Cardiovascular risk in women with non-specific chest pain (from the Women's Health Initiative Hormone Trials)
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Authors
Robinson, Jennifer G.Wallace, Robert
Limacher, Marian C.
Ren, Hong
Cochrane, Barbara B.
Wassertheil-Smoller, Sylvia
Ockene, Judith K.
Blanchette, Patricia L.
Ko, Marcia G.
UMass Chan Affiliations
Department of Medicine, Division of Preventive and Behavioral MedicineDocument Type
Journal ArticlePublication Date
2008-09-15Keywords
AgedCardiovascular Diseases
Chest Pain
Contraceptive Agents, Female
Diabetes Mellitus
*Estrogen Replacement Therapy
Estrogens
Estrogens, Conjugated (USP)
Female
Hospitalization
Humans
Hypertension
Medroxyprogesterone Acetate
Middle Aged
Myocardial Revascularization
Proportional Hazards Models
Prospective Studies
Randomized Controlled Trials as Topic
Risk
Life Sciences
Medicine and Health Sciences
Women's Studies
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Show full item recordAbstract
Women discharged with diagnoses of nonspecific chest pain (NSCP) may be at increased risk for subsequent coronary artery disease (CAD) events. The influence of hormone therapy on NSCP is unknown. The Women's Health Initiative (WHI) enrolled postmenopausal women aged 50 to 79 years. The duration of follow-up was 7.1 years in the WHI Estrogen-Alone trial (E-Alone) and 5.6 years in the WHI Estrogen Plus Progestin trial (E+P). After excluding women with previous cardiovascular disease, 9,427 women in E-Alone and 15,105 women in E+P were included in this analysis. NSCP, defined as having a primary hospital discharge diagnosis of NSCP by International Classification of Diseases, Ninth Revision, code, was reported in 322 women in E-Alone and 249 in E+P. Risks for subsequent CAD events were estimated using intent-to-treat Cox proportional-hazards models stratified by clinic and adjusted for age and other risk factors. In the fully adjusted models of the combined trials, women with NSCP had a twofold greater risk for subsequent nonfatal CAD events, including nonfatal myocardial infarction (2.3% vs 1.7%, hazard ratio [HR] 2.10, 95% confidence interval [CI] 1.11 to 3.98), revascularization (3.5% vs 2.6%, HR 1.99, 95% CI 1.20 to 3.30), and hospitalized angina (3.7% vs 2.3%, HR 2.39, 95% CI 1.46 to 3.92). Hormone therapy did not appear to have a significant effect on either the incidence of NSCP hospitalizations (E-Alone: HR 1.04, 95% CI 0.81 to 1.32; E+P: HR 0.78, 95% CI 0.59 to 1.02) or the risk for a subsequent CAD event. In conclusion, a hospitalization for NSCP doubles the risk for a subsequent CAD event in postmenopausal women over the next 5 to 7 years and identifies them as candidates for aggressive risk factor treatment.Source
Am J Cardiol. 2008 Sep 15;102(6):693-9. Epub 2008 Jul 2. Link to article on publisher's siteDOI
10.1016/j.amjcard.2007.12.044Permanent Link to this Item
http://hdl.handle.net/20.500.14038/50961PubMed ID
18773990Related Resources
Link to Article in PubMedae974a485f413a2113503eed53cd6c53
10.1016/j.amjcard.2007.12.044