Association of Remdesivir Treatment With Mortality Among Hospitalized Adults With COVID-19 in the United States

被引:42
作者
Chokkalingam, Anand P. [1 ,2 ]
Hayden, Jennifer [3 ]
Goldman, Jason D. [4 ,5 ]
Li, Hu [1 ]
Asubonteng, Julius [1 ]
Mozaffari, Essy [6 ]
Bush, Christopher [3 ]
Wang, Jocelyn R. [3 ]
Kong, Amanda [3 ]
Osinusi, Anu O. [7 ]
Gottlieb, Robert L. [8 ,9 ,10 ,11 ]
机构
[1] Gilead Sci Inc, Real World Evidence, 353 Lakeside Dr, Foster City, CA 94404 USA
[2] Univ Calif Berkeley, Sch Publ Hlth, Div Epidemiol, Berkeley, CA 94720 USA
[3] Aetion Inc, New York, NY USA
[4] Providence St Joseph Hlth, Swedish Med Ctr, Swedish Ctr Res & Innovat, Seattle, WA USA
[5] Univ Washington, Div Allerg Infect & Dis, Seattle, WA 98195 USA
[6] Gilead Sci Inc, Med Affairs, 353 Lakeside Dr, Foster City, CA 94404 USA
[7] Gilead Sci Inc, Clin Dev, 353 Lakeside Dr, Foster City, CA 94404 USA
[8] Baylor Univ, Med Ctr, Dallas, TX USA
[9] Baylor Scott & White Heart & Vasc Hosp, Dallas, TX USA
[10] Baylor Scott & White Heart Hosp, Plano, TX USA
[11] Baylor Scott & White Res Inst, Dallas, TX USA
关键词
SURVIVAL ANALYSIS; RECOMMENDATIONS; MODEL;
D O I
10.1001/jamanetworkopen.2022.44505
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IMPORTANCE SARS-CoV-2, which causes COVID-19, poses considerable morbidity and mortality risks. Studies using data collected during routine clinical practice can supplement randomized clinical trials to provide needed evidence, especially during a global pandemic, and can yield markedly larger sample sizes to assess outcomes for important patient subgroups. OBJECTIVE To evaluate the association of remdesivir treatment with inpatient mortality among patients with COVID-19 outside of the clinical trial setting. DESIGN, SETTING, AND PARTICIPANTS A retrospective cohort study in US hospitals using health insurance claims data linked to hospital chargemaster data from December 1, 2018, to May 3, 2021, was conducted among 24 856 adults hospitalized between May 1, 2020. and May 3, 2021, with newly diagnosed COVID-19 who received remdesivir and 24 856 propensity score-matched control patients. EXPOSURE Remdesivir treatment. MAIN OUTCOMES AND MEASURES All-cause inpatient mortality within 28 days of the start of remdesivir treatment for the remdesivir-exposed group or the matched index date for the control group. RESULTS A total of 24 856 remdesivir-exposed patients (12 596 men [50.7%]; mean [SD] age, 66.8 [15.4] years) and 24 856 propensity score-matched control patients (12 621men [50.8%1 mean [SD] age, 66.8 [15.4] years) were included in the study. Median follow-up was 6 days (IQR, 4-11 days) in the remdesivir group and 5 days (IQR, 2-10 days) in the control group. There were 3557 mortality events (14.3%) in the remdesivir group and 3775 mortality events (15.2%) in the control group. The 28-day mortality rate was 0.5 per person-month in the remdesivir group and 0.6 per person-month in the control group. Remdesivir treatment was associated with a statistically significant 17% reduction in inpatient mortality among patients hospitalized with COVID-19 compared with propensity score-matched control patients (hazard ratio, 0.83 [95% CI, 0.79-0.87]). CONCLUSIONS AND RELEVANCE In this retrospective cohort study using health insurance claims and hospital chargemaster data, remdesivir treatment was associated with a significantly reduced inpatient mortality overall among patients hospitalized with COVID-19. Results of this analysis using data collected during routine clinical practice and state-of-the-art methods complement results from randomized clinical trials. Future areas of research include assessing the association of remdesivir treatment with inpatient mortality during the circulation of different variants and relative to time from symptom onset.
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页数:12
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