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! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | [[Wolff-Parkinson-White syndrome resident survival guide#Management|Management]]
! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | [[Wolff-Parkinson-White syndrome resident survival guide#Management|Management]]
:[[Wolff-Parkinson-White syndrome resident survival guide#Long-term Management|Long-term Management]]
:[[Wolff-Parkinson-White syndrome resident survival guide#Long-term Management|Long-term Management]]
:[[Wolff-Parkinson-White syndrome resident survival guide#Wolff-Parkinson-White syndrome with Atrial Fibrillation|WPW with AF]]
:[[Wolff-Parkinson-White syndrome resident survival guide#Wolff-Parkinson-White syndrome with atrial fibrillation|WPW with AF]]
|-
|-
! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | [[Wolff-Parkinson-White syndrome resident survival guide#Do's|Do's]]
! style="font-size: 80%; padding: 0 5px; background: #DCDCDC" align=left | [[Wolff-Parkinson-White syndrome resident survival guide#Do's|Do's]]
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{{familytree  | G01 | | G02 | | | | G01= <div style="float: left; text-align: left; width: 24em; padding:1em;">  '''Treatment'''<br>
{{familytree  | G01 | | G02 | | | | G01= <div style="float: left; text-align: left; width: 24em; padding:1em;">  '''Treatment'''<br>
❑ Use [[vagal maneuvers]] ([[ACC AHA guidelines classification scheme|class I, level of evidence B]])<br>
❑ Use [[vagal maneuvers]] ([[ACC AHA guidelines classification scheme|class I, level of evidence B]])<br>
:❑ [[Carotid sinus massage]] <br>  
:❑ [[Carotid sinus massage]] <br>
:❑ [[Valsalva maneuver]] <br>
:❑ [[Valsalva maneuver]] <br>
<br>''If not effective initiate IV AV nodal blocking agent''<br><br>
<br>''If not effective initiate IV AV nodal blocking agent''<br><br>
❑ Administer [[adenosine]] 6 mg IV followed by 10 cc of saline solution ([[ACC AHA guidelines classification scheme|class I, level of evidence A]])<br>
❑ Administer [[adenosine]] 6 mg given as a rapid intravenous bolus (administered over a 1-2 second period) ([[ACC AHA guidelines classification scheme|class I, level of evidence A]])<br>
: ❑ If initial dose not effective, administer a second dose of 12 mg <br>
: ❑ If initial dose not effective, administer a second dose of 12 mg. This 12 mg dose may be repeated a second time if required.<br>  
:<span style="font-size:85%;color:red">Contraindications: second- or third-degree A-V block, sinus node disease</span><br>
:<span style="font-size:85%;color:red">Contraindications: second- or third-degree A-V block, sinus node disease</span><br>
<br>''If not effective''<br><br>
<br>''If not effective''<br><br>
❑ Administer [[verapamil]], given in boluses of 5 mg every two to three minutes up to cumulative 15 mg ([[ACC AHA guidelines classification scheme|class I, level of evidence A]])<br>
❑ Administer [[verapamil]], boluses of 5 mg to acumulate 15 mg. ([[ACC AHA guidelines classification scheme|class I, level of evidence A]])<br>
:❑ Additional ECG monitoring should be perforemed in patients with renal insufficiency<br>
:❑ Use lower doses to reach the same level in patients with reanal impairment<br>
:❑ Give 20% of the dose to patients with hepatic insuficiency<br>
:<span style="font-size:85%;color:red">Contraindications: hypotension (systolic pressure less than 90 mm Hg) or cardiogenic shock, patients with known hypersensitivity to verapamil hydrochloride</span><br>
:<span style="font-size:85%;color:red">Contraindications: hypotension (systolic pressure less than 90 mm Hg) or cardiogenic shock, patients with known hypersensitivity to verapamil hydrochloride</span><br>
<br>''If not effective''<br><br>
<br>''If not effective''<br><br>
❑ Administer [[procainamide]], given 100 mg diluted to 100mg/ml as infusions at a rate of 50 mg per minute, every 5 minutes the arrhythmiais suppressed or until 500 mg has been administered.If the arrhythmya is not controlled wait 10 minutes or longer to administer new dosage. ([[ACC AHA guidelines classification scheme|class I, level of evidence B]])<br>  
❑ Administer [[procainamide]], given 100 mg diluted to 100mg/ml as infusions at a rate of 50 mg per minute, every 5 minutes the arrhythmiais suppressed or until 500 mg has been administered.If the arrhythmya is not controlled wait 10 minutes or longer to administer new dosage. ([[ACC AHA guidelines classification scheme|class I, level of evidence B]])<br>
:❑ Must monitor blood pressure every 5 to 10 minnutes <br>
:❑ Blood pressure should be monitored with the patient supine during parenteral, especially intravenous administration. <br>
:❑ Reduce the loading dose to 12 mg/kg in severe renal impairment<br>
