Show simple item record

Device‐detected nonsustained ventricular tachycardia in adult congenital heart disease without tetralogy of fallot

dc.contributor.authorDoctor, Pezad
dc.contributor.authorAggarwal, Sanjeev
dc.contributor.authorLawrence, David K.
dc.contributor.authorGupta, Pooja
dc.contributor.authorSingh, Gautam K.
dc.contributor.authorMadhavan, Malini
dc.contributor.authorSriram, Chenni S.
dc.date.accessioned2022-04-08T18:06:21Z
dc.date.available2023-04-08 14:06:20en
dc.date.available2022-04-08T18:06:21Z
dc.date.issued2022-03
dc.identifier.citationDoctor, Pezad; Aggarwal, Sanjeev; Lawrence, David K.; Gupta, Pooja; Singh, Gautam K.; Madhavan, Malini; Sriram, Chenni S. (2022). "Device‐detected nonsustained ventricular tachycardia in adult congenital heart disease without tetralogy of fallot." Pacing and Clinical Electrophysiology 45(3): 302-313.
dc.identifier.issn0147-8389
dc.identifier.issn1540-8159
dc.identifier.urihttps://hdl.handle.net/2027.42/172063
dc.description.abstractObjectivesTo evaluate any association between non‐sustained ventricular tachycardia (NSVT) detected by intra‐cardiac device and clinical outcomes in repaired adult congenital heart disease (ACHD) without tetralogy of Fallot (TOF).BackgroundNSVT portends a higher risk of serious ventricular tachyarrhythmia in TOF. However its clinical significance when incidentally detected by implantable cardiac device is not well elucidated in non‐TOF ACHD cohort.MethodsWe performed a single center, retrospective, longitudinal follow‐up study in repaired ACHD (≥18 years) patients without TOF who hosted a pacemaker or automatic implantable cardiac defibrillator (AICD). The cohort was divided based on presence/absence of device detected NSVT. The primary end‐point was a composite of sustained ventricular tachycardia (VT), ventricular fibrillation (VF), or sudden cardiac death (SCD).ResultsOne hundred fifty eight patients (male 56.3%, median [IQR] age of 35 [28–43] years at last follow‐up] with longitudinal post‐implant follow‐up duration of 8 (5–12) years were included. NSVT was detected in 52 (33%) patients. The primary composite end‐point was more frequent in NSVT group [11.5% vs. 2.8%; p = .04]. Patients with NSVT were (i) older at the time of initial implant (age 25 vs. 18 years, p = .011) and more frequently demonstrated (ii) systemic ventricular dysfunction (44% vs. 26%; p = .015), as well as (iii) history of ventriculotomy (38% vs. 21%; p = .017).ConclusionsIn our repaired ACHD cohort, we noted a significant association between device‐detected‐NSVT and the primary composite end‐point of sustained VT/VF or SCD. Systemic ventricular dysfunction and history of ventriculotomy were more frequent in the NSVT group and likely constituted the clinical milieu.
dc.publisherLittle Brown
dc.publisherWiley Periodicals, Inc.
dc.subject.otheradult congenital heart disease
dc.subject.otherimplantable cardiac device
dc.subject.othernonsustained ventricular tachycardia
dc.subject.othersudden cardiac death
dc.titleDevice‐detected nonsustained ventricular tachycardia in adult congenital heart disease without tetralogy of fallot
dc.typeArticle
dc.rights.robotsIndexNoFollow
dc.subject.hlbsecondlevelPhysiology
dc.subject.hlbtoplevelHealth Sciences
dc.description.peerreviewedPeer Reviewed
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/172063/1/pace14420.pdf
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/172063/2/pace14420_am.pdf
dc.identifier.doi10.1111/pace.14420
dc.identifier.sourcePacing and Clinical Electrophysiology
dc.identifier.citedreferenceKhairy P, Van Hare GF, Balaji S, et al. PACES/HRS expert consensus statement on the recognition and management of arrhythmias in adult congenital heart disease: developed in partnership between the Pediatric and Congenital Electrophysiology Society (PACES) and the Heart Rhythm Society (HRS). Endorsed by the governing bodies of PACES, HRS, the American College of Cardiology (ACC), the American Heart Association (AHA), the European Heart Rhythm Association (EHRA), the Canadian Heart Rhythm Society (CHRS), and the International Society for Adult Congenital Heart Disease (ISACHD). Heart Rhythm. 2014; 11: 102 – 165.
