Abstract

Objective: To report 2-year results of sonography-guided transcervical fibroid ablation (TFA) using the Sonata® system in women with symptomatic uterine fibroids.Design: This is a prospective multicenter single-arm interventional trial.Methods: Premenopausal women with up to 10 clinically relevant uterine fibroids, each ranging from 1 to 5 cm in diameter, were treated with sonography-guided TFA on an outpatient basis and returned for regular follow-up visits for 2 years. Assessed outcomes included changes in symptom severity, heath-related quality of life, general health status, work and activity limitations, treatment satisfaction, adverse events, surgical reintervention, and occurrence of pregnancy and associated outcomes.Results: Among 147 enrolled women, 125 (85%) returned for follow-up at 2 years. Compared with baseline, symptom severity decreased from 55 ± 19 to 24 ± 18 (p < 0.001), health-related quality of life increased from 40 ± 21 to 83 ± 19 (p < 0.001), and EuroQol 5-Dimension scores increased from 0.72 ± 0.21 to 0.89 ± 0.14 (p < 0.001). Overall treatment satisfaction at 2 years was 94%. The mean percentage of missed work time, overall work impairment, and activity impairment significantly decreased at follow-up. Through 2 years, surgical reintervention for heavy menstrual bleeding was performed in 5.5% of patients. One singleton pregnancy occurred with a normal peripartum outcome.Conclusions: TFA treatment with the Sonata system provides significant clinical improvement through 2 years postablation, with a low incidence of surgical reintervention. Other favorable outcomes included a rapid return to work and substantial improvements in quality of life, symptom severity, work productivity, and activity levels.

Highlights

  • Uterine fibroids are a highly prevalent gynecologic condition and can be identified in at least 70% of women by the age of 50 years.[1]

  • To characterize longer term safety and efficacy results with this procedure, we present 2-year results from this pivotal trial of sonographyguided transcervical RF ablation in women with symptomatic uterine fibroids

  • The clinical trial was performed under an investigational device exemption (IDE) approved by the Food and Drug Administration (FDA) in the United States and the Federal Commission for Protection against Health Risks (COFEPRIS) in Mexico

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Summary

Introduction

Uterine fibroids are a highly prevalent gynecologic condition and can be identified in at least 70% of women by the age of 50 years.[1].

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