Background Cardiovascular MRI benefits from improved SNR-efficiency at ≥3T [1,]2, but is subject to other sources of error, which require careful consideration when transitioning from primary use of 1.5T scanners. For example, chemical shift-induced PC-MRI errors [3] are increased at 3T compared to 1.5T. Chemical shift causes the complex perivascular fat signal to chemically shift into the vessel lumen and superposes with the complex blood (water) signal, thereby corrupting the phase (velocity) estimate. Chemical shift errors can be minimized by increasing the bandwidth (reduces the magnitude of the shifted fat signal), and by using an in-phase TE (TEIN, ensures fat and water are in-phase). Shorter TEs improve SNR, therefore it is advantageous that the minimum TEIN (TEIN,MIN) at 3T is 2.46ms, which is substantially shorter than TEIN,MIN=4.92ms at 1.5T, but such short TEs cannot be attained with conventional flowcompensated/flow-encoded (FCFE) velocity encoding strategies. The objective was to design a velocity encoding strategy void of conventional FCFE gradients that instead achieves through-plane velocity sensitivity using the slice select gradient, which yields a non-zero first gradient moment (M1 )f or the first PC-MRI TR: M1,1=X. The slice-select refocusing gradient (SSRG) lobe is time-shifted for the second TR to produce M1,2=X+Y, such that ΔM1=Y=πg -1 VENC -1 .W e hypothesize that the proposed SSRG velocity encoding scheme, will permit the use of TEIN,MIN for chemical shift insensitive PC-MRI measures at 3T that are both faster and have improved SNR. Methods