dc.identifier.citedreferenceEscudero C, Khairy P, Sanatani S. Electrophysiologic considerations in congenital heart disease and their relationship to heart failure. Can J Cardiol. 2013; 29: 821 – 829.
dc.identifier.citedreferenceGallego P, Gonzalez AE, Sanchez‐Recalde A, et al. Incidence and predictors of sudden cardiac arrest in adults with congenital heart defects repaired before adult life. Am J Cardiol. 2012; 110: 109 – 117.
dc.identifier.citedreferenceKhairy P, Marelli AJ. Clinical use of electrocardiography in adults with congenital heart disease. Circulation. 2007; 116: 2734 – 2746.
dc.identifier.citedreferenceKhairy P, Landzberg MJ, Gatzoulis MA, et al. Value of programmed ventricular stimulation after tetralogy of Fallot repair: a multicenter study. Circulation. 2004; 109: 1994 – 2000.
dc.identifier.citedreferenceKhairy P, Harris L, Landzberg MJ, et al. Implantable cardioverter‐defibrillators in tetralogy of Fallot. Circulation. 2008; 117: 363 – 370.
dc.identifier.citedreferenceTeuwen CP, Ramdjan TT, Götte M, et al. Non‐sustained ventricular tachycardia in patients with congenital heart disease: an important sign? Int J Cardiol. 2016; 206: 158 – 163.
dc.identifier.citedreferenceFrancia P, Santini D, Musumeci B, et al. Clinical impact of nonsustained ventricular tachycardia recorded by the implantable cardioverter‐defibrillator in patients with hypertrophic cardiomyopathy. J Cardiovasc Electrophysiol. 2014; 25 ( 11 ): 1180 – 1187.
dc.identifier.citedreferenceJiménez‐Candil J, Hernández J, Perdiguero P, et al. Prognostic significance of nonsustained ventricular tachycardia episodes occurring early after implantable cardioverter‐defibrillator implantation among patients with left ventricular dysfunction. Am J Cardiol. 2016; 118 ( 10 ): 1503 – 1510.
dc.identifier.citedreferenceD.G. Katritsis, A.J. Camm. Nonsustained ventricular tachycardia: where do we stand? Eur Heart J. 2004; 25: 1093 – 1099
dc.identifier.citedreferenceZipes DP, Camm AJ, Borggrefe M, et al.; European Heart Rhythm Association and the Heart Rhythm Society. ACC/AHA/ESC 2006 guidelines for management of patients with ventricular arrhythmias and the prevention of sudden cardiac death‐executive summary: a report of the American College of Cardiology/American Heart Association Task Force and the European Society of Cardiology Committee for Practice Guidelines. Eur Heart J. 2006; 27: 2099 – 2140.
dc.identifier.citedreferenceThe Criteria Committee of the New York Heart Association Nomenclature and Criteria for Diagnosis of Diseases of the Heart and Blood Vessels. Boston: Little Brown, 1964
dc.identifier.citedreferenceHunt SA, Baker DW, Chin MH et al ACC/AHA Guidelines for the evaluation and management of chronic heart failure in the adult: executive summary a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee to Revise the 1995 Guidelines for the Evaluation and Management of Heart Failure). Circulation. 2001; 104 ( 24 ), 2996 – 3007.
dc.identifier.citedreferenceLang RM, Badano LP, Mor‐Avi V, et al. Recommendations for cardiac chamber quantification by echocardiography in adults: an update from the American Society of Echocardiography and the European Association of Cardiovascular Imaging. J Am Soc Echocardiogr. 2015; 28 ( 1 ): 1 – 39.
