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Title:
The Effect of Human Growth Hormone Treatment on the Development of Slipped Capital Femoral Epiphysis: A Cohort Analysis With 6 Years of Follow-up
Author:
Mittal, Mehul BBA; Momtaz, David BS, MPH; Gonuguntla, Rishi BA; Singh, Aaron BA; Dave, Dhyan BS; Mohseni, Mahshid MD; Torres-Izquierdo, Beltran MD; Schaibley, Claire BS; Hosseinzadeh, Pooya MD
Journal:
Journal of Pediatric Orthopaedics
Date:
April 2024
Reference:
44(4):p e344-e350, DOI: 10.1097/BPO.0000000000002618
Level Of Evidence:
III
# of Patients:
HGH cohort: 36,791 patients under 18 years receiving HGH therapy
Control group: Matched 1:1 cohort of patients not receiving HGH therapy
Study Type:
Therapeutic retrospective cohort study
Location:
Multicenter database analysis using the TriNetX research database
Summary:
This study investigated the association between human growth hormone (HGH) therapy and the risk of developing slipped capital femoral epiphysis (SCFE) in children. Using a large dataset and propensity score matching, the researchers analyzed the incidence of SCFE in children receiving HGH therapy compared to those who did not receive it.
Methods:
Retrospective review of patient records from January 2003 to December 2022. Propensity score matching was employed to compare HGH and no-HGH cohorts. SCFE development was identified using International Classification of Diseases (ICD) codes. Risk ratios (RR) and hazard ratios were calculated to evaluate associations.
Exclusions:
Not specified
Results:
HGH cohort showed a significantly increased risk of SCFE compared to the no-HGH cohort (RR: 3.5, 95% CI: 2.073, 5.909, P<0.001). Patients with >10 HGH prescriptions had a higher risk of SCFE than those with ≤10 prescriptions (RR: 1.914, 95% CI: 1.160, 3.159, P=0.010). Increased hazard of SCFE development was identified with HGH therapy (hazard ratio: 2.627, 95% CI: 1.555, 4.437, P<0.001).
Conclusions:
This study provides robust evidence that HGH therapy is associated with an increased risk of SCFE in children, with a dose-dependent relationship. Enhanced monitoring for SCFE should be considered in patients receiving HGH therapy.
Relevance:
Limitations:
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