The document describes a standardized neuroimaging protocol that includes various magnetic resonance imaging sequences for the brain. It provides details on the acquisition parameters for sequences such as T2-weighted, T1-weighted, FLAIR, DUAL echo, and others. The protocol is designed to obtain all common contrasts with preset procedures using flexible parameters to optimize image quality and scan time for different field strengths.
The document describes a standardized neuroimaging protocol that includes various magnetic resonance imaging sequences for the brain. It provides details on the acquisition parameters for sequences such as T2-weighted, T1-weighted, FLAIR, DUAL echo, and others. The protocol is designed to obtain all common contrasts with preset procedures using flexible parameters to optimize image quality and scan time for different field strengths.
The document describes a standardized neuroimaging protocol that includes various magnetic resonance imaging sequences for the brain. It provides details on the acquisition parameters for sequences such as T2-weighted, T1-weighted, FLAIR, DUAL echo, and others. The protocol is designed to obtain all common contrasts with preset procedures using flexible parameters to optimize image quality and scan time for different field strengths.
The document describes a standardized neuroimaging protocol that includes various magnetic resonance imaging sequences for the brain. It provides details on the acquisition parameters for sequences such as T2-weighted, T1-weighted, FLAIR, DUAL echo, and others. The protocol is designed to obtain all common contrasts with preset procedures using flexible parameters to optimize image quality and scan time for different field strengths.
looks at MR Standard brain imaging Preset procedures:
• all common contrasts available
• all scan techniques available • three orthogonal orientations • use of flexible matrix to obtain square pixels, choice based on compromise between signal to noise ratio and scan time Standard brain imaging T2W/SE echo 1 T2W/TSE PDW/TSE DUAL/TSE T2/FLAIR T2/FLAIR long TR T2W/FFE T2/GRASE T2W/SE-EPI T1W/SE T1W/IR T1W/FFE Standard brain imaging T2W/SE echo 2 T2W/TSE PDW/TSE DUAL/TSE T2/FLAIR T2/FLAIR long TR T2W/FFE T2/GRASE T2W/SE-EPI T1W/SE T1W/IR T1W/FFE Standard brain imaging T2W/SE T2W/TSE PDW/TSE DUAL/TSE T2/FLAIR T2/FLAIR long TR T2W/FFE T2/GRASE T2W/SE-EPI T1W/SE T1W/IR T1W/FFE Standard brain imaging T2W/SE T2W/TSE PDW/TSE DUAL/TSE T2/FLAIR T2/FLAIR long TR T2W/FFE T2/GRASE T2W/SE-EPI T1W/SE T1W/IR T1W/FFE Standard brain imaging T2W/SE T2W/TSE PDW/TSE DUAL/TSE echo 1 T2/FLAIR T2/FLAIR long TR T2W/FFE T2/GRASE T2W/SE-EPI T1W/SE T1W/IR T1W/FFE Standard brain imaging T2W/SE T2W/TSE PDW/TSE DUAL/TSE echo 2 T2/FLAIR T2/FLAIR long TR T2W/FFE T2/GRASE