Factores de riesgo de luxación de cadera presentes en neonatos de un hospital infantil

Marco Tulio Mahecha-Toro , Víctor Alejandro Vargas-Martínez , Gabriel Ochoa-Del-Portillo , Jerson Alfonso Hernández-Vargas , Gustavo Andrés Zamora-Vásquez , Claudia Castellanos-Peñaranda
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Abstract

Introduction

Developmental Dysplasia of the Hip (DDH) has significant repercussions on health if it is not diagnosed and treated in a timely manner. The purpose of this research is to describe the risk factors and prevalence for DDH in children born between 01/01/2016 and 12/31/2019 in a Children's Hospital in Bogotá, Colombia.

Materials and methods

Descriptive cross-sectional study. The Developmental Hip Dislocation (DHD) was clinically evaluated through Ortolani, Barlow and Galeazzi's signs, exploring the possible association with family history in the first and second degree of consanguinity. 2 × 2 contingency tables were created and the X2 test or Fisher's exact test was applied, considering a statistical significance of (p < 0.05). The information was taken from the DHD screening program database. The descriptive analysis was performed with Stata15 and SPSS20.

Results

3193 neonates meet the inclusion criteria. 49.5% are female. 7.1% had a family history of DHD in the first degree of consanguinity, 5% in the second degree of consanguinity, and 9.1% had a breech presentation. Clinical evaluation for the detection of DHD was positive in 0.41% (n = 13). A prevalence of 2.2× every 1000 live births was documented.

Conclusions

No association between sex and history of first degree of consanguinity was documented, but and an association with second degree history was founded. The estimated prevalence in a single hospital highlights the importance of strengthening and expanding screening programs.

Level of evidence: III. Descriptive study of transverse cut.

儿童医院新生儿髋关节脱位的危险因素
如果不及时诊断和治疗,发育性髋关节发育不良(DDH)会对健康产生重大影响。本研究的目的是描述2016年1月1日至2019年12月31日在哥伦比亚波哥大儿童医院出生的儿童DDH的危险因素和患病率。材料与方法描述性横断面研究。通过Ortolani, Barlow和Galeazzi的征象对发育性髋关节脱位(DHD)进行临床评估,探讨其与家族一级和二级血缘史的可能关联。制作2 × 2列联表,采用X2检验或Fisher精确检验,考虑(p <0.05)。这些信息来自DHD筛查项目数据库。采用Stata15和SPSS20进行描述性分析。结果3193例新生儿符合纳入标准。49.5%是女性。7.1%的人有一级血缘史,5%的人有二级血缘史,9.1%的人有臀位表现。临床评价DHD检测阳性率为0.41% (n = 13)。记录的患病率为每1000例活产2.2例。结论性别与一级血缘史无相关性,但与二级血缘史有相关性。单家医院的估计患病率突出了加强和扩大筛查计划的重要性。证据水平:III。横切的描述性研究。
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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