoring, recording the ECG lying and immediately on standing, and/or exercise treadmill testing can be useful for establishing a diagnosis and monitoring the response to therapy. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with suspected long QT syndrome, ambulatory electrocardiographic monitoring, recording the ECG lying and immediately on standing, and/or exercise treadmill testing can be useful for establishing a diagnosis and monitoring the response to therapy. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LemonChiffon" |'''"2.''' In asymptomatic patients with long QT syndrome and a resting QTc less than 470 ms, chronic therapy with a beta blocker is reasonable. ''([[ | | bgcolor="LemonChiffon" |'''"2.''' In asymptomatic patients with long QT syndrome and a resting QTc less than 470 ms, chronic therapy with a beta blocker is reasonable. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIb]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |'''"1.''' In asymptomatic patients with long QT syndrome and a resting QTc greater than 500 ms while receiving a beta blocker, intensification of therapy with medications (guided by consideration of the particular long QT syndrome type), left cardiac sympathetic denervation or an ICD may be considered. ''([[ | | bgcolor="LemonChiffon" |'''"1.''' In asymptomatic patients with long QT syndrome and a resting QTc greater than 500 ms while receiving a beta blocker, intensification of therapy with medications (guided by consideration of the particular long QT syndrome type), left cardiac sympathetic denervation or an ICD may be considered. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightCoral" | [[ | | colspan="1" style="text-align:center; background:LightCoral" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class III - Harm]] | ||
|- | |- | ||
| bgcolor="LightCoral" |'''"1.''' In patients with long QT syndrome, QT-prolonging medications are potentially harmful. ''([[ | | bgcolor="LightCoral" |'''"1.''' In patients with long QT syndrome, QT-prolonging medications are potentially harmful. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 540: | Line 540: | ||
| ''' Recommendations for Catecholaminergic Polymorphic Ventricular Tachycardia ''' | | ''' Recommendations for Catecholaminergic Polymorphic Ventricular Tachycardia ''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with catecholaminergic polymorphic ventricular tachycardia, a beta blocker is recommended.''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with catecholaminergic polymorphic ventricular tachycardia, a beta blocker is recommended.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with catecholaminergic polymorphic ventricular tachycardia and recurrent sustained VT or syncope, while receiving adequate or maximally tolerated beta blocker, treatment intensification with either combination medication therapy (e.g., beta blocker, flecainide), left cardiac sympathetic denervation,and/or an ICD is recommended.''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with catecholaminergic polymorphic ventricular tachycardia and recurrent sustained VT or syncope, while receiving adequate or maximally tolerated beta blocker, treatment intensification with either combination medication therapy (e.g., beta blocker, flecainide), left cardiac sympathetic denervation,and/or an ICD is recommended.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with catecholaminergic polymorphic ventricular tachycardia and with clinical VT or exertional syncope, genetic counseling and genetic testing are reasonable. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with catecholaminergic polymorphic ventricular tachycardia and with clinical VT or exertional syncope, genetic counseling and genetic testing are reasonable. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 557: | Line 557: | ||
| ''' Recommendations for Brugada Syndrome ''' | | ''' Recommendations for Brugada Syndrome ''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In asymptomatic patients with only inducible type 1 Brugada electrocardiographic pattern, observation without therapy is recommended.''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In asymptomatic patients with only inducible type 1 Brugada electrocardiographic pattern, observation without therapy is recommended.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''2.''' In patients with Brugada syndrome with spontaneous type 1 Brugada electrocardiographic pattern and cardiac arrest, sustained VA or a recent history of syncope presumed due to VA, an ICD is recommended if a meaningful survival of greater than 1 year is expected.''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''2.''' In patients with Brugada syndrome with spontaneous type 1 Brugada electrocardiographic pattern and cardiac arrest, sustained VA or a recent history of syncope presumed due to VA, an ICD is recommended if a meaningful survival of greater than 1 year is expected.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''3.''' In patients with Brugada syndrome experiencing recurrent ICD shocks for polymorphic VT, intensification of therapy with quinidine or catheter ablation is recommended.''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''3.''' In patients with Brugada syndrome experiencing recurrent ICD shocks for polymorphic VT, intensification of therapy with quinidine or catheter ablation is recommended.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''4.''' In patients with spontaneous type 1 Brugada electrocardiographic pattern and symptomatic VA who either are not candidates for or decline an ICD, quinidine or catheter ablation is recommended.''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''4.''' In patients with spontaneous type 1 Brugada electrocardiographic pattern and symptomatic VA who either are not candidates for or decline an ICD, quinidine or catheter ablation is recommended.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with suspected Brugada syndrome in the absence of a spontaneous type 1 Brugada electrocardiographic pattern, a pharmacological challenge using a sodium channel blocker can be useful for diagnosis. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with suspected Brugada syndrome in the absence of a spontaneous type 1 Brugada electrocardiographic pattern, a pharmacological challenge using a sodium channel blocker can be useful for diagnosis. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIb]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with asymptomatic Brugada syndrome and a spontaneous type 1 Brugada electrocardiographic pattern, an electrophysiological study with programmed ventricular stimulation using single and double extrastimuli may be considered for further risk stratification. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with asymptomatic Brugada syndrome and a spontaneous type 1 Brugada electrocardiographic pattern, an electrophysiological study with programmed ventricular stimulation using single and double extrastimuli may be considered for further risk stratification. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LemonChiffon" |'''"2.''' In patients with suspected or established Brugada syndrome, genetic counseling and genetic testing may be useful to facilitate cascade screening of relatives . ''([[ | | bgcolor="LemonChiffon" |'''"2.''' In patients with suspected or established Brugada syndrome, genetic counseling and genetic testing may be useful to facilitate cascade screening of relatives . ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-EO]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 584: | Line 584: | ||
| ''' Recommendations for Early Repolarization Syndrome ''' | | ''' Recommendations for Early Repolarization Syndrome ''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In asymptomatic patients with an early repolarization pattern on ECG, observation without treatment is recommended.''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In asymptomatic patients with an early repolarization pattern on ECG, observation without treatment is recommended.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |'''"2.''' In patients with early repolarization pattern on ECG and cardiac arrest or sustained VA, an ICD is recommended.''([[ | | bgcolor="LightGreen" |'''"2.''' In patients with early repolarization pattern on ECG and cardiac arrest or sustained VA, an ICD is recommended.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightCoral" | [[ | | colspan="1" style="text-align:center; background:LightCoral" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class III - No Benefit]] | ||
|- | |- | ||
| bgcolor="LightCoral" |'''"1.''' In patients with early repolarization pattern on ECG, genetic testing is not recommended. ''([[ | | bgcolor="LightCoral" |'''"1.''' In patients with early repolarization pattern on ECG, genetic testing is not recommended. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 601: | Line 601: | ||
| ''' Recommendations for Short QT Syndrome ''' | | ''' Recommendations for Short QT Syndrome ''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In asymptomatic patients with a short QTc interval, observation without treatment is recommended.''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In asymptomatic patients with a short QTc interval, observation without treatment is recommended.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |'''"2.''' In patients with short QT syndrome who have a cardiac arrest or sustained VA, an ICD is recommended if meaningful survival greater than 1 year is expected.''([[ | | bgcolor="LightGreen" |'''"2.''' In patients with short QT syndrome who have a cardiac arrest or sustained VA, an ICD is recommended if meaningful survival greater than 1 year is expected.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with short QT syndrome and recurrent sustained VA, treatment with quinidine can be useful. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with short QT syndrome and recurrent sustained VA, treatment with quinidine can be useful. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-LD]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''2.''' In patients with short QT syndrome and VT/VF storm, isoproterenol infusion can be effective. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''2.''' In patients with short QT syndrome and VT/VF storm, isoproterenol infusion can be effective. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-LD]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIb]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with short QT syndrome, genetic testing may be considered to facilitate screening of first-degree relatives. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with short QT syndrome, genetic testing may be considered to facilitate screening of first-degree relatives. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-EO]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 624: | Line 624: | ||
