Cardiac catheterization pre-procedure evaluation resident survival guide: Difference between revisions
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{{CMG}}; {{AE}} {{YD}} | {{CMG}}; {{AE}} {{YD}}; {{TA}} | ||
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! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | [[Cardiac catheterization pre-procedure evaluation resident survival guide#Do's|Do's]] | ! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | [[Cardiac catheterization pre-procedure evaluation resident survival guide#Do's|Do's]] | ||
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! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | [[Cardiac catheterization pre-procedure evaluation resident survival guide# | ! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | [[Cardiac catheterization pre-procedure evaluation resident survival guide#Don'ts|Don'ts]] | ||
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==Cardiac Catheterization Pre-procedure Evaluation== | ==Cardiac Catheterization Pre-procedure Evaluation== | ||
<span style="font-size:85%">Boxes in red signify that an urgent management is needed.</span> | |||
<span style="font-size:85%">'''Abbreviations:''' '''ASA:''' [[American society of anesthesiologists]]; '''BP:''' [[Blood Pressure]]; '''CCS:''' [[Canadian cardiovascular society]]; '''CrCl:''' [[Creatinine clearance]]; '''CXR:''' [[Chest X-ray]]; '''DNI:''' [[Do not intubate]]; '''DNR:''' [[Do not resuscitate]]; '''ECG:''' [[Electrocardiogram]]; '''eGFR:''' [[estimated glomerular filtration rate]]; '''HR:'''[[Heart rate]]; '''INR:''' [[International normalized ratio]]; '''LMWH:''' [[Low molecular weight heparin]]; '''LV:''' [[Left ventricle]]; '''LVED:''' [[Left ventricular ejection fraction]]; '''NOAC:''' [[Novel oral anticoagulant]]; '''NPO:''' [[Nothing per os]]; '''PMI:''' [[Point of maximal impulse]]; '''PT:''' [[Prothrombin time]]; '''RR:''' [[Respiratory rate]]; '''SpO2:''' [[Oxygen saturation]]; '''T:''' [[Temperature]]; '''VT:''' [[Ventricular tachycardia]]</span> | |||
{{familytree/start}} | {{familytree/start}} | ||
{{familytree | | | A01 | | | | | | | | | | | | | | | | | | | | | | | |A01=Is cardiac catheterization an emergency?}} | {{familytree | | | A01 | | | | | | | | | | | | | | | | | | | | | | | |A01=Is cardiac catheterization an emergency?}} | ||
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{{familytree | | | | | C02 | | | | | | | | | | | | | | | | | | | | | |C02=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Confirm that the patient has ANY of the following indications for cardiac catheterization'''<br><br> | {{familytree | | | | | C02 | | | | | | | | | | | | | | | | | | | | | |C02=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Confirm that the patient has ANY of the following indications for cardiac catheterization'''<br><br> | ||
'''''Left heart catheterization'''''<br> | '''''Left heart catheterization'''''<br> | ||
❑ | ❑ CCS class III (i.e. symptoms with everyday living activities) or class IV [[angina]] (i.e. inability to perform any activity without angina or angina at rest) despite medical therapy, '''OR'''<br> | ||
❑ Angina plus systolic dysfunction, '''OR'''<br> | ❑ Angina plus [[systolic dysfunction]], '''OR'''<br> | ||
❑ Uncertain diagnosis following non-invasive test and need to confirm diagnosis, '''OR'''<br> | ❑ Uncertain diagnosis following [[non-invasive test]] and need to confirm diagnosis, '''OR'''<br> | ||
❑ Systolic dysfunction with unexplained cause, '''OR'''<br> | ❑ [[Systolic dysfunction]] with unexplained cause, '''OR'''<br> | ||
❑ Survivor of sudden cardiac death, polymorphic VT, or sustained monomorphic VT, '''OR'''<br> | ❑ Survivor of [[sudden cardiac death]], [[polymorphic VT]], or [[sustained monomorphic VT]], '''OR'''<br> | ||
❑ Suspected spasm or non-atherosclerotic cause of ischemia, '''OR'''<br> | ❑ Suspected [[coronary spasm|spasm]] or non-atherosclerotic cause of ischemia, '''OR'''<br> | ||
❑ High-risk stress test finding, defined as '''ANY''' of following <ref name="pmid22326193">{{cite journal| author=Marso SP, Teirstein PS, Kereiakes DJ, Moses J, Lasala J, Grantham JA| title=Percutaneous coronary intervention use in the United States: defining measures of appropriateness. | journal=JACC Cardiovasc Interv | year= 2012 | volume= 5 | issue= 2 | pages= 229-35 | pmid=22326193 | doi=10.1016/j.jcin.2011.12.004 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22326193 }} </ref>:<br> | ❑ High-risk [[stress test]] finding, defined as '''ANY''' of following <ref name="pmid22326193">{{cite journal| author=Marso SP, Teirstein PS, Kereiakes DJ, Moses J, Lasala J, Grantham JA| title=Percutaneous coronary intervention use in the United States: defining measures of appropriateness. | journal=JACC Cardiovasc Interv | year= 2012 | volume= 5 | issue= 2 | pages= 229-35 | pmid=22326193 | doi=10.1016/j.jcin.2011.12.004 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22326193 }} </ref>:<br> | ||
:❑ Resting LVEF < 35% | :❑ Resting [[LVEF]] < 35% | ||
:❑ High-risk treadmill score (≤ 11) | :❑ High-risk [[treadmill score]] (≤ 11) | ||
:❑ Severe exercise LVEF < 35% | :❑ Severe [[exercise LVEF]] < 35% | ||
:❑ Stress-induced large perfusion defect | :❑ Stress-induced large [[perfusion defect]] | ||
:❑ Stress-induced multiple perfusion | :❑ Stress-induced multiple [[perfusion defect]]s | ||
:❑ Large, fixed perfusion defect with LV dilation OR increased lung uptake | :❑ Large, fixed perfusion defect with [[LV dilation]] OR increased [[lung uptake]] | ||
:❑ LV dilation or increased lung uptake | :❑ [[LV dilation]] or increased [[lung uptake]] | ||
:❑ Stress-induced moderate perfusion defect with LV dilation or increased lung uptake<br><br> | :❑ Stress-induced moderate perfusion defect with [[LV dilation]] or increased [[lung uptake]]<br><br> | ||
'''''Right heart catheterization'''''<br> | '''''Right heart catheterization'''''<br> | ||
❑ Patient in shock with unknown volume status<br> | ❑ Patient in [[shock]] with unknown volume status<br> | ||
❑ Cardiogenic shock<br> | ❑ [[Cardiogenic shock]]<br> | ||
