Infra-Hisian Block: Difference between revisions
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===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>. | |||
* [[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]] | |||
* [[Bacterial endocarditis]] | |||
* [[Myocarditis]] | |||
* [[hypothermia|Severe hypothermia]] | |||
===Common Causes=== | |||
* [[Acute rheumatic fever]] | |||
* [[Bacterial endocarditis]]<ref name="pmid27585419">{{cite journal |vauthors=Kamatani T, Akizuki A, Kondo S, Shirota T |title=Second-Degree Atrioventricular Block Occurring After Tooth Extraction |journal=Anesth Prog |volume=63 |issue=3 |pages=156–9 |date=Fall 2016 |pmid=27585419 |pmc=5011958 |doi=10.2344/15-00042.1 |url=}}</ref> | |||
* [[aortic stenosis|Calcific aortic stenosis]] | |||
* [[Digoxin]] | |||
* [[Dilated cardiomyopathy]] | |||
* [[Diltiazem]] | |||
* [[Vasovagal syncope#Cardioinhibitory Response|Enhanced vagal tone]] | |||
* [[HCM]] | |||
* [[Hypertension]] | |||
* [[Iatrogenic]] after surgical correction of [[VSD]], [[tetralogy of Fallot]], and [[endocardial cushion defect]] | |||
* [[ST elevation MI|Inferior ST elevation MI]] | |||
* [[mitral valve sclerosis|Massive calcification of the mitral annulus]] | |||
* [[Myocarditis]] | |||
* [[PR interval|Normal variants]]<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> | |||
* [[chest trauma|Penetrating and non-penetrating trauma of the chest]] | |||
* [[Lev's disease|Sclerodegenerative disease of the electrical conduction system]] | |||
* [[Verapamil]] | |||
* [[Beta blocker|β blockers]] | |||
===Causes by Organ System=== | |||
{|style="width:80%; height:100px" border="1" | |||
|style="height:100px"; style="width:25%" border="1" bgcolor="LightSteelBlue" | '''Cardiovascular''' | |||
|style="height:100px"; style="width:75%" border="1" bgcolor="Beige" | [[Acute myocardial infarction]], [[acute rheumatic fever]], [[ASD]], [[dilated cardiomyopathy]], [[Ebstein's anomaly]], [[Carotid sinus hypersensitivity|hypersensitive carotid sinus syndrome]], [[hypertension]], [[hypertrophic cardiomyopathy]], [[Lev's disease]], [[myocardial bridging]], [[myocarditis]], [[PR interval|normal variants]], [[Aortic valve replacement|post aortic valve replacement]], [[catheter ablation|post catheter ablation for arrhythmias]], [[ventricular septal defect surgery|post closure of a ventricular septal defect]], [[mitral valve replacement|post mitral valve replacement]], [[tetralogy of Fallot]], [[endocardial cushion defect]], [[transposition of the great vessels]], [[valvular heart disease]], [[VSD]] | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Chemical / poisoning''' | |||
|bgcolor="Beige"| No underlying causes | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Dermatologic''' | |||
|bgcolor="Beige"| No underlying causes | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Drug Side Effect''' | |||
|bgcolor="Beige"| [[Amiodarone]], [[beta-blockers]], [[digitalis]], [[calcium channel blockers]], [[cholinesterase inhibitor|cholinesterase inhibitors]], [[disopyramide]], [[dofetilide]], [[dolasetron]], [[donepezil]], [[eslicarbazepine acetate]], [[fesoterodine]], [[fingolimod]], [[flecainide]], [[ibutilide]], [[lacosamide]], [[magnesium]], [[paliperidone]], [[pramipexole]], [[procainamide]], [[propafenone]], [[propoxyphene]], [[quinidine]], [[sotalol]], [[terodiline]] | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Ear Nose Throat''' | |||
|bgcolor="Beige"| No underlying causes | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Endocrine''' | |||
|bgcolor="Beige"| [[Hyperthyroidism]], [[myxedema]], [[periodic paralysis|thyrotoxic periodic paralysis]] | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Environmental''' | |||
|bgcolor="Beige"| [[Hypothermia]] | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Gastroenterologic''' | |||
|bgcolor="Beige"| [[Hemochromatosis]] | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Genetic''' | |||
