RESUMO
Vasospastic angina (VSA), or variant angina, is an under-recognized cause of chest pain and myocardial infarction, especially in Western countries. VSA leads to a declined quality of life and is associated with increased morbidity and mortality. Currently, the diagnosis of VSA relies on invasive testing that requires the direct intracoronary administration of ergonovine or acetylcholine. However, invasive vasoreactivity testing is underutilized. Several non-invasive imaging alternatives have been proposed to screen for VSA. This review aims to discuss the strengths and limitations of available non-invasive imaging tests for vasospastic angina.
Assuntos
Vasoespasmo Coronário , Humanos , Qualidade de Vida , Ergonovina , Eletrocardiografia , Acetilcolina , Angiografia Coronária/métodosRESUMO
BACKGROUND: Myocardial viability and quantification of regional myocardial blood flow (MBF) are important for the diagnosis of heart disease. Positron emission tomography is the current gold standard for determining myocardial viability, but most positron-emitting perfusion tracers require an on-site cyclotron. Rubidium-82 ((82)Rb) is a myocardial perfusion tracer that is produced using an on-site generator. This study investigates (82)Rb-measured MBF in canine models of stunned and infarcted myocardium compared with selected measurements obtained concurrently using microspheres. METHODS: Myocardial stunning and infarction were created in canines by occluding the left anterior descending for 15 min and 2 h, respectively. Stunning was produced in all animals; six animals were reperfused after the 2 h occlusion, whereas the other six animals remained occluded permanently. Regional MBF was measured in each group during rest and dobutamine stress at acute and chronic (8 weeks postinsult) time points using dynamic (82)Rb perfusion imaging and radioactively labeled microspheres. RESULTS: Average resting MBF with microspheres and Rb was 0.68+/-0.02 versus 0.73+/-0.01 (P<0.001) in nonischemic tissue, and 0.53+/-0.03 versus 0.42+/-0.02 (P<0.001) in the region-at-risk tissue, respectively. Average MBF during stress with microspheres and Rb was 2.78+/-0.15 versus 3.53+/-0.16 (P<0.05) in the nonischemic tissue, and 1.90+/-0.20 versus 2.31+/-0.26 (P = NS) in the region-at-risk tissue, respectively. CONCLUSION: Despite the small significant differences, the dynamic (82)Rb measurements provide estimates of MBF in stunned and acutely and chronically infarcted tissue at rest and during hyperemia that correspond with clinical interpretation.
Assuntos
Circulação Coronária , Microesferas , Infarto do Miocárdio/diagnóstico por imagem , Infarto do Miocárdio/fisiopatologia , Miocárdio Atordoado/diagnóstico por imagem , Miocárdio Atordoado/fisiopatologia , Radioisótopos de Rubídio , Animais , Modelos Animais de Doenças , Cães , Coração/diagnóstico por imagem , Coração/fisiopatologia , Hiperemia/diagnóstico por imagem , Hiperemia/fisiopatologia , Tomografia por Emissão de Pósitrons , DescansoRESUMO
BACKGROUND: Our objectives were to investigate the accuracy of global and regional left ventricular (LV) function parameters determined from gated fluorine 18 deoxyglucose (FDG) positron emission tomography (PET) and to determine whether this approach complements viability imaging data for tissue characterization. Nongated FDG-PET is a clinical standard for viability imaging, but LV function is often determined with other techniques, which increases patient burden, expenditure, and co-registration errors. Better tissue characterization may be achieved if data were acquired with one test. Methods and results Forty-eight patients with LV dysfunction (including 35 with ejection fraction [EF] =35%) underwent perfusion/FDG imaging with gating of the FDG images and radionuclide angiography (RNA) 6 +/- 6 days apart. Regional function (wall motion/thickening) and viability pattern (normal, mismatch, nontransmural scar, and transmural scar) were determined for 301 segments. Global EFs from FDG-PET (29.3% +/- 11.5%) and RNA (31.1% +/- 10.4%) were well correlated: EF(FDG-PET) = 0.91 x EF(RNA) + 0.91 (r = 0.83, P <.00001). Regional wall motion concordance between PET and RNA with three wall motion scores was 67% with moderate agreement (kappa = 0.50, P <.001). PET viability was also determined for each segment. The relative frequency of normal motion compared with abnormal motion decreased with worsening viability classification. Of the normal segments, 96 of 139 (69%) had reduced wall motion, suggesting repetitively stunned myocardium. Segments classified as normal or mismatch had a higher frequency of normal wall thickening (65% and 52%) than wall motion (31% and 17%). No segments classified as transmural scar exhibited normal wall thickening. CONCLUSION: Gated FDG-PET accurately measures global LV function. Regional function can also be determined with reasonable accuracy. This approach also provides precise co-registration of function with metabolic information and thus improved tissue characterization of the myocardium. Gated FDG-PET has the potential to assist in optimizing management of this patient population.