In vivo feasibility of image-guided transvaginal focused ultrasound therapy for the treatment of intracavitary fibroids
Fertility and Sterility, ISSN: 0015-0282, Vol: 82, Issue: 3, Page: 723-730
2004
- 26Citations
- 21Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations26
- Citation Indexes26
- 26
- CrossRef18
- Captures21
- Readers21
- 21
Article Description
To determine the feasibility of uterine tissue ablation in vivo using a transvaginal focused ultrasound applicator guided by ultrasound imaging. Randomized in vivo animal study. Academic research environment. Healthy anesthetized sheep. Uterine treatment location was determined using a computerized targeting system. Five sonications 10 seconds in duration and averaging 2,000 W/cm 2 of focal ultrasound intensity were applied in each animal's uterus. Animals were euthanized either immediately or 2, 7, or 30 days post-treatment. Gross and microscopic analysis of the dissected uterus was used to quantitatively and qualitatively determine the ablated region and treatment side effects. Treatments resulted in coagulative necrosis. Histopathological analysis showed that over 7 days, inflammatory cells appeared and smooth muscle bundles regenerated. By day 30, treated tissues healed and scar tissue formed. None of the animals showed abnormal behavior or medical problems. Complications in three animals were damage to the vaginal wall and colon, possibly due to inadequate applicator cooling and an empty bladder during treatment. Transvaginal image-guided high-intensity focused ultrasound has potential for treating uterine fibroids. Further safety testing of this treatment will prepare it for human use.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0015028204009835; http://dx.doi.org/10.1016/j.fertnstert.2004.01.049; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=4544226721&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/15374721; https://linkinghub.elsevier.com/retrieve/pii/S0015028204009835; https://dx.doi.org/10.1016/j.fertnstert.2004.01.049
Elsevier BV
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