Key result
Inpatient dalteparin and outpatient dabigatran are linked to a ~1% DVT rate after joint replacement.
Why the study?
Hip and knee arthroplasty surgery is associated with increased risk of DVT and PE, and optimal postoperative anticoagulation protocols remain under evaluation.
Does a protocol of inpatient subcutaneous Dalteparin followed by discharge on low-dose oral Dabigatran prevent VTE in patients undergoing total hip or knee arthroplasty?
Observational (n=337)
No
Does a protocol of inpatient subcutaneous Dalteparin followed by discharge on low-dose oral Dabigatran prevent VTE in patients undergoing total hip or knee arthroplasty?
A modified protocol of inpatient dalteparin followed by outpatient low-dose dabigatran showed low rates of VTE post-arthroplasty, though randomized trials are needed.
NICE post-arthroplasty VTE prophylaxis guidance warrants reappraisal; leaves open optimal agent, dose, and duration in contemporary practice.
BACKGROUND: Venous Thrombo-embolic disease is currently a hot topic especially in the UK. 25,000 patients per year die of Pulmonary Emboli (PE) in the United Kingdom (UK). Hip and knee arthroplasty surgery is associated with an increased rate of deep vein thrombosis (DVT) and pulmonary embolus (PE). The National Institute for Clinical Excellence (NICE) guidelines introduced in January 2010 recommended use of subcutaneous heparin or an oral anticoagulant (Dabigatran or Rivaroxiban) for 10-14 days post knee and 28-35 days post hip arthroplasty. In our unit we were keen on the advantages of an oral anticoagulant post arthroplasty in terms of patient compliance, and avoiding the need for self administered injection in the community. METHODS: We analysed all the notes, blood results and imaging of patients undergoing total hip or knee arthroplasty and present 1 year's data using a regime of subcutaneous Dalteparin whilst an inpatient, followed by discharge on oral Dabigatran at a low dose (150 mg once daily). RESULTS: There were 337 patients over 1 year with hip and knee arthroplasty, with a 1.19% rate of DVT with no PEs and 1 death due to an unrelated cause. There was a transfusion rate of 11.57% with 1.19% patients taken back to theatre for evacuation of haematomas. There were no reported adverse effects of Dabigatran. CONCLUSION: Our treatment protocol is a novel practical approach for VTE prophylaxis in hip and knee replacement patients. This approach shows promising data but no definitive evidence to warrant wide-spread use of this new regime. This data can act as a foundation for larger randomised clinical trials.
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Subramanian et al. (2012) conducted an observational in Joint replacement surgery (hip and knee arthroplasty) (n=337). Subcutaneous Dalteparin followed by oral Dabigatran was evaluated on Deep vein thrombosis (DVT) rate. A modified VTE prophylaxis protocol using inpatient subcutaneous Dalteparin followed by outpatient oral Dabigatran 150 mg resulted in a 1.19% DVT rate and no pulmonary embolisms in patients undergoing joint replacement.
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