Blair Eve, Langdon Katherine, McIntyre Sarah, Lawrence David, Watson Linda
Telethon Kids Institute, PO Box 855, West Perth, 6872, WA, Australia.
University of Western Australia, Crawley, 6009, WA, Australia.
BMC Neurol. 2019 Jun 4;19(1):111. doi: 10.1186/s12883-019-1343-1.
Likely duration of survival of children described as having cerebral palsy is of considerable interest to individuals with cerebral palsy, their families, carers, health professionals, health economists and insurers. The aim of this paper is to describe patterns of survival and mortality to the sixth decade in a geographically defined population of people with cerebral palsy stratified according to the clinical description of their impairments in early childhood.
Identifiers of persons born in Western Australia 1956-2011, registered with cerebral palsy on the Western Australian Register of Developmental Anomalies and surviving at least 12 months, were linked to the Australian National Death Index in December 2014. Patterns of mortality were investigated using survival analysis methods.
Of 3185 eligible persons, 436 (13.7%) had died. Of that sample the 22% with the mildest impairment had survival patterns similar to the general population. Mortality increased with increasing severity of impairment. Of 349 (75%) with available cause of death data, 58.6% were attributed to respiratory causes, including 171 (49%) to pneumonia at a mean age of 14.6 (sd 13.4) years of which 77 (45%) were attributed to aspiration. For the most severely impaired, early childhood mortality increased in succeeding decades of birth cohorts from 1950s to 1990 with 20% dying by 4 years of age in the 1981-1990 birth cohort; it then decreased for subsequent birth cohorts, 20% mortality not being attained until 15 years of age. However by 20 years of age mortality of the most severely impaired born in the 1991-2000 birth cohort exceeded that of all other birth cohorts. Remaining life expectancies by age to 50 years have been estimated for two strata with more severe impairments.
For 22% of individuals with cerebral palsy with mild impairment survival to 58 years is similar to that of the general population. Since 1990 mortality for those with severe cerebral palsy in Western Australia has tended to shift from childhood to early adulthood.
脑瘫患儿的可能存活时长是脑瘫患者本人、其家人、护理人员、健康专家、卫生经济学家及保险公司相当关注的问题。本文旨在描述在一个按童年早期损伤临床描述分层的、地理区域界定明确的脑瘫患者群体中,至第六个十年的存活和死亡模式。
1956年至2011年在西澳大利亚出生、在西澳大利亚发育异常登记处登记为脑瘫且存活至少12个月的人员标识符,于2014年12月与澳大利亚国家死亡指数相链接。使用生存分析方法调查死亡模式。
在3185名符合条件的人员中,436人(13.7%)已经死亡。在该样本中,损伤最轻微的22%的人员的存活模式与普通人群相似。死亡率随损伤严重程度的增加而上升。在有死亡原因数据的349人(75%)中,58.6%归因于呼吸原因,其中包括因肺炎导致的171人(49%),平均年龄为14.6岁(标准差13.4),其中77人(45%)归因于误吸。对于损伤最严重的患者,从20世纪50年代到90年代出生队列的后续几十年中,幼儿死亡率上升,在1981年至1990年出生队列中,20%的患者在4岁前死亡;随后出生队列的死亡率下降,直到15岁才达到20%的死亡率。然而,到20岁时,1991年至2000年出生队列中损伤最严重的患者的死亡率超过了所有其他出生队列。已针对两个损伤更严重的分层估计了至50岁的剩余预期寿命。
22%的轻度损伤脑瘫患者存活至58岁,与普通人群相似。自1990年以来,西澳大利亚严重脑瘫患者的死亡率倾向于从儿童期转移到成年早期。