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Unfractionated heparin administration in patients treated with bivalirudin during primary percutaneous coronary intervention is associated lower mortality and target lesion thrombosis : a report from the Swedish Coronary Angiography and Angioplasty Registry (SCAAR)

Koutouzis, Michael (författare)
Lagerqvist, Bo, 1952- (författare)
Uppsala universitet,Uppsala kliniska forskningscentrum (UCR),Kardiologi
James, Stefan, 1964- (författare)
Uppsala universitet,Uppsala kliniska forskningscentrum (UCR),Kardiologi
visa fler...
Omerovic, Elmir (författare)
Matejka, Göran (författare)
Grip, Lars (författare)
Albertsson, Per (författare)
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 (creator_code:org_t)
2011-04-12
2011
Engelska.
Ingår i: Heart. - : BMJ. - 1355-6037 .- 1468-201X. ; 97:18, s. 1484-1488
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Background: Bivalirudin reduces bleeding events and is associated with a lower mortality than the combination of unfractionated heparin (UFH) and glycoprotein IIb/IIIa inhibitor during primary percutaneous coronary intervention (PCI). However, the effect of adding UFH in patients with ST elevation myocardial infarction (STEMI) treated with bivalirudin during primary PCI is unknown.Methods: Patients enrolled in the national Swedish Coronary Angiography and Angioplasty Registry who underwent primary PCI due to STEMI with bivalirudin as anticoagulant were evaluated. Patients were divided into two groups: those treated with bivalirudin only and those treated with bivalirudin plus a bolus dose of UFH.Results: 2996 patients were included in the study: 1928 (64%) received only bivalirudin and 1068 (36%) received bivalirudin plus a bolus dose of UFH. The primary combined endpoint of death or target lesion thrombosis at 30 days occurred more often in the bivalirudin group (11.3% vs 6.5%, OR 0.55, 95% CI 0.41 to 0.72, p<0.001). This difference remained significant after adjustment (HR 0.64, 95% CI 0.44 to 0.95, p=0.03). Death at 30 days and definite target lesion thrombosis at 30 days did not differ between the two groups after adjustment (9.2% vs 5.1%, adjusted HR 0.66, 95% CI 0.42 to 1.03, p=0.07 and 2.3% vs 1.5%, adjusted HR 0.59, 95% CI 0.27 to 1.33, p=0.21, respectively).Conclusion: An additional bolus dose of UFH is associated with a lower rate of death or definite target lesion thrombosis at 30 days in patients undergoing primary PCI with bivalirudin as anticoagulant.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)

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MEDICINE
MEDICIN

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