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采用可调式经闭孔男性系统治疗男性压力性尿失禁:一项多中心伊比利亚研究结果。

Treatment of male stress urinary incontinence with the adjustable transobturator male system: Outcomes of a multi-center Iberian study.

机构信息

Hospital Universitario de Getafe, Universidad Europea de Madrid, Madrid, Spain.

Centro Hospitalar São João, Oporto, Porto, Portugal.

出版信息

Neurourol Urodyn. 2018 Apr;37(4):1458-1466. doi: 10.1002/nau.23474. Epub 2018 Jan 9.

Abstract

AIM

To evaluate effectiveness and safety of the adjustable transobturator male system (ATOMS) for male stress urinary incontinence (SUI).

MATERIAL AND METHODS

A retrospective multicenter study was conducted in nine Iberian institutions using a board-approved database for 215 patients intervened between 2012 and 2017, with no case excluded. Continence status, patient satisfaction, number, and grade of complications (Clavien-Dindo) and factors affecting dry rate at adjustment were evaluated. Multivariate analysis defined the population at best success rate. Incontinence recurrence due to device failure and/or explant was evaluated and Kaplan-Meier curve for durability performed.

RESULTS

Adjustment was achieved at a mean 1.4 ± 1.9 fillings. Dry-rate after adjustment was 80.5% (96.2% mild and 75.3% moderate-severe), 121 (56.3%) used no pads, and 52 (24.2%) a security pad with urine loss under 10 mL. Mean basal daily pad-test and pad-count decreased from 484 ± 372.3 mL and 3.9 ± 2 pads to 63.5 ± 201.2 mL and 0.9 ± 1.5pads (both P < 0.0001). Satisfaction rate was 85.1% (94.3% mild and 82.1% moderate-severe). Factors associated to dryness were: lesser severity of SUI (P < .0001), absence of radiotherapy (P = 0.0002) and device generation (P = 0.05). Multivariate analysis revealed absence of radiation (OR = 3.12; 1.36-7.19), mild (OR = 19.61; 3.95-100), and moderate (OR = 2.48; 1.1-5.59) SUI were independent predictors. Complications presented in 33(15.35%); 66.7% grade 1, 9.1% grade 2, and 24.2% grade 3. At 24.3 ± 15 mo mean follow-up device was explanted in seven (3.25%) and SUI worsened after adjustment in nine (4.2%). Dry-rate at follow-up was 73% and durability of device in dry patients at adjustment was 89.8% (82.9-94) at 2-years.

CONCLUSIONS

This study confirms ATOMS device is safe and achieves high treatment efficacy and patient satisfaction in a multicenter setting. Significantly better results are achieved in less severe and non-irradiated cases. Durability of the device is reassuring in the short-term.

摘要

目的

评估可调经闭孔男性系统(ATOMS)治疗男性压力性尿失禁(SUI)的有效性和安全性。

材料与方法

本研究采用回顾性多中心研究方法,纳入了 2012 年至 2017 年间在 9 家伊比利亚机构接受治疗的 215 例患者,所有患者均未被排除。评估了患者的控尿状态、满意度、并发症的数量和等级(Clavien-Dindo)以及影响调整后干燥率的因素。多变量分析确定了最佳成功率人群。评估了因器械故障和/或植入物而导致的尿失禁复发情况,并绘制了耐用性 Kaplan-Meier 曲线。

结果

平均调整 1.4±1.9 次即可完成。调整后干燥率为 80.5%(轻度为 96.2%,中度至重度为 75.3%),121 例(56.3%)患者不再使用尿垫,52 例(24.2%)患者使用安全垫,且尿液丢失量小于 10ml。平均基础每日尿垫测试和尿垫计数分别从 484±372.3ml 和 3.9±2 片减少到 63.5±201.2ml 和 0.9±1.5 片(均 P<0.0001)。满意度为 85.1%(轻度为 94.3%,中度至重度为 82.1%)。与干燥相关的因素为:SUI 严重程度较轻(P<0.0001)、无放疗(P=0.0002)和器械代次(P=0.05)。多变量分析显示,无放疗(OR=3.12;1.36-7.19)、轻度(OR=19.61;3.95-100)和中度(OR=2.48;1.1-5.59)SUI 是独立的预测因素。33 例(15.35%)患者出现了并发症,其中 66.7%为 1 级,9.1%为 2 级,24.2%为 3 级。在 24.3±15 个月的平均随访期间,7 例(3.25%)患者需要取出装置,9 例(4.2%)患者在调整后 SUI 恶化。随访时干燥率为 73%,调整后干燥患者的装置耐用性在 2 年内为 89.8%(82.9-94)。

结论

本研究证实 ATOMS 装置在多中心环境中安全且疗效显著,患者满意度高。在较轻和未接受放疗的病例中,结果明显更好。该装置的短期耐用性令人安心。

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