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quantitative blood flow evaluation of vasodilation-stress compared with dobutamine-stress in patients with end-stage liver disease using 82 rb pet/ct
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نویسنده
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abele jonathan t. ,raubenheimer monique ,bain vincent g. ,wandzilak greg ,alhulaimi naji ,coulden richard ,dekemp robert a. ,klein ran ,williams randall g. ,warshawski robert s. ,lalonde lucille d.
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منبع
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journal of nuclear cardiology - 2020 - دوره : 27 - شماره : 6 - صفحه:2048 -2059
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چکیده
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Our aim was to determine if end-stage liver disease (esld) is associated with an attenuated response to vasodilator-stress or dobutamine-stress using 82rb-pet mpi with blood flow quantification. pre-liver transplant patients who had a normal dipyridamole-stress (n = 27) or dobutamine-stress (n = 26) 82rb pet/ct mpi study with no identifiable coronary artery calcium were identified retrospectively and compared to a prospectively identified low-risk of liver disease dipyridamole-stress control group (n = 20). the dipyridamole-stress liver disease group had a lower myocardial flow reserve (mfr) (1.89 ± 0.79) than the control group (2.79 ± 0.96, p < .05). the dobutamine-stress group had a higher mfr than both other groups (3.69 ± 1.49, p < .05). a moderate negative correlation between meld score and mfr was demonstrated for the dipyridamole-stress liver disease group (r = − 0.473, p < .05). this correlation was not observed for the dobutamine-stress liver disease group (r = − 0.253, p = .21). the liver failure group as a whole (n = 53) had a higher resting myocardial blood flow (0.97 ± 0.33 ml/min/g) than the control group (0.82 ± 0.26, p < .05). dipyridamole demonstrates an attenuated vasodilatory response in esld patients compared to a non-esld control group related to higher resting blood flow and comparatively reduced stress blood flow. dobutamine does not demonstrate this effect implying it be the preferred pharmacologic mpi stress agent for esld patients.
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کلیدواژه
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pet ,myocardial blood flow ,mpi ,vasodilators ,dobutamine ,cad
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آدرس
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university of alberta, 2a2.42 walter c mackenzie health sciences centre, department of radiology and diagnostic imaging, canada, university of alberta, faculty of medicine and dentistry, canada, university of alberta, liver unit, department of medicine, canada, university of alberta, department of radiology and diagnostic imaging, canada, university of alberta, division of cardiology, department of medicine, canada, university of alberta, department of radiology and diagnostic imaging, canada, university of ottawa, division of cardiology, department of medicine, canada, university of ottawa, division of nuclear medicine, department of medicine, canada, university of alberta, division of cardiology, department of medicine, canada, university of alberta, department of radiology and diagnostic imaging, canada, university of alberta, division of cardiology, department of medicine, canada
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Authors
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