Dember Laura M, Beck Gerald J, Allon Michael, Delmez James A, Dixon Bradley S, Greenberg Arthur, Himmelfarb Jonathan, Vazquez Miguel A, Gassman Jennifer J, Greene Tom, Radeva Milena K, Braden Gregory L, Ikizler T Alp, Rocco Michael V, Davidson Ingemar J, Kaufman James S, Meyers Catherine M, Kusek John W, Feldman Harold I
Boston University, School of Medicine, Renal Section, EBRC 504, 650 Albany St, Boston, Massachusetts 02118, USA.
JAMA. 2008 May 14;299(18):2164-71. doi: 10.1001/jama.299.18.2164.
The arteriovenous fistula is the preferred type of vascular access for hemodialysis because of lower thrombosis and infection rates and lower health care expenditures compared with synthetic grafts or central venous catheters. Early failure of fistulas due to thrombosis or inadequate maturation is a barrier to increasing the prevalence of fistulas among patients treated with hemodialysis. Small, inconclusive trials have suggested that antiplatelet agents may reduce thrombosis of new fistulas.
To determine whether clopidogrel reduces early failure of hemodialysis fistulas.
DESIGN, SETTING, AND PARTICIPANTS: Randomized, double-blind, placebo-controlled trial conducted at 9 US centers composed of academic and community nephrology practices in 2003-2007. Eight hundred seventy-seven participants with end-stage renal disease or advanced chronic kidney disease were followed up until 150 to 180 days after fistula creation or 30 days after initiation of dialysis, whichever occurred later.
Participants were randomly assigned to receive clopidogrel (300-mg loading dose followed by daily dose of 75 mg; n = 441) or placebo (n = 436) for 6 weeks starting within 1 day after fistula creation.
The primary outcome was fistula thrombosis, determined by physical examination at 6 weeks. The secondary outcome was failure of the fistula to become suitable for dialysis. Suitability was defined as use of the fistula at a dialysis machine blood pump rate of 300 mL/min or more during 8 of 12 dialysis sessions.
Enrollment was stopped after 877 participants were randomized based on a stopping rule for intervention efficacy. Fistula thrombosis occurred in 53 (12.2%) participants assigned to clopidogrel compared with 84 (19.5%) participants assigned to placebo (relative risk, 0.63; 95% confidence interval, 0.46-0.97; P = .018). Failure to attain suitability for dialysis did not differ between the clopidogrel and placebo groups (61.8% vs 59.5%, respectively; relative risk, 1.05; 95% confidence interval, 0.94-1.17; P = .40).
Clopidogrel reduces the frequency of early thrombosis of new arteriovenous fistulas but does not increase the proportion of fistulas that become suitable for dialysis. Trial Registration clinicaltrials.gov Identifier: NCT00067119.
动静脉内瘘是血液透析首选的血管通路类型,因为与合成移植物或中心静脉导管相比,其血栓形成和感染率较低,医疗费用也较低。因血栓形成或成熟不足导致的内瘘早期失功是阻碍血液透析患者中内瘘普及率提高的一个障碍。小型、无定论的试验表明,抗血小板药物可能会减少新内瘘的血栓形成。
确定氯吡格雷是否能减少血液透析内瘘的早期失功。
设计、地点和参与者:2003年至2007年在美国9个中心进行的随机、双盲、安慰剂对照试验,这些中心包括学术和社区肾脏病医疗单位。877名终末期肾病或晚期慢性肾病参与者被随访至内瘘建立后150至180天或开始透析后30天,以较晚者为准。
参与者在瘘管建立后1天内开始随机分配接受氯吡格雷(负荷剂量300mg,随后每日剂量75mg;n = 441)或安慰剂(n = 436),持续6周。
主要结局是瘘管血栓形成,在6周时通过体格检查确定。次要结局是瘘管未能变得适合透析。适合的定义是在12次透析疗程中的8次中,瘘管在透析机血泵速率为300mL/min或更高时使用。
根据干预效果的停止规则,在877名参与者随机分组后试验停止。分配到氯吡格雷组的参与者中有53人(12.2%)发生瘘管血栓形成,而分配到安慰剂组的有84人(19.5%)(相对风险,0.63;95%置信区间,0.46 - 0.97;P = 0.018)。氯吡格雷组和安慰剂组在未能达到适合透析的情况方面没有差异(分别为61.8%和59.5%;相对风险,1.05;95%置信区间,0.94 - 1.17;P = 0.40)。
氯吡格雷可降低新动静脉内瘘早期血栓形成的频率,但不会增加适合透析的内瘘比例。试验注册 clinicaltrials.gov 标识符:NCT00067119。