Opuntia 仙人掌提取物对住院中度 COVID-19 感染的影响:随机对照试验

Q4 Medicine
Zeinab Siami, Somayeh Mansoury
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引用次数: 0

摘要

背景:由于 COVID-19 大流行的高负荷及其超常的死亡率,以及文献中报道的仙人掌化合物的一些抗病毒作用,本研究旨在评估 Opuntia 仙人掌对 COVID-19 感染者和疾病症状的影响。研究方法这是一项随机对照试验研究。将转诊至伊朗卡拉季伊玛目阿里医院的 COVID-19 感染患者随机分为干预组和对照组。所有患者均接受基于最新指南的标准治疗方案。干预组患者每天服用 250 毫升欧蓬子提取物糖浆。除标准治疗外,对照组只接受标准治疗。对两组患者的咳嗽、呼吸困难、肌痛、头痛、乏力等症状进行每日评估和比较。结果52 名患者参与了研究。干预组患者的平均住院时间明显缩短;与对照组相比,干预组患者血氧饱和度低于 93%、发热、无嗅、咳嗽、头痛、头晕、肌痛、呼吸困难、胸痛和厌食的发生率明显降低(P<0.05)。结论仙人掌提取物可改善 COVID-19 患者的病情,使患者的症状得到改善,缩短住院时间。此外,患者组大多数症状和体征的持续时间明显缩短。还需要更多的临床试验来证实这一点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Effect of Opuntia Cactus Extract on Hospitalized Moderate COVID-19 Infection: A Randomized Controlled Trial
Background: Due to the high load of the COVID-19 pandemic and its extraordinary mortality rate and some antiviral effects of cactus compounds reported in the literature, the present study aimed to assess the effect of Opuntia cactus on patients with COVID-19 infection and symptoms of disease. Methods: This is a randomized controlled trial study. Patients with COVID-19 infection who were referred to Imam Ali hospital, located in Karaj, Iran, were randomly divided into intervention and control groups. All patients received a standard treatment regimen based on the latest guidelines. Patients in the intervention group received 250 mL of Opuntia extract syrup daily. In addition to standard treatment, the control group received only the standard regimen. Patients’ symptoms including coughing, dyspnea, myalgia, headache, weakness, etc., were estimated daily and compared between the two groups. Results: Fifty-two patients participated in the study. The average length of hospital stays was significantly shorter in the intervention group; also, blood oxygen saturation below 93%, fever, anosmia, coughing, headache, dizziness, myalgia, dyspnea, chest pain, and anorexia were significantly less frequent in the intervention group compared to the control group (P<0.05). Conclusion: Opuntia cactus extract can improve the condition of COVID-19 patients due to symptomatic improvement in patients and decreased hospital stays. Moreover, the duration of most signs and symptoms significantly decreased in the patient group. More clinical trials are also necessary to approve this.
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