Obstetrics and Gynecology, University of Naples, Naples, Italy.
Department of Molecular and Developmental Medicine, University of Siena, Siena, Italy.
Ultrasound Obstet Gynecol. 2018 Jan;51(1):134-141. doi: 10.1002/uog.17398.
To evaluate, in patients who underwent Fallopian-tube sterilization by hysteroscopic insertion of an Essure® device, the feasibility and accuracy of three-dimensional (3D) transvaginal sonography (TVS) to check the position of the device and 3D hysterosalpingo-foam sonography (3D-HyFoSy) using contrast-enhanced gel foam to assess consequent tubal occlusion.
This was a prospective multicenter study conducted from June 2012 to July 2014 in four Italian centers, which included 50 women who underwent hysteroscopic Essure microinsert placement in a total of 95 Fallopian tubes. Placement of the microinserts was performed in an outpatient setting following standard procedure recommendations. All patients underwent transvaginal 3D-HyFoSy and hysterosalpingography (HSG) approximately 12-14 weeks after the procedure. The position of the devices was first checked on 3D-TVS and classified according to specific criteria (Positions A, B, C and D). Then, 3D-HyFoSy with ExEm® gel foam as the ultrasound contrast agent was performed to confirm tubal occlusion by the absence of contrast agent within the tubes and/or around the ovaries. To evaluate the feasibility of 3D-HyFoSy, consecutive volume acquisitions were performed while injecting the gel foam. After sonographic evaluation, women underwent HSG to assess the success of sterilization, as standard methodology. Side effects and pain evoked during and after 3D-HyFoSy and HSG were evaluated using a numeric pain rating scale.
On 3D-TVS, 10 devices (10.5%) were in Position A, two (2.1%) in Position B, 59 (62.1%) in Position C and 24 (25.3%) in Position D. During 3D-HyFoSy, tubal occlusion was observed in 89 of 95 tubes (93.7%). In the six cases in which the passage of the contrast was observed, one device (16.7%) was in Position B, one device (16.7%) in Position D and four devices (66.7%) were found to lie in Position C. Tubal patency was confirmed at HSG with a concordance rate of 100%. The mean pain score associated with 3D-HyFoSy was significantly lower than that on HSG.
3D-TVS with HyFoSy allows accurate assessment of the position of Essure microinserts and tubal occlusion. It can be considered a safe, reliable, non-invasive alternative to HSG. Copyright © 2017 ISUOG. Published by John Wiley & Sons Ltd.
评估在接受宫腔镜插入 Essure®装置进行输卵管绝育的患者中,三维(3D)经阴道超声(TVS)检查装置位置的可行性和准确性,以及使用对比增强凝胶泡沫的 3D 子宫输卵管泡沫声像图(3D-HyFoSy)评估随后的输卵管阻塞。
这是 2012 年 6 月至 2014 年 7 月在意大利的四个中心进行的一项前瞻性多中心研究,包括 50 名在总共 95 条输卵管中接受宫腔镜 Essure 微植入的女性。微插入的放置是在门诊环境下按照标准程序建议进行的。所有患者在手术后约 12-14 周均接受经阴道 3D-HyFoSy 和子宫输卵管造影术(HSG)检查。首先在 3D-TVS 上检查设备的位置,并根据特定标准进行分类(位置 A、B、C 和 D)。然后,使用 ExEm®凝胶泡沫作为超声造影剂进行 3D-HyFoSy,以确认输卵管阻塞,方法是在管内和/或卵巢周围无造影剂。为了评估 3D-HyFoSy 的可行性,在注入凝胶泡沫的同时连续进行体积采集。超声评估后,女性接受 HSG 以评估绝育的成功率,作为标准方法。使用数字疼痛评分量表评估 3D-HyFoSy 和 HSG 期间和之后的副作用和疼痛。
在 3D-TVS 上,10 个设备(10.5%)位于位置 A,2 个(2.1%)位于位置 B,59 个(62.1%)位于位置 C,24 个(25.3%)位于位置 D。在 3D-HyFoSy 中,95 个管中的 89 个(93.7%)观察到输卵管阻塞。在观察到造影剂通过的 6 个病例中,1 个设备(16.7%)位于位置 B,1 个设备(16.7%)位于位置 D,4 个设备(66.7%)位于位置 C。HSG 证实了输卵管通畅,符合率为 100%。与 HSG 相比,3D-HyFoSy 相关的平均疼痛评分显著降低。
3D-TVS 联合 HyFoSy 可准确评估 Essure 微植入物的位置和输卵管阻塞情况。它可以被认为是一种安全、可靠、非侵入性的 HSG 替代方法。版权所有©2017 ISUOG。由 John Wiley & Sons Ltd 出版。