VENOUS THROMBOEMBOLIC COMPLICATIONS IN BURN PATIENTS RECEIVING HEPARIN OR ENOXAPARIN AS PROPHYLAXIS
Author(s)
Bushwitz J1, LeClaire A2, He J3, Mozingo D21Barnes-Jewish Hospital, St. Louis, MO, USA, 2Shands at the University of Florida, Gainesville, FL, USA, 3University of Florida, Gainesville, FL, USA
OBJECTIVES: To examine the comparative effectiveness of heparin 5000 units given subcutaneously twice a day or three times a day, enoxaparin 30 mg given subcutaneously twice a day, and enoxaparin 40 mg given subcutaneously daily for the prevention of venous thromboembolism in burn patients. METHODS: A retrospective cohort study was conducted by using the hospital claims database. All adult patients were included if they were admitted to Shands hospital between January 1, 1998 and September 30, 2008, had primary diagnoses of burn, and received either subcutaneous heparin or enoxaparin for VTE prophylaxis. The primary outcome was a VTE event, which was identified by using a previously validated ICD-9 coding algorithm and further confirmed by chart review for radiographic evidence. RESULTS: A total of 1111 patients were included. Seven patients (0.63%) experienced VTE events: 5 (0.83%) received heparin, 1 (0.92%) received enoxaparin 30 mg, and 1 (0.25%) received enoxaparin 40 mg. There were no incidences of heparin-induced thrombocytopenia identified in any group. CONCLUSIONS: The VTE incidence is low in burn patients receiving pharmacological prophylaxis. Both heparin and enoxaparin appear to be equally effective in preventing VTE complications in this patient population.
Conference/Value in Health Info
2010-05, ISPOR 2010, Atlanta, GA, USA
Value in Health, Vol. 13, No. 3 (May 2010)
Code
PCV20
Topic
Clinical Outcomes
Topic Subcategory
Comparative Effectiveness or Efficacy
Disease
Cardiovascular Disorders, Respiratory-Related Disorders