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Interventional therapies and in-hospital outcomes in acute coronary syndromes complicated by von Willebrand disease.

Authors :
Fogarty, P. F.
Blair, A.
Vega, R.
Matthai, W. H.
Gimotty, P. A.
Source :
Haemophilia. May2017, Vol. 23, p400-407. 8p.
Publication Year :
2017

Abstract

Introduction von Willebrand disease ( VWD) is one of the most common inherited bleeding disorders. Aim Investigate the impact of the VWD bleeding tendency on in-hospital management of acute coronary syndromes ( ACS). Methods Using discharge data from the National Inpatient Sample ( NIS), the features of presentation and in-hospital treatment among ACS hospital discharges with and without a VWD diagnosis were investigated. A total of 264 case discharges and 705 860 control discharges were identified. Results and Conclusions There was a significantly higher percentage of women among the case discharges compared to the control discharges (59.5% and 39.4%, respectively; P < 0.001). The rate of medical therapy alone [i.e. avoidance of percutaneous coronary intervention ( PCI) or coronary artery bypass grafting ( CABG)] was significantly higher among unstable angina cases than controls (55.0% vs. 46.4%; P = 0.01), and among cases undergoing PCI, bare-metal stents ( BMS) were utilized in preference to drug-eluting stents ( DES) (adjusted OR = 3.5); P < 0.001). No difference in in-hospital death was identified, but reported bleeding among discharges that underwent CABG was higher in cases compared to controls (12.9% vs. 5.2%; P = 0.047). Although medical and interventional management of ACS appears to be well tolerated in the majority of hospitalized patients with VWD, the gender ratio is reversed, interventions and DES are utilized less frequently and procedure-related bleeding may be increased, calling for further study. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13518216
Volume :
23
Database :
Academic Search Index
Journal :
Haemophilia
Publication Type :
Academic Journal
Accession number :
123107959
Full Text :
https://doi.org/10.1111/hae.13149