Audit of safety and quality of the use of enoxaparin for anticoagulation in continuous renal replacement therapy

Crit Care Resusc. 2011 Mar;13(1):24-7.

Abstract

Objective: To evaluate the safety and efficacy of enoxaparin for anticoagulation during continuous renal replacement therapy (CRRT).

Design: Six-month prospective audit on filter life, anti-Xa activity and bleeding complications among patients undergoing continuous venovenous haemodiafiltration with 1.5mg/kg enoxaparin per 24 hours. The audit was conducted between June and December 2009.

Results: Thirteen patients were included. The median overall filter survival time was 22 hours (range, 2-176 hours). Two patients experienced minor bleeding events, but there were no major bleeding events. Systemic activity of enoxaparin was demonstrated, with a significant rise in median anti-Xa activity between assays before and during filtration (0.00 [range, 0.00-0.13] v 0.31 [range, 0.07-1.26] anti-Xa U/mL; P = 0.03).

Conclusions: Enoxaparin at 1.5mg/kg/24 h appears to be effective for circuit anticoagulation in CRRT and provides significant systemic anticoagulation. Further research is required to evaluate its safety, particularly in the absence of routine anti-Xa monitoring.

Publication types

  • Comparative Study
  • Evaluation Study

MeSH terms

  • APACHE
  • Adult
  • Aged
  • Aged, 80 and over
  • Anticoagulants / therapeutic use*
  • Enoxaparin / therapeutic use*
  • Hemofiltration
  • Humans
  • Intensive Care Units
  • Kidney Diseases / mortality
  • Kidney Diseases / therapy*
  • Length of Stay
  • Male
  • Middle Aged
  • Prospective Studies
  • Renal Replacement Therapy*
  • Time Factors

Substances

  • Anticoagulants
  • Enoxaparin