Exercise and pharmacologic stress-induced interlead T-wave heterogeneity analysis to detect clinically significant coronary artery stenosis.


Journal

International journal of cardiology
ISSN: 1874-1754
Titre abrégé: Int J Cardiol
Pays: Netherlands
ID NLM: 8200291

Informations de publication

Date de publication:
01 01 2020
Historique:
received: 18 06 2019
revised: 08 07 2019
accepted: 22 07 2019
pubmed: 16 8 2019
medline: 24 11 2020
entrez: 16 8 2019
Statut: ppublish

Résumé

Despite widespread use of ETT and vasodilator-stress with myocardial perfusion imaging (MPI) for noninvasive detection of flow-limiting coronary artery disease, there is continued need to improve diagnostic accuracy. We examined whether measurement of interlead T-wave heterogeneity (TWH) during exercise tolerance testing (ETT) or pharmacologic stress testing improves detection of stenoses in large epicardial coronary arteries. All 137 patients at our institution who underwent diagnostic coronary angiography within 0 to 5 days after ETT (N = 81) or dipyridamole IV infusion (N = 58) in 2016 were studied, including 2 patients with both tests. Cases (N = 93) had angiographically significant stenosis (≥50% of left main or ≥ 70% of an epicardial coronary artery ≥2 mm in diameter); controls (N = 44) did not. TWH, i.e., interlead splay of T waves, was determined by second central moment analysis from precordial leads by an investigator blinded to angiographic results. At rest, TWH levels were similar for cases and controls. ETT and dipyridamole stress testing increased TWH by 69% (p < 0.0001) and 27% (p < 0.0001), respectively, in cases. In controls, TWH did not change. Areas under the ROC curves for TWH increase for any flow-limiting coronary artery stenosis were 0.737 (p < 0.0001) for ETT and 0.818 (p < 0.0001) for dipyridamole stress testing. By contrast, neither ST-segment changes during ETT (p = 0.12) nor MPI during dipyridamole stress testing (p = 0.60) discriminated cases from controls. TWH measurement is a novel method that improves detection of angiographically confirmed flow-limiting stenoses in large epicardial coronary arteries during both ETT and MPI during pharmacologic stress testing with dipyridamole.

Sections du résumé

BACKGROUND
Despite widespread use of ETT and vasodilator-stress with myocardial perfusion imaging (MPI) for noninvasive detection of flow-limiting coronary artery disease, there is continued need to improve diagnostic accuracy. We examined whether measurement of interlead T-wave heterogeneity (TWH) during exercise tolerance testing (ETT) or pharmacologic stress testing improves detection of stenoses in large epicardial coronary arteries.
METHODS
All 137 patients at our institution who underwent diagnostic coronary angiography within 0 to 5 days after ETT (N = 81) or dipyridamole IV infusion (N = 58) in 2016 were studied, including 2 patients with both tests. Cases (N = 93) had angiographically significant stenosis (≥50% of left main or ≥ 70% of an epicardial coronary artery ≥2 mm in diameter); controls (N = 44) did not. TWH, i.e., interlead splay of T waves, was determined by second central moment analysis from precordial leads by an investigator blinded to angiographic results.
RESULTS
At rest, TWH levels were similar for cases and controls. ETT and dipyridamole stress testing increased TWH by 69% (p < 0.0001) and 27% (p < 0.0001), respectively, in cases. In controls, TWH did not change. Areas under the ROC curves for TWH increase for any flow-limiting coronary artery stenosis were 0.737 (p < 0.0001) for ETT and 0.818 (p < 0.0001) for dipyridamole stress testing. By contrast, neither ST-segment changes during ETT (p = 0.12) nor MPI during dipyridamole stress testing (p = 0.60) discriminated cases from controls.
CONCLUSIONS
TWH measurement is a novel method that improves detection of angiographically confirmed flow-limiting stenoses in large epicardial coronary arteries during both ETT and MPI during pharmacologic stress testing with dipyridamole.

Identifiants

pubmed: 31412992
pii: S0167-5273(19)33137-7
doi: 10.1016/j.ijcard.2019.07.066
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

32-38

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Anderson C Silva (AC)

Beth Israel Deaconess Medical Center, Department of Medicine, Division of Cardiovascular Medicine, Boston, MA, United States of America; Harvard School of Public Health, Department of Environmental Sciences, Boston, MA, United States of America; Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.

Victor Z de Antonio (VZ)

Beth Israel Deaconess Medical Center, Department of Medicine, Division of Cardiovascular Medicine, Boston, MA, United States of America; Harvard School of Public Health, Department of Environmental Sciences, Boston, MA, United States of America; Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.

Jakub Sroubek (J)

Beth Israel Deaconess Medical Center, Department of Medicine, Division of Cardiovascular Medicine, Boston, MA, United States of America; Harvard Medical School, Department of Medicine, Boston, MA, United States of America.

Ernest Gervino (E)

Beth Israel Deaconess Medical Center, Department of Medicine, Division of Cardiovascular Medicine, Boston, MA, United States of America; Harvard Medical School, Department of Medicine, Boston, MA, United States of America.

Kalon Ho (K)

Beth Israel Deaconess Medical Center, Department of Medicine, Division of Cardiovascular Medicine, Boston, MA, United States of America; Harvard Medical School, Department of Medicine, Boston, MA, United States of America.

Sofia A Medeiros (SA)

Beth Israel Deaconess Medical Center, Department of Medicine, Division of Cardiovascular Medicine, Boston, MA, United States of America; Harvard School of Public Health, Department of Environmental Sciences, Boston, MA, United States of America; Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.

Fernanda Tessarolo Silva (FT)

Beth Israel Deaconess Medical Center, Department of Medicine, Division of Cardiovascular Medicine, Boston, MA, United States of America; Harvard School of Public Health, Department of Environmental Sciences, Boston, MA, United States of America; Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.

Giovanna C Pedreira (GC)

Beth Israel Deaconess Medical Center, Department of Medicine, Division of Cardiovascular Medicine, Boston, MA, United States of America; Harvard School of Public Health, Department of Environmental Sciences, Boston, MA, United States of America; Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.

Fernando G Stocco (FG)

Beth Israel Deaconess Medical Center, Department of Medicine, Division of Cardiovascular Medicine, Boston, MA, United States of America; Harvard School of Public Health, Department of Environmental Sciences, Boston, MA, United States of America; Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.

Bruce D Nearing (BD)

Beth Israel Deaconess Medical Center, Department of Medicine, Division of Cardiovascular Medicine, Boston, MA, United States of America; Harvard Medical School, Department of Medicine, Boston, MA, United States of America.

Richard L Verrier (RL)

Beth Israel Deaconess Medical Center, Department of Medicine, Division of Cardiovascular Medicine, Boston, MA, United States of America; Harvard School of Public Health, Department of Environmental Sciences, Boston, MA, United States of America; Harvard Medical School, Department of Medicine, Boston, MA, United States of America. Electronic address: rverrier@bidmc.harvard.edu.

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