Loading…
Prognostic value of phase analysis on gated single photon emission computed tomography in patients with cardiac sarcoidosis
We aimed to determine the correlation between phase analysis, reflecting the heterogeneity of perfusion defects, and the dyssynchrony of the left ventricle wall motion, and adverse cardiac events in cardiac sarcoidosis (CS) patients. Fifty-seven consecutive patients with diagnosed CS (64 [IQR 55–71]...
Saved in:
Published in: | Journal of nuclear cardiology 2021-02, Vol.28 (1), p.128-136 |
---|---|
Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | We aimed to determine the correlation between phase analysis, reflecting the heterogeneity of perfusion defects, and the dyssynchrony of the left ventricle wall motion, and adverse cardiac events in cardiac sarcoidosis (CS) patients.
Fifty-seven consecutive patients with diagnosed CS (64 [IQR 55–71] years old, 14 males), who underwent 18F-FDG PET/CT and ECG-gated SPECT, were studied. FDG PET was analysed to measure cardiac metabolic volume (CMV), and total lesion glycolysis (TLG). The SPECT findings, such as LVEF, Summed Rest Score (SRS), bandwidth (BW) were evaluated.
The median of BW was 56° (IQR 40–95). BW showed a strong inverse correlation with LVEF (r = − 0.60, P < 0.0001), and positive correlation with SRS (r = 0.82, P < 0.0001). However, there were no significant correlations between BW and CMV or TLG. The Kaplan–Meier curves revealed a significantly higher rate of MACE in the high BW group (BW > 56°) than the low BW group (BW ≤ 56°) (15.1%/years vs. 4.4%/years, P = 0.025). In multivariable analysis, BW was a significant independent predictor of MACE (P = 0.015).
Phase analysis on gated SPECT was a significant and independent predictor of MACE in patients with CS. |
---|---|
ISSN: | 1071-3581 1532-6551 |
DOI: | 10.1007/s12350-019-01660-9 |