Safety of Provocative Testing With Intracoronary Acetylcholine and Implications for Standard Protocols.


Journal

Journal of the American College of Cardiology
ISSN: 1558-3597
Titre abrégé: J Am Coll Cardiol
Pays: United States
ID NLM: 8301365

Informations de publication

Date de publication:
21 06 2022
Historique:
received: 04 03 2022
accepted: 29 03 2022
entrez: 16 6 2022
pubmed: 17 6 2022
medline: 22 6 2022
Statut: ppublish

Résumé

Heterogeneity in diagnostic criteria and provocation protocols has posed challenges in understanding the safety of coronary provocation testing with intracoronary acetylcholine (ACh) for the contemporary diagnosis of epicardial and microvascular spasm. We examined the safety of testing and subgroup differences in procedural risks based on ethnicity, diagnostic criteria, and provocation protocols. PubMed and Embase were searched in November 2021 to identify original articles reporting procedural complications associated with intracoronary ACh administration. The primary outcome was the pooled estimate of the incidence of major complications including death, myocardial infarction, ventricular tachycardia/fibrillation, and shock. A total of 16 studies with 12,585 patients were included in the meta-analysis. The overall pooled estimate of the incidence of major complications was 0.5% (95% CI: 0.0%-1.3%) without any reports of death. Exploratory subgroup analyses revealed that the pooled incidence of major complications was significantly higher in the studies that followed the contemporary diagnosis criteria for epicardial spasm defined as ≥90% diameter reduction (1.0%; 95% CI: 0.3%-2.0%) but significantly lower in Western populations (0.0%; 95% CI: 0.0%-0.45%). The rate of positive epicardial spasm and the incidence of major complications were similar between provocation protocols using the maximum ACh doses of 100 μg and 200 μg. Intracoronary ACh administration for the contemporary diagnosis of epicardial and microvascular spasm is a safe procedure. Moreover, excellent safety records are observed in Western populations primarily presenting with myocardial ischemia and/or infarction with nonobstructive coronary arteries. This study will help standardize ACh testing to improve clinical diagnosis and ensure procedural safety.

Sections du résumé

BACKGROUND
Heterogeneity in diagnostic criteria and provocation protocols has posed challenges in understanding the safety of coronary provocation testing with intracoronary acetylcholine (ACh) for the contemporary diagnosis of epicardial and microvascular spasm.
OBJECTIVES
We examined the safety of testing and subgroup differences in procedural risks based on ethnicity, diagnostic criteria, and provocation protocols.
METHODS
PubMed and Embase were searched in November 2021 to identify original articles reporting procedural complications associated with intracoronary ACh administration. The primary outcome was the pooled estimate of the incidence of major complications including death, myocardial infarction, ventricular tachycardia/fibrillation, and shock.
RESULTS
A total of 16 studies with 12,585 patients were included in the meta-analysis. The overall pooled estimate of the incidence of major complications was 0.5% (95% CI: 0.0%-1.3%) without any reports of death. Exploratory subgroup analyses revealed that the pooled incidence of major complications was significantly higher in the studies that followed the contemporary diagnosis criteria for epicardial spasm defined as ≥90% diameter reduction (1.0%; 95% CI: 0.3%-2.0%) but significantly lower in Western populations (0.0%; 95% CI: 0.0%-0.45%). The rate of positive epicardial spasm and the incidence of major complications were similar between provocation protocols using the maximum ACh doses of 100 μg and 200 μg.
CONCLUSIONS
Intracoronary ACh administration for the contemporary diagnosis of epicardial and microvascular spasm is a safe procedure. Moreover, excellent safety records are observed in Western populations primarily presenting with myocardial ischemia and/or infarction with nonobstructive coronary arteries. This study will help standardize ACh testing to improve clinical diagnosis and ensure procedural safety.

Identifiants

pubmed: 35710187
pii: S0735-1097(22)04822-7
doi: 10.1016/j.jacc.2022.03.385
pmc: PMC8972358
pii:
doi:

Substances chimiques

Acetylcholine N9YNS0M02X

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2367-2378

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 Dr Samuels has a consulting agreement with Abbott Vascular; and serves as a consultant and on the Speakers Bureau for Abbott Vascular and Philips. Dr Parikh has a consulting agreement with Abbott Vascular; and serves on the advisory boards of Abbott Vascular, Boston Scientific, and Medtronic. Dr Wei has a consulting agreement with and serves on the advisory board of Abbott Vascular. Drs Moses, Fearon, Henry, Tremmel, and Kobayashi have consulting agreements with Abbott Vascular. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Auteurs

Tatsunori Takahashi (T)

Department of Medicine, Jacobi Medical Center, Albert Einstein College of Medicine, Bronx, New York, USA.

Bruce A Samuels (BA)

Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California, USA.

Weijia Li (W)

Department of Medicine, Jacobi Medical Center, Albert Einstein College of Medicine, Bronx, New York, USA.

Manish A Parikh (MA)

Division of Cardiology, NewYork-Presbyterian Brooklyn Methodist Hospital, Weill Cornell Medicine, Brooklyn, New York, USA.

Janet Wei (J)

Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California, USA.

Jeffery W Moses (JW)

Department of Cardiology, Columbia University Medical Center, New York, New York, USA.

William F Fearon (WF)

Division of Cardiovascular Medicine, Stanford University Medical Center, Stanford, California, USA.

Timothy D Henry (TD)

The Carl and Edyth Lindner Center for Research and Education at The Christ Hospital, Cincinnati, Ohio, USA.

Jennifer A Tremmel (JA)

Division of Cardiovascular Medicine, Stanford University Medical Center, Stanford, California, USA.

Yuhei Kobayashi (Y)

Division of Cardiology, NewYork-Presbyterian Brooklyn Methodist Hospital, Weill Cornell Medicine, Brooklyn, New York, USA. Electronic address: dxl9003@med.cornell.edu.

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