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Intra-patient reproducibility of myocardial SPECT imaging with 201Tl
Background To define the physical and clinical reproducibility of 201 Tl myocardial perfusion SPECT (MPS), this study assesses the variation between two repeated rest 201 Tl MPS with repositioning only, with a two-hour time interval and with phantom measurements as a reference. Methods Three anthrop...
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Published in: | Journal of nuclear cardiology 2009, Vol.16 (1), p.97-104 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Background
To define the physical and clinical reproducibility of
201
Tl myocardial perfusion SPECT (MPS), this study assesses the variation between two repeated rest
201
Tl MPS with repositioning only, with a two-hour time interval and with phantom measurements as a reference.
Methods
Three anthropomorphic thorax phantoms were filled with
201
Tl. For each phantom five repeated
201
Tl MPS were obtained. In addition, in 20 patients repeated
201
Tl rest-MPS and in 26 patients early and delayed
201
Tl rest-MPS were performed. Quantitative analysis was done using MunichHeart. Statistical methods were used to calculate variability. Visual analysis was performed by 2 independent observers.
Results
The average variation between repeated phantom MPS was 0.5% (95% confidence interval (CI): −0.4% to 1.4%). For patient scans this was −5.0% (95% CI: −2.5% to −7.5%) and between early and delayed
201
Tl MPS −15.5% (95% CI: −11.7% to −19.3%). Visual assessment revealed no clinical significant differences between rest
201
Tl and repeated or delayed
201
Tl MPS.
Conclusions
Repositioning in phantom
201
Tl MPS does not cause significant variation. Repeated
201
Tl MPS in patients shows 5.0% decrease of
201
Tl in 30 minutes, which increases to 15% during a two-hour time interval without quantitative or visual regional differences. This decrease indicates a time-related washout of
201
Tl, but does not change clinical diagnosis. |
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ISSN: | 1071-3581 1532-6551 |
DOI: | 10.1007/s12350-008-9011-7 |