澳大利亚的大脑性麻痹:1995-2016 年的出生率以及居住地偏远程度的差异:一项基于人口的登记研究。

IF 6.7 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Hayley Smithers-Sheedy, Emma Waight, Shona Goldsmith, Sue Reid, Catherine Gibson, Heather Scott, Linda Watson, Megan Auld, Fiona Kay, Clare Wiltshire, Gina Hinwood, Annabel Webb, Tanya Martin, Nadia Badawi, Sarah McIntyre, the ACPR Group
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引用次数: 0

摘要

研究目的考察澳大利亚脑瘫出生率的最新变化;根据居住地的偏远程度考察脑瘫儿童的功能活动能力:基于人口的登记研究;澳大利亚脑瘫登记(ACPR)数据分析:主要结果测量指标:出生时脑瘫患病率的变化:主要结果测量指标:出生时脑瘫患病率的变化,出生前或围产期(子宫内至出生后第28天)脑瘫患病率的变化,包括总体患病率和按胎龄组(小于28周、28-31周、32-36周、37周或以上)划分的患病率,以及新生儿出生后(第29天至两岁)脑瘫患病率的变化;按居住地偏远程度划分的粗大运动功能分类:1995-2016年期间出生的10 855名脑瘫患儿的数据,其中6258名为男孩(57.7%)。在有完整病例确认的三个州(南澳大利亚州、维多利亚州和西澳大利亚州),脑瘫的出生流行率从1995-1996年的每千名活产婴儿2.1例(95%置信区间[CI],1.9-2.4)下降到2015-2016年的每千名活产婴儿1.5例(95%置信区间,1.3-1.7)。出生前或围产期获得性脑瘫的出生流行率从每1000例活产中2.0例(95% CI,1.7-2.3)下降到1.4例(95% CI,1.2-1.6);除32-36周外,所有孕周的出生流行率均出现了统计学意义上的显著下降。新生儿出生后获得性脑瘫的发病率从每 1000 例活产中 0.15 例(95% CI,0.11-0.21 例)下降到 0.08 例(95% CI,0.05-0.12 例),但没有统计学意义。总体而言,3.4%的脑瘫儿童(307名儿童)生活在偏远或非常偏远的地区,这一比例高于所有澳大利亚人(2.0%);这些地区需要轮椅代步的儿童比例(31.3%)高于大城市或地区的脑瘫儿童比例(各为26.1%):结论:1995-2016年间,澳大利亚的脑瘫出生率明显下降,这反映了孕产妇和围产期护理进步所带来的影响。我们的研究结果突出表明,有必要在澳大利亚全国范围内为妇女提供公平、文化安全的产前服务,并为脑瘫患者提供健康和残疾服务。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cerebral palsy in Australia: birth prevalence, 1995–2016, and differences by residential remoteness: a population-based register study

Cerebral palsy in Australia: birth prevalence, 1995–2016, and differences by residential remoteness: a population-based register study

Objective

To examine recent changes in the birth prevalence of cerebral palsy in Australia; to examine the functional mobility of children with cerebral palsy by residential remoteness.

Study design

Population-based register study; analysis of Australian Cerebral Palsy Register (ACPR) data.

Setting, participants

Children with cerebral palsy born in Australia, 1995–2016, and included in the ACPR at the time of the most recent state/territory data provision (31 July 2022).

Main outcome measures

Change in birth prevalence of cerebral palsy, of cerebral palsy acquired pre- or perinatally (in utero to day 28 after birth), both overall and by gestational age group (less than 28, 28–31, 32–36, 37 or more weeks), and of cerebral palsy acquired post-neonatally (day 29 to two years of age); gross motor function classification by residential remoteness.

Results

Data for 10 855 children with cerebral palsy born during 1995–2016 were available, 6258 of whom were boys (57.7%). The birth prevalence of cerebral palsy in the three states with complete case ascertainment (South Australia, Victoria, Western Australia) declined from 2.1 (95% confidence interval [CI], 1.9–2.4) cases per 1000 live births in 1995–1996 to 1.5 (95% CI, 1.3–1.7) cases per 1000 live births in 2015–2016. The birth prevalence of pre- or perinatally acquired cerebral palsy declined from 2.0 (95% CI, 1.7–2.3) to 1.4 (95% CI, 1.2–1.6) cases per 1000 live births; statistically significant declines were noted for all gestational ages except 32–36 weeks. The decline in birth prevalence of post-neonatally acquired cerebral palsy, from 0.15 (95% CI, 0.11–0.21) to 0.08 (95% CI, 0.05–0.12) cases per 1000 live births, was not statistically significant. Overall, 3.4% of children with cerebral palsy (307 children) lived in remote or very remote areas, a larger proportion than for all Australians (2.0%); the proportion of children in these areas who required wheelchairs for mobility was larger (31.3%) than that of children with cerebral palsy in major cities or regional areas (each 26.1%).

Conclusions

The birth prevalence of cerebral palsy declined markedly in Australia during 1995–2016, reflecting the effects of advances in maternal and perinatal care. Our findings highlight the need to provide equitable, culturally safe access to antenatal services for women, and to health and disability services for people with cerebral palsy, across Australia.

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来源期刊
Medical Journal of Australia
Medical Journal of Australia 医学-医学:内科
CiteScore
9.40
自引率
5.30%
发文量
410
审稿时长
3-8 weeks
期刊介绍: The Medical Journal of Australia (MJA) stands as Australia's foremost general medical journal, leading the dissemination of high-quality research and commentary to shape health policy and influence medical practices within the country. Under the leadership of Professor Virginia Barbour, the expert editorial team at MJA is dedicated to providing authors with a constructive and collaborative peer-review and publication process. Established in 1914, the MJA has evolved into a modern journal that upholds its founding values, maintaining a commitment to supporting the medical profession by delivering high-quality and pertinent information essential to medical practice.
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