T2W/SE-EPI T1W/SE T1W/IR T1W/FFE Standard brain imaging T2W/SE T2W/TSE PDW/TSE DUAL/TSE T2/FLAIR T2/FLAIR long TR T2W/FFE T2/GRASE T2W/SE-EPI T1W/SE T1W/IR T1W/FFE Standard brain imaging T2W/SE T2W/TSE PDW/TSE DUAL/TSE T2/FLAIR T2/FLAIR long TR T2W/FFE T2/GRASE T2W/SE-EPI T1W/SE T1W/IR T1W/FFE Standard brain imaging T2W/SE T2W/TSE PDW/TSE DUAL/TSE T2/FLAIR T2/FLAIR long TR T2W/FFE T2/GRASE T2W/SE-EPI T1W/SE T1W/IR T1W/FFE Standard brain imaging T2W/SE T2W/TSE PDW/TSE DUAL/TSE T2/FLAIR T2/FLAIR long TR T2W/FFE T2/GRASE T2W/SE-EPI T1W/SE T1W/IR T1W/FFE Standard brain imaging T2W/SE T2W/TSE PDW/TSE DUAL/TSE T2/FLAIR T2/FLAIR long TR T2W/FFE T2/GRASE T2W/SE-EPI T1W/SE T1W/IR T1W/FFE Standard brain imaging T2W/SE T2W/TSE PDW/TSE DUAL/TSE T2/FLAIR T2/FLAIR long TR T2W/FFE T2/GRASE T2W/SE-EPI T1W/SE T1W/IR T1W/FFE Standard brain imaging T2W/SE T2W/TSE PDW/TSE DUAL/TSE T2/FLAIR T2/FLAIR long TR T2W/FFE T2/GRASE T2W/SE-EPI T1W/SE T1W/IR T1W/FFE Standard brain imaging T2W/SE T2W/TSE PDW/TSE DUAL/TSE T2/FLAIR T2/FLAIR long TR T2W/FFE T2/GRASE T2W/SE-EPI T1W/SE T1W/IR T1W/FFE Standard brain imaging T2W/TSE sagital T1W/SE sagital T1W/3D/FFE coronal T1W/3D/TFE coronal T1W/3D/SPIR T1W/3D/WATS T2W/3D/SPIR STIR/TSE STIR/long TE Standard brain imaging T2W/TSE sagital T1W/SE sagital T1W/3D/FFE coronal T1W/3D/TFE coronal T1W/3D/SPIR T1W/3D/WATS T2W/3D/SPIR STIR/TSE STIR/long TE Standard brain imaging T2W/TSE sagital T1W/SE sagital T1W/3D/FFE coronal T1W/3D/TFE coronal T1W/3D/SPIR T1W/3D/WATS T2W/3D/SPIR STIR/TSE STIR/long TE Standard brain imaging T2W/TSE sagital T1W/SE sagital T1W/3D/FFE coronal T1W/3D/TFE coronal T1W/3D/SPIR T1W/3D/WATS T2W/3D/SPIR STIR/TSE STIR/long TE Standard brain imaging T2W/TSE sagital T1W/SE sagital T1W/3D/FFE coronal T1W/3D/TFE coronal T1W/3D/SPIR T1W/3D/WATS T2W/3D/SPIR STIR/TSE STIR/long TE Standard brain imaging T2W/TSE sagital T1W/SE sagital T1W/3D/FFE coronal T1W/3D/TFE coronal T1W/3D/SPIR T1W/3D/WATS T2W/3D/SPIR STIR/TSE STIR/long TE Standard brain imaging T2W/TSE sagital T1W/SE sagital T1W/3D/FFE coronal T1W/3D/TFE coronal T1W/3D/SPIR T1W/3D/WATS T2W/3D/SPIR STIR/TSE STIR/long TE Standard brain imaging T2W/TSE sagital T1W/SE sagital T1W/3D/FFE coronal T1W/3D/TFE coronal T1W/3D/SPIR T1W/3D/WATS T2W/3D/SPIR STIR/TSE STIR/long TE Standard brain imaging T2W/TSE sagital T1W/SE sagital T1W/3D/FFE coronal T1W/3D/TFE coronal T1W/3D/SPIR T1W/3D/WATS T2W/3D/SPIR STIR/TSE STIR/long TE T2W/SE Method = MS SE TR = shortest ( 2219 - 2400 ms ) TE first = 20 ms TE second = 90 ms Orientation = transverse / RL FOV / RFOV = 230 / 80 Matrix = 256 Scan perc. = 80 Slices = 22 ( 1.0T, 1.5T ) 20 ( 0.5 T ) Thk / gap = 5.0 / 1.0 ( 1.0T, 1.5T ) 6.0 / 1.0 ( 0.5T ) REST =0 Flow comp. = yes NSA =1 Scan time = 6:03 - 6:16 min Acq. resolution = 1.12 x 0.9 mm T2W/TSE ethod = MS