Lower Mortality Risk Associated With Remdesivir plus Dexamethasone Versus Dexamethasone Alone for the Treatment of Patients Hospitalized for COVID-19

被引:5
|
作者
Mozaffari, Essy [1 ]
Chandak, Aastha [2 ]
Gottlieb, Robert L. [3 ,4 ,5 ,6 ]
Chima-Melton, Chidinma [7 ]
Berry, Mark [8 ]
Oppelt, Thomas [9 ]
Okulicz, Jason F. [1 ]
Amin, Alpesh N. [10 ]
Welte, Tobias [11 ]
Sax, Paul E. [12 ]
Kalil, Andre C. [13 ]
机构
[1] Gilead Sci, Global Med Affairs, Foster City, CA USA
[2] Certara, Evidence & Access, New York, NY USA
[3] Baylor Univ, Med Ctr, Dept Internal Med, Dallas, TX USA
[4] Baylor Scott & White Heart & Vasc Hosp, Dallas, TX USA
[5] Baylor Scott & White Heart Hosp, Plano, TX USA
[6] Baylor Scott & White Res Inst, Dallas, TX USA
[7] Tele ICU Inc, Los Angeles, CA USA
[8] Gilead Sci, Real World Evidence, Foster City, CA USA
[9] Gilead Sci, US Med Affairs, Foster City, CA USA
[10] Univ Calif Irvine, Div Hosp Med & Palliat Med, Dept Med, Irvine, CA USA
[11] Hannover Med Sch, Dept Pulmonol & Infect Dis, Hannover, Germany
[12] Harvard Med Sch, Brigham & Womens Hosp, Div Infect Dis, Boston, MA USA
[13] Univ Nebraska Med Ctr, Dept Internal Med, Div Infect Dis, 985400 Nebraska Med Ctr, Omaha, NE 68198 USA
关键词
COVID-19; guidelines; real-world data; mortality; propensity score matching; inverse probability of treatment weighting; data science; remdesivir;
D O I
10.1093/cid/ciae477
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Treatment guidelines were developed early in the pandemic when much about coronavirus disease 2019 (COVID-19) was unknown. Given the evolution of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), real-world data can provide clinicians with updated information. The objective of this analysis was to assess mortality risk in patients hospitalized for COVID-19 during the Omicron period receiving remdesivir + dexamethasone versus dexamethasone alone. Methods. A large, multicenter US hospital database was used to identify adult patients hospitalized with a primary discharge diagnosis of COVID-19 flagged as "present-on-admission" and treated with remdesivir + dexamethasone or dexamethasone alone between December 2021 and April 2023. Patients were matched using 1:1 propensity score matching and stratified by baseline oxygen requirements. Cox proportional hazards model was used to assess time to 14- and 28-day in-hospital all-cause mortality. Results. A total of 33 037 patients were matched, with most patients >= 65 years old (72%), White (78%), and non-Hispanic (84%). Remdesivir + dexamethasone was associated with lower mortality risk versus dexamethasone alone across all baseline oxygen requirements at 14-days (no supplemental oxygen charges: adjusted hazard ratio [95% confidence interval {CI}]: 0.79 [.72-.87], low flow oxygen: 0.70 [.64-.77], high flow oxygen/non-invasive ventilation: 0.69 [.62-.76], invasive mechanical ventilation/extracorporeal membrane oxygen (IMV/ECMO): 0.78 [.64-.94]), with similar results at 28-days. Conclusions. Remdesivir + dexamethasone was associated with a significant reduction in 14- and 28-day mortality compared to dexamethasone alone in patients hospitalized for COVID-19 across all levels of baseline respiratory support, including IMV/ECMO. However, the use of remdesivir + dexamethasone still has low clinical practice uptake. In addition, these data suggest a need to update the existing guidelines.
引用
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页数:9
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