AVNRT pathophysiology: Difference between revisions

Jump to navigation Jump to search
No edit summary
No edit summary
 
(7 intermediate revisions by 4 users not shown)
Line 1: Line 1:
__NOTOC__
__NOTOC__
{{AVNRT}}
{{AVNRT}}
{{CMG}}
{{CMG}} ; {{AE}} {{RG}}


==Overview==
==Overview==
AVNRT occurs when a [[cardiac arrhythmia#re-entry|reentry]] circuit forms within or just next to the [[AV node|atrioventricular node]].  The circuit usually involves two anatomical pathways: the fast pathway and the slow pathway, which are both in the [[right atrium]]. The slow pathway (which is usually targeted for ablation) is located inferiorly and slightly posterior to the [[AV node]], often following the anterior margin of the [[coronary sinus]]. The fast pathway is usually located just superior and posterior to the [[AV node]].  These pathways are formed from tissue that behaves very much like the AV node, and some authors regard them as ''part of'' the AV node.  In the usual form of AVNRT, the conduction from the atrium to the ventricle is down the slow pathway, and the retrograde conduction from the ventricle to the atrium is up the fast pathway.
AVNRT occurs when a [[cardiac arrhythmia#re-entry|reentry]] circuit forms within or just next to the [[AV node|atrioventricular node]].  The circuit usually involves two anatomical pathways: the fast pathway and the slow pathway, which are both in the [[right atrium]]. The slow pathway (which is usually targeted for ablation) is located inferiorly and slightly posterior to the [[AV node]], often following the anterior margin of the [[coronary sinus]]. The fast pathway is usually located just superior and posterior to the [[AV node]].  These pathways are formed from tissue that behaves very much like the AV node, and some authors regard them as ''part of'' the AV node.  In the usual form of AVNRT, the conduction from the atrium to the ventricle is down the slow pathway, and the retrograde conduction from the ventricle to the atrium is up the fast pathway.
==Pathophysiology==
===Electrophysiologic Triggers===
====Premature Atrial Complex====
The most common trigger for an episode of AVNRT is when an [[atrial premature complex]] (APC) approaches the fast pathway, and is blocked due to the longer refractory period of this pathway, and instead conducts down the slow pathway.  As the impulse goes down the slow pathway, the fast pathway recovers, and allows the impulse to conduct backward or retrograde toward the atrium. It then re-enters the atrial entrance of the slow pathway and the cycle repeats itself.<ref name="ManiPavri2014">{{cite journal|last1=Mani|first1=Bhalaghuru Chokkalingam|last2=Pavri|first2=Behzad B.|title=Dual Atrioventricular Nodal Pathways Physiology: A Review of Relevant Anatomy, Electrophysiology, and Electrocardiographic Manifestations|journal=Indian Pacing and Electrophysiology Journal|volume=14|issue=1|year=2014|pages=12–25|issn=09726292|doi=10.1016/S0972-6292(16)30711-2}}</ref>


==Electrophysiologic Triggers==
====Premature Ventricular Complex====
===Premature Atrial Complex===
The second most common mechanism whereby AVNRT is triggered is via the entry of a [[premature ventricular complex]] down either the slow conducting pathway (similar to a [[premature atrial complex]] above) or down the rapidly conducting pathway.
The most common trigger for an episode of AVNRT is when an [[atrial premature complex]] (APC) approaches the fast pathway, and is blocked due to the longer refractory period of this pathway, and instead conducts down the slow pathway. As the impulse goes down the slow pathway, the fast pathway recovers, and allows the impulse to conduct backward or retrograde toward the atrium. It then re-enters the atrial entrance of the slow pathway and the cycle repeats itself.
==Genetics==
 
* There are certain types of cardiac arrhythmia that are shown to have a genetic basis.
**[[Wolff-Parkinson-White syndrome]] has an [[autosomal dominant]] inheritance model.<ref name="VidailletPressley1987">{{cite journal|last1=Vidaillet|first1=Humberto J.|last2=Pressley|first2=Joyce C.|last3=Henke|first3=Elizabeth|last4=Harrell|first4=Frank E.|last5=German|first5=Lawrence D.|title=Familial Occurrence of Accessory Atrioventricular Pathways (Preexcitation Syndrome)|journal=New England Journal of Medicine|volume=317|issue=2|year=1987|pages=65–69|issn=0028-4793|doi=10.1056/NEJM198707093170201}}</ref>
** familial lone atrial fibrillation which is classified as "channelopathies" and is characterized by autosomal dominant inheritance, corresponding to a locus on chromosome 10.<ref name="BrugadaTapscott1997">{{cite journal|last1=Brugada|first1=Ramon|last2=Tapscott|first2=Terry|last3=Czernuszewicz|first3=Grazyna Z.|last4=Marian|first4=A.J.|last5=Iglesias|first5=Anna|last6=Mont|first6=Lluis|last7=Brugada|first7=Josep|last8=Girona|first8=Josep|last9=Domingo|first9=Anna|last10=Bachinski|first10=Linda L.|last11=Roberts|first11=Robert|title=Identification of a Genetic Locus for Familial Atrial Fibrillation|journal=New England Journal of Medicine|volume=336|issue=13|year=1997|pages=905–911|issn=0028-4793|doi=10.1056/NEJM199703273361302}}</ref>
* However, whether a genetic mechanism also contributes to the development of AVNRT has not been well known, but it is shown that offspring of affected patient is at 3.4% increased risk to develop the disease.  


