Leegwater Emiel, Dol Lisa, Benard Menno R, Roelofsen Eveline E, Delfos Nathalie M, van der Feltz Machteld, Mollema Femke P N, Bosma Liesbeth B E, Visser Loes E, Ottens Thomas H, van Burgel Nathalie D, Arbous Sesmu M, El Bouazzaoui Lahssan H, Knevel Rachel, Groenwold Rolf H H, de Boer Mark G J, Visser Leo G, Rosendaal Frits R, Wilms Erik B, van Nieuwkoop Cees
Department of Hospital Pharmacy, Haga Teaching Hospital, Els Borst-Eilersplein 275, 2545 AA, The Hague, The Netherlands.
Apotheek Haagse Ziekenhuizen, The Hague, The Netherlands.
Infect Dis Ther. 2023 Oct;12(10):2471-2484. doi: 10.1007/s40121-023-00874-2. Epub 2023 Oct 6.
Remdesivir is a registered treatment for hospitalised patients with COVID-19 that has moderate clinical effectiveness. Anecdotally, some patients' respiratory insufficiency seemed to recover particularly rapidly after initiation of remdesivir. In this study, we investigated if this rapid improvement was caused by remdesivir, and which patient characteristics might predict a rapid clinical improvement in response to remdesivir.
This was a multicentre observational cohort study of hospitalised patients with COVID-19 who required supplemental oxygen and were treated with dexamethasone. Rapid clinical improvement in response to treatment was defined by a reduction of at least 1 L of supplemental oxygen per minute or discharge from the hospital within 72 h after admission. Inverse probability of treatment-weighted logistic regression modelling was used to assess the association between remdesivir and rapid clinical improvement. Secondary endpoints included in-hospital mortality, ICU admission rate and hospitalisation duration.
Of 871 patients included, 445 were treated with remdesivir. There was no influence of remdesivir on the occurrence of rapid clinical improvement (62% vs 61% OR 1.05, 95% CI 0.79-1.40; p = 0.76). The in-hospital mortality was lower (14.7% vs 19.8% OR 0.70, 95% CI 0.48-1.02; p = 0.06) for the remdesivir-treated patients. Rapid clinical improvement occurred more often in patients with low C-reactive protein (≤ 75 mg/L) and short duration of symptoms prior to hospitalisation (< 7 days) (OR 2.84, 95% CI 1.07-7.56).
Remdesivir generally does not increase the incidence of rapid clinical improvement in hospitalised patients with COVID-19, but it might have an effect in patients with short duration of symptoms and limited signs of systemic inflammation.
瑞德西韦是一种已注册用于治疗住院COVID-19患者的药物,具有中等临床疗效。据传闻,一些患者在开始使用瑞德西韦后呼吸功能不全似乎恢复得特别快。在本研究中,我们调查了这种快速改善是否由瑞德西韦引起,以及哪些患者特征可能预测对瑞德西韦治疗有快速临床改善。
这是一项针对需要补充氧气并接受地塞米松治疗的住院COVID-19患者的多中心观察性队列研究。对治疗的快速临床改善定义为入院后72小时内每分钟补充氧气量减少至少1升或出院。采用治疗加权逆概率逻辑回归模型评估瑞德西韦与快速临床改善之间的关联。次要终点包括住院死亡率、入住ICU率和住院时间。
在纳入的871例患者中,445例接受了瑞德西韦治疗。瑞德西韦对快速临床改善的发生率没有影响(62%对61%,OR 1.05,95%CI 0.79-1.40;p = 0.76)。接受瑞德西韦治疗的患者住院死亡率较低(14.7%对19.8%,OR 0.70,95%CI 0.48-1.02;p = 0.06)。C反应蛋白水平低(≤75mg/L)且住院前症状持续时间短(<7天)的患者更常出现快速临床改善(OR 2.84,95%CI 1.07-7.56)。
瑞德西韦一般不会增加住院COVID-19患者快速临床改善的发生率,但可能对症状持续时间短且全身炎症迹象有限的患者有效果。