Sunil Mankad
Mayo Clinic
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Featured researches published by Sunil Mankad.
Circulation | 2004
B. Delia Johnson; Leslee J. Shaw; Steven D. Buchthal; C. Noel Bairey Merz; Hee-Won Kim; Katherine N. Scott; Mark Doyle; Marian B. Olson; Carl J. Pepine; Jan A. Den Hollander; Barry L. Sharaf; William J. Rogers; Sunil Mankad; John R. Forder; Sheryl F. Kelsey; Gerald M. Pohost
Background—We previously reported that 20% of women with chest pain but without obstructive coronary artery disease (CAD) had stress-induced reduction in myocardial phosphocreatine–adenosine triphosphate ratio by phosphorus-31 nuclear magnetic resonance spectroscopy (abnormal MRS), consistent with myocardial ischemia. The prognostic implications of these findings are unknown. Methods and Results—Women referred for coronary angiography for suspected myocardial ischemia underwent MRS handgrip stress testing and follow-up evaluation. These included (1) n= 60 with no CAD/normal MRS, (2) n= 14 with no CAD/abnormal MRS, and (3) n= 352 a reference group with CAD. Cardiovascular events were death, myocardial infarction, heart failure, stroke, other vascular events, and hospitalization for unstable angina. Cumulative freedom from events at 3 years was 87%, 57%, and 52% for women with no CAD/normal MRS, no CAD/abnormal MRS, and CAD, respectively (P < 0.01). After adjusting for CAD and cardiac risk factors, a phosphocreatine–adenosine triphosphate ratio decrease of 1% increased the risk of a cardiovascular event by 4% (P = 0.02). The higher event rate in women with no CAD/abnormal MRS was primarily due to hospitalization for unstable angina, which is associated with repeat catheterization and higher healthcare costs. Conclusions—Among women without CAD, abnormal MRS consistent with myocardial ischemia predicted cardiovascular outcome, notably higher rates of anginal hospitalization, repeat catheterization, and greater treatment costs. Further evaluation into the underlying pathophysiology and possible treatment options for women with evidence of myocardial ischemia but without CAD is indicated.
Circulation | 2006
Leslee J. Shaw; C. Noel Bairey Merz; Carl J. Pepine; Steven E. Reis; Vera Bittner; Kevin E. Kip; Sheryl F. Kelsey; Marian B. Olson; B. Delia Johnson; Sunil Mankad; Barry L. Sharaf; William J. Rogers; Gerald M. Pohost; George Sopko
Background— Coronary angiography is one of the most frequently performed procedures in women; however, nonobstructive (ie, <50% stenosis) coronary artery disease (CAD) is frequently reported. Few data exist regarding the type and intensity of resource consumption in women with chest pain after coronary angiography. Methods and Results— A total of 883 women referred for coronary angiography were prospectively enrolled in the National Institutes of Health–National Heart, Lung, and Blood Institute–sponsored Women’s Ischemia Syndrome Evaluation (WISE). Cardiovascular prognosis and cost data were collected. Direct (hospitalizations, office visits, procedures, and drug utilization) and indirect (out-of-pocket, lost productivity, and travel) costs were estimated through 5 years of follow-up. Among 883 women, 62%, 17%, 11%, and 10% had nonobstructive and 1-vessel, 2-vessel, and 3-vessel CAD, respectively. Five-year cardiovascular death or myocardial infarction rates ranged from 4% to 38% for women with nonobstructive to 3-vessel CAD (P<0.0001). Five-year rates of hospitalization for chest pain occurred in 20% of women with nonobstructive CAD, increasing to 38% to 55% for women with 1-vessel to 3-vessel CAD (P<0.0001). The volume of repeat catheterizations or angina hospitalizations was 1.8-fold higher in women with nonobstructive versus 1-vessel CAD after 1 year of follow-up (P<0.0001). Drug treatment was highest for those with nonobstructive or 1-vessel CAD (P<0.0001). The proportion of costs for anti-ischemic therapy was higher for women with nonobstructive CAD (15% versus 12% for 1-vessel to 3-vessel CAD; P=0.001). For women with nonobstructive CAD, average lifetime cost estimates were
Circulation | 2010
Jasmine Grewal; Rakesh M. Suri; Sunil Mankad; Akiko Tanaka; Douglas W. Mahoney; Hartzell V. Schaff; Fletcher A. Miller; Maurice Enriquez-Sarano
767 288 (95% CI,
Journal of The American Society of Echocardiography | 2009