|bgcolor="Beige"| [[Emery-Dreifuss muscular dystrophy]], [[Fabry disease]], [[glycogenosis type 2b]], [[Neuromuscular disease|hereditary neuromuscular disease]], [[Kearns-Sayre syndrome]] | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Hematologic''' | |||
|bgcolor="Beige"| [[Multiple myeloma]] [[Lymphoma]]<ref name="pmid27200273">{{cite journal |vauthors=Menicagli F, Lanza A, Sbrocca F, Baldi A, Spugnini EP |title=A case of advanced second-degree atrioventricular block in a ferret secondary to lymphoma |journal=Open Vet J |volume=6 |issue=1 |pages=68–70 |date=2016 |pmid=27200273 |pmc=4833871 |doi=10.4314/ovj.v6i1.10 |url=}}</ref> | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Iatrogenic''' | |||
|bgcolor="Beige"| [[aortic valve replacement|Post aortic valve replacement]], [[catheter ablation|post catheter ablation for arrhythmias]], [[ventricular septal defect surgery|post closure of a ventricular septal defect]], [[mitral valve replacement|post mitral valve replacement]] | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Infectious Disease''' | |||
|bgcolor="Beige"| [[Acute rheumatic fever]], [[Chagas disease]], [[diphtheria]], [[Lyme disease]], [[myocarditis]], [[neonatal lupus erythematosus]], [[protozoa|protozoal infection]], [[sarcoidosis]], [[SLE]], [[tuberculosis]] | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Musculoskeletal / Ortho''' | |||
|bgcolor="Beige"| [[Ankylosing spondylitis]], [[Neuromuscular disease|hereditary neuromuscular disease]], [[Kearns-Sayre syndrome]], [[mitochondrial DNA|mitochondrial genome inherited conditions]], [[muscular dystrophy]] | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Neurologic''' | |||
|bgcolor="Beige"| [[Vasovagal syncope#Cardioinhibitory Response|Enhanced vagal tone]] | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Nutritional / Metabolic''' | |||
|bgcolor="Beige"| [[Fabry disease]], [[glycogenosis type 2b]] | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Obstetric/Gynecologic''' | |||
|bgcolor="Beige"| No underlying causes | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Oncologic''' | |||
|bgcolor="Beige"| [[Multiple myeloma]] | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Opthalmologic''' | |||
|bgcolor="Beige"| No underlying causes | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Overdose / Toxicity''' | |||
|bgcolor="Beige"| No underlying causes | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Psychiatric''' | |||
|bgcolor="Beige"| No underlying causes | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Pulmonary''' | |||
|bgcolor="Beige"| [[Sarcoidosis]] | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Renal / Electrolyte''' | |||
|bgcolor="Beige"| [[Hyperkalemia]], [[hypokalemia]] | |||
|-bgcolor="LightSteelBlue" | |||
| '''Rheum / Immune / Allergy''' | |||
|bgcolor="Beige"| [[Ankylosing spondylitis]], [[dermatomyositis]], [[rheumatoid arthritis]], [[scleroderma]], [[SLE]] | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Sexual''' | |||
|bgcolor="Beige"| No underlying causes | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Trauma''' | |||
|bgcolor="Beige"| No underlying causes | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Urologic''' | |||
|bgcolor="Beige"| No underlying causes | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Dental''' | |||
|bgcolor="Beige"| No underlying causes | |||
|- | |||
|-bgcolor="LightSteelBlue" | |||
| '''Miscellaneous''' | |||
|bgcolor="Beige"| [[Amyloidosis]], [[degenerative diseases]] | |||
|- | |||
|} | |||
===Causes in Alphabetical Order=== | |||
{{col-begin|width=80%}} | |||
{{col-break|width=33%}} | |||
* [[Acute myocardial infarction]] | |||
* [[Acute rheumatic fever]] | |||
* [[Amyloidosis]] | |||
* [[Ankylosing spondylitis]] | |||
* [[ASD]] | |||
* [[Bacterial endocarditis]] | |||
* [[Beta-blockers]] | |||
* [[Calcific aortic stenosis]] | |||
* [[Calcium channel blockers]] | |||
* [[Cardiac glycosides]] | |||
* [[Cardiac tumors]] | |||
* [[Chagas disease]] | |||
* [[Cholinesterase inhibitors]] | |||
* [[Clonidine]] | |||
