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Efficacy and safety of dabigatran etexilate for the prevention of venous thromboembolism following total hip or knee arthroplasty. A meta-analysis

Wolowacz, S. E. (författare)
Roskell, N. S. (författare)
Plumb, J. M. (författare)
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Caprini, J. A. (författare)
Eriksson, Bengt I., 1946 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences
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 (creator_code:org_t)
2009
2009
Engelska.
Ingår i: Thrombosis and Haemostasis. - 0340-6245. ; 101:1, s. 77-85
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Dabigatran etexilate has been investigated in three phase III trials for the prevention of venous thromboembolism (VTE). Health technology assessment agencies increasingly require meta-analyses of all relevant evidence for an intervention, if appropriate. The objective of this study was to perform a meta-analysis of efficacy and safety data for the recommended dose of dabigatran etexilate, 220 mg once daily (od), for VTE prophylaxis after total knee arthroplasty (TKA) and total hip arthroplasty (THA), and discuss the appropriateness of combining the data. Risk ratios (RR) for VTE and bleed end-points were estimated using fixed and random effects meta-analysis. Analyses were performed combining RE-MODEL and RE-NOVATE, which compared dabigatran etexilate with enoxaparin 40 mg od after TKA and THA, respectively, and also including RE-MOBILIZE, which compared dabigatran etexilate with enoxaparin 30 mg twice daily after TKA. Tests for statistical heterogeneity were performed using the Chi-squared statistic. No significant differences were detected between dabigatran etexilate and enoxaparin in any of the end-points analysed, either in the two trial analysis (all p > 0.15), or when all three trials were combined ( all p > 0.30). RRs (random effects) for the composite end-point total VTE and all-cause mortality were 0.95 [95% confidence intervals 0.82 - 1.10] and 1.05 [0.87 - 1.26] in the two and three trial analyses, respectively. Meta-analysis of RE-MODEL and RE-NOVATE supported the conclusions of the individual trials that dabigatran etexilate is non-inferior to enoxaparin 40 mg od, with a similar safety profile. Meta-analysis of all three trials found no significant differences between treatments in any of the end-points analysed. Heterogeneity between the trials cannot be ruled out.

Ämnesord

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

Nyckelord

Administration
Oral
Anticoagulants/administration & dosage/adverse effects/*therapeutic use
Arthroplasty
Replacement
Hip/*adverse effects
Arthroplasty
Replacement
Knee/*adverse effects
Benzimidazoles/administration & dosage/adverse effects/*therapeutic use
Clinical Trials
Phase III as Topic
Drug Administration Schedule
Enoxaparin/administration & dosage/adverse effects/*therapeutic use
Hemorrhage/chemically induced
Humans
Pyridines/administration & dosage/adverse effects/*therapeutic use
Risk Assessment
Treatment Outcome
Venous Thromboembolism/etiology/mortality/*prevention & control

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Av författaren/redakt...
Wolowacz, S. E.
Roskell, N. S.
Plumb, J. M.
Caprini, J. A.
Eriksson, Bengt ...
Om ämnet
MEDICIN OCH HÄLSOVETENSKAP
MEDICIN OCH HÄLS ...
och Klinisk medicin
och Kirurgi
Artiklar i publikationen
Thrombosis and H ...
Av lärosätet
Göteborgs universitet

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