| ''' Recommendations for Ventricular Arrhythmia in the Structurally Normal Heart ''' | | ''' Recommendations for Ventricular Arrhythmia in the Structurally Normal Heart ''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with symptomatic PVCs in an otherwise normal heart, treatment with a beta blocker or nondihydropyradine calcium channel blocker is useful to reduce recurrent arrhythmias and improve symptoms.''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with symptomatic PVCs in an otherwise normal heart, treatment with a beta blocker or nondihydropyradine calcium channel blocker is useful to reduce recurrent arrhythmias and improve symptoms.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-R]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with symptomatic VA in an otherwise normal heart, treatment with an antiarrhythmic medication is reasonable to reduce recurrent symptomatic arrhythmias and improve symptoms if beta blockers and nondihydropyradine calcium channel blockers are ineffective or not tolerated. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with symptomatic VA in an otherwise normal heart, treatment with an antiarrhythmic medication is reasonable to reduce recurrent symptomatic arrhythmias and improve symptoms if beta blockers and nondihydropyradine calcium channel blockers are ineffective or not tolerated. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-R]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 639: | Line 639: | ||
| ''' Recommendations for Outflow Tract Ventricular Arrhythmia ''' | | ''' Recommendations for Outflow Tract Ventricular Arrhythmia ''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with symptomatic outflow tract VA in an otherwise normal heart for whom antiarrhythmic medications are ineffective, not tolerated, or not the patient’s preference, catheter ablation is useful.''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with symptomatic outflow tract VA in an otherwise normal heart for whom antiarrhythmic medications are ineffective, not tolerated, or not the patient’s preference, catheter ablation is useful.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |'''"2.''' In patients with symptomatic outflow tract VT in an otherwise normal heart, a beta blocker or a calcium channel blocker is useful.''([[ | | bgcolor="LightGreen" |'''"2.''' In patients with symptomatic outflow tract VT in an otherwise normal heart, a beta blocker or a calcium channel blocker is useful.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 652: | Line 652: | ||
| ''' Recommendation for Papillary Muscle VA (PVCs and VT) ''' | | ''' Recommendation for Papillary Muscle VA (PVCs and VT) ''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with symptomatic VA arising from the papillary muscles for whom antiarrhythmic medications are ineffective, not tolerated, or not the patient’s preference, catheter ablation is useful.''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with symptomatic VA arising from the papillary muscles for whom antiarrhythmic medications are ineffective, not tolerated, or not the patient’s preference, catheter ablation is useful.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 663: | Line 663: | ||
| ''' Recommendations for Interfascicular Reentrant VT (Belhassen Tachycardia) ''' | | ''' Recommendations for Interfascicular Reentrant VT (Belhassen Tachycardia) ''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with verapamil-sensitive, idiopathic LVT related to interfascicular reentry for whom antiarrhythmic medications are ineffective, not tolerated, or not the patient’s preference, catheter ablation is useful.''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with verapamil-sensitive, idiopathic LVT related to interfascicular reentry for whom antiarrhythmic medications are ineffective, not tolerated, or not the patient’s preference, catheter ablation is useful.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''2.''' In patients with sustained hemodynamically tolerated verapamil-sensitive, idiopathic LVT related to interfascicular reentry, intravenous verapamil is recommended for VT termination.''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''2.''' In patients with sustained hemodynamically tolerated verapamil-sensitive, idiopathic LVT related to interfascicular reentry, intravenous verapamil is recommended for VT termination.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with recurrent verapamil-sensitive idiopathic LVT, chronic therapy with oral verapamil can be useful. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with recurrent verapamil-sensitive idiopathic LVT, chronic therapy with oral verapamil can be useful. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-LD]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 680: | Line 680: | ||
| ''' Recommendations for Idiopathic Polymorphic VT/VF ''' | | ''' Recommendations for Idiopathic Polymorphic VT/VF ''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In young patients (<40 years of age) with unexplained SCA, unexplained near drowning, or recurrent exertional syncope, who do not have ischemic or other structural heart disease, further evaluation for genetic arrhythmia syndromes is recommended.''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In young patients (<40 years of age) with unexplained SCA, unexplained near drowning, or recurrent exertional syncope, who do not have ischemic or other structural heart disease, further evaluation for genetic arrhythmia syndromes is recommended.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''2.''' In patients resuscitated from SCA due to idiopathic polymorphic VT or VF, an ICD is recommended if meaningful survival greater than 1 year is expected.''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''2.''' In patients resuscitated from SCA due to idiopathic polymorphic VT or VF, an ICD is recommended if meaningful survival greater than 1 year is expected.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''3.''' For patients with recurrent episodes of idiopathic VF initiated by PVCs with a consistent QRS morphology, catheter ablation is useful.''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''3.''' For patients with recurrent episodes of idiopathic VF initiated by PVCs with a consistent QRS morphology, catheter ablation is useful.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 695: | Line 695: | ||
| ''' Recommendations for Fremature Ventricular Complexes ''' | | ''' Recommendations for Fremature Ventricular Complexes ''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' For patients who require arrhythmia suppression for symptoms or declining ventricular function suspected to be due to frequent PVCs (generally >15% of beats and predominately of 1 morphology) and for whom antiarrhythmic medications are ineffective, not tolerated, or not the patient’s preference, catheter ablation is useful.''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' For patients who require arrhythmia suppression for symptoms or declining ventricular function suspected to be due to frequent PVCs (generally >15% of beats and predominately of 1 morphology) and for whom antiarrhythmic medications are ineffective, not tolerated, or not the patient’s preference, catheter ablation is useful.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with PVC-induced cardiomyopathy, pharmacological treatment (e.g., beta blocker, amiodarone) is reasonable to reduce recurrent arrhythmias and improve symptoms and LV function. ''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with PVC-induced cardiomyopathy, pharmacological treatment (e.g., beta blocker, amiodarone) is reasonable to reduce recurrent arrhythmias and improve symptoms and LV function. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 710: | Line 710: | ||
| ''' Recommendations for Pregnancy ''' | | ''' Recommendations for Pregnancy ''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In mothers with long QT syndrome, a beta blocker should be continued during pregnancy and throughout the postpartum period including in women who are breastfeeding.''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In mothers with long QT syndrome, a beta blocker should be continued during pregnancy and throughout the postpartum period including in women who are breastfeeding.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |'''"2.''' In the pregnant patient with sustained VA, electrical cardioversion is safe and effective and should be used with standard electrode configuration.''([[ | | bgcolor="LightGreen" |'''"2.''' In the pregnant patient with sustained VA, electrical cardioversion is safe and effective and should be used with standard electrode configuration.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-EO]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In pregnant patients needing an ICD or VT ablation, it is reasonable to undergo these procedures during pregnancy, preferably after the first trimester.''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In pregnant patients needing an ICD or VT ablation, it is reasonable to undergo these procedures during pregnancy, preferably after the first trimester.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 727: | Line 727: | ||
| ''' Recommendations for Older Patients With Comorbidities ''' | | ''' Recommendations for Older Patients With Comorbidities ''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' For older patients and those with significant comorbidities, who meet indications for a primary prevention ICD, an ICD is reasonable if meaningful survival of greater than 1 year is expected.''([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' For older patients and those with significant comorbidities, who meet indications for a primary prevention ICD, an ICD is reasonable if meaningful survival of greater than 1 year is expected.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 740: | Line 740: | ||