:❑ Dosage should be adjusted in every individual case for renal insuficiency<br>
:❑ Reduce the dosage to 50% in hepatic impaiment<br>
:<span style="font-size:85%;color:red">Contraindications: complete heart block, lupus erythematosus, idiosyncratic hypersensitivity, torsades de pointes</span><br>
:<span style="font-size:85%;color:red">Contraindications: complete heart block, lupus erythematosus, idiosyncratic hypersensitivity, torsades de pointes</span><br>
</div> |
</div> |
G02= <div style="float: left; text-align: left; width: 24em; padding:1em;"> '''Treatment'''<br>
G02= <div style="float: left; text-align: left; width: 24em; padding:1em;"> '''Treatment'''<br>
❑ Administer:
❑ Administer:
:❑ [[Ibutilide]] is the prefered treatment, 1 mg in an infusion over 10 minutes ([[ACC AHA guidelines classification scheme|class I, level of evidence B]])<br>
:❑ [[Ibutilide]] IV infusion of 1 mg given over 10 minutes ([[ACC AHA guidelines classification scheme|class I, level of evidence B]])<br>
::❑ If the tachycardia is not controlled give another 1 mg infusion over 10 minutes <br>
::❑ Repeat the dosage if the tachycardia continues <br>
::<span style="font-size:85%;color:red">Contraindications: hypersensitivity to ibutilide or any component of the formulation, QTc >440 msec</span><br>
::<span style="font-size:85%;color:red">Contraindications: hypersensitivity to ibutilide or any component of the formulation, QTc >440 msec</span><br>
<br>''Or''<br><br>
<br>''Or''<br><br>
:❑ [[Procainamide]] <br> 20 to 50 mg/minute until the arrythmia is controlled or reach 17 mg/kg ([[ACC AHA guidelines classification scheme|class I, level of evidence B]])<br>
:❑ [[Procainamide]] 100 mg diluted to 100mg/ml given in infusions of 50 mg per minute, every 5 minutes untill the arrhythmia is suppressed or until 500 mg has been administered.If the arrhythmya is not controlled wait 10 minutes or longer to administer new dosage. ([[ACC AHA guidelines classification scheme|class I, level of evidence B]])<br>
::❑ Must monitor blood pressure every 5 to 10 minnutes <br>
::❑ Blood pressure should be monitored with the patient supine during parenteral, especially intravenous administration. <br>
::❑ Reduce the loading dose to 12 mg/kg in severe renal impairment<br>
::❑ Dosage should be adjusted in every individual case for renal insuficiency<br>
::❑ Reduce the dosage to 50% in hepatic impaiment <br>
::<span style="font-size:85%;color:red">Contraindications: complete heart block, lupus erythematosus, idiosyncratic hypersensitivity, torsades de pointes</span><br>
::<span style="font-size:85%;color:red">Contraindications: complete heart block, lupus erythematosus, idiosyncratic hypersensitivity, torsades de pointes</span><br>
❑ [[Adenosine]] should be used with caution because may produce [[AF]]<br>
❑ [[Adenosine]] should be used with caution because may produce [[AF]]<br>
:❑ Administer 6 mg (initial dose) that could be followed by 12 mg if initial dose not effective<br>
:❑ 6 mg given as a rapid intravenous bolus (administered over a 1-2 second period)<br>
:❑ Administer IV followed by 10 cc of saline solution<br>
: ❑ If initial dose not effective, administer a second dose of 12 mg. This 12 mg dose may be repeated a second time if required.<br>
:<span style="font-size:85%;color:red">Contraindications: second- or third-degree A-V block, sinus node disease</span><br>
:<span style="font-size:85%;color:red">Contraindications: second- or third-degree A-V block, sinus node disease</span><br>
</div>}}
</div>}}
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{{familytree | | | |,|-|-|^|-|-|.| | | | | |}}
{{familytree | | | |,|-|-|^|-|-|.| | | | | |}}
{{familytree | | | C01 | | | | C02 | | | | | C01= <div style="float: left; text-align: left; width: 24em; padding:1em;"> '''Orthodromic AVRT'''<br>
{{familytree | | | C01 | | | | C02 | | | | | C01= <div style="float: left; text-align: left; width: 24em; padding:1em;"> '''Orthodromic AVRT'''<br>
❑ [[Antiarrhythmic agent|class IC antiarrhythmic drugs]] such as [[flecainide]] and [[propofenone]] <br>
❑ [[Antiarrhythmic agent|Class IC antiarrhythmic drugs]] such as [[flecainide]] and [[propofenone]] <br>
❑ [[Beta blockers]] are used as second-line therapy<br>
❑ [[Beta blockers]] are used as second-line therapy<br>
❑ [[Antiarrhythmic agent|class IA antiarrhythmic drugs]] such as [[procainamide]] and [[quinidine]] can be used but are less efective than [[Antiarrythmic agent|class IC antiarrhythmic drugs]]<br>
❑ [[Antiarrhythmic agent|Class IA antiarrhythmic drugs]] such as [[procainamide]] and [[quinidine]] can be used but are less efective than [[Antiarrythmic agent|class IC antiarrhythmic drugs]]<br>
❑ [[Amiodarone]] is very efective in supresing orthodromic AVRT, but has too many adverse efects such as: pulmonary and hepatic toxicity<br>
