Kang Diana, Han Julia, Neuberger Molly M, Moy M Louis, Wallace Sheila A, Alonso-Coello Pablo, Dahm Philipp
Department of Urology, University of California Los Angeles, 200 Medical Plaza, Suite 140 PMB 252, Los Angeles, CA, USA, 90025.
Cochrane Database Syst Rev. 2015 Mar 18;2015(3):CD010217. doi: 10.1002/14651858.CD010217.pub2.
Transurethral radiofrequency collagen denaturation is a relatively novel, minimally invasive device-based intervention used to treat individuals with urinary incontinence (UI). No systematic review of the evidence supporting its use has been published to date.
To evaluate the efficacy of transurethral radiofrequency collagen denaturation, compared with other interventions, in the treatment of women with UI.Review authors sought to compare the following.• Transurethral radiofrequency collagen denaturation versus no treatment/sham treatment.• Transurethral radiofrequency collagen denaturation versus conservative physical treatment.• Transurethral radiofrequency collagen denaturation versus mechanical devices (pessaries for UI).• Transurethral radiofrequency collagen denaturation versus drug treatment.• Transurethral radiofrequency collagen denaturation versus injectable treatment for UI.• Transurethral radiofrequency collagen denaturation versus other surgery for UI.
We conducted a systematic search of the Cochrane Incontinence Group Specialised Register (searched 19 December 2014), EMBASE and EMBASE Classic (January 1947 to 2014 Week 50), Google Scholar and three trials registries in December 2014, along with reference checking. We sought to identify unpublished studies by handsearching abstracts of major gynaecology and urology meetings, and by contacting experts in the field and the device manufacturer.
Randomised and quasi-randomised trials of transurethral radiofrequency collagen denaturation versus no treatment/sham treatment, conservative physical treatment, mechanical devices, drug treatment, injectable treatment for UI or other surgery for UI in women were eligible.
We screened search results and selected eligible studies for inclusion. We assessed risk of bias and analysed dichotomous variables as risk ratios (RRs) with 95% confidence intervals (CIs) and continuous variables as mean differences (MDs) with 95% CIs. We rated the quality of evidence using the GRADE (Grading of Recommendations Assessment, Development and Evaluation) approach.
We included in the analysis one small sham-controlled randomised trial of 173 women performed in the United States. Participants enrolled in this study had been diagnosed with stress UI and were randomly assigned to transurethral radiofrequency collagen denaturation (treatment) or a sham surgery using a non-functioning catheter (no treatment). Mean age of participants in the 12-month multi-centre trial was 50 years (range 22 to 76 years).Of three patient-important primary outcomes selected for this systematic review, the number of women reporting UI symptoms after intervention was not reported. No serious adverse events were reported for the transurethral radiofrequency collagen denaturation arm or the sham treatment arm during the 12-month trial. Owing to high risk of bias and imprecision, we downgraded the quality of evidence for this outcome to low. The effect of transurethral radiofrequency collagen denaturation on the number of women with an incontinence quality of life (I-QOL) score improvement ≥ 10 points at 12 months was as follows: RR 1.11, 95% CI 0.77 to 1.62; participants = 142, but the confidence interval was wide. For this outcome, the quality of evidence was also low as the result of high risk of bias and imprecision.We found no evidence on the number of women undergoing repeat continence surgery. The risk of other adverse events (pain/dysuria (RR 5.73, 95% CI 0.75 to 43.70; participants = 173); new detrusor overactivity (RR 1.36, 95% CI 0.63 to 2.93; participants = 173); and urinary tract infection (RR 0.95, 95% CI 0.24 to 3.86; participants = 173) could not be established reliably as the trial was small. Evidence was insufficient for assessment of whether use of transurethral radiofrequency collagen denaturation was associated with an increased rate of urinary retention, haematuria and hesitancy compared with sham treatment in 173 participants. The GRADE quality of evidence for all other adverse events with available evidence was low as the result of high risk of bias and imprecision.We found no evidence to inform comparisons of transurethral radiofrequency collagen denaturation with conservative physical treatment, mechanical devices, drug treatment, injectable treatment for UI or other surgery for UI.
