TY - JOUR
T1 - Dobutamine stress echocardiography
T2 - Sensitivity, specificity, and predictive value for future cardiac events
AU - Afridi, Imran
AU - Quin̂ones, Miguel A.
AU - Zoghbi, William A.
AU - Cheirif, Jorge
N1 - Funding Information:
From the Section of Cardiology, Department College of Medicine, Veterans Administration tational assistance was provided by the CLINFO RR-00350 from the Division of Research Resources, Health, Bethesda, Md. Received for publication Sept. 3, 1993; accepted Reprint requests: Jorge Cheirif B., MD, Section of Cardiology, Clinic, 1516 Jefferson Highway, New Orleans, LA 70121. Copyright Q 1994 by Mosby-Year Book, Inc. 0002~8703/94/$3.00+ 0 4/l/537.%7 of Internal Medicine, Baylor Hospital, Houston. Compu-project, funded by grant National Institutes of
Copyright:
Copyright 2014 Elsevier B.V., All rights reserved.
PY - 1994/6
Y1 - 1994/6
N2 - We conducted a retrospective study to determine whether dobutamine stress echocardiography (DE) can be used for risk stratification of patients with known or suspected coronary artery disease (CAD). The study population consisted of 77 patients who underwent DE at our institution. The protocol consisted of an echocardiogram at baseline followed by imaging during intravenous dobutamine infusion starting at 10 μg/kg/min with increments of 10 μg/kg/min every 3 minutes to a maximum dose of 40 μg/kg/min. The reasons for performing DE included preoperative cardiac evaluation (30), chest pain (23), assessment of ischemia (18), and suspected restenosis (6). DE was classified according to wall motion response as normal (before and during DE), fixed abnormal (abnormal before with no change during DE), or ischemic (new wall-motion abnormality during DE). Mean duration of follow-up was 10 months. Cardiac events occurred in 14 patients. These included congestive heart failure in seven patients, myocardial infarction in six, and cardiac death in one. A normal wall-motion response (n = 40) was associated with a low incidence of cardiac events (5%), whereas 5 of 10 patients (50%) with an ischemic response had events. The risk of cardiac events was intermediate (26%) in patients with fixed abnormal wall motion. Overall sensitivity of DE for predicting future cardiac events was 85%. In 45 patients who underwent coronary angiography within 2 months of DE, the test detected CAD with a sensitivity of 71%. In conclusion, the wall-motion response during DE may be used for identifying patients at high risk for future cardiac events.
AB - We conducted a retrospective study to determine whether dobutamine stress echocardiography (DE) can be used for risk stratification of patients with known or suspected coronary artery disease (CAD). The study population consisted of 77 patients who underwent DE at our institution. The protocol consisted of an echocardiogram at baseline followed by imaging during intravenous dobutamine infusion starting at 10 μg/kg/min with increments of 10 μg/kg/min every 3 minutes to a maximum dose of 40 μg/kg/min. The reasons for performing DE included preoperative cardiac evaluation (30), chest pain (23), assessment of ischemia (18), and suspected restenosis (6). DE was classified according to wall motion response as normal (before and during DE), fixed abnormal (abnormal before with no change during DE), or ischemic (new wall-motion abnormality during DE). Mean duration of follow-up was 10 months. Cardiac events occurred in 14 patients. These included congestive heart failure in seven patients, myocardial infarction in six, and cardiac death in one. A normal wall-motion response (n = 40) was associated with a low incidence of cardiac events (5%), whereas 5 of 10 patients (50%) with an ischemic response had events. The risk of cardiac events was intermediate (26%) in patients with fixed abnormal wall motion. Overall sensitivity of DE for predicting future cardiac events was 85%. In 45 patients who underwent coronary angiography within 2 months of DE, the test detected CAD with a sensitivity of 71%. In conclusion, the wall-motion response during DE may be used for identifying patients at high risk for future cardiac events.
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U2 - 10.1016/0002-8703(94)90378-6
DO - 10.1016/0002-8703(94)90378-6
M3 - Article
C2 - 8197976
AN - SCOPUS:0028246432
SN - 0002-8703
VL - 127
SP - 1510
EP - 1515
JO - American Heart Journal
JF - American Heart Journal
IS - 6
ER -