Pulseless ventricular tachycardia history and symptoms: Difference between revisions

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==Overview==
==Overview==
Pulseless ventricular tachycardia may be symptomatic or asymptomatic. In a young patient with a family history of sudden death, immediate evaluation for an inherited ventricular syndrome is recommended. If symptomatic, the ventricular rate, durations of tachycardia, and the presence of underlying disease determine the kind of symptoms that present.
Pulseless ventricular tachycardia may be symptomatic or asymptomatic. In a young patient with a family history of sudden death, immediate evaluation for an inherited ventricular syndrome is recommended. If symptomatic, the ventricular rate, duration of tachycardia, and the presence of underlying disease determine the kind of symptoms that present.


==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].
*Symptoms of [disease name] include [symptom 1], [symptom 2], and [symptom 3]. 
===History===
===History===
Patients with [disease name]] may have a positive history of:
In young patients with a positive family history of sudden death, evaluation for inherited arrhythmia syndromes is warranted.<ref name="pmid27484660">{{cite journal |vauthors=Baldzizhar A, Manuylova E, Marchenko R, Kryvalap Y, Carey MG |title=Ventricular Tachycardias: Characteristics and Management |journal=Crit Care Nurs Clin North Am |volume=28 |issue=3 |pages=317–29 |date=September 2016 |pmid=27484660 |doi=10.1016/j.cnc.2016.04.004 |url=}}</ref> Inherited arrhythmia disorders include:
*[History finding 1]
*[[Long QT syndrome|Congenital long QT]] (LQT)<ref name="pmid234667">{{cite journal |vauthors=Schwartz PJ, Periti M, Malliani A |title=The long Q-T syndrome |journal=Am. Heart J. |volume=89 |issue=3 |pages=378–90 |date=March 1975 |pmid=234667 |doi=10.1016/0002-8703(75)90089-7 |url=}}</ref>
*[History finding 2]
*[[Brugada syndrome]] (BrS)<ref name="pmid24568830">{{cite journal |vauthors=Chockalingam P, Wilde AA |title=Inherited arrhythmia syndromes leading to sudden cardiac death in the young: a global update and an Indian perspective |journal=Indian Heart J |volume=66 Suppl 1 |issue= |pages=S49–57 |date=2014 |pmid=24568830 |pmc=4237302 |doi=10.1016/j.ihj.2013.11.008 |url=}}</ref>
*[History finding 3]
*[[Hypertrophic cardiomyopathy]]
*[[Arrhythmogenic right ventricular dysplasia]] (ARVD)
*[[Short QT syndrome|Congenital short QT intervals]] (SQT)<ref name="pmid23994779">{{cite journal |vauthors=Priori SG, Wilde AA, Horie M, Cho Y, Behr ER, Berul C, Blom N, Brugada J, Chiang CE, Huikuri H, Kannankeril P, Krahn A, Leenhardt A, Moss A, Schwartz PJ, Shimizu W, Tomaselli G, Tracy C, Ackerman M, Belhassen B, Estes NA, Fatkin D, Kalman J, Kaufman E, Kirchhof P, Schulze-Bahr E, Wolpert C, Vohra J, Refaat M, Etheridge SP, Campbell RM, Martin ET, Quek SC |title=Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes |journal=Europace |volume=15 |issue=10 |pages=1389–406 |date=October 2013 |pmid=23994779 |doi=10.1093/europace/eut272 |url=}}</ref>
*[[Early repolarization syndrome]]
*[[Ventricular fibrillation, idiopathic|Idiopathic ventricular fibrillation]] (IVF)<ref name="pmid2202193">{{cite journal |vauthors=Viskin S, Belhassen B |title=Idiopathic ventricular fibrillation |journal=Am. Heart J. |volume=120 |issue=3 |pages=661–71 |date=September 1990 |pmid=2202193 |doi=10.1016/0002-8703(90)90025-s |url=}}</ref>


===Common Symptoms===
=== Symptoms===
Common symptoms of [disease] include:
*Pulseless ventricular tachycardia can be symptomatic or asymptomatic.
*[Symptom 1]
*If symptomatic, the ventricular rate, duration of tachycardia, and the presence of underlying [[heart disease]] determine the kind of symptoms that present.
*[Symptom 2]
*On initial presentation, patients with impending [[pulseless ventricular tachycardia]] may present with signs of inadequate [[cardiac perfusion]] such as <ref name="pmid21593723">{{cite journal |vauthors=Barsheshet A, Goldenberg I |title=Cardiovascular syncope: diagnostic approach and risk assessment |journal=Minerva Med. |volume=102 |issue=3 |pages=223–38 |date=June 2011 |pmid=21593723 |doi= |url=}}</ref> <ref name="pmid10532503">{{cite journal |vauthors=Moss AJ, Robinson JL, Gessman L, Gillespie R, Zareba W, Schwartz PJ, Vincent GM, Benhorin J, Heilbron EL, Towbin JA, Priori SG, Napolitano C, Zhang L, Medina A, Andrews ML, Timothy K |title=Comparison of clinical and genetic variables of cardiac events associated with loud noise versus swimming among subjects with the long QT syndrome |journal=Am. J. Cardiol. |volume=84 |issue=8 |pages=876–9 |date=October 1999 |pmid=10532503 |doi=10.1016/s0002-9149(99)00458-0 |url=}}</ref>
*[Symptom 3]
**[[chest pain]],
 
