Key result
Native T1-mapping accurately delineated the edema-based area-at-risk compared to T2-mapping, and post-contrast T1-mapping accurately quantified acute MI size.
Why the study?
Does T1-mapping accurately quantify area-at-risk and infarct size compared to conventional T2-mapping and LGE in STEMI patients?
Observational (n=28)
No
Does T1-mapping accurately quantify area-at-risk and infarct size compared to conventional T2-mapping and LGE in STEMI patients?
Answers are grounded in this paper and cite their sources.
T1-mapping can accurately quantify both edema-based area-at-risk and acute infarct size in STEMI patients, potentially shortening CMR scan duration by 15-20 minutes.
BACKGROUND: A comprehensive cardiovascular magnetic resonance (CMR) in reperfused ST-segment myocardial infarction (STEMI) patients can be challenging to perform and can be time-consuming. We aimed to investigate whether native T1-mapping can accurately delineate the edema-based area-at-risk (AAR) and post-contrast T1-mapping and synthetic late gadolinium (LGE) images can quantify MI size at 1.5 T. Conventional LGE imaging and T2-mapping could then be omitted, thereby shortening the scan duration. METHODS: Twenty-eight STEMI patients underwent a CMR scan at 1.5 T, 3 ± 1 days following primary percutaneous coronary intervention. The AAR was quantified using both native T1 and T2-mapping. MI size was quantified using conventional LGE, post-contrast T1-mapping and synthetic magnitude-reconstructed inversion recovery (MagIR) LGE and synthetic phase-sensitive inversion recovery (PSIR) LGE, derived from the post-contrast T1 maps. RESULTS: 0.97; ICC 0.986 (0.969-0.993); bias -0.1 ± 4.2% LV). There were excellent correlation and inter-method agreement with no bias, between MI size by conventional LGE, synthetic MagIR LGE (bias 0.2 ± 2.2%LV, P = 0.35), synthetic PSIR LGE (bias 0.4 ± 2.2% LV, P = 0.060) and post-contrast T1-mapping (bias 0.3 ± 1.8% LV, P = 0.10). The mean scan duration was 58 ± 4 min. Not performing T2 mapping (6 ± 1 min) and conventional LGE (10 ± 1 min) would shorten the CMR study by 15-20 min. CONCLUSIONS: T1-mapping can accurately quantify both the edema-based AAR (using native T1 maps) and acute MI size (using post-contrast T1 maps) in STEMI patients without major cardiovascular risk factors. This approach would shorten the duration of a comprehensive CMR study without significantly compromising on data acquisition and would obviate the need to perform T2 maps and LGE imaging.
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Bulluck et al. (2016) conducted an observational in ST-segment elevation myocardial infarction (n=28). Native T1-mapping vs. T2-mapping was evaluated on Area-at-risk (% of left ventricle) (ICC 0.986, 95% CI 0.969-0.993, p=0.72). Native T1-mapping accurately delineated the edema-based area-at-risk compared to T2-mapping, and post-contrast T1-mapping accurately quantified acute MI size.
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