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__NOTOC__
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{{SI}}
{{Infra-Hisian Block}}
{{CMG}} '''Associate Editor-In-Chief:''' {{S.M.}}
{{CMG}}; '''Associate Editor-In-Chief:''' {{S.M.}}


==Overview==
==Overview==
Infra-Hisian blocks are defined as impaired conduction in the [[electrical system of the heart]] that occur below the [[AV node]].
Infra-Hisian [[Blocking (statistics)|block]] is defined as an impaired [[Conduction System|conduction]] in the [[electrical system of the heart]] that occurs below the [[atrioventricular node]].


==Historical Perspective==
==Historical Perspective==
Line 40: Line 40:


==Pathophysiology==
==Pathophysiology==
===Normal Cardiac Conduction===
# The [[normal]] [[cardiac]] [[Conduction System|conduction]] proceeds in a way so as to allow [[Time constant|time]] for the [[atrium]] to [[Relaxation|relax]] during [[atrial]] [[diastole]].
# The [[electrical]] [[Impulse (psychology)|impulse]] [[Generation|generated]] in the [[SA node]] travels through the [[Internodal segment|internodal]] pathways towards the [[AV node]].
# The [[Conduction System|conduction]] through the [[Atrioventricular node|AV node]] is [[Slow|slowed]] down as it travels through it. This decrease in [[velocity]] of [[Conduction System|conduction]] allows [[Time constant|time]] for the [[atrium]] to [[Contraction|contract]] ahead of the [[ventricle]] so that the [[blood]] from the [[atria]] can fill up the [[ventricles]] through the [[atrioventricular valves]].
# As the [[Impulse (psychology)|impulse]] [[Flow|flows]] through the [[Compact tissue|compact]] [[Atrioventricular node|AV node]], it rapidly [[Conductance|conducts]] through the [[ventricular]] [[myocardial]] [[Cells (biology)|cells]]. Once the [[depolarization]] is complete, the [[ventricle]] [[Relaxation|relaxes]] during [[diastole]] in [[Preparation (dental)|preparation]] for the next [[Impulse (psychology)|impulse]].


* [[Mobitz type II]] [[second degree AV block]], in which the PR interval remains unchanged prior to a P wave that fails to conduct to the ventricles.
===Anatomy===
*It almost always results from conduction system disease below the level of the AV node, occurring in the bundle of His in approximately 20 percent of cases and in the bundle branches in the remainder.
* The [[Conduction System|conduction system]] of [[heart]] consists of [[Specialize|specialized]] [[Cells (biology)|cells]] designed to [[Conductance|conduct]] [[electrical]] [[Impulse (psychology)|impulse]] faster than the surrounding [[myocardial]] [[Cells (biology)|cells]].
*Patients with bundle branch involvement also have axis shifts and QRS widening depending upon the location of the block.
*[[Anatomical|Anatomically]], the [[Atrioventricular node|AV node]] is [[Division (biology)|divided]] into three [[Region of interest|regions]] as follows:
*In addition, at least two-thirds of patients with this disorder also have bifascicular or even trifascicular disease.
**'''[[Transitional cell]] zone''': This is the [[Region of interest|region]] where the [[Internodal segment|internodal]] [[atrial]] pathways merge with the [[Compact tissue|compact]] [[Atrioventricular node|AV node]].
*Mobitz type I and Mobitz type II second degree AV block cannot be differentiated from the ECG when 2:1 AV block is present.
**'''[[Compact tissue|Compact]] [[Atrioventricular node|AV node]]''': This [[Region of interest|region]] is [[Location parameter|located]] at the [[apex]] of the [[triangle of Koch]], which is formed by the [[ostium]] of [[coronary sinus]], [[tricuspid]] [[Annulus (mycology)|annulus]] and the [[tendon of Todaro]].
*In this situation, every other P wave is non-conducted and there is no opportunity to observe for the constant PR interval that is characteristic of Mobitz type II second degree AV block.
**'''[[Penetration|Penetrating]] portion of the [[Atrioventricular|AV]] [[Bundle branch|bundle]]''': This [[Region of interest|region]] enters the [[tendon of Todaro]] and runs within the [[fibrous]] [[body]] of the [[interventricular septum|membranous interventricular septum]] and eventually [[Division (biology)|divides]] at the crest of the [[interventricular septum|muscular interventricular septum]] into right and left branches.
* The [[Left bundle branch block|left bundle branch]] [[Penetrance|penetrates]] the [[Membrane|membranous]] portion of the [[interventricular septum]] and [[Division (biology)|divides]] into several smaller branches. Parts of the [[Left bundle branch block|left bundle branch]] include a pre-[[Division (biology)|divisional]] [[Segment (linguistics)|segment]], [[anterior]] [[fascicle]]/hemibundle and [[posterior]] [[fascicle]]/hemibundle. Rarely a [[median]] [[fascicle]] is [[Presenting symptom|present]] in some [[Heart|hearts]].
** The [[anterior]] [[fascicle]] supplies the [[anterior]] [[papillary muscle]] and the [[Purkinje System|Purkinje network]] of the [[Anterior|antero]]-[[lateral]] [[Surface anatomy|surface]] of the [[left ventricle]].
** The [[posterior]] [[fascicle]] supplies the [[posterior]] [[papillary muscle]] and the [[Purkinje System|Purkinje network]] of the [[Posterior|postero]]-inferior [[Surface anatomy|surface]] of the [[left ventricle]].
**[[Left bundle branch block|Left bundle branch]] receives its [[blood]] supply from [[left anterior descending artery]].
{|
|
[[Image:Conduction system of the heart.png|thumb|200px|none|Conduction system of the heart]]
|
[[Image:AV node.png|thumb|500px|none|Structure of the heart's conduction system]]
|
|}


* Conduction delay in Mobitz type II second degree block is almost always infra-nodal (His bundle [20%], bundle branches or fascicles).
===Pathophysiology of Mobitz type II second degree AV block===
* Usually the morphology of the QRS complex is wide, except when the site of block is the His bundle.
* [[Mobitz type II]] [[second degree AV block]] is [[Characterization (mathematics)|characterized]] by a [[PR interval]] that remains unchanged with occasional [[Drop (liquid)|dropped]] [[Beats per minute|beats]] prior to a [[P wave]] that [[Failure|fails]] to [[conduct]] to the [[ventricles]] as [[Comparability|compared]] to the gradually [[Prolonged PR-interval|prolonging PR interval]] in [[Mobitz type I]].
* In this variant of second degree heart block the PR interval is constant with occasional dropped beats as compared to the gradually prolonging PR interval in Mobitz type I.
*[[ECG]] findings include intermittently non-[[Conduct|conducted]] [[P wave]]s not preceded by [[PR prolongation]] and not followed by [[PR interval|PR]] [[shortening]].
* Bifascicular or trifascicular disease is seen in two thirds of the patients with Mobitz type II.<ref name="pmid6544636">{{cite journal| author=Puech P, Wainwright RJ| title=Clinical electrophysiology of atrioventricular block. | journal=Cardiol Clin | year= 1983 | volume= 1 | issue= 2 | pages= 209-24 | pmid=6544636 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=6544636  }}</ref><ref name="pmid8445186">{{cite journal |vauthors=Wogan JM, Lowenstein SR, Gordon GS |title=Second-degree atrioventricular block: Mobitz type II |journal=J Emerg Med |volume=11 |issue=1 |pages=47–54 |date=1993 |pmid=8445186 |doi=10.1016/0736-4679(93)90009-v |url=}}</ref>
*It almost always [[Result|results]] from a [[Conduction system disease|disease of the conduction system]] below the [[Level of measurement|level]] of [[Atrioventricular node|AV node]], occurring in the [[bundle of His]] in approximately 20% of the [[Case-based reasoning|cases]] and in the [[Bundle branch|bundle branches]] in the remainder.
*Type 2 second degree AV block, also known as Mobitz II is almost always a disease of the distal conduction system ([[electrical conduction system of the heart|His-Purkinje System]]).
*[[Dependent variable|Depending]] upon the [[Location parameter|location]] of the [[Heart block|block]], [[patients]] having [[bundle branch]] involvement also have [[axis]] shifts and [[QRS]] widening.
*At least two-thirds of the [[patients]] with [[Mobitz type II]] [[second degree AV block]] have [[Bifascicular block|bifascicular]] or even [[Trifascicular heart block|trifascicular]] [[disease]].<ref name="pmid6544636">{{cite journal| author=Puech P, Wainwright RJ| title=Clinical electrophysiology of atrioventricular block. | journal=Cardiol Clin | year= 1983 | volume= 1 | issue= 2 | pages= 209-24 | pmid=6544636 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=6544636  }}</ref><ref name="pmid8445186">{{cite journal |vauthors=Wogan JM, Lowenstein SR, Gordon GS |title=Second-degree atrioventricular block: Mobitz type II |journal=J Emerg Med |volume=11 |issue=1 |pages=47–54 |date=1993 |pmid=8445186 |doi=10.1016/0736-4679(93)90009-v |url=}}</ref>
*In the presence of 2:1 [[Atrioventricular block|AV block]], [[Mobitz type I]] and [[Mobitz type II AV block|Mobitz type II]] [[second degree AV block]] cannot be [[Differentiate|differentiated]] on the basis of [[electrocardiographic]] findings. In such cases, every other [[P wave]] is non-[[Conduct|conducted]] without a chance to [[Observation|observe]] the [[constant]] [[PR interval]] that is [[Characteristic impedance|characteristic]] of [[Mobitz type II AV block|Mobitz type II]] [[second degree AV block]].
*The [[Conduction System|conduction]] delay seen in [[Mobitz type II AV block|Mobitz type II]] [[second degree block]] is almost always at the infra-[[Nodal (protein)|nodal]] level involving the [[distal]] [[Conduction system disease|conduction system]] ([[His bundle]] (20%), [[Bundle branch|bundle branches]] or/and [[fascicles]]).


*Although the terms infranodal block or infrahisian block are often applied to this disorder, they are not synonymous with it.  
*Although often both the [[Term logic|terms]], [[Infranodal Wenkebach-type block|infranodal block]] or infrahisian [[Heart block|block]] are applied to [[Mobitz type II]] [[second degree AV block]], they are not [[Synonymous substitution|synonymous]] with it.


:*Infranodal block and [[infra-Hisian block]] are terms which refer to the anatomic location of the block, whereas
:*[[Infranodal Wenkebach-type block|Infranodal]] [[Heart block|block]] and [[infra-Hisian block]] are [[Term logic|terms]] which [[Reference|refer]] to the [[anatomic]] [[Location parameter|location]] of the [[Heart block|block]], whereas
:*Mobitz II refers to an electrocardiographic pattern associated with block at these levels.<ref name="pmid29850368">{{cite journal |vauthors=Li X, Xue Y, Wu H |title=A Case of Atrioventricular Block Potentially Associated with Right Coronary Artery Lesion and Ticagrelor Therapy Mediated by the Increasing Adenosine Plasma Concentration |journal=Case Rep Vasc Med |volume=2018 |issue= |pages=9385017 |date=2018 |pmid=29850368 |pmc=5933017 |doi=10.1155/2018/9385017 |url=}}</ref>
:*[[Mobitz II]] [[Reference|refers]] to an [[electrocardiographic]] [[pattern]] [[Association (statistics)|associated]] with [[Heart block|block]] at these [[Leveling effect|levels]].<ref name="pmid29850368">{{cite journal |vauthors=Li X, Xue Y, Wu H |title=A Case of Atrioventricular Block Potentially Associated with Right Coronary Artery Lesion and Ticagrelor Therapy Mediated by the Increasing Adenosine Plasma Concentration |journal=Case Rep Vasc Med |volume=2018 |issue= |pages=9385017 |date=2018 |pmid=29850368 |pmc=5933017 |doi=10.1155/2018/9385017 |url=}}</ref>


*Mobitz II heart block is characterized on a surface [[ECG]] by intermittently non-conducted [[P wave]]s not preceded by [[PR prolongation]] and not followed by PR shortening.
===Pathophysiology of LBBB===
*The medical significance of this type of [[AV block]] is that it may progress rapidly to [[complete heart block]], in which no escape rhythm may emerge.  
* Unlike [[right bundle branch block]] ([[RBBB]]), [[left bundle branch block]] completely modifies the way of [[depolarization]] of the [[Electrical conduction system of the heart|conduction system of the heart]].  
*In this case, the person may experience a [[Stokes-Adams attack]], [[cardiac arrest]], or [[sudden cardiac death]].
*In [[Left bundle branch block|LBBB]] the [[Activation energy|activation]] of [[interventricular septum]] is from right to left due to uninterrupted [[Conductance|conduction]] in the [[Right bundle branch block|RBB]].
*The definitive treatment for this form of AV Block is an [[implanted pacemaker]].<ref name="pmid29275956">{{cite journal |vauthors=Fu Md J, Bhatta L |title=Lyme carditis: Early occurrence and prolonged recovery |journal=J Electrocardiol |volume=51 |issue=3 |pages=516–518 |date=2018 |pmid=29275956 |doi=10.1016/j.jelectrocard.2017.12.035 |url=}}</ref><ref name="pmid28823599">{{cite journal |vauthors=Tuohy S, Saliba W, Pai M, Tchou P |title=Catheter ablation as a treatment of atrioventricular block |journal=Heart Rhythm |volume=15 |issue=1 |pages=90–96 |date=January 2018 |pmid=28823599 |doi=10.1016/j.hrthm.2017.08.015 |url=}}</ref>
* Then the [[electrical]] [[Impulse (psychology)|impulse]] propagates [[inferiorly]] to the left [[Result|resulting]] in delayed [[depolarization]] and [[Activation energy|activation]] of the [[left ventricle]] especially the left [[lateral]] wall.<ref name="pmid17385703">{{cite journal |author=Francia P, Balla C, Paneni F, Volpe M |title=Left bundle-branch block--pathophysiology, prognosis, and clinical management |journal=Clinical Cardiology |volume=30 |issue=3 |pages=110–5 |year=2007 |month=March |pmid=17385703 |doi=10.1002/clc.20034 |url=}}</ref>
* In [[Left bundle branch block|LBBB]], the right to left [[Activation energy|activation]] of the [[septum]] [[causes]] a small negative deflection ([[Q wave]]) in [[lead]] [[V1-morph|V<sub>1</sub>]] and a [[positive]] deflection ([[R wave]]) in [[lead]] V<sub>6</sub>.
*The [[right ventricle]] [[Depolarization|depolarizes]] earlier than the [[left ventricle]] giving an [[R wave]] in [[lead]] [[V1-morph|V<sub>1</sub>]] and an [[S wave]] in [[lead]] V<sub>6</sub>.
*Subsequent delayed [[depolarization]] of the [[left ventricle]] [[Result|results]] in an [[S wave]] in [[lead]] [[V1-morph|V<sub>1</sub>]] and another [[R wave]] in [[lead]] V<sub>6</sub>.


