Department of Nephrology, Erasme Hospital, Université Libre de Bruxelles, Brussels, Belgium.
Am J Kidney Dis. 2013 Mar;61(3):459-65. doi: 10.1053/j.ajkd.2012.10.014. Epub 2012 Dec 8.
Hemodialysis (HD) tunneled cuffed catheters may be fitted with neutral-valve closed-system connectors. Such connectors, which are flushed with saline solution and used for 3 consecutive HD sessions, provide a mechanically closed positive-pressure barrier and potentially may be useful to prevent catheter-related bacteremia and dysfunction.
Single-center randomized controlled trial.
SETTING & PARTICIPANTS: 66 adult HD patients with a tunneled cuffed catheter.
Neutral-valve closed-system connector (Tego Needlefree Hemodialysis Connector) versus trisodium citrate, 46.7%, locking solution (Citra-Lock; control group).
Primary composite outcome was the incidence rate of catheter-related dysfunction or bacteremia. Secondary outcomes were the separate incidence rates of catheter-related dysfunction and bacteremia and the cost of both procedures.
Catheter dysfunction was defined as the requirement of urokinase and/or a mean blood flow ≤250 mL/min during 2 consecutive HD sessions. Catheter-related bacteremia was defined as ≥2 positive blood cultures. Time of catheter use was calculated and the incidence rate of complications was expressed per 100 person-years.
66 patients were followed up for a median of 86 (IQR, 29-200) days. The composite primary outcome was not significantly reduced in the closed-system-connector intervention group versus the citrate-locking-solution control group (63.56 vs 71.51 per 100 person-years; P = 0.3). Catheter dysfunction in the intervention group was not decreased versus controls (59.59 vs 51.64 per 100-person-years; P = 0.9). Only 6 catheter-related bacteremia events were identified, one in the intervention group (3.97 vs 19.86 per 100 person-years; P = 0.06).
Small size of the patient population and single-center study.
Superiority of the closed-system connector in terms of prevention of the primary efficacy end point compared to the standard locking solution was not observed. Further evaluation in a larger study is suggested.
血液透析(HD)隧道带袖套的导管可能配备中性阀密闭系统连接器。这种连接器用生理盐水冲洗,用于连续 3 次 HD 治疗,提供机械密闭正压屏障,可能有助于预防导管相关性菌血症和功能障碍。
单中心随机对照试验。
66 例成人隧道带袖套的导管患者。
中性阀密闭系统连接器(Tego 无针血液透析连接器)与枸橼酸钠 46.7%,锁定溶液(Citra-Lock;对照组)。
主要复合终点是导管相关性功能障碍或菌血症的发生率。次要结局是导管相关性功能障碍和菌血症的发生率以及两种程序的成本。
导管功能障碍定义为在连续 2 次 HD 治疗中需要尿激酶和/或平均血流<250ml/min。导管相关性菌血症定义为≥2 次阳性血培养。计算导管使用时间,并按每 100 人年的发生率表示并发症的发生率。
66 例患者中位随访 86(IQR,29-200)天。密闭系统连接器干预组与枸橼酸钠锁定溶液对照组复合主要结局无显著降低(63.56 与 71.51/100 人年;P=0.3)。干预组导管功能障碍与对照组无差异(59.59 与 51.64/100 人年;P=0.9)。仅发现 6 例导管相关性菌血症事件,其中 1 例发生在干预组(3.97 与 19.86/100 人年;P=0.06)。
患者人群规模小和单中心研究。
与标准锁定溶液相比,密闭系统连接器在预防主要疗效终点方面的优势没有得到观察。建议在更大的研究中进一步评估。