===Premature Ventricular Complex===
The second most common mechanism whereby AVNRT is triggered is via the entry of a [[premature ventricular complex]] down either the slow conducting pathway (similar to a [[premature atrial complex]] above) or down the rapidly conducting pathway.
==References==
==References==
{{Reflist|2}}
{{Reflist|2}}
{{WH}}
{{WS}}
[[CME Category::Cardiology]]


[[Category:Cardiology]]
[[Category:Cardiology]]

Latest revision as of 17:31, 10 April 2020

AVNRT Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating AVNRT from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diaagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X-ray

Echocardiography and Ultrasound

CT Scan

MRI

Other Imaging Findings

Other Diagnostic Studies

Treatment

Overview

Medical Treatment

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Case Studies

Case #1

AVNRT pathophysiology On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of AVNRT pathophysiology

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on AVNRT pathophysiology

CDC on AVNRT pathophysiology

AVNRT pathophysiology in the news

Blogs on AVNRT pathophysiology

Directions to Hospitals Treating AVNRT

Risk calculators and risk factors for AVNRT pathophysiology

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] ; Associate Editor(s)-in-Chief: Ramyar Ghandriz MD[2]

Overview

AVNRT occurs when a reentry circuit forms within or just next to the atrioventricular node. The circuit usually involves two anatomical pathways: the fast pathway and the slow pathway, which are both in the right atrium. The slow pathway (which is usually targeted for ablation) is located inferiorly and slightly posterior to the AV node, often following the anterior margin of the coronary sinus. The fast pathway is usually located just superior and posterior to the AV node. These pathways are formed from tissue that behaves very much like the AV node, and some authors regard them as part of the AV node. In the usual form of AVNRT, the conduction from the atrium to the ventricle is down the slow pathway, and the retrograde conduction from the ventricle to the atrium is up the fast pathway.

Pathophysiology

Electrophysiologic Triggers

Premature Atrial Complex

The most common trigger for an episode of AVNRT is when an atrial premature complex (APC) approaches the fast pathway, and is blocked due to the longer refractory period of this pathway, and instead conducts down the slow pathway. As the impulse goes down the slow pathway, the fast pathway recovers, and allows the impulse to conduct backward or retrograde toward the atrium. It then re-enters the atrial entrance of the slow pathway and the cycle repeats itself.[1]

Premature Ventricular Complex

The second most common mechanism whereby AVNRT is triggered is via the entry of a premature ventricular complex down either the slow conducting pathway (similar to a premature atrial complex above) or down the rapidly conducting pathway.

Genetics

  • There are certain types of cardiac arrhythmia that are shown to have a genetic basis.
  • However, whether a genetic mechanism also contributes to the development of AVNRT has not been well known, but it is shown that offspring of affected patient is at 3.4% increased risk to develop the disease.

References

  1. Mani, Bhalaghuru Chokkalingam; Pavri, Behzad B. (2014). "Dual Atrioventricular Nodal Pathways Physiology: A Review of Relevant Anatomy, Electrophysiology, and Electrocardiographic Manifestations". Indian Pacing and Electrophysiology Journal. 14 (1): 12–25. doi:10.1016/S0972-6292(16)30711-2. ISSN 0972-6292.
  2. Vidaillet, Humberto J.; Pressley, Joyce C.; Henke, Elizabeth; Harrell, Frank E.; German, Lawrence D. (1987). "Familial Occurrence of Accessory Atrioventricular Pathways (Preexcitation Syndrome)". New England Journal of Medicine. 317 (2): 65–69. doi:10.1056/NEJM198707093170201. ISSN 0028-4793.
  3. Brugada, Ramon; Tapscott, Terry; Czernuszewicz, Grazyna Z.; Marian, A.J.; Iglesias, Anna; Mont, Lluis; Brugada, Josep; Girona, Josep; Domingo, Anna; Bachinski, Linda L.; Roberts, Robert (1997). "Identification of a Genetic Locus for Familial Atrial Fibrillation". New England Journal of Medicine. 336 (13): 905–911. doi:10.1056/NEJM199703273361302. ISSN 0028-4793.

Template:WH Template:WS CME Category::Cardiology