The impact of body mass index on heterotopic ossification
- Waleed Fouad Mourad(corresponding author),
- Satya Packianathan,
- Rania A. Shourbaji,
- Zhen Zhang,
- Mathew Graves,
- Majid A. Khan
- Yeshiva University,
- University of Mississippi,
- Continuum Health Partners, Inc.,
- Jackson State University
Sustainable Development Goals
- SDG 3 Good Health and Well
Abstract
Purpose: To analyze the impact of different body mass index (BMI) as a surrogate marker for heterotopic ossification (HO) in patients who underwent surgical repair (SR) for displaced acetabular fractures (DAF) followed by radiation therapy (RT). Methods and Materials: This is a single-institution retrospective study of 395 patients. All patients underwent SR for DAF followed by RT ± indomethacin. All patients received postoperative RT, 7 Gy, within 72 h. The patients were separated into four groups based on their BMI: <18.5, 18.5-24.9, 25-29.9, and >30. The end point of this study was to evaluate the efficacy of RT ± indomethacin in preventing HO in patients with different BMI. Results: Analysis of BMI showed an increasing incidence of HO with increasing BMI: <18.5, (0%) 0/6 patients; 18.5-24.9 (6%), 6 of 105 patients developed HO; 25-29.9 (19%), 22 of 117; >30 (31%), 51 of 167. Chi-square and multivariate logistic regression analysis showed that the correlation between odds of HO and BMI is significant, p < 0.0001. As the BMI increased, the risk of HO and Brooker Classes 3, 4 HO increased. The risk of developing HO is 1.0× (10%) more likely among those with higher BMI compared with those with lower BMI. For a one-unit increase in BMI the log odds of HO increases by 1.0, 95% CI (1.06-1.14). Chi-square test shows no significant difference among all other factors and HO (e.g., indomethacin, race, gender). Conclusions: Despite similar surgical treatment and prophylactic measures (RT ± indomethacin), the risk of HO appears to significantly increase in patients with higher BMI after DAF. Higher single-fraction doses or multiple fractions and/or combination therapy with nonsteroidal inflammatory drugs may be of greater benefit to these patients.
Publication Information
Output type
Original language
English (US)Pages from-to (Number of pages)
Pages e831-e836Journal (Volume, Issue Number)
International Journal of Radiation Oncology Biology Physics (Volume 82, Issue 5)Publication milestones
- Published - 04/01/2012
Publication status
ISSN
0360-3016Publication IDs
- Scopus: 84862808518
- PubMed: 22365623