Jasmine Grewal; Sunil Mankad; William K. Freeman; Roger L. Click; Rakesh M. Suri; Martin D. Abel; Jae K. Oh; Patricia A. Pellikka; Gillian C. Nesbitt; Imran S. Syed; Sharon L. Mulvagh; Fletcher A. Miller
708 480 to
American Journal of Cardiology | 1998
John Gorcsan; Anita Deswal; Sunil Mankad; William A. Mandarino; Christine M. Mahler; Nobuo Yamazaki; William E. Katz
826 097) and ranged from
Journal of the American College of Cardiology | 2000
Christopher M. Kramer; Walter J. Rogers; Sunil Mankad; Therese M. Theobald; Diana L Pakstis; Yong-Lin Hu
1 001 493 to
Nephrology Dialysis Transplantation | 2010
Sean M. Bagshaw; Dinna N. Cruz; Nadia Aspromonte; Luciano Daliento; Federico Ronco; Geoff Sheinfeld; Stefan D. Anker; Inder S. Anand; Rinaldo Bellomo; Tomas Berl; Ilona Bobek; Andrew Davenport; Mikko Haapio; Hans L. Hillege; Andrew A. House; Nevin Katz; Alan S. Maisel; Sunil Mankad; Peter A. McCullough; Alexandre Mebazaa; Alberto Palazzuoli; Piotr Ponikowski; Andrew D. Shaw; Sachin Soni; Giorgio Vescovo; Nereo Zamperetti; Pierluigi Zanco; Claudio Ronco
1 051 302 for women with 1-vessel to 3-vessel CAD (P=0.0003). Conclusions— Symptom-driven care is costly even for women with nonobstructive CAD. Our lifetime estimates for costs of cardiovascular care identify a significant subset of women who are unaccounted for within current estimates of the economic burden of coronary heart disease.
International Journal of Cardiovascular Imaging | 2009
Gillian C. Nesbitt; Sunil Mankad; Jae K. Oh
Background— Mitral annulus is a complex structure of poorly understood physiology. Full-volume real-time 3-dimensional transesophageal echocardiography offers a unique opportunity to completely image and quantify mitral annulus size and motion. Methods and Results— Real-time 3-dimensional transesophageal echocardiography of the mitral valve was acquired in 32 patients with myxomatous valve disease (MVD) and moderate to severe regurgitation, 15 normal control subjects, and 10 patients with ischemic mitral regurgitation of identical body surface area. Mitral annular dimensions (circumference, area, anteroposterior and intercommissural diameters, height, and ratio of height to intercommissural diameter ratio, which appraises annular saddle-shape depth) were measured throughout the cardiac cycle with dedicated quantification software. Compared with direct surgical measurement, 3-dimensional anterior annular dimension provided reliable measurements (mean difference, 0.1±0.1 mm; P=0.73; 95% confidence interval, ±4.4 mm). Annular dimensions were larger in MVD patients compared with control subjects in diastole (all P<0.05). Normal annulus displayed early-systolic anteroposterior (P<0.001) and area (P=0.04) contraction, increased height (P<0.001), and deeper saddle shape (ratio of height to intercommissural diameter, 15±1% to 21±1%; P<0.001), whereas intercommissural diameter was unchanged (P=0.30). In contrast, MVD showed early-systolic intercommissural dilatation (P=0.02) and no area contraction (P=0.99), height increase (P=0.11), or saddle-shape deepening (P=0.35). Late-systolic MVD annular saddle shape deepened but annular area excessively enlarged (P<0.04) as a result of persistent intercommissural widening (P<0.02). MVD annulus also contrasts with ischemic mitral regurgitation annulus, which, despite similar anteroposterior enlargement, is narrower and essentially adynamic. After MVD repair, the annulus remained dynamic without systolic saddle-shape accentuation (P=0.30). Conclusions— Real-time 3-dimensional transesophageal echocardiography provides insights into normal, dynamic mitral annulus function with early-systolic area contraction and saddle-shape deepening contributing to mitral competency. MVD annulus is also dynamic but considerably different with loss of early-systolic area contraction and saddle-shape deepening despite similar magnitude of ventricular contraction, suggestive of ventricular-annular decoupling. Subsequent area enlargement may contribute to mitral incompetence. After mitral repair, MVD annulus remains dynamic without systolic saddle-shape accentuation. Thus, real-time 3-dimensional transesophageal echocardiography provides new insights that allow the refining of mitral pathophysiology concepts and repair strategies.
