4.5 Article

Global prevalence of cerebral palsy: A systematic analysis

期刊

DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
卷 64, 期 12, 页码 1494-1506

出版社

WILEY
DOI: 10.1111/dmcn.15346

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资金

  1. Cerebral Palsy Alliance, Australia
  2. Public Health Agency Northern Ireland
  3. South-Eastern Norway Regional Health Authority
  4. Public Health Agency France
  5. National Institute of Health and Medical Research

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The study determined trends and estimates of cerebral palsy prevalence in different regions and globally through systematic analysis and meta-analyses. Birth prevalence of CP declined significantly in Europe and Australia while data from low- and middle-income countries indicated higher prevalence rates.
Aim To determine trends and current estimates in regional and global prevalence of cerebral palsy (CP). Method A systematic analysis of data from participating CP registers/surveillance systems and population-based prevalence studies (from birth year 1995) was performed. Quality and risk of bias were assessed for both data sources. Analyses were conducted for pre-/perinatal, postnatal, neonatal, and overall CP. For each region, trends were statistically classified as increasing, decreasing, heterogeneous, or no change, and most recent prevalence estimates with 95% confidence intervals (CI) were calculated. Meta-analyses were conducted to determine current birth prevalence estimates (from birth year 2010). Results Forty-one regions from 27 countries across five continents were represented. Pre-/perinatal birth prevalence declined significantly across Europe and Australia (11 out of 14 regions), with no change in postneonatal CP. From the limited but increasing data available from regions in low- and middle-income countries (LMICs), birth prevalence for pre-/perinatal CP was as high as 3.4 per 1000 (95% CI 3.0-3.9) live births. Following meta-analyses, birth prevalence for pre-/perinatal CP in regions from high-income countries (HICs) was 1.5 per 1000 (95% CI 1.4-1.6) live births, and 1.6 per 1000 (95% CI 1.5-1.7) live births when postneonatal CP was included. Interpretation The birth prevalence estimate of CP in HICs declined to 1.6 per 1000 live births. Data available from LMICs indicated markedly higher birth prevalence.

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