Ultrasound-guided thread-release of the first extensor compartment of the hand: initial experience in the anatomical model
Author Block: L. Lechner, S. A. Jengojan, P. Sorgo, G. Bodner, V. Moser, L. Hirtler; Vienna/AT
Purpose: The objective of this study was to develop and evaluate a minimally-invasive ultrasound-guided thread-release technique for safely and effectively decompressing the first extensor compartment in anatomical specimens.
Methods or Background: De Quervain’s tenosynovitis is a common disabling condition of the hand, arising due to the compression of the tendons in the first extensor compartment. If conservative treatments fail, surgical intervention is required. In recent years, minimally-invasive ultrasound-guided procedures, especially for carpal tunnel syndrome and trigger finger, are on the rise. However, thus far the thread technique was not studied in the release of the first extensor compartment for possible future treatment of De Quervain´s tenosynovitis in an anatomical or clinical setting.
For this study, we developed a protocol for the minimally-invasive ultrasound-guided thread-release and performed it prospectively on ten fresh cadaveric hands. Subsequently, the specimens were dissected and assessed by an experienced anatomist regarding efficacy and safety of the procedure. Ultrasound visibility, degree of transection, and unnecessary damage to surrounding neurovascular structures were documented.
Results or Findings: Ultrasound visibility was sufficient in all specimens. Out of ten interventions, a complete release was achieved in nine cases. Slight, clinically irrelevant, lesions on the underlying extensor tendons were observed in one case. Macroscopically visible neurovascular structures were not harmed in any case.
Conclusion: Real-time ultrasound-guided thread-release is a reliable and safe minimally-invasive method for releasing the first extensor compartment in anatomical specimens while protecting the surrounding structures.
Limitations: This study was conducted on anatomical specimens. Thus, results may differ in the clinical setting. Due to cadaver availability, the initial sample size was limited. Therefore, further anatomical and clinical trials are warranted.
Funding for this study: No funding was received for this study.
Has your study been approved by an ethics committee? Yes
Ethics committee - additional information: This study was approved by the Ethics Committee at the Medical University of Vienna.