van Gastel D M, Maassen L W, Van Erp M A J M, Coolen A L W M, Thurkow A L, Koks C A M, Veersema S, Bongers M Y
Facts Views Vis Obgyn. 2024 Dec;16(4):441-447. doi: 10.52054/FVVO.16.4.050.
The Adiana® Permanent Contraception System was a hysteroscopic tubal occlusion device but was withdrawn from the market in 2012.
To evaluate the safety, feasibility and efficacy of the Adiana hysteroscopic tubal occlusion.
A prospective observational multicentre cohort study of 300 women undergoing hysteroscopic sterilisation using the Adiana® was conducted in the Netherlands between 2009 and 2012. All procedures were performed using the same study protocol. Three months after bilateral placement a hysterosalpingography (HSG) was performed to confirm tubal occlusion. In 2018-2020 follow-up questionnaires were sent to all women.
The primary outcome was the success rate of the Adiana tubal occlusion technique. Successful tubal occlusion was defined as an uneventful procedure with occluded fallopian tubes according to the HSG after 3 months. Secondary outcomes were the success rate of the device placement, the number of complications during placement and the pregnancy rate.
Bilateral placement of Adiana devices was achieved in 93.5% of cases. Bilateral confirmed occlusion by HSG was accomplished in 87.9% of cases with successful Adiana placement. This was 77.1% in the intention-to-treat group. Complications and side effects were reported in 4.4% of women. The pregnancy rate was 3.6% in women with proven bilateral tubal occlusion.
Hysteroscopic tubal occlusion using the Adiana technology is associated with a pregnancy rate of 3.6%. Although this technology was removed from the commercial market, this evaluation of the Adiana technology could provide useful information for the development of potential new, more effective hysteroscopic tubal occlusion devices.
WHAT’S NEW?: Hysteroscopic tubal occlusion techniques are no longer available on the market. This evaluation of Adiana could provide useful information for the development of potential new hysteroscopic tubal occlusion devices.
Adiana®永久性避孕系统是一种宫腔镜输卵管阻塞装置,但已于2012年退出市场。
评估Adiana宫腔镜输卵管阻塞术的安全性、可行性和有效性。
2009年至2012年在荷兰对300名使用Adiana®进行宫腔镜绝育术的女性进行了一项前瞻性观察性多中心队列研究。所有手术均按照相同的研究方案进行。双侧放置三个月后进行子宫输卵管造影(HSG)以确认输卵管阻塞。在2018 - 2020年向所有女性发送了随访问卷。
主要结局是Adiana输卵管阻塞技术的成功率。成功的输卵管阻塞定义为术后3个月根据HSG显示输卵管闭塞且手术顺利。次要结局是装置放置成功率、放置过程中的并发症数量和妊娠率。
93.5%的病例实现了双侧放置Adiana装置。在成功放置Adiana的病例中,87.9%通过HSG确认双侧闭塞。在意向性治疗组中这一比例为77.1%。4.4%的女性报告有并发症和副作用。在已证实双侧输卵管闭塞的女性中,妊娠率为3.6%。
使用Adiana技术的宫腔镜输卵管阻塞术的妊娠率为3.6%。尽管该技术已退出商业市场,但对Adiana技术的评估可为开发潜在的新型、更有效的宫腔镜输卵管阻塞装置提供有用信息。
宫腔镜输卵管阻塞技术已不在市场上。对Adiana的评估可为开发潜在的新型宫腔镜输卵管阻塞装置提供有用信息。