TY - JOUR
T1 - Regional variability in the myocardial clearance of thallium-201 and its importance in determining the presence or absence of coronary artery disease
AU - Kaul, Sanjiv
AU - Newell, John B.
AU - Pohast, Gerald M.
AU - Okada, Robert D.
AU - Boucher, Charles A.
N1 - Funding Information:
From the eral Hospital and Harvard Medical School, Boston, Massachusetts and the *Division of Cardiology, University of Virginia School of Medicine, Char lottesville, Virginia. This study was supported in part by Grants HL 26215, HL 32953 and HL 07416 from the National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland. Dr. Okada is an Established Texas. Presented in part at the 35th Annual Scientific Sessions of the American College of Cardiology, Atlanta, Georgia, March 1986. Manuscript received December 10, 1985; revised manuscript received February 10, 1986, accepted February 18, 1986.
PY - 1986
Y1 - 1986
N2 - There are several limitations in using absolute myocardial clearance of thallium-201 for the detection of coronary artery disease. Noncardiac factors such as peak exercise heart rate and blood level of thallium can affect its absolute myocardial clearance. However, because all myocardial segments in a given heart are exposed to the same noncardiac factors, a relative difference in myocardial clearance of thallium between segments could reflect the presence of coronary artery disease. Accordingly, myocardial clearance of thallium was analyzed in 370 patients. Patients in Group I (n = 45) had less than 1% probability of having coronary artery disease, patients in Group II (n = 44) had normal coronary arteries and patients in Group III (n = 281) had coronary artery disease. Although mean myocardial clearance of thallium in 15 myocardial segments in three views in Group I subjects was 3.4 ± 0.7 hours, the variability between the slowest and fastest clearing segments in the same subject was as much as 98%. This variability was systematic, suggesting technical reasons associated with imaging as the cause of the variability: 78% of the slowest clearing segments were basal whereas 53% of the fastest clearing segments were apical (p < 0.01). When Group II and HI patients were compared based on Group I values, the absolute myocardial clearance of thallium had a sensitivity and specificity of 92 and 16%, respectively. However, when myocardial clearance of thallium was considered abnormal in a segment only if the rate was 98% slower than that in the fastest clearing segment in the same patient, sensitivity and specificity changed to 69 and 86%, respectively (p < 0.01). When the latter values were provided for logistic regression analysis, myocardial clearance of thallium was at par with redistribution and lung/heart ratio for the detection of coronary artery disease. In conclusion: 1) there is significant regional variability in the myocardial clearance of thallium, even in normal subjects, probably as a result of factors related to imaging techniques; 2) when myocardial clearance of thallium is considered abnormal after comparison with the fastest clearing segment in the myocardium, its diagnostic utility improves significantly; and 3) although the initial impetus for using myocardial clearance of thallium to detect coronary artery disease was its ability to measure absolute values, its use as a relative variable optimizes its diagnostic utility.
AB - There are several limitations in using absolute myocardial clearance of thallium-201 for the detection of coronary artery disease. Noncardiac factors such as peak exercise heart rate and blood level of thallium can affect its absolute myocardial clearance. However, because all myocardial segments in a given heart are exposed to the same noncardiac factors, a relative difference in myocardial clearance of thallium between segments could reflect the presence of coronary artery disease. Accordingly, myocardial clearance of thallium was analyzed in 370 patients. Patients in Group I (n = 45) had less than 1% probability of having coronary artery disease, patients in Group II (n = 44) had normal coronary arteries and patients in Group III (n = 281) had coronary artery disease. Although mean myocardial clearance of thallium in 15 myocardial segments in three views in Group I subjects was 3.4 ± 0.7 hours, the variability between the slowest and fastest clearing segments in the same subject was as much as 98%. This variability was systematic, suggesting technical reasons associated with imaging as the cause of the variability: 78% of the slowest clearing segments were basal whereas 53% of the fastest clearing segments were apical (p < 0.01). When Group II and HI patients were compared based on Group I values, the absolute myocardial clearance of thallium had a sensitivity and specificity of 92 and 16%, respectively. However, when myocardial clearance of thallium was considered abnormal in a segment only if the rate was 98% slower than that in the fastest clearing segment in the same patient, sensitivity and specificity changed to 69 and 86%, respectively (p < 0.01). When the latter values were provided for logistic regression analysis, myocardial clearance of thallium was at par with redistribution and lung/heart ratio for the detection of coronary artery disease. In conclusion: 1) there is significant regional variability in the myocardial clearance of thallium, even in normal subjects, probably as a result of factors related to imaging techniques; 2) when myocardial clearance of thallium is considered abnormal after comparison with the fastest clearing segment in the myocardium, its diagnostic utility improves significantly; and 3) although the initial impetus for using myocardial clearance of thallium to detect coronary artery disease was its ability to measure absolute values, its use as a relative variable optimizes its diagnostic utility.
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U2 - 10.1016/S0735-1097(86)80097-3
DO - 10.1016/S0735-1097(86)80097-3
M3 - Editorial
C2 - 3711537
AN - SCOPUS:0022621231
SN - 0735-1097
VL - 8
SP - 95
EP - 100
JO - Journal of the American College of Cardiology
JF - Journal of the American College of Cardiology
IS - 1
ER -