TSE NOTE: R = shortest ( 4121 - 4518 ms ) E = 100 ms Long TR and TE for high SE factor = 10 - 15, linear signal of CSF. rientation = transverse / RL OV / RFOV = 230 / 80 atrix = 384 ( 1.0T, 1.5T ) 256 ( 0.5T ) can perc = 80 ices = 22 ( 1.0T, 1.5T ) 20 ( 0.5 T ) hk / gap = 5.0 / 1.0 ( 1.0T, 1.5T ) 6.0 / 1.0 ( 0.5T ) EST =0 SA =3 can time = 3:21 - 3:38 min cq. resolution = 0.75 x 0.6 mm ( 1.0T, 1.5T ) 1.12 x 0.9 mm ( 0.5T ) PDW/TSE ethod = MS TSE NOTE: R = 1800 ms E = 30 ms TR of 1800 ms for relatively SE factor = 3, linear low signal of CSF. rientation = transverse / RL OV / RFOV = 230 / 80 Low turbo factor to minimize atrix = 384 ( 1.0T, 1.5T ) T2-influence. 256 ( 0.5T ) can perc = 80 Profile order linear to reduce ices = 22 ( 1.0T, 1.5T ) blurring. 20 ( 0.5 T ) hk / gap = 5.0 / 1.0 ( 1.0T, 1.5T ) 6.0 / 1.0 ( 0.5T ) EST =0 SA = 2 ( 1.0T, 1.5T ) = 3 ( 0.5T ) can time = 4:53 min cq. resolution = 0.75 x 0.6 mm ( 1.0T, 1.5T ) 1.12 x 0.9 mm ( 0.5T ) DUAL/TSE ethod = MS TSE NOTE: R = 2200 ms E first = 20 ms TR of 2200 ms for relatively E second = 100 ms low signal of CSF. SE factor = 14 rientation = transverse / RL Profile order low-high for first echo, OV / RFOV = 230 / 80 reversed linear for second atrix = 384 ( 1.0T, 1.5T ) 256 ( 0.5T ) echo. can perc = 80 ices = 22 ( 1.0T, 1.5T ) 20 ( 0.5 T ) hk / gap = 5.0 / 1.0 ( 1.0T, 1.5T ) 6.0 / 1.0 ( 0.5T ) EST =0 SA = 2 ( 1.0T, 1.5T ) = 3 ( 0.5T ) can time = 4:53 - 5:03 min cq. resolution = 0.75 x 0.6 mm ( 1.0T, 1.5T ) 1.12 x 0.9 mm ( 0.5T ) T2W/FLAIR ethod = MS IR-TSE NOTE: R = 6000 ms ( 1.0T, 1.5T ) 5000 ms ( 0.5T ) TI determines contrast between E = 100 ms gray and white matter ( amount 1 = 2000 ms ( 1.0T, 1.5T ) 1900 ms ( 0.5T ) of T1-relaxation ). SE factor = 18, linear To avoid flow artifacts, scan must rientation = transverse / RL OV / RFOV = 230 / 80 be divided in two or more atrix = 256 packages. can perc = 80 ices = 22 ( 1.0T, 1.5T ) 20 ( 0.5 T ) hk / gap = 5.0 / 1.0 ( 1.0T, 1.5T ) 6.0 / 1.0 ( 0.5T EST =0 SA = 2 ( 1.0T, 1.5T ) ( 0.5T ) can time = 3:48 - 4:40 min cq. resolution = 1.12 x 0.9 mm FLAIR/long TR ethod = MS IR-TSE NOTE: R = 11.000 ms E = 140 ms TI determines contrast between 1 = 2800 ms gray and white matter ( amount SE factor = 27 - 40 rientation = transverse / RL of T1-relaxation ). Longer TI OV / RFOV = 230 / 80 results in better T2-weighted atrix = 256 can perc = 80 contrast between gray and ices = 22 ( 1.0T, 1.5T ) white matter. 