Safety and efficacy of sonographically guided high-intensity focused ultrasound for symptomatic uterine fibroids: preliminary study of a modified protocol

We aimed to assess the safety and efficacy of sonographically guided high-intensity focused ultrasound for treating patients with symptomatic uterine fibroids using a modified protocol. This work was part of an ongoing prospective phase 1 study. Twenty patients with 22 symptomatic fibroids were trea...

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Veröffentlicht in:Journal of ultrasound in medicine 2014-10, Vol.33 (10), p.1811-1818
Hauptverfasser: Leung, Joyce H Y, Yu, Simon C H, Cheung, Eva C W, Wong, Alyssa S W, Tong, Mabel M B, Ho, Stella S Y, Leung, Vivian Y F, Ahuja, Anil T
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container_end_page 1818
container_issue 10
container_start_page 1811
container_title Journal of ultrasound in medicine
container_volume 33
creator Leung, Joyce H Y
Yu, Simon C H
Cheung, Eva C W
Wong, Alyssa S W
Tong, Mabel M B
Ho, Stella S Y
Leung, Vivian Y F
Ahuja, Anil T
description We aimed to assess the safety and efficacy of sonographically guided high-intensity focused ultrasound for treating patients with symptomatic uterine fibroids using a modified protocol. This work was part of an ongoing prospective phase 1 study. Twenty patients with 22 symptomatic fibroids were treated with sonographically guided high-intensity focused ultrasound under no anesthesia. The modified protocol consisted of repeated and shortened (
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This work was part of an ongoing prospective phase 1 study. Twenty patients with 22 symptomatic fibroids were treated with sonographically guided high-intensity focused ultrasound under no anesthesia. The modified protocol consisted of repeated and shortened (&lt;25 minutes) treatment sessions of high-input acoustic intensity (1000-1500 W/cm(2)) and intensified sonication pulses (1500-2000) at each spot. The primary end points were periprocedural complications. The secondary end points were symptomatic improvement and radiologic evidence of treatment responses, including the degree of fibroid infarction and volume shrinkage 3 months after treatment. Symptomatic improvement was assessed by a pain score, a pictorial chart menstrual score, the Urogenital Distress Inventory short form, and the Incontinence Impact Questionnaire short form. The degree of fibroid infarction was assessed by the nonperfused ratio on contrast-enhanced magnetic resonance imaging, defined as the ratio of the nonperfused fibroid volume to the total fibroid volume. Nineteen patients tolerated the treatment well, with no major adverse events. One patient who received treatment for a fibroid located within 6 cm from the skin had third-degree skin burns at 2 sites of 1 cm in diameter. Fibroid-related abdominal pain, pictorial chart, Urogenital Distress Inventory, and Incontinence Impact Questionnaire scores were significantly improved (P &lt; .05). The median nonperfused ratio at 3 months was 20% (95% confidence interval, 5%-32.5%). Median volume shrinkage at 3 months was 17.2% (95% confidence interval, 4.3%-26.6%). Sonographically guided high-intensity focused ultrasound using a modified protocol may be safe and effective for symptomatic uterine fibroids in selected patients to avoid skin burns.</description><identifier>ISSN: 0278-4297</identifier><identifier>EISSN: 1550-9613</identifier><identifier>DOI: 10.7863/ultra.33.10.1811</identifier><identifier>PMID: 25253828</identifier><language>eng</language><publisher>England</publisher><subject>Adult ; Contrast Media - administration &amp; dosage ; Female ; High-Intensity Focused Ultrasound Ablation - adverse effects ; High-Intensity Focused Ultrasound Ablation - methods ; Humans ; Leiomyoma - pathology ; Leiomyoma - surgery ; Magnetic Resonance Imaging ; Meglumine - administration &amp; dosage ; Middle Aged ; Organometallic Compounds - administration &amp; dosage ; Pain Measurement ; Prospective Studies ; Surveys and Questionnaires ; Time Factors ; Treatment Outcome ; Ultrasonography, Interventional ; Uterine Neoplasms - pathology ; Uterine Neoplasms - surgery</subject><ispartof>Journal of ultrasound in medicine, 2014-10, Vol.33 (10), p.1811-1818</ispartof><rights>2014 by the American Institute of Ultrasound in Medicine.