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Updated: Nov 4, 2025

Direct Mouse Trauma/Burn Model of Heterotopic Ossification
Published on: August 6, 2015
Primary Versus Secondary Radiotherapy for Heterotopic Ossification Prevention About the Elbow
Joseph S Geller1, Paul R Allegra2, Crystal S Seldon3
1University of Miami Miller School of Medicine, Miami, FL; and.
Objectives:
To examine the efficacy and safety of radiotherapy for the prevention of heterotopic ossification (HO) about the elbow.
Design:
Retrospective chart review.
Setting:
Level 1 trauma center.
Patients/Participants:
Two hundred and twenty-nine patients who received prophylactic radiotherapy (XRT) over a 15-year period were identified. Patients were included if they received XRT to the elbow joint and had at least 12 weeks of follow-up after XRT. Fifty-four patients were ultimately included.
Intervention:
All patients were treated with a single dose of 7 Gy. Ninety-eight percentage of patients received XRT within 24 hours after surgery, and all patients received XRT within 72 hours after surgery.
Main Outcomes Measurements:
The primary study measures evaluated were the presence or absence of clinically symptomatic HO and the presence of radiographic HO after XRT to the elbow joint.
Results:
Eighteen patients were treated with XRT after a traumatic injury requiring surgery (primary prophylaxis), and 36 were treated with XRT after excision surgery to remove HO which had already formed (secondary prophylaxis). In the primary cohort, 16.7% developed symptomatic HO after XRT and 11.1% required surgery to resect the heterotopic bone. In the secondary cohort, 11.1% developed symptomatic HO after surgery and XRT and 5.5% required resection surgery. No secondary malignancies were identified.
Conclusions:
Our findings suggest that XRT for elbow HO may be safe and effective for both primary and secondary HO. XRT for HO was not shown to be associated with radiation-induced sarcoma in this series, at least in the short term. Further study in a large patient population with extended follow-up is required to better characterize populations at high risk for development of HO and secondary malignancy.
Level Of Evidence:
Prognostic Level III. See Instructions for Authors for a complete description of levels of evidence.

