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Volume 50, Issue 3, Pages 433-440 (September 2007)


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Warfarin Anticoagulation in Hemodialysis Patients: A Systematic Review of Bleeding Rates

Meghan J. Elliott, BSc1, Deborah Zimmerman, MD, MSc2, Rachel M. Holden, MD1Corresponding Author Informationemail address

Received 1 January 2007; accepted 15 June 2007. published online 07 August 2007.

Refers to article:
Anticoagulation for Chronic Atrial Fibrillation in Hemodialysis Patients: Which Fruit From the Decision Tree?
Kevin C. Abbott, Robert T. Neff, Erin M. Bohen, Rajeev Narayan
American Journal of Kidney Diseases
September 2007 (Vol. 50, Issue 3, Pages 345-348)
Full Text | Full-Text PDF (82 KB)
Background

Despite common use of warfarin, the bleeding risk associated with this treatment in hemodialysis (HD) patients is unknown.

Study Design

Systematic review.

Selection Criteria for Studies

Inclusion criteria were case series, cohort studies, and randomized controlled trials in dialysis patients that examined the bleeding risk associated with warfarin use compared with no warfarin or subcutaneous heparin. Studies with fewer than 10 subjects, case reports, abstracts lacking complete data sets, review articles, and editorials were excluded.

Predictor

Warfarin use compared with no warfarin or subcutaneous heparin.

Outcomes

Data for bleeding were reported as rates: number of bleeding episodes per number of patient-years of warfarin exposure or follow-up.

Results

Of 79 articles and abstracts, 5 met inclusion criteria and 3 more could be added after investigators provided additional information. All studies were of HD patients, and 7 of 8 evaluated the use of warfarin for the prevention of HD access thrombosis. Intensity of anticoagulation varied. Meta-analysis was not possible because of study heterogeneity. Studies of full-intensity anticoagulation and the 1 randomized controlled trial of low-intensity anticoagulation showed major bleeding episode rates ranging from 0.1 to 0.54 events/patient-year of warfarin exposure. These rates are approximately twice as high as those of HD patients receiving either no warfarin or subcutaneous heparin.

Limitations

This review is based largely on data from observational studies in which bleeding rates may be confounded by comorbidity. Relatively small sample sizes may provide imprecise estimates of rates.

Conclusion

Low- and full-intensity anticoagulation use in HD patients is associated with a significant bleeding risk, which has to be balanced against any potential benefit of therapy. This has to be considered carefully when prescribing warfarin to HD patients.

1 Division of Nephrology, Queen’s University, Kingston, Ontario, Canada

2 Division of Nephrology, University of Ottawa, Ottawa, Ontario, Canada.

Corresponding Author InformationAddress correspondence to Rachel M. Holden, MD, 3048C Etherington Hall, Queen’s University, Kingston, Ontario, Canada K7L 2V6.

 Originally published online as doi:10.1053/j.ajkd.2007.06.017 on August 9, 2007.

PII: S0272-6386(07)00950-X

doi:10.1053/j.ajkd.2007.06.017


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