Cochrane Response, Cochrane, London, UK.
Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK.
Cochrane Database Syst Rev. 2021 Nov 17;11(11):CD008521. doi: 10.1002/14651858.CD008521.pub6.
Rotavirus is a common cause of diarrhoea, diarrhoea-related hospital admissions, and diarrhoea-related deaths worldwide. Rotavirus vaccines prequalified by the World Health Organization (WHO) include Rotarix (GlaxoSmithKline), RotaTeq (Merck), and, more recently, Rotasiil (Serum Institute of India Ltd.), and Rotavac (Bharat Biotech Ltd.).
To evaluate rotavirus vaccines prequalified by the WHO for their efficacy and safety in children.
On 30 November 2020, we searched PubMed, the Cochrane Infectious Diseases Group Specialized Register, CENTRAL (published in the Cochrane Library), Embase, LILACS, Science Citation Index Expanded, Social Sciences Citation Index, Conference Proceedings Citation Index-Science, Conference Proceedings Citation Index-Social Science & Humanities. We also searched the WHO ICTRP, ClinicalTrials.gov, clinical trial reports from manufacturers' websites, and reference lists of included studies, and relevant systematic reviews.
We selected randomized controlled trials (RCTs) conducted in children that compared rotavirus vaccines prequalified for use by the WHO with either placebo or no intervention.
Two authors independently assessed trial eligibility and assessed risk of bias. One author extracted data and a second author cross-checked them. We combined dichotomous data using the risk ratio (RR) and 95% confidence interval (CI). We stratified the analyses by under-five country mortality rate and used GRADE to evaluate evidence certainty.
Sixty trials met the inclusion criteria and enrolled a total of 228,233 participants. Thirty-six trials (119,114 participants) assessed Rotarix, 15 trials RotaTeq (88,934 participants), five trials Rotasiil (11,753 participants), and four trials Rotavac (8432 participants). Rotarix Infants vaccinated and followed up for the first year of life In low-mortality countries, Rotarix prevented 93% of severe rotavirus diarrhoea cases (14,976 participants, 4 trials; high-certainty evidence), and 52% of severe all-cause diarrhoea cases (3874 participants, 1 trial; moderate-certainty evidence). In medium-mortality countries, Rotarix prevented 79% of severe rotavirus diarrhoea cases (31,671 participants, 4 trials; high-certainty evidence), and 36% of severe all-cause diarrhoea cases (26,479 participants, 2 trials; high-certainty evidence). In high-mortality countries, Rotarix prevented 58% of severe rotavirus diarrhoea cases (15,882 participants, 4 trials; high-certainty evidence), and 27% of severe all-cause diarrhoea cases (5639 participants, 2 trials; high-certainty evidence). Children vaccinated and followed up for two years In low-mortality countries, Rotarix prevented 90% of severe rotavirus diarrhoea cases (18,145 participants, 6 trials; high-certainty evidence), and 51% of severe all-cause diarrhoea episodes (6269 participants, 2 trials; moderate-certainty evidence). In medium-mortality countries, Rotarix prevented 77% of severe rotavirus diarrhoea cases (28,834 participants, 3 trials; high-certainty evidence), and 26% of severe all-cause diarrhoea cases (23,317 participants, 2 trials; moderate-certainty evidence). In high-mortality countries, Rotarix