Treatment methods for post-traumatic elbow stiffness caused by heterotopic ossification. Academic Article uri icon

Overview

abstract

  • HYPOTHESIS: Heterotopic ossification (HO) is a common complication of surgically treated elbow fractures that can inhibit range of motion and impair quality of life. Although there are many treatment methods for HO, there is a lack of consensus as to the best option. We hypothesized that contracture release combined with Botox injection would lead to improved functional outcome scores when compared with current treatment methods. METHODS: A retrospective review was conducted of patients who presented to a single surgeon with HO secondary to elbow fracture between 2005 and 2018. A total of 59 patients were identified who met inclusion criteria. Data were classified into 3 groups: contracture release (control - CR), Botox injection with CR (Botox + CR), and radiation therapy with CR (CR + RT). Range of motion measurements were obtained, including flexion, extension, pronation, and supination. RESULTS: A total of 30 patients (30 of 59, 50.8%) received CR, 6 (6 of 59, 9.2%) were treated with CR + RT, and 23 (23 of 59, 40.0%) had CR + Botox. There was a significant difference between pre- and postoperative arc of motion for both CR + RT (P < .01) and CR + Botox (P < .01). In addition, there was a significant difference in pre- and postoperative extension for patients who received intraoperative Botox injections (P < .05). There was no significant difference between pre- and postoperative motion nor extension in the CR group. CONCLUSION: Intraoperative Botox injection with CR is an effective method in the treatment of post-traumatic elbow stiffness caused by HO.

publication date

  • July 1, 2020

Research

keywords

  • Botulinum Toxins, Type A
  • Elbow Joint
  • Fractures, Bone
  • Joint Capsule Release
  • Neuromuscular Agents
  • Ossification, Heterotopic

Identity

Scopus Document Identifier

  • 85086384832

Digital Object Identifier (DOI)

  • 10.1016/j.jse.2020.02.026

PubMed ID

  • 32553438

Additional Document Info

volume

  • 29

issue

  • 7