Section for Health Equity Studies & Migration, Department of General Practice & Health Services Research, Heidelberg University Hospital, Marsilius-Arkaden, Heidelberg, Germany.
Clinical Reader in Infectious Disease Epidemiology, Wolfson Institute of Population Health, Queen Mary University of London, London, United Kingdom.
PLoS Med. 2023 Jan 31;20(1):e1004030. doi: 10.1371/journal.pmed.1004030. eCollection 2023 Jan.
Post-migration follow-up of migrants identified to be at-risk of developing tuberculosis during the initial screening is effective, but programmes vary across countries. We aimed to review main strategies applied to design follow-up programmes and analyse the effect of key programme characteristics on reported coverage (i.e., proportion of migrants screened among those eligible for screening) or yields (i.e., proportion of active tuberculosis among those identified as eligible for follow-up screening).
We performed a systematic review and meta-analysis of studies reporting yields of follow-up screening programmes. Studies were included if they reported the rate of tuberculosis disease detected in international migrants through active case finding strategies and applied a post-migration follow-up (defined as one or more additional rounds of screening after finalising the initial round). For this, we retrieved all studies identified by Chan and colleagues for their systematic review (in their search until January 12, 2017) and included those reporting from active follow-up programmes. We then updated the search (from January 12, 2017 to September 30, 2022) using Medline and Embase via Ovid. Data were extracted on reported coverage, yields, and key programme characteristics, including eligible population, mode of screening, time intervals for screening, programme providers, and legal frameworks. Differences in follow-up programmes were tabulated and synthesised narratively. Meta-analyses in random effect models and exploratory analysis of subgroups showed high heterogeneity (I2 statistic > 95.0%). We hence refrained from pooling, and estimated yields and coverage with corresponding 95% confidence intervals (CIs), stratified by country, legal character (mandatory versus voluntary screening), and follow-up scheme (one-off versus repetitive screening) using forest plots for comparison and synthesis. Of 1,170 articles, 24 reports on screening programmes from 7 countries were included, with considerable variation in eligible populations, time intervals of screening, and diagnostic protocols. Coverage varied, but was higher than 60% in 15 studies, and tended to be lower in voluntary compared to compulsory programmes, and higher in studies from the United States of America, Israel, and Australia. Yield varied within and between countries and ranged between 53.05 (31.94 to 82.84) in a Dutch study and 5,927.05 (4,248.29 to 8,013.71) in a study from the United States. Of 15 estimates with narrow 95% CIs for yields, 12 were below 1,500 cases per 100,000 eligible migrants. Estimates of yields in one-off follow-up programmes tended to be higher and were surrounded by less uncertainty, compared to those in repetitive follow-up programmes. Yields in voluntary and mandatory programmes were comparable in magnitude and uncertainty. The study is limited by the heterogeneity in the design of the identified screening programmes as effectiveness, coverage and yields also depend on factors often underreported or not known, such as baseline incidence in the respective population, reactivation rate, educative and administrative processes, and consequences of not complying with obligatory measures.
Programme characteristics of post-migration follow-up screening for prevention and control of tuberculosis as well as coverage and yield vary considerably. Voluntary programmes appear to have similar yields compared with mandatory programmes and repetitive screening apparently did not lead to higher yields compared with one-off screening. Screening strategies should consider marginal costs for each additional round of screening.
在初始筛查中发现有患结核病风险的移民进行移民后随访是有效的,但各国的方案各不相同。我们旨在回顾用于设计随访方案的主要策略,并分析关键方案特征对报告覆盖率(即筛查合格者中接受筛查的移民比例)或检出率(即被确定有资格接受随访筛查的移民中活动性结核病的比例)的影响。
我们对报告随访筛查方案检出率的研究进行了系统回顾和荟萃分析。如果研究报告了通过主动病例发现策略在国际移民中发现的结核病发病率,并应用了移民后随访(定义为在完成第一轮筛查后进行一轮或多轮额外筛查),则将其纳入研究。为此,我们检索了 Chan 及其同事在其系统综述中确定的所有研究(在其截至 2017 年 1 月 12 日的搜索中),并纳入了报告开展主动随访方案的研究。然后,我们使用 Ovid 中的 Medline 和 Embase 更新了检索(从 2017 年 1 月 12 日至 2022 年 9 月 30 日)。我们提取了报告的覆盖率、检出率和关键方案特征的数据,包括合格人群、筛查方式、筛查时间间隔、方案提供者和法律框架。我们对随访方案的差异进行了制表和叙述性综合。随机效应模型的荟萃分析和亚组探索性分析显示存在高度异质性(I2 统计量>95.0%)。因此,我们避免了合并,并使用森林图对报告覆盖率和检出率进行估计,并按国家、法律特征(强制性与自愿性筛查)和随访方案(一次性与重复性筛查)进行分层,以进行比较和综合,得出相应的 95%置信区间(CI)。在 1,170 篇文章中,有 24 篇来自 7 个国家的筛查方案报告被纳入,合格人群、筛查时间间隔和诊断方案存在较大差异。覆盖率有所不同,但在 15 项研究中超过 60%,且在自愿性方案中低于强制性方案,在美国、以色列和澳大利亚的研究中较高。检出率在国家内和国家间存在差异,在一项荷兰研究中为 53.05(31.94 至 82.84),在一项来自美国的研究中为 5,927.05(4,248.29 至 8,013.71)。在 15 项检出率的估计值中,有 12 项低于每 100,000 名合格移民 1,500 例。一次性随访方案的检出率估计值较高,不确定性较小,而重复性随访方案的检出率估计值则较低。自愿性和强制性方案的检出率在幅度和不确定性方面相当。该研究受到所确定的筛查方案设计的异质性的限制,因为有效性、覆盖率和检出率还取决于通常未报告或未知的因素,例如各自人群中的基线发病率、再激活率、教育和行政过程以及不遵守强制性措施的后果。
移民后结核病防治随访筛查的方案特征、覆盖率和检出率差异很大。自愿性方案的检出率似乎与强制性方案相当,且重复性筛查与一次性筛查相比并未导致更高的检出率。筛查策略应考虑每增加一轮筛查的边际成本。