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{{familytree/start}}
{{familytree/start}}
{{familytree | | | | | | A01 | | | | | A01= '''Long term management'''}}
{{familytree | | | | | | A01 | | | | | A01= '''Long term management'''}}
{{familytree | | | |,|-|-|^|-|-|.| | |}}
{{familytree | |,|-|-|-|-|+|-|-|-|-|-|-|.| | |}}
{{familytree | | | B01 | | | | B02 | | B01= <div style="float: left; text-align: left; width: 24em; padding:1em;"> '''Single or infrequent episodes'''<br>
{{familytree | B01 | | | B02 | | | | | B03 | | B01= <div style="float: left; text-align: left; width: 24em; padding:1em;"> '''Single or infrequent episodes'''<br>
❑ No treatment ([[ACC AHA guidelines classification scheme|class I, level of evidence C]]) <br>
❑ No treatment ([[ACC AHA guidelines classification scheme|class I, level of evidence C]]) <br>
❑ [[Vagal maneuvers]] ([[ACC AHA guidelines classification scheme|class I, level of evidence B]]) <br>
❑ [[Vagal maneuvers]] ([[ACC AHA guidelines classification scheme|class I, level of evidence B]]) <br>
❑ Single-dose oral therapy (Pill-in-the-pocket) ([[ACC AHA guidelines classification scheme|class I, level of evidence B]]): <br>
:❑ [[Verapamil]] <br>
:❑ [[Diltiazem]] <br>
:❑ [[Beta blockers]], such as: [[Propanolol]] <br>
❑ [[Catheter ablation]] ([[ACC AHA guidelines classification scheme|class IIa, level of evidence B]]) <br>
❑ [[Catheter ablation]] ([[ACC AHA guidelines classification scheme|class IIa, level of evidence B]]) <br>
❑ Avoid the use of [[Digoxin]] ([[ACC AHA guidelines classification scheme|class III, level of evidence C]])
❑ Avoid the use of [[Digoxin]] ([[ACC AHA guidelines classification scheme|class III, level of evidence C]])
</div> |
</div> |
B02= <div style="float: left; text-align: left; width: 24em; padding:1em;"> '''Asymptomatic''' <br>
B02= <div style="float: left; text-align: left; width: 24em; padding:1em;"> '''Prevention of recurrent AVRT'''<br>
</div> |
B03= <div style="float: left; text-align: left; width: 24em; padding:1em;"> '''Asymptomatic''' <br>
❑ No treatment ([[ACC AHA guidelines classification scheme|class I, level of evidence C]]) <br>
❑ No treatment ([[ACC AHA guidelines classification scheme|class I, level of evidence C]]) <br>
❑ [[Catheter ablation]] ([[ACC AHA guidelines classification scheme|class IIa, level of evidence B]]) <br>
❑ [[Catheter ablation]] ([[ACC AHA guidelines classification scheme|class IIa, level of evidence B]]) <br>
</div>}}
{{familytree | | | |,|-|-|^|-|-|.| | | | | |}}
{{familytree | | | C01 | | | | C02 | | | | | C01= <div style="float: left; text-align: left; width: 24em; padding:1em;"> '''Orthodromic AVRT'''<br>
❑ [[Antiarrhythmic agent|class IC antiarithmic drugs]] such as [[flecainide]] and [[propofenone]] <br>
❑ [[Beta blockers]] are used as second-line therapy<br>
❑ [[Antiarrhythmic agent|class IA antiarithmic drugs]] such as [[procainamide]] and [[quinidine]] can be used but are less efective than [[Antiarrythmic agent|class IC antiarithmic drugs]]<br>
❑ [[Amiodarone]] is very efective in supresing orthodromic AVRT, but has too many adverse efects such as: pulmonary and hepatic toxicity.
❑ Avoid the chronic treatment with [[verapamil]] or [[digoxin]]<br>
</div> |
C02= <div style="float: left; text-align: left; width: 24em; padding:1em;"> '''Antidromic AVRT'''<br>
❑ [[Catheter ablation]] is the prefered therapy <br>
❑ Medical therapy: reserved to patients who are not candidates or feeruse to the intervention.
:❑ [[Antiarrhythmic agent|class IC antiarithmic drugs]] such as [[flecainide]] and [[propofenone]] <br>
:❑ [[Antiarrythmic agent|class IA antiarithmic drugs]] such as [[procainamide]] and [[quinidine]] can be used but are less efective than [[Antiarrythmic agents|class IC antiarithmic drugs]]<br>
:❑ [[Amiodarone]] is also efective, but it should be reserved for patients who doesn't respond to [[Antiarrhythmic agent|class IC antiarithmic drugs]] and [[Antiarrythmic agent|class IA antiarithmic drugs]], or catheter ablation was ineffective. <br>
</div>}}
</div>}}
{{familytree/end}}
{{familytree/end}}

Revision as of 19:02, 24 March 2014

.


Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Wolff-Parkinson-White Syndrome Resident Survival Guide Microchapters
Overview
Causes
Diagnosis
Management
Long-term Management
WPW with AF
Do's
Don'ts

Overview

Wolff-Parkinson-White syndrome (WPW) is a syndrome of pre-excitation of the ventricles of the heart due to an accessory pathway known as the Bundle of Kent. The diagnosis is made when a patient with pre-existing WPW patern in the ECG, developes an arrythmia which involves an accessory pathway. The treatment is focused on recovering sinus rythm. Atrial Fibrillation in a patient with WPW is lifethretening and should be managed urgently.

Causes

Life Threatening Causes

Life-threatening causes include conditions which result in death or permanent disability within 24 hours if left untreated. Wolff-Parkinson-White syndrome can be a life-threatening condition and must be treated as such irrespective of the underlying cause.

Common Causes

WPW is a congenic disease

Diagnosis

Shown below is an algorithm summarizing the initial approach to Wolff-Parkinson-White syndrome according to the 2003 ACC/AHA/ESC guidelines for the management of patients with supraventricular arrhythmias.[1]

AVRT: AV reentrant tachycardia

 
 
 
Characterize the symptoms:

❑ Asymptomatic
Palpitations
Dyspnea
Fatigue
Chest discomfort
Lightheadedness
Polyuria
Characterize the timing of the symptoms:
❑ Onset
❑ Duration
❑ Frequency

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Examine the patient:

Vitals
❑ Monitor the blood pressure: patient may be hypotensive
❑ Monitor the heart rate: symptomatic patients usually present with heart rates between 150-250 beats per minute (bpm)
❑ Patient may apear cool and diaphoretic
Cardiovascular
❑ Normal heart examination in most cases
❑ Elevated heart rate
Respiratory
❑ Lung auscultation: search for crackles

 
 
 
 
 
 
 
 
 
 
 
 
 
 
Order studies:
❑ Order and monitor the ECG

❑ Order an ECG
Echocardiography: evaluate cardiac function and dimentions, search for assciated contitions such as:

Hypertrophic cardiomyopathy
Ebstein's anomaly of the tricuspid valve
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Orthodromic AVRT

The impulse travels from the atrium to the ventricle through the AV node and returns to the atrium through the accessory pathway. 90-95% of WPW
❑ Narrow QRS complexes
❑ Ventricular rate between 150-250 bpm (or more) usually regular
❑ PR interval less than one half of the tachycardia RR interval

 
 
 
Antidromic AVRT

The impulse travels from the atrium to the ventricle through the accessory pathway and from the ventricle to the atrium through the AV node. Less than 10% of WPW
❑ Wide QRS complexes
❑ Ventricular rate between 150-250 bpm (or more) usually regular
❑ PR interval more than one half of the tachycardia RR interval

 
 
 

Management

Shown below is an algorithm summarizing the initial approach to Wolff-Parkinson-White syndrome according to the 2003 ACC/AHA/ESC guidelines for the management of patients with supraventricular arrhythmias.[1]

 
 
 
 
 
Initial approach

❑ Determine blood pressure
❑ Determine heart rate
❑ If possible, catheter ablation (class I, level of evidence B)

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Stable patient
 
 
 
Unstable patient
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
❑ Assess the ECG
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Orthodromic AVRT
 
Antidromic AVRT
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Treatment.

❑ Use Vagal maneuvers (class I, level of evidence B)

Carotid sinus massage
Valsalva maneuver


If not effective initiate IV AV nodal blocking agent

❑ Administer Adenosine, 6 mg (initial dose) that could be followed by 12 mg if initial dose not effective.

❑ Administer IV followed by 10 cc of saline solution (class I, level of evidence A)
Contraindications: second- or third-degree A-V block, sinus node disease


If not effective

❑ Administer Verapamil, given in boluses of 5 mg every two to three minutes up to cumulative 15 mg (class I, level of evidence A).

❑ Additional ECG monitoring should be perforemed in patients with renal insufficiency.
❑ In cirrhosis, reduce dose to 20% and 50% of normal
Contraindications: hypotension (systolic pressure less than 90 mm Hg) or cardiogenic shock, patients with known hypersensitivity to verapamil hydrochloride


If not effective

❑ Administer Procainamide, give intravenusly 20 to 50 mg/minute until the arrythmia is controlled or reach 17 mg/kg.

❑ Must monitor blood pressure every 5 to 10 minnutes (class I, level of evidence B).
❑ Reduce the loading dose to 12 mg/kg in severe renal impairment.
❑ Reduce the dosage to 50% in hepatic impaiment
Contraindications: complete heart block, lupus erythematosus, idiosyncratic hypersensitivity, torsades de pointes
 
Treatment.