| '''Digoxin''' | | '''Digoxin''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' Administration of digoxin antibodies is recommended for patients who present with sustained VA potentially due to digoxin toxicity.''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' Administration of digoxin antibodies is recommended for patients who present with sustained VA potentially due to digoxin toxicity.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| '''Medication-Induced QT Prolongation and Torsades de Pointes''' | | '''Medication-Induced QT Prolongation and Torsades de Pointes''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightGreen" |[[ | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''2.''' In patients with recurrent torsades de pointes associated with acquired QT prolongation and bradycardia that cannot be suppressed with intravenous magnesium administration, increasing the heart rate with atrial or ventricular pacing or isoproterenol are recommended to suppress the arrhythmia.''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''2.''' In patients with recurrent torsades de pointes associated with acquired QT prolongation and bradycardia that cannot be suppressed with intravenous magnesium administration, increasing the heart rate with atrial or ventricular pacing or isoproterenol are recommended to suppress the arrhythmia.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''3.''' For patients with QT prolongation due to a medication, hypokalemia, hypomagnesemia, or other acquired factor and recurrent torsades de pointes, administration of intravenous magnesium sulfate is recommended to suppress the arrhythmia.''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''3.''' For patients with QT prolongation due to a medication, hypokalemia, hypomagnesemia, or other acquired factor and recurrent torsades de pointes, administration of intravenous magnesium sulfate is recommended to suppress the arrhythmia.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-LD]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''4.''' For patients with torsades de pointes associated with acquired QT prolongation, potassium repletion to 4.0 mmol per L or more and magnesium repletion to normal values (e.g., ≥2.0 mmol/L) are beneficial.''([[ | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''4.''' For patients with torsades de pointes associated with acquired QT prolongation, potassium repletion to 4.0 mmol per L or more and magnesium repletion to normal values (e.g., ≥2.0 mmol/L) are beneficial.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-LD]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| '''Sodium Channel Blocker–Related Toxicity''' | | '''Sodium Channel Blocker–Related Toxicity''' | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients taking sodium channel blockers who present with elevated defibrillation or pacing thresholds, discontinuing the presumed responsible medication or reprogramming the device can be useful to restore effective device therapy.''<nowiki>([[ | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients taking sodium channel blockers who present with elevated defibrillation or pacing thresholds, discontinuing the presumed responsible medication or reprogramming the device can be useful to restore effective device therapy.''<nowiki>([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-LD]])</nowiki>'' <nowiki>"</nowiki> | ||
|- | |- | ||
| colspan="1" style="text-align:center; background:LightCoral" | [[ | | colspan="1" style="text-align:center; background:LightCoral" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class III - Harm]] | ||
|- | |- | ||
| bgcolor="LightCoral" |'''"1.''' In patients with congenital or acquired long QT syndrome, QT-prolonging medications are potentially harmful. ''([[ | | bgcolor="LightCoral" |'''"1.''' In patients with congenital or acquired long QT syndrome, QT-prolonging medications are potentially harmful. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|} | |} | ||
Line 771: | Line 771: | ||
| ''' Recommendations for Adult Congenital Heart Disease ''' | | ''' Recommendations for Adult Congenital Heart Disease ''' | ||
|- | |- | ||
| ''' | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' Adult patients with repaired complex congenital heart disease presenting with frequent, complex, or sustained VA, or unexplained syncope should undergo evaluation for potential residual anatomic or coronary abnormalities.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''2.''' In patients with adult congenital heart disease and complex or sustained VA in the presence of important residual hemodynamic lesions, treatment of hemodynamic abnormalities with catheter or surgical intervention as feasible is indicated prior to consideration of ablation or an ICD.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''3.''' In patients with adult congenital heart disease and hemodynamically unstable VT, an ICD is recommended after evaluation and appropriate treatment for residual lesions/ventricular dysfunction if meaningful survival of greater than 1 year is expected.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''4.''' In patients with adult congenital heart disease with SCA due to VT or VF in the absence of reversible causes, an ICD is recommended if meaningful survival of greater than 1 year is expected.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | |||
|- | |||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | |||
|- | |||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In adults with repaired tetralogy of Fallot physiology with high-risk characteristics and frequent VA, an electrophysiological study can be useful to evaluate the risk of sustained VT/VF.''<nowiki>''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])</nowiki>'' <nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''2.''' In adults with repaired tetralogy of Fallot physiology and inducible VT/VF or spontaneous sustained VT, implantation of an ICD is reasonable.''<nowiki>''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])</nowiki>'' <nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''3.''' In patients with adult congenital heart disease with recurrent sustained monomorphic VT or recurrent ICD shocks for VT, catheter ablation can be effective.''<nowiki>''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]]])</nowiki>'' <nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''4.''' In adults with repaired severe complexity adult congenital heart disease and frequent or complex VA, a beta blocker can be beneficial to reduce the risk of SCA.''<nowiki>''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])</nowiki>'' <nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''5.''' In patients with repaired moderate or severe complexity adult congenital heart disease with unexplained syncope and at least moderate ventricular dysfunction or marked hypertrophy, either ICD implantation or an electrophysiological study with ICD implantation for inducible sustained VA is reasonable if meaningful survival of greater than 1 year is expected.''<nowiki>''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])</nowiki>'' <nowiki>"</nowiki> | |||
|- | |||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIb]] | |||
|- | |||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with adult congenital heart disease and severe ventricular dysfunction (LVEF <35%) and symptoms of heart failure despite GDMT or additional risk factors, ICD implantation may be considered if meaningful survival of greater than 1 year is expected.''<nowiki>''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])</nowiki>'' <nowiki>"</nowiki> | |||
|- | |||
| colspan="1" style="text-align:center; background:LightCoral" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class III - Harm]] | |||
|- | |||
| bgcolor="LightCoral" |'''"1.''' In patients with adult congenital heart disease who have asymptomatic VA, prophylactic antiarrhythmic therapy with class Ic medications (i.e., flecainide, propafenone) or amiodarone is potentially harmful. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | |||
|} | |||
===Defibrillators Other than Transvenous Implantable Cardioverter Defibrillators (ICDs)=== | |||
{| class="wikitable" style="width:80%" | |||
|- | |||
| ''' Subcutaneous Implantable Cardioverter-Defibrillator ''' | |||
|- | |||
| colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | |||
|- | |||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients who meet criteria for an ICD who have inadequate vascular access or are at high risk for infection, and in whom pacing for bradycardia or VT termination or as part of CRT is neither needed nor anticipated, a subcutaneous implantable cardioverter-defibrillator is recommended.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | |||
|- | |||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | |||
|- | |||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients who meet indication for an ICD, implantation of a subcutaneous implantable cardioverter-defibrillator is reasonable if pacing for bradycardia or VT termination or as part of CRT is neither needed nor anticipated.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | |||
|- | |||
| colspan="1" style="text-align:center; background:LightCoral" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class III - Harm]] | |||
|- | |||
| bgcolor="LightCoral" |'''"1.''' In patients with an indication for bradycardia pacing or CRT, or for whom antitachycardia pacing for VT termination is required, a subcutaneous implantable cardioverter-defibrillator should not be implanted. ''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | |||
|} | |||
===Wearable Cardioverter-Defibrillator=== | |||
{| class="wikitable" style="width:80%" | |||
|- | |||
| ''' Recommendations for Wearable Cardioverter-Defibrillator ''' | |||
|- | |||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | |||
|- | |||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with an ICD and a history of SCA or sustained VA in whom removal of the ICD is required (as with infection), the wearable cardioverter- defibrillator is reasonable for the prevention of SCD.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | |||