==Causes==
===Pathophysiology of RBBB===
*[[Right bundle branch block]] occurs when the [[electrical]] [[Impulse (psychology)|impulse]] is not [[Conductance|conducted]] along the [[Right bundle branch block|right bundle branch]].
* As the [[Conduction System|conduction]] along the [[Left bundle branch block|left bundle branch]] remains unaffected, the [[electrical]] [[Impulse (psychology)|impulse]] [[Travel medicine|travels]] [[Normal|normally]] within the [[septum]] from left to right.
* However, the [[right ventricular]] [[contraction]] occurs [[Comparability|comparatively]] [[Slow|slowly]] giving the [[Characteristic impedance|characteristic]] 'M' [[pattern]] on the [[electrocardiogram]].
 
====Genetics====
*[[Familial]] [[Case-based reasoning|cases]] of [[right bundle branch block]] have been [[Observation|observed]] in 4 Lebanese [[Family|families]] and the [[Abnormality (behavior)|abnormality]] was mapped to [[chromosome 19]].
* There is a [[subset]] of [[patients]] with [[Brugada syndrome]] who have [[mutations]] in [[SCN5A]], the [[gene]] [[Encoding (memory)|encoding]] for the [[Voltage-gated sodium channel|voltage-gated cardiac sodium channel]].
 
====Associated Syndromes====
*[[Duchenne muscular dystrophy]]
*[[Myotonic dystrophy]]: Other [[EKG]] findings include:
**[[First-degree AV block]]
**[[Left anterior fascicular block]]
**[[Intraventricular conduction delay]]
**[[Arrhythmias]]
*[[Stokes-Adams attacks]]
*[[Kearns-Sayre Syndrome]]
*[[Brugada syndrome]]
 
====Pseudo Right Bundle Branch Block====
'''[[Brugada syndrome]]:'''


The potential etiologies of Mobitz type II second degree AV block include reversible (both pathologic and iatrogenic) and idiopathic causes that are similar to other degrees of AV block (table 1). Common potentially reversible causes include:
*[[Brugada syndrome]] is due to a [[channelopathy]] [[Mediated transport|mediated]] by the [[SCN5A]] [[gene]].
* The [[Right bundle branch block|RBBB]] [[pattern]] seen in [[patients]] of [[Brugada syndrome]] is not actually [[Right bundle branch block|RBBB]] but instead it is due to a [[repolarization]] [[Abnormality (behavior)|abnormality]]. Therefore, the [[Right bundle branch block|RBBB]] like [[pattern]] seen in [[Brugada syndrome]] is [[Reference|referred]] to as a 'pseudo [[right bundle branch block]]'.
*[[EKG]] findings include [[ST-segment elevation]] in [[Lead|leads]] [[V1-morph|V1]]-[[V3 loop|V3]].
*[[Cocaine]] [[Consumer/Survivor/Ex-Patient Movement|consumption]] and/or the [[Usage analysis|use]] of the [[antiarrhythmic]] [[propafenone]] may unmask the [[EKG]] findings seen in [[Brugada syndrome]].<ref name="pmid23613002">{{cite journal |author=Yildiz BS, Gungor H, Gul I, Bilgin M, Zoghi M, Akilli A |title=Is a drug-challenge test with propafenone adequate to exclude Brugada syndrome? |journal=Cardiovascular Journal of Africa |volume=24 |issue=2 |pages=e4–6 |year=2013 |pmid=23613002 |doi=10.5830/CVJA-2012-068 |url=}}</ref>


●Pathologic – Myocardial ischemia (acute or chronic) involving the conduction system, cardiomyopathy (eg, amyloidosis, sarcoidosis), myocarditis (eg, Lyme disease), endocarditis with abscess formation, hyperkalemia, and hypervagotonia.
==Causes==
===Mobitz type II second degree AV block causes===


●Iatrogenic – Medication-related (AV nodal blocking medications), post-cardiac surgery, post-catheter ablation, post-transcatheter aortic valve implantation.
*[[Mobitz type II AV block|Mobitz type II]] [[second degree AV block]] is [[Rare|rarely]] seen in the [[patients]] without any [[Underlying representation|underlying]] [[heart disease]].
*The most common [[causes]] of [[Mobitz type II]] [[second degree AV block]] include:
** Reversible [[causes]] (both [[Pathological|pathologic]] and [[iatrogenic]])
**[[Idiopathic]] [[causes]] similar to other [[Degree (angle)|degrees]] of [[Atrioventricular block|AV block]] such as [[idiopathic]] progressive [[Cardiac conduction disorder|cardiac conduction disease]] with [[myocardial]] [[fibrosis]] and/or [[sclerosis]] [[Affect|affecting]] the [[Conduction system disease|conduction system]].


Mobitz type II second degree AV block is rarely seen in patients without underlying heart disease. When identifiable, the reversible causes most commonly associated with Mobitz type II second degree AV block are myocardial infarction with ischemia of the AV node and medications that alter conduction through the AV node (eg, digoxin, beta blockers, calcium channel blockers). When no specific reversible cause is identified, the block is often felt to be related to idiopathic progressive cardiac conduction disease with myocardial fibrosis and/or sclerosis that affects the conduction system.
* Details of all the possible [[etiologies]] are given in the table below:


{| class="wikitable"
{| class="wikitable"
|+Major causes of atrioventricular (AV) block
|+Major reversible causes of atrioventricular (AV) block
!'''Physiologic and pathophysiologic'''
! colspan="2" style="background: #4479BA; width: 200px;" | {{fontcolor|#FFF|'''Physiologic and pathophysiologic'''}}
!
|-
|-
|Increased vagal tone
|style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" |Increased [[vagal]] [[Tone (linguistics)|tone]]
|
|
* Also known as hypervagotonia
|-
|-
|Ischemic heart disease, including acute myocardial infarction
|style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" |[[Ischemic heart disease]]
|
|
*[[Acute]] or [[chronic]] [[myocardial infarction]]/[[ischemia]] involving the [[Conduction system disease|conduction system.]]
|-
|-
| rowspan="2" |Progressive cardiac conduction system disease
|style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" |Progressive [[Cardiac conduction disorder|cardiac conduction system disease]]
|With fibrosis and/or sclerosis (Lenegre disease)
|[[Association (statistics)|Associated]] with:
 
*[[Calcification]] in [[Lev's disease]]
*[[Fibrosis]] and/or [[sclerosis]] in [[Lenegre's Disease|Lenegre's disease]]
|-
|-
|With calcification (Lev disease)
|style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" |[[Infections]]
|-
|Infections (eg, viral myocarditis, Lyme carditis)
|
|
*[[Viral myocarditis]]
*[[Lyme carditis]]
*[[Endocarditis]] with [[abscess]] [[Formation matrix|formation]]
|-
|-
| rowspan="2" |Cardiomyopathy
|style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" |[[Cardiomyopathy]]
|Infiltrative processes (eg, sarcoidosis, amyloidosis, hemochromatosis, malignancy, etc)
|[[Infiltration (medical)|Infiltrative]] [[Process (anatomy)|processes]] such as:
 
*[[Sarcoidosis]]
*[[Hemochromatosis]]
*[[Amyloidosis]]
*[[Malignancy]]
 
Other non-[[Ischemic cardiomyopathy|ischemic cardiomyopathies]] include:
 
*[[Idiopathic]]
*[[Infectious]]
|-
|-
|Other non-ischemic cardiomyopathies (eg, idiopathic, infectious, etc)
|style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" |[[Congenital]] [[Atrioventricular block|AV block]]
|
* It is [[Related changes|related]] to [[Structural biology|structural]] [[congenital heart disease]]
*It occurs as a part of [[neonatal lupus syndrome]]
|-
|-
| rowspan="2" |Congenital AV block
|style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" |Other [[Reversible cell|reversible]] [[causes]]
|Related to structural congenital heart disease
|
*[[Hyperkalemia]]
* Severe [[Hypothyroidism|hypo]]- or [[hyperthyroidism]]
*[[Degenerative]] [[Neuromuscular disease|neuromuscular diseases]]
*[[Trauma]]
|-
|-
|As part of neonatal lupus syndrome
| colspan="2" style="background: #4479BA; width: 200px;" | {{fontcolor|#FFF|'''Iatrogenic'''}}
|-
|-
| rowspan="4" |Other
|style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" |[[Drugs]] (altering [[Conduction System|conduction]] through [[Atrioventricular node|AV node]])
|Hyperkalemia
|
*[[Beta-blockers]]
*[[Digoxin]]
*[[Calcium channel blockers]]
*[[Adenosine]]
*[[Antiarrhythmic drugs]]
|-
|-
|severe hypo- or hyperthyroidism
|style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" |[[Cardiac surgery]]
|-
|
|trauma
* Post [[valvular]] [[surgery]]
|-
* Post-[[Surgery|surgical]] [[Correction (newspaper)|correction]] of [[congenital heart disease]]
|degenerative neuromuscular diseases
|-
| colspan="2" |'''Iatrogenic'''
|-
| rowspan="5" |Drugs
|Beta blockers
|-
|calcium channel blockers
|-
|digoxin
|-
|antiarrhythmic drugs
|-
|adenosine
|-
| colspan="2" |Transcatheter aortic valve implantation
|-
|-
| rowspan="2" |Cardiac surgery
| colspan="2" style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" |[[Catheter ablation]] of [[arrhythmias]]
|Post valvular surgery
|-
|-
|post surgical correction of congenital heart disease
| colspan="2" style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" |[[Alcohol septal ablation]] for [[hypertrophic cardiomyopathy]]
|-
|-
|Catheter ablation of arrhythmias
| colspan="2" style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" |Transcatheter [[Closure (psychology)|closure]] of [[ventricular septal defect]]
|
|-
|-
|Alcohol septal ablation for hypertrophic cardiomyopathy
| colspan="2" style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" |Post-[[transcatheter aortic valve implantation]]
|
|-
|Transcatheter closure of ventricular septal defect
|
|}
|}


===Life Threatening Causes===
===Life Threatening Causes===
Life-threatening conditions can result in death or permanent disability within 24 hours if left untreated<ref name="pmid29493981">{{cite journal |vauthors=Mangi MA, Jones WM, Napier L |title= |journal= |volume= |issue= |pages= |date= |pmid=29493981 |doi= |url=}}</ref>.
[[Life]]-threatening [[conditions]] can [[result]] in death or permanent [[disability]] within 24 hours if left untreated.<ref name="pmid29493981">{{cite journal |vauthors=Mangi MA, Jones WM, Napier L |title= |journal= |volume= |issue= |pages= |date= |pmid=29493981 |doi= |url=}}</ref>
 
* [[Acute myocardial infarction]]<ref name="pmid30227965">{{cite journal |vauthors=Misumida N, Ogunbayo GO, Kim SM, Abdel-Latif A, Ziada KM, Elayi CS |title=Frequency and Significance of High-Degree Atrioventricular Block and Sinoatrial Node Dysfunction in Patients With Non-ST-Elevation Myocardial Infarction |journal=Am. J. Cardiol. |volume=122 |issue=10 |pages=1598–1603 |date=November 2018 |pmid=30227965 |doi=10.1016/j.amjcard.2018.08.001 |url=}}</ref><ref name="pmid23224264">{{cite journal |vauthors=Barold SS, Herweg B |title=Second-degree atrioventricular block revisited |journal=Herzschrittmacherther Elektrophysiol |volume=23 |issue=4 |pages=296–304 |date=December 2012 |pmid=23224264 |doi=10.1007/s00399-012-0240-8 |url=}}</ref>
* [[Acute myocardial infarction]]<ref name="pmid30227965">{{cite journal |vauthors=Misumida N, Ogunbayo GO, Kim SM, Abdel-Latif A, Ziada KM, Elayi CS |title=Frequency and Significance of High-Degree Atrioventricular Block and Sinoatrial Node Dysfunction in Patients With Non-ST-Elevation Myocardial Infarction |journal=Am. J. Cardiol. |volume=122 |issue=10 |pages=1598–1603 |date=November 2018 |pmid=30227965 |doi=10.1016/j.amjcard.2018.08.001 |url=}}</ref><ref name="pmid23224264">{{cite journal |vauthors=Barold SS, Herweg B |title=Second-degree atrioventricular block revisited |journal=Herzschrittmacherther Elektrophysiol |volume=23 |issue=4 |pages=296–304 |date=December 2012 |pmid=23224264 |doi=10.1007/s00399-012-0240-8 |url=}}</ref>
* [[Acute rheumatic fever]]
* [[Acute rheumatic fever]]
Line 160: Line 216:
* [[HCM]]
* [[HCM]]
* [[Hypertension]]
* [[Hypertension]]
* [[Iatrogenic]] after surgical correction of [[VSD]], [[tetralogy of Fallot]], and [[endocardial cushion defect]]
* [[Iatrogenic]] after [[Surgery|surgical]] [[Correction (newspaper)|correction]] of [[VSD]], [[tetralogy of Fallot]], and [[endocardial cushion defect]]
* [[ST elevation MI|Inferior ST elevation MI]]
* [[ST elevation MI|Inferior ST elevation MI]]
* [[mitral valve sclerosis|Massive calcification of the mitral annulus]]
* [[mitral valve sclerosis|Massive calcification of the mitral annulus]]
Line 177: Line 233:
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Chemical / poisoning'''
| '''Chemical / poisoning'''
|bgcolor="Beige"| No underlying causes
|bgcolor="Beige"| No [[Underlying representation|underlying]] [[causes]]
|-
|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Dermatologic'''
| '''Dermatologic'''
|bgcolor="Beige"| No underlying causes
|bgcolor="Beige"| No [[Underlying representation|underlying]] [[causes]]
|-
|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
Line 189: Line 245:
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Ear Nose Throat'''
| '''Ear Nose Throat'''
|bgcolor="Beige"| No underlying causes
|bgcolor="Beige"| No [[Underlying representation|underlying]] [[causes]]
|-  
|-  
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
Line 233: Line 289:
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Obstetric/Gynecologic'''
| '''Obstetric/Gynecologic'''
|bgcolor="Beige"| No underlying causes
|bgcolor="Beige"| No [[Underlying representation|underlying]] [[causes]]
|-
|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
Line 241: Line 297:
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Opthalmologic'''
| '''Opthalmologic'''
|bgcolor="Beige"| No underlying causes
|bgcolor="Beige"| No [[Underlying representation|underlying]] [[causes]]
|-
|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Overdose / Toxicity'''
| '''Overdose / Toxicity'''
|bgcolor="Beige"| No underlying causes
|bgcolor="Beige"| No [[Underlying representation|underlying]] [[causes]]
|-
|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Psychiatric'''
| '''Psychiatric'''
|bgcolor="Beige"| No underlying causes
|bgcolor="Beige"| No [[Underlying representation|underlying]] [[causes]]
|-
|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
Line 265: Line 321:
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Sexual'''
| '''Sexual'''
|bgcolor="Beige"| No underlying causes
|bgcolor="Beige"| No [[Underlying representation|underlying]] [[causes]]
|-
|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Trauma'''
| '''Trauma'''
|bgcolor="Beige"| No underlying causes
|bgcolor="Beige"| No [[Underlying representation|underlying]] [[causes]]
|-
|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Urologic'''
| '''Urologic'''
|bgcolor="Beige"| No underlying causes
|bgcolor="Beige"| No [[Underlying representation|underlying]] [[causes]]
|-
|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
| '''Dental'''
| '''Dental'''
|bgcolor="Beige"| No underlying causes
|bgcolor="Beige"| No [[Underlying representation|underlying]] [[causes]]
|-
|-
|-bgcolor="LightSteelBlue"
|-bgcolor="LightSteelBlue"
Line 377: Line 433:
* [[sex linkage|X-linked inherited  conditions]]
* [[sex linkage|X-linked inherited  conditions]]
{{col-end}}
{{col-end}}
*'''For causes of [[Left bundle branch block]], click [[Left bundle branch block causes|here]].'''
*'''For causes of [[Right bundle branch block]], click [[Right bundle branch block causes|here]].'''