prevented 35% of severe rotavirus diarrhoea cases (13,768 participants, 2 trials; moderate-certainty evidence), and 17% of severe all-cause diarrhoea cases (2764 participants, 1 trial; high-certainty evidence). RotaTeq Infants vaccinated and followed up for the first year of life In low-mortality countries, RotaTeq prevented 97% of severe rotavirus diarrhoea cases (5442 participants, 2 trials; high-certainty evidence). In medium-mortality countries, RotaTeq prevented 79% of severe rotavirus diarrhoea cases (3863 participants, 1 trial; low-certainty evidence). In high-mortality countries, RotaTeq prevented 57% of severe rotavirus diarrhoea cases (6775 participants, 2 trials; high-certainty evidence), but there is probably little or no difference between vaccine and placebo for severe all-cause diarrhoea (1 trial, 4085 participants; moderate-certainty evidence). Children vaccinated and followed up for two years In low-mortality countries, RotaTeq prevented 96% of severe rotavirus diarrhoea cases (5442 participants, 2 trials; high-certainty evidence). In medium-mortality countries, RotaTeq prevented 79% of severe rotavirus diarrhoea cases (3863 participants, 1 trial; low-certainty evidence). In high-mortality countries, RotaTeq prevented 44% of severe rotavirus diarrhoea cases (6744 participants, 2 trials; high-certainty evidence), and 15% of severe all-cause diarrhoea cases (5977 participants, 2 trials; high-certainty evidence). We did not identify RotaTeq studies reporting on severe all-cause diarrhoea in low- or medium-mortality countries. Rotasiil Rotasiil has not been assessed in any RCT in countries with low or medium child mortality. Infants vaccinated and followed up for the first year of life In high-mortality countries, Rotasiil prevented 48% of severe rotavirus diarrhoea cases (11,008 participants, 2 trials; high-certainty evidence), and resulted in little to no difference in severe all-cause diarrhoea cases (11,008 participants, 2 trials; high-certainty evidence). Children vaccinated and followed up for two years In high-mortality countries, Rotasiil prevented 44% of severe rotavirus diarrhoea cases (11,008 participants, 2 trials; high-certainty evidence), and resulted in little to no difference in severe all-cause diarrhoea cases (11,008 participants, 2 trials; high-certainty evidence). Rotavac Rotavac has not been assessed in any RCT in countries with low or medium child mortality. Infants vaccinated and followed up for the first year of life In high-mortality countries, Rotavac prevented 57% of severe rotavirus diarrhoea cases (6799 participants, 1 trial; moderate-certainty evidence), and 16% of severe all-cause diarrhoea cases (6799 participants, 1 trial; moderate-certainty evidence). Children vaccinated and followed up for two years In high-mortality countries, Rotavac prevented 54% of severe rotavirus diarrhoea cases (6541 participants, 1 trial; moderate-certainty evidence); no Rotavac studies have reported on severe all-cause diarrhoea at two-years follow-up. Safety No increased risk of serious adverse events (SAEs) was detected with Rotarix (103,714 participants, 31 trials; high-certainty evidence), RotaTeq (82,502 participants, 14 trials; moderate to high-certainty evidence), Rotasiil (11,646 participants, 3 trials; high-certainty evidence), or Rotavac (8210 participants, 3 trials; moderate-certainty evidence). Deaths were infrequent and the analysis had insufficient evidence to show an effect on all-cause mortality. Intussusception was rare. AUTHORS' CONCLUSIONS: Rotarix, RotaTeq, Rotasiil, and Rotavac prevent episodes of rotavirus diarrhoea. The relative effect estimate is smaller in high-mortality than in low-mortality countries, but more episodes are prevented in high-mortality settings as the baseline risk is higher. In high-mortality countries some results suggest lower efficacy in the second year. We found no increased risk of serious adverse events, including intussusception, from any of the prequalified rotavirus vaccines.
轮状病毒是导致全球腹泻、腹泻相关住院和腹泻相关死亡的常见原因。世界卫生组织(WHO)预认证的轮状病毒疫苗包括 Rotarix(葛兰素史克)、RotaTeq(默克),以及最近的 Rotasiil(印度血清研究所有限公司)和 Rotavac( Bharat Biotech Ltd.)。
评估 WHO 预认证的轮状病毒疫苗在儿童中的疗效和安全性。
2020 年 11 月 30 日,我们检索了 PubMed、Cochrane 传染病组专业注册库、Cochrane 图书馆中的 CENTRAL、Embase、LILACS、科学引文索引扩展版、社会科学引文索引、会议论文引文索引-科学、会议论文引文索引-社会科学与人文科学。我们还检索了 WHO 国际临床试验注册平台、ClinicalTrials.gov、来自制造商网站的临床试验报告,以及纳入研究的相关系统评价。
我们选择了在儿童中进行的随机对照试验(RCT),这些试验比较了 WHO 预认证的轮状病毒疫苗与安慰剂或无干预措施的效果。
两名作者独立评估了试验的纳入标准和偏倚风险。一名作者提取数据,另一名作者交叉核对。我们使用风险比(RR)和 95%置信区间(CI)合并二分类数据。我们根据五岁以下儿童死亡率进行分层分析,并使用 GRADE 评估证据确定性。
60 项试验符合纳入标准,共纳入 228233 名参与者。36 项试验(119114 名参与者)评估了 Rotarix,15 项试验评估了 RotaTeq(88934 名参与者),5 项试验评估了 Rotasiil(11753 名参与者),4 项试验评估了 Rotavac(8432 名参与者)。Rotarix 接种并随访一岁以下儿童在低死亡率国家,Rotarix 预防了 93%的严重轮状病毒腹泻病例(4 项试验,14976 名参与者;高确定性证据)和 52%的严重全因腹泻病例(1 项试验,3874 名参与者;中确定性证据)。在中死亡率国家,Rotarix 预防了 79%的严重轮状病毒腹泻病例(4 项试验,31671 名参与者;高确定性证据)和 36%的严重全因腹泻病例(2 项试验,26479 名参与者;高确定性证据)。在高死亡率国家,Rotarix 预防了 58%的严重轮状病毒腹泻病例(4 项试验,15882 名参与者;高确定性证据)和 27%的严重全因腹泻病例(2 项试验,5639 名参与者;高确定性证据)。接种并随访两年的儿童在低死亡率国家,Rotarix 预防了 90%的严重轮状病毒腹泻病例(6 项试验,18145 名参与者;高确定性证据)和 51%的严重全因腹泻发作(2 项试验,6269 名参与者;中确定性证据)。在中死亡率国家,Rotarix 预防了 77%的严重轮状病毒腹泻病例(3 项试验,28834 名参与者;高确定性证据)和 26%的严重全因腹泻病例(2 项试验,23317 名参与者;中确定性证据)。在高死亡率国家,Rotarix 预防了 35%的严重轮状病毒腹泻病例(2 项试验,13768 名参与者;中确定性证据)和 17%的严重全因腹泻病例(1 项试验,2764 名参与者;高确定性证据)。RotaTeq 接种并随访一岁以下儿童在低死亡率国家,RotaTeq 预防了 97%的严重轮状病毒腹泻病例(2 项试验,5442 名参与者;高确定性证据)。在中死亡率国家,RotaTeq 预防了 79%的严重轮状病毒腹泻病例(1 项试验,3863 名参与者;低确定性证据)。在高死亡率国家,RotaTeq 预防了 57%的严重轮状病毒腹泻病例(2 项试验,6775 名参与者;高确定性证据),但疫苗与安慰剂在严重全因腹泻方面可能差异不大(1 项试验,4085 名参与者;中确定性证据)。接种并随访两年的儿童在低死亡率国家,RotaTeq 预防了 96%的严重轮状病毒腹泻病例(2 项试验,5442 名参与者;高确定性证据)。在中死亡率国家,RotaTeq 预防了 79%的严重轮状病毒腹泻病例(1 项试验,3863 名参与者;低确定性证据)。在高死亡率国家,RotaTeq 预防了 44%的严重轮状病毒腹泻病例(2 项试验,6744 名参与者;高确定性证据)和 15%的严重全因腹泻病例(2 项试验,5977 名参与者;高确定性证据)。我们未发现报告低死亡率或中死亡率国家严重全因腹泻的 RotaTeq 研究。Rotasiil 尚未在高儿童死亡率国家的任何 RCT 中进行评估。接种并随访一岁以下儿童在高死亡率国家,Rotasiil 预防了 48%的严重轮状病毒腹泻病例(2 项试验,11008 名参与者;高确定性证据)和严重全因腹泻病例(2 项试验,11008 名参与者;高确定性证据)。接种并随访两年的儿童在高死亡率国家,Rotasiil 预防了 44%的严重轮状病毒腹泻病例(2 项试验,11008 名参与者;高确定性证据)和严重全因腹泻病例(2 项试验,11008 名参与者;高确定性证据)。Rotavac 尚未在低死亡率或中死亡率国家的任何 RCT 中进行评估。接种并随访一岁以下儿童在高死亡率国家,Rotavac 预防了 57%的严重轮状病毒腹泻病例(1 项试验,6799 名参与者;中确定性证据)和严重全因腹泻病例(1 项试验,6799 名参与者;中确定性证据)。接种并随访两年的儿童在高死亡率国家,Rotavac 预防了 54%的严重轮状病毒腹泻病例(1 项试验,6541 名参与者;中确定性证据);没有 Rotavac 研究报告两年随访时的严重全因腹泻情况。安全性没有增加严重不良事件(SAE)的风险(31 项试验,103714 名参与者;高确定性证据)、RotaTeq(14 项试验,82502 名参与者;中到高确定性证据)、Rotasiil(3 项试验,11646 名参与者;高确定性证据)或 Rotavac(3 项试验,8210 名参与者;中确定性证据)。死亡事件很少见,分析没有足够的证据表明全因死亡率有影响。肠套叠罕见。作者结论:Rotarix、RotaTeq、Rotasiil 和 Rotavac 可预防轮状病毒腹泻。相对效果估计在高死亡率国家较小,但在高死亡率国家中,由于基线风险较高,可预防的腹泻病例更多。在高死亡率国家,一些结果表明第二年的疗效较低。我们没有发现任何预认证的轮状病毒疫苗会增加严重不良事件(包括肠套叠)的风险。