先天性大动脉矫正转位(ccTGA)的模式、表现和治疗结果的可变性:一项系统综述和荟萃分析。

Josephat M Chinawa, Awoere T Chinawa T, Ndubuisi A Uwaezuoke, Peter D Igoche
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引用次数: 0

摘要

背景:先天性纠正性大动脉转位(ccTGA)是一种罕见的先天性心脏病,在治疗方法上各地区报道不一。该荟萃分析旨在记录先天性大动脉转位(ccTGA)治疗的模式、表现和结果的不同地区差异。方法:meta分析使用ccTGA发表文章的搜索引擎。这包括PubMed、b谷歌Scholar、Web of Science、Medline和Africa journal online。2001年至2024年间发表的文章被招募,其中最后一次搜索是在2024年8月完成的。通过PRISMA(系统评价和荟萃分析首选报告项目)对选定的文章进行突出显示和筛选。采用I2统计量评估统计异质性。结果:从最初的480次引用中筛选出51篇全文。在进一步筛选不完整的数据、病例报告、非英语报告文学和尸检结果研究后,共有37项研究被进一步从51项研究中排除。最终的14项研究发表在PRISMA上。在所选研究中发现的显著异质性证明了统计显著性。结论:本综述显示ccTGA患儿表现出不同的染色体相关特征。管理选择是针对高指数的怀疑,早期干预和及时的手术护理,以避免许多并发症,跟随疾病。
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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The variability in pattern, presentation, and outcomes in the management of congenital corrected transposition of the great artery (ccTGA): A Systematic Review and Meta-analysis.

Background: Congenitally corrected transposition of the great arteries (ccTGA) is a rare congenital heart disease with varying regional reports in management approach. The meta-analysis is aimed to document various regional differences in the pattern, presentation, and outcomes in the management of congenitally corrected transposition of the great artery(ccTGA).

Methodology: Search engines for published articles on ccTGA were used in the meta-analysis. This includes PubMed, Google Scholar, Web of Science, Medline, and Africa journal online. Articles published between 2001 and 2024 were recruited of which the last search was done in August 2024. Selected articles were highlighted and screened by means of PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses). Statistical heterogeneity was assessed with the I2 statistics.

Results: Fifty-one full articles were screened from the initial four hundred and eighty citations. A total of 37 studies were further excluded from the 51 studies after further screening for incomplete data, case reports, non-English language reportage, and studies from autopsy findings. The resultant 14 studies were presented in PRISMA. The statistical significance was observed as evidenced by the significance heterogeneity identified in the selected studies.

Conclusion: The review had shown that children with ccTGA presented with varying features with some chromosomal correlates. Management options are directed towards a high index of suspicion, early intervention, and prompt surgical care to avert the numerous complications that follow the disease.

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