Department of Nephrology, Poitiers University Hospital, Poitiers, France.
Laboratory of Hematology, Poitiers University Hospital, Poitiers, France.
Hemodial Int. 2022 Jul;26(3):314-322. doi: 10.1111/hdi.13004. Epub 2022 Jan 10.
Low-molecular weight heparins (LMWH) are widely used for preventing clotting during hemodialysis (HD). Although injection in the venous blood line is recommended to avoid initial loss of LMWH through the dialyzer, LMWH is still frequently administered in the arterial blood line at the start of dialysis. This study aimed to compare the safety and efficacy of the same enoxaparin dose administered through the venous blood line or arterial blood line. We also evaluated antifactor Xa (aXa) activity according to the injection route and dialysis modalities: high-flux (HF) HD, medium cut-off (MCO) HD, and online hemodiafiltration (OL-HDF). Forty-three patients were studied over 18 consecutive dialysis sessions using a fixed enoxaparin dose (20 or 40 mg), first administered through the arterial blood line bolus and then through the venous blood line for another 18 sessions. Compared to arterial blood line administration, venous blood line bolus resulted in a significant increase in median post-dialysis aXa activity: 0.16 (0.1-0.6) IU/ml versus 0.31 (0.1-1.3) IU/ml, respectively, p = 0.006. After arterial blood line bolus of 40 mg enoxaparin, median post-dialysis aXa activity was significantly lower with OL-HDF compared to HF-HD: 0.14 (0.1-0.35) versus 0.32 (0.15-0.49), p = 0.02. A trend for lower clotting within lines and bubble trap using venous blood line bolus was observed. In conclusion, venous blood line enoxaparin injection is safe in OL-HDF patients. However, in HF-HD and MCO-HD, venous blood line injection of 40 mg enoxaparin may increase overdosing risk. Thus, aXa activity should be monitored in HF-HD and MCO-HD patients at risk of bleeding and/or on vitamin K antagonists and careful surveillance is required when administering a 40 mg enoxaparin dose through the venous blood line route.
低分子肝素(LMWH)广泛用于预防血液透析(HD)期间的凝血。尽管建议将其注入静脉血路以避免 LMWH 最初通过透析器丢失,但在开始透析时,LMWH 仍经常注入动脉血路。本研究旨在比较通过静脉血路或动脉血路给予相同依诺肝素剂量的安全性和疗效。我们还根据注射途径和透析方式评估抗因子 Xa(aXa)活性:高通量(HF)HD、中截留(MCO)HD 和在线血液透析滤过(OL-HDF)。43 例患者在连续 18 次透析过程中使用固定剂量的依诺肝素(20 或 40mg)进行研究,首先通过动脉血路推注,然后再通过静脉血路进行另外 18 次透析。与动脉血路给药相比,静脉血路推注可显著增加中位透析后 aXa 活性:分别为 0.16(0.1-0.6)IU/ml 和 0.31(0.1-1.3)IU/ml,p=0.006。在动脉血路推注 40mg 依诺肝素后,与 HF-HD 相比,OL-HDF 中中位透析后 aXa 活性显著降低:0.14(0.1-0.35)vs 0.32(0.15-0.49),p=0.02。观察到使用静脉血路推注时线内和气泡捕集器的凝块形成倾向较低。总之,OL-HDF 患者静脉血路依诺肝素注射是安全的。然而,在 HF-HD 和 MCO-HD 中,静脉血路注射 40mg 依诺肝素可能会增加用药过量的风险。因此,HF-HD 和 MCO-HD 中存在出血风险和/或正在使用维生素 K 拮抗剂的患者应监测 aXa 活性,并且需要谨慎监测通过静脉血路途径给予 40mg 依诺肝素剂量。