4.7 Article

Identification of Risk Factors in the Development of Heterotopic Ossification After Primary Total Hip Arthroplasty

期刊

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
卷 107, 期 9, 页码 E3944-E3952

出版社

ENDOCRINE SOC
DOI: 10.1210/clinem/dgac249

关键词

heterotopic ossification; hip surgery; hip arthroplasty; prophylaxis

资金

  1. National Institutes of Health [R01AR073015, T32DK007418]
  2. UCSF Department of Medicine
  3. National Center for Advancing Translational Sciences, National Institutes of Health, through UCSF-CTSI [KL2 TR001870]
  4. Zuckerberg San Francisco General Hospital Department of Medicine

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This study investigated the risk factors for heterotopic ossification (HO) after hip arthroplasty. The results showed that patients with underlying osteoporosis, vitamin D deficiency, spine disease, diabetes, amenorrhea, postmenopausal status, parathyroid disorders, and history of pathologic fracture were more likely to develop HO. Black/African American race, osteoporosis, spine disease, and low estrogen states were identified as significant predictors for HO development. Perioperative nonsteroidal anti-inflammatory drug (NSAID) treatment was negatively correlated with HO formation. These findings suggest that certain patient populations may benefit from HO prophylaxis, such as perioperative NSAIDs.
Purpose: Heterotopic ossification (HO) is a process by which bone forms abnormally in soft tissues. Known risk factors for developing HO include male sex, spinal cord injury, trauma, and surgery. We investigated additional risk factors in the development of HO after hip arthroplasty. Methods: We performed a retrospective review of electronic medical records of 4070 individuals who underwent hip arthroplasty from September 2010 to October 2019 at the University of California, San Francisco Hospital. Demographics, anthropometrics, medications, and comorbid conditions were used in logistic regression analysis to identify factors associated with the development of HO. Results: A total of 2541 patients underwent primary hip arthroplasty in the analyzed timeframe (46.04% men, mean age at procedure: 62.13 +/- 13.29 years). The incidence of postsurgical HO was 3% (n = 80). A larger proportion of individuals who developed HO had underlying osteoporosis (P < 0.001), vitamin D deficiency (P < 0.001), spine disease (P < 0.001), type 1 or 2 diabetes (P < 0.001), amenorrhea (P = 0.037), postmenopausal status (P < 0.001), parathyroid disorders (P = 0.011), and history of pathologic fracture (P = 0.005). Significant predictors for HO development were Black/African American race [odds ratio (OR) 2.97 P= 0.005], preexisting osteoporosis (OR 2.72, P= 0.001), spine disease (OR 2.04, P= 0.036), and low estrogen states (OR 1.99, P= 0.025). In the overall group, 75.64% received perioperative nonsteroidal anti-inflammatory drugs (NSAIDs), which negatively correlated with HO formation (OR 0.39, P = 0.001). Conclusions: We identified new factors potentially associated with an increased risk of developing HO after primary hip arthroplasty, including African American race, osteoporosis, and low estrogen states.These patients may benefit from HO prophylaxis, such as perioperative NSAIDs.

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