AUTHORS' CONCLUSIONS: It is not known whether transurethral radiofrequency collagen denaturation, as compared with sham treatment, improves patient-reported symptoms of UI. Evidence is insufficient to show whether the procedure improves disease-specific quality of life. Evidence is also insufficient to show whether the procedure causes serious adverse events or other adverse events in comparison with sham treatment, and no evidence was found for comparison with any other method of treatment for UI.
经尿道射频胶原变性术是一种相对新颖的、基于微创设备的干预措施,用于治疗尿失禁(UI)患者。迄今为止,尚未发表对支持其应用的证据进行的系统评价。
评估经尿道射频胶原变性术与其他干预措施相比,在治疗女性尿失禁方面的疗效。综述作者试图比较以下方面。
• 经尿道射频胶原变性术与不治疗/假治疗。
• 经尿道射频胶原变性术与保守物理治疗。
• 经尿道射频胶原变性术与机械装置(用于尿失禁的子宫托)。
• 经尿道射频胶原变性术与药物治疗。
• 经尿道射频胶原变性术与用于尿失禁的注射治疗。
• 经尿道射频胶原变性术与其他尿失禁手术。
我们对Cochrane尿失禁小组专业注册库(2014年12月19日检索)、EMBASE及EMBASE经典数据库(1947年1月至2014年第50周)、谷歌学术进行了系统检索,并于2014年12月检索了三个试验注册库,同时进行参考文献核对。我们试图通过手工检索主要妇科和泌尿外科学术会议的摘要、联系该领域专家及设备制造商来识别未发表的研究。
经尿道射频胶原变性术与不治疗/假治疗、保守物理治疗、机械装置、药物治疗、用于尿失禁的注射治疗或其他女性尿失禁手术的随机和半随机试验符合纳入标准。
我们筛选检索结果并选择符合纳入标准的研究。我们评估偏倚风险,并将二分变量分析为具有95%置信区间(CIs)的风险比(RRs),将连续变量分析为具有95% CIs的平均差(MDs)。我们使用GRADE(推荐分级评估、制定与评价)方法对证据质量进行评级。
我们纳入分析的是在美国进行的一项针对173名女性的小型假对照随机试验。参与本研究的受试者被诊断为压力性尿失禁,并被随机分配至经尿道射频胶原变性术(治疗组)或使用无功能导管的假手术(未治疗组)。在这项为期12个月的多中心试验中,受试者的平均年龄为50岁(范围22至76岁)。在本次系统评价选择的三个对患者重要的主要结局中,未报告干预后报告尿失禁症状的女性数量。在为期12个月的试验中,经尿道射频胶原变性术组或假治疗组均未报告严重不良事件。由于偏倚风险高且结果不精确,我们将该结局的证据质量降为低质量。经尿道射频胶原变性术对12个月时失禁生活质量(I-QOL)评分改善≥10分的女性数量的影响如下:RR 1.11,95% CI 0.77至1.62;受试者 = 142,但置信区间较宽。对于该结局,由于偏倚风险高且结果不精确,证据质量也为低质量。我们未找到关于接受重复尿失禁手术的女性数量的证据。由于试验规模小,其他不良事件(疼痛/排尿困难(RR 5.73,95% CI 0.75至43.70;受试者 = 173);新发逼尿肌过度活动(RR 1.36,95% CI 0.63至2.93;受试者 = 173);以及尿路感染(RR 0.95,95% CI 0.24至3.86;受试者 = 173))的风险无法可靠确定。对于173名受试者,与假治疗相比,使用经尿道射频胶原变性术是否与尿潴留、血尿和排尿犹豫发生率增加相关的证据不足。由于偏倚风险高且结果不精确,所有其他有可用证据的不良事件的GRADE证据质量均为低质量。我们未找到证据来比较经尿道射频胶原变性术与保守物理治疗、机械装置、药物治疗、用于尿失禁的注射治疗或其他尿失禁手术。
与假治疗相比,经尿道射频胶原变性术是否能改善患者报告的尿失禁症状尚不清楚。证据不足以表明该手术是否能改善疾病特异性生活质量。与假治疗相比,也没有足够的证据表明该手术是否会导致严重不良事件或其他不良事件,并且未找到与任何其他尿失禁治疗方法进行比较的证据。