Differential associations of beta-blockers with hemorrhagic events for chronic heart failure patients on warfarin

被引:14
作者
Berlowitz, Dan R.
Miller, Donald R.
Oliveria, Susan A.
Cunningham, Fran
Gomez-Caminero, Andres
Rothendler, James A.
机构
[1] Bedford VA Hosp, CHQOER, Bedford, MA 01730 USA
[2] Boston Univ, Sch Publ Hlth, Boston, MA 02215 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY 10021 USA
[4] Edward Hines Vet Adm Med Ctr, Pharm Benefits Management Strateg Healthcare Grp, Chicago, IL USA
[5] GlaxoSmithKline Inc, Worldwide Epidemiol, Collegeville, PA USA
关键词
adrenergic beta-antagonist; heart failure; congestive; warfarin; hemorrhage;
D O I
10.1002/pds.1301
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Purpose Beta-blockers have many different physiologic effects that could potentially influence the risk of hemorrhagic events in chronic heart failure patients (CHF) on warfarin. We examined how different beta-blockers vary in their associated risk of a hemorrhagic event. Methods We used databases from the Department of Veterans Affairs (VA) that contain information on medications prescribed, diagnoses, and hospitalizations. We identified patients with CHF on warfarin and either metoprolol, carvedilol, atenolol, or no beta-blocker during 1999-2001. We modeled time to first hemorrhagic event using a Cox proportional hazards model, adjusting for age, ethnicity, comorbidities, and other factors. INR levels were examined in a subsample of 3546 patients. Results We identified 66988 CHF patients on warfarin. Hemorrhagic events occurred in 15.3% of the sample and, in 3.8% of the sample, the hemorrhage was considered severe. Compared to patients on carvedilol, the hazards ratio for a new hemorrhagic event was 1.25 (1.17, 1.34) for no beta-blocker, 1.27 (1.18, 1.38) for atenolol, and 1.38 (1.28, 1.48) for rnetoprolol. No differences in INR levels were evident among the four groups. Conclusions The risk for a hemorrhagic event among CHF patients on warfarin may be affected by beta-blocker use and varies depending on which beta-blocker is prescribed. Copyright (c) 2006 John Wiley & Sons, Ltd.
引用
收藏
页码:799 / 807
页数:9
相关论文
共 37 条
[1]   Validation of diagnoses of peptic ulcers and bleeding from administrative databases: A multi-health maintenance organization study [J].
Andrade, SE ;
Gurwitz, JH ;
Chan, KA ;
Donahue, JG ;
Beck, A ;
Boles, M ;
Buist, DSM ;
Goodman, M ;
LaCroix, AZ ;
Levin, TR ;
Platt, R .
JOURNAL OF CLINICAL EPIDEMIOLOGY, 2002, 55 (03) :310-313
[2]  
BAX ND, 1984, BR J CLIN PHARM S1, V17, P85
[3]   Identifying hypertension-related comorbidities from administrative data: What's the optimal approach? [J].
Borzecki, AM ;
Wong, AT ;
Hickey, EC ;
Ash, AS ;
Berlowitz, DR .
AMERICAN JOURNAL OF MEDICAL QUALITY, 2004, 19 (05) :201-206
[4]   A NEW METHOD OF CLASSIFYING PROGNOSTIC CO-MORBIDITY IN LONGITUDINAL-STUDIES - DEVELOPMENT AND VALIDATION [J].
CHARLSON, ME ;
POMPEI, P ;
ALES, KL ;
MACKENZIE, CR .
JOURNAL OF CHRONIC DISEASES, 1987, 40 (05) :373-383
[5]   A randomized trial of the angiotensin-receptor blocker valsartan in chronic heart failure [J].
Cohn, JN ;
Tognoni, G .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 345 (23) :1667-1675
[6]   Drug therapy - The management of chronic heart failure [J].
Cohn, JN .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (07) :490-498
[7]   The effectiveness of early endoscopy for upper gastrointestinal hemorrhage - A community-based analysis [J].
Cooper, GS ;
Chak, A ;
Connors, AF ;
Harper, DL ;
Rosenthal, GE .
MEDICAL CARE, 1998, 36 (04) :462-474
[8]   ADAPTING A CLINICAL COMORBIDITY INDEX FOR USE WITH ICD-9-CM ADMINISTRATIVE DATABASES [J].
DEYO, RA ;
CHERKIN, DC ;
CIOL, MA .
JOURNAL OF CLINICAL EPIDEMIOLOGY, 1992, 45 (06) :613-619
[9]   Long-term ACE-inhibitor therapy in patients with heart failure or left-ventricular dysfunction:: a systematic overview of data from individual patients [J].
Flather, MD ;
Yusuf, S ;
Kober, L ;
Pfeffer, M ;
Hall, A ;
Murray, G ;
Torp-Pedersen, C ;
Ball, S ;
Pogue, J ;
Moyé, L ;
Braunwald, E .
LANCET, 2000, 355 (9215) :1575-1581
[10]  
GASSER JA, 1991, J CARDIOVASC PHARM, V18, pS29, DOI 10.1097/00005344-199106184-00007