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Initial Results 
at Georgetown University Medical Center

Georgetown University Medical Center began a study to evaluate UAE in July of 1997 and as of May 1, 1999, we had treated 96 patients. The clinical and imaging results in the first 61 patients were reported at the Annual SCVIR Meeting in Orlando, Florida in March of 1999. We have submitted these results for publication. The abstract from the presentation and the paper is given below.

Abstract

Initial Results from Uterine Fibroid Embolization for Symptomatic Leiomyomata.

James B. Spies M.D., Anthony R. Scialli M.D., Reena C. Jha M.D., Izumi Imaoka M.D., Susan M. Ascher M.D., Vivian M. Fraga M.D., Klemens H. Barth M.D.

From the Departments of Radiology (JBS, RCJ, II, SMA, KHB) and Obstetrics and Gynecology (ARS,VMF) of Georgetown University Medical Center.

Objective: To evaluate the safety and short term efficacy of uterine fibroid embolization (UFE) in patients with symptomatic uterine fibroids.

Methods: Bilateral UFE was performed in 61 patients with symptomatic uterine leiomyomata over a 16 month period. Imaging was performed before the procedure and at three months and one year afterward. Questionnaires were obtained at regular intervals post-procedure to assess patient outcome.

Results: All procedures but one were technically successful. Mean clinical follow-up was 8.7 months. Minor complications occurred in five patients during the follow-up period. All were treated without permanent sequelae.

Menstrual bleeding was improved in 89%, with 81% of patients moderately to markedly improved. Pelvic pain and pressure was improved in 96% of patients, with moderate to marked improvement in 79%. At initial imaging follow-up (mean 4.4 months post-procedure), median uterine volume decreased 34% (P=.0001) and the median dominant fibroid volume decreased 50 % (P=.0001). Imaging at one year (mean 12.3 months) post-procedure showed continued reduction with a median uterine volume reduction of 48 % (P=.0002) and median dominant fibroid volume decrease of 78% (P=.0002).

Conclusion: In our initial clinical experience, UAE appears to be effective in controlling symptoms and substantially reducing fibroid volume with few complications.

 


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