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通过新生儿筛查诊断为中链酰基辅酶 A 脱氢酶缺乏症的儿童的卫生服务利用:加拿大安大略省的一项队列研究。

Health services use among children diagnosed with medium-chain acyl-CoA dehydrogenase deficiency through newborn screening: a cohort study in Ontario, Canada.

机构信息

School of Epidemiology and Public Health, Faculty of Medicine, University of Ottawa, 600 Peter Morand Cr, Ottawa, ON, K1G 5Z3, Canada.

Ottawa Hospital Research Institute, University of Ottawa, Ottawa, Canada.

出版信息

Orphanet J Rare Dis. 2019 Mar 22;14(1):70. doi: 10.1186/s13023-019-1001-0.

Abstract

BACKGROUND

We describe early health services utilization for children diagnosed with medium-chain acyl-CoA dehydrogenase (MCAD) deficiency through newborn screening in Ontario, Canada, relative to a screen negative comparison cohort.

METHODS

Eligible children were identified via newborn screening between April 1, 2006 and March 31, 2010. Age-stratified rates of physician encounters, emergency department (ED) visits and inpatient hospitalizations to March 31, 2012 were compared using incidence rate ratios (IRR) and incidence rate differences (IRD). We used negative binomial regression to adjust IRRs for sex, gestational age, birth weight, socioeconomic status and rural/urban residence.

RESULTS

Throughout the first few years of life, children with MCAD deficiency (n = 40) experienced statistically significantly higher rates of physician encounters, ED visits, and hospital stays compared with the screen negative cohort. The highest rates of ED visits and hospitalizations in the MCAD deficiency cohort occurred from 6 months to 2 years of age (ED use: 2.1-2.5 visits per child per year; hospitalization: 0.5-0.6 visits per child per year), after which rates gradually declined.

CONCLUSIONS

This study confirms that young children with MCAD deficiency use health services more frequently than the general population throughout the first few years of life. Rates of service use in this population gradually diminish after 24 months of age.

摘要

背景

我们描述了通过安大略省新生儿筛查诊断为中链酰基辅酶 A 脱氢酶 (MCAD) 缺乏症的儿童在早期的健康服务利用情况,与筛查阴性的对照组进行了比较。

方法

通过 2006 年 4 月 1 日至 2010 年 3 月 31 日之间的新生儿筛查确定符合条件的儿童。使用发病率比率 (IRR) 和发病率差异 (IRD) 比较 2012 年 3 月 31 日前儿童与医生的接触、急诊就诊和住院的年龄分层率。我们使用负二项回归来调整性别、胎龄、出生体重、社会经济地位和农村/城市居住情况对 IRR 的影响。

结果

在生命的头几年,与筛查阴性组相比,患有 MCAD 缺乏症的儿童(n=40)与医生的接触、急诊就诊和住院的比率明显更高。MCAD 缺乏症患儿的 ED 就诊和住院率最高发生在 6 个月至 2 岁(ED 使用:每名儿童每年 2.1-2.5 次就诊;住院:每名儿童每年 0.5-0.6 次就诊),此后逐渐下降。

结论

这项研究证实,在生命的头几年,患有 MCAD 缺乏症的幼儿比一般人群更频繁地使用医疗服务。在 24 个月后,该人群的服务使用率逐渐下降。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/519d/6431026/4a61792ca15b/13023_2019_1001_Fig1_HTML.jpg

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