❑ Diagnosis of follow-up of pulmonary artery hypertension<br> | ❑ Diagnosis of follow-up of [[pulmonary artery hypertension]]<br> | ||
❑ Patients with advanced cardiopulmonary diseases who require surgery<br> | ❑ Patients with advanced [[cardiopulmonary diseases]] who require surgery<br> | ||
:❑ Left-to-right shunt<br> | :❑ [[Left-to-right shunt]]<br> | ||
:❑ Valvular disease<br> | :❑ [[Valvular disease]]<br> | ||
:❑ Pulmonary artery hypertension<br> | :❑ [[Pulmonary artery hypertension]]<br> | ||
:❑ Congenital heart disease</div> | :❑ [[Congenital heart disease]]</div> | ||
}} | }} | ||
{{familytree | | | | | |!| | | | | | | | | | | | | | | | | | | | | | |}} | {{familytree | | | | | |!| | | | | | | | | | | | | | | | | | | | | | |}} | ||
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'''''History of Present Illness'''''<br> | '''''History of Present Illness'''''<br> | ||
❑ Age<br> | ❑ [[Age]]<br> | ||
❑ Chest pain or chest discomfort<br> | ❑ [[Chest pain]] or [[chest discomfort]]<br> | ||
❑ Onset of symptoms<br> | ❑ Onset of symptoms<br> | ||
❑ Sensation of heaviness, tightness, pressure, or squeezing<br> | ❑ Sensation of [[heaviness]], [[tightness]], [[pressure]], or [[squeezing]]<br> | ||
❑ Duration of each episode<br> | ❑ Duration of each episode<br> | ||
❑ Radiation to the left arm, jaw, neck, right arm, back or epigastrium<br> | ❑ Radiation to the [[left arm]], [[jaw]], [[neck]], [[right arm]], [[back]], or [[epigastrium]]<br> | ||
❑ Timing of symptoms (morning vs. evening vs. wake patient at night)<br> | ❑ Timing of symptoms (morning vs. evening vs. wake patient at night)<br> | ||
❑ Alleviating | ❑ [[Alleviating factor]]s (e.g. [[medication]]s or [[rest]])<br> | ||
❑ Exacerbating | ❑ [[Exacerbating factor]]s<br> | ||
❑ Association of symptoms | ❑ Association of symptoms with food intake<br> | ||
❑ Palpitations<br> | ❑ [[Palpitations]]<br> | ||
❑ Nausea or vomiting<br> | ❑ [[Nausea]] or [[vomiting]]<br> | ||
❑ Sweating<br> | ❑ [[Sweating]]<br> | ||
❑ Dyspnea<br> | ❑ [[Dyspnea]]<br> | ||
❑ Orthopnea<br> | ❑ [[Orthopnea]]<br> | ||
❑ Dizziness<br> | ❑ [[Dizziness]]<br> | ||
❑ Weakness of extremities<br> | ❑ [[Weakness]] of extremities<br> | ||
❑ Numbness | ❑ [[Numbness]] or [[tingling]] of extremities<br> | ||
❑ Lightheadedness<br> | ❑ [[Lightheadedness]]<br> | ||
❑ Syncope or presyncope<br> | ❑ [[Syncope]] or [[presyncope]]<br> | ||
❑ Increased frequency of symptoms<br> | ❑ Increased frequency of symptoms<br> | ||
❑ Worsening of | ❑ Worsening of [[severity]]<br> | ||
❑ Previous episodes<br> | ❑ Previous episodes<br> | ||
❑ Recent | ❑ Recent [[infection]]s<br> | ||
❑ Fever<br> | ❑ [[Fever]]<br> | ||
❑ Weight or appetite | ❑ [[Weight change|Weight]] or [[appetite change]]s<br> | ||
❑ Stress<br> | ❑ [[Stress]]<br> | ||
❑ Fatigue<br><br> | ❑ [[Fatigue]]<br><br> | ||
'''''Possible Symptom Triggers'''''<br> | '''''Possible Symptom Triggers'''''<br> | ||
❑ Physical exertion<br> | ❑ [[Physical exertion]]<br> | ||
❑ Air pollution or fine particulate matter<br> | ❑ [[Air pollution]] or fine particulate matter<br> | ||
❑ Recent infection<br> | ❑ Recent [[infection]]<br> | ||
❑ Heavy meal intake<br> | ❑ [[Heavy meal intake]]<br> | ||
❑ Cocaine<br> | ❑ [[Cocaine]]<br> | ||
❑ Marijuana<br><br> | ❑ [[Marijuana]]<br><br> | ||
'''''Cardiovascular Risk Factors'''''<br> | '''''Cardiovascular Risk Factors'''''<br> | ||
❑ Known CAD (review available | ❑ Known [[CAD]] (review available [[cardiac catheterization]]s or [[CABG]] reports)<br> | ||
❑ Smoking history<br> | ❑ [[Smoking]] history<br> | ||
❑ Baseline blood pressure (Duration, antihypertensive therapy, compliance with medications)<br> | ❑ Baseline [[blood pressure]] (Duration, [[antihypertensive therapy]], compliance with medications)<br> | ||
❑ History of diabetes mellitus (Duration, DM control, compliance, antidiabetic | ❑ History of [[diabetes mellitus]] (Duration, DM control, compliance, [[antidiabetic medication]]s, recent [[HbA1C]], screening for [[Microvascular complications of diabetes|microvascular]] and [[Macrovascular complications of diabetes|macrovascular]] DM [[Complications of diabetes|complications]])<br> | ||
❑ Dyslipidemia<br> | ❑ [[Dyslipidemia]]<br> | ||
❑ Obesity (BMI > 30 kg/m2)<br><br> | ❑ [[Obesity]] ([[BMI]]> 30 kg/m2)<br><br> | ||
'''''Past Medical History'''''<br> | '''''Past Medical History'''''<br> | ||
❑ Congenital heart disease<br> | ❑ [[Congenital heart disease]]<br> | ||
❑ Left to right | ❑ [[Left to right shunt]]s<br> | ||
❑ Dextrocardia<br> | ❑ [[Dextrocardia]]<br> | ||
❑ Situs inversus<br> | ❑ [[Situs inversus]]<br> | ||
❑ History of renal disease (CrCl < 60 mL/min)? Does the patient currently have a stable renal function?<br> | ❑ History of [[renal disease]] ([[CrCl]] < 60 mL/min)? Does the patient currently have a [[stable renal function]]?<br> | ||
❑ History of bleeding tendency<br> | ❑ History of [[bleeding tendency]]<br> | ||
❑ Known significant anemia (Hct < 30%)<br> | ❑ Known significant [[anemia]] (Hct < 30%)<br> | ||
❑ History of heparin-induced thrombocytopenia (HIT)<br> | ❑ History of [[heparin-induced thrombocytopenia]] (HIT)<br> | ||
❑ History of pulmonary disease<br> | ❑ History of [[pulmonary disease]]<br> | ||
❑ History of major surgery in the past month<br> | ❑ History of [[major surgery]] in the past month<br> | ||
❑ Anticipated major surgery in the next year<br><br> | ❑ Anticipated [[major surgery]] in the next year<br><br> | ||
'''''Medications'''''<br> | '''''Medications'''''<br> | ||
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❑ Prescribed drug<br> | ❑ Prescribed drug<br> | ||
❑ Home oxygen therapy<br> | ❑ Home [[oxygen therapy]]<br> | ||
❑ Over-the-counter | ❑ [[Over-the-counter drug]]s<br> | ||
❑ | ❑ [[Herb]]s and [[supplement]]s<br> | ||
❑ Administration of ANY of the following medications within the last 48 hours prior to catheterization?<br> | ❑ Administration of ANY of the following medications within the last 48 hours prior to catheterization?<br> | ||
:❑ Aspirin | :❑ [[Aspirin]] | ||
:❑ Clopidogrel | :❑ [[Clopidogrel]] | ||
