TY - JOUR
T1 - Regional citrate versus heparin anticoagulation for continuous renal replacement therapy
T2 - A meta-analysis of randomized controlled trials
AU - Wu, Mei Yi
AU - Hsu, Yung Ho
AU - Bai, Chyi Huey
AU - Lin, Yuh Feng
AU - Wu, Chih Hsiung
AU - Tam, Ka Wai
PY - 2012/6
Y1 - 2012/6
N2 - Background: Anticoagulation of the extracorporeal circuit is required in continuous renal replacement therapy (CRRT). Heparin is the classic choice for anticoagulation, although it may increase the risk of bleeding. Regional citrate anticoagulation reduces the risk of bleeding, but may cause hypocalcemia and metabolic disturbances. Study Design: Systematic review and meta-analysis of randomized controlled trials (RCTs). Setting & Population: Patients admitted to the intensive care unit with acute kidney injury that required CRRT. Selection Criteria for Studies: RCTs regardless of publication status or language. Intervention: Regional citrate versus heparin anticoagulation in CRRT. Outcomes: The primary outcomes were circuit survival time, the occurrence of major bleeding defined as a site of gross bleeding with a decrease in blood pressure or requiring transfusion of 2 or more units of red blood cells, metabolic alkalosis, hypocalcemia, and thrombocytopenia. The secondary outcome was cost. Results: 6 RCTs with 488 patients were identified. Citrate anticoagulation was associated with a significant decrease in bleeding (RR, 0.34; 95% CI, 0.17-0.65). Circuit survival time, the incidence of metabolic alkalosis, and thrombocytopenia showed no significant difference between groups. Hypocalcemia was more common in patients receiving citrate, although no clinical adverse event was reported in the included studies. Limitations: Significant heterogeneity in the primary outcome. Conclusion: The efficacy of citrate and heparin anticoagulation for CRRT was similar. However, citrate anticoagulation decreased the risk of bleeding with no significant increase in the incidence of metabolic alkalosis. We recommend citrate as an anticoagulation agent in patients who require CRRT but are at high risk of bleeding.
AB - Background: Anticoagulation of the extracorporeal circuit is required in continuous renal replacement therapy (CRRT). Heparin is the classic choice for anticoagulation, although it may increase the risk of bleeding. Regional citrate anticoagulation reduces the risk of bleeding, but may cause hypocalcemia and metabolic disturbances. Study Design: Systematic review and meta-analysis of randomized controlled trials (RCTs). Setting & Population: Patients admitted to the intensive care unit with acute kidney injury that required CRRT. Selection Criteria for Studies: RCTs regardless of publication status or language. Intervention: Regional citrate versus heparin anticoagulation in CRRT. Outcomes: The primary outcomes were circuit survival time, the occurrence of major bleeding defined as a site of gross bleeding with a decrease in blood pressure or requiring transfusion of 2 or more units of red blood cells, metabolic alkalosis, hypocalcemia, and thrombocytopenia. The secondary outcome was cost. Results: 6 RCTs with 488 patients were identified. Citrate anticoagulation was associated with a significant decrease in bleeding (RR, 0.34; 95% CI, 0.17-0.65). Circuit survival time, the incidence of metabolic alkalosis, and thrombocytopenia showed no significant difference between groups. Hypocalcemia was more common in patients receiving citrate, although no clinical adverse event was reported in the included studies. Limitations: Significant heterogeneity in the primary outcome. Conclusion: The efficacy of citrate and heparin anticoagulation for CRRT was similar. However, citrate anticoagulation decreased the risk of bleeding with no significant increase in the incidence of metabolic alkalosis. We recommend citrate as an anticoagulation agent in patients who require CRRT but are at high risk of bleeding.
KW - Citrate
KW - anticoagulation
KW - continuous renal replacement therapy
KW - heparin
KW - meta-analysis
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U2 - 10.1053/j.ajkd.2011.11.030
DO - 10.1053/j.ajkd.2011.11.030
M3 - Article
C2 - 22226564
AN - SCOPUS:84858793574
SN - 0272-6386
VL - 59
SP - 810
EP - 818
JO - American Journal of Kidney Diseases
JF - American Journal of Kidney Diseases
IS - 6
ER -