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Sökning: WFRF:(Hantel Stefan) > (2011) > Oral dabigatran ver...

Oral dabigatran versus enoxaparin for thromboprophylaxis after primary total hip arthroplasty (RE-NOVATE II*). A randomised, double-blind, non-inferiority trial.

Eriksson, Bengt I., 1946 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper, Avdelningen för ortopedi,Institute of Clinical Sciences, Department of Orthopaedics
Dahl, Ola E (författare)
Huo, Michael H (författare)
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Kurth, Andreas A (författare)
Hantel, Stefan (författare)
Hermansson, Karin (författare)
Schnee, Janet M (författare)
Friedman, Richard J (författare)
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 (creator_code:org_t)
2011
2011
Engelska.
Ingår i: Thrombosis and haemostasis. - 0340-6245 .- 2567-689X. ; 105:4, s. 721-9
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • This trial compared the efficacy and safety of oral dabigatran, a direct thrombin inhibitor, versus subcutaneous enoxaparin for extended thromboprophylaxis in patients undergoing total hip arthroplasty. A total of 2,055 patients were randomised to 28-35 days treatment with oral dabigatran, 220 mg once-daily, starting with a half-dose 1-4 hours after surgery, or subcutaneous enoxaparin 40 mg once-daily, starting the evening before surgery. The primary efficacy outcome was a composite of total venous thromboembolism [VTE] (venographic or symptomatic) and death from all-causes. The main secondary composite outcome was major VTE (proximal deep-vein thrombosis or non-fatal pulmonary embolism) plus VTE-related death. The main safety outcome was major bleeding. In total, 2,013 were treated, of whom 1,577 operated patients were included in the primary efficacy analysis. The primary efficacy outcome occurred in 7.7% of the dabigatran group versus 8.8% of the enoxaparin group, risk difference (RD) -1.1% (95%CI -3.8 to 1.6%); p<0.0001 for the pre-specified non-inferiority margin. Major VTE plus VTE-related death occurred in 2.2% of the dabigatran group versus 4.2% of the enoxaparin group, RD -1.9% (-3.6% to -0.2%); p=0.03. Major bleeding occurred in 1.4% of the dabigatran group and 0.9% of the enoxaparin group (p=0.40). The incidence of adverse events, including liver enzyme elevations and cardiac events, during treatment was similar between the groups. Extended prophylaxis with oral dabigatran 220 mg once-daily was as effective as subcutaneous enoxaparin 40 mg once-daily in reducing the risk of VTE after total hip arthroplasty, and superior to enoxaparin for reducing the risk of major VTE. The risk of bleeding and safety profiles were similar.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kirurgi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Surgery (hsv//eng)

Nyckelord

Administration
Oral
Aged
Anticoagulants
administration & dosage
adverse effects
Antithrombins
administration & dosage
adverse effects
Arthroplasty
Replacement
Hip
mortality
Benzimidazoles
administration & dosage
adverse effects
Double-Blind Method
Enoxaparin
administration & dosage
adverse effects
Female
Hemorrhage
etiology
Humans
Injections
Subcutaneous
Male
Middle Aged
Postoperative Complications
Survival Analysis
Venous Thromboembolism
etiology
mortality
prevention & control
Venous Thrombosis
etiology
mortality
prevention & control
beta-Alanine
administration & dosage
adverse effects
analogs & derivatives

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