20 ( 0.5 T ) Increased TR for correct zero- hk / gap = 5.0 / 1.0 ( 1.0T, 1.5T ) 6.0 / 1.0 ( 0.5T ) crossing point. EST =0 Long TE for heavy T2-weighting. SA =3 can time = 4:02 - 5:52 min¹ To avoid flow artifacts, scan must cq. resolution = 1.12 x 0.9 mm be divided in two or more packages. T2W/FFE ethod = MS FFE NOTE: R = shortest ( 664 - 799 ms ) E = I.p., 23.02 ms ( 0.5T, 1.5T ) Combination of TR and small flip 20.7 ms ( 1.0T ) angle to reduce T1-influence. p angle = 18 rientation = transverse / RL FFE is sensitive to flow. Flow OV / RFOV = 230 / 80 compensation is set to yes. atrix = 256 can perc = 80 T2-FFE is sensitive for suscep- ices = 22 ( 1.0T, 1.5T ) tibility, useful to detect haemor- 20 ( 0.5T ) raghe. hk / gap = 5.0 / 1.0 ( 1.0T, 1.5T ) 6.0 / 1.0 ( 0.5T ) EST =0 ow comp. = yes SA =2 can time = 3:37 - 4:41 min cq. resolution = 0.98 x 0.78 mm T2W/GRASE ethod = MS GRASE NOTE: R = shortest ( 5554 - 5685 ms ) E = 120 ms Lower turbo factor gives reduced SE factor = 6 - 8, linear MTC-effects compared to PI factor =3 PIR = yes TSE, resulting in better T2- rientation = transverse / RL weighted contrast between gray OV / RFOV = 230 / 80 atrix = 256 - 384 dep. on available software options and white matter. can perc = 80 Use of EPI readout gives higher ices = 22 ( 1.0T, 1.5T ) sensitivity for haemosiderin. 20 ( 0.5 T ) hk / gap = 5.0 / 1.0 ( 1.0T, 1.5T ) EPI readout results in larger water 6.0 / 1.0 ( 0.5T ) fat shift. SPIR is used. EST =0 SA = 3 ( 1.0T, 1.5T ) ( 0.5T ) can time = 2:46 - 3:31 min cq. resolution = 0.75 x 0.6 mm ( 1.0T, 1.5T ) 1.12 x 0.9 mm ( 0.5T ) T2/SE-EPI ethod = MS SE-EPI NOTE: R = shortest ( 2717 - 3270 ms ) E = 90 ms Contrast comparable to normal PI factor = 13 T2W/SE. PIR = yes rientation = transverse / RL EPI factor of 13 gives very fast OV / RFOV = 230 / 80 scan, sensitive for haemorraghe. atrix = 256 can perc = 80 EPI readout results in large water ices = 22 ( 1.0T, 1.5T ) fat shift. SPIR is used. 20 ( 0.5 T ) hk / gap = 5.0 / 1.0 ( 1.0T, 1.5T ) 6.0 / 1.0 ( 0.5T ) EST =0 SA =3 can time = 1:45 - 2:02 min cq. resolution = 1.12 x 0.9 mm T1W/SE ethod = MS SE NOTE: R = shortest ( 582 - 593 ms ) E = 15 ms For fat suppression, SPIR and rientation = transverse / RL autoshim can be added. Change OV / RFOV = 230 / 80 atrix = 256 TR to user defined 550 ms. can perc = 80 ProSet can be used for fat sup- ices = 22 ( 1.0T, 1.5T ) 20 ( 0.5 T ) pression as well. hk / gap = 5.0 / 1.0 ( 1.0T, 1.5T ) MTC on resonance prepuls can be 6.0 / 1.0 ( 0.5T ) added. TR will increase. If EST =0 SA =2 necessary, set to shortest. can time = 2:57 - 3:11 min cq. resolution = 1.12 x 0.9 mm T1W/IR ethod = MS IR-TSE NOTE: R = shortest ( 3092 - 3104 ms ) E = 15 ms TI of 400 ms to obtain very good 1 = 400 ms T1-weighted contrast between SE factor = 5, low-high rientation = coronal / RL gray and white matter. OV / RFOV = 200 / 80 ( 1.0T, 1.5T ) Profile order low-high for short 230 / 80 ( 0.5T ) atrix = 336 ( 1.0T, 1.5T ) effective TE. Small turbo factor 256 ( 0.5T ) to avoid blurring. can perc = 80 ices = 20 hk / gap = 6.0 / 1.2 EST =0 SA = 2 ( 1.0T, 1.5T ) ( 0.5T ) can time = 4:29 - 5:10 min cq. resolution = 0.75 x 0.6 mm ( 1.0T, 