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

IF 1.6 Q4 HEALTH CARE SCIENCES & SERVICES
Sissel Hegdahl Oversand, Tomislav Dimoski, Rune Svenningsen
{"title":"Improving long-term postoperative pain monitoring and follow-up for women undergoing incontinence mesh surgery: a quality improvement initiative.","authors":"Sissel Hegdahl Oversand, Tomislav Dimoski, Rune Svenningsen","doi":"10.1136/bmjoq-2025-003346","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>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.</p><p><strong>Local problem: </strong>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.</p><p><strong>Methods: </strong>A quality improvement project (2022-2023), initiated by NFIR, included seven hospitals selected for surgical volume, location and follow-up performance.</p><p><strong>Interventions: </strong>(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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusions: </strong>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.</p>","PeriodicalId":9052,"journal":{"name":"BMJ Open Quality","volume":"14 3","pages":""},"PeriodicalIF":1.6000,"publicationDate":"2025-07-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12306378/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMJ Open Quality","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1136/bmjoq-2025-003346","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"HEALTH CARE SCIENCES & SERVICES","Score":null,"Total":0}
引用次数: 0

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.

Abstract Image

改善妇女接受失禁补片手术的长期术后疼痛监测和随访:一项质量改进倡议。
背景:压力性尿失禁(SUI)影响许多女性,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状SUI植入物是有效的,但由于长期疼痛等并发症引起了人们的担忧。在挪威,不充分的随访和不一致的疼痛登记阻碍了准确的患病率估计。本研究旨在提高吊带手术后疼痛记录和标准化随访。当地问题:挪威女性失禁登记处(NFIR)推荐的3年常规术后控制由于财政原因被公立医院取消。2017年,接受吊带手术的患者中,只有不到50%的人接受了随访,其中只有一半包括疼痛数据。这可能会低估疼痛的普遍性,并阻碍质量的提高。方法:由nir发起的质量改进项目(2022-2023),根据手术量、位置和随访情况选择7家医院。干预措施:(1)在2019年4月1日至2020年3月31日期间,对SUI补片手术进行为期3年的结构化电话随访,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,跟踪发病和持续时间。(4)规范患者术后疼痛信息。通过基线、项目中期和最终阶段的主要数据分析,对NFIR疼痛变量进行了细化。结果:随访率超过80%,所有患者均有疼痛数据记录。自我报告持续疼痛的比例为4.3%。经临床评估,1.9%归因于网状植入物。3例患者(0.7%)需要治疗,1例需要部分去除补片。部门间随访的可变性降低,NFIR疼痛监测被修正为精确。结论:以电话为基础的随访改善了疼痛记录,减少了部门差异。虽然疼痛的患病率很低,但系统的随访和精确的监测仍然至关重要。未来的工作应探索电子跟踪并保持部门间协作,为类似的医疗保健挑战提供一个模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
BMJ Open Quality
BMJ Open Quality Nursing-Leadership and Management
CiteScore
2.20
自引率
0.00%
发文量
226
审稿时长
20 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信