Left ventricular non-compaction in paediatrics: a novel semi-automated imaging technique bridging imaging findings and clinical outcomes

Author:

Tadros Hanna J1ORCID,Doan Tam T1,Pednekar Amol S2,Masand Prakash M3,Spinner Joseph A1,Schlingmann Tobias R1,Pignatelli Ricardo1,Noel Cory V4,Wilkinson James C1ORCID

Affiliation:

1. Section of Cardiology, Department of Pediatrics, Baylor College of Medicine , 6651 Main St, Legacy Tower, E1920, 77030 Houston, TX , USA

2. Department of Radiology, Cincinnati Children’s Hospital Medical Center , Cincinnati, OH , USA

3. Department of Radiology, Baylor College of Medicine , Houston, TX , USA

4. Pediatric Cardiology of Alaska, Seattle Children’s Hospital , Anchorage, AK , USA

Abstract

Abstract Aims We set out to design a reliable, semi-automated, and quantitative imaging tool using cardiac magnetic resonance (CMR) imaging that captures LV trabeculations in relation to the morphologic endocardial and epicardial surface, or perimeter-derived ratios, and assess its diagnostic and prognostic utility. Methods and results We queried our institutional database between January 2008 and December 2018. Non-compacted (NC)-to-compacted (C) (NC/C) myocardium ratios were calculated and our tool was used to calculate fractal dimension (FD), total mass ratio (TMR), and composite surface ratios (SRcomp). NC/C, FD, TMR, and SRcomp were assessed in relation to LVNC diagnosis and outcomes. Univariate hazard ratios with cut-offs were performed using clinically significant variables to find ‘at-risk’ patients and imaging parameters were compared in ‘at-risk’ patients missed by Petersen Index (PI). Ninety-six patients were included. The average time to complete the semi-automated measurements was 3.90 min (SEM: 0.06). TMR, SRcomp, and NC/C were negatively correlated with LV ejection fraction (LVEF) and positively correlated with indexed LV end-systolic volumes (iLVESVs), with TMR showing the strongest correlation with LVEF (−0.287; P = 0.005) and SRcomp with iLVESV (0.260; P = 0.011). We found 29 ‘at-risk’ patients who were classified as non-LVNC by PI and hence, were missed. When compared with non-LVNC and ‘low-risk’ patients, only SRcomp differentiated between both groups (1.91 SEM 0.03 vs. 1.80 SEM 0.03; P = 0.019). Conclusion This method of semi-automatic calculation of SRcomp captured changes in at-risk patients missed by standard methods, was strongly correlated with LVEF and LV systolic volumes and may better capture outcome events.

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine,Radiology, Nuclear Medicine and imaging,General Medicine

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