Adam M. Rogers
University of Michigan
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Featured researches published by Adam M. Rogers.
Circulation | 2011
Adam M. Rogers; Luke K. Hermann; Anna M. Booher; Christoph Nienaber; David M. Williams; Ella A. Kazerooni; James B. Froehlich; Patrick T. O'Gara; Daniel Montgomery; Jeanna V. Cooper; Kevin M. Harris; Stuart Hutchison; Arturo Evangelista; Eric M. Isselbacher; Kim A. Eagle
Background— In 2010, the American Heart Association and American College of Cardiology released guidelines for the diagnosis and management of patients with thoracic aortic disease, which identified high-risk clinical features to assist in the early detection of acute aortic dissection. The sensitivity of these risk markers has not been validated. Methods and Results— We examined patients enrolled in the International Registry of Acute Aortic Dissection from 1996 to 2009. The number of patients with confirmed acute aortic dissection who presented with 1 or more of 12 proposed clinical risk markers was determined. An aortic dissection detection (ADD) risk score of 0 to 3 was calculated on the basis of the number of risk categories (high-risk predisposing conditions, high-risk pain features, high-risk examination features) in which patients met criteria. The ADD risk score was tested for sensitivity. Of 2538 patients with acute aortic dissection, 2430 (95.7%) were identified by 1 or more of 12 proposed clinical risk markers. With the use of the ADD risk score, 108 patients (4.3%) were identified as low risk (ADD score 0), 927 patients (36.5%) were intermediate risk (ADD score 1), and 1503 patients (59.2%) were high risk (ADD score 2 or 3). Among 108 patients with no clinical risk markers present (ADD score 0), 72 had chest x-rays recorded, of which 35 (48.6%) demonstrated a widened mediastinum. Conclusions— The clinical risk markers proposed in the 2010 thoracic aortic disease guidelines and their application as part of the ADD risk score comprise a highly sensitive clinical tool for the detection of acute aortic dissection.
American Heart Journal | 2009
Bill P.C. Hsieh; Adam M. Rogers; Beeya Na; Alan H.B. Wu; Nelson B. Schiller; Mary A. Whooley
BACKGROUND The significance of troponin elevation and clinical utility of troponin testing in ambulatory patients with coronary artery disease (CAD) have not been examined. We sought to investigate the prevalence and prognostic value of cardiac troponin T (cTnT) elevation in a population with stable CAD. METHODS We studied 987 patients with stable CAD enrolled in the Heart & Soul study who had plasma cTnT measurements before performing exercise treadmill testing. RESULTS Of the studied population, 58 patients or 6.2% had detectable cTnT levels, >or=0.01 ng/mL (0.01-0.72 ng/mL). During a mean follow-up period of 4.3 (0.1-6.5) years, 58.6% of participants with detectable cTnT had cardiovascular events compared with 22.5% of those without detectable cTnT (hazard ratio [HR] 3.8, 95% CI 2.6-5.4, P < .001). This association remained strong after adjustment for traditional risk factors and C-reactive protein (HR 2.0, 95% CI 1.3-3.1, P = .002). However, after further adjustment for N-terminal pro-B-type natriuretic peptide and echocardiographic parameters of left ventricular function, cTnT elevation was not an independent predictor of cardiovascular events (HR 1.3, 95% CI, 0.8-2.3, P = .28). CONCLUSIONS In ambulatory patients with stable CAD, the prevalence of cTnT elevation was 6.2%. Cardiac troponin T elevation detected using the conventional troponin assay was associated with increased risk of adverse cardiovascular outcomes, but its prognostic value was not incremental over N-terminal pro-B-type natriuretic peptide and echocardiographic evidence of cardiac abnormalities.
Circulation | 2011
Adam M. Rogers; Luke K. Hermann; Anna M. Booher; Christoph Nienaber; David M. Williams; Ella A. Kazerooni; James B. Froehlich; Patrick T. O'Gara; Daniel Montgomery; Jeanna V. Cooper; Kevin M. Harris; Stuart Hutchison; Arturo Evangelista; Eric M. Isselbacher; Kim A. Eagle
Background— In 2010, the American Heart Association and American College of Cardiology released guidelines for the diagnosis and management of patients with thoracic aortic disease, which identified high-risk clinical features to assist in the early detection of acute aortic dissection. The sensitivity of these risk markers has not been validated. Methods and Results— We examined patients enrolled in the International Registry of Acute Aortic Dissection from 1996 to 2009. The number of patients with confirmed acute aortic dissection who presented with 1 or more of 12 proposed clinical risk markers was determined. An aortic dissection detection (ADD) risk score of 0 to 3 was calculated on the basis of the number of risk categories (high-risk predisposing conditions, high-risk pain features, high-risk examination features) in which patients met criteria. The ADD risk score was tested for sensitivity. Of 2538 patients with acute aortic dissection, 2430 (95.7%) were identified by 1 or more of 12 proposed clinical risk markers. With the use of the ADD risk score, 108 patients (4.3%) were identified as low risk (ADD score 0), 927 patients (36.5%) were intermediate risk (ADD score 1), and 1503 patients (59.2%) were high risk (ADD score 2 or 3). Among 108 patients with no clinical risk markers present (ADD score 0), 72 had chest x-rays recorded, of which 35 (48.6%) demonstrated a widened mediastinum. Conclusions— The clinical risk markers proposed in the 2010 thoracic aortic disease guidelines and their application as part of the ADD risk score comprise a highly sensitive clinical tool for the detection of acute aortic dissection.