==Epidemiology and Demographics==
==Epidemiology and Demographics==
Line 389: Line 448:
*[[Men]] and [[women]] are [[Affect|affected]] [[Equalism|equally]] by [[second degree AV block]].
*[[Men]] and [[women]] are [[Affect|affected]] [[Equalism|equally]] by [[second degree AV block]].


==Risk factors==
==Risk Factors==


* Common [[risk factors]] [[Association (statistics)|associated]] with [[second degree AV block]] include the following:<ref name="pmid11988196">{{cite journal| author=Meimoun P, Zeghdi R, D'Attelis N, Berrebi A, Braunberger E, Deloche A | display-authors=etal| title=Frequency, predictors, and consequences of atrioventricular block after mitral valve repair. | journal=Am J Cardiol | year= 2002 | volume= 89 | issue= 9 | pages= 1062-6 | pmid=11988196 | doi=10.1016/s0002-9149(02)02276-2 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11988196  }}</ref><ref name="pmid119881962">{{cite journal| author=Meimoun P, Zeghdi R, D'Attelis N, Berrebi A, Braunberger E, Deloche A | display-authors=etal| title=Frequency, predictors, and consequences of atrioventricular block after mitral valve repair. | journal=Am J Cardiol | year= 2002 | volume= 89 | issue= 9 | pages= 1062-6 | pmid=11988196 | doi=10.1016/s0002-9149(02)02276-2 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11988196  }}</ref><ref name="pmid31125096">{{cite journal |vauthors=Kerola T, Eranti A, Aro AL, Haukilahti MA, Holkeri A, Junttila MJ, Kenttä TV, Rissanen H, Vittinghoff E, Knekt P, Heliövaara M, Huikuri HV, Marcus GM |title=Risk Factors Associated With Atrioventricular Block |journal=JAMA Netw Open |volume=2 |issue=5 |pages=e194176 |date=May 2019 |pmid=31125096 |pmc=6632153 |doi=10.1001/jamanetworkopen.2019.4176 |url=}}</ref><ref name="pmid8447272">{{cite journal |vauthors=Schoeller R, Andresen D, Büttner P, Oezcelik K, Vey G, Schröder R |title=First- or second-degree atrioventricular block as a risk factor in idiopathic dilated cardiomyopathy |journal=Am. J. Cardiol. |volume=71 |issue=8 |pages=720–6 |date=March 1993 |pmid=8447272 |doi=10.1016/0002-9149(93)91017-c |url=}}</ref>
* Common [[risk factors]] [[Association (statistics)|associated]] with [[second degree AV block]] include the following:<ref name="pmid11988196">{{cite journal| author=Meimoun P, Zeghdi R, D'Attelis N, Berrebi A, Braunberger E, Deloche A | display-authors=etal| title=Frequency, predictors, and consequences of atrioventricular block after mitral valve repair. | journal=Am J Cardiol | year= 2002 | volume= 89 | issue= 9 | pages= 1062-6 | pmid=11988196 | doi=10.1016/s0002-9149(02)02276-2 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11988196  }}</ref><ref name="pmid119881962">{{cite journal| author=Meimoun P, Zeghdi R, D'Attelis N, Berrebi A, Braunberger E, Deloche A | display-authors=etal| title=Frequency, predictors, and consequences of atrioventricular block after mitral valve repair. | journal=Am J Cardiol | year= 2002 | volume= 89 | issue= 9 | pages= 1062-6 | pmid=11988196 | doi=10.1016/s0002-9149(02)02276-2 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11988196  }}</ref><ref name="pmid31125096">{{cite journal |vauthors=Kerola T, Eranti A, Aro AL, Haukilahti MA, Holkeri A, Junttila MJ, Kenttä TV, Rissanen H, Vittinghoff E, Knekt P, Heliövaara M, Huikuri HV, Marcus GM |title=Risk Factors Associated With Atrioventricular Block |journal=JAMA Netw Open |volume=2 |issue=5 |pages=e194176 |date=May 2019 |pmid=31125096 |pmc=6632153 |doi=10.1001/jamanetworkopen.2019.4176 |url=}}</ref><ref name="pmid8447272">{{cite journal |vauthors=Schoeller R, Andresen D, Büttner P, Oezcelik K, Vey G, Schröder R |title=First- or second-degree atrioventricular block as a risk factor in idiopathic dilated cardiomyopathy |journal=Am. J. Cardiol. |volume=71 |issue=8 |pages=720–6 |date=March 1993 |pmid=8447272 |doi=10.1016/0002-9149(93)91017-c |url=}}</ref>
Line 396: Line 455:
**[[Acute myocardial infarction]]
**[[Acute myocardial infarction]]
** Prior [[cardiac surgery]]
** Prior [[cardiac surgery]]
** Older [[age]]
**[[Old age|Older age]]
**[[Heart attack]] or [[coronary artery disease]]
**[[Heart attack]] or [[coronary artery disease]]
**[[Cardiomyopathy]]
**[[Cardiomyopathy]]
Line 407: Line 466:
** After [[open heart surgery]]
** After [[open heart surgery]]


==Natural History, Complications, and Prognosis==
==Natural History, Complications and Prognosis==
===Natural History===
===Natural History===
* Mobitz II second degree Av block is due to block inferior to the AV node (infra-Hisian structures) and it progresses to complete heart block.<ref name="pmid463945">{{cite journal |vauthors=Rodstein M, Wolloch L, Iuster Z |title=The natural history intraventricular conduction disturbances in the aged: an analysis of the developing second and third degree heart block with clinical pathological correlations |journal=Am. J. Med. Sci. |volume=277 |issue=2 |pages=179–88 |date=1979 |pmid=463945 |doi=10.1097/00000441-197903000-00006 |url=}}</ref>
*[[Mobitz II]] [[second degree AV block]] is due to the [[Blocking (statistics)|block]] [[Inferior angle|inferior]] to the [[Atrioventricular node|AV node]] (infra-Hisian [[Structure factor|structures]]) and it rapidly progresses to a [[complete heart block]] in which no escape [[rhythm]] may emerge.<ref name="pmid463945">{{cite journal |vauthors=Rodstein M, Wolloch L, Iuster Z |title=The natural history intraventricular conduction disturbances in the aged: an analysis of the developing second and third degree heart block with clinical pathological correlations |journal=Am. J. Med. Sci. |volume=277 |issue=2 |pages=179–88 |date=1979 |pmid=463945 |doi=10.1097/00000441-197903000-00006 |url=}}</ref>


===Complications===
===Complications===
Line 415: Line 474:
* [[Stokes-Adams syndrome]]
* [[Stokes-Adams syndrome]]
* [[Syncope]]<ref name="pmid29493981">{{cite journal |vauthors=Mangi MA, Jones WM, Napier L |title= |journal= |volume= |issue= |pages= |date= |pmid=29493981 |doi= |url=}}</ref>
* [[Syncope]]<ref name="pmid29493981">{{cite journal |vauthors=Mangi MA, Jones WM, Napier L |title= |journal= |volume= |issue= |pages= |date= |pmid=29493981 |doi= |url=}}</ref>
*Dizziness
*[[Dizziness]]
*Chest pain
*[[Chest pain]]
*Death
*Death


===Prognosis===
===Prognosis===
*[[Mobitz II]], as it involves the infra nodal structures, carries the risk of progression to complete heart block and carries an unfavorable prognosis.<ref name="pmid11988196">{{cite journal| author=Meimoun P, Zeghdi R, D'Attelis N, Berrebi A, Braunberger E, Deloche A | display-authors=etal| title=Frequency, predictors, and consequences of atrioventricular block after mitral valve repair. | journal=Am J Cardiol | year= 2002 | volume= 89 | issue= 9 | pages= 1062-6 | pmid=11988196 | doi=10.1016/s0002-9149(02)02276-2 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11988196  }}</ref>
*[[Mobitz II]], as it involves the [[Infranodal Wenkebach-type block|infra-nodal]] [[Structure factor|structures]], [[Carrying capacity|carries]] the [[RiskMetrics|risk]] of progression to [[complete heart block]] and [[Carrying capacity|carries]] an unfavorable [[prognosis]].<ref name="pmid11988196">{{cite journal| author=Meimoun P, Zeghdi R, D'Attelis N, Berrebi A, Braunberger E, Deloche A | display-authors=etal| title=Frequency, predictors, and consequences of atrioventricular block after mitral valve repair. | journal=Am J Cardiol | year= 2002 | volume= 89 | issue= 9 | pages= 1062-6 | pmid=11988196 | doi=10.1016/s0002-9149(02)02276-2 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11988196  }}</ref>


==Diagnosis==
==Diagnosis==
===Diagnostic Study of Choice===
===Diagnostic Study of Choice===
* [[Electrocardiography]] (ECG) is employed to determine the type of [[second-degree atrioventricular]] (AV) block present<ref name="pmid29493981">{{cite journal |vauthors=Mangi MA, Jones WM, Napier L |title= |journal= |volume= |issue= |pages= |date= |pmid=29493981 |doi= |url=}}</ref><ref name="pmid22813399">{{cite journal |vauthors=Thiruganasambandamoorthy V, Hess EP, Turko E, Tran ML, Wells GA, Stiell IG |title=Defining abnormal electrocardiography in adult emergency department syncope patients: the Ottawa Electrocardiographic Criteria |journal=CJEM |volume=14 |issue=4 |pages=248–58 |date=July 2012 |pmid=22813399 |doi= |url=}}</ref><ref name="pmid23224264">{{cite journal |vauthors=Barold SS, Herweg B |title=Second-degree atrioventricular block revisited |journal=Herzschrittmacherther Elektrophysiol |volume=23 |issue=4 |pages=296–304 |date=December 2012 |pmid=23224264 |doi=10.1007/s00399-012-0240-8 |url=}}</ref>.
* [[Electrocardiography]] ([[ECG]]) is employed to determine the type of [[Second-degree AV block|second-degree atrioventricular (AV) block]] [[Presenting symptom|present]]<ref name="pmid29493981">{{cite journal |vauthors=Mangi MA, Jones WM, Napier L |title= |journal= |volume= |issue= |pages= |date= |pmid=29493981 |doi= |url=}}</ref><ref name="pmid22813399">{{cite journal |vauthors=Thiruganasambandamoorthy V, Hess EP, Turko E, Tran ML, Wells GA, Stiell IG |title=Defining abnormal electrocardiography in adult emergency department syncope patients: the Ottawa Electrocardiographic Criteria |journal=CJEM |volume=14 |issue=4 |pages=248–58 |date=July 2012 |pmid=22813399 |doi= |url=}}</ref><ref name="pmid23224264">{{cite journal |vauthors=Barold SS, Herweg B |title=Second-degree atrioventricular block revisited |journal=Herzschrittmacherther Elektrophysiol |volume=23 |issue=4 |pages=296–304 |date=December 2012 |pmid=23224264 |doi=10.1007/s00399-012-0240-8 |url=}}</ref>.
* Follow-up [[ECG]]s and [[cardiac]] monitoring are appropriate<ref name="pmid25080840">{{cite journal |vauthors=Barold SS, Van Heuverswyn FE, Timmers L, Stroobandt RX |title=Mobitz type II second-degree atrioventricular block during dobutamine stress echocardiography. True or false? |journal=Echocardiography |volume=31 |issue=7 |pages=799–801 |date=August 2014 |pmid=25080840 |doi=10.1111/echo.12577 |url=}}</ref>.
* Follow-up [[ECG]]s and [[cardiac monitoring]] are [[Appropriate Use Criteria|appropriate]].<ref name="pmid25080840">{{cite journal |vauthors=Barold SS, Van Heuverswyn FE, Timmers L, Stroobandt RX |title=Mobitz type II second-degree atrioventricular block during dobutamine stress echocardiography. True or false? |journal=Echocardiography |volume=31 |issue=7 |pages=799–801 |date=August 2014 |pmid=25080840 |doi=10.1111/echo.12577 |url=}}</ref>
* Routine imaging studies are not required. However, if [[myocarditis]] is a concern, [[echocardiography]] may be indicated<ref name="pmid29850368">{{cite journal |vauthors=Li X, Xue Y, Wu H |title=A Case of Atrioventricular Block Potentially Associated with Right Coronary Artery Lesion and Ticagrelor Therapy Mediated by the Increasing Adenosine Plasma Concentration |journal=Case Rep Vasc Med |volume=2018 |issue= |pages=9385017 |date=2018 |pmid=29850368 |pmc=5933017 |doi=10.1155/2018/9385017 |url=}}</ref><ref name="pmid29275956">{{cite journal |vauthors=Fu Md J, Bhatta L |title=Lyme carditis: Early occurrence and prolonged recovery |journal=J Electrocardiol |volume=51 |issue=3 |pages=516–518 |date=2018 |pmid=29275956 |doi=10.1016/j.jelectrocard.2017.12.035 |url=}}</ref>.
* Routine [[imaging studies]] are not required. However, if [[myocarditis]] is a concern, [[echocardiography]] may be [[Indication (medicine)|indicated]].<ref name="pmid29850368">{{cite journal |vauthors=Li X, Xue Y, Wu H |title=A Case of Atrioventricular Block Potentially Associated with Right Coronary Artery Lesion and Ticagrelor Therapy Mediated by the Increasing Adenosine Plasma Concentration |journal=Case Rep Vasc Med |volume=2018 |issue= |pages=9385017 |date=2018 |pmid=29850368 |pmc=5933017 |doi=10.1155/2018/9385017 |url=}}</ref><ref name="pmid29275956">{{cite journal |vauthors=Fu Md J, Bhatta L |title=Lyme carditis: Early occurrence and prolonged recovery |journal=J Electrocardiol |volume=51 |issue=3 |pages=516–518 |date=2018 |pmid=29275956 |doi=10.1016/j.jelectrocard.2017.12.035 |url=}}</ref>
* If [[myocardial ischemia]] is a concern, a chest radiograph may be indicated<ref name="pmid29083636">{{cite journal |vauthors=Kashou AH, Goyal A, Nguyen T, Chhabra L |title= |journal= |volume= |issue= |pages= |date= |pmid=29083636 |doi= |url=}}</ref>.
* If [[myocardial ischemia]] is a concern, a [[chest radiograph]] may be [[Indication (medicine)|indicated]].<ref name="pmid29083636">{{cite journal |vauthors=Kashou AH, Goyal A, Nguyen T, Chhabra L |title= |journal= |volume= |issue= |pages= |date= |pmid=29083636 |doi= |url=}}</ref>