:❑ | :❑ [[Prasugrel]] | ||
:❑[[Ticagrelor]] | |||
:❑ Phosphodiesterase | :❑ [[Metformin]] | ||
:❑ Other [[oral antidiabetic agent]]s | |||
:❑ [[Insulin]] injections | |||
:❑ [[Phosphodiesterase inhibitor]]s (e.g. [[Tadalafil]], [[sildenafil]], or [[vardenafil]]) | |||
:❑ Warfarin. If yes, what is most recent INR? | :❑ [[Warfarin]]. If yes, what is most recent INR? | ||
:❑ Low molecular weight heparin (LMWH). If yes, when was last dose? | :❑ [[Unfractionated heparin]] or [[Low molecular weight heparin]] (LMWH). If yes, when was last dose? | ||
:❑ Other chronic | :❑ Other chronic [[anticoagualant]]s (e.g. [[dabigatran]], [[NOAC]]s)<br><br> | ||
'''''Allergies'''''<br> | '''''Allergies'''''<br> | ||
❑ List of allergies, including severity and manifestations (pruritus, rash, hives, stridor, or anaphylactic shock)<br> | ❑ List of allergies, including severity and manifestations ([[pruritus]], [[rash]], [[hives]], [[stridor]], or [[anaphylactic shock]])<br> | ||
❑ Known drug allergies | ❑ Known [[Drug allergy|drug allergies]] | ||
:❑ Allergy to aspirin or history of nasal | :❑ Allergy to [[aspirin]] or history of [[nasal polyp]]s or [[aspirin desensitization]] | ||
:❑ Allergy to heparin | :❑ Allergy to [[heparin]] | ||
:❑ Allergy to | :❑ Allergy to [sedative]]s | ||
:❑ Other drug allergies | :❑ Other [[Drug allergy|drug allergies]] | ||
:❑ Contrast allergy | :❑ [[Contrast allergy]] | ||
:❑ Latex allergy | :❑ [[Latex allergy]] | ||
:❑ Allergy to | :❑ [[Shellfish allergy|Allergy to shellfish]] (controversial association between shellfish allergy and contrast allergy) | ||
:❑ Other known environmental and food allergies<br><br> | :❑ Other known environmental and food allergies<br><br> | ||
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'''''Family History'''''<br> | '''''Family History'''''<br> | ||
❑ Family history of premature cardiovascular | ❑ Family history of premature [[cardiovascular disease]]s<br><br> | ||
'''''Social and Sexual History'''''<br> | '''''Social and Sexual History'''''<br> | ||
❑ Healthcare proxy and available family members for patient care<br> | ❑ [[Healthcare proxy]] and available family members for patient care<br> | ||
❑ Barrier to tolerate or adhere to dual antiplatelet therapy (DAPT) or follow-up visits<br> | ❑ Barrier to tolerate or adhere to [[dual antiplatelet therapy]] (DAPT) or follow-up visits<br> | ||
❑ Pregnancy or possible pregnancy<br><br> | ❑ [[Pregnancy]] or possible pregnancy<br><br> | ||
'''''Advanced Directives'''''<br> | '''''Advanced Directives'''''<br> | ||
❑ DNR status<br> | ❑ [[Do not resuscitate|DNR]] status<br> | ||
❑ DNI status</div>}} | ❑ [[Do not intubate|DNI]] status</div>}} | ||
{{familytree | | | | | |!| | | | | | | | | | | | | | | | | | | | | | |}} | {{familytree | | | | | |!| | | | | | | | | | | | | | | | | | | | | | |}} | ||
{{familytree | | | | | E01 | | | | | | | | | | | | | | | | | | | | | |E01=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Examine the patient'''<br><br> | {{familytree | | | | | E01 | | | | | | | | | | | | | | | | | | | | | |E01=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Examine the patient'''<br><br> | ||
❑ Vital signs, including BP, HR, RR, T, room air SpO2<br> | ❑ [[Vital signs]], including [[Blood pressure|BP]], [[Heart rate|HR]], [[Respiratory rate|RR]], [[Temperature|T]], room air [[Oxygen saturation|SpO2]]<br> | ||
❑ Height (in meters), weight (in kilograms), and body mass index (BMI)<br> | ❑ [[Height]] (in meters), [[weight]] (in kilograms), and [[body mass index]] (BMI)<br> | ||
❑ Level of consciousness, orientation, and ability to cooperate and communicate<br><br> | ❑ Level of [[consciousness]], [[orientation]], and ability to cooperate and communicate<br><br> | ||
'''''Skin'''''<br> | '''''Skin'''''<br> | ||
❑ Xanthelesma or xanthoma (suggestive of dyslipidemia)<br> | ❑ [[Xanthelesma]] or [[xanthoma]] (suggestive of [[dyslipidemia]])<br> | ||
❑ Edema (suggestive of congestive heart failure)<br> | ❑ [[Edema]] (suggestive of renal insufficiency or [[congestive heart failure]])<br> | ||
❑ Acral and/or central cyanosis<br><br> | ❑ [[Acral cyanosis|Acral]] and/or [[central cyanosis]]<br><br> | ||
'''''HEENT'''''<br> | '''''HEENT'''''<br> | ||
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❑ Modified Mallampati score<br> | ❑ Modified Mallampati score<br> | ||
:❑ Class I: Soft palate, uvula, fauces, pillars visible | :❑ Class I: [[Soft palate]], [[uvula]], [[fauces]], [[pillars]] visible | ||
:❑ Class II: Soft palate, uvula, fauces visible | :❑ Class II: [[Soft palate]], [[uvula]], [[fauces]] visible | ||
:❑ Class III: Soft palate, base of uvula present | :❑ Class III: [[Soft palate]], base of [[uvula]] present | ||
:❑ Class IV: Only hard palate visible<br><br> | :❑ Class IV: Only [[hard palate]] visible<br><br> | ||
'''''Cardiothoracic'''''<br> | '''''Cardiothoracic'''''<br> | ||
❑ Auscultation of heart sounds (including number of sounds, pitch, interval, murmurs, gallops, or rubs) over 4 precordial regions in sitting position (stethoscope diaphragm) and auscultation of mitral area while in left lateral decubitus position (stethoscope bell)<br> | ❑ Auscultation of heart sounds (including number of sounds, pitch, interval, murmurs, gallops, or rubs) over 4 precordial regions in sitting position (stethoscope diaphragm) and auscultation of [[mitral area]] while in [[left lateral decubitus]] position (stethoscope bell)<br> | ||
:❑ Normal S1 and S2 | :❑ Normal S1 and S2 | ||
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:❑ Murmur may be physiologic or may suggest valvulopathy or hemodynamic derangement (e.g. anemia) | :❑ Murmur may be physiologic or may suggest valvulopathy or hemodynamic derangement (e.g. anemia) | ||
:❑ Pericardial friction rub may suggest pericarditis<br> | :❑ [[Pericardial friction rub]] may suggest [[pericarditis]]<br> | ||
❑ Point of maximal impulse (PMI) (normally one, non-sustained, tapping impulse per cardiac cycle located less than 2-3 cm from midclavicular line at 5th intercostal space)<br> | ❑ [[Point of maximal impulse]] (PMI) (normally one, non-sustained, tapping impulse per cardiac cycle located less than 2-3 cm from [[midclavicular line]] at 5th intercostal space)<br> | ||
