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Maves infectious diseases and critical care medicine services

1Infectious Diseases and Critical Care Medicine Services, Naval Medical Center, San Diego, California, USA, and 2Department of Medicine, Uniformed Services University, Bethesda, Maryland,

USA

[1]. The National Institutes of Health
(NIH) and Infectious Diseases Society of

corporation of remdesivir into the IDSA

in the mind at the same time, and

America (IDSA) have produced guide- and NIH guidelines. More recently, how-
lines that differ in some areas of emphasis
but are in agreement in most areas of

Crack-Up,” February 1936

overlap, such as recommending gluco- Solidarity was an open-label, prag-

The coronavirus disease 2019 (COVID-

corticoids and remdesivir for the treat-
ment of severe disease [2, 3]. The World
Health Organization (WHO) has pro-
duced its own living guideline document,

19) pandemic is the defining event of our

which differs from the IDSA and NIH

were randomized to receive remde sivir,

recommendations in some key areas [4]. hydroxychloroquine,
Significant among these is a recommen- co-formulated lopinavir-ritonavir, inter-

dation against the use of remdesivir.

feron in combination with lopinavir-

to help us make decisions regarding the

The NIH-sponsored Adaptive
COVID-19 Treatment Trial (ACTT) is
an ongoing, multicenter, international

in-hospital mortality, with initiation of

has improved since those first desperate

trial of COVID-19 therapeutics. The first
iteration of ACTT, known as ACTT-1,
randomized hospitalized patients with At the conclusion of the study, death oc-

research.

COVID-19 to receive remdesivir vs

curred in 301 of 2743 (12.5%) patients

placebo for up to 10 days, with time to
recovery as the primary endpoint [5].

COVID-19. The first, the Surviving

After monitoring 1063 participants for

the results of ACTT-1, patients receiving

28 days after enrollment, ACTT-1 re-
ported a reduction in the time to re-

core critical care interventions such as

covery with the use of remdesivir, from

patients (59%).

15 days with placebo to 10 days with
remdesivir. Mortality was lower with
remdesivir in ACTT-1 but did not meet
Received 30 December 2020; editorial decision 3 January statistical significance. This benefit of

IDSA and NIH guidelines vs the WHO

2021; published online 25 January 2021.

remdesivir was most marked in patients guidelines. I suggest that we should con-
Correspondence: R. C. Maves, Naval Medical Center, 34800 Bob
with hypoxemia requiring only low-flow sider not whether one trial or one guide-
supplemental oxygen (<15 L/minute),
whereas patients requiring mechanical

be true. The answer lies in the different

Society of America 2021. This work is written by (a) US

ventilation did not show any meaningful information obtained from homoge-

EDITORIAL COMMENTARY • cid 2021:XX (XX XXXX) • 1

7. Landoni G, Comis M, Conte M, et al. Mortality in 9. Andrews B, Semler MW, Muchemwa L, et al. Effect

multicenter critical care trials: an analysis of interven-

of an early resuscitation protocol on in-hospital

43:1559–68.

tension: a randomized clinical trial. JAMA 2017;

Group. Mortality after fluid bolus in African chil-

10. Law AC, Stevens JP, Walkey AJ. National trends in

lation for severe COVID-19: a randomized phase

1994-2014. Crit Care Med 2019; 47:1493–6.

196:359–66.

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