Department of Global Health, Boston University School of Public Health, Boston, Massachusetts, USA.
Hospital de Especialidades CMN SXXI Instituto Mexicano del Seguro Social Ciudad de México, Mexico City, Mexico.
BMJ Glob Health. 2023 May;8(5). doi: 10.1136/bmjgh-2022-010962.
Several countries in Latin America conducted mass distribution of COVID-19 kits intended to treat mild COVID-19, thereby preventing excess hospitalisations. Many of the kits contained ivermectin, an antiparasitic medicine that was not approved at the time for the treatment of COVID-19. The study objective was to compare the timing of the publication of scientific evidence about the efficacy of ivermectin for COVID-19 with the timeline of distribution of COVID-19 kits in eight Latin American countries and to analyse whether evidence was used to justify ivermectin distribution.
We conducted a systematic review of randomised controlled trials (RCTs) published on the efficacy of ivermectin or ivermectin as adjuvant therapy on mortality from, or as prevention for, COVID-19. Each RCT was assessed using the Cochrane Grading of Recommendations, Assessment, Development and Evaluations (GRADE). Information on the timing and justification of government decisions was collected through a systematic search of leading newspapers and government press releases.
After removing the duplicates and abstracts without full text, 33 RCTs met our inclusion criteria. According to GRADE, the majority had a substantial risk of bias. Many government officials made claims that ivermectin was effective and safe in the prevention or treatment of COVID-19, despite the lack of published evidence.
All eight governments distributed COVID-19 kits to their populations despite the absence of high-quality evidence on the efficacy of ivermectin for prevention, hospitalisation and mortality in COVID-19 patients. Lessons learnt from this situation could be used to strengthen government institutions' capacities to implement evidence-informed public health policies.
拉丁美洲的几个国家开展了 COVID-19 试剂盒的大规模分发,旨在治疗轻症 COVID-19,从而防止过度住院。许多试剂盒中含有伊维菌素,一种当时未被批准用于治疗 COVID-19 的抗寄生虫药物。本研究的目的是比较伊维菌素治疗 COVID-19 的疗效的科学证据发表时间与八个拉丁美洲国家 COVID-19 试剂盒分发时间的关系,并分析是否有证据支持伊维菌素的分发。
我们对发表的关于伊维菌素治疗 COVID-19 或作为 COVID-19 死亡率或预防的辅助治疗的疗效的随机对照试验(RCT)进行了系统评价。每个 RCT 都使用 Cochrane 分级推荐、评估、发展和评估(GRADE)进行评估。通过对主要报纸和政府新闻稿的系统搜索,收集了有关政府决策的时间和理由的信息。
在去除重复项和没有全文的摘要后,有 33 项 RCT 符合我们的纳入标准。根据 GRADE,大多数 RCT 存在较大的偏倚风险。尽管缺乏已发表的证据,许多政府官员仍声称伊维菌素在预防或治疗 COVID-19 方面有效且安全。
尽管缺乏高质量的证据表明伊维菌素在预防、住院和 COVID-19 患者死亡率方面的疗效,但所有八个政府都向其民众分发了 COVID-19 试剂盒。从这种情况中吸取的经验教训可以用于加强政府机构实施循证公共卫生政策的能力。