❑ [[Amiodarone]] shoul be reserved as is equally efective than [[Antiarrhythmic agent|Class IC antiarrhythmic drugs]] but has more adverse effects<br>
❑ Avoid the chronic treatment with [[verapamil]] or [[digoxin]]<br>
❑ Avoid the chronic treatment with [[verapamil]] or [[digoxin]]<br>
</div> |
</div> |
C02= <div style="float: left; text-align: left; width: 24em; padding:1em;"> '''Antidromic AVRT'''<br>
C02= <div style="float: left; text-align: left; width: 24em; padding:1em;"> '''Antidromic AVRT'''<br>
❑ [[Catheter ablation]] is the prefered therapy <br>
❑ [[Catheter ablation]] should be ofered to every patient <br>
❑ Medical therapy: reserved to patients who are not candidates or feeruse to the intervention.
❑ Medical therapy:
:❑ [[Antiarrhythmic agent|class IC antiarrhythmic drugs]] such as [[flecainide]] and [[propofenone]] <br>
:❑ [[Antiarrhythmic agent|class IC antiarrhythmic drugs]] such as [[flecainide]] and [[propofenone]] <br>
:❑ [[Antiarrythmic agent|class IA antiarrhythmic drugs]] such as [[procainamide]] and [[quinidine]] can be used but are less efective than [[Antiarrythmic agents|class IC antiarithmic drugs]]<br>
:❑ [[Antiarrythmic agent|class IA antiarrhythmic drugs]] such as [[procainamide]] and [[quinidine]] can be used but are less efective than [[Antiarrythmic agents|class IC antiarithmic drugs]]<br>
Line 234: Line 231:
{{familytree | C01 | | | | C02 | | | | C01=  <div style="float: left; text-align: left; width: 27em; padding:1em;">
{{familytree | C01 | | | | C02 | | | | C01=  <div style="float: left; text-align: left; width: 27em; padding:1em;">
❑ Restore sinus rythm ([[ACC AHA guidelines classification scheme|class I, level of evidence C]])<br>
❑ Restore sinus rythm ([[ACC AHA guidelines classification scheme|class I, level of evidence C]])<br>
:❑ [[Ibutilide]] administer 1 mg in an infusion over 10 minutes, if the tachycardia is not controlled give another 1 mg infusion over 10 minutes ([[ACC AHA guidelines classification scheme|class I, level of evidence C]])<br>
:❑ [[Ibutilide]] IV infusion of 1 mg given over 10 minutes. Repeat the dosage if the tachycardia continues ([[ACC AHA guidelines classification scheme|class I, level of evidence C]])<br>
::<span style="font-size:85%;color:red">Contraindications: hypersensitivity to ibutilide or any component of the formulation, QTc >440 msec</span><br>
::<span style="font-size:85%;color:red">Contraindications: hypersensitivity to ibutilide or any component of the formulation, QTc >440 msec</span><br>
<br>''Or''<br><br>
<br>''Or''<br><br>
:❑ [[Procainamide]] administer 20 to 50 mg/minute until the arrythmia is controlled or reach 17 mg/kg ([[ACC AHA guidelines classification scheme|class I, level of evidence B]])<br>
:❑ [[Procainamide]] 100 mg diluted to 100mg/ml given in infusions of 50 mg per minute, every 5 minutes untill the arrhythmia is suppressed or until 500 mg has been administered.If the arrhythmya is not controlled wait 10 minutes or longer to administer new dosage. ([[ACC AHA guidelines classification scheme|class I, level of evidence B]])<br>
::❑ Must monitor blood pressure every 5 to 10 minnutes <br>
::❑ Blood pressure should be monitored with the patient supine during parenteral, especially intravenous administration. <br>
::❑ Reduce the loading dose to 12 mg/kg in severe renal impairment<br>
::❑ Dosage should be adjusted in every individual case for renal insuficiency<br>
::❑ Reduce the dosage to 50% in hepatic impaiment <br>
::<span style="font-size:85%;color:red">Contraindications: complete heart block, lupus erythematosus, idiosyncratic hypersensitivity, torsades de pointes</span><br>
::<span style="font-size:85%;color:red">Contraindications: complete heart block, lupus erythematosus, idiosyncratic hypersensitivity, torsades de pointes</span><br>
<br>''Or''<br><br>
<br>''Or''<br><br>
:❑ [[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 ([[ACC AHA guidelines classification scheme|class IIb, level of evidence B]])<br>
:❑ [[Amiodarone]], Loading doses of 800 to 1,600 mg/day are required for 1 to 3 weeks (occasionally longer) until initial therapeutic response occurs. ([[ACC AHA guidelines classification scheme|class IIb, level of evidence B]])<br>
::<span style="font-size:85%;color:red">Contraindications: cardiogenic shock, severe sinus-node dysfunction</span><br>
::<span style="font-size:85%;color:red">Contraindications: cardiogenic shock, severe sinus-node dysfunction</span><br>
❑ Avoid AV blocking agents ([[ACC AHA guidelines classification scheme|class III, level of evidence B]]), such as:<br>
❑ Avoid AV blocking agents ([[ACC AHA guidelines classification scheme|class III, level of evidence B]]), such as:<br>

