The impact of heterotopic ossification prophylaxis after surgical fixation of acetabular fractures: national treatment patterns and related outcomes

The PREP-IT Investigators, Executive Committee, Steering Committee, Adjudication Committee, Data and Safety Monitoring Committee, Research Methodology Core, Patient Centred Outcomes Core, Orthopaedic Surgery Core, Operating Room Core, Infectious Disease Core, Military Core, McMaster University Methods Center (Hamilton, ON), University of Maryland School of Medicine Administrative Center (Baltimore, MD), University of Maryland School of Pharmacy, The PATIENTS Program (Baltimore, MD), PREP-IT Clinical Sites, Lead Clinical Site (Aqueous-PREP and PREPARE), University of Maryland School of Medicine, R Adams Cowley Shock Trauma Center, Baltimore, MD, Aqueous-PREP and PREPARE, Hamilton Health Sciences – General Site, Hamilton, ON, Prisma Health - Upstate, Greenville, SCIU Health Methodist Hospital, Indianapolis, IN, San Antonio Military Medical Center, San Antonio, TX, University of California, San Francisco, San Francisco, CA, Aqueous-PREP, Vanderbilt Medical Center, Nashville, TN, University of Florida, Gainesville, FL, McGovern Medical School at UTHealth Houston, Houston, TX, Wright State University, Dayton, OH, Banner University Medical Center – Tucson, Tucson, AZ, The CORE Institute, Phoenix, AZ, Vall d'Hebron University Hospital, Barcelona, Spain, Hospital Universitari Parc Tauli, Barcelona, Spain, PREPARE, FRASER HEALTH AUTHORITY/Royal Columbian Hospital, New Westminster, BC, Inova Fairfax Medical Campus, Falls Church, VA, Wake Forest Baptist Health, Winston-Salem, NC, MetroHealth Medical Center, Cleveland, OH, University of Utah, Salt Lake City, Utah, University of Mississippi Medical Center, Jackson, MS, Sanford Health, Sioux Falls, SD, Dartmouth-Hitchcock Medical Center, Lebanon, NH, Carolinas Medical Center, Atrium Health Musculoskeletal Institute, Charlotte, NC, University of Maryland, Capital Region Health, Largo, MD, University of Wisconsin Madison, Madison, WI, Duke University Hospital, Durham, NC, Brigham Women's Hospital, Boston, MA, University of Pennsylvania, Philadelphia, PA, Massachusetts General Hospital, Boston, MA, Bryan Medical Center, Lincoln, Nebraska, University of Cincinnati, Cincinnati, OH, Cedars-Sinai Medical Center, Los Angeles, CA, University of California, Irvine, Orange, CA

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1 Scopus citations

Abstract

Background: Heterotopic ossification (HO) is a common complication after surgical fixation of acetabular fractures. Numerous strategies have been employed to prevent HO formation, but results are mixed and optimal treatment strategy remains controversial. The purpose of the study was to describe current national heterotopic ossification (HO) prophylaxis patterns among academic trauma centers, determine the association between prophylaxis type and radiographic HO, and identify if heterogeneity in treatment effects exist based on outcome risk strata. Methods: We used data from a subset of participants enrolled in the Pragmatic Randomized Trial Evaluating Pre-Operative Alcohol Skin Solutions in Fractured Extremities (PREPARE) trial. We included only patients with closed AO-type 62 acetabular fractures that were surgically treated via a posterior (Kocher-Langenbeck), combined anterior and posterior, or extensile exposure. PREPARE Clinical Trial Registration Number: NCT03523962 Patient population This cohort study was nested within the Pragmatic Randomized Trial Evaluating Pre-Operative Alcohol Skin Solutions in Fractured Extremities (PREPARE) trial. The PREPARE trial is a multicenter cluster-randomized crossover trial evaluating the effectiveness of two alcohol-based pre-operative antiseptic skin solutions. All PREPARE trial clinical centers that enrolled at least one patient with a closed AO-type 62 acetabular fracture were invited to participate in the nested study. Results: 277 patients from 20 level 1 and level 2 trauma centers in the U.S. and Canada were included in this study. 32 patients (12%) received indomethacin prophylaxis, 100 patients (36%) received XRT prophylaxis, and 145 patients (52%) received no prophylaxis. Administration of XRT was associated with a 68% reduction in the adjusted odds of overall HO (OR 0.32, 95% CI, 0.14 – 0.69, p = 0.005). The overall severe HO (Brooker classes III or IV) rate was 8% for the entire cohort; XRT reduced the rate of severe HO in high-risk patients only (p=0.03). Conclusion: HO prophylaxis patterns after surgical fixation of acetabular fractures have changed dramatically over the last two decades. Most centers included in this study did not administer HO prophylaxis. XRT was associated with a marked reduction in the rate of overall HO and the rate of severe HO in high-risk patients. Randomized trials are needed to fully elucidate the potential benefit of XRT. PREPARE Clinical Trial Registration Number: NCT03523962.

Original languageEnglish
Pages (from-to)1693-1701
Number of pages9
JournalInjury
Volume54
Issue number6
DOIs
StatePublished - Jun 2023

Keywords

  • Acetabular fractures
  • Heterotopic ossification
  • Indomethacin prophylaxis
  • XRT prophylaxis

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