Effects of acute hormone therapy on recurrent ischemia in postmenopausal women with unstable angina
Steven P. Schulman, MD*,*,
David R. Thiemann, MD*,
Pamela Ouyang, MD, FACC*,
Nisha C. Chandra, MD*,
Douglas S. Schulman, MD, FACC
,
Steven E. Reis, MD, FACC
,
Michael Terrin, MD
,
Sandra Forman, MA
,
Cicero Piva de Albuquerque, MD||,
Raymond D. Bahr, MD, FACC¶,
Susan N. Townsend, BSN*,
Rosalie Cosgriff, RCT* and
Gary Gerstenblith, MD, FACC*
* Johns Hopkins Medical Institutions, Baltimore, Maryland, USA
Allegheny General Hospital, Pittsburgh, Pennsylvania USA
University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA
Maryland Medical Research Institute, Baltimore, Maryland, USA
|| Unidade Coronariana-InCor, Sao Paulo, Brazil
¶ St. Agnes Medical Center, Baltimore, Maryland USA

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Figure 1 The rates of in-hospital death, myocardial infarction (MI), emergency percutaneous intervention (PCI) and emergency coronary artery bypass surgery (CABG) are shown for patients randomized to each group. Patients underwent revascularization for recurrent ischemic symptoms or high-risk presentation. There were no differences in hospital events among the three randomized groups, p = 0.91. E = conjugated equine estrogen; MPA = medroxyprogesterone; PLBO = placebo.
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Figure 2 Six-month rates of death or nonfatal myocardial infarction among the three randomized groups. Event rates did not differ, p = 0.97. E = conjugated equine estrogen; MPA = medroxyprogesterone; PLBO = placebo.
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Figure 3 Six-month rates of death, nonfatal myocardial infarction or need for revascularization (coronary artery bypass surgery or percutaneous intervention) among the three randomized groups. Most of the events occurred early, and hormone therapy did not reduce the adverse event rate, p = 0.98. E = conjugated equine estrogen; MPA = medroxyprogesterone; PLBO = placebo.
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Copyright © 2002 by the American College of Cardiology Foundation.