Canadian surveillance study of complex regional pain syndrome in children
- PMID: 34799536
- PMCID: PMC9100430
- DOI: 10.1097/j.pain.0000000000002482
Canadian surveillance study of complex regional pain syndrome in children
Abstract
This study describes the minimum incidence of pediatric complex regional pain syndrome (CRPS), clinical features, and treatments recommended by pediatricians and pain clinics in Canada. Participants in the Canadian Paediatric Surveillance Program reported new cases of CRPS aged 2 to 18 years monthly and completed a detailed case reporting questionnaire from September 2017 to August 2019. Descriptive analysis was completed, and the annual incidence of CRPS by sex and age groupings was estimated. A total of 198 cases were reported to the Canadian Paediatric Surveillance Program, and 168 (84.8%) met the case definition. The minimum Canadian incidence of CRPS is estimated at 1.14/100,000 (95% confidence interval 0.93-1.35/100,000) children per year. Incidence was highest among girls 12 years and older (3.10, 95% confidence interval 2.76-3.44/100,000). The mean age of CRPS diagnosis was 12.2 years (SD = 2.4), with the mean time from symptom onset to diagnosis of 5.6 months (SD = 9.9) and no known inciting event for 19.6% of cases. Most cases had lower limb involvement (79.8%). Nonsteroidal anti-inflammatory drugs (82.7%) and acetaminophen (66.0%) were prescribed more commonly than antiepileptic drugs (52.3%) and antidepressants (32.0%). Referrals most commonly included physical therapy (83.3%) and multidisciplinary pain clinics (72.6%); a small number of patients withdrew from treatment because of pain exacerbation (5.3%). Pain education was recommended for only 65.6% of cases. Treatment variability highlights the need for empiric data to support treatment of pediatric CRPS and development of treatment consensus guidelines.
Copyright © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the International Association for the Study of Pain.
Conflict of interest statement
K. Baerg reports royalties from Brush Education and serves on the Board of Directors, Saskatchewan Pain Society Inc., outside the submitted work. S. M. Tupper serves as the Chair, Board of Directors, Saskatchewan Pain Society Inc., outside the submitted work. L. M. Chu reports he is a paid employee in the Department of Pediatrics, related to the submitted work. N. Cooke has nothing to disclose. B. D. Dick has nothing to disclose. M.-J. Doré-Bergeron has nothing to disclose. S. Findlay serves as Co-Chair, Ontario Chronic Pain Network, outside the submitted work. P. M. Ingelmo has nothing to disclose. C. Lamontagne has nothing to disclose. G. Mesaroli reports funding from RESTRACOMP Clinician Scientist Training Program and Frederick Banting and Charles Best Canada Graduate Scholarship (CGS-M) from the Canadian Institutes of Health Research (CIHR), outside the submitted work. T. F. Oberlander has nothing to disclose. R. Poolacherla has nothing to disclose. A. O. Spencer has nothing to disclose. J. Stinson has nothing to disclose. G. A. Finley serves on the Executive Board, Canadian Pain Society, outside the submitted work.
References
-
- Abu-Arafeh H, Abu-Arafeh I. Complex regional pain syndrome in children: a systematic review of clinical features and movement disorders. Pain Manag 2017;7:133–40. - PubMed
-
- Abu-Arafeh H, Abu-Arafeh I. Complex regional pain syndrome in children: incidence and clinical characteristics. Arch Dis Child 2016;101:719–23. - PubMed
-
- Agrawal SK, Rittey CD, Harrower NA, Goddard JM, Mordekar SR. Movement disorders associated with complex regional pain syndrome in children. Dev Med Child Neurol 2009;51:557–62. - PubMed
-
- Bayle-Iniguez X, Audouin-Pajot C, Sales de Gauzy J, Munzer C, Murgier J, Accadbled F. Complex regional pain syndrome type I in children. Clinical description and quality of life. Orthop Traumatol Surg Res 2015;101:745–8. - PubMed
-
- Brown S, Johnston B, Amaria K, Watkins J, Campbell F, Pehora C, McGrath P. A randomized controlled trial of amitriptyline versus gabapentin for complex regional pain syndrome type I and neuropathic pain in children. Scand J Pain 2016;13:156–63. - PubMed
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous
