瑞德西韦联合地塞米松与单独地塞米松治疗需要补充氧气治疗的冠状病毒病2019 (COVID-19)患者:一项前瞻性对照非随机研究

Aldo Marrone, Riccardo Nevola, Ausilia Sellitto, Domenico Cozzolino, Ciro Romano, Giovanna Cuomo, Concetta Aprea, Michelangelo X Palou Schwartzbaum, Carmen Ricozzi, Simona Imbriani, Luca Rinaldi, Klodian Gjeloshi, Andrea Padula, Roberta Ranieri, Carolina Ruosi, Luciana Agnese Meo, Marianna Abitabile, Francesca Cinone, Caterina Carusone, Luigi Elio Adinolfi
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引用次数: 20

摘要

背景:瑞德西韦是一种用于治疗冠状病毒病2019 (COVID-19)的抗病毒药物,可以改善一些临床结果。地塞米松已被证明在降低死亡率方面有效。据推测,这两种药物联合使用可以提高死亡率。我们评估了联合用药对需要氧气治疗的COVID-19患者死亡率的影响。方法:设计前瞻性准实验研究,包括两个独立的序贯对照队列,一组接受瑞地西韦-地塞米松治疗,另一组单独接受地塞米松治疗。所有需要补充氧气治疗的COVID-19患者均连续入组。死亡率幂的样本量是先验计算的。主要终点是30天死亡率和病毒清除率差异。次要终点是住院时间、呼吸衰竭改善(PO2/FiO2)和炎症指标(纤维蛋白原、CRP、中性粒细胞/淋巴细胞比值、d -二聚体)的差异。Kaplan-Meier曲线和log-rank检验用于评估组间死亡率的显著差异。结果:共纳入151例COVID-19患者(瑞德西韦/地塞米松组76例,单用地塞米松组75例)。在基线时,两组在人口学、临床和实验室特征上没有观察到差异。与单独使用地塞米松相比,瑞德西韦/地塞米松组的病毒清除速度更快(中位6天vs 16天;结论:与单独使用地塞米松相比,瑞德西韦/地塞米松治疗可显著降低死亡率、住院时间和更快地清除SARS-CoV-2。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Remdesivir Plus Dexamethasone Versus Dexamethasone Alone for the Treatment of Coronavirus Disease 2019 (COVID-19) Patients Requiring Supplemental O2 Therapy: A Prospective Controlled Nonrandomized Study.

Background: Remdesivir is an antiviral used to treat coronavirus disease 2019 (COVID-19), which improves some clinical outcomes. Dexamethasone has been shown to be effective in reducing mortality. It has been hypothesized that combination of these two drugs can improve mortality. We evaluated the effect of combination on mortality of COVID-19 patients requiring O2 therapy.

Methods: A prospective quasi-experimental study, including two independent, sequential controlled cohorts, one received remdesivir-dexamethasone and the other dexamethasone alone, was designed. All COVID-19 patients requiring supplemental O2 therapy were enrolled consecutively. The sample size to power mortality was a priori calculated. The primary endpoints were 30-day mortality and viral clearance differences. Secondary endpoints were differences in hospitalization times, improvement in respiratory failure (PO2/FiO2) and inflammatory indices (fibrinogen, CRP, neutrophil/lymphocyte ratio, D-Dimer). Kaplan-Meier curves and the log-rank test were used to evaluate significant differences in mortality between groups.

Results: In total, 151 COVID-19 patients were enrolled (remdesivir/dexamethasone group, 76, and dexamethasone alone, 75). No differences in demographic, clinical, and laboratory characteristics were observed between the 2 groups at baseline. Faster viral clearance occurred in the remdesivir/dexamethasone group compared to dexamethasone alone (median 6 vs 16 days; P < .001). The 30-day mortality in the remdesivir/dexamethasone group was 1.3%, whereas in dexamethasone alone was 16% (P < .005). In the remdesivir/dexamethasone group compared to dexamethasone alone there was a reduction in hospitalization days (P < .0001) and a faster improvement in both respiratory function and inflammatory markers.

Conclusions: Remdesivir/dexamethasone treatment is associated with significant reduction in mortality, length of hospitalization, and faster SARS-CoV-2 clearance, compared to dexamethasone alone.

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