===History and Symptoms===
===History and Symptoms===
* History from patients with second degree AV block should involve asking about the following:<ref name="pmid7405798">{{cite journal |vauthors=Zeppilli P, Fenici R, Sassara M, Pirrami MM, Caselli G |title=Wenckebach second-degree A-V block in top-ranking athletes: an old problem revisited |journal=Am. Heart J. |volume=100 |issue=3 |pages=281–94 |date=September 1980 |pmid=7405798 |doi=10.1016/0002-8703(80)90140-4 |url=}}</ref><ref name="pmid29083636">{{cite journal| author=| title=StatPearls | journal= | year= 2020 | volume=  | issue=  | pages=  | pmid=29083636 | doi= | pmc= | url= }}</ref>
*[[History and Physical examination|History]] from [[patients]] with [[second degree AV block]] should involve [[Ask a question|asking]] about the following:<ref name="pmid7405798">{{cite journal |vauthors=Zeppilli P, Fenici R, Sassara M, Pirrami MM, Caselli G |title=Wenckebach second-degree A-V block in top-ranking athletes: an old problem revisited |journal=Am. Heart J. |volume=100 |issue=3 |pages=281–94 |date=September 1980 |pmid=7405798 |doi=10.1016/0002-8703(80)90140-4 |url=}}</ref><ref name="pmid29083636">{{cite journal| author=| title=StatPearls | journal= | year= 2020 | volume=  | issue=  | pages=  | pmid=29083636 | doi= | pmc= | url= }}</ref>
** Congenital cardiac disease
**[[Congenital heart disease]]
** Current heart condition  
**[[Current]] [[heart condition]]
** Recent or previous cardiac procedures  
**[[Recent changes|Recent]] or previous [[cardiac]] [[Procedure|procedures]]
** History of medications
**[[History and Physical examination|History]] of [[medications]]
* Most people with Wenckebach (Type I Mobitz) do not show symptoms.<ref name="pmid11988196">{{cite journal| author=Meimoun P, Zeghdi R, D'Attelis N, Berrebi A, Braunberger E, Deloche A | display-authors=etal| title=Frequency, predictors, and consequences of atrioventricular block after mitral valve repair. | journal=Am J Cardiol | year= 2002 | volume= 89 | issue= 9 | pages= 1062-6 | pmid=11988196 | doi=10.1016/s0002-9149(02)02276-2 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11988196  }} </ref><ref name="pmid29493981">{{cite journal |vauthors=Mangi MA, Jones WM, Napier L |title= |journal= |volume= |issue= |pages= |date= |pmid=29493981 |doi= |url=}}</ref>
* Most [[People's Solidarity|people]] with [[Wenckebach]] ([[Type I Mobitz]]) do not show [[symptoms]].<ref name="pmid11988196">{{cite journal| author=Meimoun P, Zeghdi R, D'Attelis N, Berrebi A, Braunberger E, Deloche A | display-authors=etal| title=Frequency, predictors, and consequences of atrioventricular block after mitral valve repair. | journal=Am J Cardiol | year= 2002 | volume= 89 | issue= 9 | pages= 1062-6 | pmid=11988196 | doi=10.1016/s0002-9149(02)02276-2 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11988196  }} </ref><ref name="pmid29493981">{{cite journal |vauthors=Mangi MA, Jones WM, Napier L |title= |journal= |volume= |issue= |pages= |date= |pmid=29493981 |doi= |url=}}</ref>
* If the sinus rate is slow and only few beats are conducted (higher grade blocks) there may be a significantly [[reduced cardiac output]].
* If the [[sinus]] [[rate]] is [[slow]] and only [[Fewmets|few]] [[Beats per minute|beats]] are [[Conductance|conducted]] (higher [[Grading (tumors)|grade]] [[Blocking (statistics)|blocks]]) there may be a [[Significant figure|significantly]] [[reduced cardiac output]].
*Usual symptoms in such patients include:<ref name="pmid6373268">{{cite journal |vauthors=Bexton RS, Camm AJ |title=Second degree atrioventricular block |journal=Eur. Heart J. |volume=5 Suppl A |issue= |pages=111–4 |date=March 1984 |pmid=6373268 |doi=10.1093/eurheartj/5.suppl_a.111 |url=}}</ref><ref name="pmid8445186">{{cite journal |vauthors=Wogan JM, Lowenstein SR, Gordon GS |title=Second-degree atrioventricular block: Mobitz type II |journal=J Emerg Med |volume=11 |issue=1 |pages=47–54 |date=1993 |pmid=8445186 |doi=10.1016/0736-4679(93)90009-v |url=}}</ref>
*Usual [[symptoms]] in such [[patients]] include:<ref name="pmid6373268">{{cite journal |vauthors=Bexton RS, Camm AJ |title=Second degree atrioventricular block |journal=Eur. Heart J. |volume=5 Suppl A |issue= |pages=111–4 |date=March 1984 |pmid=6373268 |doi=10.1093/eurheartj/5.suppl_a.111 |url=}}</ref><ref name="pmid8445186">{{cite journal |vauthors=Wogan JM, Lowenstein SR, Gordon GS |title=Second-degree atrioventricular block: Mobitz type II |journal=J Emerg Med |volume=11 |issue=1 |pages=47–54 |date=1993 |pmid=8445186 |doi=10.1016/0736-4679(93)90009-v |url=}}</ref>
**[[Light-headedness]]
**[[Light-headedness]]
**[[Dizziness]]
**[[Dizziness]]
**[[Fainting]]
**[[Fainting]]
**[[Fatigue]]
**[[Fatigue]]
**[[Heart failure]] symptoms
**[[Heart failure]] [[symptoms]]
**[[Pre-syncope]]
**[[Pre-syncope]]
**[[Syncope]]
**[[Syncope]]


===Physical Examination===
===Physical Examination===
*Patients with Mobitz II can appear asymptomatic as well. However, in more cases they may be in distress or progress to the more severe third degree AV block.  
*[[Patients]] with [[Mobitz II]] can [[Appearance|appear]] [[asymptomatic]] as well. However, in more [[Case-based reasoning|cases]] they may be in [[distress]] or progress to the more severe [[third degree AV block]].
*Patients may appear pale in cases of bradycardia with decreased cardiac output.<ref name="pmid4701376">{{cite journal| author=Rosen KM, Dhingra RC, Loeb HS, Rahimtoola SH| title=Chronic heart block in adults. Clinical and electrophysiological observations. | journal=Arch Intern Med | year= 1973 | volume= 131 | issue= 5 | pages= 663-72 | pmid=4701376 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=4701376  }}</ref>
*[[Patients]] may [[Appearance|appear]] [[Pale skin color|pale]] in [[Case-based reasoning|cases]] of [[bradycardia]] with decreased [[cardiac output]].<ref name="pmid4701376">{{cite journal| author=Rosen KM, Dhingra RC, Loeb HS, Rahimtoola SH| title=Chronic heart block in adults. Clinical and electrophysiological observations. | journal=Arch Intern Med | year= 1973 | volume= 131 | issue= 5 | pages= 663-72 | pmid=4701376 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=4701376  }}</ref>
* Bradycardia with an irregular pulse<ref name="pmid699934">{{cite journal |vauthors=Schneider MD, Roller DH, Morganroth J, Josephson ME |title=The syndromes of familial atrioventricular block with sinus bradycardia: prognostic indices, electrophysiologic and histopathologic correlates |journal=Eur J Cardiol |volume=7 |issue=5-6 |pages=337–51 |date=July 1978 |pmid=699934 |doi= |url=}}</ref>
*[[Bradycardia]] with an [[irregular pulse]]<ref name="pmid699934">{{cite journal |vauthors=Schneider MD, Roller DH, Morganroth J, Josephson ME |title=The syndromes of familial atrioventricular block with sinus bradycardia: prognostic indices, electrophysiologic and histopathologic correlates |journal=Eur J Cardiol |volume=7 |issue=5-6 |pages=337–51 |date=July 1978 |pmid=699934 |doi= |url=}}</ref>
*Lightheadedness  
*[[Lightheadedness]]
*Hypotension<ref name="pmid27642736">{{cite journal |vauthors=Trappe HJ |title=[Consciousness disorders from cardiological view] |language=German |journal=Dtsch. Med. Wochenschr. |volume=141 |issue=19 |pages=1361–9 |date=September 2016 |pmid=27642736 |doi=10.1055/s-0042-103177 |url=}}</ref>
*[[Hypotension]]<ref name="pmid27642736">{{cite journal |vauthors=Trappe HJ |title=[Consciousness disorders from cardiological view] |language=German |journal=Dtsch. Med. Wochenschr. |volume=141 |issue=19 |pages=1361–9 |date=September 2016 |pmid=27642736 |doi=10.1055/s-0042-103177 |url=}}</ref>
*Syncope or presyncope
*[[Syncope]] or [[presyncope]]
*Jugular venous distension  
*[[Jugular venous distension]]
*Bibasilar crackles in patients with exacerbated heart failure
*Bibasilar [[crackles]] in [[patients]] with exacerbated [[heart failure]]
*Peripheral edema
*[[Peripheral edema]]


===Laboratory Findings===
===Laboratory Findings===
Patients with second degree AV block should be checked for the following laboratory tests:<ref name="pmid1008977">{{cite journal| author=Gupta PK, Lichstein E, Chadda KD| title=Chronic His bundle block. Clinical, electrocardiographic, electrophysiological, and follow-up studies on 16 patients. | journal=Br Heart J | year= 1976 | volume= 38 | issue= 12 | pages= 1343-9 | pmid=1008977 | doi=10.1136/hrt.38.12.1343 | pmc=483178 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1008977  }}</ref>
[[Patients]] with [[second degree AV block]] should be [[Check|checked]] for the following [[laboratory]] [[Test|tests]]:<ref name="pmid1008977">{{cite journal| author=Gupta PK, Lichstein E, Chadda KD| title=Chronic His bundle block. Clinical, electrocardiographic, electrophysiological, and follow-up studies on 16 patients. | journal=Br Heart J | year= 1976 | volume= 38 | issue= 12 | pages= 1343-9 | pmid=1008977 | doi=10.1136/hrt.38.12.1343 | pmc=483178 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1008977  }}</ref>
* Serum [[electrolytes]]
*[[Serum electrolyte|Serum electrolytes]]
* [[Calcium]]  
* [[Calcium]]  
* [[Magnesium]]  
* [[Magnesium]]  
* [[Myocardial]] enzymes in patients with [[myocardial infarction]]
* [[Myocardial]] [[enzymes]] in [[patients]] with [[myocardial infarction]]
* [[Myocarditis]] related laboratory tests as the following:<ref name="pmid18532885">{{cite journal| author=Steere AC, McHugh G, Damle N, Sikand VK| title=Prospective study of serologic tests for lyme disease. | journal=Clin Infect Dis | year= 2008 | volume= 47 | issue= 2 | pages= 188-95 | pmid=18532885 | doi=10.1086/589242 | pmc=5538270 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=18532885  }}</ref>  
* [[Myocarditis]] [[Related phenomena|related]] [[laboratory]] [[Test|tests]] as the following:<ref name="pmid18532885">{{cite journal| author=Steere AC, McHugh G, Damle N, Sikand VK| title=Prospective study of serologic tests for lyme disease. | journal=Clin Infect Dis | year= 2008 | volume= 47 | issue= 2 | pages= 188-95 | pmid=18532885 | doi=10.1086/589242 | pmc=5538270 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=18532885  }}</ref>  
**[[Lyme]] titres
**[[Lyme]] [[Titre|titres]]
** [[HIV]] tests
**[[HIV test|HIV tests]]
** [[PCR]] for [[enteroviruses]]
**[[PCR]] for [[enteroviruses]]
** [[Chagas]] titres
**[[Chagas]] [[Titre|titres]]


===Electrocardiogram===
===Electrocardiogram===
* There are intermittent blocked [[P wave]]s
* There are intermittent [[Blocking (statistics)|blocked]] [[P wave]]s.
* In the conducted beats, the [[PR interval]]s remain constant
* In the [[Conductance|conducted]] [[Beats per minute|beats]], the [[PR interval]]s remain [[constant]].
* The PR is fairly constant except that slight shortening may occur in the first beat after the blocked cycle. This is the result of improved conduction following the block
* The [[PR]] is fairly [[constant]] except that slight [[shortening]] may occur in the first [[Beats per minute|beat]] after the [[Blocking (statistics)|blocked]] [[Cycle (gene)|cycle]]. This is the [[result]] of improved [[Conduction System|conduction]] following the [[Blocking (statistics)|block]].
* Most patients with type II second-degree AV block have associated bundle branch block.
* Most [[patients]] with type II [[second-degree AV block]] have [[Association (statistics)|associated]] [[bundle branch block]].
* In these instances the block is usually located distal to the [[His bundle]], in approximately 27 to 35% of patients however, the lesion is located in the His bundle itself, and a narrow complex may be inscribed. <br>
* In these instances, the [[Blocking (statistics)|block]] is usually [[Location parameter|located]] [[distal]] to the [[His bundle]]. However, in approximately 27% to 35% of the [[patients]], the [[lesion]] is [[Location parameter|located]] in the [[His bundle]] itself, and a narrow [[Complex (chemistry)|complex]] may be inscribed. <br>
* 2:1 AV Block:
* 2:1 [[Atrioventricular block|AV Block]]:
:*Impossible to determine whether the second-degree AV block is type I or type II.
 
:*A long rhythm strip is helpful to document any change in the behavior of the conduction ratio
:*Impossible to determine whether the [[second-degree AV block]] is type I or type II.
:*When the atrial rate is increased by exercise or by [[atropine]], the AV block in type I tends to decrease and that in type II tends to increase
:*A long [[rhythm]] strip is helpful to [[Document classification|document]] any [[Change detection|change]] in the [[behavior]] of the [[Conduction System|conduction]] [[ratio]].
:*When the [[atrial]] [[rate]] is increased by [[exercise]] or by [[atropine]], the [[Atrioventricular block|AV block]] in type I tends to decrease and that in type II tends to increase.