* [[Degenerative diseases]] | |||
* [[Dermatomyositis]] | |||
* [[Digitalis]] | |||
* [[Digoxin]] | |||
* [[Dilated cardiomyopathy]] | |||
* [[Diltiazem]] | |||
* [[Diphtheria]] | |||
* [[Disopyramide]] | |||
* [[Dolasetron]] | |||
* [[Donepezil]] | |||
* [[Ebstein's anomaly]] | |||
* [[Electrolyte disturbances]] | |||
* [[Emery-Dreifuss muscular dystrophy]] | |||
* [[Endocarditis]] | |||
* [[vagus nerve|Enhanced vagal tone in athletes]] | |||
{{col-break|width=33%}} | |||
* [[Eslicarbazepine acetate]] | |||
* [[Fabry disease]] | |||
* [[Fesoterodine]] | |||
* [[Fingolimod]] | |||
* [[Glycogenosis type 2b]] | |||
* [[HCM]] | |||
* [[Neuromuscular disease|Hereditary neuromuscular disease]] | |||
* [[Hodgkin lymphoma]] | |||
* [[Hyperkalaemia]] | |||
* [[Carotid sinus hypersensitivity|Hypersensitive carotid sinus syndrome]] | |||
* [[Hyperthyroidism]] | |||
* [[Hypokalaemia]] | |||
* [[Hypothermia]] | |||
* [[Ibutilide]] | |||
* [[Ischemic heart disease]] | |||
* [[Kearns-Sayre syndrome]] | |||
* [[Labetalol]] | |||
* [[Lacosamide]] | |||
* [[Lanatoside C]] | |||
* [[Lenegre's disease]] | |||
* [[Lev's disease]] | |||
* [[Lyme disease]] | |||
* [[Mitochondrial DNA|Mitochondrial genome inherited conditions]] | |||
* [[Multiple myeloma]] | |||
* [[Muscular dystrophy]] | |||
* [[Myocardial bridging]] | |||
* [[Myocarditis]] | |||
* [[Myotonic dystrophy]] | |||
* [[Myxedema]] | |||
{{col-break|width=33%}} | |||
* [[Neonatal lupus erythematosus]] | |||
* [[prolonged PR interval|Normal variants of PR prolongation]] | |||
* [[Paliperidone]] | |||
* [[aortic valve replacement|Post aortic valve replacement]] | |||
* [[catheter ablation|Post catheter ablation for arrhythmias]] | |||
* [[Ventricular septal defect surgery|Post closure of a ventricular septal defect]] | |||
* [[mitral valve replacement|Post mitral valve replacement]] | |||
* [[Procainamide]] | |||
* [[Propoxyphene]] | |||
* [[Propranolol]] | |||
* [[Protozoa|Protozoal infection]] | |||
* [[Quinidine]] | |||
* [[Quinine]] | |||
* [[Rheumatic fever|Rheumatic mitral valve disease]] | |||
* [[Sarcoidosis]] | |||
* [[SLE]] | |||
* [[Systemic sclerosis]] | |||
* [[Terodiline]] | |||
* [[Tetralogy of Fallot]] | |||
* [[periodic paralysis|Thyrotoxic periodic paralysis]] | |||
* [[Tolterodine]] | |||
* [[Transposition of the great vessels]] | |||
* [[vagus nerve|Vagal maneuvers]] | |||
* [[Valsalva maneuvers]] | |||
* [[Valvular heart disease]] | |||
* [[Verapamil]] | |||
* [[VSD]] | |||
* [[sex linkage|X-linked inherited conditions]] | |||
{{col-end}} | |||
==Differentiating ((Page name)) from other Diseases== | ==Differentiating ((Page name)) from other Diseases== |
Revision as of 22:50, 21 April 2020
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor-In-Chief: Sara Mohsin, M.D.[2]
Overview
Infra-Hisian blocks are defined as impaired conduction in the electrical system of the heart that occur below the AV node.
Classification
Infrahisian block describes block of the distal conduction system. Types of infrahisian block include:
Of these types of infrahisian block, Mobitz II heart block is considered most important because of the possible progression to complete heart block.
Pathophysiology
Mobitz type II second degree AV block 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. 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. Patients with bundle branch involvement also have axis shifts and QRS widening depending upon the location of the block. In addition, at least two-thirds of patients with this disorder also have bifascicular or even trifascicular disease. Mobitz type I and Mobitz type II second degree AV block cannot be differentiated from the ECG when 2:1 AV block is present. 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.
Causes
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:
●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.
●Iatrogenic – Medication-related (AV nodal blocking medications), post-cardiac surgery, post-catheter ablation, post-transcatheter aortic valve implantation.
