Ailsa Hospital, NHS Ayrshire & Arran, Ayr, UK.
Neurourol Urodyn. 2011 Sep;30(7):1208-12. doi: 10.1002/nau.21063. Epub 2011 May 11.
People requiring long-term bladder draining with an indwelling catheter can experience catheter blockage. Regimens involving different solutions can be used to wash out catheters with the aim of preventing blockage.
To determine if certain washout regimens (including no washout) are better than others in terms of effectiveness, acceptability, complications, quality of life, and economics for the management of long-term indwelling urinary catheters in adults.
We searched the Cochrane Incontinence Group Specialized Trials Register (searched April 30, 2009), MEDLINE (January 1966 to April 2009), MEDLINE In-Process (April 30, 2009), EMBASE (January 1980 to April 2009), and CINAHL (December 1981 to April 2009). Additionally, we examined all reference lists of identified trials and contacted manufacturers and researchers in the field.
All randomized and quasi-randomized trials comparing catheter washout policies (e.g., washout vs. no washout, different washout solutions, frequency, duration, volume, concentration, method of administration) in adults (16 years and above) in any setting (i.e., hospital, nursing/residential home, community) with an indwelling urethral or suprapubic catheter in place for more than 28 days.
Data were extracted by three reviewers independently and compared. Disagreements were resolved by discussion. Data were processed as described in the Cochrane Handbook. If the trial data were not fully reported, clarification was sought from the authors. For categorical outcomes, the numbers reporting an outcome were related to the numbers at risk in each group to derive a risk ratio (RR). For continuous outcomes, means, and standard deviations were used to derive weighted mean differences (WMD). No meta-analysis of study results was possible.
Five trials met the inclusion criteria involving 242 patients (132 completed) in two cross-over and three parallel-group randomized controlled trials. Only three of the eight comparisons pre-stated in the review protocol were addressed in these trials. Some trials addressed more than one comparison (e.g., washout vs. no washout and one type of washout solution vs. another). The analyses reported for the two cross-over trials were inappropriate as they were based on differences between groups rather than differences within individuals receiving sequential interventions. Two parallel-group trials had limited value: one combined results for suprapubic and urethral catheters and one had data on only four participants. Only one trial was free of significant methodological limitations, but its sample size was small. Three trials compared no washout with one or more washout solution (saline or acidic solutions) and authors tended to conclude no difference in clinical outcomes between washout and no washout. In the one trial which had data of sufficient quality to allow interpretation, no difference was detected between washout and no washout groups in the rate of symptomatic urinary tract infection or time to first catheter change. Three trials compared different types of solution: saline versus acidic solutions (two trials); saline versus acidic solution versus antibiotic solution (one trial). Authors tended to report no difference between different washout solutions but the data were too few to support their conclusions. The one trial which warranted consideration concluded no difference between saline and an acidic solution in terms of symptomatic urinary tract infections or time to first catheter change.
The data from five trials comparing differing washout policies were sparse and trials were generally of poor quality or poorly reported. The evidence was too scant to conclude whether or not washouts were beneficial. Further rigorous, high quality trials with adequate power to detect any benefit from washout rather than no washout being performed are required in the first instance. After that, trials comparing different washout solutions, washout volumes, frequencies/timings, and routes of administration are needed.
需要长期留置导尿管的患者可能会出现导管堵塞。冲洗导管的方案涉及不同的溶液,目的是预防堵塞。
确定在成人长期留置导尿管管理方面,冲洗方案(包括不冲洗)在有效性、可接受性、并发症、生活质量和经济学方面是否优于其他方案。
我们检索了 Cochrane 尿失禁组专业试验注册库(2009 年 4 月 30 日检索)、MEDLINE(1966 年 1 月至 2009 年 4 月)、MEDLINE 正在处理(2009 年 4 月 30 日)、EMBASE(1980 年 1 月至 2009 年 4 月)和 CINAHL(1981 年 12 月至 2009 年 4 月)。此外,我们还检查了所有确定试验的参考文献,并联系了该领域的制造商和研究人员。
所有比较成人(16 岁及以上)留置导尿管冲洗方案(如冲洗与不冲洗、不同冲洗溶液、冲洗频率、持续时间、冲洗量、冲洗浓度、冲洗方法)的随机和半随机试验,在任何环境(即医院、护理/养老院、社区)中,留置导尿管超过 28 天。
数据由三位评审员独立提取,并进行比较。有分歧的地方通过讨论解决。数据处理按照 Cochrane 手册的说明进行。如果试验数据没有完全报告,则向作者寻求澄清。对于分类结果,报告结局的人数与每组的风险人数相关,以得出风险比(RR)。对于连续结果,使用均值和标准差得出加权均数差(WMD)。由于研究结果的多样性,不可能进行meta 分析。
五项试验符合纳入标准,涉及 242 名患者(132 名完成),其中两项为交叉试验,三项为平行组随机对照试验。只有八项比较中的三项在研究方案中预先提出。这些试验中的一些比较了多个方案(如冲洗与不冲洗和一种冲洗溶液与另一种冲洗溶液)。两项交叉试验报告的分析不恰当,因为它们基于组间差异,而不是个体接受连续干预时的差异。两项平行组试验价值有限:一项结合了耻骨上和尿道导管的结果,另一项只有 4 名参与者的数据。只有一项试验没有明显的方法学限制,但样本量较小。三项试验比较了不冲洗与一种或多种冲洗溶液(盐水或酸性溶液),作者倾向于得出冲洗与不冲洗在临床结局方面无差异的结论。在一项试验中,有足够质量的数据可以进行解释,在症状性尿路感染的发生率或首次更换导管的时间方面,冲洗组和不冲洗组之间没有差异。三项试验比较了不同类型的溶液:盐水与酸性溶液(两项试验);盐水与酸性溶液与抗生素溶液(一项试验)。作者倾向于报告不同冲洗溶液之间无差异,但数据太少,无法支持他们的结论。一项值得考虑的试验得出的结论是,在症状性尿路感染或首次更换导管的时间方面,盐水和酸性溶液之间无差异。
五项比较不同冲洗方案的试验数据稀少,试验质量普遍较差或报告不佳。证据太少,无法得出冲洗是否有益的结论。首先需要进行更多严格、高质量、有足够效能的试验,以检测冲洗而非不冲洗是否有益。在此之后,需要比较不同的冲洗溶液、冲洗量、冲洗频率/时间以及冲洗途径的试验。