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Swinging the pendulum: lessons learned from public discourse concerning hydroxychloroquine and COVID-19

  • Sebastian E. Sattui
    ,
  • Jean W. Liew
    ,
  • Elizabeth R. Graef
    ,
  • Ariella Coler-Reilly
    ,
  • Francis Berenbaum
    ,
  • Alí Duarte-García
*Corresponding author for this work
  • Hospital for Special Surgery - New York
    ,
  • University of Washington
    ,
  • Harvard Medical School
    ,
  • Washington University School of Medicine in St. Louis
    ,
  • Sorbonne Université
    ,
  • Mayo Clinic
Research Output:
Contribution to journal
Article
Peer-review

Open access

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Journal (Volume, Issue Number)

Expert Review of Clinical Immunology

Publication milestones

  • Published - 2020

Publication status

Published - 2020

ISSN

1744-666X

Publication IDs

  • Scopus: 85087739693
  • PubMed: 32620062

Abstract

Introduction: Several months into the COVID-19 pandemic, safe and effective treatments against this global health disaster have yet to be identified. Clinical research trials around the world are underway testing a wide array of possible medications. In particular, the off-label use of hydroxychloroquine for COVID-19 prophylaxis and treatment has created many unprecedented challenges for the scientific community and the public. Areas covered: We critically assessed major events from February - May 2020 that contributed to widespread use of hydroxychloroquine for the treatment and prophylaxis of COVID-19. We aimed to explore how opinions towards hydroxychloroquine may shift from early enthusiasm (based on in vitro and preliminary clinical data) to the hope for a miracle cure (through communication and promotion of questionable results) and, finally, to a rise of skepticism as more in-depth analyses are emerging. Expert opinion: Mindful and rigorous acquisition of data, as well as its interpretation, are essential to an effective pandemic response. The rapid and premature promotion of results has had major implications for global crisis management, even creating distrust among the public. It is crucial for the medical and scientific community to incorporate the lessons learned from this situation.

Funding Details

S Sattui is supported by the Vasculitis Clinical Research Consortium (VCRC)/Vasculitis Foundation Fellowship. The VCRC is part of the Rare Diseases Clinical Research Network, an initiative of the Office of Rare Diseases Research, National Center for Advancing Translational Science (NCATS). The VCRC is funded through collaboration between NCATS and the National Institute of Arthritis and Musculoskeletal and Skin Diseases (U54 AR057319). No conflicts of interest or competing interests, and no funding relevant to this manuscript. J Liew is supported by a grant from the NIH/NIAMS outside of the submitted work. No conflicts of interest or competing interests relevant to this manuscript. F Berenbaum reports personal fees from Boehringer, Bone Therapeutics, Expanscience, Galapagos, Gilead, GSK, Merck Sereno, MSD, Nordic, Novartis, Pfizer, Regulaxis, Roche, Sandoz, Sanofi, Servier, UCB, Peptinov, TRB Chemedica, and 4P Pharma outside of the submitted work. No funding relevant to this manuscript. M Ugarte-Gil is supported by grants from Pfizer and Janssen outside of the submitted work. No conflicts of interest or competing interests, and no funding relevant to this manuscript. M Konig is supported by NIH/NIAMS T32AR048522, and received personal fees from Bristol-Myers Squibb and Celltrion, unrelated to the submitted work. No conflicts of interest or competing interests. P Korsten reports personal fees from GlaxoSmithKline, Sanofi-Aventis, Pfizer, AbbVie, Novartis Pharma, Lilly, and Bristol-Myers Squibb outside of the submitted work. No funding relevant to this manuscript. M Putman is supported by the Rheumatology Research Foundation outside of the submitted work. No conflicts of interest or competing interests. P Robinson reports personal fees from Abbvie, Eli Lilly, Janssen, Novartis, Pfizer, Roche and UCB and research grant funding from Janssen, Novartis and UCB all outside of this work. A Kim is supported by grants from NIH/NIAMS, Rheumatology Research Foundation, and GlaxoSmithKline as well as personal fees from Exagen Diagnostics, Inc. and GlaxoSmithKline outside of the submitted work. J Sparks is supported by grants from NIH/NIAID/Autoimmune Centers of Excellence, Rheumatology Research Foundation, the Brigham Research Institute, and the R. Bruce and Joan M. Mickey Research Scholar Fund as well as personal fees from Bristol-Myers Squibb, Gilead, Inova, Janssen, and Optum outside of the submitted work. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.
FundersFunding numbers
Autoimmune Centers of Excellence
-
NIH
-
NIAID
-
NIAMS
U54 AR057319, T32AR048522, K23AR069688
Pfizer
-
GSK
-
Novartis
-
Gilead Sciences
-
NCATS
-
RRF
-
VF
-
BRI
-
Janssen Pharmaceuticals
-
UCB
-
VCRC
-

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