Colditz G A, Berkey C S, Mosteller F, Brewer T F, Wilson M E, Burdick E, Fineberg H V
Technology Assessment Group, Harvard School of Public Health, Boston, MA 02115, USA.
Pediatrics. 1995 Jul;96(1 Pt 1):29-35.
To quantify the efficacy of vaccination of infants with bacillus Calmette-Guérin (BCG) against tuberculosis.
MEDLINE with index terms BCG vaccine, tuberculosis, and human; lists of all known studies provided by experts at the Centers for Disease Control and Prevention, the World Health Organization, and other organizations.
A total of 1264 articles and abstracts were reviewed for details on BCG vaccination, the availability of concurrent vaccinated and unvaccinated groups, and a tuberculosis outcome. Seventy articles were reviewed in depth for method of vaccine allocation used to create comparable groups, age at vaccination of study participants, comparability of surveillance and follow-up of recipient and concurrent control groups in trials, an appropriately defined control group in case-control studies, and outcome measures (tuberculosis cases and/or deaths). Five prospective trials and eleven case-control studies of vaccination during infancy were included in the present analyses.
We recorded study design, age range of study population, number of patients enrolled, efficacy of vaccine, location of the study, and a series of items to assess the potential for bias in study design, follow-up, and diagnosis. We extracted or computed vaccine efficacy by years since vaccination wherever possible. At least two readers independently extracted data and evaluated data validity.
The relative risk (RR) or odds ratio (OR) for tuberculosis in vaccinated versus unvaccinated infants was the measure of vaccine efficacy analyzed. A random-effects method estimated a weighted average RR or OR from data extracted from the trials and case-control studies. The protective effect was then computed by 1-RR or 1-OR. Overall, the protective effect of vaccination against cases of tuberculosis was 0.74 (95% confidence interval [95% CI], 0.62 to 0.83) when estimated from four randomized controlled trials, and 0.52 (95% CI, 0.38 to 0.64) when estimated from nine case-control studies. Five trials reporting deaths from tuberculosis showed a BCG protective effect of 0.65 (95% CI, 0.12 to 0.86), five studies reporting on meningitis showed a protective effect of 0.64 (95% CI, 0.30 to 0.82), and three studies of disseminated tuberculosis showed a protective effect of 0.78 (95% CI, 0.58 to 0.88). Three case-control studies included separate results for laboratory-confirmed cases of tuberculosis. These studies documented a protective effect of 0.83 (95% CI, 0.58 to 0.93). In a random-effects regression model of the nine case-control studies, study validity score explained 15% of the heterogeneity among study-estimated protective effects, suggesting that better studies reported greater efficacy. Three trials and six case-control studies provided some age-specific information that allowed us to examine the duration of BCG efficacy. Most of this evidence suggested that BCG efficacy may persist through 10 years after infant vaccination.
BCG vaccination of newborns and infants significantly reduces the risk of tuberculosis--by over 50%, on average. Protection has been observed across many populations, study designs, and forms of tuberculosis. Rates of protection against cases that are confirmed by laboratory tests, reflecting reduced error in disease classification and consequently more accurate estimates of BCG efficacy, are highest at 83%.
量化婴儿接种卡介苗(BCG)预防结核病的效果。
MEDLINE,检索词为卡介苗疫苗、结核病和人类;疾病控制与预防中心、世界卫生组织及其他组织的专家提供的所有已知研究列表。
共查阅了1264篇文章和摘要,以获取卡介苗接种的详细信息、同时存在接种组和未接种组的情况以及结核病结局。对70篇文章进行了深入审查,内容包括用于创建可比组的疫苗分配方法、研究参与者的接种年龄、试验中接受者和同期对照组监测与随访的可比性、病例对照研究中适当定义的对照组以及结局指标(结核病例和/或死亡)。本分析纳入了5项婴儿期接种疫苗的前瞻性试验和11项病例对照研究。
我们记录了研究设计、研究人群的年龄范围、入组患者数量、疫苗效果、研究地点以及一系列用于评估研究设计、随访和诊断中偏倚可能性的项目。只要有可能,我们就按接种后的年份提取或计算疫苗效力。至少两名读者独立提取数据并评估数据有效性。
分析接种疫苗与未接种疫苗婴儿患结核病的相对风险(RR)或比值比(OR)作为疫苗效力的衡量指标。采用随机效应方法从试验和病例对照研究中提取的数据估计加权平均RR或OR。然后通过1-RR或1-OR计算保护效果。总体而言,从4项随机对照试验估计,接种疫苗预防结核病例的保护效果为0.74(95%置信区间[95%CI],0.62至0.83),从9项病例对照研究估计为0.52(95%CI,0.38至0.64)。5项报告结核病死亡情况的试验显示卡介苗的保护效果为0.65(95%CI,0.12至0.86),5项报告脑膜炎情况的研究显示保护效果为0.64(95%CI,0.30至0.82),3项播散性结核病研究显示保护效果为0.78(95%CI,0.58至0.88)。3项病例对照研究包括实验室确诊结核病例的单独结果。这些研究记录的保护效果为0.83(95%CI,0.58至0.93)。在9项病例对照研究的随机效应回归模型中,研究效度评分解释了研究估计的保护效果之间15%的异质性,这表明质量更好的研究报告的效力更高。3项试验和6项病例对照研究提供了一些特定年龄的信息,使我们能够研究卡介苗效力的持续时间。这些证据大多表明,婴儿接种卡介苗后,其效力可能持续10年。
新生儿和婴儿接种卡介苗可显著降低结核病风险——平均降低超过50%。在许多人群、研究设计和结核病类型中均观察到了保护作用。针对实验室确诊病例的保护率最高,为83%,这反映出疾病分类误差减少,从而对卡介苗效力的估计更为准确。