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Ann Thorac Surg 2005;80:1063-1066
© 2005 The Society of Thoracic Surgeons


Original article: General thoracic

Clinical Experience in 397 Consecutive Thoracoscopic Sympathectomies

King F. Kwong, MD * , Lindsay B. Cooper, BS, Leslie A. Bennett, RN, BSN, Whitney Burrows, MD, Ziv Gamliel, MD, Mark J. Krasna, MD

Department of Surgery, Division of Thoracic Surgery, University of Maryland School of Medicine, Baltimore, Maryland

Accepted for publication March 18, 2005.

* Address reprint requests to Dr Kwong, Division of Thoracic Surgery, University of Maryland School of Medicine, 22 S Greene St, Rm N4E35, Baltimore, MD 21201 (Email: kkwong{at}smail.umaryland.edu).

Presented at the Fiftieth Annual Meeting of the Southern Thoracic Surgical Association, Bonita Springs, FL, Nov 13–15, 2003.

BACKGROUND: The purpose of this study is to evaluate the safety and efficacy of thoracoscopic sympathectomy for the treatment of hyperhidrosis, blushing, reflex sympathetic dystrophy, and digital ischemia.

METHODS: We conducted a retrospective review of 202 patients who underwent thoracoscopic sympathectomy at the University of Maryland from March 1992 to April 2003.

RESULTS: Three hundred ninety-seven procedures were performed on 202 patients (105 women, 97 men). Mean age was 29 years (range, 9 to 65). Indications for surgery included hyperhidrosis, facial blushing, digital ischemia, and reflex sympathetic dystrophy. Synchronous bilateral sympathectomies were performed in 194 patients; right side alone (n = 6); left side alone (n = 1); 1 patient had staged bilateral sympathectomies. Single incision with lung isolation technique was used. There was no mortality. Preoperative symptoms resolved completely or significantly improved in greater than 90% of patients. One patient with reflex sympathetic dystrophy recurred and 1 patient with hyperhidrosis complained of significant compensatory sweating. Compensatory sweating to a lesser degree occurred in approximately one third of patients. Complications included asymptomatic pleural effusion (n = 1), pneumothorax (n = 1), and reoperation for chylothorax that was identified early (n = 1). In 2 patients treated for facial blushing, Horner’s syndrome developed postoperatively; 1 of them subsequently underwent blepharoplasty. In 3 patients, hyperesthesias developed at the incision.

CONCLUSIONS: Thoracoscopic sympathectomy can be performed safely and with excellent results. Compensatory sweating is the main side effect, although significant complaints from this are rare. Horner’s syndrome remains an extremely uncommon complication as a result of thoracoscopic sympathectomy at our institution.




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