The Weight of Evidence From Electrophysiology, Observational, and Cardiovascular End Point Studies Demonstrates the Safety of Azithromycin

Increased use of azithromycin (AZ) in treating infections associated with coronavirus disease 2019 (COVID‐19) and reports of increased incidence of prolonged corrected QT (QTc) interval associated with AZ used with hydroxychloroquine prompted us to review the latest evidence in the literature, prese...

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Main Authors: Jack Cook, Milton L. Pressler, Bharat Damle, Demissie Alemayehu, Charles A. Knirsch
Format: Article
Language:English
Published: Wiley 2021-01-01
Series:Clinical and Translational Science
Online Access:https://doi.org/10.1111/cts.12867
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spelling doaj-a614d481d60242c8bcf4c4c26c354a112021-02-11T20:06:35ZengWileyClinical and Translational Science1752-80541752-80622021-01-0114110611210.1111/cts.12867The Weight of Evidence From Electrophysiology, Observational, and Cardiovascular End Point Studies Demonstrates the Safety of AzithromycinJack Cook0Milton L. Pressler1Bharat Damle2Demissie Alemayehu3Charles A. Knirsch4Pfizer Global Research and Development Groton Connecticut USAPfizer Global Research and Development New York New York USAPfizer Global Research and Development New York New York USAPfizer Global Research and Development New York New York USAPfizer Global Research and Development New York New York USAIncreased use of azithromycin (AZ) in treating infections associated with coronavirus disease 2019 (COVID‐19) and reports of increased incidence of prolonged corrected QT (QTc) interval associated with AZ used with hydroxychloroquine prompted us to review the latest evidence in the literature, present additional analyses of human cardiovascular (CV) electrophysiology studies, and to describe sequential steps in research and development that were undertaken to characterize the benefit‐risk profile of AZ. Combined QTc findings from electrocardiograms taken during oral and i.v. pharmacokinetic‐pharmacodynamic studies of AZ suggest that clinically meaningful QTc prolongation is unlikely. Findings from several observational studies were heterogeneous and not as consistent as results from at least two large randomized controlled trials (RCTs). The QTc findings presented and observational data from studies with large numbers of events are not consistent with either a proarrhythmic action of AZ or an increase in frequency of CV deaths. Well‐powered RCTs do not suggest a presence of increased risk of CV or sudden cardiac death after short‐term or protracted periods of AZ usage, even in patients at higher risk from pre‐existing coronary disease.https://doi.org/10.1111/cts.12867
collection DOAJ
language English
format Article
sources DOAJ
author Jack Cook
Milton L. Pressler
Bharat Damle
Demissie Alemayehu
Charles A. Knirsch
spellingShingle Jack Cook
Milton L. Pressler
Bharat Damle
Demissie Alemayehu
Charles A. Knirsch
The Weight of Evidence From Electrophysiology, Observational, and Cardiovascular End Point Studies Demonstrates the Safety of Azithromycin
Clinical and Translational Science
author_facet Jack Cook
Milton L. Pressler
Bharat Damle
Demissie Alemayehu
Charles A. Knirsch
author_sort Jack Cook
title The Weight of Evidence From Electrophysiology, Observational, and Cardiovascular End Point Studies Demonstrates the Safety of Azithromycin
title_short The Weight of Evidence From Electrophysiology, Observational, and Cardiovascular End Point Studies Demonstrates the Safety of Azithromycin
title_full The Weight of Evidence From Electrophysiology, Observational, and Cardiovascular End Point Studies Demonstrates the Safety of Azithromycin
title_fullStr The Weight of Evidence From Electrophysiology, Observational, and Cardiovascular End Point Studies Demonstrates the Safety of Azithromycin
title_full_unstemmed The Weight of Evidence From Electrophysiology, Observational, and Cardiovascular End Point Studies Demonstrates the Safety of Azithromycin
title_sort weight of evidence from electrophysiology, observational, and cardiovascular end point studies demonstrates the safety of azithromycin
publisher Wiley
series Clinical and Translational Science
issn 1752-8054
1752-8062
publishDate 2021-01-01
description Increased use of azithromycin (AZ) in treating infections associated with coronavirus disease 2019 (COVID‐19) and reports of increased incidence of prolonged corrected QT (QTc) interval associated with AZ used with hydroxychloroquine prompted us to review the latest evidence in the literature, present additional analyses of human cardiovascular (CV) electrophysiology studies, and to describe sequential steps in research and development that were undertaken to characterize the benefit‐risk profile of AZ. Combined QTc findings from electrocardiograms taken during oral and i.v. pharmacokinetic‐pharmacodynamic studies of AZ suggest that clinically meaningful QTc prolongation is unlikely. Findings from several observational studies were heterogeneous and not as consistent as results from at least two large randomized controlled trials (RCTs). The QTc findings presented and observational data from studies with large numbers of events are not consistent with either a proarrhythmic action of AZ or an increase in frequency of CV deaths. Well‐powered RCTs do not suggest a presence of increased risk of CV or sudden cardiac death after short‐term or protracted periods of AZ usage, even in patients at higher risk from pre‐existing coronary disease.
url https://doi.org/10.1111/cts.12867
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