|- | |||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIb]] | |||
|- | |||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients at an increased risk of SCD but who are not ineligible for an ICD, such as awaiting cardiac transplant, having an LVEF of 35% or less and are within 40 days from an MI, or have newly diagnosed NICM, revascularization within the past 90 days, myocarditis or secondary cardiomyopathy or a systemic infection, wearable cardioverter-defibrillator may be reasonable.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | |||
|} | |||
===Special Considerations for Catheter Ablation=== | |||
{| class="wikitable" style="width:80%" | |||
|- | |||
| ''' Recommendations for Catheter Ablation ''' | |||
|- | |||
| colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | |||
|- | |||
| bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with bundle-branch reentrant VT, catheter ablation is useful for reducing the risk of recurrent VT and ICD shocks .''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-LD]])'' <nowiki>"</nowiki> | |||
|- | |||
| colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | |||
|- | |||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In patients with structural heart disease who have failed endocardial catheter ablation, epicardial catheter ablation can be useful for reducing the risk of recurrent monomorphic VT.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | |||
|} | |||
===Postmortem Evaluation of Sudden Cardiac Death (SCD)=== | |||
{| class="wikitable" style="width:80%" | |||
|- | |- | ||
| | | ''' Recommendations for Postmortem Evaluation of SCD ''' | ||
|- | |- | ||
| | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>''' | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In victims of SCD without obvious causes, a standardized cardiac-specific autopsy is recommended.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LightGreen" |<nowiki>"</nowiki>''' | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''2.''' In first-degree relatives of SCD victims who were 40 years of age or younger, cardiac evaluation is recommended, with genetic counseling and genetic testing performed as indicated by clinical findings.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| | | colspan="1" style="text-align:center; background:LemonChiffon" | [[ACC AHA guidelines classification scheme#Classification of Recommendations|Class IIa]] | ||
|- | |- | ||
| | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''1.''' In victims of SCD with an autopsy that implicates a potentially heritable cardiomyopathy or absence of structural disease, suggesting a potential cardiac channelopathy, postmortem genetic testing is reasonable.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor="LemonChiffon" |<nowiki>"</nowiki>''' | | bgcolor="LemonChiffon" |<nowiki>"</nowiki>'''2.''' In victims of SCD with a previously identified phenotype for a genetic arrhythmia-associated disorder, but without genotyping prior to death, postmortem genetic testing can be useful for the purpose of family risk profiling.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-LD]])'' <nowiki>"</nowiki> | ||
|} | |||
===Terminal Care=== | |||
{| class="wikitable" style="width:80%" | |||
|- | |- | ||
| | | ''' Recommendations for Terminal Care ''' | ||
|- | |- | ||
| | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| bgcolor=" | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' At the time of ICD implantation or replacement, and during advance care planning, patients should be informed that their ICD shock therapy can be deactivated at any time if it is consistent with their goals and preferences.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-EO]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor=" | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''2.''' In patients with refractory HF symptoms, refractory sustained VA, or nearing the end of life from other illness, clinicians should discuss ICD shock deactivation and consider the patients’ goals and preferences.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-EO]])'' <nowiki>"</nowiki> | ||
|} | |||
===Shared Decision-Making=== | |||
{| class="wikitable" style="width:80%" | |||
|- | |- | ||
| | | ''' Recommendations for Shared Decision-Making ''' | ||
|- | |- | ||
| | | colspan="1" style="text-align:center; background:LightGreen" |[[ACC AHA guidelines classification scheme#Classification of Recommendations|Class I]] | ||
|- | |- | ||
| | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''1.''' In patients with VA or at increased risk for SCD, clinicians should adopt a shared decision-making approach in which treatment decisions are based not only on the best available evidence but also on the patients’ health goals, preferences, and values.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|- | |- | ||
| bgcolor=" | | bgcolor="LightGreen" |<nowiki>"</nowiki>'''2.''' Patients considering implantation of a new ICD or replacement of an existing ICD for a low battery should be informed of their individual risk of SCD and nonsudden death from HF or noncardiac conditions and the effectiveness, safety, and potential complications of the ICD in light of their health goals, preferences and values.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]])'' <nowiki>"</nowiki> | ||
|} | |} |
Latest revision as of 15:31, 2 November 2017
Template:Ventricular Arrhythmias ACC -2017
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1],Associate Editor(s)-in-Chief: Arzu Kalayci, M.D. [2]
2017 AHA/ACC/HRS Guideline for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death
General Evaluation of Patients With Documented or Suspected Ventricular Arrhythmias
History and Physical Examination
Class I |
"1. Patients presenting with syncope for which VA is documented, or thought to be a likely cause, should be hospitalized for evaluation, monitoring, and management. (Level of Evidence: B-NR) " |
Noninvasive Evaluation
12-lead ECG and Exercise Testing
Class I |
"1. In patients with sustained, hemodynamically stable, wide complex tachycardia, a 12-lead ECG during tachycardia should be obtained. (Level of Evidence: B-NR) " |
"2. In patients with VA symptoms associated with exertion, suspected ischemic heart disease, or catecholaminergic polymorphic ventricular tachycardia, exercise treadmill testing is useful to assess for exercise-induced VA. (Level of Evidence: B-NR) " |
"3. In patients with suspected or documented VA, a 12-lead ECG should be obtained in sinus rhythm to look for evidence of heart disease. (Level of Evidence: B-NR) " |
Ambulatory Electrocardiography |
"1. Ambulatory electrocardiographic monitoring is useful to evaluate whether symptoms, including palpitations, presyncope, or syncope, are caused by VA. (Level of Evidence: B-NR) " |
Implanted Cardiac Monitors |
Class IIa |
"1. In patients with sporadic symptoms (including syncope) suspected to be related to VA, implanted cardiac monitors can be useful. (Level of Evidence: B-R) " |
Noninvasive Cardiac Imaging |
Class I |
"1. In patients with known or suspected VA that may be associated with underlying structural heart disease or a risk of SCA, echocardiography is recommended for evaluation of cardiac structure and function. (Level of Evidence: B-NR) " |
Class IIa |
"1. In patients presenting with VA who are suspected of having structural heart disease, cardiac magnetic resonance imaging (MRI) or computed tomography (CT) can be useful to detect and characterize underlying structural heart disease. (Level of Evidence: C-EO) " |
Biomarkers |
Class IIa |
"1. In patients presenting with VA who are suspected of having structural heart disease, cardiac magnetic resonance imaging (MRI) or computed tomography (CT) can be useful to detect and characterize underlying structural heart disease. (Level of Evidence: B-NR) " |
Genetic Considerations in Arrhythmia Syndromes |
Class I |
"1. In patients and family members in whom genetic testing for risk stratification for SCA or SCD is recommended, genetic counselling in beneficial. (Level of Evidence: C-EO) " |
Invasive Cardiac Imaging: Cardiac Catheterization or CT Angiography |
"1. In patients who have recovered from unexplained SCA, CT or invasive coronary angiography is useful to confirm the presence or absence of ischemic heart disease and guide decisions for myocardial revascularization. (Level of Evidence: C-EO) " |
Electrophysiological Study for VA |
Class IIa |
"1. In patients with ischemic cardiomyopathy, NICM, or adult congenital heart disease who have syncope or other VA symptoms and who do not meet indications for a primary prevention ICD, an electrophysiological study can be useful for assessing the risk of sustained VT. (Level of Evidence: B-R) " |
Class III - No Benefit |
"1. In patients who meet criteria for ICD implantation, an electrophysiological study for the sole reason of inducing VA is not indicated for risk stratification. (Level of Evidence: B-R) " |
"1. In patients who meet criteria for ICD implantation, an electrophysiological study for the sole reason of inducing VA is not indicated for risk stratification. (Level of Evidence: B-NR) " |
Preventing SCD With HF Medications |
Class I |
"1. In patients with HFrEF (LVEF ≤40%), treatment with a beta blocker, a mineralocorticoid receptor antagonist and either an angiotensin-converting enzyme inhibitor, an angiotensin-receptor blocker, or an angiotensin receptor- neprilysin inhibitor is recommended to reduce SCD and all-cause mortality. (Level of Evidence: A) " |
Surgery and Revascularization Procedures in Patients With Ischemic Heart Disease |
Class I |
"1. Patients with sustained VA and survivors of SCA should be evaluated for ischemic heart disease, and should be revascularized as appropriate. (Level of Evidence: B-NR) " |
"1. In patients with anomalous origin of a coronary artery suspected to be the cause of SCA, repair or revascularization is recommended. (Level of Evidence: C-EO) " |
Surgery for Arrhythmia Management |
Class IIb |
"1. In patients with monomorphic VT refractory to antiarrhythmic medications and attempts at catheter ablation, surgical ablation may be reasonable. (Level of Evidence: C-LD) " |
Autonomic Modulation |
Class IIa |
