Evidence map›Paper›PMID 39775879›Full record

ArticlePaediatric and perinatal epidemiology2025

Postneonatal Cerebral Palsy in Europe: Prevalence and Clinical Characteristics According to Contributory Events: An SCPE Study.

Malika Delobel-Ayoub, Virginie Ehlinger, Dana Klapouszczak, Anja Troha Gergeli, Elodie Sellier, Katalin Hollody, Daniel Virella, Torstein Vik, Célia Perret, Nicolas Vidart d'Egurbide Bagazgoïtia and 2 more

Abstract read
In one paragraph

Article in Paediatric and perinatal epidemiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Malika Delobel-AyoubChildhood Disability Registry in Haute-Garonne, University Hospital, Toulouse, France.ORCID https://orcid.org/0000-0002-0090-8313
Virginie EhlingerChildhood Disability Registry in Haute-Garonne, University Hospital, Toulouse, France.
Dana KlapouszczakChildhood Disability Registry in Haute-Garonne, University Hospital, Toulouse, France.
Anja Troha GergeliDepartment of Child, Adolescent & Developmental Neurology, University Children's Hospital Ljubljana, Ljubljana, Slovenia.
Elodie SellierGrenoble Alpes University, CNRS, Grenoble INP, CHU Grenoble Alpes, TIMC-IMAG, Grenoble, France.
Katalin HollodyDepartment of Paediatrics, University of Pecs, Medical School, Pecs, Hungary.
Daniel VirellaNeonatology Intensive Care Unit/Research Centre, Central Lisbon Hospital, Lisbon, Portugal.
Torstein VikThe Norwegian University of Science and Technology, NTNU, Trondheim, Norway.
Célia PerretCERPOP, UMR1295 Toulouse University, Inserm, Paul Sabatier University, Toulouse, France.
Nicolas Vidart d'Egurbide BagazgoïtiaCERPOP, UMR1295 Toulouse University, Inserm, Paul Sabatier University, Toulouse, France.
Karen HorridgeDepartment of Education, University of Sunderland, Sunderland, UK.
Catherine ArnaudChildhood Disability Registry in Haute-Garonne, University Hospital, Toulouse, France.ORCID https://orcid.org/0000-0002-4002-802X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPostneonatal cerebral palsy (PNCP) is rare and requires large databases to be studied over time.

objectivesTo 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).

methodsThe 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.

resultsThe 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.

conclusionOur 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.

Indexed as

Cerebral PalsyChild, PreschoolEuropeFemaleHumansInfantInfant, NewbornMalePrevalenceaetiologyclassificationcomplicationsepidemiologypostneonatal cerebral palsy

Identifiers

PMID39775879
PMCPMC11997238

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.