Psychosomatic Medicine | 2004
Thomas Rutledge; Steven E. Reis; Marian B. Olson; Jane F. Owens; Sherel F. Kelsey; Carl J. Pepine; Sunil Mankad; William J. Rogers; C. Noel Bairey Merz; George Sopko; Carol E. Cornell; Barry L. Sharaf; Karen A. Matthews
BACKGROUND The aims of this study were to evaluate the feasibility of real-time 3-dimensional (3D) transesophageal echocardiography in the intraoperative assessment of mitral valve (MV) pathology and to compare this novel technique with 2-dimensional (2D) transesophageal echocardiography. METHODS Forty-two consecutive patients undergoing MV repair for mitral regurgitation (MR) were studied prospectively. Intraoperative 2D and 3D transesophageal echocardiographic (TEE) examinations were performed using a recently introduced TEE probe that provides real-time 3D imaging. Expert echocardiographers blinded to 2D TEE findings assessed the etiology of MR on 3D transesophageal echocardiography. Similarly, experts blinded to 3D TEE findings assessed 2D TEE findings. Both were compared with the anatomic findings reported by the surgeon. RESULTS At the time of surgical inspection, ischemic MR was identified in 12% of patients, complex bileaflet myxomatous disease in 31%, and specific scallop disease in 55%. Three-dimensional TEE image acquisition was performed in a short period of time (60 +/- 18 seconds) and was feasible in all patients, with optimal (36%) or good (33%) imaging quality in the majority of cases. Three-dimensional TEE imaging was superior to 2D TEE imaging in the diagnosis of P1, A2, A3, and bileaflet disease (P < .05). CONCLUSIONS Real-time 3D transesophageal echocardiography is a feasible method for identifying specific MV pathology in the setting of complex disease and can be expeditiously used in the intraoperative evaluation of patients undergoing MV repair.
Circulation | 2002
Steven E. Reis; Marian B. Olson; Linda P. Fried; Virginia Reeser; Sunil Mankad; Carl J. Pepine; Richard Kerensky; C. Noel Bairey Merz; B.L. Sharaf; George Sopko; William J. Rogers; Richard Holubkov
Low-dose dobutamine echocardiography has been clinically useful in myocardial viability studies, although routine visual assessment of wall motion is subjective. The objective was to quantify the incremental myocardial response to low-dose dobutamine infusion using a new semiautomated tissue Doppler (TD) analysis system and to compare these data with routine echocardiographic measures in the same subjects. Twelve subjects had TD and routine echocardiographic studies at baseline and during 10-minute stages of dobutamine infusion at 1, 2, 3, and 5 microg/kg/min. Color TD video data were converted to a digital velocity matrix (4.5 velocity data points/mm at 500 Hz) for analysis of mitral annular velocity, endocardial velocity, and velocity gradient at each stage. Posterior wall percent thickening and ejection fraction were calculated from the routine images. Mitral annular peak systolic velocity significantly increased with only 1 microg/kg/min of dobutamine from 69 +/- 9 to 77 +/- 7 mm/s (p <0.05 vs baseline), and further incremental increases occurred with each subsequent dose. Anteroseptal and posterior wall peak endocardial velocity increased with 2 microg/kg/min of dobutamine from 33 +/- 7 to 46 +/- 15 mm/s and 50 +/- 9 to 61 +/- 10 mm/s, respectively (p <0.01 vs baseline) and further increased with 5 microg/kg/min (p <0.0001 vs 3 microg/kg/min). Posterior wall peak systolic gradient also increased with 2 microg/kg/min of dobutamine from 3.1 +/- 0.6 to 5.4 +/- 1.6 s(-1) (p <0.05 vs baseline). Routine measures of percent wall thickening or ejection fraction did not detect increases until the 3 microg/kg/min dose. TD can detect subtle alterations in contractility induced by low-dose dobutamine and has the potential to quantify regional ventricular function objectively.