Table 4.
Study | Methods | Reference technique | Accuracy results |
---|---|---|---|
Ku et al. [47] | In vitro | LDV, theoretical calculations | Excellent accuracy, good correlation (no reported values) |
Recirculating steady flow phantom (25.4 mm diameter) | |||
Debatin et al. [50] | In vitro | True flow | Flow error: 42.1 ± 10.3% (16-frame cine PC-MRI), − 10.4 ± 17.3% (1-frame 2D PC-MRI), − 2.4 ± 2.5% (6-frame triads PC-MRI) |
Flow phantom | |||
Siegel et al. [45] | In vitro | LDV | Velocity error < 30% (provided high SNR, low TE, thick slices) |
Stenotic flow phantom | |||
Lee et al. [44] | In vitro | Doppler US | Peak systolic velocity: SEE = 5.3 cm/s (fast PC vs Doppler US), 4.6 cm/s (cine PC vs Doppler US); minimum diastolic velocity: r = 0.74 (fast PC vs Doppler US) |
Flow phantoms (10 mm diameter) with 0, 50, 75% stenosis | |||
Hoppe et al. [43] | In vitro | Doppler US guidewire | Flow: r = 0.95 |
Flow phantoms with varying concentric stenosis | |||
King et al. [35] | In vitro | True flow | Steady flow: R2 = (0.77–0.99), relative flow error = (1.5–112)% according to pixel resolution [(0.8–3.6) mm]; pulsatile flow: error = (0.6–4.1)% (5 mm diameter) (1.4–13.8)% (2 mm diameter) |
Steady flow phantoms (3–11 mm diameter) + pulsatile flow phantoms (2 and 5 mm diameter) | |||
Hollnagel et al. [46] | In vitro | LDV, CFD | Maximum velocity: RMSE = 6.55% (internal cerebral artery, PC-MRI vs LDV), 8.02% (internal cerebral artery, PC-MRI vs CFD), 9.34% (anterior cerebral artery, PC-MRI vs LDV), 10.35% (anterior cerebral artery, PC-MRI vs CFD) |
Flow phantom | |||
Dambreville et al. [41] | In vitro | True flow | Steady flow: CCC = 0.992, mean flow error = 6.0 mL/min; pulsative flow: CCC = 0.996, mean flow error = − 6.7 mL/min |
Steady flow phantoms (3–11 mm diameter) + pulsatile-flow phantoms with additional 2.1 mm diameter channel | |||
Khodarahmi et al. [48] | In vitro | PIV | Steady flow: CC > 0.99, pulsatile flow: CC > 0.96 |
Flow phantom with varying concentric stenosis | |||
Spithoven et al. [42] | In vitro | True flow | Flow: CC = 0.969 (6–8 mm diameter) |
Flow phantoms (5–8 mm diameter) | |||
Sommer et al. [19] | In vivo | PAH clearance | RBF: r = 0.63 (artery), r = 0.76 (vein) |
9 HVs | |||
Lundin et al. [53] | In vivo | PAH clearance | Good agreement (no reported values) |
14 HVs | |||
Wolf et al. [52] | In vivo | PAH clearance | RBF error = 39 mL/min (95% CI − 100 to 177) (Venc = 100), 69 mL/min (95% CI − 31 to 169) (Venc = 150); |
10 HVs | |||
Debatin et al. [50] | In vivo | PAH clearance | Mean RBF error = 2.8 ± 7.1% (6-frame triads PC-MRI), 28.5 ± 28.2% (16-frame), − 11.6 ± 14.9% (1-frame) |
8 HVs | |||
Myers et al. [1] | In vivo | PAH clearance | RBF error = 20 mL/min (95% CI − 214 to 254), r = 0.91 |
14 renal transplant recipients | |||
Cortsen et al. [49] | In vivo | PAH clearance, 99mTc-DTPA scintigraphy | RBF: r = 0.68 |
8 CKD patients | |||
Sommer et al. [51] | In vivo | PAH clearance | Mean RBF error = (0–95) mL/min, RBF bias = (− 1.3 to 10)%, 95% CI = ± (17.6–26.5)%, based on cine PC-MRI sequences (segmented k space, rapid spiral) |
18 HVs | |||
de Haan et al. [55] | In vivo | 133Xenon Washout | RBF: r = 0.69; CC = 0.51 |
71 kidneys from patients with suspected renovascular hypertension | |||
Spithoven et al. [42] | In vivo | Hip clearance | RBF: r = 0.81 |
21 ADPKD patients |
PC, phase contrast; Venc, velocity encoding; PIV, particle image velocimetry; Hip, 131I-hippuran; SEE, standard error of the estimate; US, ultrasound; SNR, signal-to-noise ratio; ICC, intraclass correlation coefficient; RMSE, root mean squared error; CFD, computational fluid dynamics; LDV, laser Doppler velocimetry; RBF, renal blood flow; HVs, healthy volunteers; ADPKD, autosomal dominant polycystic kidney disease; CKD, chronic kidney disease; PAH, para-aminohippurate; CV, coefficient of variation; CI, confidence interval; TE, echo time; CCC, concordance correlation coefficient