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.
Physiologic and pathophysiologic | |
---|---|
Increased vagal tone | |
Ischemic heart disease, including acute myocardial infarction | |
Progressive cardiac conduction system disease | With fibrosis and/or sclerosis (Lenegre disease) |
With calcification (Lev disease) | |
Infections (eg, viral myocarditis, Lyme carditis) | |
Cardiomyopathy | Infiltrative processes (eg, sarcoidosis, amyloidosis, hemochromatosis, malignancy, etc) |
Other non-ischemic cardiomyopathies (eg, idiopathic, infectious, etc) | |
Congenital AV block | Related to structural congenital heart disease |
As part of neonatal lupus syndrome | |
Other | Hyperkalemia |
severe hypo- or hyperthyroidism | |
trauma | |
degenerative neuromuscular diseases | |
Iatrogenic | |
Drugs | Beta blockers |
calcium channel blockers | |
digoxin | |
antiarrhythmic drugs | |
adenosine | |
Transcatheter aortic valve implantation | |
Cardiac surgery | Post valvular surgery |
post surgical correction of congenital heart disease | |
Catheter ablation of arrhythmias | |
Alcohol septal ablation for hypertrophic cardiomyopathy | |
Transcatheter closure of ventricular septal defect |
Life Threatening Causes
Life-threatening conditions can result in death or permanent disability within 24 hours if left untreated[1].
- Acute myocardial infarction[2][3]
- Acute rheumatic fever
- Bacterial endocarditis
- Myocarditis
- Severe hypothermia
Common Causes
- Acute rheumatic fever
- Bacterial endocarditis[4]
- Calcific aortic stenosis
- Digoxin
- Dilated cardiomyopathy
- Diltiazem
- Enhanced vagal tone
- HCM
- Hypertension
- Iatrogenic after surgical correction of VSD, tetralogy of Fallot, and endocardial cushion defect
- Inferior ST elevation MI
- Massive calcification of the mitral annulus
- Myocarditis
- Normal variants[5]
- Penetrating and non-penetrating trauma of the chest
- Sclerodegenerative disease of the electrical conduction system
- Verapamil
- β blockers
Causes by Organ System
Causes in Alphabetical Order
Differentiating ((Page name)) from other Diseases
[Disease name] must be differentiated from other diseases that cause [clinical feature 1], [clinical feature 2], and [clinical feature 3], such as [differential dx1], [differential dx2], and [differential dx3].
OR
[Disease name] must be differentiated from [[differential dx1], [differential dx2], and [differential dx3].
Epidemiology and Demographics
The incidence/prevalence of [disease name] is approximately [number range] per 100,000 individuals worldwide.
OR
In [year], the incidence/prevalence of [disease name] was estimated to be [number range] cases per 100,000 individuals worldwide.
OR
In [year], the incidence of [disease name] is approximately [number range] per 100,000 individuals with a case-fatality rate of [number range]%.
Patients of all age groups may develop [disease name].
OR
The incidence of [disease name] increases with age; the median age at diagnosis is [#] years.
OR
[Disease name] commonly affects individuals younger than/older than [number of years] years of age.
OR
[Chronic disease name] is usually first diagnosed among [age group].
OR
[Acute disease name] commonly affects [age group].
There is no racial predilection to [disease name].
OR
[Disease name] usually affects individuals of the [race 1] race. [Race 2] individuals are less likely to develop [disease name].
[Disease name] affects men and women equally.
OR
[Gender 1] are more commonly affected by [disease name] than [gender 2]. The [gender 1] to [gender 2] ratio is approximately [number > 1] to 1.
The majority of [disease name] cases are reported in [geographical region].
OR
[Disease name] is a common/rare disease that tends to affect [patient population 1] and [patient population 2].
Risk Factors
There are no established risk factors for [disease name].
OR
The most potent risk factor in the development of [disease name] is [risk factor 1]. Other risk factors include [risk factor 2], [risk factor 3], and [risk factor 4].
OR
Common risk factors in the development of [disease name] include [risk factor 1], [risk factor 2], [risk factor 3], and [risk factor 4].
OR
Common risk factors in the development of [disease name] may be occupational, environmental, genetic, and viral.
Screening
There is insufficient evidence to recommend routine screening for [disease/malignancy].
OR
According to the [guideline name], screening for [disease name] is not recommended.
