澳大利亚Treacher Collins综合征住院总人口数描述

Mohammed Junaid, Linda Slack-Smith, Kingsley Wong, Gareth Baynam, Hanny Calache, Timothy Hewitt, Helen Leonard
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引用次数: 4

摘要

目的:描述澳大利亚诊断为Treacher Collins综合征(TCS)的总体住院模式和人口统计学特征。数据来源:主要诊断为TCS (ICD10-AM-Q87.04)的住院病人(公立和私立)的人口汇总数据(ICD10-AM-Q87.04)来自澳大利亚卫生和福利研究所国家医院发病率数据库,为期11年(2002-2013年)。主要结局指标:主要结局指标是医院分离率(HSR),通过每年医院分离次数除以估计的常住人口来计算。经年龄和性别调整后的高铁发病率趋势采用负二项回归表示为年变化百分比,与年龄和性别的相关性表示为发病率比。结果:在确定的244例入院患者中,我们观察到在11年期间高铁发生率增加了4.55%(95%置信区间[CI] -1.78, 11.29)。婴儿期发生率较高(1.87 [95% CI 1.42, 2.42]),随着年龄的增长显著下降。每次发作的平均住院时间为6.09天(95% CI 5.78, 6.40),但女性和婴儿的住院时间更长。结论:研究结果表明住院率增加,特别是在婴儿和女性中,这可能与早期气道干预程序有关,可能受性别特异性疾病严重程度和TCS表型变异性的影响。对TCS表型的认识和基因检测的改善可能会支持更个性化和更有效的护理。总人口管理数据为更好地了解罕见颅面疾病的健康负担提供了潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Description of Total Population Hospital Admissions for Treacher Collins Syndrome in Australia.

Objective: To describe patterns and demographic characteristics of total-population hospital admissions with a diagnosis of Treacher Collins syndrome (TCS) in Australia.

Data source: Population summary data for inpatient hospitals admissions (public and private) with a principal diagnosis of TCS (ICD10-AM-Q87.04) were obtained from the Australian Institute of Health and Welfare National Hospital Morbidity Database for a 11-year period (2002-2013).

Main outcome measures: The primary outcome was hospital separation rate (HSR), calculated by dividing the number of hospital separations by estimated resident population per year. Trends in HSR s adjusted for age and sex were investigated by negative binomial regression presented as annual percent change and the association of rates with age and sex was expressed as incidence rate ratio.

Results: In 244 admissions identified, we observed an increase of 4.55% (95% confidence interval [CI] -1.78, 11.29) in HSR's over the 11-year period. Rates were higher during infancy (1.87 [95% CI 1.42, 2.42]), declining markedly with increasing age. The average length of hospital stay was 6.09 days (95% CI 5.78, 6.40) per episode, but longer for females and infants.

Conclusions: Findings indicate an increase in hospitalization rates, especially among infants and females which potentially relates to early airway intervention procedures possibly influenced by sex specific-disease severity and phenotypic variability of TCS. Awareness of the TCS phenotype and improved access to genetic testing may support more personalized and efficient care. Total-population administrative data offers a potential to better understand the health burden of rare craniofacial diseases.

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