Key result
Highly accelerated compressed sensing CMR yields lower strain and volumetric parameters than conventional cine acquisitions.
Why the study?
Highly accelerated compressed sensing-based sequences were developed for faster CMR acquisitions, but intersoftware and interacquisition differences across postprocessing software remained unclear.
Do feature-tracking strain parameters differ between highly accelerated compressed sensing-based sequences and conventional cine sequences in cardiac magnetic resonance imaging?
Observational (n=106)
Do feature-tracking strain parameters differ between highly accelerated compressed sensing-based sequences and conventional cine sequences in cardiac magnetic resonance imaging?
p-value: p=<0.02
Highly accelerated compressed sensing CMR sequences yield significantly lower magnitudes of strain and volumetric parameters compared to conventional cine, highlighting the need for sequence-specific awareness during follow-up.
Sequence-specific reference values needed for compressed sensing CMR strain/volumes; leaves open clinical impact and prospective validation.
BACKGROUND: Cardiac magnetic resonance imaging protocols have been adapted to fit the needs for faster, more efficient acquisitions, resulting in the development of highly accelerated, compressed sensing-based (CS) sequences. The aim of this study was to evaluate intersoftware and interacquisition differences for postprocessing software applied to both CS and conventional cine sequences. MATERIALS AND METHODS: A total of 106 individuals (66 healthy volunteers, 40 patients with dilated cardiomyopathy, 51% female, 38±17 y) underwent cardiac magnetic resonance at 3T with retrospectively gated conventional cine and CS sequences. Postprocessing was performed using 2 commercially available software solutions and 1 research prototype from 3 different developers. The agreement of clinical and feature-tracking strain parameters between software solutions and acquisition types was assessed by Bland-Altmann analyses and intraclass correlation coefficients. Differences between softwares and acquisitions were assessed using Kruskal-Wallis analysis of variances. In addition, receiver operating characteristic curve-derived cutoffs were used to evaluate whether sequence-specific cutoffs influence disease classification. RESULTS: There were significant intersoftware ( P <0.002 for all except LV end-diastolic volume per body surface area) and interacquisition differences ( P <0.02 for all except end-diastolic volume per body surface area from Neosoft, left ventricular mass per body surface area from cvi42 and TrufiStrain and global circumferential strain from Neosoft). However, the intraclass correlation coefficients between acquisitions were strong-to-excellent for all parameters (all ≥0.81). In comparing individual softwares to a pooled mean, Bland-Altmann analyses revealed smaller magnitudes of bias for cine acquisition than for CS acquisition. In addition, the application of conventional cutoffs to CS measurements did not result in the false reclassification of patients. CONCLUSION: Significantly lower magnitudes of strain and volumetric parameters were observed in retrospectively gated CS acquisitions, despite strong-to-excellent agreement amongst software solutions and acquisition types. It remains important to be aware of the acquisition type in the context of follow-up examinations, where different cutoffs might lead to misclassifications.
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Halfmann et al. (2023) conducted an observational in Healthy volunteers and dilated cardiomyopathy (n=106). Highly accelerated compressed sensing-based (CS) sequences vs. Retrospectively gated conventional cine sequences was evaluated on Intersoftware and interacquisition differences in clinical and feature-tracking strain parameters (p=<0.02). Highly accelerated compressed sensing-based CMR sequences yielded significantly lower magnitudes of strain and volumetric parameters compared to conventional cine acquisitions (P<0.02).
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