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Safety of hydroxychloroquine, alone and in combination with azithromycin, in light of rapid wide-spread use for COVID-19: a multinational, network cohort and self-controlled case series study

Authors :
A Prats Uribe
Sergio Fernandez-Bertolin
Lin Zhang
Sarah Seager
Peter R. Rijnbeek
Oleg Zhuk
Azza Shoaibi
Daniel R. Morales
Edward Burn
Anthony G. Sena
J van der Lei
T Duarte-Salles
Michael E. Matheny
Abrahao
Sajan Khosla
M. de Wilde
Seamus Kent
Sathappan Smk.
Paras P. Mehta
R Gowtham
Jill Hardin
Martijn J. Schuemie
Jenna Reps
Spyros Kolovos
Aedín C. Culhane
H Morgan-Stewart
Fredrik Nyberg
Thamir M. Alshammari
Kristine E. Lynch
Patricia Biedermann
Danielle Newby
Kristina Fišter
Rupa Makadia
Andrea V. Margulis
Seng Chan You
Osaid Alser
Laura Hester
George Hripcsak
A Londhe
Rae Woong Park
Christophe G. Lambert
Heba Alghoul
J Weaves
Matthew E. Spotnitz
Jennifer C E Lane
Haini Wen
C Torre
D Prieto Alhambra
David Vizcaya
Joel N. Swerdel
Mitchell M. Conover
A Daydov
Marc A. Suchard
Anna Ostropolets
Paula Casajust
Dmitry Dymshyts
Christian G. Reich
Scott L. DuVall
Kristin Kostka
M Mossveld
Patrick B. Ryan
consortium, OHDSI-COVID-19
Source :
medRxiv
Publication Year :
2020
Publisher :
Cold Spring Harbor Laboratory, 2020.

Abstract

BackgroundHydroxychloroquine has recently received Emergency Use Authorization by the FDA and is currently prescribed in combination with azithromycin for COVID-19 pneumonia. We studied the safety of hydroxychloroquine, alone and in combination with azithromycin.MethodsNew user cohort studies were conducted including 16 severe adverse events (SAEs). Rheumatoid arthritis patients aged 18+ and initiating hydroxychloroquine were compared to those initiating sulfasalazine and followed up over 30 days. Self-controlled case series (SCCS) were conducted to further establish safety in wider populations. Separately, SAEs associated with hydroxychloroquine- azithromycin (compared to hydroxychloroquine-amoxicillin) were studied. Data comprised 14 sources of claims data or electronic medical records from Germany, Japan, Netherlands, Spain, UK, and USA. Propensity score stratification and calibration using negative control outcomes were used to address confounding. Cox models were fitted to estimate calibrated hazard ratios (CalHRs) according to drug use. Estimates were pooled where I2ResultsOverall, 956,374 and 310,350 users of hydroxychloroquine and sulfasalazine, and 323,122 and 351,956 users of hydroxychloroquine-azithromycin and hydroxychloroquine-amoxicillin were included. No excess risk of SAEs was identified when 30-day hydroxychloroquine and sulfasalazine use were compared. SCCS confirmed these findings. However, when azithromycin was added to hydroxychloroquine, we observed an increased risk of 30-day cardiovascular mortality (CalHR2.19 [1.22- 3.94]), chest pain/angina (CalHR 1.15 [95% CI 1.05-1.26]), and heart failure (CalHR 1.22 [95% CI 1.02- 1.45])ConclusionsShort-term hydroxychloroquine treatment is safe, but addition of azithromycin may induce heart failure and cardiovascular mortality, potentially due to synergistic effects on QT length. We call for caution if such combination is to be used in the management of Covid-19.Trial registration numberRegistered with EU PAS; Reference number EUPAS34497 (http://www.encepp.eu/encepp/viewResource.htm?id=34498). The full study protocol and analysis source code can be found at https://github.com/ohdsi-studies/Covid19EstimationHydroxychloroquine.Funding sourcesThis research received partial support from the National Institute for Health Research (NIHR) Oxford Biomedical Research Centre (BRC) and Senior Research Fellowship (DPA), US National Institutes of Health, Janssen Research & Development, IQVIA, and by a grant from the Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI), funded by the Ministry of Health & Welfare, Republic of Korea [grant number: HI16C0992]. Personal funding included Versus Arthritis [21605] (JL), MRC-DTP [MR/K501256/1] (JL), MRC and FAME (APU). The European Health Data & Evidence Network has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 806968. The JU receives support from the European Union’s Horizon 2020 research and innovation programme and EFPIA. No funders had a direct role in this study. The views and opinions expressed are those of the authors and do not necessarily reflect those of the Clinician Scientist Award programme, NIHR, NHS or the Department of Health, England.

Details

Database :
OpenAIRE
Journal :
medRxiv
Accession number :
edsair.doi.dedup.....4f684079ea0ee1943e9d4b828f862cb8