Literature DB >> 18192468

Leiomyoma infarction after uterine artery embolization: a prospective randomized study comparing tris-acryl gelatin microspheres versus polyvinyl alcohol microspheres.

Gary P Siskin1, Avi Beck, Michael Schuster, Kenneth Mandato, Meridith Englander, Allen Herr.   

Abstract

PURPOSE: To determine the degree of leiomyoma infarction after uterine artery embolization (UAE) performed with tris-acryl gelatin microspheres or polyvinyl alcohol (PVA) microspheres.
MATERIALS AND METHODS: Patients determined to be candidates and scheduled for UAE were randomized prospectively to receive tris-acryl gelatin microspheres or PVA microspheres. The manufacturers' recommended technique was used for both products during the UAE procedures (including the recently described refined protocol for PVA microspheres). All patients underwent magnetic resonance (MR) imaging of the pelvis with contrast agent enhancement before and after the UAE procedure. On the postprocedural MR study, the degree of tumor infarction was assessed on postcontrast images. These findings were classified as follows: 100% infarction, 90%-99% infarction, 50%-89% infarction, and less than 50% infarction. Treatment failure was defined by enhancement of more than 10% of a patient's entire tumor burden.
RESULTS: A total of 53 patients were enrolled in this study. Twenty-seven (mean age, 44.9 years) received PVA microspheres and 26 (mean age, 45.1 years) received tris-acryl gelatin microspheres. There were no significant differences in the preprocedural uterine volume, dominant tumor volume, location of dominant tumor, and presenting symptoms between populations. In the PVA microsphere group, treatment failure was seen in eight patients (29.6%). In the tris-acryl gelatin microsphere group, treatment failure was seen in one patient (3.8%), which was a significant difference between groups (P < or = .025).
CONCLUSIONS: There was a significantly greater degree of tumor infarction in patients treated with tris-acryl gelatin microspheres during UAE than in patients who received PVA microspheres administered in accordance with a newly refined protocol. Given the known risk of recurrence in patients with persistent tumor enhancement after UAE, it is concluded that tris-acryl gelatin microspheres should be the preferred agent for UAE at this time.

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Year:  2008        PMID: 18192468     DOI: 10.1016/j.jvir.2007.08.034

Source DB:  PubMed          Journal:  J Vasc Interv Radiol        ISSN: 1051-0443            Impact factor:   3.464


  13 in total

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Authors:  Md Mohosin Rana; Marites P Melancon
Journal:  Biomimetics (Basel)       Date:  2022-06-10

6.  Tri-acryl gelatin microsphere is better than polyvinyl alcohol in the treatment of uterine myomas with uterine artery embolization.

Authors:  Yu Gao; Fang Jiang; Xinbo Wang
Journal:  Int J Clin Exp Med       Date:  2015-06-15

7.  Uterine fibroid embolisation for symptomatic uterine fibroids: a survey of clinical practice in Europe.

Authors:  Marianne J Voogt; Mark J Arntz; Paul N M Lohle; Willem P Th M Mali; Leo E H Lampmann
Journal:  Cardiovasc Intervent Radiol       Date:  2010-09-21       Impact factor: 2.740

8.  Uterine artery embolization in patients with a large fibroid burden: long-term clinical and MR follow-up.

Authors:  Albert J Smeets; Robbert J Nijenhuis; Willem Jan van Rooij; Emilie A M Weimar; Peter F Boekkooi; Leo E H Lampmann; Harry A M Vervest; Paul N M Lohle
Journal:  Cardiovasc Intervent Radiol       Date:  2010-01-12       Impact factor: 2.740

9.  Efficacies of uterine artery embolization for symptomatic uterine fibroids using gelatin sponge: a single-center experience and literature review.

Authors:  Aska Toda; Kenjiro Sawada; Keigo Osuga; Noboru Maeda; Hiroki Higashihara; Tomoyuki Sasano; Noriyuki Tomiyama; Tadashi Kimura
Journal:  Int J Womens Health       Date:  2016-08-12

10.  Randomised trial of two embolic agents for uterine artery embolisation for fibroids: Gelfoam versus Embospheres (RAGE trial).

Authors:  R Yadavali; G Ananthakrishnan; M Sim; K Monaghan; G McNaught; I Hamoodi; F Bryden; S Lassman; J G Moss
Journal:  CVIR Endovasc       Date:  2019-01-08
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