❑ Auscultation of anterior and posterior | ❑ Auscultation of anterior and posterior [[pulmonic region]]s bilaterally<br> | ||
:❑ | :❑ [[Crackle]]s suggest [[pulmonary edema]], which might be attributed to [[congestive heart failure]] | ||
:❑ If pulmonary auscultation abnormal, egophony, tactile fremitus, and thoracic percussion may be needed<br><br> | :❑ If [[pulmonary auscultation]] is abnormal, [[egophony]], [[tactile fremitus]], and [[thoracic percussion]] may be needed<br><br> | ||
'''''Vascular'''''<br> | '''''Vascular'''''<br> | ||
❑ | ❑ [[Pulse]]s of both upper extremities ([[Radial artery|radial]], [[Ulnar artery|ulnar]], [[Brachial artery|brachial]]) and lower extremities ([[dorsalis pedis]], [[posterior tibial]], [[Popliteal artery|popliteal]])<br> | ||
❑ Femoral | ❑ [[Femoral pulse]]s bilaterally<br> | ||
❑ Femoral auscultation bilaterally for | ❑ [[Femoral auscultation]] bilaterally for [[bruit]]s<br> | ||
❑ Modified Allen test bilaterally to evaluate adequacy of radial access<br> | ❑ Modified Allen test bilaterally to evaluate adequacy of radial access<br> | ||
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'''''Neurological'''''<br> | '''''Neurological'''''<br> | ||
❑ Upper/lower extremity motor strength | ❑ Upper/lower extremity [[motor strength]]<br> | ||
❑ | ❑ Upper/lower extremity [[sensory exam]]<br> | ||
❑ | ❑ [[Spasticity]] or [[rigidity]]<br> | ||
❑ | ❑ [[Deep tendon reflexes]]<br> | ||
❑ | ❑ Bilateral [[Babinski]]<br> | ||
❑ Coordination and cerebellar | ❑ [[Cranial nerves]] assessment<br> | ||
❑ Coordination and [[cerebellar exam]]s ([[Finger to nose]], [[Romberg]], [[heel to shin]], [[alternating movement]])<br> | |||
❑ Gait</div>}} | ❑ [[Gait]]</div>}} | ||
{{familytree | | | | | |!| | | | | | | | | | | | | | | | | | | | | | |}} | {{familytree | | | | | |!| | | | | | | | | | | | | | | | | | | | | | |}} | ||
{{familytree | | | | | F01 | | | | | | | | | | | | | | | | | | | | | |F01=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Provide appropriate counseling before catheterization'''<br><br> | {{familytree | | | | | F01 | | | | | | | | | | | | | | | | | | | | | |F01=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Provide appropriate counseling before catheterization'''<br><br> | ||
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''Warfarin''<br> | ''Warfarin''<br> | ||
❑ Hold warfarin for at least 2 to 6 days before elective coronary angiography (to prevent bleeding)<br> | ❑ Hold [[warfarin]] for at least 2 to 6 days before elective coronary angiography (to prevent bleeding)<br> | ||
❑ Confirm INR < 1.8 (preferable INR < 1.4) within 24 hours before arterial puncture<br> | ❑ Confirm [[INR]] < 1.8 (preferable INR < 1.4) within 24 hours before arterial puncture<br> | ||
❑ Restart warfarin 12 to 24 hours following catheterization (warfarin requires 2 to 3 days for INR to become therapeutic range)<br> | ❑ Restart [[warfarin]] 12 to 24 hours following catheterization (warfarin requires 2 to 3 days for INR to become therapeutic range)<br> | ||
❑ Consider heparin bridging 3 days before planned catheterization for high risk patients to prevent prolonged subtherapeutic INR<br> | ❑ Consider [[heparin bridging]] 3 days before planned catheterization for high risk patients to prevent prolonged subtherapeutic INR<br> | ||
:❑ Therapeutic dose LMWH 1 mg/kg | :❑ Therapeutic dose [[LMWH]] 1 mg/kg [[subcutaneous]]ly twice daily for high-risk patients who are not at high risk of bleeding | ||
:❑ Intermediate dose LMWH 40 mg | :❑ Intermediate dose [[LMWH]] 40 mg [[subcutaneous]]ly twice daily for high-risk patients at high risk of bleeding<br><br> | ||
''Novel Oral Anticoagulants''<br> | ''Novel Oral Anticoagulants''<br> | ||
❑ Hold NOAC before catheterization as follow<br> | ❑ Hold [[NOAC]] before catheterization as follow<br> | ||
❑ Rivaroxaban: Hold rivaroxaban for 2 days in patients with low bleeding risk OR for 3 days in patients with high bleeding risk<br> | ❑ [[Rivaroxaban]]: Hold rivaroxaban for 2 days in patients with low bleeding risk OR for 3 days in patients with high bleeding risk<br> | ||
❑ Apixaban: Hold apixaban for 2 days in patients with low bleeding risk OR for 3 days in patients with high bleeding risk<br> | ❑ [[Apixaban]]: Hold apixaban for 2 days in patients with low bleeding risk OR for 3 days in patients with high bleeding risk<br> | ||
❑ If patient does not develop any hematoma, restart NOAC 1 day after the catheterization for patients with low bleeding risk OR 2-3 days after the catheterization for patients with high bleeding risk<br><br> | ❑ If patient does not develop any hematoma, restart NOAC 1 day after the catheterization for patients with low bleeding risk OR 2-3 days after the catheterization for patients with high bleeding risk<br><br> | ||
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''Dabigatran''<br> | ''Dabigatran''<br> | ||
❑ Hold dabigatran based on renal function as shown below<br> | ❑ Hold [[dabigatran]] based on renal function as shown below<br> | ||
:❑ CrCl > 50 ml/min: Hold dabigatran for 1 day if low/intermediate bleeding risk or 3 days if high bleeding risk (e.g. major surgery) | :❑ [[CrCl]] > 50 ml/min: Hold dabigatran for 1 day if low/intermediate bleeding risk or 3 days if high bleeding risk (e.g. major surgery) | ||
:❑ CrCl between 30 and 50 ml/min: Hold dabigatran for 3 days if low/intermediate bleeding risk or 5 days if high bleeding risk (e.g. major surgery) | :❑ CrCl between 30 and 50 ml/min: Hold dabigatran for 3 days if low/intermediate bleeding risk or 5 days if high bleeding risk (e.g. major surgery) | ||
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''LMWH''<br> | ''LMWH''<br> | ||
❑ Hold LMWH for 12 hours before cardiac catheterization<br> | ❑ Hold [[LMWH]] for 12 hours before cardiac catheterization<br> | ||
❑ Resume LMWH 12-24 hours following cardiac catheterization<br><br> | ❑ Resume LMWH 12-24 hours following cardiac catheterization<br><br> | ||
