Open Access
CC BY 4.0 · Arch Plast Surg 2024; 51(01): 110-117
DOI: 10.1055/a-2179-3911
Hand/Peripheral Nerve
Case Report

Serious Complications of the Percutaneous A1 Pulley Release: Case Reports and Literature Review

1   Department of Plastic and Reconstructive Surgery, Gwangmyeong Sungae General Hospital, Gwangmyeong, Republic of Korea
,
1   Department of Plastic and Reconstructive Surgery, Gwangmyeong Sungae General Hospital, Gwangmyeong, Republic of Korea
,
1   Department of Plastic and Reconstructive Surgery, Gwangmyeong Sungae General Hospital, Gwangmyeong, Republic of Korea
,
1   Department of Plastic and Reconstructive Surgery, Gwangmyeong Sungae General Hospital, Gwangmyeong, Republic of Korea
,
1   Department of Plastic and Reconstructive Surgery, Gwangmyeong Sungae General Hospital, Gwangmyeong, Republic of Korea
,
1   Department of Plastic and Reconstructive Surgery, Gwangmyeong Sungae General Hospital, Gwangmyeong, Republic of Korea
› Author Affiliations
Preview

Abstract

Percutaneous first annular pulley (A1 pulley) release, which has been increasingly used to treat trigger fingers, has been widely established as a safe and simple procedure. Multiple studies have reported positive results of percutaneous A1 pulley release. In this study, however, we report cases of patients who developed complications after undergoing percutaneous A1 pulley release at local clinics. A total of six patients visited our hospital for infectious complications after percutaneous A1 pulley release. Various sequelae such as damage to normal structures, insufficient procedure, and tissue necrosis were observed during the exploration. A retrospective study was conducted to identify the cause and trend of the observed complications by instruments (HAKI knife or needle). In the HAKI knife group, there was a tendency for damage to normal structures, while in the needle group, an insufficient release or serious soft tissue necrosis was observed. Based on these cases, our findings confirm the existence and characteristics of infectious complications following the percutaneous A1 pulley release. We further identify that the type of instrument used predicts the nature of complications. Thus, reliable and skilled performance of the procedure by experts is essential for safe treatment.

Authors' Contributions

Conceptualization: D.C.L., Data curation: H.H.L., K.J.L.

Methodology: J.S.K., S.Y.R., Writing - original draft: H.H.L.

Writing - review & editing: D.C.L., S.H.K.


Ethical Approval

The study protocol was approved by the Ethics Review Board of our hospital (IRB no. KIRB 2022-N-005), and informed consent was obtained from all patients prior to the procedure.


Patient Consent

Written and informed consent was obtained from patients.




Publication History

Received: 04 April 2023

Accepted: 19 September 2023

Accepted Manuscript online:
21 September 2023

Article published online:
07 February 2024

© 2024. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)

Thieme Medical Publishers, Inc.
333 Seventh Avenue, 18th Floor, New York, NY 10001, USA