Myocardial flow reserve estimation with contemporary CZT-SPECT and 99mTc-tracers lacks precision for routine clinical application

被引:15
作者
Renaud, Jennifer M. [1 ]
Poitrasson-Riviere, Alexis [1 ]
Hagio, Tomoe [1 ]
Moody, Jonathan B. [1 ]
Arida-Moody, Liliana [2 ,3 ]
Ficaro, Edward P. [1 ,2 ,3 ]
Murthy, Venkatesh L. [2 ,3 ]
机构
[1] INVIA Med Imaging Solut, Ann Arbor, MI 48108 USA
[2] Univ Michigan, Frankel Cardiovasc Ctr, Dept Internal Med, Div Cardiovasc Med, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Radiol, Div Nucl Med, Ann Arbor, MI 48109 USA
关键词
Myocardial flow reserve; coronary flow reserve; myocardial perfusion imaging; SPECT; CORONARY-ARTERY-DISEASE; BLOOD-FLOW; DYNAMIC SPECT; QUANTIFICATION; PERFUSION; OPTIMIZATION; VALIDATION; SYSTEM;
D O I
10.1007/s12350-021-02761-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background PET myocardial flow reserve (MFR) has established diagnostic and prognostic value. Technological advances have now enabled SPECT MFR quantification. We investigated whether SPECT MFR precision is sufficient for clinical categorization of patients. Methods Validation studies vs invasive flow measurements and PET MFR were reviewed to determine global SPECT MFR thresholds. Studies vs PET and a SPECT MFR repeatability study were used to establish imprecision in SPECT MFR measurements as the standard deviation of the difference between SPECT and PET MFR, or test-retest SPECT MFR. Simulations were used to evaluate the impact of SPECT MFR imprecision on confidence of clinically relevant categorization. Results Based on validation studies, the typical PET MFR categories were used for SPECT MFR classification (< 1.5, 1.5-2.0, > 2.0). Imprecision vs PET MFR ranged from 0.556 to 0.829, and test-retest imprecision was 0.781-0.878. Simulations showed correct classification of up to only 34% of patients when 1.5 <= true MFR <= 2.0. Categorization with high confidence (> 80%) was only achieved for extreme MFR values (< 1.0 or > 2.5), with correct classification in only 15% of patients in a typical lab with MFR of 1.8 +/- 0.5. Conclusions Current SPECT-derived estimates of MFR lack precision and require further optimization for clinical risk stratification.
引用
收藏
页码:2078 / 2089
页数:12
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