Revision as of 18:24, 25 March 2014

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Hilda Mahmoudi M.D., M.P.H.[2]; Alonso Alavarado, MD

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) its a condition 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 the accessory pathway. The treatment is focused on recovering sinus rythm. Atrial fibrillation in a patient with WPW is life threatening and should be managed urgently.

Causes

Life Threatening Causes

Wolff-Parkinson-White syndrome can be a life-threatening condition and must be treated as such irrespective of the underlying cause.

Common Causes

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]

Abbreviations: AVRT: AV reentrant tachycardia; BP: Blood pressure; AF: Atrial fibrilation HF: Heart failure LVH: Left ventricle hypertension; ECG: Electrocardiography

 
 
 
Characterize the symptoms:

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

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Examine the patient:

Appearance of the patient
❑ Cool and diaphoretic


Vitals
Heart rate:

Tachycardic (150-250 beats per minute (bpm))
❑ Rhythm:
❑ Rhytmic (most of the cases)
❑ Arrhythmic (suggestive of AF)

Blood pressure: hypotensive or normal BP


Cardiovascular
❑ Normal heart examination in most cases
Tricuspid regurgitation murmur (suggestive of Ebstein's anomaly)
S4 (suggestive of LVH)


Respiratory
Rales (suggestive of HF)

 
 
 
 
 
 
 
 
 
 
 
 
 
 
Order studies:

ECG
Echocardiography to evaluate cardiac function and dimentions, search for assciated conditions 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


EKG findings:
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


EKG findings:
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]

 
 
 
 
 
Determine if the patient has any unstable sign or symptom

Chest pain
Congestive heart failure
Hypotension
Loss of consciousness
Seizures

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
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 given as a rapid intravenous bolus (administered over a 1-2 second period) (class I, level of evidence A)

❑ If initial dose not effective, administer a second dose of 12 mg. This 12 mg dose may be repeated a second time if required.
Contraindications: second- or third-degree A-V block, sinus node disease


If not effective

❑ Administer verapamil, boluses of 5 mg to acumulate 15 mg. (class I, level of evidence A)

❑ Use lower doses to reach the same level in patients with reanal impairment
Contraindications: hypotension (systolic pressure less than 90 mm Hg) or cardiogenic shock, patients with known hypersensitivity to verapamil hydrochloride


If not effective

❑ Administer procainamide, given 100 mg diluted to 100mg/ml as infusions at a rate of 50 mg per minute, every 5 minutes the arrhythmiais suppressed or until 500 mg has been administered.If the arrhythmya is not controlled wait 10 minutes or longer to administer new dosage. (class I, level of evidence B)

