Epidemiological burden of inborn errors of metabolism in low- and middle-income countries: a systematic review protocol.

IF 1.5 Q3 HEALTH CARE SCIENCES & SERVICES JBI evidence synthesis Pub Date : 2024-09-13 DOI:10.11124/JBIES-23-00540
Kavita Kachroo, Annie NithiyaVathani Johnson, S A K Moinudeen, Jitendra Sharma, Cheryl Holly
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Abstract

Objective: This systematic review examines the evidence on the incidence and prevalence of inborn errors of metabolism (IEMs) in low- and middle-income countries (LMICs).

Introduction: IEMs are a set of conditions that can either be inherited or result from spontaneous mutations. Although each condition is rare in isolation, various specific disorders within the IEM group have an estimated global prevalence of 50.9 per 100,000 live births. A precise estimate of the prevalence and incidence of IEM in LMICs can help determine the necessity for extensive newborn screening programs.

Inclusion criteria: This review will cover studies conducted in LMICs, reporting on IEMs in infants and children under the age of 5 years. Studies that calculate birth prevalence and incidence of IEM will be included. Studies that provide information on the causes, clinical characteristics, treatment, case fatality rates, mortality rates, and other outcomes will also be considered.

Methods: The databases to be searched include PubMed, MEDLINE (Ovid), Embase (Ovid), CINAHL (EBSCOhost), Scopus, and gray literature sources. No date or language restrictions will be applied. Our search will encompass analytical and descriptive observational studies, which will be critically appraised by 2 independent reviewers. Data will be extracted using JBI data extraction tools. If sufficient data are available, a meta-analysis will be performed. Alternatively, if data are limited, we will present our findings in narrative format using tables and figures.

Review registration: PROSPERO CRD42023457421.

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中低收入国家先天性代谢错误的流行病学负担:系统审查协议。
摘要本系统综述研究了中低收入国家(LMICs)先天性代谢异常(IEMs)发病率和流行率的相关证据:导言:先天性代谢异常是一系列可遗传或由自发突变引起的疾病。虽然每种疾病单独来看都很罕见,但 IEM 组中的各种特定疾病在全球的发病率估计为每 10 万名活产婴儿中有 50.9 例。准确估计 IEM 在低收入和中等收入国家的流行率和发病率有助于确定是否有必要开展广泛的新生儿筛查计划:本综述将涵盖在低收入和中等收入国家进行的、报告 5 岁以下婴儿和儿童中 IEMs 的研究。将包括计算新生儿肠道疾病出生率和发病率的研究。提供病因、临床特征、治疗、病死率、死亡率和其他结果信息的研究也在考虑之列:检索的数据库包括 PubMed、MEDLINE (Ovid)、Embase (Ovid)、CINAHL (EBSCOhost)、Scopus 和灰色文献来源。没有日期或语言限制。我们的检索将包括分析性和描述性观察研究,这些研究将由两名独立审稿人进行严格评估。将使用 JBI 数据提取工具提取数据。如果有足够的数据,将进行荟萃分析。或者,如果数据有限,我们将使用表格和图表以叙述的形式呈现我们的研究结果:PREMCORD42023457421。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
JBI evidence synthesis
JBI evidence synthesis Nursing-Nursing (all)
CiteScore
4.50
自引率
3.70%
发文量
218
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