OR
According to the [guideline name], screening for [disease name] by [test 1] is recommended every [duration] among patients with [condition 1], [condition 2], and [condition 3].
Natural History, Complications, and Prognosis
If left untreated, [#]% of patients with [disease name] may progress to develop [manifestation 1], [manifestation 2], and [manifestation 3].
OR
Common complications of [disease name] include [complication 1], [complication 2], and [complication 3].
OR
Prognosis is generally excellent/good/poor, and the 1/5/10-year mortality/survival rate of patients with [disease name] is approximately [#]%.
Diagnosis
Diagnostic Study of Choice
The diagnosis of [disease name] is made when at least [number] of the following [number] diagnostic criteria are met: [criterion 1], [criterion 2], [criterion 3], and [criterion 4].
OR
The diagnosis of [disease name] is based on the [criteria name] criteria, which include [criterion 1], [criterion 2], and [criterion 3].
OR
The diagnosis of [disease name] is based on the [definition name] definition, which includes [criterion 1], [criterion 2], and [criterion 3].
OR
There are no established criteria for the diagnosis of [disease name].
History and Symptoms
The majority of patients with [disease name] are asymptomatic.
OR
The hallmark of [disease name] is [finding]. A positive history of [finding 1] and [finding 2] is suggestive of [disease name]. The most common symptoms of [disease name] include [symptom 1], [symptom 2], and [symptom 3]. Common symptoms of [disease] include [symptom 1], [symptom 2], and [symptom 3]. Less common symptoms of [disease name] include [symptom 1], [symptom 2], and [symptom 3].
Physical Examination
Patients with [disease name] usually appear [general appearance]. Physical examination of patients with [disease name] is usually remarkable for [finding 1], [finding 2], and [finding 3].
OR
Common physical examination findings of [disease name] include [finding 1], [finding 2], and [finding 3].
OR
The presence of [finding(s)] on physical examination is diagnostic of [disease name].
OR
The presence of [finding(s)] on physical examination is highly suggestive of [disease name].
Laboratory Findings
An elevated/reduced concentration of serum/blood/urinary/CSF/other [lab test] is diagnostic of [disease name].
OR
Laboratory findings consistent with the diagnosis of [disease name] include [abnormal test 1], [abnormal test 2], and [abnormal test 3].
OR
[Test] is usually normal among patients with [disease name].
OR
Some patients with [disease name] may have elevated/reduced concentration of [test], which is usually suggestive of [progression/complication].
OR
There are no diagnostic laboratory findings associated with [disease name].
Electrocardiogram
There are no ECG findings associated with [disease name].
OR
An ECG may be helpful in the diagnosis of [disease name]. Findings on an ECG suggestive of/diagnostic of [disease name] include [finding 1], [finding 2], and [finding 3].
References
- ↑ Mangi MA, Jones WM, Napier L. PMID 29493981. Missing or empty
|title=
(help) - ↑ Misumida N, Ogunbayo GO, Kim SM, Abdel-Latif A, Ziada KM, Elayi CS (November 2018). "Frequency and Significance of High-Degree Atrioventricular Block and Sinoatrial Node Dysfunction in Patients With Non-ST-Elevation Myocardial Infarction". Am. J. Cardiol. 122 (10): 1598–1603. doi:10.1016/j.amjcard.2018.08.001. PMID 30227965.
- ↑ Barold SS, Herweg B (December 2012). "Second-degree atrioventricular block revisited". Herzschrittmacherther Elektrophysiol. 23 (4): 296–304. doi:10.1007/s00399-012-0240-8. PMID 23224264.
- ↑ Kamatani T, Akizuki A, Kondo S, Shirota T (Fall 2016). "Second-Degree Atrioventricular Block Occurring After Tooth Extraction". Anesth Prog. 63 (3): 156–9. doi:10.2344/15-00042.1. PMC 5011958. PMID 27585419.
- ↑ Wogan JM, Lowenstein SR, Gordon GS (1993). "Second-degree atrioventricular block: Mobitz type II". J Emerg Med. 11 (1): 47–54. doi:10.1016/0736-4679(93)90009-v. PMID 8445186.
- ↑ Menicagli F, Lanza A, Sbrocca F, Baldi A, Spugnini EP (2016). "A case of advanced second-degree atrioventricular block in a ferret secondary to lymphoma". Open Vet J. 6 (1): 68–70. doi:10.4314/ovj.v6i1.10. PMC 4833871. PMID 27200273.