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''Phosphodiesterase inhibitors''<br> | ''Phosphodiesterase inhibitors''<br> | ||
❑ Hold sildenafil/tadalafil/vardenafil for at least 2 days before elective | ❑ Hold [[sildenafil]]/[[tadalafil]]/[[vardenafil]] for at least 2 days before elective cardiac catheterization<br> | ||
❑ Restart sildenafil/tadalafil/vardenafil one day after catheterization</div>}} | ❑ Restart sildenafil/tadalafil/vardenafil one day after catheterization</div>}} | ||
{{familytree | | | | | |!| | | | | | | | | | | | | | | | | | | | | | |}} | {{familytree | | | | | |!| | | | | | | | | | | | | | | | | | | | | | |}} | ||
{{familytree | | | | | G01 | | | | | | | | | | | | | | | | | | | | | |G01=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Identify ASA physical status'''<br> | {{familytree | | | | | G01 | | | | | | | | | | | | | | | | | | | | | |G01=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Identify ASA physical status'''<br> | ||
❑ 1=Healthy individual with no systemic | ❑ 1=Healthy individual with no [[systemic disease]]s<br> | ||
❑ 2=Mild systemic disease<br> | ❑ 2=Mild [[systemic disease]]<br> | ||
❑ 3=Severe systemic disease<br> | ❑ 3=Severe [[systemic disease]]<br> | ||
❑ 4=Severe systemic disease that poses a constant | ❑ 4=Severe [[systemic disease]] that poses a constant threat to the patient’s life<br> | ||
❑ 5=Moribund patient not expected to survive | ❑ 5=[[Moribund patient]] not expected to survive without the operation/procedure<br> | ||
❑ 6=Patient declared brain-dead or whose organs are being removed for donation</div>}} | ❑ 6=Patient declared brain-dead or whose organs are being removed for donation</div>}} | ||
{{familytree | | | |,|-|^|-|.| | | | | | | | | | | | | | | | | | | | |}} | {{familytree | | | |,|-|^|-|.| | | | | | | | | | | | | | | | | | | | |}} | ||
{{familytree | | | I01 | | I02 | | | | | | | | | | | | | | | | | | | |I01=ASA physical status ≥ 4|I02=ASA physical status < 4}} | {{familytree | | | I01 | | I02 | | | | | | | | | | | | | | | | | | | |I01=[[ASA physical status]] ≥ 4|I02=[[ASA physical status]] < 4}} | ||
{{familytree | | | |!| | | |!| | | | | | | | | | | | | | | | | | | | |}} | {{familytree | | | |!| | | |!| | | | | | | | | | | | | | | | | | | | |}} | ||
{{familytree | | | J01 | | |!| | | | | | | | | | | | | | | | | | | | |J01=Consult anesthesia}} | {{familytree | | | J01 | | |!| | | | | | | | | | | | | | | | | | | | |J01=Consult [[anesthesia]]}} | ||
{{familytree | | | |`|-|v|-|'| | | | | | | | | | | | | | | | | | | | |}} | {{familytree | | | |`|-|v|-|'| | | | | | | | | | | | | | | | | | | | |}} | ||
{{familytree | | | | | K01 | | | | | | | | | | | | | | | | | | | | | |K01=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Perform pre-procedure routine work-up'''<br> | {{familytree | | | | | K01 | | | | | | | | | | | | | | | | | | | | | |K01=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Perform pre-procedure routine work-up'''<br> | ||
❑ Complete blood count (CBC)<br> | ❑ [[Complete blood count]] (CBC)<br> | ||
❑ Platelet count (Administration of unfractionated heparin, low molecular weight | ❑ [[Platelet count]] (Administration of [[unfractionated heparin]], [[low molecular weight heparin]], and parenteral [[glycoprotein 2b3a inhibitor]]s are associated with thrombocytopenia. [[Thrombocytopenia]] is a contraindication to the administration of parenteral glycoprotein 2b3a inhibitors)<br> | ||
❑ Electrolytes panel<br> | ❑ [[Electrolytes panel]]<br> | ||
❑ Baseline serum creatinine and BUN. Calculate and record estimated creatinine clearance/eGFR (creatinine clearance/eGFR may significantly be different from true GFR in patients with unstable renal function) <br> | ❑ Baseline serum [[creatinine]] and [[BUN]]. Calculate and record estimated [[creatinine clearance]]/[[eGFR]] (creatinine clearance/eGFR may significantly be different from true GFR in patients with unstable [[renal function]]) <br> | ||
❑ Glycemia<br> | ❑ [[Glycemia]]<br> | ||
❑ | ❑ [[ß-HCG]] within 2 weeks of procedure for women of child-bearing age<br> | ||
❑ Baseline ECG within 24 hours of procedure | ❑ Baseline [[ECG]] within 24 hours of procedure | ||
:❑ Assess baseline ischemic changes | :❑ Assess baseline ischemic changes | ||
:❑ Presence of baseline bundle branch block (BBB) (Cardiac catheterization may damage HIS | :❑ Presence of baseline [[bundle branch block]] (BBB) (Cardiac catheterization may damage HIS system and induce BBB)<br> | ||
❑ PT/INR within 24 hours, especially if patient is receiving warfarin (INR > 1.8 is a relative contraindication of cardiac catheterization)<br> | ❑ [[PT]]/[[INR]] within 24 hours, especially if patient is receiving [[warfarin]] (INR > 1.8 is a relative contraindication of cardiac catheterization)<br> | ||
❑ CXR if patient suspected to have pulmonary edema or other diseases</div>}} | ❑ [[CXR]] if patient suspected to have pulmonary edema or other diseases</div>}} | ||
{{familytree | | | | | |!| | | | | | | | | | | | | | | | | | | | | | |}} | {{familytree | | | | | |!| | | | | | | | | | | | | | | | | | | | | | |}} | ||
{{familytree | | | | | L01 | | | | | | | | | | | | | | | | | | | | | |L01=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Address relevant and significant comorbidities'''<br><br> | {{familytree | | | | | L01 | | | | | | | | | | | | | | | | | | | | | |L01=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Address relevant and significant comorbidities'''<br><br> | ||
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❑ Prolonged INR (>1.8) 24 hours prior to procedure<br> | ❑ Prolonged INR (>1.8) 24 hours prior to procedure<br> | ||
:❑ Administer low-dose vitamin K 1-2 mg PO | :❑ Administer low-dose [[vitamin K]] 1-2 mg PO | ||
:❑ Repeat INR and confirm new INR < 1.8 (preferable INR ≤ 1.4). If INR still > 1.8 | :❑ Repeat INR and confirm new INR < 1.8 (preferable INR ≤ 1.4). If INR still > 1.8 | ||
