Anticoagulation strategies in continuous renal replacement therapy

被引:67
作者
Legrand, Matthieu [1 ,2 ]
Tolwani, Ashita [3 ]
机构
[1] UCSF, Sch Med, Dept Anesthesia & Perioperat Care, Div Crit Care Med, San Francisco, CA USA
[2] INI CRCT Network, Nancy, France
[3] Univ Alabama Birmingham, Div Nephrol, Dept Internal Med, Birmingham, AL USA
关键词
anticoagulation; citrate; continuous renal replacement therapy;
D O I
10.1111/sdi.12959
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
The most common anticoagulant options for continuous renal replacement therapy (CRRT) include unfractionated heparin (UFH), regional citrate anticoagulation (RCA), and no anticoagulation. Less common anticoagulation options include UFH with protamine reversal, low-molecular weight heparin (LMWH), thrombin antagonists, and platelet inhibiting agents. The choice of anticoagulant for CRRT should be determined by patient characteristics, local expertise, and ease of monitoring. The Kidney Disease Improving Global Outcomes (KDIGO) acute kidney injury guidelines recommend using RCA rather than UFH in patients who do not have contraindications to citrate and are with or without increased risk of bleeding. Monitoring should include evaluation of the anticoagulant effect, circuit life, filter efficacy, and complications.
引用
收藏
页码:416 / 422
页数:7
相关论文
共 29 条
[1]   Citrate versus heparin anticoagulation for continuous renal replacement therapy: an updated meta-analysis of RCTs [J].
Bai, Ming ;
Zhou, Meilan ;
He, Lijie ;
Ma, Feng ;
Li, Yangping ;
Yu, Yan ;
Wang, Pengbo ;
Li, Li ;
Jing, Rui ;
Zhao, Lijuan ;
Sun, Shiren .
INTENSIVE CARE MEDICINE, 2015, 41 (12) :2098-2110
[2]   Inability of the activated partial thromboplastin time to predict heparin levels - Time to reassess guidelines for heparin assays [J].
Baker, BA ;
Adelman, MD ;
Smith, PA ;
Osborn, JC .
ARCHIVES OF INTERNAL MEDICINE, 1997, 157 (21) :2475-2479
[3]   Bioenergetic gain of citrate anticoagulated continuous hemodiafiltration-a comparison between 2 citrate modalities and unfractionated heparin [J].
Balik, Martin ;
Zakharchenko, Mykhaylo ;
Leden, Pavel ;
Otahal, Michal ;
Hruby, Jan ;
Polak, Ferdinand ;
Rusinova, Katerina ;
Stach, Zdenek ;
Tokarik, Monika ;
Vavrova, Jaroslava ;
Jabor, Antonin ;
Oudemans-van Straaten, Heleen M. .
JOURNAL OF CRITICAL CARE, 2013, 28 (01) :87-95
[4]  
BLAUFOX MD, 1966, T AM SOC ART INT ORG, V12, P207
[5]   Citrate anticoagulation for extracorporeal circuits: Effects on whole blood coagulation activation and clot formation [J].
Calatzis, A ;
Toepfer, M ;
Schramm, W ;
Spannagl, M ;
Schiffl, H .
NEPHRON, 2001, 89 (02) :233-236
[6]   ANTICOAGULANT ACTION OF HEPARIN [J].
DAMUS, PS ;
HICKS, M ;
ROSENBERG, RD .
NATURE, 1973, 246 (5432) :355-357
[7]   Nadroparin versus dalteparin anticoagulation in high-volume, continuous venovenous hemofiltration: A double-blind, randomized, crossover study [J].
de Pont, ACJM ;
Oudemans-van Straaten, HM ;
Roozendaal, KJ ;
Zandstra, DF .
CRITICAL CARE MEDICINE, 2000, 28 (02) :421-425
[8]  
Greaves M, 2002, THROMB HAEMOSTASIS, V87, P163
[9]   Citrate plasma levels in patients under regional anticoagulation in continuous venovenous hemofiltration [J].
Hetzel, Gerd R. ;
Taskaya, Gediz ;
Sucker, Christoph ;
Hennersdorf, Marcus ;
Grabensee, Bernd ;
Schmitz, Michael .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2006, 48 (05) :806-811
[10]   Heparin and low-molecular-weight heparin - Mechanisms of action, pharmacokinetics, dosing, monitoring, efficacy, and safety [J].
Hirsh, J ;
Warkentin, TE ;
Shaughnessy, SG ;
Anand, SS ;
Halperin, JL ;
Raschke, R ;
Granger, C ;
Ohman, EM ;
Dalen, JE .
CHEST, 2001, 119 (01) :64S-94S