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改善接受尿失禁补片手术女性的术后长期疼痛监测与随访:一项质量改进举措。

Improving long-term postoperative pain monitoring and follow-up for women undergoing incontinence mesh surgery: a quality improvement initiative.

作者信息

Oversand Sissel Hegdahl, Dimoski Tomislav, Svenningsen Rune

机构信息

Gynecology, Oslo University Hospital, Oslo, Norway

Gynecology, Oslo University Hospital, Oslo, Norway.

出版信息

BMJ Open Qual. 2025 Jul 27;14(3):e003346. doi: 10.1136/bmjoq-2025-003346.

Abstract

BACKGROUND

Stress urinary incontinence (SUI) affects many women, often resulting from childbirth-related injuries. Synthetic mesh SUI implants, popular since the 1990s, are effective but have raised concerns due to complications like long-term pain. In Norway, insufficient follow-up and inconsistent pain registration hinder accurate prevalence estimates. This study aimed to enhance pain registration and standardise follow-ups after sling surgery.

LOCAL PROBLEM

Routine 3-year postoperative controls, recommended by the Norwegian Female Incontinence Registry (NFIR) have been deprioritised by public hospitals for financial reasons. Less than 50% of patients undergoing sling surgeries in 2017 received follow-ups, with only half including pain data. This risks underestimating pain prevalence and impedes quality improvements.

METHODS

A quality improvement project (2022-2023), initiated by NFIR, included seven hospitals selected for surgical volume, location and follow-up performance.

INTERVENTIONS

(1) Structured 3-year telephone follow-ups with pain registration for SUI mesh surgeries between 1 April 2019 and 31 March 2020. (2) Mandatory clinical examinations for patients reporting persistent pain. (3) Improved NFIR pain monitoring to track onset and persistence. (4) Standardised patient information on postoperative pain.The NFIR pain variable was refined, with main data analyses at baseline, mid-project and finalisation.

RESULTS

Follow-up rates exceeded 80%, with pain data documented for all. Persistent pain was self-reported by 4.3%. After clinical evaluations, 1.9% could be attributed to the mesh implant. Three patients (0.7%) required treatment, one needed partial mesh removal. Interdepartmental follow-up variability decreased, and NFIR pain monitoring was revised for precision.

CONCLUSIONS

Telephone-based follow-ups improved pain documentation and reduced departmental variability. Although pain prevalence was low, systematic follow-ups and refined monitoring remain crucial. Future efforts should explore electronic follow-ups and maintain interdepartmental collaboration, providing a model for similar healthcare challenges.

摘要

背景

压力性尿失禁(SUI)影响着许多女性,通常由分娩相关损伤引起。自20世纪90年代以来流行的合成网片SUI植入物是有效的,但由于长期疼痛等并发症而引发了担忧。在挪威,随访不足和疼痛登记不一致阻碍了准确的患病率估计。本研究旨在加强疼痛登记并规范吊带手术后的随访。

当地问题

挪威女性尿失禁登记处(NFIR)建议的术后3年常规检查因经济原因被公立医院置于次要地位。2017年接受吊带手术的患者中,不到50%接受了随访,其中只有一半包括疼痛数据。这有可能低估疼痛患病率,并阻碍质量改进。

方法

NFIR发起的一项质量改进项目(2022 - 2023年),包括根据手术量、地点和随访表现选择的七家医院。

干预措施

(1)对2019年4月1日至2020年3月31日期间接受SUI网片手术的患者进行结构化的3年电话随访,并进行疼痛登记。(2)对报告持续疼痛的患者进行强制性临床检查。(3)改进NFIR疼痛监测以跟踪疼痛的发作和持续情况。(4)规范患者关于术后疼痛的信息。NFIR疼痛变量得到完善,主要数据分析在基线、项目中期和结束时进行。

结果

随访率超过80%,所有患者都记录了疼痛数据。4.3%的患者自我报告有持续疼痛。经过临床评估,1.9%可归因于网片植入物。三名患者(0.7%)需要治疗,一名患者需要部分取出网片。部门间随访差异减小,NFIR疼痛监测进行了修订以提高精度。

结论

基于电话的随访改善了疼痛记录并减少了部门差异。尽管疼痛患病率较低,但系统的随访和完善的监测仍然至关重要。未来的努力应探索电子随访并维持部门间合作,为类似的医疗挑战提供一个模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1ba/12306378/3994fb0cccba/bmjoq-14-3-g001.jpg

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