❑ Administer:

Ibutilide is the prefered treatment, 1 mg in an infusion over 10 minutes (class I, level of evidence B)
❑ If the tachycardia is not controlled give another 1 mg infusion over 10 minutes
Contraindications: hypersensitivity to ibutilide or any component of the formulation, QTc >440 msec


Or

Procainamide
20 to 50 mg/minute until the arrythmia is controlled or reach 17 mg/kg (class I, level of evidence B)
❑ Must monitor blood pressure every 5 to 10 minnutes
❑ Reduce the loading dose to 12 mg/kg in severe renal impairment
❑ Reduce the dosage to 50% in hepatic impaiment
Contraindications: complete heart block, lupus erythematosus, idiosyncratic hypersensitivity, torsades de pointes

Adenosine should be used with caution because may produce AF

❑ Administer 6 mg (initial dose) that could be followed by 12 mg if initial dose not effective
❑ Administer IV followed by 10 cc of saline solution
Contraindications: second- or third-degree A-V block, sinus node disease
 
 
 


Long-term Management

 
 
 
 
 
Long term management
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Prevention of recurrent AVRT
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Orthodromic AVRT

class IC antiarithmic drugs such as flecainide and propofenone
Beta blockers are used as second-line therapy
class IA antiarithmic drugs such as procainamide and quinidine can be used but are less efective than class IC antiarithmic drugs
Amiodarone is very efective in supresing orthodromic AVRT, but has too many adverse efects such as: pulmonary and hepatic toxicity. ❑ Avoid the chronic treatment with verapamil or digoxin

 
 
 
Antidromic AVRT

Catheter ablation is the prefered therapy
❑ Medical therapy: reserved to patients who are not candidates or feeruse to the intervention.

class IC antiarithmic drugs such as flecainide and propofenone
class IA antiarithmic drugs such as procainamide and quinidine can be used but are less efective than class IC antiarithmic drugs
Amiodarone is also efective, but it should be reserved for patients who doesn't respond to class IC antiarithmic drugs and class IA antiarithmic drugs, or catheter ablation was ineffective.
 
 
 
 

Wolff-Parkinson-White syndrome with Atrial fibrillation

Shown below is an algorithm summarizing the managment of Wolff-Parkinson-White syndrome with Atrial fibrillation according to the ACC/AHA/ESC 2006 Guidelines for the Management of Patients with Atrial Fibrillation.[2]

 
 
 
Initial approach

❑ Control ventricular response
❑ If possible: terminate AF
❑ If possible: catheter ablation of the accessory pathway (class I, level of evidence B)

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Stable patient
 
 
 
Unstable patient
 
 
 
 
 
 
 
 
 
 
 
 
 
 

❑ Restore sinus rythm (class I, level of evidence C)

Ibutilide administer 1 mg in an infusion over 10 minutes, if the tachycardia is not controlled give another 1 mg infusion over 10 minutes (class I, level of evidence C)
Contraindications: hypersensitivity to ibutilide or any component of the formulation, QTc >440 msec


Or

Procainamide administer 20 to 50 mg/minute until the arrythmia is controlled or reach 17 mg/kg (class I, level of evidence B)
❑ Must monitor blood pressure every 5 to 10 minnutes
❑ Reduce the loading dose to 12 mg/kg in severe renal impairment
❑ Reduce the dosage to 50% in hepatic impaiment
Contraindications: complete heart block, lupus erythematosus, idiosyncratic hypersensitivity, torsades de pointes


Or

Amiodarone, administer 5-7 mg/kg over 30-60 minutes (initial dose), then 1.2-1.8 g daily continuous infusion or in divided oral doses until 10 g total (class IIb, level of evidence B)
Contraindications: cardiogenic shock, severe sinus-node dysfunction

❑ Avoid AV blocking agents (class III, level of evidence B), such as:

❑ Digitalis glycosides
❑ Nondihydropyridine calcium channel antagonists
 
 
 
 
 
 

Do's

❑ Perform catheter ablation of the accessory pathway if possible (class I, level of evidence B).
❑ Electrical cardioversion can be performed in cases of WPW with AF with rapid ventricular response (class II, level of evidence A).
❑ In asymptomatic patients, either no intervantion (class I, level of evidence C) or catheter ablation (class IIb, level of evidence B) could be performed.

Don'ts

❑ Aoid the usage of AV blocking agents in patients with WPW and AF as they will promote conduction down the accessory pathway (class III, level of evidence B).

References

  1. 1.0 1.1 "ACC/AHA/ESC Guidelines for the Management of Patients With Supraventricular Arrhythmias—Executive Summary". Retrieved 15 August 2013.
  2. Fuster, V.; Rydén, LE.; Cannom, DS.; Crijns, HJ.; Curtis, AB.; Ellenbogen, KA.; Halperin, JL.; Le Heuzey, JY.; Kay, GN. (2006). "ACC/AHA/ESC 2006 Guidelines for the Management of Patients with Atrial Fibrillation: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines and the European Society of Cardiology Committee for Practice Guidelines (Writing Committee to Revise the 2001 Guidelines for the Management of Patients With Atrial Fibrillation): developed in collaboration with the European Heart Rhythm Association and the Heart Rhythm Society". Circulation. 114 (7): e257–354. doi:10.1161/CIRCULATIONAHA.106.177292. PMID 16908781. Unknown parameter |month= ignored (help)


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