"1. In patients with symptomatic, non–life-threatening VA, treatment with a beta blocker is reasonable. (Level of Evidence: C-LD) " |
Class IIb |
"1. In patients with VT/VF storm in whom a beta blocker, other antiarrhythmic medications, and catheter ablation are ineffective, not tolerated, or not possible, cardiac sympathetic denervation may be reasonable. (Level of Evidence: C-LD) " |
Acute Management of Specific Ventricular Arrhythmia
Recommendations for Management of Cardiac Arrest |
Class I |
"1. CPR should be performed in patients in cardiac arrest. according to published basic and advanced cardiovascular life support algorithms. (Level of Evidence: A) " |
"2. In patients with hemodynamically unstable VA that persist or recur after a maximal energy shock, intravenous amiodarone should be administered to attempt to achieve a stable rhythm after further defibrillation. (Level of Evidence: A) " |
"3. Patients presenting with VA with hemodynamic instability should undergo direct current cardioversion. (Level of Evidence: A) " |
"4. In patients with polymorphic VT or VF with ST-elevation MI, angiography with emergency revascularization is recommended. (Level of Evidence: B-NR) " |
"5. Patients with a wide-QRS tachycardia should be presumed to have VT if the diagnosis is unclear. (Level of Evidence: C-EO) " |
Class IIa |
"1. In patients with hemodynamically stable VT, administration of intravenous procainamide can be useful to attempt to terminate VT. (Level of Evidence: A) " |
"2. In patients with a witnessed cardiac arrest due to VF or polymorphic VT that is unresponsive to CPR, defibrillation, and vasopressor therapy, intravenous lidocaine can be beneficia. (Level of Evidence: B-R) " |
"3. In patients with polymorphic VT due to myocardial ischemia, intravenous beta blockers can be useful. (Level of Evidence: B-R) " |
"4. In patients with a recent MI who have VT/VF that repeatedly recurs despite direct current cardioversion and antiarrhythmic medications (VT/VF storm), an intravenous beta blocker can be useful. (Level of Evidence: B-NR) " |
Class IIb |
"1. In patients in cardiac arrest, administration of epinephrine (1 mg every 3 to 5 minutes) during CPR may be reasonable. (Level of Evidence: A) " |
"2. In patients with hemodynamically stable VT, administration of intravenous amiodarone or sotalol may be considered to attempt to terminate VT. (Level of Evidence: B-R) " |
Class III - No Benefit |
"1. In patients with cardiac arrest,administration of high-dose epinephrine (>1mg boluses) compared with standard doses is not beneficial. (Level of Evidence: A) " |
"2. In patients with cardiac arrest,administration of high-dose epinephrine (>1mg boluses) compared with standard doses is not beneficial. (Level of Evidence: A) " |
Class III - Harm |
"3. In patients with suspected AMI, prophylactic administration of lidocaine or high dose amiodarone for the prevention of VT is potentially harmful. (Level of Evidence: B-R) " |
"4. In patients with a wide QRS complex tachycardia of unknown origin, calcium channel blockers (e.g., verapamil and diltiazem) are potentially harmful . (Level of Evidence: C-LD) " |
Ongoing Management of Ventricular Arrhythmia (VA) and Sudden Cardiac Death (SCD) Risk Related to Specific Disease States
Secondary Prevention of SCD in Patients With Ischemic Heart Disease
Recommendations for Secondary Prevention of SCD in Patients With Ischemic Heart Disease |
Class I |
"1. In patients with ischemic heart disease, who either survive SCA due to VT/VF or experience hemodynamically unstable VT (LOE: B-R) or stable VT (LOE: B- NR) not due to reversible causes, an ICD is recommended if meaningful survival greater than 1 year is expected. (Level of Evidence: B-R / B-NR) " |
"2. Value Statement: Intermediate Value (LOE: B-R)
A transvenous ICD provides intermediate value in the secondary prevention of SCD particularly when the patient’s risk of death due to a VA is deemed high and the risk of nonarrhythmic death (either cardiac or noncardiac) is deemed low based on the patient’s burden of comorbidities and functional status. |
Class I |
"3. In patients with ischemic heart disease and unexplained syncope who have inducible sustained monomorphic VT on electrophysiological study, an ICD is recommended if meaningful survival of greater than 1 year is expected. (Level of Evidence: B-NR) " |
Coronary Artery Spasm
Recommendations for Patients With Coronary Artery Spasm |
Class I |
"1. In patients with VA due to coronary artery spasm, treatment with maximally tolerated doses of a calcium channel blocker and smoking cessation are indicated to reduce recurrent ischemia and VA. (Level of Evidence: B-NR) " |
Class IIa |
"1. In patients resuscitated from SCA due to coronary artery spasm in whom medical therapy is ineffective or not tolerated, an ICD is reasonable if meaningful survival of greater than 1 year is expected. (Level of Evidence: B-NR) " |
Class IIb |
"1. In patients resuscitated from SCA due to coronary artery spasm, an ICD in addition to medical therapy may be reasonable if meaningful survival of greater than 1 year is expected. (Level of Evidence: B-NR) " |
Primary Prevention of SCD in Patients With Ischemic Heart Disease
Recommendations for Primary Prevention of SCD in Patients With Ischemic Heart Disease |
Class I |
"1. In patients with LVEF of 35% or less that is due to ischemic heart disease who are at least 40 days’ post-MI and at least 90 days postrevascularization, and with NYHA class II or III HF despite GDMT, an ICD is recommended if meaningful survival of greater than 1 year is expected. (Level of Evidence: A) " |
"2. In patients with LVEF of 30% or less that is due to ischemic heart disease who are at least 40 days’ post-MI and at least 90 days postrevascularization, and with NYHA class I HF despite GDMT, an ICD is recommended if meaningful survival of greater than 1 year is expected. (Level of Evidence: A) " |
"3.Value Statement: High Value (LOE: B-R)
A transvenous ICD provides high value in the primary prevention of SCD particularly when the patient’s risk of death due to a VA is deemed high and the risk of nonarrhythmic death (either cardiac or noncardiac) is deemed low based on the patient’s burden of comorbidities and functional status. |
Class I |
"1. In patients with NSVT due to prior MI, LVEF of 40% or less and inducible sustained VT or VF at electrophysiological study, an ICD is recommended if meaningful survival of greater than 1 year is expected. (Level of Evidence: B-R) " |
Class IIa |
"1. In nonhospitalized patients with NYHA class IV symptoms who are candidates for cardiac transplantation or an LVAD, an ICD is reasonable if meaningful survival of greater than 1 year is expected. (Level of Evidence: B-NR) " |
Class III - No Benefit |
"1. An ICD is not indicated for NYHA class IV patients with medication-refractory HF who are not also candidates for cardiac transplantation, an LVAD, or a CRT defibrillator that incorporates both pacing and defibrillation capabilities. (Level of Evidence: C-EO) " |
Treatment and Prevention of Recurrent VA in Patients With Ischemic Heart Disease
Recommendations for Treatment of Recurrent VA in Patients With Ischemic Heart Disease |
Class I |
"1. In patients with ischemic heart disease and recurrent VA, with significant symptoms or ICD shocks despite optimal device programming and ongoing treatment with a beta blocker, amiodarone or sotalol is useful to suppress recurrent VA. (Level of Evidence: B-R) " |
"2. In patients with prior MI and recurrent episodes of symptomatic sustained VT, or who present with VT or VF storm and have failed or are intolerant of amiodarone (LOE: B-R) or other antiarrhythmic medications (LOE: B-NR) catheter ablation is recommended . (Level of Evidence: B-R / B-NR) " |
Class IIb |
"1. In patients with ischemic heart disease and ICD shocks for sustained monomorphic VT or symptomatic sustained monomorphic VT that is recurrent, or hemodynamically tolerated, catheter ablation as first-line therapy may be considered to reduce recurrent VA. (Level of Evidence: C-LD) " |
Class III - Harm |
"1. In patients with prior MI, class IC antiarrhythmic medications (e.g., flecainide and propafenone) should not be used. (Level of Evidence: B-R) " |
"2. In patients with incessant VT or VF, an ICD should not be implanted until sufficient control of the VA is achieved to prevent repeated ICD shocks. (Level of Evidence: C-LD) " |
Class III - No benefit |
"3. In patients with ischemic heart disease and sustained monomorphic VT, coronary revascularization alone is an ineffective therapy to prevent recurrent VT. (Level of Evidence: C-LD) " |
Nonischemic Cardiomyopathy (NICM)
Recommendations for Patients With NICM |
Class I |
"1. In patients with suspected NICM from myocardial infiltrative processes, cardiac MRI with late gadolinium enhancement is useful for diagnosis. (Level of Evidence: B-NR) " |
Class IIa |
"1. In patients with suspected NICM, cardiac MRI with late gadolinium enhancement can be useful for assessing risk of SCA/SCD. (Level of Evidence: B-NR) " |
"1. In patients with NICM who develop conduction disease or LV dysfunction at less than 40 years of age, or who have a family history of NICM or SCD in a first-degree relative (<50 years of age), genetic counseling and genetic testing are reasonable to detect a heritable disease that may clarify prognosis and facilitate cascade screening of relatives. (Level of Evidence: C-EO) " |
Secondary Prevention of SCD in Patients With NICM
Recommendations for Secondary Prevention of SCD in Patients With NICM |
Class I |
"1. In patients with NICM who either survive SCA due to VT/VF or experience hemodynamically unstable VT (LOE: B-R) or stable VT (LOE: B-NR) not due to reversible causes, an ICD is recommended if meaningful survival greater than 1 year is expected. (Level of Evidence: B-R / B-NR) " |
Class IIa |
"1. In patients with NICM who experience syncope presumed to be due to VA and who do not meet indications for a primary prevention ICD, an ICD or an electrophysiological study for risk stratification for SCD can be beneficial if meaningful survival greater than 1 year is expected. (Level of Evidence: B-NR) " |
Class IIb |
"1. In patients with NICM who survive a cardiac arrest, have sustained VT, or have symptomatic VA who are ineligible for an ICD (due to a limited life-expectancy and/or functional status or lack of access to an ICD), amiodarone may be considered for prevention of SCD. (Level of Evidence: B-R) " |
