Botulinum Toxin Injection for Internal Rotation Contractures in Brachial Plexus Birth Palsy. A Minimum 5-Year

Bouke J Duijnisveld1, Marie S van Wijlen-Hempel, Simone Hogendoorn

  • 1Departments of *Orthopaedics ‡Neurosurgery †Rehabilitation, Leiden University Medical Center, Leiden, The Netherlands.

Insights

Botulinum toxin A (BTX-A) injections in the subscapular muscle can improve external rotation and reduce the need for surgery in brachial plexus birth palsy patients. However, relapses occur in 67% of patients within 5 years.

Area of Science:

  • Orthopedics
  • Pediatric Surgery
  • Neurology

Background:

  • Brachial plexus birth palsy often causes shoulder internal rotation contractures due to muscle imbalance.
  • Botulinum toxin A (BTX-A) is investigated as a treatment for these contractures.

Purpose of the Study:

  • To evaluate the efficacy of BTX-A injections in the subscapular (SC) muscle.
  • To assess the impact on shoulder external rotation and the requirement for tendon transfer surgery.

Main Methods:

  • A prospective comparative study involved 15 patients receiving BTX-A injections and 67 historical controls.
  • Patients received BTX-A (2 IU/kg) in the SC muscle under general anesthesia.
  • Evaluated passive external rotation, need for surgery, glenohumeral deformity, and muscle degeneration.

Main Results:

  • BTX-A group showed improved passive external rotation (from -1° to 32°) at 3 months, with 6 patients needing surgery versus 66 in the control group.
  • At 5 years, 10 BTX-A patients required surgery, with a hazard ratio of 4.0 for relapse compared to controls.
  • Less SC muscle degeneration was observed in good responders to BTX-A treatment.

Conclusions:

  • BTX-A injections in the SC muscle can decrease internal rotation contractures and reduce the need for tendon transfer surgery.
  • A significant relapse rate (67%) was observed at 5 years post-treatment.
  • Identifying optimal patient candidates, considering factors like glenohumeral deformity and SC muscle degeneration, is crucial for future BTX-A treatment strategies.
Abstract

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