Size and location of posterior wall fragment on CT can predict hip instability in a cadaveric model

Theerachai Apivatthakakul1, Jason L Koerner2, Sutiwat Luangsod3

  • 1Department of Orthopaedics, Faculty of Medicine, Chiang Mai University, Thailand; Excellence Center in Osteology Research and Training Center, Chiang Mai University.

Injury
|April 1, 2021
PubMed

Insights

Posterior wall acetabular fractures with fragment sizes of 20% and 25% were unstable at a 40° fracture angle. Even a 15% fragment size became unstable at a 60° fracture angle, indicating fragment size and angle impact hip stability.

Area of Science:

  • Orthopedic surgery
  • Biomechanics
  • Trauma research

Background:

  • Hip instability is a complication of posterior wall acetabular fractures.
  • Predicting instability is crucial for surgical planning and patient outcomes.
  • Previous research has not fully identified factors influencing hip stability in these fractures.

Purpose of the Study:

  • To determine the influence of posterior wall fracture fragment size (FS) and fracture angle (FA) on hip joint stability.
  • To establish a CT-based measurement for predicting hip instability in posterior wall acetabular fractures.

Main Methods:

  • Utilized six human cadavers (12 hips) with pre-procedure CT evaluation.
  • Randomized specimens into three groups based on FS (15%, 20%, 25%).
  • Assessed hip stability under anesthesia, increasing FA from 40° in 20° increments until instability occurred.

Main Results:

  • A 15% FS with a 40° FA demonstrated stability in all hips.
  • Increasing FA to 60° in the 15% FS group resulted in instability (subluxation or dislocation).
  • All hips with 20% and 25% FS were unstable at a 40° FA.

Conclusions:

  • A posterior wall fracture fragment size of 15% and fracture angle of 40° were found to be stable.
  • Increasing fragment size or fracture angle led to instability.
  • CT-based measurements of FS and FA can help predict hip instability in posterior wall acetabular fractures, requiring further clinical validation.
Abstract

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