Primary Prevention of SCD in Patients With NICM
Recommendations for Primary Prevention of SCD in Patients With NICM |
Class I |
"1. In patients with NICM, HF with NYHA class II–III symptoms and an LVEF of 35% or less, despite GDMT, an ICD is recommended if meaningful survival of greater than 1 year is expected. (Level of Evidence: A) " |
Class IIa |
"1. In patients with NICM due to a Lamin A/C mutation who have 2 or more risk factors (NSVT, LVEF <45%, nonmissense mutation, and male sex), an ICD can be beneficial if meaningful survival of greater than 1 year is expected. (Level of Evidence: B-NR) " |
Class IIb |
"1. In patients with NICM, HF with NYHA class I symptoms and an LVEF of 35% or less, despite GDMT, an ICD may be considered if meaningful survival of greater than 1 year is expected. (Level of Evidence: B-R) " |
Class III - No benefit |
"1. In patients with medication-refractory NYHA class IV HF who are not also candidates for cardiac transplantation, an LVAD, or a CRT defibrillator that incorporates both pacing and defibrillation capabilities, an ICD should not be implanted. (Level of Evidence: C-EO) " |
Treatment of Recurrent VA in Patients With NICM
Recommendations for Treatment of Recurrent VA in Patients With NICM |
Class IIa |
"1. In patients with NICM and an ICD who experience spontaneous VA or recurrent appropriate shocks despite optimal device programming and treatment with a beta blocker, amiodarone or sotalol can be beneficial. (Level of Evidence: B-R) " |
"2. In patients with NICM and recurrent sustained monomorphic VT who fail or are intolerant of antiarrhythmic medications, catheter ablation can be useful for reducing recurrent VT and ICD shocks. (Level of Evidence: B-NR) " |
Arrhythmogenic Right Ventricular Cardiomyopathy
Recommendations for Arrhythmogenic Right Ventricular Cardiomyopathy |
Class I |
"1. In selected first-degree relatives of patients with arrhythmogenic right ventricular cardiomyopathy, clinical screening for the disease is recommended along with genetic counseling and genetic testing, if the proband has a disease causing mutation. (Level of Evidence: B-NR) " |
"2. In patients with suspected arrhythmogenic right ventricular cardiomyopathy and VA or electrocardiographic abnormalities, cardiac MRI is useful for establishing a diagnosis and for risk stratification. (Level of Evidence: B-NR) " |
"3. In patients with arrhythmogenic right ventricular cardiomyopathy and an additional marker of increased risk of SCD (resuscitated SCA, sustained VT, significant ventricular dysfunction with RVEF or LVEF ≤35%), an ICD is recommended if meaningful survival greater than 1 year is expected. (Level of Evidence: B-NR) " |
"4. In patients with arrhythmogenic right ventricular cardiomyopathy and VA, a beta blocker is recommended.(Level of Evidence: B-NR) " |
"4. In patients with a clinical diagnosis of arrhythmogenic right ventricular cardiomyopathy , avoiding intensive exercise is recommended.(Level of Evidence: B-NR) " |
Class IIa |
"1. In patients with clinically diagnosed or suspected arrhythmogenic right ventricular cardiomyopathy , genetic counseling and genetic testing can be useful for diagnosis and for gene-specific targeted family screening. (Level of Evidence: B-NR) " |
"2. In patients with arrhythmogenic right ventricular cardiomyopathy and syncope presumed due to VA, an ICD can be useful if meaningful survival greater than 1 year is expected. (Level of Evidence: B-NR) " |
"3. In patients with clinical evidence of arrhythmogenic right ventricular cardiomyopathy but not VA, a beta blocker can be useful. (Level of Evidence: B-NR) " |
"4. In patients with arrhythmogenic right ventricular cardiomyopathy and recurrent symptomatic sustained VT in whom a beta blocker is ineffective or not tolerated, catheter ablation with availability of a combined endocardial/epicardial approach can be beneficial . (Level of Evidence: B-NR) " |
"5. Inpatientswithsuspectedarrhythmogenicrightventricularcardiomyopathy, a signal averaged ECG can be useful for diagnosis and risk stratification . (Level of Evidence: B-NR) " |
Class IIb |
"1. In asymptomatic patients with clinical evidence of arrhythmogenic right ventricular cardiomyopathy , an electrophysiological study may be considered for risk stratification. (Level of Evidence: B-NR) " |
Hypertrophic Cardiomyopathy
Recommendations for Hypertrophic Cardiomyopathy |
Class I |
"1. In patients with HCM, SCD risk stratification should be performed at the time of initial evaluation and periodically thereafter. (Level of Evidence: B-NR) " |
"2. In patients with HCM who have survived an SCA due to VT or VF, or have spontaneous sustained VT causing syncope or hemodynamic compromise, an ICD is recommended if meaningful survival greater than 1 year is expected. (Level of Evidence: B-NR) " |
"3. In first-degree relatives of patients with HCM, an ECG and echocardiogram shouldbeperformed. (Level of Evidence: B-NR) " |
"4. In first-degree relatives of patients with HCM due to a known causative mutation, genetic counseling and mutation-specific genetic testing are recommended. (Level of Evidence: B-NR) " |
Class IIa |
"1. In patients with clinically suspected or diagnosed HCM, genetic counseling and genetic testing are reasonable. (Level of Evidence: B-NR) " |
"2. In patients with HCM and 1 or more of the following risk factors, an ICD is reasonable if meaningful survival of greater than 1 year is expected:
a. Maximum LV wall thickness ≥30 mm (LOE: B-NR) b. SCD in 1 or more first-degree relatives presumably caused by HCM (LOE: C-LD) c. 1 or more episodes of unexplained syncope within the preceding 6 months (LOE: C-LD). (Level of Evidence: B-NR / C-LD) " |
"3. In patients with HCM who have spontaneous NSVT (LOE: C-LD) or an abnormal blood pressure response with exercise (LOE: B-NR), who also have additional SCD risk modifiers or high risk features, an ICD is reasonable if meaningful survival greater than 1 year is expected. (Level of Evidence: B-NR / C-LD) " |
Class IIb |
"1. In patients with HCM who have NSVT (LOE: B-NR) or an abnormal blood pressure response with exercise (LOE: B-NR) but do not have any other SCD risk modifiers, an ICD may be considered, but its benefit is uncertain. (Level of Evidence: B-NR) " |
"2. In patients with HCM and a history of sustained VT or VF, amiodarone may be considered when an ICD is not feasible or not preferred by the patient. (Level of Evidence: C-LD) " |
Class III - No benefit |
"1. In patients with HCM, an invasive electrophysiological study with programmed ventricular stimulation should not be performed for risk stratification. (Level of Evidence: B-NR) " |
"2. In patients with an identified HCM genotype in the absence of SCD risk factors, an ICD should not be implanted. (Level of Evidence: B-NR) " |
Myocarditis
Recommendations for Myocarditis |
Class I |
"1. In patients with life-threatening VT or VF associated with confirmed or clinically suspected myocarditis, referral to centers with mechanical hemodynamic support and advanced arrhythmia management is recommended. (Level of Evidence: C-LD) " |
Class IIb |
"1. In patients with giant cell myocarditis with VF or hemodynamically unstable VT treated according to GDMT, an ICD and/or an anti arrhythmic medication may be considered if meaningful survival of greater than 1 year is expected. (Level of Evidence: C-LD) " |
Cardiac Sarcoidosis
Recommendations for Cardiac Sarcoidosis |
Class I |
"1. In patients with cardiac sarcoidosis who have sustained VT or are survivors of sudden cardiac arrest (SCA) or have an LVEF of 35% or less, an ICD is recommended, if meaningful survival of greater than 1 year is expected. (Level of Evidence: B-NR) " |
Class IIa |
"1. In patients with cardiac sarcoidosis and LVEF greater than 35% who have syncope and/or evidence of myocardial scar by cardiac MRI or positron emission tomographic (PET) scan, and/or have an indication for permanent pacing implantation of an ICD is reasonable, provided that meaningful survival of greater than 1 year is expected. (Level of Evidence: B-NR) " |
"2. In patients with cardiac sarcoidosis and LVEF greater than 35%, it is reasonable to perform an electrophysiological study and to impant an ICD, if sustained VA is inducible, provided that meaningful survival of greater than 1 year is expected. (Level of Evidence: C-LD) " |
"3. In patients with cardiac sarcoidosis who have an indication for permanent pacing, implantation of an ICD can be beneficial. (Level of Evidence: C-LD) " |
"4. In patients with cardiac sarcoidosis with frequent symptomatic VA and evidence of myocardial inflammation, immunosuppression in combination with antiarrhythmic medication therapy can be useful to reduce VA burden. (Level of Evidence: C-LD) " |
Heart Failure (HR)
Recommendation for Heart Failure With Reduced Ejection Fraction |
Class IIa |
"1. In patients with HFrEF who are awaiting heart transplant and who otherwise would not qualify for an ICD (e.g., NYHA class IV and/or use of inotropes) with a plan to discharge home, an ICD is reasonable. (Level of Evidence: B-NR) " |
Left Ventricular Assist Device (LVAD)
Recommendation for Patients With an LVAD |
Class IIa |
"1. In patients with an LVAD and sustained VA, an ICD can be beneficial. (Level of Evidence: C-LD) " |
Implantable Cardioverter Defibrillator (ICD) Use After Heart Transplantation
Recommendation for ICD Use After Heart Transplantation |
Class IIb |
"1. In patients with a heart transplant and severe allograft vasculopathy with LV dysfunction, an ICD may be reasonable if meaningful survival of greater than 1 year is expected. (Level of Evidence: B-NR) " |
Neuromuscular Disorders
Recommendations for Neuromuscular Disorders |
Class I |
"1. In patients with neuromuscular disorders, primary and secondary prevention ICDs are recommended for the same indications as for patients with NICM if meaningful survival of greater than 1 year is expected. (Level of Evidence: B-NR) " |
Class IIa |
"1. In patients with Emery-Dreifuss and limb-girdle type IB muscular dystrophies with progressive cardiac involvement, an ICD is reasonable if a meaningful survival of greater than 1 year is expected. (Level of Evidence: B-NR) " |
"2. In patients with muscular dystrophy, follow-up for development of cardiac involvement is reasonable, even if the patient is asymptomatic at presentation. (Level of Evidence: B-NR) " |
Class IIb |