----
----
Shown below is an electrocardiogram of a 12 lead EKG with a 2:1 AV block.
Shown below is an [[electrocardiogram]] of a 12 [[lead]] [[EKG]] with a 2:1 [[Atrioventricular block|AV block]].
[[File:2to1AVBlock1.jpg|center|500px]]
[[File:2to1AVBlock1.jpg|center|500px]]
Copyleft image obtained courtesy of ECGpedia, http://en.ecgpedia.org/wiki/Main_Page
Copyleft image obtained, courtesy of ECGpedia, http://en.ecgpedia.org/wiki/Main_Page
----
----


Shown below is an electrocardiogram of a type II second degree AV block (Mobitz type II).
Shown below is an [[electrocardiogram]] of a type II [[second degree AV block]] ([[Mobitz type II AV block|Mobitz type II]]).
[[File:Rhythm Mobitz.png|center|500px]]
[[File:Rhythm Mobitz.png|center|500px]]
Copyleft image obtained courtesy of ECGpedia, http://en.ecgpedia.org/wiki/Main_Page
Copyleft image obtained, courtesy of ECGpedia, http://en.ecgpedia.org/wiki/Main_Page
----
----
==Treatment==
==Treatment==
===Medical therapy for Mobitz II===
===Medical therapy for Mobitz II===
* Correction of reversible causes of the block such as ischemia, medications, and vagotonic conditions should be considered<ref name="pmid29850368">{{cite journal |vauthors=Li X, Xue Y, Wu H |title=A Case of Atrioventricular Block Potentially Associated with Right Coronary Artery Lesion and Ticagrelor Therapy Mediated by the Increasing Adenosine Plasma Concentration |journal=Case Rep Vasc Med |volume=2018 |issue= |pages=9385017 |date=2018 |pmid=29850368 |pmc=5933017 |doi=10.1155/2018/9385017 |url=}}</ref>.
*[[Correction (newspaper)|Correction]] of [[Reversible cell|reversible]] [[causes]] of the [[Blocking (statistics)|block]] such as [[ischemia]], [[medications]], and [[Vagotonic agents|vagotonic]] [[conditions]] should be considered.<ref name="pmid29850368">{{cite journal |vauthors=Li X, Xue Y, Wu H |title=A Case of Atrioventricular Block Potentially Associated with Right Coronary Artery Lesion and Ticagrelor Therapy Mediated by the Increasing Adenosine Plasma Concentration |journal=Case Rep Vasc Med |volume=2018 |issue= |pages=9385017 |date=2018 |pmid=29850368 |pmc=5933017 |doi=10.1155/2018/9385017 |url=}}</ref>
* Treatment may also include medicines to control [[blood pressure]] and [[atrial fibrillation]], as well as lifestyle and dietary changes to reduce risk factors associated with [[myocardial infarction|heart attack]] and [[stroke]]<ref name="pmid26745972">{{cite journal |vauthors=Schernthaner C, Kraus J, Danmayr F, Hammerer M, Schneider J, Hoppe UC, Strohmer B |title=Short-term pacemaker dependency after transcatheter aortic valve implantation |journal=Wien. Klin. Wochenschr. |volume=128 |issue=5-6 |pages=198–203 |date=March 2016 |pmid=26745972 |doi=10.1007/s00508-015-0906-4 |url=}}</ref>.
*[[Treatments|Treatment]] may also include [[Medicine|medicines]] to [[control]] [[blood pressure]] and [[atrial fibrillation]], as well as [[lifestyle]] and [[dietary]] [[Change detection|changes]] to [[Reduced|reduce]] the [[risk factors]] [[Association (statistics)|associated]] with [[myocardial infarction|heart attack]] and [[stroke]].<ref name="pmid26745972">{{cite journal |vauthors=Schernthaner C, Kraus J, Danmayr F, Hammerer M, Schneider J, Hoppe UC, Strohmer B |title=Short-term pacemaker dependency after transcatheter aortic valve implantation |journal=Wien. Klin. Wochenschr. |volume=128 |issue=5-6 |pages=198–203 |date=March 2016 |pmid=26745972 |doi=10.1007/s00508-015-0906-4 |url=}}</ref>
* Treatment in emergency situations are [[atropine]] and an [[external pacer]].<ref name="pmid23224264">{{cite journal |vauthors=Barold SS, Herweg B |title=Second-degree atrioventricular block revisited |journal=Herzschrittmacherther Elektrophysiol |volume=23 |issue=4 |pages=296–304 |date=December 2012 |pmid=23224264 |doi=10.1007/s00399-012-0240-8 |url=}}</ref><ref name="pmid8445186">{{cite journal |vauthors=Wogan JM, Lowenstein SR, Gordon GS |title=Second-degree atrioventricular block: Mobitz type II |journal=J Emerg Med |volume=11 |issue=1 |pages=47–54 |date=1993 |pmid=8445186 |doi=10.1016/0736-4679(93)90009-v |url=}}</ref>
*[[Treatments|Treatment]] in [[emergency]] situations are [[atropine]] and an [[external pacer]].<ref name="pmid23224264">{{cite journal |vauthors=Barold SS, Herweg B |title=Second-degree atrioventricular block revisited |journal=Herzschrittmacherther Elektrophysiol |volume=23 |issue=4 |pages=296–304 |date=December 2012 |pmid=23224264 |doi=10.1007/s00399-012-0240-8 |url=}}</ref><ref name="pmid8445186">{{cite journal |vauthors=Wogan JM, Lowenstein SR, Gordon GS |title=Second-degree atrioventricular block: Mobitz type II |journal=J Emerg Med |volume=11 |issue=1 |pages=47–54 |date=1993 |pmid=8445186 |doi=10.1016/0736-4679(93)90009-v |url=}}</ref>


====Contraindicated medications====
====Contraindicated medications====
Line 501: Line 561:
|MedCond = Second degree AV block(except in patients with a functioning artificial pacemaker)<ref name="pmid26115830">{{cite journal |vauthors=Brignole M, Deharo JC, Guieu R |title=Syncope and Idiopathic (Paroxysmal) AV Block |journal=Cardiol Clin |volume=33 |issue=3 |pages=441–7 |date=August 2015 |pmid=26115830 |doi=10.1016/j.ccl.2015.04.012 |url=}}</ref><ref name="pmid11229299">{{cite journal |vauthors=Kelkar PN |title=Atenolol induced high grade AV block |journal=J Assoc Physicians India |volume=46 |issue=8 |pages=748, 751 |date=August 1998 |pmid=11229299 |doi= |url=}}</ref>|Adenosine|Atenolol|Betaxolol|Bisoprolol|Brimonidine tartrate and Timolol maleate|Carteolol|Diltiazem|Disopyramide|Dronedarone|Fingolimod|Flecainide|Metoprolol|Mexiletine|Nadolol|Nebivolol|Penbutolol|Pindolol|Propranolol|Sotalol|Timolol|Labetalol}}<ref name="pmid15234417">{{cite journal |vauthors=Zeltser D, Justo D, Halkin A, Rosso R, Ish-Shalom M, Hochenberg M, Viskin S |title=Drug-induced atrioventricular block: prognosis after discontinuation of the culprit drug |journal=J. Am. Coll. Cardiol. |volume=44 |issue=1 |pages=105–8 |date=July 2004 |pmid=15234417 |doi=10.1016/j.jacc.2004.03.057 |url=}}</ref>
|MedCond = Second degree AV block(except in patients with a functioning artificial pacemaker)<ref name="pmid26115830">{{cite journal |vauthors=Brignole M, Deharo JC, Guieu R |title=Syncope and Idiopathic (Paroxysmal) AV Block |journal=Cardiol Clin |volume=33 |issue=3 |pages=441–7 |date=August 2015 |pmid=26115830 |doi=10.1016/j.ccl.2015.04.012 |url=}}</ref><ref name="pmid11229299">{{cite journal |vauthors=Kelkar PN |title=Atenolol induced high grade AV block |journal=J Assoc Physicians India |volume=46 |issue=8 |pages=748, 751 |date=August 1998 |pmid=11229299 |doi= |url=}}</ref>|Adenosine|Atenolol|Betaxolol|Bisoprolol|Brimonidine tartrate and Timolol maleate|Carteolol|Diltiazem|Disopyramide|Dronedarone|Fingolimod|Flecainide|Metoprolol|Mexiletine|Nadolol|Nebivolol|Penbutolol|Pindolol|Propranolol|Sotalol|Timolol|Labetalol}}<ref name="pmid15234417">{{cite journal |vauthors=Zeltser D, Justo D, Halkin A, Rosso R, Ish-Shalom M, Hochenberg M, Viskin S |title=Drug-induced atrioventricular block: prognosis after discontinuation of the culprit drug |journal=J. Am. Coll. Cardiol. |volume=44 |issue=1 |pages=105–8 |date=July 2004 |pmid=15234417 |doi=10.1016/j.jacc.2004.03.057 |url=}}</ref>
===Surgery for Mobitz II===
===Surgery for Mobitz II===
* Type II Mobitz (symptomatic or asymptomatic) is by itself an indication for insertion of a pacemaker. Other indications include<ref name="pmid30412709">{{cite journal |vauthors=Kusumoto FM, Schoenfeld MH, Barrett C, Edgerton JR, Ellenbogen KA, Gold MR, Goldschlager NF, Hamilton RM, Joglar JA, Kim RJ, Lee R, Marine JE, McLeod CJ, Oken KR, Patton KK, Pellegrini CN, Selzman KA, Thompson A, Varosy PD |title=2018 ACC/AHA/HRS Guideline on the Evaluation and Management of Patients With Bradycardia and Cardiac Conduction Delay: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines and the Heart Rhythm Society |journal=J. Am. Coll. Cardiol. |volume=74 |issue=7 |pages=e51–e156 |date=August 2019 |pmid=30412709 |doi=10.1016/j.jacc.2018.10.044 |url=}}</ref><ref name="pmid7471363">{{cite journal |vauthors=Strasberg B, Amat-Y-Leon F, Dhingra RC, Palileo E, Swiryn S, Bauernfeind R, Wyndham C, Rosen KM |title=Natural history of chronic second-degree atrioventricular nodal block |journal=Circulation |volume=63 |issue=5 |pages=1043–9 |date=May 1981 |pmid=7471363 |doi=10.1161/01.cir.63.5.1043 |url=}}</ref>:
====Definitive treatment-Pacemaker insertion====
*[[Mobitz type II AV block|Type II Mobitz]] ([[symptomatic]] or [[asymptomatic]]) is by itself an [[Indication (medicine)|indication]] for [[insertion]] of a [[pacemaker]] (definitive [[Treatments|treatment]]). Other [[Indication (medicine)|indications]] include:<ref name="pmid29275956">{{cite journal |vauthors=Fu Md J, Bhatta L |title=Lyme carditis: Early occurrence and prolonged recovery |journal=J Electrocardiol |volume=51 |issue=3 |pages=516–518 |date=2018 |pmid=29275956 |doi=10.1016/j.jelectrocard.2017.12.035 |url=}}</ref><ref name="pmid28823599">{{cite journal |vauthors=Tuohy S, Saliba W, Pai M, Tchou P |title=Catheter ablation as a treatment of atrioventricular block |journal=Heart Rhythm |volume=15 |issue=1 |pages=90–96 |date=January 2018 |pmid=28823599 |doi=10.1016/j.hrthm.2017.08.015 |url=}}</ref><ref name="pmid30412709">{{cite journal |vauthors=Kusumoto FM, Schoenfeld MH, Barrett C, Edgerton JR, Ellenbogen KA, Gold MR, Goldschlager NF, Hamilton RM, Joglar JA, Kim RJ, Lee R, Marine JE, McLeod CJ, Oken KR, Patton KK, Pellegrini CN, Selzman KA, Thompson A, Varosy PD |title=2018 ACC/AHA/HRS Guideline on the Evaluation and Management of Patients With Bradycardia and Cardiac Conduction Delay: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines and the Heart Rhythm Society |journal=J. Am. Coll. Cardiol. |volume=74 |issue=7 |pages=e51–e156 |date=August 2019 |pmid=30412709 |doi=10.1016/j.jacc.2018.10.044 |url=}}</ref><ref name="pmid7471363">{{cite journal |vauthors=Strasberg B, Amat-Y-Leon F, Dhingra RC, Palileo E, Swiryn S, Bauernfeind R, Wyndham C, Rosen KM |title=Natural history of chronic second-degree atrioventricular nodal block |journal=Circulation |volume=63 |issue=5 |pages=1043–9 |date=May 1981 |pmid=7471363 |doi=10.1161/01.cir.63.5.1043 |url=}}</ref>:
**[[Myotonic dystrophy]]
**[[Myotonic dystrophy]]
** [[Kearns-Sayre syndrome]]
** [[Kearns-Sayre syndrome]]
** [[Erb's dystrophy]]
** [[Erb's dystrophy]]
** [[Peroneal muscular atrophy]]. These neuromuscular disorders have a high potential for unpredictable rapid progression to [[complete heart block]].
** [[Peroneal muscular atrophy]]. These [[Neuromuscular disorder|neuromuscular disorders]] have a high [[potential]] for unpredictable rapid progression to [[complete heart block]].
* Implantation of permanent pacemakers in both asymptomatic and symptomatic patients is usually done. Asymptomatic Mobitz II are prone to be converted to symptomatic or [[third degree heart block]]. Thus, they should be considered for a pacemaker even if asymptomatic.
*[[Implantation]] of [[Permanent pacemaker|permanent pacemakers]] in both [[asymptomatic]] and [[symptomatic]] [[patients]] is usually [[done]]. [[Asymptomatic]] [[Mobitz II]] are [[prone]] to be converted to [[symptomatic]] or [[third degree heart block]]. Thus, they should be considered for a [[pacemaker]] even if [[asymptomatic]].
* A dual chamber DDD pacemaker is preferred over a single chambered VVI pacemakers as it maintains physiologic AV synchrony.
* A dual chamber [[DDD]] [[pacemaker]] is [[Preferences|preferred]] over a single chambered VVI [[Pacemaker|pacemakers]] as it maintains [[physiologic]] [[Atrioventricular|AV]] [[Synchronicity|synchrony]].
* A dual-chamber [[artificial pacemaker]] is a type of device that typically listens for a pulse from the [[SA node]] and sends a pulse to the [[AV node]] at an appropriate interval, essentially completing the connection between the two nodes. Pacemakers in this role are usually programmed to enforce a minimum heart rate and to record instances of [[atrial flutter]] and [[atrial fibrillation]].
* A dual-chamber [[artificial pacemaker]] is a type of device that typically listens for a [[pulse]] from the [[SA node]] and sends a [[pulse]] to the [[AV node]] at an appropriate [[Interval (mathematics)|interval]], essentially completing the connection between the two [[Node (physics)|nodes]]. [[Pacemaker|Pacemakers]] in this role are usually programmed to enforce a [[minimum]] [[heart rate]] and to record instances of [[atrial flutter]] and [[atrial fibrillation]].


==Prevention==
==Prevention==
Line 514: Line 575:
*[[Effect size|Effective]] [[Treatments|treatment]] of [[hypertension]] and [[Maintenance dose|maintenance]] of [[normal]] [[blood glucose]] [[Level of measurement|levels]] may be [[Usage analysis|useful]] [[Strategies for Improving Care|strategies]] in [[Prevention (medical)|preventing]] the [[Atrioventricular block|AV block]].
*[[Effect size|Effective]] [[Treatments|treatment]] of [[hypertension]] and [[Maintenance dose|maintenance]] of [[normal]] [[blood glucose]] [[Level of measurement|levels]] may be [[Usage analysis|useful]] [[Strategies for Improving Care|strategies]] in [[Prevention (medical)|preventing]] the [[Atrioventricular block|AV block]].