❑ Blood pressure should be monitored with the patient supine during parenteral, especially intravenous administration.
❑ Dosage should be adjusted in every individual case for renal insuficiency
Contraindications: complete heart block, lupus erythematosus, idiosyncratic hypersensitivity, torsades de pointes
 
Treatment

❑ Administer:

Ibutilide IV infusion of 1 mg given over 10 minutes (class I, level of evidence B)
❑ Repeat the dosage if the tachycardia continues
Contraindications: hypersensitivity to ibutilide or any component of the formulation, QTc >440 msec


Or

Procainamide 100 mg diluted to 100mg/ml given in infusions of 50 mg per minute, every 5 minutes untill the arrhythmia is suppressed or until 500 mg has been administered.If the arrhythmya is not controlled wait 10 minutes or longer to administer new dosage. (class I, level of evidence B)
❑ Blood pressure should be monitored with the patient supine during parenteral, especially intravenous administration.
❑ Dosage should be adjusted in every individual case for renal insuficiency
Contraindications: complete heart block, lupus erythematosus, idiosyncratic hypersensitivity, torsades de pointes

Adenosine should be used with caution because may produce AF

❑ 6 mg given as a rapid intravenous bolus (administered over a 1-2 second period)
❑ If initial dose not effective, administer a second dose of 12 mg. This 12 mg dose may be repeated a second time if required.
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 antiarrhythmic drugs such as flecainide and propofenone
Beta blockers are used as second-line therapy
Class IA antiarrhythmic drugs such as procainamide and quinidine can be used but are less efective than class IC antiarrhythmic drugs
Amiodarone shoul be reserved as is equally efective than Class IC antiarrhythmic drugs but has more adverse effects
❑ Avoid the chronic treatment with verapamil or digoxin

 
 
 
Antidromic AVRT

Catheter ablation should be ofered to every patient
❑ Medical therapy:

class IC antiarrhythmic drugs such as flecainide and propofenone
class IA antiarrhythmic 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 antiarrhythmic drugs and class IA antiarrhythmic 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 IV infusion of 1 mg given over 10 minutes. Repeat the dosage if the tachycardia continues (class I, level of evidence C)
Contraindications: hypersensitivity to ibutilide or any component of the formulation, QTc >440 msec


Or

Procainamide 100 mg diluted to 100mg/ml given in infusions of 50 mg per minute, every 5 minutes untill the arrhythmia is suppressed or until 500 mg has been administered.If the arrhythmya is not controlled wait 10 minutes or longer to administer new dosage. (class I, level of evidence B)
❑ Blood pressure should be monitored with the patient supine during parenteral, especially intravenous administration.
❑ Dosage should be adjusted in every individual case for renal insuficiency
Contraindications: complete heart block, lupus erythematosus, idiosyncratic hypersensitivity, torsades de pointes


Or

Amiodarone, Loading doses of 800 to 1,600 mg/day are required for 1 to 3 weeks (occasionally longer) until initial therapeutic response occurs. (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:

Digoxin
Nondihydropyridine calcium channel antagonists: verapamil, diltizem
 
 
 
 
 
 

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.
❑ Prescribe propofenone over flecainide for the prevention of recurrence orthodromic AVRT as it has also a mild beta blocking activity.
❑ Schedule exccercise stress test and electrophysiology tests for the sudden cardiac death stratification (class IIa, level of evidence B).
❑ Consider catheter ablation in asymptomatic patients with structural heart disease (class IIb, level of evidence C)

Don'ts

❑ Don't use AV blocking agents in patients with WPW and antidromic AVRT as it will promote promote conduction down the accessory pathway (class III, level of evidence C).[3] [4] [5]
❑ Avoid the usage of AV blocking agents in patients with WPW and AF (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)
  3. Garratt, C.; Antoniou, A.; Ward, D.; Camm, AJ. (1989). "Misuse of verapamil in pre-excited atrial fibrillation". Lancet. 1 (8634): 367–9. PMID 2563516. Unknown parameter |month= ignored (help)
  4. Gulamhusein, S.; Ko, P.; Carruthers, SG.; Klein, GJ. (1982). "Acceleration of the ventricular response during atrial fibrillation in the Wolff-Parkinson-White syndrome after verapamil". Circulation. 65 (2): 348–54. PMID 7053894. Unknown parameter |month= ignored (help)
  5. McGovern, B.; Garan, H.; Ruskin, JN. (1986). "Precipitation of cardiac arrest by verapamil in patients with Wolff-Parkinson-White syndrome". Ann Intern Med. 104 (6): 791–4. PMID 3706931. Unknown parameter |month= ignored (help)


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