Journal of the American College of Cardiology | 2011
Shyamli Sinha; Santi Trimarchi; Daniel Montgomery; Elise M. Woznicki; David Corteville; Adam M. Rogers; Himanshu J. Patel; Anna M. Booher; Christoph Nienaber; Mark E. Peterson; Reed E. Pyeritz; Eva Kline-Rogers; Eduardo Bossone; Thomas T. Tsai; Kim A. Eagle
Results: Reasons for NS management included: prohibitive comorbidities 151 (59.0%), advanced age 69 ( 27.0%, average age 81.0±7.0), patient preference 37 (14.5%) , and intramural hematoma of arch or descending aorta 26 (10.0%) and 12 (4.7%, respectively). In-hospital mortality was higher for NS (56.3% vs. 21.5%, p < 0.001). Data was separated into tertiles based on time of incident dissection. The % of NS patients and inhospital mortality of all TA-AAD patients decreased over this time span (Table).
Circulation | 2011
Adam M. Rogers; Luke K. Hermann; Anna M. Booher; Christoph Nienaber; David M. Williams; Ella A. Kazerooni; James B. Froehlich; Patrick T. O'Gara; Daniel Montgomery; Jeanna V. Cooper; Kevin M. Harris; Stuart Hutchison; Arturo Evangelista; Eric M. Isselbacher; Kim A. Eagle
Background— In 2010, the American Heart Association and American College of Cardiology released guidelines for the diagnosis and management of patients with thoracic aortic disease, which identified high-risk clinical features to assist in the early detection of acute aortic dissection. The sensitivity of these risk markers has not been validated. Methods and Results— We examined patients enrolled in the International Registry of Acute Aortic Dissection from 1996 to 2009. The number of patients with confirmed acute aortic dissection who presented with 1 or more of 12 proposed clinical risk markers was determined. An aortic dissection detection (ADD) risk score of 0 to 3 was calculated on the basis of the number of risk categories (high-risk predisposing conditions, high-risk pain features, high-risk examination features) in which patients met criteria. The ADD risk score was tested for sensitivity. Of 2538 patients with acute aortic dissection, 2430 (95.7%) were identified by 1 or more of 12 proposed clinical risk markers. With the use of the ADD risk score, 108 patients (4.3%) were identified as low risk (ADD score 0), 927 patients (36.5%) were intermediate risk (ADD score 1), and 1503 patients (59.2%) were high risk (ADD score 2 or 3). Among 108 patients with no clinical risk markers present (ADD score 0), 72 had chest x-rays recorded, of which 35 (48.6%) demonstrated a widened mediastinum. Conclusions— The clinical risk markers proposed in the 2010 thoracic aortic disease guidelines and their application as part of the ADD risk score comprise a highly sensitive clinical tool for the detection of acute aortic dissection.
American Heart Journal | 2007
Adam M. Rogers; Vijay S. Ramanath; Mary Grzybowski; Arthur Riba; Sandeep M. Jani; Rajendra H. Mehta; Anthony C. De Franco; Robert Parrish; Stephen Skorcz; Patricia L. Baker; Jessica D. Faul; Benrong Chen; Canopy Roychoudhury; Mary Anne Elma; Kristi Mitchell; James B. Froehlich; Cecelia Montoye; Kim A. Eagle
American Heart Journal | 2010
Adesuwa Olomu; Mary Grzybowski; Vijay S. Ramanath; Adam M. Rogers; Bonnie Motyka Vautaw; Benrong Chen; Canopy Roychoudhury; Elizabeth A. Jackson; Kim A. Eagle
Journal of The American Society of Echocardiography | 2008
Adam M. Rogers; Nelson B. Schiller
Journal of the American College of Cardiology | 2012
Hasan K. Siddiqi; Eric M. Isselbacher; Toru Suzuki; Daniel Montgomery; Linda Pape; Rossella Fattori; Patrick T. O'Gara; Guillaume Jondeau; Emil Missov; Alberto Forteza; Eduardo Bossone; Alan T. Hirsch; Adam M. Rogers; Christoph Nienaber; Kim A. Eagle
The American Journal of Medicine | 2012
Palaniappan Muthappan; Adam M. Rogers; Kim A. Eagle