INSERM, Centre d'Investigations Cliniques 9501, Institut lorrain du Cœur et des Vaisseaux Louis Mathieu, Vandoeuvre lès Nancy, France.
Trials. 2013 Jun 1;14:163. doi: 10.1186/1745-6215-14-163.
Anticoagulation for chronic dialysis patients with contraindications to heparin administration is challenging. Current guidelines state that in patients with increased bleeding risks, strategies that can induce systemic anticoagulation should be avoided. Heparin-free dialysis using intermittent saline flushes is widely adopted as the method of choice for patients at risk of bleeding, although on-line blood predilution may also be used. A new dialyzer, Evodial (Gambro, Lund, Sweden), is grafted with unfractionated heparin during the manufacturing process and may allow safe and efficient heparin-free hemodialysis sessions. In the present trial, Evodial was compared to standard care with either saline flushes or blood predilution.
The HepZero study is the first international (seven countries), multicenter (10 centers), randomized, controlled, open-label, non-inferiority (and if applicable subsequently, superiority) trial with two parallel groups, comprising 252 end-stage renal disease patients treated by maintenance hemodialysis for at least 3 months and requiring heparin-free dialysis treatments. Patients will be treated during a maximum of three heparin-free dialysis treatments with either saline flushes or blood predilution (control group), or Evodial. The first heparin-free dialysis treatment will be considered successful when there is: no complete occlusion of air traps or dialyzer rendering dialysis impossible; no additional saline flushes to prevent clotting; no change of dialyzer or blood lines because of clotting; and no premature termination (early rinse-back) because of clotting.The primary objectives of the study are to determine the effectiveness of the Evodial dialyzer, compared with standard care in terms of successful treatments during the first heparin-free dialysis. If the non-inferiority of Evodial is demonstrated then the superiority of Evodial over standard care will be tested. The HepZero study results may have major clinical implications for patient care.
ClinicalTrials.gov NCT01318486.
对于肝素给药禁忌的慢性透析患者,抗凝治疗具有挑战性。当前指南指出,对于出血风险增加的患者,应避免使用可诱导全身抗凝的策略。肝素免费透析使用间歇性盐水冲洗被广泛应用于出血风险患者,尽管在线血液预稀释也可能被使用。一种新型透析器 Evodial( Gambro,Lund,瑞典)在制造过程中接枝未分级肝素,可实现安全有效的肝素免费血液透析。在本试验中,Evodial 与盐水冲洗或血液预稀释的标准护理进行比较。
HepZero 研究是第一项国际(七个国家)、多中心(10 个中心)、随机、对照、开放标签、非劣效(如果适用,随后进行优效性)试验,包括 252 名接受维持性血液透析治疗至少 3 个月且需要肝素免费透析治疗的终末期肾病患者。患者将在最多三次肝素免费透析治疗中接受治疗,分别使用盐水冲洗或血液预稀释(对照组)或 Evodial。第一次肝素免费透析治疗成功的标准是:没有空气陷阱或透析器完全阻塞导致透析无法进行;不需要额外的盐水冲洗以防止凝血;不需要因为凝血而更换透析器或血液管路;并且没有因为凝血而提前终止(早期冲洗回)。该研究的主要目的是确定 Evodial 透析器与标准护理相比,在第一次肝素免费透析期间治疗成功的效果。如果证明 Evodial 具有非劣效性,则将测试 Evodial 优于标准护理的优越性。HepZero 研究结果可能对患者护理具有重要的临床意义。
ClinicalTrials.gov NCT01318486。