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Personalized Models for Injected Activity Levels in SPECT Myocardial Perfusion Imaging

Ramon, Albert Juan
Yang, Yongyi
Pretorius, P. Hendrik
Johnson, Karen L.
King, Michael A
Wernick, Miles N.
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Journal Article
Publication Date
2018-12-06
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Abstract

We propose a patient-specific ("personalized") approach for tailoring the injected activities to individual patients in order to achieve dose reduction in SPECT-myocardial perfusion imaging (MPI). First, we develop a strategy to determine the minimum dose levels required for each patient in a large set of clinical acquisitions (857 subjects) such that the reconstructed images are sufficiently similar to that obtained at conventional clinical dose. We then apply machine learning models to predict the required dose levels on an individual basis based on a set of patient attributes which include body measurements and various clinical variables. We demonstrate the personalized dose models for two commonly used reconstruction methods in clinical SPECT-MPI: 1) conventional filtered backprojection (FBP) with post-filtering, and 2) ordered-subsets expectation-maximization (OS-EM) with corrections for attenuation, scatter and resolution, and evaluate their performance in perfusion-defect detection by using the clinical Quantitative Perfusion SPECT (QPS) software package. The results indicate that the achieved dose reduction can vary greatly among individuals from their conventional clinical dose, and that the personalized dose models can achieve further reduction on average compared to a global (non-patient specific) dose reduction approach. In particular, the average personalized dose level can be reduced to 58% and 54% of the full clinical dose, respectively, for FBP and OS-EM reconstruction, while without deteriorating the accuracy in perfusion-defect detection. Furthermore, with the average personalized dose further reduced to only 16% of full dose, OS-EM can still achieve a detection accuracy level comparable to that of FBP with full dose.

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IEEE Trans Med Imaging. 2018 Dec 6. doi: 10.1109/TMI.2018.2885319. Link to article on publisher's site

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10.1109/TMI.2018.2885319
PubMed ID
30530358
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