|
Thrombosis Journal 2011
Meta regression analysis to indirectly compare dalteparin to enoxaparin for the prevention of venous thromboembolic events following total hip replacementAbstract: A literature search was conducted from January 1980 to November 2009 for randomized trials evaluating dalteparin or enoxaparin prophylaxis in THR patients. In trials where a common control was used (e.g. placebo), indirect statistical comparisons between dalteparin and enoxaparin were performed using meta regression analysis with active drug as the primary independent variable.A total of nine placebo controlled enoxaparin (n = 5) and dalteparin (n = 4) trials met the inclusion criteria. THR patients treated with enoxaparin or dalteparin had a 50% VTE risk reduction compared to the placebo control (RR = 0.50, p < 0.001). This benefit was achieved without a significant increase in the risk for major bleeds (RR = 1.19, p = 0.76), heparin induced thrombocytopenia (HIT) (RR = 1.13, p = 0.83) or death (RR = 0.72, p = 0.59). The indirect comparison was not able to find significant differences between enoxaparin and dalteparin in terms of VTEs (p = 0.36), major bleeds (p = 0.45), HIT (p = 0.48) and death (p = 0.86).The findings suggested comparable safety and efficacy between dalteparin and enoxaparin in TKR patients. Therefore, treatment decisions should be based on other considerations, such as patient or physician preference, ease of administration and cost.Deep vein thrombosis (DVT) and pulmonary embolism (PE) are manifestations of venous thromboembolic events (VTE). The primary cause of a PE is a DVT. Following invasive procedures such as orthopedic surgery, patients are at risk for developing a DVT and subsequent PE.1 This is a major clinical concern because PE can be fatal in 70% of cases, usually within the first few hours [1]. DVT and PE can also be common events in hospitalized patients. In one claims based study, it was determined that 0.64% (i.e. 32,193 cases) of all patients discharged from evaluated U.S. hospitals between 1998 to 2004 had DVT or PE as the primary discharge diagnosis, and 26,159 (0.52%) had DVT or PE as a secondary discharge diagnosis [2]. In t
|