==Differentiating Infra-Hisian Block From Other Diseases==
==Differentiating Infra-Hisian Block from other Diseases==
<br />
<br />
{| class="wikitable"
{| class="wikitable"
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! align="center" style="background:#4479BA; color: #FFFFFF;" + |Co-existing Conditions
! align="center" style="background:#4479BA; color: #FFFFFF;" + |Co-existing Conditions
|-
|-
! rowspan="3" |Atrioventricular block<ref name="pmid311250962">{{cite journal| author=Kerola T, Eranti A, Aro AL, Haukilahti MA, Holkeri A, Junttila MJ et al.| title=Risk Factors Associated With Atrioventricular Block. | journal=JAMA Netw Open | year= 2019 | volume= 2 | issue= 5 | pages= e194176 | pmid=31125096 | doi=10.1001/jamanetworkopen.2019.4176 | pmc=6632153 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=31125096  }}</ref>
! rowspan="3" |[[Atrioventricular block]]<ref name="pmid311250962">{{cite journal| author=Kerola T, Eranti A, Aro AL, Haukilahti MA, Holkeri A, Junttila MJ et al.| title=Risk Factors Associated With Atrioventricular Block. | journal=JAMA Netw Open | year= 2019 | volume= 2 | issue= 5 | pages= e194176 | pmid=31125096 | doi=10.1001/jamanetworkopen.2019.4176 | pmc=6632153 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=31125096  }}</ref>
![[First degree AV block|First degree]] <ref name="pmid8734740">{{cite journal| author=Barold SS| title=Indications for permanent cardiac pacing in first-degree AV block: class I, II, or III? | journal=Pacing Clin Electrophysiol | year= 1996 | volume= 19 | issue= 5 | pages= 747-51 | pmid=8734740 | doi=10.1111/j.1540-8159.1996.tb03355.x | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8734740  }}</ref><ref name="pmid15233485">{{cite journal| author=Upshaw CB| title=Comparison of the prevalence of first-degree atrioventricular block in African-American and in Caucasian patients: an electrocardiographic study III. | journal=J Natl Med Assoc | year= 2004 | volume= 96 | issue= 6 | pages= 756-60 | pmid=15233485 | doi= | pmc=2568382 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15233485  }}</ref>
![[First degree AV block|First degree]] <ref name="pmid8734740">{{cite journal| author=Barold SS| title=Indications for permanent cardiac pacing in first-degree AV block: class I, II, or III? | journal=Pacing Clin Electrophysiol | year= 1996 | volume= 19 | issue= 5 | pages= 747-51 | pmid=8734740 | doi=10.1111/j.1540-8159.1996.tb03355.x | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8734740  }}</ref><ref name="pmid15233485">{{cite journal| author=Upshaw CB| title=Comparison of the prevalence of first-degree atrioventricular block in African-American and in Caucasian patients: an electrocardiographic study III. | journal=J Natl Med Assoc | year= 2004 | volume= 96 | issue= 6 | pages= 756-60 | pmid=15233485 | doi= | pmc=2568382 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15233485  }}</ref>
|
|
Line 534: Line 595:
|
|
|
|
* Normal  
*[[Normal]]
|
|
* Prolonged PR interval (>200 msec)
*[[Prolonged PR interval]] (>200 [[Millisecond|msec]])
|
|
* Less than 0.12 seconds, consistent, and normal in morphology.
* Less than 0.12 [[Second|seconds]], consistent, and [[normal]] in [[Morphology (biology)|morphology]].
|
|
* No treatment required
* No [[Treatments|treatment]] required


<br />
<br />
|
|
* Prevalence: 650 to 1600 per 100,000 individuals in the united states.  
*[[Prevalence]]: 650 to 1600 per 100,000 [[Individual growth|individuals]] in the [[United States]].
| rowspan="3" |<br />
| rowspan="3" |<br />


Line 552: Line 613:
*[[Sarcoidosis]]
*[[Sarcoidosis]]
*[[Lyme disease]]
*[[Lyme disease]]
* Defenerative muscle disorders as [[Lev's disease]] and [[Lenegre's disease]].
*[[Degenerative disease|Degenerative]] [[muscle]] [[disorders]] as [[Lev's disease]] and [[Lenegre's disease]].
* Overly active [[vagus nerve]].
* Overly active [[vagus nerve]].
|-
|-
![[Second degree AV block|Second degree]]<ref name="pmid2191578">{{cite journal| author=Zehender M, Meinertz T, Keul J, Just H| title=ECG variants and cardiac arrhythmias in athletes: clinical relevance and prognostic importance. | journal=Am Heart J | year= 1990 | volume= 119 | issue= 6 | pages= 1378-91 | pmid=2191578 | doi=10.1016/s0002-8703(05)80189-9 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2191578  }}</ref><ref name="pmid1176840">{{cite journal| author=Friedman HS, Gomes JA, Haft JI| title=An analysis of Wenckebach periodicity. | journal=J Electrocardiol | year= 1975 | volume= 8 | issue= 4 | pages= 307-15 | pmid=1176840 | doi=10.1016/s0022-0736(75)80003-3 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1176840  }}</ref>
![[Second degree AV block|Second degree]]<ref name="pmid2191578">{{cite journal| author=Zehender M, Meinertz T, Keul J, Just H| title=ECG variants and cardiac arrhythmias in athletes: clinical relevance and prognostic importance. | journal=Am Heart J | year= 1990 | volume= 119 | issue= 6 | pages= 1378-91 | pmid=2191578 | doi=10.1016/s0002-8703(05)80189-9 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2191578  }}</ref><ref name="pmid1176840">{{cite journal| author=Friedman HS, Gomes JA, Haft JI| title=An analysis of Wenckebach periodicity. | journal=J Electrocardiol | year= 1975 | volume= 8 | issue= 4 | pages= 307-15 | pmid=1176840 | doi=10.1016/s0022-0736(75)80003-3 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1176840  }}</ref>
|
|
* Regular irregular  
* Regular [[Irregular heart rhythms|irregular]]
|
|
|
|
* Normal
*[[Normal]]
|
|
* Mobtiz I: Progressive PR prolongation  
*[[Mobitz I|Mobtiz I]]: Progressive [[PR prolongation]]
*Mobitz II: Normal PR interval  
*[[Mobitz II]]: [[Normal]] [[PR interval]]
|QRS is normal but dropped as the following:  
|[[QRS complex|QRS]] is [[normal]] but [[Drop (liquid)|dropped]] as the following:  


