The suitability of gamma camera coincidence systems for nitrogen 13-labeled ammonia myocardial perfusion imaging: A quantitative comparison with full-ring PET |
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Authors: | Fergus I. McKiddie Howard G. Gemmell E. Joyce Davidson Andrew Welch Mohaned Egred |
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Affiliation: | Department of Bio-medical Physics and Bio-engineering, University of Aberdeen, Grampian University Hospitals NHS Trust, Foresterhill, United Kongdom. f.mckiddie@biomed.abdn.ac.uk |
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Abstract: | BACKGROUND: The aim of this study was to examine the quality of nitrogen 13-labeled ammonia (NH(3)) perfusion data from coincidence-capable gamma camera positron emission tomography (GC-PET) systems compared with that from full-ring positron emission tomography (FR-PET). METHODS AND RESULTS: The performance parameters of the GC-PET system were examined and found adequate for imaging at the activity levels used clinically. We studied 15 patients who underwent stress and rest N-13-labeled NH(3) perfusion imaging on FR-PET and GC-PET systems. Quantitative analysis of perfusion values showed that GC-PET uptake was significantly lower than FR-PET uptake in 67.6% of segments. Bland-Altman analysis showed that the mean difference between FR-PET and GC-PET values was from 5.3% to 5.9%. Stress FR-PET identified 49 segments as having impaired perfusion, 46 (93.9%) of which were also identified by GC-PET. Fifty-six additional segments were identified as abnormal by GC-PET. These findings indicated a general overestimation of defect size on GC-PET. Analysis of the degree of perfusion reduction also found that GC-PET tended to overestimate defect contrast. These findings are similar to those previously found by workers examining fluorine 18-fluorodeoxyglucose uptake by both techniques. CONCLUSIONS: Good concordance was shown between GC-PET and FR-PET systems for N-13-labeled NH(3) perfusion imaging, although further work is required to optimize the technique. |
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Keywords: | Gamma camera coincidence imaging positron emission tomography nitrogen 13– labeled ammonia myocardial perfusion myocardial viability |
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