Kosa Sarah D, Al-Jaishi Ahmed A, Moist Louise, Lok Charmaine E
Department of Clinical Epidemiology and Biostatistics, McMaster University, 28 Undercliffe Avenue, Hamilton, ON, Canada, L8P 2H1.
Cochrane Database Syst Rev. 2015 Sep 30;2015(9):CD007013. doi: 10.1002/14651858.CD007013.pub2.
Haemodialysis treatment requires reliable vascular access. Optimal access is provided via functional arteriovenous fistula (fistula), which compared with other forms of vascular access, provides superior long-term patency, requires few interventions, has low thrombosis and infection rates and cost. However, it has been estimated that between 20% and 60% of fistulas never mature sufficiently to enable haemodialysis treatment. Mapping blood vessels using imaging technologies before surgery may identify vessels that are most suitable for fistula creation.
We compared the effect of conducting routine radiological imaging evaluation for vascular access creation preoperatively with standard care without routine preoperative vessel imaging on fistula creation and use.
We searched Cochrane Kidney and Transplant's Specialised Register to 14 April 2015 through contact with the Trials' Search Co-ordinator using search terms relevant to this review.
We included randomised controlled trials (RCTs) that enrolled adult participants (aged ≥ 18 years) with chronic or end-stage kidney disease (ESKD) who needed fistulas (both before dialysis and after dialysis initiation) that compared fistula maturation rates relating to use of imaging technologies to map blood vessels before fistula surgery with standard care (no imaging).
Two authors assessed study quality and extracted data. Dichotomous outcomes, including fistula creation, maturation and need for catheters at dialysis initiation, were expressed as risk ratios (RR) with 95% confidence intervals (CI). Continuous outcomes, such as numbers of interventions required to maintain patency, were expressed as mean differences (MD). We used the random-effects model to measure mean effects.
Four studies enrolling 450 participants met our inclusion criteria. Overall risk of bias was judged to be low in one study, unclear in two, and high in one.There was no significant differences in the number of fistulas that were successfully created (4 studies, 433 patients: RR 1.06, 95% CI 0.95 to 1.28; I² = 76%); the number of fistulas that matured at six months (3 studies, 356 participants: RR 1.11, 95% CI 0.98 to 1.25; I² = 0%); number of fistulas that were used successfully for dialysis (2 studies, 286 participants: RR 1.12, 95% CI 0.99 to 1.28; I² = 0%); the number of patients initiating dialysis with a catheter (1 study, 214 patients: RR 0.66, 95% CI 0.42 to 1.04); and in the rate of interventions required to maintain patency (1 study, 70 patients: MD 14.70 interventions/1000 patient-days, 95% CI -7.51 to 36.91) between the use of preoperative imaging technologies compared with standard care (no imaging).
AUTHORS' CONCLUSIONS: Based on four small studies, preoperative vessel imaging did not improve fistula outcomes compared with standard care. Adequately powered prospective studies are required to fully answer this question.
血液透析治疗需要可靠的血管通路。最佳的血管通路是通过功能性动静脉内瘘(内瘘)实现的,与其他形式的血管通路相比,内瘘具有更高的长期通畅率,所需干预少,血栓形成和感染率低且成本低。然而,据估计,20%至60%的内瘘从未充分成熟到能够进行血液透析治疗。术前使用成像技术对血管进行造影可能会识别出最适合创建内瘘的血管。
我们比较了术前对血管通路创建进行常规放射学成像评估与不进行常规术前血管成像的标准护理在创建和使用内瘘方面的效果。
我们通过与试验检索协调员联系,使用与本综述相关的检索词,检索了截至2015年4月14日的Cochrane肾脏和移植专业注册库。
我们纳入了随机对照试验(RCT),这些试验纳入了成年参与者(年龄≥18岁),患有慢性或终末期肾病(ESKD),需要内瘘(透析前和开始透析后),比较了在瘘管手术前使用成像技术对血管进行造影与标准护理(无成像)相关的内瘘成熟率。
两位作者评估了研究质量并提取了数据。二分结果,包括内瘘创建、成熟以及透析开始时对导管的需求,以风险比(RR)及95%置信区间(CI)表示。连续结果,如维持通畅所需的干预次数,以平均差(MD)表示。我们使用随机效应模型来衡量平均效应。
四项纳入450名参与者的研究符合我们的纳入标准。一项研究中总体偏倚风险被判定为低,两项为不清楚,一项为高。在成功创建的内瘘数量(4项研究,433例患者:RR 1.06,95% CI 0.95至1.28;I² = 76%)、六个月时成熟的内瘘数量(3项研究,356名参与者:RR 1.11,95% CI 0.98至1.25;I² = 0%)、成功用于透析的内瘘数量(2项研究,286名参与者:RR 1.12,95% CI 0.99至1.28;I² = 0%)、开始透析时使用导管的患者数量(1项研究,214例患者:RR 0.66,95% CI 0.42至1.04)以及维持通畅所需的干预率(1项研究,70例患者:MD 14.70次干预/1000患者日,95% CI -7.51至36.91)方面,术前成像技术与标准护理(无成像)之间没有显著差异。
基于四项小型研究,与标准护理相比,术前血管成像并未改善内瘘的结果。需要进行足够样本量的前瞻性研究来充分回答这个问题。