Delobel-Ayoub Malika, Ehlinger Virginie, Klapouszczak Dana, Troha Gergeli Anja, Sellier Elodie, Hollody Katalin, Virella Daniel, Vik Torstein, Perret Célia, Vidart d'Egurbide Bagazgoïtia Nicolas, Horridge Karen, Arnaud Catherine
Childhood Disability Registry in Haute-Garonne, University Hospital, Toulouse, France.
CERPOP, UMR1295 Toulouse University, Inserm, Paul Sabatier University, Toulouse, France.
Paediatr Perinat Epidemiol. 2025 Mar;39(3):287-298. doi: 10.1111/ppe.13164. Epub 2025 Jan 7.
Postneonatal cerebral palsy (PNCP) is rare and requires large databases to be studied over time.
To study the time trend of prevalence of PNCP overall and by cause, and to describe the clinical characteristics of children with PNCP according to cause and compared with children with pre/peri/neonatal CP (PPNCP).
The Surveillance of Cerebral Palsy in Europe (SCPE) database was used. Primary events (the first known chronological event in the causal chain) were classified according to the SCPE classification (six main and 19 sub-categories). Prevalence trends for children born during 1976-2012 were modelled using multilevel generalised linear models. The clinical characteristics of PNCP and PPNCP cases born after 1998 were reported as proportions.
The prevalence rates of PNCP were 1.76 (95% confidence interval (CI) 1.37, 2.23) and 0.82 per 10,000 live births (95% CI 0.73, 0.92) in children born during 1976-1980 and 2006-2012, respectively. The models showed a 2% annual decline in overall prevalence (prevalence rate multiplied by 0.98 each year) and a 10% decline for infectious causes for every 5-year change. The prevalence rate in children born during 2006-2012 was 0.26 per 10,000 (95% CI 0.21, 0.32) for infectious causes, which remained the most frequent. No trend emerged for other causes. Unilateral spastic CP, associated impairments and severe gross motor dysfunction were more frequent in PNCP than in PPNCP, and PNCP showed predominantly grey matter injury (55.6%). Seventeen percent were born preterm. PNCP differed by cause, with cerebrovascular accidents presenting the least severe and hypoxic causes the most severe forms.
Our study confirms the decrease in the prevalence of PNCP in children born up to 2012, particularly for CP, due to infectious causes, which remain the most frequent. Children with PNCP had more severe presentation overall than those with PPNCP, with severity depending on the cause.
新生儿期后脑性瘫痪(PNCP)较为罕见,需要大量数据库进行长期研究。
研究PNCP总体患病率及按病因分类的患病率随时间的变化趋势,并根据病因描述PNCP患儿的临床特征,并与产前/产时/新生儿期脑瘫(PPNCP)患儿进行比较。
使用欧洲脑瘫监测(SCPE)数据库。主要事件(因果链中第一个已知的按时间顺序排列的事件)根据SCPE分类(6个主要类别和19个子类别)进行分类。使用多级广义线性模型对1976 - 2012年期间出生儿童的患病率趋势进行建模。1998年后出生的PNCP和PPNCP病例的临床特征以比例形式报告。
1976 - 1980年和2006 - 2012年期间出生儿童的PNCP患病率分别为每10000例活产1.76例(95%置信区间(CI)1.37, 2.23)和每10000例活产0.82例(95% CI 0.73, 0.92)。模型显示总体患病率每年下降2%(患病率每年乘以0.98),每5年变化,感染性病因导致的患病率下降10%。2006 - 2012年期间出生儿童中,感染性病因导致的患病率为每10000例0.26例(95% CI 0.21, 0.32),仍是最常见的病因。其他病因未呈现出趋势。PNCP中单侧痉挛性脑瘫、相关损伤和严重粗大运动功能障碍比PPNCP更常见,且PNCP主要表现为灰质损伤(55.6%)。17%为早产。PNCP因病因不同而有所差异,脑血管意外导致的形式最轻,缺氧导致的形式最严重。
我们的研究证实,截至2012年出生儿童中PNCP的患病率有所下降,尤其是因感染性病因导致的脑瘫,感染性病因仍是最常见的。PNCP患儿总体表现比PPNCP患儿更严重,严重程度取决于病因。