TY - JOUR
T1 - Clinical outcomes of focused ultrasound surgery for the treatment of uterine fibroids
AU - Stewart, Elizabeth A.
AU - Rabinovici, Jaron
AU - Tempany, Clare M.C.
AU - Inbar, Yael
AU - Regan, Leslie
AU - Gastout, Bobbie
AU - Hesley, Gina
AU - Kim, Hyun S.
AU - Hengst, Suzanne
AU - Gedroye, Wladyslaw M.
N1 - Funding Information:
Supported and funded by Insightec, Ltd., Haifa, Israel.
PY - 2006/1
Y1 - 2006/1
N2 - Objective: To assess outcomes at 6 and 12 months after magnetic resonance-guided focused ultrasound surgery (MRgFUS) for symptomatic uterine leiomyomas. Design: Multicenter clinical trial. Setting: Academic medical centers. Patient(s): Premenopausal women with symptomatic uterine leiomyomas and no plans for future pregnancy (n = 109 at 6 months and n = 82 at 12 months). Intervention(s): A single treatment session of MRgFUS for uterine fibroids. Main Outcome Measure(s): Reduction in fibroid symptoms as measured by the symptom severity score (SSS) of the Uterine Fibroid Quality-of-Life Instrument (UFS-QOL), the only validated measure of leiomyoma symptomatology. A 10-point reduction in the SSS was selected as the targeted improvement. Result(s): Seventy-one percent of women undergoing MRgFUS reached the targeted symptom reduction at 6 months, and 51% reached this at 12 months. The magnitude of improvement in SSS was greater than predicted, with subjects having a mean decrease of 39% and 36% at 6 and 12 months, respectively. This paralleled the improvement seen using the short form-36 instrument. A modest volume reduction similar in magnitude to the treated volume was seen. The incidence of adverse events was low. Conclusion(s): MRgFUS treatment results in short-term symptom reduction for women with symptomatic uterine leiomyomas with an excellent safety profile.
AB - Objective: To assess outcomes at 6 and 12 months after magnetic resonance-guided focused ultrasound surgery (MRgFUS) for symptomatic uterine leiomyomas. Design: Multicenter clinical trial. Setting: Academic medical centers. Patient(s): Premenopausal women with symptomatic uterine leiomyomas and no plans for future pregnancy (n = 109 at 6 months and n = 82 at 12 months). Intervention(s): A single treatment session of MRgFUS for uterine fibroids. Main Outcome Measure(s): Reduction in fibroid symptoms as measured by the symptom severity score (SSS) of the Uterine Fibroid Quality-of-Life Instrument (UFS-QOL), the only validated measure of leiomyoma symptomatology. A 10-point reduction in the SSS was selected as the targeted improvement. Result(s): Seventy-one percent of women undergoing MRgFUS reached the targeted symptom reduction at 6 months, and 51% reached this at 12 months. The magnitude of improvement in SSS was greater than predicted, with subjects having a mean decrease of 39% and 36% at 6 and 12 months, respectively. This paralleled the improvement seen using the short form-36 instrument. A modest volume reduction similar in magnitude to the treated volume was seen. The incidence of adverse events was low. Conclusion(s): MRgFUS treatment results in short-term symptom reduction for women with symptomatic uterine leiomyomas with an excellent safety profile.
KW - Focused ultrasound
KW - Leiomyomas
KW - Magnetic resonance imaging
UR - https://www.scopus.com/pages/publications/30344483219
U2 - 10.1016/j.fertnstert.2005.04.072
DO - 10.1016/j.fertnstert.2005.04.072
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C2 - 16412721
AN - SCOPUS:30344483219
SN - 0015-0282
VL - 85
SP - 22
EP - 29
JO - Fertility and Sterility
JF - Fertility and Sterility
IS - 1
ER -