{"title":"Orthopedic surgery after selective dorsal rhizotomy in children with cerebral palsy: A matched cohort study.","authors":"Michael H Schwartz, Andrew G Georgiadis","doi":"10.1111/dmcn.16425","DOIUrl":null,"url":null,"abstract":"<p><strong>Aim: </strong>To test whether selective dorsal rhizotomy (SDR) changes the incidence of subsequent orthopedic surgery in children with cerebral palsy.</p><p><strong>Method: </strong>This was a matched cohort study. Using historical data from a single center, we identified two groups of individuals based on their history of SDR (yes-SDR and no-SDR), matched at baseline on key clinical variables. We defined 10 orthopedic surgery categories that accounted for more than 95% of surgery recorded in our gait center database. We then fitted Kaplan-Meier estimates of cumulative incidence for each surgery, stratified according to SDR status.</p><p><strong>Results: </strong>We obtained excellent comprehensive baseline matching. Foot and ankle bone surgery and femoral derotation osteotomy exhibited 15% to 20% higher cumulative incidence after SDR. Rectus femoris transfer exhibited approximately 30% lower cumulative incidence after SDR. The remaining surgeries, including all surgeries for treating muscle contractures, were unaffected by SDR, exhibiting only small (<15%) or nonsignificant (p > 0.05, log-rank test) differences in cumulative incidence.</p><p><strong>Interpretation: </strong>SDR does not consistently lower the cumulative incidence of orthopedic surgery and does not lower the rate of surgery for muscle contracture. The mechanisms through which SDR influences subsequent surgery remain unclear, highlighting a critical area for future research.</p>","PeriodicalId":50587,"journal":{"name":"Developmental Medicine and Child Neurology","volume":" ","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2025-07-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Developmental Medicine and Child Neurology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/dmcn.16425","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Aim: To test whether selective dorsal rhizotomy (SDR) changes the incidence of subsequent orthopedic surgery in children with cerebral palsy.
Method: This was a matched cohort study. Using historical data from a single center, we identified two groups of individuals based on their history of SDR (yes-SDR and no-SDR), matched at baseline on key clinical variables. We defined 10 orthopedic surgery categories that accounted for more than 95% of surgery recorded in our gait center database. We then fitted Kaplan-Meier estimates of cumulative incidence for each surgery, stratified according to SDR status.
Results: We obtained excellent comprehensive baseline matching. Foot and ankle bone surgery and femoral derotation osteotomy exhibited 15% to 20% higher cumulative incidence after SDR. Rectus femoris transfer exhibited approximately 30% lower cumulative incidence after SDR. The remaining surgeries, including all surgeries for treating muscle contractures, were unaffected by SDR, exhibiting only small (<15%) or nonsignificant (p > 0.05, log-rank test) differences in cumulative incidence.
Interpretation: SDR does not consistently lower the cumulative incidence of orthopedic surgery and does not lower the rate of surgery for muscle contracture. The mechanisms through which SDR influences subsequent surgery remain unclear, highlighting a critical area for future research.
期刊介绍:
Wiley-Blackwell is pleased to publish Developmental Medicine & Child Neurology (DMCN), a Mac Keith Press publication and official journal of the American Academy for Cerebral Palsy and Developmental Medicine (AACPDM) and the British Paediatric Neurology Association (BPNA).
For over 50 years, DMCN has defined the field of paediatric neurology and neurodisability and is one of the world’s leading journals in the whole field of paediatrics. DMCN disseminates a range of information worldwide to improve the lives of disabled children and their families. The high quality of published articles is maintained by expert review, including independent statistical assessment, before acceptance.