Haddadzadeh Shoushtari Maryam, Raji Hanieh, Borsi Seyed Hamid, Tavakol Heshmatollah, Cheraghian Bahman, Moeinpour Mahtab
Air Pollution and Respiratory Diseases Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Department of Biostatics and Public Health, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Galen Med J. 2024 Feb 8;13:e3035. doi: 10.31661/gmj.v12i.3035. eCollection 2024.
The coronavirus disease 2019 (COVID-19) pandemic has engendered scores of deaths worldwide. Just as the development of varying procedures during the pandemic has helped inhibit the disease, none is considered a definitive treatment protocol for this problem, as each induces some clinical complications pertinent to the disease. This study thus assessed the early use of sofosbuvir in outpatients with mild COVID-19.
This randomized clinical trial study was conducted on 360 patients with mild COVID-19 infection at 17 Shahrivar Ahvaz Health Center. These patients were randomly divided into the intervention and control groups. Both the control and intervention groups received 400 mg of sofosbuvir and a placebo for seven days, respectively. After 14 days from the onset of the treatment, the duration of symptoms, the necessity of hospitalization, the mean of hospitalization duration, and mortality were assessed.
The most common symptoms in the intervention and control groups were coughs with a frequency of 46 (25.6%) and 54(30%), respectively. The two groups showed no statistically significant difference in the frequency of the first observed clinical symptom related to the disease (P=0.2). The mean days that the patients were symptomatic in the control group were 14±4.17, whereas, in the intervention group, it was 12.12±3.15 (P=0.08). The frequency of hospitalization in the control and intervention groups was 7 (3.8%) and 4 (2.22%), respectively (P=0.11). Moreover, the mean days of hospitalization in the control and the intervention groups were 4±1.1 and 3±0.8, respectively (P=0.15). In addition, the two groups had a similar frequency of hospitalization in the ICU (0) and mortality rate (0).
Sofosbuvir alone cannot play a significant role in the treatment of outpatients with mild COVID-19.
2019年冠状病毒病(COVID-19)大流行已在全球造成大量死亡。正如大流行期间各种治疗方法的发展有助于抑制该疾病一样,由于每种方法都会引发一些与该疾病相关的临床并发症,因此没有一种方法被认为是针对该问题的明确治疗方案。因此,本研究评估了索磷布韦在轻度COVID-19门诊患者中的早期使用情况。
本随机临床试验研究在阿瓦士17号沙赫里瓦尔健康中心对360例轻度COVID-19感染患者进行。这些患者被随机分为干预组和对照组。对照组和干预组分别接受400毫克索磷布韦和安慰剂,持续7天。治疗开始14天后,评估症状持续时间、住院必要性、平均住院时间和死亡率。
干预组和对照组最常见的症状均为咳嗽,频率分别为46例(25.6%)和54例(30%)。两组在与该疾病相关的首次观察到的临床症状频率上无统计学显著差异(P=0.2)。对照组患者出现症状的平均天数为14±4.17天,而干预组为12.12±3.15天(P=0.08)。对照组和干预组的住院频率分别为7例(3.8%)和4例(2.22%)(P=0.11)。此外,对照组和干预组的平均住院天数分别为4±1.1天和3±0.8天(P=0.15)。此外,两组在重症监护病房的住院频率(0)和死亡率(0)相似。
单独使用索磷布韦在治疗轻度COVID-19门诊患者中不能发挥显著作用。