dc.identifier.citedreferenceKossaify A. Echocardiographic assessment of the right ventricle, from the conventional approach to speckle tracking and three‐dimensional imaging, and insights into the "Right Way" to explore the forgotten chamber. Clin Med Insights Cardiol. 2015; 9: 65 – 75.
dc.identifier.citedreferenceZoghbi WA, Adams D, Bonow RO, et al. Recommendations for noninvasive evaluation of native valvular regurgitation: a report from the American Society of Echocardiography Developed in Collaboration with the Society for Cardiovascular Magnetic Resonance. J Am Soc Echocardiogr. 2017; 30 ( 4 ): 303 – 371.
dc.identifier.citedreferenceKoyak Z, Harris L, de Groot JR, et al. Sudden cardiac death in adult congenital heart disease. Circulation. 2012; 126 ( 16 ): 1944 – 1954.
dc.identifier.citedreferenceDiller GP, Kempny A, Liodakis E, et al. Left ventricular longitudinal function predicts life‐threatening ventricular arrhythmia and death in adults with repaired tetralogy of fallot. Circulation. 2012; 125: 2440 – 2446.
dc.identifier.citedreferenceKapel GF, Sacher F, Dekkers OM, et al. Arrhythmogenic anatomical isthmuses identified by electroanatomical mapping are the substrate for ventricular tachycardia in repaired Tetralogy of Fallot. Eur Heart J 2017; 38: 268 – 276.
dc.identifier.citedreferenceKhairy P, Aboulhosn J, Gurvitz MZ, et al. Arrhythmia burden in adults with surgically repaired tetralogy of Fallot: a multi‐institutional study. Circulation 2010; 122: 868 – 875.
dc.identifier.citedreferenceGatzoulis MA, Balaji S, Webber SA, et al. Risk factors for arrhythmia and sudden cardiac death late after repair of tetralogy of Fallot: a multicentre study. Lancet. 2000; 356: 975 – 981.
dc.identifier.citedreferenceKoyak Z, de Groot JR, Van Gelder IC, et al. Implantable cardioverter defibrillator therapy in adults with congenital heart disease: who is at risk of shocks? Circ Arrhythm Electrophysiol. 2012; 5: 101 – 110.
dc.identifier.citedreferenceSakhi R, Kauling RM, Theuns DA, et al. Early detection of ventricular arrhythmias in adults with congenital heart disease using an insertable cardiac monitor (EDVA‐CHD study). Int J Cardiol. 2020; 305: 63 – 69.
dc.identifier.citedreferenceRaphael CE, Finegold JA, Barron AJ, et al. The effect of duration of follow‐up and presence of competing risk on lifespan‐gain from implantable cardioverter defibrillator therapy: who benefits the most?. Eur Heart J. 2015; 36 ( 26 ): 1676 – 1688.
dc.identifier.citedreferenceVehmeijer JT, Koyak Z, Zwinderman AH, et al. PREVENTION‐ACHD: PRospEctiVE study on implaNTable cardioverter‐defibrillator therapy and suddeN cardiac death in adults with congenital heart disease; rationale and design. Neth Heart J. 2019; 27 ( 10 ): 474 – 479.
dc.identifier.citedreferenceSilka MJ, Hardy BG, Menashe VD, Morris CD. A population‐based prospective evaluation of risk of sudden cardiac death after operation for common congenital heart defects. J Am Coll Cardiol. 1998; 32: 245 – 251
dc.identifier.citedreferencePundi KN, Pundi KN, Johnson JN, et al. Sudden cardiac death and late arrhythmias after the Fontan operation. Congenit Heart Dis. 2017; 12 ( 1 ): 17 – 23.
dc.identifier.citedreferenceSomerville J. Grown‐up congenital heart disease–medical demands look back, look forward 2000. Thorac Cardiovasc Surg. 2001; 49: 21 – 26.
dc.working.doiNOen
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.