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. 1999 Jan;80(1):67–68. doi: 10.1136/adc.80.1.67

Four key questions that identify severe disability

J Fooks 1
PMCID: PMC1717806  PMID: 10325762

Abstract

BACKGROUND—Six hundred and four surviving children aged 2 years, who had been entered into a neonatal trial of fresh frozen plasma on the incidence of intraventricular haemorrhage, were grouped into four categories of disability based on a review by a full paediatric assessment. A 29 item questionnaire completed by the children's health visitors was used to group the children into the same categories.
AIMS—To explore whether severe disability could be identified by using only a few of the 29questions.
METHOD—The sensitivity and specificity of individual questions were used first to find the subset of questions that best identified children with severe disability. The efficacy of the four most useful questions was tested in a separate cohort of 105 children for whom health visitors had completed questionnaires at the age of 2 years, and who had similarly been assessed by a paediatrician. 
RESULTS—In the original trial cohort, the four questions correctly identified 56 of the 61 children with the most severe disabilities as assessed by the paediatrician, and seven children were falsely identified as being severely disabled. In the second cohort, the four questions correctly identified six of the seven children classified as severely disabled by the paediatrician, with no false positives.
CONCLUSION—If four such questions were included in routine child information systems at age 2 years, it might be possible to obtain useful data on the prevalence of severe disability in children.



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Selected References

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  1. Fooks J., Fritz S., Tin W., Yudkin P., Johnson A., Elbourne D., Hey E. A comparison of two methods of follow-up in a trial of prophylactic volume expansion in preterm babies. Paediatr Perinat Epidemiol. 1998 Apr;12(2):199–216. doi: 10.1046/j.1365-3016.1998.00099.x. [DOI] [PubMed] [Google Scholar]
  2. Johnson A., Goddard O., Ashurst H. Is late walking a marker of morbidity? Steering Committee, Oxford Region Child Development Project. Arch Dis Child. 1990 May;65(5):486–488. doi: 10.1136/adc.65.5.486. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Neligan G., Prudham D. Potential value of four early developmental milestones in screening children for increased risk of later retardation. Dev Med Child Neurol. 1969 Aug;11(4):423–431. doi: 10.1111/j.1469-8749.1969.tb01460.x. [DOI] [PubMed] [Google Scholar]
  4. UK collaborative randomised trial of neonatal extracorporeal membrane oxygenation. UK Collaborative ECMO Trail Group. Lancet. 1996 Jul 13;348(9020):75–82. [PubMed] [Google Scholar]
  5. Zaman S. S., Khan N. Z., Islam S., Banu S., Dixit S., Shrout P., Durkin M. Validity of the 'Ten Questions' for screening serious childhood disability: results from urban Bangladesh. Int J Epidemiol. 1990 Sep;19(3):613–620. doi: 10.1093/ije/19.3.613. [DOI] [PubMed] [Google Scholar]

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