* Mobitz I: QRS complex is dropped after a progressive lengthening of PR
*[[Mobitz I]]: [[QRS complex]] is [[Drop (liquid)|dropped]] after a progressive [[Length|lengthening]] of [[PR interval|PR]]
* Mobitz II: QRS complex is dropped after a normal PR  
*[[Mobitz II]]: [[QRS complex]] is [[Drop (liquid)|dropped]] after a [[normal]] [[PR interval|PR]]
|
|
* Can be reversed by using a pacemaker.
* Can be reversed by [[Usage analysis|using]] a [[pacemaker]].
|
|
* Prevalence: 3 per 100,000 individuals in the united states.  
*[[Prevalence]]: 3 per 100,000 [[Individual growth|individuals]] in the [[United States]].
|-
|-
![[Third degree AV block|Third degree]]<ref name="pmid14297523">{{cite journal |vauthors=OSTRANDER LD, BRANDT RL, KJELSBERG MO, EPSTEIN FH |title=ELECTROCARDIOGRAPHIC FINDINGS AMONG THE ADULT POPULATION OF A TOTAL NATURAL COMMUNITY, TECUMSEH, MICHIGAN |journal=Circulation |volume=31 |issue= |pages=888–98 |date=June 1965 |pmid=14297523 |doi=10.1161/01.cir.31.6.888 |url=}}</ref><ref name="pmid16236932">{{cite journal |vauthors=Movahed MR, Hashemzadeh M, Jamal MM |title=Increased prevalence of third-degree atrioventricular block in patients with type II diabetes mellitus |journal=Chest |volume=128 |issue=4 |pages=2611–4 |date=October 2005 |pmid=16236932 |doi=10.1378/chest.128.4.2611 |url=}}</ref>
![[Third degree AV block|Third degree]]<ref name="pmid14297523">{{cite journal |vauthors=OSTRANDER LD, BRANDT RL, KJELSBERG MO, EPSTEIN FH |title=ELECTROCARDIOGRAPHIC FINDINGS AMONG THE ADULT POPULATION OF A TOTAL NATURAL COMMUNITY, TECUMSEH, MICHIGAN |journal=Circulation |volume=31 |issue= |pages=888–98 |date=June 1965 |pmid=14297523 |doi=10.1161/01.cir.31.6.888 |url=}}</ref><ref name="pmid16236932">{{cite journal |vauthors=Movahed MR, Hashemzadeh M, Jamal MM |title=Increased prevalence of third-degree atrioventricular block in patients with type II diabetes mellitus |journal=Chest |volume=128 |issue=4 |pages=2611–4 |date=October 2005 |pmid=16236932 |doi=10.1378/chest.128.4.2611 |url=}}</ref>
Line 578: Line 639:
|
|
|
|
* Normal but no relationship between P wave and the QRS.
*[[Normal]] but no relationship between [[P wave]] and the [[QRS complex|QRS]].
* More P waves than the QRS complexes.
* More [[P waves]] than the [[QRS complexes]].
|
|
* Varies
*[[Variable|Varies]]
|
|
* Normal QRS
*[[Normal]] [[QRS complex|QRS]]
|
|
* Can be reversed by using a pacemaker.
* Can be reversed by [[Usage analysis|using]] a [[pacemaker]].
|
|
* The prevalence: 20 per 100,000 individuals worldwide.
* The [[prevalence]]: 20 per 100,000 [[Individual growth|individuals]] worldwide.
|-
|-
! colspan="2" |'''Atrial Fibrillation (AFib)<ref name="pmid24837984">{{cite journal |vauthors=Lankveld TA, Zeemering S, Crijns HJ, Schotten U |title=The ECG as a tool to determine atrial fibrillation complexity |journal=Heart |volume=100 |issue=14 |pages=1077–84 |date=July 2014 |pmid=24837984 |doi=10.1136/heartjnl-2013-305149 |url=}}</ref><ref name="pmid22518390">{{cite journal |vauthors=Harris K, Edwards D, Mant J |title=How can we best detect atrial fibrillation? |journal=J R Coll Physicians Edinb |volume=42 Suppl 18 |issue= |pages=5–22 |date=2012 |pmid=22518390 |doi=10.4997/JRCPE.2012.S02 |url=}}</ref>'''
! colspan="2" |'''[[Atrial fibrillation|Atrial Fibrillation (AFib)]]<ref name="pmid24837984">{{cite journal |vauthors=Lankveld TA, Zeemering S, Crijns HJ, Schotten U |title=The ECG as a tool to determine atrial fibrillation complexity |journal=Heart |volume=100 |issue=14 |pages=1077–84 |date=July 2014 |pmid=24837984 |doi=10.1136/heartjnl-2013-305149 |url=}}</ref><ref name="pmid22518390">{{cite journal |vauthors=Harris K, Edwards D, Mant J |title=How can we best detect atrial fibrillation? |journal=J R Coll Physicians Edinb |volume=42 Suppl 18 |issue= |pages=5–22 |date=2012 |pmid=22518390 |doi=10.4997/JRCPE.2012.S02 |url=}}</ref>'''
|
|
* Irregularly irregular
*[[Irregularly irregular pulse|Irregularly irregular]]
|
|
* On a 10-second 12-lead [[The electrocardiogram|EKG]] strip, multiply number of [[QRS complexes]] by 6
* On a 10-[[second]] [[12-lead ECG|12-lead EKG]] [[Stripping|strip]], multiply [[number]] of [[QRS complexes]] by 6
|
|
* Absent
* Absent
*Fibrillatory waves
*[[Fibrillation|Fibrillatory]] [[waves]]
|
|
* Absent
* Absent
|
|
* Less than 0.12 seconds, consistent, and normal in morphology in the absence of aberrant conduction
* Less than 0.12 [[Second|seconds]], consistent, and [[normal]] in [[Morphology (biology)|morphology]] in the absence of aberrant [[Conduction System|conduction]]
|
|
* Does not break with [[adenosine]] or [[vagal maneuvers]]
* Does not break with [[adenosine]] or [[vagal maneuvers]]
|
|
* 2.7–6.1 million people in the United States have AFib
* 2.7–6.1 million [[People's Solidarity|people]] in the [[United States]] have [[Atrial fibrillation|AFib]]
* 2% of people younger than age 65 have AFib, while about 9% of people aged 65 years or older have AFib
* 2% of [[People's Solidarity|people]] [[Young adult|younger]] than [[age]] 65 have [[Atrial fibrillation|AFib]], while about 9% of [[People's Solidarity|people]] aged 65 [[Year|years]] or [[Old age|older]] have [[Atrial fibrillation|AFib]]
|
|
* Elderly
*[[Elderly]]
* Following [[Coronary artery bypass surgery|bypass surgery]]
* Following [[Coronary artery bypass surgery|bypass surgery]]
*[[Mitral valve disease]]
*[[Mitral valve disease]]
Line 620: Line 681:
! colspan="2" |'''[[Atrial Flutter]]'''<ref name="pmid28835836">{{cite journal |vauthors=Cosío FG |title=Atrial Flutter, Typical and Atypical: A Review |journal=Arrhythm Electrophysiol Rev |volume=6 |issue=2 |pages=55–62 |date=June 2017 |pmid=28835836 |pmc=5522718 |doi=10.15420/aer.2017.5.2 |url=}}</ref>
! colspan="2" |'''[[Atrial Flutter]]'''<ref name="pmid28835836">{{cite journal |vauthors=Cosío FG |title=Atrial Flutter, Typical and Atypical: A Review |journal=Arrhythm Electrophysiol Rev |volume=6 |issue=2 |pages=55–62 |date=June 2017 |pmid=28835836 |pmc=5522718 |doi=10.15420/aer.2017.5.2 |url=}}</ref>
|
|
* Regular or Irregular
* Regular or [[Irregular heart rhythms|Irregular]]
|
|
* 75 (4:1 block), 100 (3:1 block) and 150 (2:1 block) beats per minute (bpm), but 150 is more common
* 75 (4:1 [[Blocking (statistics)|block]]), 100 (3:1 [[Blocking (statistics)|block]]) and 150 (2:1 [[Blocking (statistics)|block]]) [[beats per minute]] ([[Beats per minute|bpm]]), but 150 is more common
|
|
* Sawtooth pattern of P waves at 250 to 350 bpm
* Sawtooth [[pattern]] of [[P waves]] at 250 to 350 [[Beats per minute|bpm]]
*Biphasic deflection in V1
*[[Biphasic]] deflection in [[V1-morph|V1]]
|
|
* Varies depending upon the magnitude of the block, but is short
*[[Variable|Varies]] [[Dependent variable|depending]] upon the [[Magnitude (mathematics)|magnitude]] of the [[Blocking (statistics)|block]], but is short
|
|
* Less than 0.12 seconds, consistent, and normal in morphology
* Less than 0.12 [[Second|seconds]], consistent, and [[normal]] in [[morphology]]
|
|
* Conduction may vary in response to drugs and maneuvers dropping the rate from 150 to 100 or to 75 bpm
*[[Conduction System|Conduction]] may [[Variable|vary]] in [[Response element|response]] to [[drugs]] and maneuvers [[Drop (liquid)|dropping]] the [[rate]] from 150 to 100 or to 75 [[Beats per minute|bpm]]
|
|
*[[Incidence]]: 88 per 100,000 individuals
*[[Incidence]]: 88 per 100,000 [[Individual growth|individuals]]
|
|
*[[Elderly]]
*[[Elderly]]
Line 642: Line 703:
* Regular
* Regular
|
|
* 140-280 bpm
* 140-280 [[Beats per minute|bpm]]
|
|
*Slow-Fast AVNRT:
*[[Slow]]-[[Fast and wide|Fast]] [[AV nodal reentrant tachycardia|AVNRT]]:
**Pseudo-S wave in leads II, III, and AVF
**Pseudo-[[S wave]] in [[Lead|leads]] II, III, and AVF
**Pseudo-R' in lead V1.
**Pseudo-[[R wave|R]]' in [[lead]] V1.
*Fast-Slow AVNRT
*[[Fast and wide|Fast]]-[[Slow]] [[AV nodal reentrant tachycardia|AVNRT]]
**[[P waves]] between the [[QRS complex|QRS]] and [[T waves]] (QRS-P-T complexes)
**[[P waves]] between the [[QRS complex|QRS]] and [[T waves]] ([[QRS complex|QRS]]-[[P wave|P]]-[[T wave|T]] [[Complex (chemistry)|complexes]])
*Slow-Slow AVNRT
*[[Slow]]-[[Slow]] [[AV nodal reentrant tachycardia|AVNRT]]
**Late [[P waves]] after a [[QRS complex|QRS]]
**Late [[P waves]] after a [[QRS complex|QRS]]
**Often appears as [[atrial tachycardia]].
**Often [[Appearance|appears]] as [[atrial tachycardia]].
*Inverted, superimposed on or buried within the [[QRS complex]] (pseudo R prime in V1/pseudo S wave in inferior leads)
*[[Inverted P wave|Inverted]], [[Superimposition|superimposed]] on or buried within the [[QRS complex]] (pseudo [[R wave|R]] [[Prime ECG|prime]] in [[V1-morph|V1]]/pseudo [[S wave]] in [[Inferior angle|inferior]] [[Lead|leads]])
|
|
* Absent ([[P wave]] can appear after the QRS complex and before the T wave, and in atypical AVNRT, the [[P wave]] can appear just before the [[QRS complex]])
* Absent ([[P wave]] can [[Appearance|appear]] after the [[QRS complex]] and before the [[T wave]], and in [[Atypical AV nodal reentrant tachycardia|atypical AVNRT]], the [[P wave]] can [[Appearance|appear]] just before the [[QRS complex]])
|
|
* Less than 0.12 seconds, consistent, and normal in morphology in the absence of aberrant conduction
* Less than 0.12 [[Second|seconds]], consistent, and [[normal]] in [[Morphology (biology)|morphology]] in the absence of aberrant [[Conduction System|conduction]]
*[[QRS complex alternans|QRS alternans]] may be present
*[[QRS complex alternans|QRS alternans]] may be [[Presenting symptom|present]]
|
|
* May break with [[adenosine]] or [[vagal maneuvers]]
* May break with [[adenosine]] or [[vagal maneuvers]]
Line 668: Line 729:
! colspan="2" |'''[[Multifocal atrial tachycardia|Multifocal Atrial Tachycardia]]<ref name="pmid2570520">{{cite journal |vauthors=Scher DL, Arsura EL |title=Multifocal atrial tachycardia: mechanisms, clinical correlates, and treatment |journal=Am. Heart J. |volume=118 |issue=3 |pages=574–80 |date=September 1989 |pmid=2570520 |doi=10.1016/0002-8703(89)90275-5 |url=}}</ref><ref name="pmid11884328">{{cite journal |vauthors=Goodacre S, Irons R |title=ABC of clinical electrocardiography: Atrial arrhythmias |journal=BMJ |volume=324 |issue=7337 |pages=594–7 |date=March 2002 |pmid=11884328 |pmc=1122515 |doi=10.1136/bmj.324.7337.594 |url=}}</ref>'''
! colspan="2" |'''[[Multifocal atrial tachycardia|Multifocal Atrial Tachycardia]]<ref name="pmid2570520">{{cite journal |vauthors=Scher DL, Arsura EL |title=Multifocal atrial tachycardia: mechanisms, clinical correlates, and treatment |journal=Am. Heart J. |volume=118 |issue=3 |pages=574–80 |date=September 1989 |pmid=2570520 |doi=10.1016/0002-8703(89)90275-5 |url=}}</ref><ref name="pmid11884328">{{cite journal |vauthors=Goodacre S, Irons R |title=ABC of clinical electrocardiography: Atrial arrhythmias |journal=BMJ |volume=324 |issue=7337 |pages=594–7 |date=March 2002 |pmid=11884328 |pmc=1122515 |doi=10.1136/bmj.324.7337.594 |url=}}</ref>'''
|
|
* Irregular
*[[Irregular heart rhythms|Irregular]]
|
|
*[[Atrial]] rate is > 100 beats per minute
*[[Atrial]] [[rate]] is > 100 [[beats per minute]]
|
|
* Varying morphology from at least three different foci
* Varying [[morphology]] from at least three [[Difference (philosophy)|different]] [[Focus (optics)|foci]]
* Absence of one dominant atrial pacemaker, can be mistaken for [[atrial fibrillation]] if the [[P waves]] are of low amplitude
* Absence of one [[dominant]] [[Atrial|atria]]<nowiki/>l [[pacemaker]], can be mistaken for [[atrial fibrillation]] if the [[P waves]] are of low [[amplitude]]
|
|
* Variable [[PR interval|PR intervals]], RR intervals, and PP intervals
*[[Variable]] [[PR interval|PR intervals]], [[RR interval|RR intervals]], and [[PP interval|PP intervals]]
|
|
* Less than 0.12 seconds, consistent, and normal in morphology
* Less than 0.12 [[Second|seconds]], consistent, and [[normal]] in [[Morphology (biology)|morphology]]
|
|
* Does not terminate with [[adenosine]] or [[vagal maneuvers]]
* Does not [[Termination signal|terminate]] with [[adenosine]] or [[vagal maneuvers]]
|
|
* 0.05% to 0.32% of [[electrocardiograms]] in general hospital admissions
* 0.05% to 0.32% of [[electrocardiograms]] in general [[hospital]] [[Admission note|admissions]]
|
|
*[[Elderly]]
*[[Elderly]]
*[[Chronic obstructive pulmonary disease]] ([[Chronic obstructive pulmonary disease|COPD]])
*[[Chronic obstructive pulmonary disease]] ([[Chronic obstructive pulmonary disease|COPD]])
|-
|-
! colspan="2" |'''Paroxysmal Supraventricular Tachycardia'''
! colspan="2" |'''Paroxysmal [[Supraventricular tachycardia|Supraventricular Tachycardia]]'''
|
|
* Regular
* Regular
|
|
* 150 and 240 bpm
* 150 and 240 [[Beats per minute|bpm]]
|
|
* Absent
* Absent
Line 697: Line 758:
* Absent
* Absent
|
|
* Narrow complexes (< 0.12 s)
*[[Narrow complex tachycardia|Narrow complexes]] (< 0.12 [[Second|s]])
|
|
* Breaks with [[vagal maneuvers]], [[adenosine]], [[diving reflex]], [[oculocardiac reflex]]
* Breaks with [[vagal maneuvers]], [[adenosine]], [[diving reflex]], [[oculocardiac reflex]]
Line 711: Line 772:
! colspan="2" |'''[[Premature atrial contraction|Premature Atrial Contractrions]] ([[Premature atrial contraction|PAC]])'''<ref name="pmid26316525">{{cite journal |vauthors=Lin CY, Lin YJ, Chen YY, Chang SL, Lo LW, Chao TF, Chung FP, Hu YF, Chong E, Cheng HM, Tuan TC, Liao JN, Chiou CW, Huang JL, Chen SA |title=Prognostic Significance of Premature Atrial Complexes Burden in Prediction of Long-Term Outcome |journal=J Am Heart Assoc |volume=4 |issue=9 |pages=e002192 |date=August 2015 |pmid=26316525 |pmc=4599506 |doi=10.1161/JAHA.115.002192 |url=}}</ref><ref name="pmid18063110">{{cite journal |vauthors=Strasburger JF, Cheulkar B, Wichman HJ |title=Perinatal arrhythmias: diagnosis and management |journal=Clin Perinatol |volume=34 |issue=4 |pages=627–52, vii–viii |date=December 2007 |pmid=18063110 |pmc=3310372 |doi=10.1016/j.clp.2007.10.002 |url=}}</ref>
! colspan="2" |'''[[Premature atrial contraction|Premature Atrial Contractrions]] ([[Premature atrial contraction|PAC]])'''<ref name="pmid26316525">{{cite journal |vauthors=Lin CY, Lin YJ, Chen YY, Chang SL, Lo LW, Chao TF, Chung FP, Hu YF, Chong E, Cheng HM, Tuan TC, Liao JN, Chiou CW, Huang JL, Chen SA |title=Prognostic Significance of Premature Atrial Complexes Burden in Prediction of Long-Term Outcome |journal=J Am Heart Assoc |volume=4 |issue=9 |pages=e002192 |date=August 2015 |pmid=26316525 |pmc=4599506 |doi=10.1161/JAHA.115.002192 |url=}}</ref><ref name="pmid18063110">{{cite journal |vauthors=Strasburger JF, Cheulkar B, Wichman HJ |title=Perinatal arrhythmias: diagnosis and management |journal=Clin Perinatol |volume=34 |issue=4 |pages=627–52, vii–viii |date=December 2007 |pmid=18063110 |pmc=3310372 |doi=10.1016/j.clp.2007.10.002 |url=}}</ref>
|
|
* Regular except when disturbed by premature beat(s)
* Regular except when disturbed by [[premature]] [[Beats per minute|beat(s)]]
|
|
* 80-120 bpm
* 80-120 [[Beats per minute|bpm]]
|
|
* Upright
* Upright
|
|
* > 0.12 second
* > 0.12 [[second]]
* May be shorter than that in normal sinus rhythm (NSR) if the origin of PAC is located closer to the AV node
* May be shorter than that in [[normal sinus rhythm]] ([[Normal sinus rhythm|NSR]]) if the [[origin]] of [[PAC]] is [[Location parameter|located]] closer to the [[Atrioventricular node|AV node]]
*Ashman’s Phenomenon:
*[[Ashman phenomenon|Ashman’s phenomenon]]:
**[[Premature atrial contraction|PAC]] displaying a [[right bundle branch block]] pattern
**[[Premature atrial contraction|PAC]] displaying a [[right bundle branch block]] [[pattern]]
|
|
* Usually narrow (< 0.12 s)
* Usually narrow (< 0.12 [[Second|s]])
|
|
* Breaks with [[vagal maneuvers]], [[adenosine]], [[diving reflex]], [[oculocardiac reflex]]
* Breaks with [[vagal maneuvers]], [[adenosine]], [[diving reflex]], [[oculocardiac reflex]]
Line 740: Line 801:
* Regular
* Regular
|
|
* Atrial rate is nearly 300 bpm and ventricular rate is at 150 bpm
*[[Atrial]] [[rate]] is nearly 300 [[Beats per minute|bpm]] and [[ventricular]] [[rate]] is at 150 [[Beats per minute|bpm]]
|
|
* With [[orthodromic]] conduction due to a bypass tract, the [[P wave]] generally follows the [[QRS complex]], whereas in [[AVNRT]], the [[P wave]] is generally buried in the [[QRS complex]].
* With [[orthodromic]] [[Conduction System|conduction]] due to a [[bypass tract]], the [[P wave]] [[Generalization|generally]] follows the [[QRS complex]], whereas in [[AVNRT]], the [[P wave]] is generally buried in the [[QRS complex]].
|
|
* Less than 0.12 seconds
* Less than 0.12 [[Second|seconds]]
|
|
* A [[delta wave]] and evidence of [[ventricular]] pre-excitation if there is conduction to the ventricle via ante-grade conduction down an accessory pathway
* A [[delta wave]] and [[evidence]] of [[ventricular]] [[pre-excitation]] if there is [[Conduction System|conduction]] to the [[ventricle]] via ante-grade [[Conduction System|conduction]] down an [[accessory pathway]]
* A [[delta wave]] and pre-excitation may not be present because bypass tracts do not conduct ante-grade.
* A [[delta wave]] and [[pre-excitation]] may not be [[Presenting symptom|present]] because [[Bypass tract|bypass tracts]] do not [[conduct]] ante-grade.
|
|
* May break in response to [[procainamide]], [[adenosine]], [[vagal maneuvers]]
* May break in [[Response element|response]] to [[procainamide]], [[adenosine]], [[vagal maneuvers]]
|
|
* Worldwide [[prevalence]] of [[Wolff-Parkinson-White syndrome|WPW syndrome]] is 100 - 300 per 100,000
* Worldwide [[prevalence]] of [[Wolff-Parkinson-White syndrome|WPW syndrome]] is 100 - 300 per 100,000
|
|
*[[Ebstein's anomaly]]
*[[Ebstein's anomaly]]
*[[Mitral valve prolapse]]: This cardiac disorder, if present, is associated with left-sided accessory pathways.
*[[Mitral valve prolapse]]: This [[cardiac]] [[Disorder (medicine)|disorder]], if [[Presenting symptom|present]], is [[Association (statistics)|associated]] with left-sided [[accessory pathways]].
*[[Hypertrophic cardiomyopathy]]: This disorder is associated with familial/inherited form of [[Wolff-Parkinson-White syndrome|WPW syndrome]].
*[[Hypertrophic cardiomyopathy]]: This [[Disorder (medicine)|disorder]] is [[Association (statistics)|associated]] with [[familial]]/[[inherited]] form of [[Wolff-Parkinson-White syndrome|WPW syndrome]].
*[[Hypokalemic periodic paralysis]]
*[[Hypokalemic periodic paralysis]]
*[[Pompe disease]]
*[[Pompe disease]]
*[[Tuberous sclerosis]]
*[[Tuberous sclerosis]]
|-
|-
! colspan="2" |'''[[Ventricular fibrillation|Ventricular Fibrillation]] (VF)'''<ref name="pmid27899944">{{cite journal |vauthors=Glinge C, Sattler S, Jabbari R, Tfelt-Hansen J |title=Epidemiology and genetics of ventricular fibrillation during acute myocardial infarction |journal=J Geriatr Cardiol |volume=13 |issue=9 |pages=789–797 |date=September 2016 |pmid=27899944 |pmc=5122505 |doi=10.11909/j.issn.1671-5411.2016.09.006 |url=}}</ref><ref name="pmid11334828">{{cite journal |vauthors=Samie FH, Jalife J |title=Mechanisms underlying ventricular tachycardia and its transition to ventricular fibrillation in the structurally normal heart |journal=Cardiovasc. Res. |volume=50 |issue=2 |pages=242–50 |date=May 2001 |pmid=11334828 |doi=10.1016/s0008-6363(00)00289-3 |url=}}</ref><ref name="pmid20142817">{{cite journal |vauthors=Adabag AS, Luepker RV, Roger VL, Gersh BJ |title=Sudden cardiac death: epidemiology and risk factors |journal=Nat Rev Cardiol |volume=7 |issue=4 |pages=216–25 |date=April 2010 |pmid=20142817 |pmc=5014372 |doi=10.1038/nrcardio.2010.3 |url=}}</ref>
! colspan="2" |'''[[Ventricular fibrillation|Ventricular Fibrillation]] ([[Ventricular fibrillation|VF]])'''<ref name="pmid27899944">{{cite journal |vauthors=Glinge C, Sattler S, Jabbari R, Tfelt-Hansen J |title=Epidemiology and genetics of ventricular fibrillation during acute myocardial infarction |journal=J Geriatr Cardiol |volume=13 |issue=9 |pages=789–797 |date=September 2016 |pmid=27899944 |pmc=5122505 |doi=10.11909/j.issn.1671-5411.2016.09.006 |url=}}</ref><ref name="pmid11334828">{{cite journal |vauthors=Samie FH, Jalife J |title=Mechanisms underlying ventricular tachycardia and its transition to ventricular fibrillation in the structurally normal heart |journal=Cardiovasc. Res. |volume=50 |issue=2 |pages=242–50 |date=May 2001 |pmid=11334828 |doi=10.1016/s0008-6363(00)00289-3 |url=}}</ref><ref name="pmid20142817">{{cite journal |vauthors=Adabag AS, Luepker RV, Roger VL, Gersh BJ |title=Sudden cardiac death: epidemiology and risk factors |journal=Nat Rev Cardiol |volume=7 |issue=4 |pages=216–25 |date=April 2010 |pmid=20142817 |pmc=5014372 |doi=10.1038/nrcardio.2010.3 |url=}}</ref>
|
|
* Irregular
*[[Irregular heart rhythms|Irregular]]
|
|
* 150 to 500 bpm
* 150 to 500 [[Beats per minute|bpm]]
|
|
* Absent
* Absent
Line 770: Line 831:
* Absent
* Absent
|
|
* Absent (R on T phenomenon in the setting of ischemia)
* Absent ([[R wave|R]] on [[T wave|T]] [[Phenomenology|phenomenon]] in the [[Set|setting]] of [[ischemia]])
|
|
* Does not break in response to [[procainamide]], [[adenosine]], [[vagal maneuvers]]
* Does not break in response to [[procainamide]], [[adenosine]], [[vagal maneuvers]]
|
|
* 3-12% cases of [[acute myocardial infarction]] (AMI)
* 3-12% [[Case-based reasoning|cases]] of [[acute myocardial infarction]] ([[Acute myocardial infarction|AMI]])
* Out of 356,500 out of hospital cardiac arrests, 23% have VF as initial rhythm
* Out of 356,500 out of [[hospital]] [[Cardiac arrest|cardiac arrests]], 23% have [[Ventricular fibrillation|VF]] as initial [[rhythm]]
|
|
*[[Myocardial ischemia]] / [[Myocardial infarction|infarction]]
*[[Myocardial ischemia]] / [[Myocardial infarction|infarction]]
*[[Cardiomyopathy]]
*[[Cardiomyopathy]]
* Channelopathies e.g. Long QT (acquired / congenital)
*[[Channelopathies]] [[Example 1|e.g]]. [[Long QT syndrome|Long QT]] ([[acquired]] / [[congenital]])
*Electrolyte abnormalities ([[hypokalemia]]/[[hyperkalemia]], [[hypomagnesemia]])
*[[Electrolyte abnormalities]] ([[hypokalemia]]/[[hyperkalemia]], [[hypomagnesemia]])
*[[Aortic stenosis]]
*[[Aortic stenosis]]
*[[Aortic dissection]]
*[[Aortic dissection]]
*[[Myocarditis]]
*[[Myocarditis]]
*[[Cardiac tamponade]]
*[[Cardiac tamponade]]
* Blunt trauma (Commotio Cordis)
*[[Blunt trauma]] ([[Commotio cordis|Commotio Cordis]])
*[[Sepsis]]
*[[Sepsis]]
*[[Hypothermia]]
*[[Hypothermia]]
Line 796: Line 857:
* Regular
* Regular
|
|
* > 100 bpm (150-200 bpm common)
* > 100 [[Beats per minute|bpm]] (150-200 [[Beats per minute|bpm]] common)
|
|
* Absent
* Absent
Line 802: Line 863:


