Toobaie Asra, Yousef Yasmine, Balvardi Saba, St-Louis Etienne, Baird Robert, Guadagno Elena, Poenaru Dan
Division of Pediatric General and Thoracic Surgery, The Montreal Children's Hospital, McGill University Health Centre, Montreal, Quebec, Canada.
Department of Surgery, The University of British Colombia, Vancouver, BC, Canada.
J Pediatr Surg. 2019 May;54(5):1089-1093. doi: 10.1016/j.jpedsurg.2019.01.034. Epub 2019 Feb 2.
In the absence of robust data from low- and middle-income countries (LMICs), most disease burden estimates and related resource allocation choices are based on historic Northern demographics. We hypothesize that significant discrepancies exist between directly reported LMIC data and surrogate high-income country (HIC) disease burden estimates of correctible congenital anomalies.
Nine online databases were searched for studies reporting incidence and prevalence data on surgically correctible congenital anomalies in LMICs between 2006 and 2017. Two independent reviewers screened titles and abstracts, with a third adjudicating discrepancies. Selected studies were reviewed and analyzed.
Of 10,128 identified articles, 98 were extracted for full-text review, and 41 were included, representing 21 LMICs and 18 conditions. Study types included community surveys (34%), prospective (22%) and retrospective (17%) multi-site data, registries (12%), single-site data (12%), and systematic reviews (5%). Data collection periods were 1 to 10 years. The pooled epidemiologic data varied systematically from existing HIC literature, with the incidence of disease being generally lower in LMICs.
Marked discrepancies exist between reported epidemiological data in LMICs and HIC literature, in part owing to varying quality of data collection in LMICs. Robust population-based surveys are needed to accurately estimate the burden of surgically correctable congenital anomalies in LMICs.
Level V, expert opinion without explicit critical appraisal.
由于缺乏来自低收入和中等收入国家(LMICs)的有力数据,大多数疾病负担估计以及相关资源分配选择是基于历史上北方地区的人口统计数据。我们推测,在低收入和中等收入国家直接报告的数据与替代高收入国家(HIC)对可矫正先天性异常的疾病负担估计之间存在显著差异。
检索了九个在线数据库,以查找2006年至2017年间报告低收入和中等收入国家可手术矫正先天性异常发病率和患病率数据的研究。两名独立评审员筛选标题和摘要,由第三名评审员裁决差异。对选定的研究进行了审查和分析。
在10,128篇已识别的文章中,提取了98篇进行全文审查,纳入了41篇,代表21个低收入和中等收入国家以及18种疾病。研究类型包括社区调查(34%)、前瞻性(22%)和回顾性(17%)多地点数据、登记处(12%)、单地点数据(12%)和系统评价(5%)。数据收集期为1至10年。汇总的流行病学数据与现有的高收入国家文献存在系统性差异,低收入和中等收入国家的疾病发病率普遍较低。
低收入和中等收入国家报告的流行病学数据与高收入国家文献之间存在明显差异,部分原因是低收入和中等收入国家数据收集质量不同。需要进行有力的基于人群的调查,以准确估计低收入和中等收入国家可手术矫正先天性异常的负担。
V级,无明确批判性评价的专家意见。