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巴西上肢先天畸形的患病率:一项描述性横断面研究。

Prevalence of Congenital Anomalies of the Upper Limbs in Brazil: a descriptive cross-sectional study.

机构信息

Hand Surgeon, Department of Orthopedics and Traumatology, Escola Paulista de Medicina - Universidade Federal de São Paulo (EPM-UNIFESP), São Paulo (SP), Brazil.

Adjunct Professor, Department of Orthopedics and Traumatology. Discipline of Hand and Upper Limb Surgery, Escola Paulista de Medicina - Universidade Federal de São Paulo (EPMUNIFESP), São Paulo (SP), Brazil.

出版信息

Sao Paulo Med J. 2024 Jun 17;142(6):e2023349. doi: 10.1590/1516-3180.2023.0349.R1.08042024. eCollection 2024.

DOI:10.1590/1516-3180.2023.0349.R1.08042024
PMID:38896746
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11185865/
Abstract

BACKGROUND

Congenital Anomalies of the Upper Limb (CAUL) are a group of structural or functional abnormalities that develop during intrauterine life and can lead to limb dysfunction.

OBJECTIVES

To analyze the prevalence of congenital anomalies of the upper limbs in Brazil and assess maternal and neonatal variables.

DESIGN AND SETTING

A cross-sectional, descriptive study was conducted on congenital upper limb malformations among live births across Brazil.

METHODS

The study spanned from 2010 to 2019. Data were sourced from the Department of Informatics of the Unified Health System (DATASUS) and the Live Birth Information System (SINASC) portal. Analyses focused on the information reported in field 41 of the Live Birth Declaration Form entered into the computerized system.

RESULTS

The most common anomaly in Brazil was supernumerary fingers, classified as ICD-Q69.0, affecting 11,708 children, with a prevalence of 4.02 per 10,000 live births. Mothers aged over 40 years had a 36% higher prevalence of having children with CAUL than mothers under 40 years old (OR = 1.36; 95% CI 1.19-1.56). Newborns weighing ≥ 2,499 g were 2.64 times more likely to have CAUL compared to those weighing ≥ 2,500 g (OR = 2.64; 95% CI 2.55-2.73).

CONCLUSION

There was an observed increase in the reporting of CAUL cases over the decade studied. This trend serves as an alert for health agencies, as understanding the prevalence of CAUL and its associated factors is crucial for preventive medicine.

摘要

背景

上肢先天畸形(CAUL)是一组在宫内发育过程中发生的结构或功能异常,可导致肢体功能障碍。

目的

分析巴西上肢先天畸形的流行情况,并评估母婴和新生儿变量。

设计和设置

这是一项在巴西进行的涉及活产儿上肢先天畸形的横断面描述性研究。

方法

研究时间跨度为 2010 年至 2019 年。数据来源于统一卫生系统(DATASUS)和活产信息系统(SINASC)门户的信息。分析重点是在计算机系统中输入的活产声明表第 41 字段中报告的信息。

结果

巴西最常见的上肢先天畸形是多指畸形,分类为 ICD-Q69.0,影响了 11708 名儿童,每 10000 例活产儿中有 4.02 例。年龄超过 40 岁的母亲所生孩子患有 CAUL 的患病率比年龄在 40 岁以下的母亲高 36%(OR=1.36;95%CI 1.19-1.56)。体重≥2499g 的新生儿发生 CAUL 的可能性是体重≥2500g 新生儿的 2.64 倍(OR=2.64;95%CI 2.55-2.73)。

结论

在所研究的十年中,CAUL 病例的报告呈上升趋势。这一趋势提醒了卫生机构,因为了解 CAUL 的流行情况及其相关因素对于预防医学至关重要。

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本文引用的文献

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Congenital anomalies in Rio Grande do Sul State: a time series analysis.南里奥格兰德州的先天性异常:时间序列分析
Rev Bras Epidemiol. 2019;22:e190040. doi: 10.1590/1980-549720190040. Epub 2019 Apr 29.
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Profile of congenital anomalies among live births in the municipality of Tangará da Serra, Mato Grosso, Brazil, 2006-2016.2006 - 2016年巴西马托格罗索州唐加拉达塞拉市活产儿先天性异常情况
Epidemiol Serv Saude. 2018 Oct 22;27(3):e2018008. doi: 10.5123/S1679-49742018000300017.
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Congenital limb deficiency in Japan: a cross-sectional nationwide survey on its epidemiology.日本的先天性肢体缺损:一项关于其流行病学的全国性横断面调查。
BMC Musculoskelet Disord. 2018 Jul 27;19(1):262. doi: 10.1186/s12891-018-2195-3.
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EUROCAT: an update on its functions and activities.欧洲先天性异常监测系统(EUROCAT):其功能与活动的最新情况
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PREVALENCE OF CONGENITAL ANOMALIES AND THEIR ASSOCIATED FACTORS IN NEWBORNS IN THE CITY OF SÃO PAULO FROM 2010 TO 2014.2010年至2014年圣保罗市新生儿先天性异常的患病率及其相关因素
Rev Paul Pediatr. 2017 Jan-Mar;35(1):33-38. doi: 10.1590/1984-0462/;2017;35;1;00002.
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The Prevalence of Congenital Hand and Upper Extremity Anomalies Based Upon the New York Congenital Malformations Registry.基于纽约先天性畸形登记处的先天性手部及上肢异常患病率
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Congenital upper limb deficiencies and associated malformations in Finland: a population-based study.芬兰先天性上肢缺陷及相关畸形:一项基于人群的研究。
J Hand Surg Am. 2011 Jun;36(6):1058-65. doi: 10.1016/j.jhsa.2011.03.015. Epub 2011 May 23.
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