*Absent
*Absent
*Initial [[R wave]] in V1, initial r > 40 ms in V1/V2, notched S in V1, initial R in aVR, lead II R wave peak time ≥50 ms, no RS in V1-V6, and atrioventricular dissociation
*Initial [[R wave]] in [[V1-morph|V1]], initial r > 40 [[Millisecond|ms]] in [[V1-morph|V1]]/V2, [[Notch|notched]] [[S wave|S]] in [[V1-morph|V1]], initial [[R wave|R]] in [[aVR]], [[lead]] II [[R wave]] [[Peakadilly|peak]] [[Time constant|time]] ≥50 [[Millisecond|ms]], no RS in [[V1-morph|V1]]-V6, and [[atrioventricular dissociation]]
|
|
* Wide complex, [[QRS complex|QRS]] duration > 120 milliseconds
*[[Wide complex tachycardias|Wide complex]], [[QRS complex|QRS]] duration > 120 [[Millisecond|milliseconds]]
|
|
* Does not break in response to [[procainamide]], [[adenosine]], [[vagal maneuvers]]
* Does not break in response to [[procainamide]], [[adenosine]], [[vagal maneuvers]]
|
|
* 5-10% of patients presenting with AMI
* 5-10% of [[patients]] [[Presenting symptom|presenting]] with [[Acute myocardial infarction|AMI]]
|
|
*[[Coronary artery disease]]
*[[Coronary artery disease]]
Line 814: Line 875:
*[[Cardiomyopathy]]
*[[Cardiomyopathy]]
*[[Electrolyte imbalance|Electrolyte imbalances]] (e.g., [[hypokalemia]], [[hypomagnesemia]])
*[[Electrolyte imbalance|Electrolyte imbalances]] (e.g., [[hypokalemia]], [[hypomagnesemia]])
* Inherited [[channelopathies]] (e.g., [[long-QT syndrome]])
*[[Inherited]] [[channelopathies]] (e.g., [[long-QT syndrome]])
*[[Catecholaminergic polymorphic ventricular tachycardia]]
*[[Catecholaminergic polymorphic ventricular tachycardia]]
*[[Arrhythmogenic right ventricular dysplasia]]
*[[Arrhythmogenic right ventricular dysplasia]]
*[[Myocardial infarction]]
*[[Myocardial infarction]]
*[[Torsades de pointes]] is a form of polymorphic VT that is often associated with a prolonged [[QT interval]]
*[[Torsades de pointes]] is a form of [[polymorphic VT]] that is often [[Association (statistics)|associated]] with a [[prolonged QT interval]]
|}
|}



Latest revision as of 20:59, 19 August 2020

Infra-Hisian Block Microchapters

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Epidemiology and Demographics

Risk Factors

Natural History, Complications and Prognosis

Diagnosis

Treatment

Prevention

Differentiating Infra-Hisian Block from other Diseases

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor-In-Chief: Sara Mohsin, M.D.[2]

Overview

Infra-Hisian block is defined as an impaired conduction in the electrical system of the heart that occurs below the atrioventricular node.

Historical Perspective

Classification

Classification of Infra-Hisian Block
Types of Infra-Hisian Block Sub-type
Type 2 second degree heart block (Mobitz II) _
Left bundle branch block Left anterior fascicular block
Left posterior fascicular block
Right bundle branch block _

Pathophysiology

Normal Cardiac Conduction

  1. The normal cardiac conduction proceeds in a way so as to allow time for the atrium to relax during atrial diastole.
  2. The electrical impulse generated in the SA node travels through the internodal pathways towards the AV node.
  3. The conduction through the AV node is slowed down as it travels through it. This decrease in velocity of conduction allows time for the atrium to contract ahead of the ventricle so that the blood from the atria can fill up the ventricles through the atrioventricular valves.
  4. As the impulse flows through the compact AV node, it rapidly conducts through the ventricular myocardial cells. Once the depolarization is complete, the ventricle relaxes during diastole in preparation for the next impulse.

Anatomy

Conduction system of the heart
Structure of the heart's conduction system

Pathophysiology of Mobitz type II second degree AV block

Pathophysiology of LBBB

Pathophysiology of RBBB

Genetics

Associated Syndromes

Pseudo Right Bundle Branch Block

Brugada syndrome:

Causes

Mobitz type II second degree AV block causes

  • Details of all the possible etiologies are given in the table below:
Major reversible causes of atrioventricular (AV) block
Physiologic and pathophysiologic
Increased vagal tone
  • Also known as hypervagotonia
Ischemic heart disease
Progressive cardiac conduction system disease Associated with:
Infections
Cardiomyopathy Infiltrative processes such as:

Other non-ischemic cardiomyopathies include:

Congenital AV block
Other reversible causes
Iatrogenic
Drugs (altering conduction through AV node)
Cardiac surgery
Catheter ablation of arrhythmias
Alcohol septal ablation for hypertrophic cardiomyopathy
Transcatheter closure of ventricular septal defect
Post-transcatheter aortic valve implantation

Life Threatening Causes

Life-threatening conditions can result in death or permanent disability within 24 hours if left untreated.[7]

Common Causes

Causes by Organ System

Cardiovascular Acute myocardial infarction, acute rheumatic fever, ASD, dilated cardiomyopathy, Ebstein's anomaly, hypersensitive carotid sinus syndrome, hypertension, hypertrophic cardiomyopathy, Lev's disease, myocardial bridging, myocarditis, normal variants, post aortic valve replacement, post catheter ablation for arrhythmias, post closure of a ventricular septal defect, post mitral valve replacement, tetralogy of Fallot, endocardial cushion defect, transposition of the great vessels, valvular heart disease, VSD
Chemical / poisoning No underlying causes
Dermatologic No underlying causes
Drug Side Effect Amiodarone, beta-blockers, digitalis, calcium channel blockers, cholinesterase inhibitors, disopyramide, dofetilide, dolasetron, donepezil, eslicarbazepine acetate, fesoterodine, fingolimod, flecainide, ibutilide, lacosamide, magnesium, paliperidone, pramipexole, procainamide, propafenone, propoxyphene, quinidine, sotalol, terodiline
Ear Nose Throat No underlying causes
Endocrine Hyperthyroidism, myxedema, thyrotoxic periodic paralysis
Environmental Hypothermia
Gastroenterologic Hemochromatosis
Genetic Emery-Dreifuss muscular dystrophy, Fabry disease, glycogenosis type 2b, hereditary neuromuscular disease, Kearns-Sayre syndrome
Hematologic Multiple myeloma Lymphoma[11]
Iatrogenic Post aortic valve replacement, post catheter ablation for arrhythmias, post closure of a ventricular septal defect, post mitral valve replacement
Infectious Disease Acute rheumatic fever, Chagas disease, diphtheria, Lyme disease, myocarditis, neonatal lupus erythematosus, protozoal infection, sarcoidosis, SLE, tuberculosis
Musculoskeletal / Ortho Ankylosing spondylitis, hereditary neuromuscular disease, Kearns-Sayre syndrome, mitochondrial genome inherited conditions, muscular dystrophy
Neurologic Enhanced vagal tone
Nutritional / Metabolic Fabry disease, glycogenosis type 2b
Obstetric/Gynecologic No underlying causes
Oncologic Multiple myeloma
Opthalmologic No underlying causes
Overdose / Toxicity No underlying causes
Psychiatric No underlying causes
Pulmonary Sarcoidosis
Renal / Electrolyte Hyperkalemia, hypokalemia
Rheum / Immune / Allergy Ankylosing spondylitis, dermatomyositis, rheumatoid arthritis, scleroderma, SLE
Sexual No underlying causes
Trauma No underlying causes
Urologic No underlying causes
Dental No underlying causes
Miscellaneous Amyloidosis, degenerative diseases

Causes in Alphabetical Order

Epidemiology and Demographics

Prevalence

Gender

Risk Factors

Natural History, Complications and Prognosis

Natural History

Complications

Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Patients with second degree AV block should be checked for the following laboratory tests:[27]

Electrocardiogram


Shown below is an electrocardiogram of a 12 lead EKG with a 2:1 AV block.

Copyleft image obtained, courtesy of ECGpedia, http://en.ecgpedia.org/wiki/Main_Page


Shown below is an electrocardiogram of a type II second degree AV block (Mobitz type II).

Copyleft image obtained, courtesy of ECGpedia, http://en.ecgpedia.org/wiki/Main_Page


Treatment

Medical therapy for Mobitz II

Contraindicated medications

Second degree AV block(except in patients with a functioning artificial pacemaker)[30][31] is considered an absolute contraindication to the use of the following medications:

Surgery for Mobitz II

Definitive treatment-Pacemaker insertion

Prevention

Primary Prevention

Differentiating Infra-Hisian Block from other Diseases


Arrhythmia Rhythm Rate P wave PR Interval QRS Complex Response to Maneuvers Epidemiology Co-existing Conditions
Atrioventricular block[36] First degree [37][38]
  • Regular



Second degree[12][39] QRS is normal but dropped as the following:
Third degree[40][41]
  • Regular
Atrial Fibrillation (AFib)[42][43]
  • Absent
Atrial Flutter[44]
Atrioventricular nodal reentry tachycardia (AVNRT)[45][46][47][48]
  • Regular
Multifocal Atrial Tachycardia[49][50]
Paroxysmal Supraventricular Tachycardia
  • Regular
  • 150 and 240 bpm
  • Absent
  • Hidden in QRS
  • Absent
Premature Atrial Contractrions (PAC)[51][52]
  • Upright
  • Usually narrow (< 0.12 s)
Wolff-Parkinson-White Syndrome[53][54]
  • Regular
Ventricular Fibrillation (VF)[55][56][57]
  • Absent
  • Absent
Ventricular Tachycardia[58][59]
  • Regular
  • > 100 bpm (150-200 bpm common)
  • Absent

References

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  2. Puech P, Wainwright RJ (1983). "Clinical electrophysiology of atrioventricular block". Cardiol Clin. 1 (2): 209–24. PMID 6544636.
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  4. 4.0 4.1 4.2 Li X, Xue Y, Wu H (2018). "A Case of Atrioventricular Block Potentially Associated with Right Coronary Artery Lesion and Ticagrelor Therapy Mediated by the Increasing Adenosine Plasma Concentration". Case Rep Vasc Med. 2018: 9385017. doi:10.1155/2018/9385017. PMC 5933017. PMID 29850368.
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  6. Yildiz BS, Gungor H, Gul I, Bilgin M, Zoghi M, Akilli A (2013). "Is a drug-challenge test with propafenone adequate to exclude Brugada syndrome?". Cardiovascular Journal of Africa. 24 (2): e4–6. doi:10.5830/CVJA-2012-068. PMID 23613002.
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