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c252t-543cc47fe11f598e052324b18cae2b92249a0676d6b77ebc191530325b9764163</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25253828$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Leung, Joyce H Y</creatorcontrib><creatorcontrib>Yu, Simon C H</creatorcontrib><creatorcontrib>Cheung, Eva C W</creatorcontrib><creatorcontrib>Wong, Alyssa S W</creatorcontrib><creatorcontrib>Tong, Mabel M B</creatorcontrib><creatorcontrib>Ho, Stella S Y</creatorcontrib><creatorcontrib>Leung, Vivian Y F</creatorcontrib><creatorcontrib>Ahuja, Anil T</creatorcontrib><title>Safety and efficacy of sonographically guided high-intensity focused ultrasound for symptomatic uterine fibroids: preliminary study of a modified protocol</title><title>Journal of ultrasound in medicine</title><addtitle>J Ultrasound Med</addtitle><description>We aimed to assess the safety and efficacy of sonographically guided high-intensity focused ultrasound for treating patients with symptomatic uterine fibroids using a modified protocol. 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The degree of fibroid infarction was assessed by the nonperfused ratio on contrast-enhanced magnetic resonance imaging, defined as the ratio of the nonperfused fibroid volume to the total fibroid volume. Nineteen patients tolerated the treatment well, with no major adverse events. One patient who received treatment for a fibroid located within 6 cm from the skin had third-degree skin burns at 2 sites of 1 cm in diameter. Fibroid-related abdominal pain, pictorial chart, Urogenital Distress Inventory, and Incontinence Impact Questionnaire scores were significantly improved (P &lt; .05). The median nonperfused ratio at 3 months was 20% (95% confidence interval, 5%-32.5%). Median volume shrinkage at 3 months was 17.2% (95% confidence interval, 4.3%-26.6%). 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The degree of fibroid infarction was assessed by the nonperfused ratio on contrast-enhanced magnetic resonance imaging, defined as the ratio of the nonperfused fibroid volume to the total fibroid volume. Nineteen patients tolerated the treatment well, with no major adverse events. One patient who received treatment for a fibroid located within 6 cm from the skin had third-degree skin burns at 2 sites of 1 cm in diameter. Fibroid-related abdominal pain, pictorial chart, Urogenital Distress Inventory, and Incontinence Impact Questionnaire scores were significantly improved (P &lt; .05). The median nonperfused ratio at 3 months was 20% (95% confidence interval, 5%-32.5%). Median volume shrinkage at 3 months was 17.2% (95% confidence interval, 4.3%-26.6%). Sonographically guided high-intensity focused ultrasound using a modified protocol may be safe and effective for symptomatic uterine fibroids in selected patients to avoid skin burns.</abstract><cop>England</cop><pmid>25253828</pmid><doi>10.7863/ultra.33.10.1811</doi><tpages>8</tpages></addata></record>
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subjects Adult
Contrast Media - administration & dosage
Female
High-Intensity Focused Ultrasound Ablation - adverse effects
High-Intensity Focused Ultrasound Ablation - methods
Humans
Leiomyoma - pathology
Leiomyoma - surgery
Magnetic Resonance Imaging
Meglumine - administration & dosage
Middle Aged
Organometallic Compounds - administration & dosage
Pain Measurement
Prospective Studies
Surveys and Questionnaires
Time Factors
Treatment Outcome
Ultrasonography, Interventional
Uterine Neoplasms - pathology
Uterine Neoplasms - surgery
title Safety and efficacy of sonographically guided high-intensity focused ultrasound for symptomatic uterine fibroids: preliminary study of a modified protocol
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