1.5T ) 1.12 x 0.9 mm ( 0.5T ) T1W/FFE ethod = MS FFE NOTE: R = shortest ( 182 - 258 ms ) E = shortest ( 2.3 - 3.7 ms ) Short TR in combination with large artial echo = yes flip angle for good T1-weighting. p angle = 80 rientation = coronal / RL FFE is sensitive to flow. Flow OV / RFOV = 200 / 80 ( 1.0T, 1.5T ) compensation, however, is set 230 / 80 ( 0.5T ) atrix = 336 to no for shortest possible TE. 256 ( standard grad. only ) Very short TE will hardly result can perc = 80 in intra voxel dephasing. ices = 22 hk / gap = 6.0 / 1.2 Use of 336 matrix increases EST =0 shortest TR, reducing T1- SA =2 can time = 2:18 - 3:37 min influence. cq. resolution = 0.75 x 0.6 mm 1.12 x 0.9 mm ( standard ) T2W/TSE sag ethod = MS TSE NOTE: R = shortest ( 3611 - 3689 ms ) E = 120 ms TE of 120 ms for good contrast SE factor = 16, linear between brain tissue and CSF, 12, linear ( standard ) rientation = sagittal / AP which results in better overall OV / RFOV = 180 / 100 contrast in cerebellum, brain atrix = 320 256 ( 0.5T ) stem and nerve roots. can perc = 80 ices = 15 hk / gap = 4.0 / 0.4 EST =0 SA =3 can time = 3:54 - 4:16 min cq. resolution = 0.7 x 0.56 mm 0.88 x 0.7 mm ( 0.5T ) T1W/SE sag ethod = MS SE NOTE: R = 550 ms E = 15 ms Flow compensation is set to yes. rientation = sagittal / AP This is useful when contrast OV / RFOV = 180 / 100 atrix = 320 agent is administered. 256 ( 0.5T ) can perc = 80 ices = 15 hk / gap = 4.0 / 0.4 EST =0 ow comp = yes SA =2 3 ( 0.5T ) can time = 4:43 - 5:39 min cq. resolution = 0.7 x 0.56 mm 0.88 x 0.7 mm ( 0.5T ) T1W/3D/FFE cor hod = 3D T1-FFE NOTE: = 25 ms = in phase, 4.6 ms ( 1.5T ) ProSet can be used for fat sup- 6.9 ms ( 1.0T ) pression. Change TE to shortest. 13.8 ms ( 0.5T ) al echo = yes Implemented K-space shutter no ( 0.5T ) results in actual scan percentage angle = 30 ntation = coronal / RL of 100 %. / RFOV = 180 / 100 ( 1.0T, 1.5T ) 200 / 100 ( 0.5T ) ix = 256 n perc = 80, actual 100 % es = 50 / gap = 0.7 OS T =0 comp = yes =2 n time = 5:28 min resolution = 0.7 x 0.7 mm ( 1.0T, 1.5T ) 0.78 x 0.78 mm ( 0.5T ) T1W/3D/TFE cor = 3D T1-TFE NOTE: = 20 ms = in phase, 4.6 ms ( 1.5T ) Inversion prepulse is used to 6.9 ms ( 1.0T ) obtain good T1-weighted contrast. 13.8 ms ( 0.5T ) ho = yes Compared to T1W/3D/FFE, T1- no ( 0.5T ) contrast will be slightly better, e = 25 or = 34, linear but signal to noise ratio will be ection =Y somewhat lower. ulse = invert on = coronal / RL OV = 180 / 100 ( 1.0T, 1.5T ) 200 / 100 ( 0.5T ) = 256 c = 80 = 50 = 0.7 OS =0 =1 e = 4:56 - 5:39 min lution = 0.88 x 0.7 mm ( 1.0T, 1.5T ) 0.98 x 0.78 mm ( 0.5T ) T1W/3D/SPIR ethod = 3D T1-FFE NOTE: R = shortest ( 39 - 69 ms ) E = in phase, 4.6 ms ( 1.5T ) SPIR is used to suppress high 6.9 ms ( 1.0T ) signal of retro-orbital fat. 13.8 ms ( 0.5T ) artial echo = yes TR