Early Use of Ibuprofen in Moderate Cases of COVID-19 Might be a Promising Agent to Attenuate the Severity of Disease: A Randomized Controlled Trial

A. Sobhy, Lobna A Saleh, Marwa Abdelatty, S. Refaat, M. Kamal
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引用次数: 1

Abstract

Critically ill COVID-19 patients undergoing cytokine storm are believed to have a worse prognosis and increased fatality rate. Ibuprofen is a non-steroidal anti-inflammatory drug (NSAIDs) that might prove beneficial for the early management of COVID-19 due to its immunomodulatory effects. This study aimed to assess the efficacy and safety of the early use of ibuprofen to attenuate the severity of the course of COVID-19 and improve outcomes in patients diagnosed with a moderate case of COVID-19 disease. This randomized, double-blinded prospective study was conducted from January, 2022 to May, 2022, which included a total sample size of 180 patients with moderate cases of COVID-19. The number of patients transferred to intensive care was used as a primary outcome with a proposed large effect size (0.8), alfa =0.05, and power=0.80, so 90 cases were included in each group. Secondary outcomes were inflammatory markers: C-Reactive Protein (CRP), serum ferritin, and interleukin-6 (IL-6), duration of hospital stay, and need for ICU admission. One hundred eighty patients with moderate case of COVID-19 disease were divided in a 1: 1 ratio to receive ibuprofen (IG) or paracetamol (CG). The average age of the included patients was almost 41 years. Statistically significant differences were reported between both groups in terms of improvement in cough symptoms and lymphopenia in IG compared to CG (p= 0.034 and p= 0.044, respectively). Regarding secondary outcomes, statistically, significant differences were reported between the study’s groups in terms of the mean number of patients transferred to the ICU in IG compared to the CG (p =0.0.047) and duration of hospitalization (p =0.013), with no significant differences (p > 0.9999) in the occurrence of side effects. Concerning the follow-up of the cytokine storm marker, there was a statistically significant reduction in serum cytokine marker compared to the baseline value (P < 0.05) in the same group. No statistically significant differences were observed when comparing both groups together in terms of serum ferritin level (p =0.570), serum IL-6 level (p =0.580), and CRP level (p =0.401). It can be concluded that early use of ibuprofen as adjuvant therapy in COVID-19 management is effective and safe to attenuate the severity of diseases and improve outcomes. Project manager for the Pan African Clinical Trial Registry PACTR202202880140319. Registered 9th February, 2022 - Retrospectively registered, (https://pactr.samrc.ac.za/)
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在中度COVID-19病例中早期使用布洛芬可能是一种有希望减轻疾病严重程度的药物:一项随机对照试验
新冠肺炎危重患者在经历细胞因子风暴后,预后更差,死亡率更高。布洛芬是一种非甾体抗炎药,由于其免疫调节作用,可能对COVID-19的早期治疗有益。本研究旨在评估早期使用布洛芬减轻COVID-19病程严重程度和改善诊断为中度COVID-19疾病患者预后的有效性和安全性。这项随机双盲前瞻性研究于2022年1月至2022年5月进行,总样本量为180例中度COVID-19患者。转入重症监护的患者数量作为主要结局,提出了大效应量(0.8),alpha =0.05, power=0.80,因此每组纳入90例。次要结局是炎症标志物:c -反应蛋白(CRP)、血清铁蛋白和白细胞介素-6 (IL-6)、住院时间和是否需要进入ICU。180例中度COVID-19病例按1:1的比例分成两组,分别服用布洛芬(IG)或扑热息痛(CG)。纳入患者的平均年龄几乎为41岁。IG组与CG组相比,在咳嗽症状改善和淋巴细胞减少方面,两组的差异有统计学意义(p= 0.034和p= 0.044)。次要结局方面,IG组转入ICU的平均患者数与CG组比较,差异有统计学意义(p =0.0.047),住院时间差异有统计学意义(p =0.013),副作用发生差异无统计学意义(p > 0.9999)。在细胞因子风暴标志物随访中,同组患者血清细胞因子标志物较基线值降低有统计学意义(P < 0.05)。两组患者血清铁蛋白水平(p =0.570)、血清IL-6水平(p =0.580)、CRP水平(p =0.401)比较,差异均无统计学意义。由此可见,早期使用布洛芬辅助治疗COVID-19是有效和安全的,可以减轻疾病严重程度,改善预后。泛非临床试验注册中心PACTR202202880140319项目经理。2022年2月9日注册-追溯注册,(https://pactr.samrc.ac.za/)
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