普遍临床DDH筛查辅以靶向超声在芬兰是有效的。

IF 4.4 1区 医学 Q1 ORTHOPEDICS
Emma-Sofia Luoto, Jenni Jalkanen, Ilari Kuitunen, Reijo Sund, Yrjänä Nietosvaara
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引用次数: 0

摘要

背景:根据最近的一项荟萃分析,普遍超声筛查的发育性髋关节发育不良(DDH)的晚期诊断率为每1000名儿童0.2例,这与日本使用选择性超声筛查的情况相同。我们假设芬兰目前的普遍临床筛查辅以靶向超声的方案并不亚于普遍和选择性超声筛查方案。结果:在20年的研究期间,有1,103,269名婴儿出生(中位数为每年57,214名婴儿;每年有45346到60694个婴儿)。共有6421名儿童被诊断为DDH(平均每年321名儿童;每年193至405名儿童),平均计算发病率为每1000名新生儿5.8例(95%可信区间[CI], 5.7至6.0)。结论:芬兰目前的DDH筛查项目,包括普遍的临床靶向超声筛查,与其他筛查项目相比,效果并不差。证据等级:预后III级。有关证据水平的完整描述,请参见作者说明。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Universal Clinical DDH Screening Complemented with Targeted Ultrasound Is Effective in Finland.

Background: The late diagnosis rate of developmental dysplasia of the hip (DDH) with universal ultrasound screening is 0.2 per 1,000 children according to a recent meta-analysis, which is the same as in Japan where selective ultrasound screening is used. We hypothesized that Finland's current program of universal clinical screening complemented with targeted ultrasound is noninferior to universal and selective ultrasound screening programs.

Methods: For this retrospective cohort study, we collected the number of children <15 years of age who were diagnosed with DDH (International Classification of Diseases, Tenth Revision [ICD-10] codes Q65.0-Q65.6 and Ninth Revision [ICD-9] code 7543) as their primary diagnosis after ≥3 visits to a physician. These data were obtained from the Finnish Care Register for Health Care, which collects the ICD-10 and ICD-9 codes from every medical appointment. We calculated the annual incidence of DDH diagnoses per 1,000 newborns between 2002 and 2021. Late diagnosis of DDH was defined as a finding of DDH in children aged 6 months through <15 years at the initial diagnosis who had undergone treatment under anesthesia (closed reduction and casting or surgery). We also registered the geographic, age, and sex distributions of the DDH diagnoses.

Results: During the 20-year study period, 1,103,269 babies were born (median per year, 57,214 babies; range per year, 45,346 to 60,694 babies). A total of 6,421 children had a diagnosis of DDH (mean per year, 321 children; range per year, 193 to 405 children), with a mean calculated incidence of 5.8 per 1,000 newborns (95% confidence interval [CI], 5.7 to 6.0). Altogether, 120 children aged 6 months through <15 years were treated for DDH, with little annual variation (median, 6.5 children; range, 2 to 9 children). The mean national incidence of late-diagnosed cases was 0.11 per 1,000 newborns (95% CI, 0.09 to 0.13).

Conclusions: Finland's current DDH screening program, which includes universal clinical screening with targeted ultrasound, is noninferior when compared with other screening programs.

Level of evidence: Prognostic Level III . See Instructions for Authors for a complete description of levels of evidence.

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来源期刊
CiteScore
8.90
自引率
7.50%
发文量
660
审稿时长
1 months
期刊介绍: The Journal of Bone & Joint Surgery (JBJS) has been the most valued source of information for orthopaedic surgeons and researchers for over 125 years and is the gold standard in peer-reviewed scientific information in the field. A core journal and essential reading for general as well as specialist orthopaedic surgeons worldwide, The Journal publishes evidence-based research to enhance the quality of care for orthopaedic patients. Standards of excellence and high quality are maintained in everything we do, from the science of the content published to the customer service we provide. JBJS is an independent, non-profit journal.
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