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::❑ Administer additional vitamin K 2-4 mg PO if anticipated procedure is > 24 hours later. Administer more doses of low-dose vitamin K (1-2 mg PO) if INR still high | ::❑ Administer additional vitamin K 2-4 mg PO if anticipated procedure is > 24 hours later. Administer more doses of low-dose vitamin K (1-2 mg PO) if INR still high | ||
::❑ Cancel transfemoral approach (except if emergency) if INR does not normalize in time of procedure | ::❑ Cancel [[transfemoral approach]] (except if emergency) if INR does not normalize in time of procedure | ||
::❑ Consider transradial approach if radial artery accessible to reduce risk of bleeding | ::❑ Consider transradial approach if radial artery accessible to reduce risk of bleeding | ||
::❑ Consider transfusion of fresh frozen plasma (FFP)<br> | ::❑ Consider [[transfusion]] of [[fresh frozen plasma]] (FFP)<br> | ||
❑ Renal insufficiency (CrCl < 60 ml/min)<br> | ❑ [[Renal insufficiency]] (CrCl < 60 ml/min)<br> | ||
:❑ Saline administration | :❑ [[Saline]] administration | ||
::❑ In patients with no CHF, administer 0.9% or 0.45% normal saline: 1 mL/ kg/ hour (MAX 100 ml/hour) for 12 hours before contrast '''AND''' 12 hours after contrast) in patients with no CHF | ::❑ In patients with no [[CHF]], administer 0.9% or 0.45% normal saline: 1 mL/ kg/ hour (MAX 100 ml/hour) for 12 hours before contrast '''AND''' 12 hours after contrast) in patients with no CHF | ||
::❑ In patients with CHF, administer 0.45% normal saline: 0.5 ml/kg/hr (MAX 50 ml/hr) 12 hrs before contrast '''AND''' 12 hours after contrast | ::❑ In patients with CHF, administer 0.45% normal saline: 0.5 ml/kg/hr (MAX 50 ml/hr) 12 hrs before contrast '''AND''' 12 hours after contrast | ||
:❑ Consider administration of NaHCO3 | :❑ Consider administration of [[sodium bicarbonate]] ([[NaHCO3]]) | ||
::❑ Mix 150 mEq of NaHCO3 in 1 liter of D5W in non-diabetic patients OR mix 150 mEq of NaHCO3 in 1 liter of sterile water in diabetic | ::❑ Mix 150 mEq of NaHCO3 in 1 liter of D5W in non-diabetic patients OR mix 150 mEq of NaHCO3 in 1 liter of sterile water in [[diabetic patient]]s. | ||
::❑ Administer 3 ml/kg bolus (MAX 300 ml) for 1 hour prior to procedure AND 1 mL/kg/hour (MAX 100 ml/hr) during the procedure AND 1 mg/kg/hour for 6 hours post-procedure | ::❑ Administer 3 ml/kg [[bolus]] (MAX 300 ml) for 1 hour prior to procedure AND 1 mL/kg/hour (MAX 100 ml/hr) during the procedure AND 1 mg/kg/hour for 6 hours post-procedure | ||
:❑ Follow-up serum creatinine 2 to 5 days following catheterization<br> | :❑ Follow-up serum creatinine 2 to 5 days following catheterization<br> | ||
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:❑ Regimen 1 | :❑ Regimen 1 | ||
::❑ Methylprednisolone 60 mg IV once, '''AND''' | ::❑ [[Methylprednisolone]] 60 mg IV once, '''AND''' | ||
::❑ Diphenhydramine 50 mg IV once, '''AND''' | ::❑ [[Diphenhydramine]] 50 mg IV once, '''AND''' | ||
::❑ Cimetidine 300 mg (or alternative H2 blocker) IV once | ::❑ [[Cimetidine]] 300 mg (or alternative H2 blocker) IV once | ||
:❑ Regimen 2 | :❑ Regimen 2 | ||
::❑ Prednisolone 50 mg PO at 13 hours, 7 hours, and 1 hour (total of 3 doses) before procedure</div>}} | ::❑ [[Prednisolone]] 50 mg PO at 13 hours, 7 hours, and 1 hour (total of 3 doses) before procedure</div>}} | ||
{{familytree | | | | | |!| | | | | | | | | | | | | | | | | | | | | | |}} | {{familytree | | | | | |!| | | | | | | | | | | | | | | | | | | | | | |}} | ||
{{familytree | | | | | M01 | | | | | | | | | | | | | | | | | | | | | |M01=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Confirm pre-cath checklist on the day of the procedure''' | {{familytree | | | | | M01 | | | | | | | | | | | | | | | | | | | | | |M01=<div style="float: left; text-align: left; width: 18em; padding:1em;">'''Confirm pre-cath checklist on the day of the procedure''' | ||
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'''''Antiplatelet therapy'''''<br> | '''''Antiplatelet therapy'''''<br> | ||
''Aspirin''<br> | ''Aspirin''<br> | ||
❑ Administer aspirin 325 mg PO once at least 2 hours before any cardiac catheterization procedure<br> | ❑ Administer [[aspirin]] 325 mg PO once at least 2 hours before any cardiac catheterization procedure<br> | ||
''Thienopyridine'' should be administered '''ONLY''' when there is intention for PCI or high likelihood to perform PCI during left heart catheterization. Generally, right heart catheterizations do not require administration of thienopyridine <br> | ''Thienopyridine''<br> | ||
A [[thienopyridine]] should be administered '''ONLY''' when there is intention for PCI or high likelihood to perform PCI during left heart catheterization. Generally, right heart catheterizations do not require administration of thienopyridine <br> | |||
❑ Administer '''ANY''' of the following thienopyridines at least 2 to 6 hours before the procedure ONLY when there is intention for PCI or high likelihood to perform PCI: <br> | ❑ Administer '''ANY''' of the following thienopyridines at least 2 to 6 hours before the procedure ONLY when there is intention for PCI or high likelihood to perform PCI: <br> | ||
:❑ Clopidogrel 600 mg (loading dose) PO once, '''OR''' | :❑ [[Clopidogrel]] 600 mg ([[loading dose]]) PO once, '''OR''' | ||
:❑ Prasugrel 60 mg (loading dose) PO once, '''OR''' | :❑ [[Prasugrel]] 60 mg ([[loading dose]]) PO once, '''OR''' | ||
:❑ Ticagrelor 180 mg (loading dose) PO once<br><br> | :❑ [[Ticagrelor]] 180 mg ([[loading dose]]) PO once<br><br> | ||
'''''Conscious Sedation'''''<br> | '''''Conscious Sedation'''''<br> | ||
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'''''Consider antihistamine'''''<br> | '''''Consider antihistamine'''''<br> | ||
❑ Consider administration of diphenhydramine (Bendaryl) 25 mg PO once<br><br> | ❑ Consider administration of [[diphenhydramine]] ([[Bendaryl]]) 25 mg PO once<br><br> | ||
'''''Consider anti-nausea agents'''''<br> | '''''Consider anti-nausea agents'''''<br> | ||
❑ Consider administration of ondansetron (Zofran) 4 mg IV once</div>}} | ❑ Consider administration of [[ondansetron]] ([[Zofran]]) 4 mg IV once</div>}} | ||
{{familytree | | | | | |!| | | | | | | | | | | | | | | | | | | | | | |}} | {{familytree | | | | | |!| | | | | | | | | | | | | | | | | | | | | | |}} | ||
