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 |
|
||||
|
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 | |||||
|
overlap, such as recommending gluco- | Solidarity was an open-label, prag- | |||
|
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, | |||||
|
|||||
which differs from the IDSA and NIH |
|
||||
recommendations in some key areas [4]. | hydroxychloroquine, | ||||
Significant among these is a recommen- | co-formulated lopinavir-ritonavir, inter- | ||||
|
feron in combination with lopinavir- | ||||
|
|||||
The | NIH-sponsored | Adaptive | |||
COVID-19 Treatment Trial (ACTT) is | |||||
an ongoing, multicenter, international |
|
||||
|
|||||
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- | ||||
|
|||||
COVID-19 to receive remdesivir vs |
|
||||
placebo for up to 10 days, with time to | |||||
recovery as the primary endpoint [5]. | |||||
|
|||||
After monitoring 1063 participants for |
|
||||
28 days after enrollment, ACTT-1 re- | |||||
ported a reduction in the time to re- | |||||
|
|||||
covery with the use of remdesivir, from |
|
||||
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 |
|
|||
|
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 |
|
||||
|
|||||
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 | |
---|---|---|---|
|
|
||
|
|
||
|
10. Law AC, Stevens JP, Walkey AJ. National trends in |
|
|
|
|