Movahed A, Reeves W C, Batts J, Jolly S R
Department of Medicine, East Carolina University School of Medicine, Greenville, North Carolina 27858-4354.
Clin Nucl Med. 1992 Jun;17(6):489-94. doi: 10.1097/00003072-199206000-00013.
The purpose of this study was to evaluate the significance of increased Tl-201 uptake by the lungs after oral dipyridamole testing. In conjunction with myocardial perfusion scintigraphy, intravenous dipyridamole has been recently approved as an alternative to exercise for the evaluation of coronary artery disease in patients who cannot adequately exercise, and it will largely replace oral dipyridamole testing. This study contributes to the understanding of the significance of increased lung thallium uptake during pharmacologic stress testing. Oral dipyridamole, 400 mg, was administered to 192 patients undergoing Tl-201 imaging for clinical indications. Mild adverse effects occurred in 31% of patients (chest pain, nausea, headache, or flushing). Dipyridamole had minimal hemodynamic effects. The lung/heart thallium activity ratio was determined in 152 patients. These were subdivided into four groups according to the presence or absence of ischemia, transient myocardial perfusion defect, or scar as indicated by a fixed myocardial perfusion defect. In 61 patients without transient myocardial perfusion defect or fixed myocardial perfusion defect (group 1), the lung/heart thallium activity ratio was 0.39 +/- 0.01 (mean +/- SEM). In 31 patients without transient myocardial perfusion defect but with fixed myocardial perfusion defect (group 2), the lung/heart thallium activity ratio was higher, 0.44 +/- 0.02 (P less than 0.05). In 27 patients with transient myocardial perfusion defect but no fixed myocardial perfusion defect (group 3) and in 33 patients with both transient myocardial perfusion defect and fixed myocardial perfusion defect (group 4), the lung/heart thallium activity ratio was 0.51 +/- 0.03 and 0.52 +/- 0.03, respectively, both significantly higher than either group 1 or group 2 (P less than 0.05).(ABSTRACT TRUNCATED AT 250 WORDS)
本研究的目的是评估口服双嘧达莫试验后肺摄取铊-201增加的意义。与心肌灌注闪烁显像相结合,静脉注射双嘧达莫最近已被批准作为不能充分运动的患者评估冠状动脉疾病时替代运动试验的方法,并且它将在很大程度上取代口服双嘧达莫试验。本研究有助于理解药物负荷试验期间肺摄取铊增加的意义。对192例因临床指征接受铊-201显像的患者给予400mg口服双嘧达莫。31%的患者出现轻度不良反应(胸痛、恶心、头痛或潮红)。双嘧达莫对血流动力学影响极小。对152例患者测定了肺/心铊活性比值。根据有无缺血、短暂性心肌灌注缺损或固定性心肌灌注缺损(表现为心肌灌注瘢痕)将这些患者分为四组。61例无短暂性心肌灌注缺损或固定性心肌灌注缺损的患者(第1组),肺/心铊活性比值为0.39±0.01(均值±标准误)。31例无短暂性心肌灌注缺损但有固定性心肌灌注缺损的患者(第2组),肺/心铊活性比值较高,为0.44±0.02(P<0.05)。27例有短暂性心肌灌注缺损但无固定性心肌灌注缺损的患者(第3组)和33例既有短暂性心肌灌注缺损又有固定性心肌灌注缺损的患者(第4组),肺/心铊活性比值分别为0.51±0.03和0.52±0.03,均显著高于第1组或第2组(P<0.05)。(摘要截短于250字)