Abstract
Aim: To explore data linkage and pain medication as a proxy for pain, to assess differences in pain medication between the cerebral palsy (CP) and the general populations, and to identify factors associated with pain medication in CP. Method: This cross‐sectional study linked the Northern Ireland CP Register and two administrative health care databases for people resident in Northern Ireland born between 1981 and 2008. Pain medication as a proxy was validated by replicating analyses from the Study of Participation of Children with Cerebral Palsy Living in Europe (SPARCLE) studies. Logistic regression compared pain medication in the CP and general populations. Multi‐level regression models assessed factors associated with pain medication in the CP cohort. Results: The sample size was 701 075, of whom 1430 (0.2%) were people with CP. There were 358 969 males and 340 677 females in the general population, and 810 males and 620 females in the CP population, with an age range of 4 to 31 years in both groups. The validation exercise produced results similar to the SPARCLE studies. More people with CP received pain medication (61% vs 50.9%) and had twice the odds of being prescribed opioid analgesics (odds ratio [OR]=2.81, 95% confidence interval [CI] 2.32–3.40). Among those with CP, the odds of being prescribed pain medication were higher for: females (OR=1.34, 95% CI 1.06–1.70), younger age (OR=1.60, 95% CI 1.02–2.51), Gross Motor Function Classification System level V (OR=2.60, 95% CI 1.52–4.47), seizures (OR=2.55, 95% CI 1.68–3.87), and higher deprivation score (OR=2.06, 95% CI 1.41–3.24). Interpretation: Pain medication is an effective proxy for pain. More people with CP were prescribed pain medication than the general population. Pain medication for people with CP is not only dependent on physiological and clinical characteristics, but also environmental factors. What this paper adds: Data linkage using pain medication as a proxy for experiencing pain is a valid method. People with cerebral palsy (CP) are more likely to experience pain than the general population. People with CP have over twice the odds of receiving opioids compared to the general population. The odds of being prescribed pain medication were higher for females with CP. Prescription of pain medication among those with CP is not only dependent on clinical characteristics, but also environmental factors.
Original language | English |
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Pages (from-to) | 1085-1092 |
Number of pages | 8 |
Journal | Developmental Medicine and Child Neurology |
Volume | 63 |
Issue number | 9 |
Early online date | 31 Mar 2021 |
DOIs | |
Publication status | Published - Sept 2021 |
Bibliographical note
Funding Information:We would like to thank the help provided by the staff of the Honest Broker Service, which is funded by the Business Services Organisation Northern Ireland and the Department of Health. The authors have contributed equally to the work presented here and they alone are responsible for the interpretation of the data; any views or opinions presented are solely those of the authors and do not necessarily represent those of Queen's University of Belfast, Public Health Agency Northern Ireland, the Business Service Organisation, or the Department of Health.
Publisher Copyright:
© 2021 The Authors. Developmental Medicine & Child Neurology published by John Wiley & Sons Ltd on behalf of Mac Keith Press
Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
Keywords
- Pain; Cerebral Palsy; Prescriptions; Children; Data matching
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health
- Developmental Neuroscience
- Clinical Neurology