will lengthen due to the added no ( 0.5T ) prepuls. p angle = 30 PIR = yes rientation = transverse / RL OV / RFOV = 180 / 100 ( 1.0T, 1.5T ) 200 / 100 ( 0.5T ) atrix = 256 can perc = 80, actual 100 % ices = 50 hk / gap = 0.7 OS EST =0 ow comp = yes SA =1 can time = 5:28 min cq. resolution = 0.7 x 0.7 mm ( 1.0T, 1.5T ) 0.78 x 0.78 mm ( 0.5T ) T1W/3D/WATS ethod = 3D T1-FFE NOTE: R = shortest ( 25 - 30 ms ) E = shortest ( 5.1 - 17 ms ) ProSet is used to suppress high artial echo = yes signal of retro-orbital fat. p angle = 30 oSet = water selective, 1 2 1 Water selective pulse 1 2 1 will rientation = transverse / RL result in good fat suppression. OV / RFOV = 180 / 100 ( 1.0T, 1.5T ) 200 / 100 ( 0.5T ) Pulse type influences echo time. atrix = 256 can perc = 80, actual 100 % ices = 50 hk / gap = 0.7 OS EST =0 ow comp = yes SA =2 can time = 4:14 - 5:28 min¹ cq. resolution = 0.7 x 0.7 mm ( 1.0T, 1.5T ) 0.78 x 0.78 mm ( 0.5T ) T2W/3D/SPIR ethod = 3D TSE NOTE: R = 4000 ms E = 250 ms Long TR and TE result in heavy SE factor = 62 - 74 T2-weighting. PIR = yes alfscan = yes SPIR is used to suppress signal rientation = transverse / RL of retro-orbital fat. OV / RFOV = 180 / 100 ( 1.0T, 1.5T ) 200 / 100 ( 0.5T ) Thin slices for good resolution atrix = 256 enables good deliniation of the can perc = 80 ( Power / Master ) optic nerve. 70 ( standard / Omni ) ices = 30 hk / gap = 0.7 OS EST =0 SA =1 can time = 3:40 min cq. resolution = 0.88 x 0.7 mm ( 1.0T, 1.5T ) 0.98 x 0.78 mm ( 0.5T ) STIR/TSE ethod = MS IR-TSE NOTE: R = shortest ( 1474 - 1661 ms ) E = 15 ms TI is chosen such, that signal of fat = 180 ms ( 1.5T ) will be suppressed ( field strength 165 ms ( 1.0T ) 150 ms ( 0.5T ) dependent ). SE factor = 5, low-high Profile order low-high for short rientation = transverse / RL OV / RFOV = 180 / 100 ( 1.0T, 1.5T ) effective TE. Small turbo factor 200 / 100 ( 0.5T ) to avoid blurring. atrix = 256 Avoid use of contrast agent in can perc = 80 ices = 11 combination with STIR. High hk / gap = 3.0 / 0.6 signal of gadolinium might be EST =0 SA =4 suppressed, depending on local can time = 4:06 - 4:37 min concentration. cq. resolution = 0.88 x 0.7 mm ( 1.0T, 1.5T ) 0.98 x 0.78 mm ( 0.5T ) STIR/long TE ethod = MS IR-TSE NOTE: R = 2650 ms E = 90 ms TI is chosen such, that signal of fat = 180 ms ( 1.5T ) will be suppressed ( field strength 165 ms ( 1.0T ) 150 ms ( 0.5T ) dependent ). SE factor = 17, linear Contrast is similar to T2/TSE with rientation = transverse / RL OV / RFOV = 180 / 100 ( 1.0T, 1.5T ) SPIR. Scan can be used as an 200 / 100 ( 0.5T ) alternative in case SPIR will not atrix = 256 work properly due to suscepti- can perc = 80 ices = 11 bility. hk / gap = 3.0 / 0.6 EST =0 SA =4 can time = 3:21 - 4:25 min cq. resolution = 0.88 x 0.7 mm ( 1.0T, 1.5T ) 0.98 x 0.78 mm ( 0.5T )