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Sökning: id:"swepub:oai:gup.ub.gu.se/43935" > A new oral direct t...

A new oral direct thrombin inhibitor, dabigatran etexilate, compared with enoxaparin for prevention of thromboembolic events following total hip or knee replacement: the BISTRO II randomized trial

Eriksson, Bengt I., 1946 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för de kirurgiska disciplinerna, Avdelningen för ortopedi,Institute of Surgical Sciences, Department of Orthopaedics
Dahl, O. E. (författare)
Buller, H. R. (författare)
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Hettiarachchi, R. (författare)
Rosencher, N. (författare)
Bravo, M. L. (författare)
Ahnfelt, L. (författare)
Piovella, F. (författare)
Stangier, J. (författare)
Kalebo, P. (författare)
Reilly, P. (författare)
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 (creator_code:org_t)
2005
2005
Engelska.
Ingår i: J Thromb Haemost. - 1538-7933. ; 3:1, s. 103-11
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • BACKGROUND: Dabigatran etexilate is an oral direct thrombin inhibitor undergoing evaluation for the prevention of venous thromboembolism (VTE) following orthopedic surgery. METHODS: In a multicenter, parallel-group, double-blind study, 1973 patients undergoing total hip or knee replacement were randomized to 6-10 days of oral dabigatran etexilate (50, 150 mg twice daily, 300 mg once daily, 225 mg twice daily), starting 1-4 h after surgery, or subcutaneous enoxaparin (40 mg once daily) starting 12 h prior to surgery. The primary efficacy outcome was the incidence of VTE (detected by bilateral venography or symptomatic events) during treatment. RESULTS: Of the 1949 treated patients, 1464 (75%) patients were evaluable for the efficacy analysis. VTE occurred in 28.5%, 17.4%, 16.6%, 13.1% and 24% of patients assigned to dabigatran etexilate 50, 150 mg twice daily, 300 mg once daily, 225 mg twice daily and enoxaparin, respectively. A significant dose-dependent decrease in VTE occurred with increasing doses of dabigatran etexilate (P < 0.0001). Compared with enoxaparin, VTE was significantly lower in patients receiving 150 mg twice daily [odds ratio (OR) 0.65, P = 0.04], 300 mg once daily (OR 0.61, P = 0.02) and 225 mg twice daily (OR 0.47, P = 0.0007). Compared with enoxaparin, major bleeding was significantly lower with 50 mg twice daily (0.3% vs. 2.0%, P = 0.047) but elevated with higher doses, nearly reaching statistical significance with the 300 mg once-daily dose (4.7%, P = 0.051). CONCLUSIONS: Oral administration of dabigatran etexilate, commenced early in the postoperative period, was effective and safe across a range of doses. Further optimization of the efficacy/safety balance will be addressed in future studies.

Ämnesord

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

Nyckelord

Administration
Oral
Adult
Aged
Aged
80 and over
Anticoagulants/*pharmacology
Arthroplasty
Replacement
Hip/*adverse effects
Arthroplasty
Replacement
Knee/*adverse effects
Benzimidazoles/*chemistry/*pharmacology
Dose-Response Relationship
Drug
Double-Blind Method
Enoxaparin/*pharmacology
Female
Humans
Male
Middle Aged
Odds Ratio
Postoperative Complications
Postoperative Period
Pyridines/*chemistry/*pharmacology
Regression Analysis
Thrombin/*antagonists & inhibitors
Thromboembolism/*prevention & control

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