Department of Traumatology and Acute Critical Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
Department of Respiratory Medicine and Clinical Immunology, Graduate School of Medicine, Osaka University, 2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.
J Infect Chemother. 2022 Apr;28(4):548-553. doi: 10.1016/j.jiac.2021.12.024. Epub 2021 Dec 31.
COVID-19 patients have been reported to have digestive symptoms with poor outcome. Ivermectin, an antiparasitic drug, has been used in COVID-19 patients. The objective of this study was to evaluate whether ivermectin has effects on gastrointestinal complications and ventilator-free days in ventilated patients with COVID-19.
COVID-19 patients who were mechanically ventilated in the ICU were included in this study. The ventilated patients who received ivermectin within 3 days after admission were assigned to the Ivermectin group, and the others were assigned to the Control group. Patients in the Ivermectin group received ivermectin 200 μg/kg via nasal tube. The incidence of gastrointestinal complications and ventilator-free days within 4 weeks from admission were evaluated as clinical outcomes using a propensity score with the inverse probability weighting method.
We included 88 patients in this study, of whom 39 patients were classified into the Ivermectin group, and 49 patients were classified into the Control group. The hazard ratio for gastrointestinal complications in the Ivermectin group as compared with the Control group was 0.221 (95% confidence interval [CI], 0.057 to 0.855; p = 0.029) in a Cox proportional-hazard regression model. The odds ratio for ventilator-free days as compared with the Control group was 1.920 (95% CI, 1.076 to 3.425; p = 0.027) in a proportional odds logistic regression model.
Ivermectin improved gastrointestinal complications and the number of ventilator-free days in severe COVID-19 patients undergoing mechanical ventilation. Prevention of gastrointestinal symptoms by SARS-Cov-2 might be associated with COVID-19 outcome.
有报道称 COVID-19 患者有消化系统症状且预后不良。伊维菌素是一种抗寄生虫药物,已在 COVID-19 患者中使用。本研究的目的是评估伊维菌素对 COVID-19 机械通气患者的胃肠道并发症和无呼吸机天数的影响。
本研究纳入了在 ICU 接受机械通气的 COVID-19 患者。在入院后 3 天内接受伊维菌素治疗的机械通气患者被分配到伊维菌素组,其余患者被分配到对照组。伊维菌素组患者通过鼻饲管给予伊维菌素 200μg/kg。采用逆概率加权法进行倾向评分,评估入院后 4 周内胃肠道并发症和无呼吸机天数的发生率作为临床结局。
本研究共纳入 88 例患者,其中 39 例患者被分为伊维菌素组,49 例患者被分为对照组。在 Cox 比例风险回归模型中,伊维菌素组与对照组相比,胃肠道并发症的风险比为 0.221(95%可信区间,0.057 至 0.855;p=0.029)。在比例优势逻辑回归模型中,与对照组相比,伊维菌素组无呼吸机天数的优势比为 1.920(95%可信区间,1.076 至 3.425;p=0.027)。
伊维菌素可改善重症 COVID-19 机械通气患者的胃肠道并发症和无呼吸机天数。SARS-CoV-2 引起的胃肠道症状可能与 COVID-19 结局相关。