Morgera Stanislao, Schneider Michael, Slowinski Torsten, Vargas-Hein Ortrud, Zuckermann-Becker Heidrun, Peters Harm, Kindgen-Milles Detlef, Neumayer Hans-Hellmut
Departmentsof Nephrology, University Hospital Charité Campus Mitte, Berlin, Germany.
Crit Care Med. 2009 Jun;37(6):2018-24. doi: 10.1097/CCM.0b013e3181a00a92.
Citrate anticoagulation is an excellent alternative to heparin anticoagulation for critically ill patients requiring continuous renal replacement therapy. In this article, we provide a safe and an easy-to-handle citrate anticoagulation protocol with variable treatment doses and excellent control of the acid-base status.
Prospective observational study.
University hospital.
One hundred sixty-two patients with acute renal failure requiring renal replacement therapy were enrolled in the study.
A continuous venovenous hemodialysis-based citrate anticoagulation protocol using a 4% trisodium solution, a specially designed dialysate fluid, and a continuous calcium infusion were used. The study period was 6 days. Hemofilters were changed routinely after 72 hours of treatment. The patients were grouped according to body weight, with patients below 60 kg body weight in group 1, patients with at least 60 kg and up to 90 kg body weight in group 2, and patients with a body weight of above 90 kg in group 3. Dialysate flow was adapted according to body size and matched approximately 2 L/hr for a patient with average body size. Blood flow, citrate flow, and calcium flow were adjusted according to the dialysate flow used.
Median filter run time was 61.5 hours (interquartile range: 34.5-81.1 hours). Only 5% of all hemofilters had to be changed because of clotting. The prescribed treatment dose was achieved in all patients. Acid-base and electrolyte control were excellent in all groups. In the rare cases of metabolic disarrangement during citrate anticoagulation, acid-base values were rapidly corrected by modifying either the dialysate flow or alternatively the blood flow rate. Eight patients (5%) developed signs of citrate accumulation indicated by an increase of the total calcium >3 mmol/L or a need for high calcium substitution.
We provide a safe and an easy-to-handle citrate anticoagulation protocol that allows an excellent acid-base and electrolyte control in critically ill patients with acute renal failure. The protocol can be adapted to patients' need, allowing a wide spectrum of treatment doses.
对于需要持续肾脏替代治疗的重症患者,枸橼酸盐抗凝是肝素抗凝的一种极佳替代方法。在本文中,我们提供了一种安全且易于操作的枸橼酸盐抗凝方案,该方案具有可变的治疗剂量,并能出色地控制酸碱状态。
前瞻性观察性研究。
大学医院。
162例需要肾脏替代治疗的急性肾衰竭患者纳入本研究。
采用基于持续静脉-静脉血液透析的枸橼酸盐抗凝方案,使用4%的三钠溶液、一种专门设计的透析液以及持续钙剂输注。研究期为6天。治疗72小时后常规更换血液滤过器。患者按体重分组,体重低于60 kg的患者为第1组,体重至少60 kg且最高90 kg的患者为第2组,体重超过90 kg的患者为第3组。透析液流量根据体型进行调整,平均体型患者的透析液流量约为2 L/小时。血流、枸橼酸盐流量和钙剂流量根据所用透析液流量进行调整。
滤器中位使用时间为61.5小时(四分位间距:34.5 - 81.1小时)。所有血液滤过器中仅5%因凝血而需要更换。所有患者均达到规定的治疗剂量。所有组的酸碱和电解质控制均良好。在枸橼酸盐抗凝期间罕见的代谢紊乱情况下,通过调整透析液流量或血流速率可迅速纠正酸碱值。8例患者(5%)出现枸橼酸盐蓄积迹象,表现为总钙升高>3 mmol/L或需要大量补钙。
我们提供了一种安全且易于操作的枸橼酸盐抗凝方案,该方案能在急性肾衰竭重症患者中实现出色的酸碱和电解质控制。该方案可根据患者需求进行调整,允许广泛的治疗剂量。