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澳大利亚脑瘫:1995-2016 年的出生率、居住偏远程度的差异:一项基于人群的登记研究。

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

机构信息

Cerebral Palsy Alliance Research Institute, the University of Sydney, Sydney, NSW.

Murdoch Children's Research Institute, the Royal Children's Hospital, Melbourne, VIC.

出版信息

Med J Aust. 2024 Nov 18;221(10):533-539. doi: 10.5694/mja2.52487. Epub 2024 Oct 30.

Abstract

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.

摘要

目的

研究澳大利亚脑瘫发病率的近期变化;根据居住偏远程度,研究脑瘫儿童的功能性移动能力。

研究设计

基于人群的登记研究;对澳大利亚脑瘫登记处(ACPR)数据进行分析。

地点、参与者:1995 年至 2016 年在澳大利亚出生、并在最近一次州/地区数据提供(2022 年 7 月 31 日)时被纳入 ACPR 的脑瘫儿童。

主要观察指标

脑瘫的发病率变化,包括产前或围产期获得的脑瘫(宫内至出生后 28 天),以及整体发病率和按胎龄组(不足 28 周、28-31 周、32-36 周、37 周或以上)的发病率,以及新生儿后期获得的脑瘫(出生后 29 天至 2 岁);根据居住偏远程度的总体运动功能分类。

结果

共有 10855 名 1995-2016 年出生的脑瘫儿童的数据可用,其中 6258 名为男孩(57.7%)。在三个完全确定病例的州(南澳大利亚州、维多利亚州、西澳大利亚州),脑瘫的发病率从 1995-1996 年的每 1000 例活产 2.1(95%置信区间[CI],1.9-2.4)例降至 2015-2016 年的每 1000 例活产 1.5(95%CI,1.3-1.7)例。产前或围产期获得的脑瘫的发病率从每 1000 例活产 2.0(95%CI,1.7-2.3)例降至 1.4(95%CI,1.2-1.6)例;除 32-36 周外,所有胎龄组的发病率均显著下降。新生儿后期获得的脑瘫的发病率从每 1000 例活产 0.15(95%CI,0.11-0.21)例降至 0.08(95%CI,0.05-0.12)例,但无统计学意义。总体而言,3.4%(307 名)脑瘫儿童生活在偏远或非常偏远地区,这一比例高于所有澳大利亚人(2.0%);这些地区需要轮椅移动的儿童比例(31.3%)高于主要城市或地区(各 26.1%)的脑瘫儿童。

结论

1995-2016 年期间,澳大利亚脑瘫的发病率显著下降,反映了孕产妇和围产期护理的进步的影响。我们的研究结果强调了在澳大利亚为妇女提供公平、文化安全的产前服务以及为脑瘫患者提供卫生和残疾服务的必要性。

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