"1. In patients with myotonic dystrophy type 1 with an indication for a permanent pacemaker, an ICD may be considered to minimize the risk of SCA from VT if meaningful survival of greater than 1 year is expected. (Level of Evidence: B-NR) " |
Cardiac Channelopathies
Recommendations for Cardiac Channelopathies |
Class I |
"1. In first-degree relatives of patients who have a causative mutation for long QT syndrome, catecholaminergic polymorphic ventricular tachycardia, short QT syndrome, or Brugada syndrome, genetic counseling and mutation-specific genetic testing are recommended. (Level of Evidence: B-NR) " |
"1. In patients with a cardiac channelopathy and SCA, an ICD is recommended if meaningful survival of greater than 1 year is expected. (Level of Evidence: B-NR) " |
Specific Cardiac Channelopathy Syndromes
Recommendations for Long QT Syndrome |
Class I |
"1. In patients with long QT syndrome with a resting QTc greater than 470 ms, a beta blocker is recommended. (Level of Evidence: B-NR) " |
"2. In high-risk patients with symptomatic long QT syndrome in whom a beta blocker is ineffective or not tolerated, intensification of therapy with additional medications (guided by consideration of the particular long QT syndrome type), left cardiac sympathetic denervation, and/or an ICD is recommended. (Level of Evidence: B-NR) " |
"3. In patients with long QT syndrome and recurrent appropriate ICD shocks despite maximum tolerated doses of a beta blocker, intensification of medical therapy with additional medications (guided by consideration of according to the particular long QT syndrome type) or left cardiac sympathetic denervation, is recommended. (Level of Evidence: B-NR) " |
"4. In patients with clinically diagnosed long QT syndrome, genetic counseling and genetic testing are recommended. (Level of Evidence: B-NR) " |
Class IIa |
"1. In patients with suspected long QT syndrome, ambulatory electrocardiographic monitoring, recording the ECG lying and immediately on standing, and/or exercise treadmill testing can be useful for establishing a diagnosis and monitoring the response to therapy. (Level of Evidence: B-NR) " |
"2. In asymptomatic patients with long QT syndrome and a resting QTc less than 470 ms, chronic therapy with a beta blocker is reasonable. (Level of Evidence: B-NR) " |
Class IIb |
"1. In asymptomatic patients with long QT syndrome and a resting QTc greater than 500 ms while receiving a beta blocker, intensification of therapy with medications (guided by consideration of the particular long QT syndrome type), left cardiac sympathetic denervation or an ICD may be considered. (Level of Evidence: B-NR) " |
Class III - Harm |
"1. In patients with long QT syndrome, QT-prolonging medications are potentially harmful. (Level of Evidence: B-NR) " |
Catecholaminergic Polymorphic Ventricular Tachycardia
Recommendations for Catecholaminergic Polymorphic Ventricular Tachycardia |
Class I |
"1. In patients with catecholaminergic polymorphic ventricular tachycardia, a beta blocker is recommended.(Level of Evidence: B-NR) " |
"1. In patients with catecholaminergic polymorphic ventricular tachycardia and recurrent sustained VT or syncope, while receiving adequate or maximally tolerated beta blocker, treatment intensification with either combination medication therapy (e.g., beta blocker, flecainide), left cardiac sympathetic denervation,and/or an ICD is recommended.(Level of Evidence: B-NR) " |
Class IIa |
"1. In patients with catecholaminergic polymorphic ventricular tachycardia and with clinical VT or exertional syncope, genetic counseling and genetic testing are reasonable. (Level of Evidence: B-NR) " |
Brugada Syndrome
Recommendations for Brugada Syndrome |
Class I |
"1. In asymptomatic patients with only inducible type 1 Brugada electrocardiographic pattern, observation without therapy is recommended.(Level of Evidence: B-NR) " |
"2. In patients with Brugada syndrome with spontaneous type 1 Brugada electrocardiographic pattern and cardiac arrest, sustained VA or a recent history of syncope presumed due to VA, an ICD is recommended if a meaningful survival of greater than 1 year is expected.(Level of Evidence: B-NR) " |
"3. In patients with Brugada syndrome experiencing recurrent ICD shocks for polymorphic VT, intensification of therapy with quinidine or catheter ablation is recommended.(Level of Evidence: B-NR) " |
"4. In patients with spontaneous type 1 Brugada electrocardiographic pattern and symptomatic VA who either are not candidates for or decline an ICD, quinidine or catheter ablation is recommended.(Level of Evidence: B-NR) " |
Class IIa |
"1. In patients with suspected Brugada syndrome in the absence of a spontaneous type 1 Brugada electrocardiographic pattern, a pharmacological challenge using a sodium channel blocker can be useful for diagnosis. (Level of Evidence: B-NR) " |
Class IIb |
"1. In patients with asymptomatic Brugada syndrome and a spontaneous type 1 Brugada electrocardiographic pattern, an electrophysiological study with programmed ventricular stimulation using single and double extrastimuli may be considered for further risk stratification. (Level of Evidence: B-NR) " |
"2. In patients with suspected or established Brugada syndrome, genetic counseling and genetic testing may be useful to facilitate cascade screening of relatives . (Level of Evidence: C-EO) " |
Early Repolarization “J-wave” Syndrome
Recommendations for Early Repolarization Syndrome |
Class I |
"1. In asymptomatic patients with an early repolarization pattern on ECG, observation without treatment is recommended.(Level of Evidence: B-NR) " |
"2. In patients with early repolarization pattern on ECG and cardiac arrest or sustained VA, an ICD is recommended.(Level of Evidence: B-NR) " |
Class III - No Benefit |
"1. In patients with early repolarization pattern on ECG, genetic testing is not recommended. (Level of Evidence: B-NR) " |
Short QT Syndrome
Recommendations for Short QT Syndrome |
Class I |
"1. In asymptomatic patients with a short QTc interval, observation without treatment is recommended.(Level of Evidence: B-NR) " |
"2. In patients with short QT syndrome who have a cardiac arrest or sustained VA, an ICD is recommended if meaningful survival greater than 1 year is expected.(Level of Evidence: B-NR) " |
Class IIa |
"1. In patients with short QT syndrome and recurrent sustained VA, treatment with quinidine can be useful. (Level of Evidence: C-LD) " |
"2. In patients with short QT syndrome and VT/VF storm, isoproterenol infusion can be effective. (Level of Evidence: C-LD) " |
Class IIb |
"1. In patients with short QT syndrome, genetic testing may be considered to facilitate screening of first-degree relatives. (Level of Evidence: C-EO) " |
Ventricular Arrhythmia in the Structurally Normal Heart
Recommendations for Ventricular Arrhythmia in the Structurally Normal Heart |
Class I |
"1. In patients with symptomatic PVCs in an otherwise normal heart, treatment with a beta blocker or nondihydropyradine calcium channel blocker is useful to reduce recurrent arrhythmias and improve symptoms.(Level of Evidence: B-R) " |
Class IIa |
"1. In patients with symptomatic VA in an otherwise normal heart, treatment with an antiarrhythmic medication is reasonable to reduce recurrent symptomatic arrhythmias and improve symptoms if beta blockers and nondihydropyradine calcium channel blockers are ineffective or not tolerated. (Level of Evidence: B-R) " |
Outflow Tract and Atrioventricular Annular Ventricular Arrhythmia (VA)
Recommendations for Outflow Tract Ventricular Arrhythmia |
Class I |
"1. In patients with symptomatic outflow tract VA in an otherwise normal heart for whom antiarrhythmic medications are ineffective, not tolerated, or not the patient’s preference, catheter ablation is useful.(Level of Evidence: B-NR) " |
"2. In patients with symptomatic outflow tract VT in an otherwise normal heart, a beta blocker or a calcium channel blocker is useful.(Level of Evidence: B-NR) " |
Papillary Muscle Ventricular Arrhythmia (VA)
Recommendation for Papillary Muscle VA (PVCs and VT) |
Class I |
"1. In patients with symptomatic VA arising from the papillary muscles for whom antiarrhythmic medications are ineffective, not tolerated, or not the patient’s preference, catheter ablation is useful.(Level of Evidence: B-NR) " |
Interfascicular Reentrant Ventricular Tachycardia (VT) (Belhassen Tachycardia)
Recommendations for Interfascicular Reentrant VT (Belhassen Tachycardia) |
Class I |
"1. In patients with verapamil-sensitive, idiopathic LVT related to interfascicular reentry for whom antiarrhythmic medications are ineffective, not tolerated, or not the patient’s preference, catheter ablation is useful.(Level of Evidence: B-NR) " |
"2. In patients with sustained hemodynamically tolerated verapamil-sensitive, idiopathic LVT related to interfascicular reentry, intravenous verapamil is recommended for VT termination.(Level of Evidence: B-NR) " |
Class IIa |
"1. In patients with recurrent verapamil-sensitive idiopathic LVT, chronic therapy with oral verapamil can be useful. (Level of Evidence: C-LD) " |
Idiopathic Polymorphic (Ventricular Tachycardia) VT/ Ventricular Fibrillation (VF)
Recommendations for Idiopathic Polymorphic VT/VF |
Class I |
"1. In young patients (<40 years of age) with unexplained SCA, unexplained near drowning, or recurrent exertional syncope, who do not have ischemic or other structural heart disease, further evaluation for genetic arrhythmia syndromes is recommended.(Level of Evidence: B-NR) " |
"2. In patients resuscitated from SCA due to idiopathic polymorphic VT or VF, an ICD is recommended if meaningful survival greater than 1 year is expected.(Level of Evidence: B-NR) " |
"3. For patients with recurrent episodes of idiopathic VF initiated by PVCs with a consistent QRS morphology, catheter ablation is useful.(Level of Evidence: B-NR) " |
Premature Ventricular Complexes (PVC)-Induced Cardiomyopathy
Recommendations for Fremature Ventricular Complexes |
Class I |
"1. For patients who require arrhythmia suppression for symptoms or declining ventricular function suspected to be due to frequent PVCs (generally >15% of beats and predominately of 1 morphology) and for whom antiarrhythmic medications are ineffective, not tolerated, or not the patient’s preference, catheter ablation is useful.(Level of Evidence: B-NR) " |
Class IIa |