{{familytree | | | | | O01 | | | | | | | | | | | | | | | | | | | | | |O01=Transfer patient to cath lab}} | {{familytree | | | | | O01 | | | | | | | | | | | | | | | | | | | | | |O01=Transfer patient to cath lab}} |
Latest revision as of 14:18, 20 April 2015
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Yazan Daaboul, M.D.; Turky Alkathery, M.D. [2]
Cardiac catheterization pre-procedure evaluation resident survival guide Microchapters |
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Overview |
Classification |
Pre-procedure Evaluation |
Do's |
Don'ts |
Overview
Cardiac catheterization is an endovascular procedure that aims to study cardiac function and anatomy, as well as to diagnose and treat acute cardiovascular diseases and evaluate surgical candidates. Cardiac catheterization may be either diagnostic (no intervention) or therapeutic (percutaneous coronary intervention or PCI). However, it may also be classified as coronary angiography (assess patency of coronary arteries), left heart catheterization (to assess blood flow, anatomy, and pressures in left heart chambers and to evaluate the anatomy and function of the mitral and aortic valves), or right heart catheterization (to assess blood flow, anatomy, and pressures in right heart chambers, anatomy and function of the tricuspid and pulmonic valves, pulmonary artery pressure, and pulmonary capillary wedge pressure). Determining emergency/urgency for revascularization dictates how extensive and how thorough the pre-cardiac catheterization management will be. In the case of emergencies (e.g. myocardial infarction), patient transfer to the catheterization laboratory and immediate revascularization (door-to-balloon) precede all other steps in management. In contrast, stable patients require a more extensive work-up pre-catheterization to minimize the risk of adverse events that may develop during or following the procedure.
Classification
Cardiac catheterization may be either:
- Diagnostic (no intervention), OR
- Therapeutic (percutaneous coronary intervention or PCI)
However, cardiac catheterization may also classified based on the cardiac structure in which the catheter is inserted:
Coronary Angiography
Insertion of the catheter into the coronary arteries. Coronary angiography assesses the patency of coronary arteries.
Left Heart Catheterization
Left heart catheterization (LHC) is the insertion of the catheter into the left ventricle. LHC is used to assess the following:
- Blood flow, anatomy, and pressures in left heart chambers
- The anatomy and function of the mitral and aortic valves
Right Heart Catheterization
Right heart catheterization (RHC) is the insertion of the catheter into the right ventricle and the pulmonary artery. RHC is used to assess the following:
- Blood flow, anatomy, and pressures in right heart chambers
- Anatomy and function of the tricuspid and pulmonic valves
- Pulmonary artery pressure
- Pulmonary capillary wedge pressure (PCWP)
Cardiac Catheterization Pre-procedure Evaluation
Boxes in red signify that an urgent management is needed.
Abbreviations: ASA: American society of anesthesiologists; BP: Blood Pressure; CCS: Canadian cardiovascular society; CrCl: Creatinine clearance; CXR: Chest X-ray; DNI: Do not intubate; DNR: Do not resuscitate; ECG: Electrocardiogram; eGFR: estimated glomerular filtration rate; HR:Heart rate; INR: International normalized ratio; LMWH: Low molecular weight heparin; LV: Left ventricle; LVED: Left ventricular ejection fraction; NOAC: Novel oral anticoagulant; NPO: Nothing per os; PMI: Point of maximal impulse; PT: Prothrombin time; RR: Respiratory rate; SpO2: Oxygen saturation; T: Temperature; VT: Ventricular tachycardia
Is cardiac catheterization an emergency? | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Yes | No | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Refer to management of acute coronary syndromes | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Confirm that the patient has ANY of the following indications for cardiac catheterization Left heart catheterization
Right heart catheterization ❑ Diagnosis of follow-up of pulmonary artery hypertension ❑ Patients with advanced cardiopulmonary diseases who require surgery | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Obtain a detailed history History of Present Illness ❑ Age ❑ Chest pain or chest discomfort ❑ Onset of symptoms ❑ Sensation of heaviness, tightness, pressure, or squeezing ❑ Duration of each episode ❑ Radiation to the left arm, jaw, neck, right arm, back, or epigastrium ❑ Timing of symptoms (morning vs. evening vs. wake patient at night) ❑ Alleviating factors (e.g. medications or rest) ❑ Association of symptoms with food intake ❑ Sweating ❑ Dyspnea ❑ Weakness of extremities ❑ Numbness or tingling of extremities ❑ Syncope or presyncope ❑ Increased frequency of symptoms ❑ Worsening of severity ❑ Previous episodes ❑ Recent infections ❑ Fever ❑ Weight or appetite changes ❑ Stress ❑ Fatigue Possible Symptom Triggers ❑ Air pollution or fine particulate matter ❑ Recent infection ❑ Cocaine Cardiovascular Risk Factors ❑ Known CAD (review available cardiac catheterizations or CABG reports) ❑ Smoking history ❑ Baseline blood pressure (Duration, antihypertensive therapy, compliance with medications) ❑ History of diabetes mellitus (Duration, DM control, compliance, antidiabetic medications, recent HbA1C, screening for microvascular and macrovascular DM complications) Past Medical History ❑ History of renal disease (CrCl < 60 mL/min)? Does the patient currently have a stable renal function? ❑ History of bleeding tendency ❑ Known significant anemia (Hct < 30%) ❑ History of heparin-induced thrombocytopenia (HIT) ❑ History of pulmonary disease ❑ History of major surgery in the past month ❑ Anticipated major surgery in the next year Medications ❑ Prescribed drug ❑ Home oxygen therapy ❑ Herbs and supplements ❑ Administration of ANY of the following medications within the last 48 hours prior to catheterization?
