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使用聚偏二氟乙烯网片治疗盆腔器官脱垂的骶骨阴道固定术:与聚丙烯网片的中期比较结果

Sacrocolpopexy with polyvinylidene fluoride mesh for pelvic organ prolapse: Mid term comparative outcomes with polypropylene mesh.

作者信息

Balsamo Raffaele, Illiano Ester, Zucchi Alessandro, Natale Franca, Carbone Antonio, Sio Marco De, Costantini Elisabetta

机构信息

Urology Service, University of Campania Luigi Vanvitelli, Naples, 80100, Italy; Doctorate Research Program, Magna Graecia University of Catanzaro, Catanzaro, 88100, Italy.

Department of Urology and Andrology Clinic, Department of Surgical and Biomedical Sciences, University of Perugia, Perugia, 06121, Italy.

出版信息

Eur J Obstet Gynecol Reprod Biol. 2018 Jan;220:74-78. doi: 10.1016/j.ejogrb.2017.11.018. Epub 2017 Nov 22.

Abstract

OBJECTIVE

The aim of this study was to compare the surgical, anatomical, and functional outcomes of sacrocolpopexy (SCP) using polyvinylidene fluoride (PVDF) mesh versus SCP using the standard polypropylene (PP) mesh.

STUDY DESIGN

This was a retrospective single centre case-control study including female patients who underwent laparoscopic or abdominal SCP for POP with either PP (Cousin Biotech) or PVDF (DynaMesh-PRS) mesh between March 2005 and May 2015. Anatomical outcomes were assessed by the Pelvic Organ Prolapse Quantification (POP-Q) system. Functional outcomes included voiding and storage urinary symptoms (VS and SS, respectively), urgency and stress urinary incontinence (UUI and SUI) and sexual dysfunction (SD). Symptoms and their impact on patients' quality of life (QoL) were assessed using validated questionnaires as Incontinence Impact Questionnaire (IIQ-7), Urinary Distress Inventory (UDI-6) and Female Sexual Function Index (FSFI). Global patient perception of improvement (PGI-I questionnaire) and mesh erosion rates were also recorded.

RESULTS

Of the 166 patients enrolled, 136 could be included in the analysis: 73 in the PP group and 63 in the PVDF group. The mean follow-up was 94± 17.31 months for the PP and 25.6± 13.8 months for the PVDF group. There were no statistically significant differences in patient demographics and preoperative clinical characteristics. Postoperative anatomical correction were not significantly different between the two groups. The PVDF group showed superior results in term of storage symptoms (PVDF=0% versus PP=8.2%; p=0.02) and lower rate of sexual dysfunction (PVDF=0% versus PP=16,4%; p=0.001). Only 1 patient in PP group and 2 in PVDF group (p=0.47) presented a mesh exposure. There was no statistical difference in PGI-I scores (PP=1.5±1.0 vs PVDF=1.8±0.5; p=0.40).

CONCLUSIONS

Our findings suggest that both meshes can be safely and effectively used with good anatomical outcomes. Interestingly, PVDF use was associated with significantly less storage symptoms and sexual dysfunction.

摘要

目的

本研究的目的是比较使用聚偏二氟乙烯(PVDF)网片与使用标准聚丙烯(PP)网片进行骶骨阴道固定术(SCP)的手术、解剖和功能结果。

研究设计

这是一项回顾性单中心病例对照研究,纳入了2005年3月至2015年5月间因盆腔器官脱垂(POP)接受腹腔镜或开腹SCP手术的女性患者,分别使用PP(Cousin Biotech)或PVDF(DynaMesh-PRS)网片。通过盆腔器官脱垂定量(POP-Q)系统评估解剖学结果。功能结果包括排尿和储尿症状(分别为VS和SS)、急迫性和压力性尿失禁(UUI和SUI)以及性功能障碍(SD)。使用经过验证的问卷如尿失禁影响问卷(IIQ-7)、排尿困扰量表(UDI-6)和女性性功能指数(FSFI)评估症状及其对患者生活质量(QoL)的影响。还记录了患者对改善的总体感知(PGI-I问卷)和网片侵蚀率。

结果

在纳入的166例患者中,136例可纳入分析:PP组73例,PVDF组63例。PP组的平均随访时间为94±17.31个月,PVDF组为25.6±13.8个月。患者人口统计学和术前临床特征无统计学显著差异。两组术后解剖学矫正无显著差异。PVDF组在储尿症状方面显示出更好的结果(PVDF = 0% 对比PP = 8.2%;p = 0.02),性功能障碍发生率更低(PVDF = 0% 对比PP = 16.4%;p = 0.001)。PP组仅有1例患者和PVDF组有2例患者出现网片暴露(p = 0.47)。PGI-I评分无统计学差异(PP = 1.5±1.0对比PVDF = 1.8±0.5;p = 0.40)。

结论

我们的研究结果表明,两种网片均可安全有效地使用,并取得良好的解剖学结果。有趣的是,使用PVDF与显著更少的储尿症状和性功能障碍相关。

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