"1. In patients with PVC-induced cardiomyopathy, pharmacological treatment (e.g., beta blocker, amiodarone) is reasonable to reduce recurrent arrhythmias and improve symptoms and LV function. (Level of Evidence: B-NR) " |
Pregnancy
Recommendations for Pregnancy |
Class I |
"1. In mothers with long QT syndrome, a beta blocker should be continued during pregnancy and throughout the postpartum period including in women who are breastfeeding.(Level of Evidence: B-NR) " |
"2. In the pregnant patient with sustained VA, electrical cardioversion is safe and effective and should be used with standard electrode configuration.(Level of Evidence: C-EO) " |
Class IIa |
"1. In pregnant patients needing an ICD or VT ablation, it is reasonable to undergo these procedures during pregnancy, preferably after the first trimester.(Level of Evidence: B-NR) " |
Older Patients With Comorbidities
Recommendations for Older Patients With Comorbidities |
Class IIa |
"1. For older patients and those with significant comorbidities, who meet indications for a primary prevention ICD, an ICD is reasonable if meaningful survival of greater than 1 year is expected.(Level of Evidence: B-NR) " |
Medication-Induced Arrhythmias
Recommendations for Medication-Induced Arrhythmias |
Digoxin |
Class I |
"1. Administration of digoxin antibodies is recommended for patients who present with sustained VA potentially due to digoxin toxicity.(Level of Evidence: B-NR) " |
Medication-Induced QT Prolongation and Torsades de Pointes |
Class I |
"2. In patients with recurrent torsades de pointes associated with acquired QT prolongation and bradycardia that cannot be suppressed with intravenous magnesium administration, increasing the heart rate with atrial or ventricular pacing or isoproterenol are recommended to suppress the arrhythmia.(Level of Evidence: B-NR) " |
"3. For patients with QT prolongation due to a medication, hypokalemia, hypomagnesemia, or other acquired factor and recurrent torsades de pointes, administration of intravenous magnesium sulfate is recommended to suppress the arrhythmia.(Level of Evidence: C-LD) " |
"4. For patients with torsades de pointes associated with acquired QT prolongation, potassium repletion to 4.0 mmol per L or more and magnesium repletion to normal values (e.g., ≥2.0 mmol/L) are beneficial.(Level of Evidence: C-LD) " |
Sodium Channel Blocker–Related Toxicity |
Class IIa |
"1. In patients taking sodium channel blockers who present with elevated defibrillation or pacing thresholds, discontinuing the presumed responsible medication or reprogramming the device can be useful to restore effective device therapy.([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: C-LD]]) " |
Class III - Harm |
"1. In patients with congenital or acquired long QT syndrome, QT-prolonging medications are potentially harmful. (Level of Evidence: B-NR) " |
Adult Congenital Heart Disease
Recommendations for Adult Congenital Heart Disease |
Class I |
"1. Adult patients with repaired complex congenital heart disease presenting with frequent, complex, or sustained VA, or unexplained syncope should undergo evaluation for potential residual anatomic or coronary abnormalities.(Level of Evidence: B-NR) " |
"2. In patients with adult congenital heart disease and complex or sustained VA in the presence of important residual hemodynamic lesions, treatment of hemodynamic abnormalities with catheter or surgical intervention as feasible is indicated prior to consideration of ablation or an ICD.(Level of Evidence: B-NR) " |
"3. In patients with adult congenital heart disease and hemodynamically unstable VT, an ICD is recommended after evaluation and appropriate treatment for residual lesions/ventricular dysfunction if meaningful survival of greater than 1 year is expected.(Level of Evidence: B-NR) " |
"4. In patients with adult congenital heart disease with SCA due to VT or VF in the absence of reversible causes, an ICD is recommended if meaningful survival of greater than 1 year is expected.(Level of Evidence: B-NR) " |
Class IIa |
"1. In adults with repaired tetralogy of Fallot physiology with high-risk characteristics and frequent VA, an electrophysiological study can be useful to evaluate the risk of sustained VT/VF.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]]) " |
"2. In adults with repaired tetralogy of Fallot physiology and inducible VT/VF or spontaneous sustained VT, implantation of an ICD is reasonable.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]]) " |
"3. In patients with adult congenital heart disease with recurrent sustained monomorphic VT or recurrent ICD shocks for VT, catheter ablation can be effective.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]]]) " |
"4. In adults with repaired severe complexity adult congenital heart disease and frequent or complex VA, a beta blocker can be beneficial to reduce the risk of SCA.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]]) " |
"5. In patients with repaired moderate or severe complexity adult congenital heart disease with unexplained syncope and at least moderate ventricular dysfunction or marked hypertrophy, either ICD implantation or an electrophysiological study with ICD implantation for inducible sustained VA is reasonable if meaningful survival of greater than 1 year is expected.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]]) " |
Class IIb |
"1. In patients with adult congenital heart disease and severe ventricular dysfunction (LVEF <35%) and symptoms of heart failure despite GDMT or additional risk factors, ICD implantation may be considered if meaningful survival of greater than 1 year is expected.''([[ACC AHA guidelines classification scheme#Level of Evidence|Level of Evidence: B-NR]]) " |
Class III - Harm |
"1. In patients with adult congenital heart disease who have asymptomatic VA, prophylactic antiarrhythmic therapy with class Ic medications (i.e., flecainide, propafenone) or amiodarone is potentially harmful. (Level of Evidence: B-NR) " |
Defibrillators Other than Transvenous Implantable Cardioverter Defibrillators (ICDs)
Subcutaneous Implantable Cardioverter-Defibrillator |
Class I |
"1. In patients who meet criteria for an ICD who have inadequate vascular access or are at high risk for infection, and in whom pacing for bradycardia or VT termination or as part of CRT is neither needed nor anticipated, a subcutaneous implantable cardioverter-defibrillator is recommended.(Level of Evidence: B-NR) " |
Class IIa |
"1. In patients who meet indication for an ICD, implantation of a subcutaneous implantable cardioverter-defibrillator is reasonable if pacing for bradycardia or VT termination or as part of CRT is neither needed nor anticipated.(Level of Evidence: B-NR) " |
Class III - Harm |
"1. In patients with an indication for bradycardia pacing or CRT, or for whom antitachycardia pacing for VT termination is required, a subcutaneous implantable cardioverter-defibrillator should not be implanted. (Level of Evidence: B-NR) " |
Wearable Cardioverter-Defibrillator
Recommendations for Wearable Cardioverter-Defibrillator |
Class IIa |
"1. In patients with an ICD and a history of SCA or sustained VA in whom removal of the ICD is required (as with infection), the wearable cardioverter- defibrillator is reasonable for the prevention of SCD.(Level of Evidence: B-NR) " |
Class IIb |
"1. In patients at an increased risk of SCD but who are not ineligible for an ICD, such as awaiting cardiac transplant, having an LVEF of 35% or less and are within 40 days from an MI, or have newly diagnosed NICM, revascularization within the past 90 days, myocarditis or secondary cardiomyopathy or a systemic infection, wearable cardioverter-defibrillator may be reasonable.(Level of Evidence: B-NR) " |
Special Considerations for Catheter Ablation
Recommendations for Catheter Ablation |
Class I |
"1. In patients with bundle-branch reentrant VT, catheter ablation is useful for reducing the risk of recurrent VT and ICD shocks .(Level of Evidence: C-LD) " |
Class IIa |
"1. In patients with structural heart disease who have failed endocardial catheter ablation, epicardial catheter ablation can be useful for reducing the risk of recurrent monomorphic VT.(Level of Evidence: B-NR) " |
Postmortem Evaluation of Sudden Cardiac Death (SCD)
Recommendations for Postmortem Evaluation of SCD |
Class I |
"1. In victims of SCD without obvious causes, a standardized cardiac-specific autopsy is recommended.(Level of Evidence: B-NR) " |
"2. In first-degree relatives of SCD victims who were 40 years of age or younger, cardiac evaluation is recommended, with genetic counseling and genetic testing performed as indicated by clinical findings.(Level of Evidence: B-NR) " |
Class IIa |
"1. In victims of SCD with an autopsy that implicates a potentially heritable cardiomyopathy or absence of structural disease, suggesting a potential cardiac channelopathy, postmortem genetic testing is reasonable.(Level of Evidence: B-NR) " |
"2. In victims of SCD with a previously identified phenotype for a genetic arrhythmia-associated disorder, but without genotyping prior to death, postmortem genetic testing can be useful for the purpose of family risk profiling.(Level of Evidence: C-LD) " |
Terminal Care
Recommendations for Terminal Care |
Class I |
"1. At the time of ICD implantation or replacement, and during advance care planning, patients should be informed that their ICD shock therapy can be deactivated at any time if it is consistent with their goals and preferences.(Level of Evidence: C-EO) " |
"2. In patients with refractory HF symptoms, refractory sustained VA, or nearing the end of life from other illness, clinicians should discuss ICD shock deactivation and consider the patients’ goals and preferences.(Level of Evidence: C-EO) " |
Recommendations for Shared Decision-Making |
Class I |
"1. In patients with VA or at increased risk for SCD, clinicians should adopt a shared decision-making approach in which treatment decisions are based not only on the best available evidence but also on the patients’ health goals, preferences, and values.(Level of Evidence: B-NR) " |
"2. Patients considering implantation of a new ICD or replacement of an existing ICD for a low battery should be informed of their individual risk of SCD and nonsudden death from HF or noncardiac conditions and the effectiveness, safety, and potential complications of the ICD in light of their health goals, preferences and values.(Level of Evidence: B-NR) " |