Abstract

Methods Five patients with CHD were included in this pilot study (table 2 in Figure 2). The FB MR studies were performed on a Philips Acheiva 1.5T magnet using a 5-channel phased array coil (see Table 1 in Figure 1) 1. Respiratory synchronized [1], time-resolved MRA 2. Equilibrium phase MRA 3. 3D cine SSFP 4.4D phase contrast (PC) flow imaging 5.3D whole-heart single phase SSFP (coronary) Comparative data was obtained using conventional 2D cine RT SSFP sequences [2] in the VLA, 4 chamber and short axis planes, and 2D PC imaging. Data Analysis: Image quality assessment and quantitative volumetric and flow analysis were performed by three blinded, experienced users. MRA images were graded using a semi-quantitative scale from 1-5 for relevant imaging targets in CHD [1], with 1: excellent, no limitations, and 5: non-diagnostic. The clinical scoring system for 2D and 3D cine SSFP was based on bloodmyocardial contrast, endocardial edge definition and inter-slice alignment [2]. Paired t-test analysis was performed on LV and RV volumes obtained by an experienced observer using the same software

Highlights

  • Cardiac MRI for congenital heart disease (CHD) is an operator dependent and time-intensive examination requiring real-time decision making regarding choice of sequences, planes, and acquisition parameters to adapt to unique morphological and functional variables in a given patient.relevant imaging targets in CHD [1], with 1: excellent, no limitations, and 5: non-diagnostic

  • Equilibrium phase MRA 3. 3D cine SSFP 4.4D phase contrast (PC) flow imaging 5.3D whole-heart single phase SSFP Comparative data was obtained using conventional 2D cine RT SSFP sequences [2] in the VLA, 4 chamber and short axis planes, and 2D PC imaging

  • Clinical scores for 2D SSFP were consistently better than 3D-SSFP, but 3D SSFP images were adequate for recognition of pathology in all cases (2D vs 3D: 1.5 ± 0.5 vs 1.6 ± 0.9) and had better inter-slice alignment (1.4 ± 0.5 vs 1 ± 0)

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Summary

Background

Cardiac MRI for congenital heart disease (CHD) is an operator dependent and time-intensive examination requiring real-time decision making regarding choice of sequences, planes, and acquisition parameters to adapt to unique morphological and functional variables in a given patient. Relevant imaging targets in CHD [1], with 1: excellent, no limitations, and 5: non-diagnostic. The clinical scoring system for 2D and 3D cine SSFP was based on bloodmyocardial contrast, endocardial edge definition and inter-slice alignment [2]. Paired t-test analysis was performed on LV and RV volumes obtained by an experienced observer using the same software

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