Diagnosis and treatment of synthetic mid-urethral sling complications

Helen E. O’Connell , Christopher K. Harding , Gaurav Khatri , Phyllis Glanc , Eric Bautrant , Sarah Love-Jones , Karen Ward , Henry H. Yao , Ventia Hoe , Charlotte Korte , Nicolle Germano , Sanjeevan Kalavampara , Sherif Mourad , Hashim Hashim
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Abstract

Background and Objective:

Synthetic Mid-Urethral Slings (SMUS) have been widely used with benefit to many women. Complications arise in a small proportion, occurring acutely in the perioperative stage, post-operatively and in a delayed fashion many years after implantation. Clinical trials provide data on selected patients who are as homogeneous as possible. Real world studies rarely provide detail on the denominator population from which the sample originates. Mature clinical quality registries (CQR) provide long term data on a non selected population who have undergone a procedure for a given condition. Near complete case ascertainment is the goal and there are many examples in other clinical areas.
Due to the serious and potentially life changing nature of some of the complications that may arise following SMUS, health agencies instigated action on behalf of patients to promote improvements in care.

Methods and Limitations:

The International Continence Society (ICS) assembled a multidisciplinary working group to forge this guidance. The working group includes 2 consumer advocates and relevant medical expertise. The management of complications following SMUS placement is discussed and algorithms are provided for each of the common complications of SMUS. The recommendations are based on an expert consensus derived from experience and limited data from a multiple narrative and systematic reviews of the literature. Due to a retrospective design, low cohort numbers, short follow-up and inconsistent definitions, all the studies were at high risk of bias (Figure 1).

Key Findings and Conclusions:

This overview of SMUS complications commissioned by the ICS aims to provide background literature and algorithms for management of common problems that may present, though it is not exhaustive. Problems such as recurrent urine infection and overactive bladder may have their root cause in an obstructive SMUS. The temporal link between sling implantation and onset of symptoms is not always evident and patients are not always aware that an SMUS was implanted as part of a pelvic floor procedure. Clinicians need to be assiduous in their history taking and physical examination to determine the likely root cause using imaging or other tests judiciously. Multi-disciplinary teams (MDT) are required particularly where chronic pain has developed
人工尿道中悬吊并发症的诊断与治疗
背景与目的:人工合成尿道中吊带(SMUS)已广泛应用于许多女性。并发症发生的比例很小,在围手术期、术后和植入后多年延迟发生。临床试验提供的数据来自于尽可能具有同质性的选定患者。现实世界的研究很少提供样本来源的分母总体的细节。成熟的临床质量登记(CQR)提供非选择人群的长期数据,这些人群因特定疾病接受了手术。接近完全的病例确定是目标,在其他临床领域有许多例子。由于SMUS后可能出现的一些并发症的严重和可能改变生活的性质,卫生机构代表患者采取行动,促进护理的改善。方法和局限性:国际尿失禁学会(ICS)组建了一个多学科工作组来制定本指南。该工作组包括2名消费者权益倡导者和相关的医学专家。讨论了SMUS放置后并发症的处理,并为SMUS的每种常见并发症提供了算法。这些建议是基于专家共识得出的经验和有限的数据从多种叙述和系统的文献综述。由于采用回顾性设计,队列数量少,随访时间短,定义不一致,所有的研究都存在高偏倚风险(图1)。主要发现和结论:由ICS委托进行的SMUS并发症概述旨在为可能出现的常见问题的管理提供背景文献和算法,尽管它并不详尽。诸如反复尿感染和膀胱过度活动等问题可能是梗阻性SMUS的根本原因。吊带植入与症状发作之间的时间联系并不总是很明显,患者并不总是意识到SMUS是作为骨盆底手术的一部分植入的。临床医生需要在病史记录和体格检查中勤奋,以确定可能的根本原因,使用影像学或其他检查审慎。多学科团队(MDT)是必要的,特别是在慢性疼痛已经发展
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