Allergies ❑ List of allergies, including severity and manifestations (pruritus, rash, hives, stridor, or anaphylactic shock) ❑ Known drug allergies
Family History ❑ Family history of premature cardiovascular diseases Social and Sexual History ❑ Healthcare proxy and available family members for patient care ❑ Barrier to tolerate or adhere to dual antiplatelet therapy (DAPT) or follow-up visits ❑ Pregnancy or possible pregnancy Advanced Directives ❑ DNR status | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Examine the patient ❑ Vital signs, including BP, HR, RR, T, room air SpO2 ❑ Height (in meters), weight (in kilograms), and body mass index (BMI) ❑ Level of consciousness, orientation, and ability to cooperate and communicate Skin ❑ Xanthelesma or xanthoma (suggestive of dyslipidemia) ❑ Edema (suggestive of renal insufficiency or congestive heart failure) ❑ Acral and/or central cyanosis HEENT ❑ Head and neck range of motion ❑ Modified Mallampati score
Cardiothoracic ❑ Auscultation of heart sounds (including number of sounds, pitch, interval, murmurs, gallops, or rubs) over 4 precordial regions in sitting position (stethoscope diaphragm) and auscultation of mitral area while in left lateral decubitus position (stethoscope bell)
❑ Point of maximal impulse (PMI) (normally one, non-sustained, tapping impulse per cardiac cycle located less than 2-3 cm from midclavicular line at 5th intercostal space) ❑ Auscultation of anterior and posterior pulmonic regions bilaterally
Vascular ❑ Pulses of both upper extremities (radial, ulnar, brachial) and lower extremities (dorsalis pedis, posterior tibial, popliteal) ❑ Femoral pulses bilaterally ❑ Femoral auscultation bilaterally for bruits ❑ Modified Allen test bilaterally to evaluate adequacy of radial access ❑ Carotid auscultation bilaterally ❑ Jugular venous pressure Neurological ❑ Upper/lower extremity motor strength ❑ Upper/lower extremity sensory exam ❑ Spasticity or rigidity ❑ Bilateral Babinski ❑ Cranial nerves assessment | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Provide appropriate counseling before catheterization ❑ Address individual concerns and questions ❑ Keep patient NPO at least 6 hours before elective coronary angiography Hold Certain Medications Before Procedure Warfarin ❑ Hold warfarin for at least 2 to 6 days before elective coronary angiography (to prevent bleeding) ❑ Confirm INR < 1.8 (preferable INR < 1.4) within 24 hours before arterial puncture ❑ Restart warfarin 12 to 24 hours following catheterization (warfarin requires 2 to 3 days for INR to become therapeutic range) ❑ Consider heparin bridging 3 days before planned catheterization for high risk patients to prevent prolonged subtherapeutic INR
Novel Oral Anticoagulants ❑ Hold NOAC before catheterization as follow ❑ Rivaroxaban: Hold rivaroxaban for 2 days in patients with low bleeding risk OR for 3 days in patients with high bleeding risk ❑ Apixaban: Hold apixaban for 2 days in patients with low bleeding risk OR for 3 days in patients with high bleeding risk ❑ If patient does not develop any hematoma, restart NOAC 1 day after the catheterization for patients with low bleeding risk OR 2-3 days after the catheterization for patients with high bleeding risk Dabigatran ❑ Hold dabigatran based on renal function as shown below
❑ CrCl < 30 ml/min: Hold dabigatran for 2 to 5 days if low/intermediate bleeding risk or > 5 days if high bleeding risk (e.g. major surgery) ❑ If patient does not develop any hematoma, restart dabigatran 1 day after the catheterization for patients with low bleeding risk OR 2-3 days after the catheterization for patients with high bleeding risk LMWH ❑ Hold LMWH for 12 hours before cardiac catheterization ❑ Resume LMWH 12-24 hours following cardiac catheterization Metformin ❑ Hold metformin 2 days before elective coronary angiography Phosphodiesterase inhibitors ❑ Hold sildenafil/tadalafil/vardenafil for at least 2 days before elective cardiac catheterization | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Identify ASA physical status ❑ 1=Healthy individual with no systemic diseases ❑ 2=Mild systemic disease ❑ 3=Severe systemic disease ❑ 4=Severe systemic disease that poses a constant threat to the patient’s life ❑ 5=Moribund patient not expected to survive without the operation/procedure | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
ASA physical status ≥ 4 | ASA physical status < 4 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Consult anesthesia | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Perform pre-procedure routine work-up ❑ Complete blood count (CBC) ❑ Platelet count (Administration of unfractionated heparin, low molecular weight heparin, and parenteral glycoprotein 2b3a inhibitors are associated with thrombocytopenia. Thrombocytopenia is a contraindication to the administration of parenteral glycoprotein 2b3a inhibitors) ❑ Baseline serum creatinine and BUN. Calculate and record estimated creatinine clearance/eGFR (creatinine clearance/eGFR may significantly be different from true GFR in patients with unstable renal function) ❑ Glycemia ❑ ß-HCG within 2 weeks of procedure for women of child-bearing age ❑ Baseline ECG within 24 hours of procedure
❑ PT/INR within 24 hours, especially if patient is receiving warfarin (INR > 1.8 is a relative contraindication of cardiac catheterization) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Address relevant and significant comorbidities ❑ Prolonged INR (>1.8) 24 hours prior to procedure
❑ Renal insufficiency (CrCl < 60 ml/min)
❑ Contrast allergy
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Confirm pre-cath checklist on the day of the procedure
❑ Confirm patient full name ❑ Planned procedure
❑ Appropriate history and physical examination documented in patient record ❑ Informed consent is filled within 30 days, complete, signed, and available in patient record ❑ Candidacy for DES
❑ Allergies and adverse drug reactions
❑ Medications
❑ ASA physical status available ❑ Modified mallampati score available ❑ Does patient have any contraindication to sedation? ❑ Patient's height (in meter) and weight (in kilograms) recorded?
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Administer Preprocedural Drugs Antiplatelet therapy ❑ Administer ANY of the following thienopyridines at least 2 to 6 hours before the procedure ONLY when there is intention for PCI or high likelihood to perform PCI:
Conscious Sedation
Consider antihistamine ❑ Consider administration of diphenhydramine (Bendaryl) 25 mg PO once Consider anti-nausea agents | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Transfer patient to cath lab | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Do's
- Perform a transradial approach instead of a transfemoral appraoach if radial artery is patent
- Hold anticoagulants, anti-diabetic agents, and phosphodiesterase inhibitors before the procedure
- Keep patient NPO at least 6 hours before the procedure
- Prepare the patient before the procedure if he is known to have contrast allergy, renal insufficiency, or diabetes mellitus
- Administer minimal among of contrast dye before a full injection to ensure the patient is not allergic or to confirm is adequately prepared
- Maintain the patient in a conscious state when administering sedatives
Don'ts
- Do not perform right heart catheterization (RHC) for routine management of pulmonary edema
- Do not perform RHC before a trial of intravascular volume expansion is attempted for low-risk patients
- Do not perform RHC for patients with certain cardiac tamponade, in whom RHC would delay treatment
- Do not perform RHC for patients with compensated heart failure undergoing low-risk non-cardiac surgery
- Do not administer thienopyridine if PCI will not be performed or unlikely to be performed during catheterization
- Do not remove compressive gauze at the site of injection before 24 hours of catheterization or before the patient is being discharged
- Do not insert the catheter at an infected site
- Do not perform catheterization if patient is pregnant (relative contraindication)
- Do not perform catheterization if the patient has uncontrolled hypertension or uncontrolled glycemia
References
- ↑ Marso SP, Teirstein PS, Kereiakes DJ, Moses J, Lasala J, Grantham JA (2012). "Percutaneous coronary intervention use in the United States: defining measures of appropriateness". JACC Cardiovasc Interv. 5 (2): 229–35. doi:10.1016/j.jcin.2011.12.004. PMID 22326193.