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自主研发的中国盆腔修复系统与Avaulta修复系统治疗女性盆腔器官脱垂的安全性和有效性:一项多中心、前瞻性、随机、平行组研究。

Safety and efficacy of a self-developed Chinese pelvic repair system and Avaulta repair system for the treatment of pelvic organ prolapse in women: A multicenter, prospective, randomized, parallel-group study.

作者信息

Ouyang Yiqin, Chen Rujun, Chu Lei, Liang Junhua, Zhang Xueyu, Li Li, Gao Tian, Li Huaifang, Tong Xiaowen

机构信息

Department of Gynecology and Obstetrics, Tongji Hospital of Tongji University.

The Fifth People's Hospital of Shanghai, Shanghai.

出版信息

Medicine (Baltimore). 2020 Sep 18;99(38):e22332. doi: 10.1097/MD.0000000000022332.

Abstract

The pelvic organ prolapse (POP) repair systems used in China are imported and expensive. Our aim was to compare the efficacy and safety of a self-developed pelvic floor repair system versus the Avaulta system.This was a multicenter, randomized, parallel-group, noninferiority trial of 132 patients with POP stage ≥II from the Tongji Hospital Affiliated to Tongji University and the General Hospital of Ningxia Medical University enrolled from 02/2014 to 03/2015. The patients were randomized 1:1 to POP repair using the self-developed system or the Avaulta system. Perioperative conditions, POP quantification, pelvic floor impact questionnaire-7, and prolapse quality of life questionnaires, gynecological ultrasound, and postoperative complications were compared. Patients were followed at 1.5, 3, and 6 months.According to the POP quantification scores obtained at 6 months after surgery, the cure rates of the self-developed and Avaulta groups were 98.3% and 100.0%, respectively (P > .999). At 6 months follow-up, the pelvic floor impact questionnaire-7 scores of the self-developed and Avaulta groups were both improved (P < .001 vs baseline), with no between-group difference observed (P = .488). There were no differences between the 2 groups for subjective symptoms of POP (all P > .05). There were no significant differences between the 2 groups regarding complications (all P > .05).The self-developed pelvic reconstruction system is safe and effective for the treatment of POP and improves the patients' quality of life, without difference compared to the Avaulta system.

摘要

中国使用的盆腔器官脱垂(POP)修复系统均为进口产品,价格昂贵。我们的目的是比较自主研发的盆底修复系统与Avaulta系统的疗效和安全性。

这是一项多中心、随机、平行组、非劣效性试验,共纳入了132例2014年2月至2015年3月期间来自同济大学附属同济医院和宁夏医科大学总医院的POP分期≥II期患者。患者按1:1随机分为使用自主研发系统或Avaulta系统进行POP修复两组。比较围手术期情况、POP量化、盆底影响问卷-7、脱垂生活质量问卷、妇科超声及术后并发症。在术后1.5、3和6个月对患者进行随访。

根据术后6个月获得的POP量化评分,自主研发组和Avaulta组的治愈率分别为98.3%和100.0%(P>0.999)。在6个月随访时,自主研发组和Avaulta组的盆底影响问卷-7评分均有所改善(与基线相比P<0.001),两组间未观察到差异(P=0.488)。两组在POP主观症状方面无差异(所有P>0.05)。两组在并发症方面无显著差异(所有P>0.05)。

自主研发的盆腔重建系统治疗POP安全有效,可改善患者生活质量,与Avaulta系统相比无差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7680/7505298/d15c08b50baa/medi-99-e22332-g001.jpg

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