Safety of Right and Left Ventricular Endomyocardial Biopsy in Heart Transplantation and Cardiomyopathy Patients.


Journal

JACC. Heart failure
ISSN: 2213-1787
Titre abrégé: JACC Heart Fail
Pays: United States
ID NLM: 101598241

Informations de publication

Date de publication:
12 2022
Historique:
received: 14 06 2022
revised: 08 08 2022
accepted: 11 08 2022
entrez: 1 12 2022
pubmed: 2 12 2022
medline: 6 12 2022
Statut: ppublish

Résumé

Endomyocardial biopsy (EMB) facilitates a histopathologic diagnosis with unique prognostic and therapeutic implications in both native and donor hearts. It is a relatively safe procedure, with an overall complication rate ranging from <1% to 6% depending on the experience of the operator, the clinical status of the patient, the presence or absence of left bundle branch block, the access site, and the site of procurement (right ventricular [RV] vs left ventricular [LV] approach). This study aimed to assess the incidence of procedure-related complications in a real-world population. EMBs were performed either for surveillance of rejection episodes after heart transplantation or for diagnosis of etiology of cardiomyopathy. The authors retrospectively analyzed 1,368 biopsies obtained in 561 consecutive patients between May 2011 and May 2021. Patients were stratified according to the underlying heart disease, sex, age, access site, body mass index, and RV vs LV approach. The analysis revealed an overall complication rate of 4.1%. Serious life-threatening cardiac complications occurred in <1% of EMBs, with tamponade necessitating pericardiocentesis in 0.2% and urgent cardiac surgery in 0.1% of the procedures. Minor complications occurred in 3.3% of the overall population and were more often encountered during LV EMBs (3.9%) and when the native heart was sampled (5.3%). In experienced hands, LV and RV EMB for heart transplantation rejection surveillance and cardiomyopathy diagnosis is a safe procedure with low risk of complications. Older, female patients and those undergoing native heart EMB were more prone to complications following EMB.

Sections du résumé

BACKGROUND
Endomyocardial biopsy (EMB) facilitates a histopathologic diagnosis with unique prognostic and therapeutic implications in both native and donor hearts. It is a relatively safe procedure, with an overall complication rate ranging from <1% to 6% depending on the experience of the operator, the clinical status of the patient, the presence or absence of left bundle branch block, the access site, and the site of procurement (right ventricular [RV] vs left ventricular [LV] approach).
OBJECTIVES
This study aimed to assess the incidence of procedure-related complications in a real-world population. EMBs were performed either for surveillance of rejection episodes after heart transplantation or for diagnosis of etiology of cardiomyopathy.
METHODS
The authors retrospectively analyzed 1,368 biopsies obtained in 561 consecutive patients between May 2011 and May 2021. Patients were stratified according to the underlying heart disease, sex, age, access site, body mass index, and RV vs LV approach.
RESULTS
The analysis revealed an overall complication rate of 4.1%. Serious life-threatening cardiac complications occurred in <1% of EMBs, with tamponade necessitating pericardiocentesis in 0.2% and urgent cardiac surgery in 0.1% of the procedures. Minor complications occurred in 3.3% of the overall population and were more often encountered during LV EMBs (3.9%) and when the native heart was sampled (5.3%).
CONCLUSIONS
In experienced hands, LV and RV EMB for heart transplantation rejection surveillance and cardiomyopathy diagnosis is a safe procedure with low risk of complications. Older, female patients and those undergoing native heart EMB were more prone to complications following EMB.

Identifiants

pubmed: 36456070
pii: S2213-1779(22)00468-1
doi: 10.1016/j.jchf.2022.08.005
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

963-973

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2022 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Funding Support and Author Disclosures Drs Paolisso, Esposito, Bertolone, and Fabbricatore are supported by a research grant from the CardioPaTh PhD Program. Dr De Bruyne owns minor equity in Philips Volcano, Siemens, GE Healthcare, Edwards Lifesciences, HeartFlow, Opsens, and Celiad. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Auteurs

Konstantinos Bermpeis (K)

Cardiovascular Center Aalst, OLV Hospital, Aalst, Belgium; Department of Cardiology, AHEPA University General Hospital, Thessaloniki, Greece.

Giuseppe Esposito (G)

Cardiovascular Center Aalst, OLV Hospital, Aalst, Belgium; Department of Advanced Biomedical Sciences, University of Naples Federico II, Naples, Italy.

Emanuele Gallinoro (E)

Cardiovascular Center Aalst, OLV Hospital, Aalst, Belgium; Department of Translational Medical Sciences, University of Campania Luigi Vanvitelli, Naples, Italy.

Pasquale Paolisso (P)

Cardiovascular Center Aalst, OLV Hospital, Aalst, Belgium; Department of Advanced Biomedical Sciences, University of Naples Federico II, Naples, Italy.

Dario Tino Bertolone (DT)

Cardiovascular Center Aalst, OLV Hospital, Aalst, Belgium; Department of Advanced Biomedical Sciences, University of Naples Federico II, Naples, Italy.

Davide Fabbricatore (D)

Cardiovascular Center Aalst, OLV Hospital, Aalst, Belgium; Department of Advanced Biomedical Sciences, University of Naples Federico II, Naples, Italy.

Niya Mileva (N)

Cardiovascular Center Aalst, OLV Hospital, Aalst, Belgium; Cardiology Clinic, University Hospital Alexandrovska, Sofia, Bulgaria.

Daniel Munhoz (D)

Cardiovascular Center Aalst, OLV Hospital, Aalst, Belgium.

John Buckley (J)

Cardiovascular Center Aalst, OLV Hospital, Aalst, Belgium.

Eric Wyffels (E)

Cardiovascular Center Aalst, OLV Hospital, Aalst, Belgium.

Jeroen Sonck (J)

Cardiovascular Center Aalst, OLV Hospital, Aalst, Belgium; Department of Advanced Biomedical Sciences, University of Naples Federico II, Naples, Italy.

Carlos Collet (C)

Cardiovascular Center Aalst, OLV Hospital, Aalst, Belgium.

Emanuele Barbato (E)

Cardiovascular Center Aalst, OLV Hospital, Aalst, Belgium; Department of Advanced Biomedical Sciences, University of Naples Federico II, Naples, Italy.

Bernard De Bruyne (B)

Cardiovascular Center Aalst, OLV Hospital, Aalst, Belgium; Department of Cardiology, Lausanne University Hospital, Lausanne, Switzerland.

Jozef Bartunek (J)

Cardiovascular Center Aalst, OLV Hospital, Aalst, Belgium.

Marc Vanderheyden (M)

Cardiovascular Center Aalst, OLV Hospital, Aalst, Belgium. Electronic address: marc.vanderheyden@olvz-aalst.be.

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Classifications MeSH