**[[shortness of breath]],
===Less Common Symptoms===
**[[diaphoresis]],
Less common symptoms of [disease name] include
**[[palpitations]], and
*[Symptom 1]
**[[syncope]].
*[Symptom 2]
*Physical examination may be positive for [[hypotension]], [[tachycardia]], [[tachypnea]], [[increased JVD]], and an [[S1]].
*[Symptom 3]
*Eventually, Pulseless ventricular tachycardia ensues and patients become unconscious and unresponsive with no detectable pulse.<ref name="pmid32119354">{{cite journal |vauthors=Foglesong A, Mathew D |title= |journal= |volume= |issue= |pages= |date= |pmid=32119354 |doi= |url=}}</ref>


==References==
==References==

Latest revision as of 14:35, 10 July 2020

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Aisha Adigun, B.Sc., M.D.[2]

Overview

Pulseless ventricular tachycardia may be symptomatic or asymptomatic. In a young patient with a family history of sudden death, immediate evaluation for an inherited ventricular syndrome is recommended. If symptomatic, the ventricular rate, duration of tachycardia, and the presence of underlying disease determine the kind of symptoms that present.

History

In young patients with a positive family history of sudden death, evaluation for inherited arrhythmia syndromes is warranted.[1] Inherited arrhythmia disorders include:

Symptoms

References

  1. ↑ Baldzizhar A, Manuylova E, Marchenko R, Kryvalap Y, Carey MG (September 2016). "Ventricular Tachycardias: Characteristics and Management". Crit Care Nurs Clin North Am. 28 (3): 317–29. doi:10.1016/j.cnc.2016.04.004. PMID 27484660.
  2. ↑ Schwartz PJ, Periti M, Malliani A (March 1975). "The long Q-T syndrome". Am. Heart J. 89 (3): 378–90. doi:10.1016/0002-8703(75)90089-7. PMID 234667.
  3. ↑ Chockalingam P, Wilde AA (2014). "Inherited arrhythmia syndromes leading to sudden cardiac death in the young: a global update and an Indian perspective". Indian Heart J. 66 Suppl 1: S49–57. doi:10.1016/j.ihj.2013.11.008. PMC 4237302. PMID 24568830.
  4. ↑ Priori SG, Wilde AA, Horie M, Cho Y, Behr ER, Berul C, Blom N, Brugada J, Chiang CE, Huikuri H, Kannankeril P, Krahn A, Leenhardt A, Moss A, Schwartz PJ, Shimizu W, Tomaselli G, Tracy C, Ackerman M, Belhassen B, Estes NA, Fatkin D, Kalman J, Kaufman E, Kirchhof P, Schulze-Bahr E, Wolpert C, Vohra J, Refaat M, Etheridge SP, Campbell RM, Martin ET, Quek SC (October 2013). "Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes". Europace. 15 (10): 1389–406. doi:10.1093/europace/eut272. PMID 23994779.
  5. ↑ Viskin S, Belhassen B (September 1990). "Idiopathic ventricular fibrillation". Am. Heart J. 120 (3): 661–71. doi:10.1016/0002-8703(90)90025-s. PMID 2202193.
  6. ↑ Barsheshet A, Goldenberg I (June 2011). "Cardiovascular syncope: diagnostic approach and risk assessment". Minerva Med. 102 (3): 223–38. PMID 21593723.
  7. ↑ Moss AJ, Robinson JL, Gessman L, Gillespie R, Zareba W, Schwartz PJ, Vincent GM, Benhorin J, Heilbron EL, Towbin JA, Priori SG, Napolitano C, Zhang L, Medina A, Andrews ML, Timothy K (October 1999). "Comparison of clinical and genetic variables of cardiac events associated with loud noise versus swimming among subjects with the long QT syndrome". Am. J. Cardiol. 84 (8): 876–9. doi:10.1016/s0002-9149(99)00458-0. PMID 10532503.
  8. ↑ Foglesong A, Mathew D. PMID 32119354 Check |pmid= value (help). Missing or empty |title= (help)


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