ScanFlo

Resources/Protocols

Brain MRI protocols

The highest-volume region in MRI, and where console fundamentals are built. Every specialised brain protocol is the routine exam plus a deliberate change.

Brain imaging teaches the discipline the rest of MRI depends on: consistent angulation, complete coverage, and a sequence order that puts the most time-critical information first. Learn the routine survey properly and stroke, epilepsy and tumour protocols stop being separate exams — they become variations you can reason about.

Deep-dive protocol guides

Full step-by-step protocols — positioning, per-sequence planning, parameters, artifacts and a review checklist for each study:

Studies in this region

  • Routine brain
  • Stroke
  • Epilepsy
  • Parkinson protocol
  • Cranial nerves
  • Inner ear (IAC)
  • CP angle
  • Pituitary
  • Orbits
  • CSF flow
  • Spectroscopy
  • Perfusion
  • Brain mapping
  • Tractography (DTI)
  • Functional MRI
  • MR angiography
  • MR venography
  • Vessel wall imaging
  • Neonatal quiet protocols
  • Contrast MPRAGE

Planning

  • Align axial stacks to the AC–PC line on the sagittal localizer so follow-up exams compare slice-for-slice.
  • Cover vertex to foramen magnum with no gap at the convexity — that is where subtle pathology hides from careless planning.
  • Correct head roll in the slice angulation, not by repositioning a settled patient.
  • Use an anterior–posterior phase direction on axials so flow and motion ghosts land outside the hemispheres.
  • For pituitary, IAC and orbit studies, drop to thin slices and a small field of view centred on the target — resolution beats coverage here.

Sequences by study

StudyCore additions to the routineWhy
Routine brainDWI/ADC, FLAIR, T2 TSE, T1, T2*/SWIBroad contrast variety for general survey
StrokeDWI early, SWI, MRA, perfusion if availableInfarct age, hemorrhage exclusion, vessel status
EpilepsyThin coronal T2/FLAIR angled to hippocampi, 3D T1Mesial temporal sclerosis and subtle cortical lesions
PituitaryThin sagittal & coronal T1 pre/post, dynamic contrastMicroadenoma detection needs resolution and timing
IAC / CP angleHeavily T2-weighted 3D thin-slice, post-contrast T1Nerve and small tumour visualisation
OrbitsFat-suppressed T2 and post-contrast T1, thin slicesFat suppression separates lesion from orbital fat
MRA / MRVTime-of-flight or contrast angiography, MIP reconstructionsArterial or venous anatomy without catheters

Representative parameters

Ranges, not commandments — field strength, coil and vendor move the numbers. What must not move is understanding why each sits where it does.

SequenceTR (ms)TE (ms)Notes
T1 SE400–6508–15Short/short — anatomy and subacute blood
T2 TSE3000–600080–120Long/long — most pathology
FLAIR8000–1100080–140TI ≈ 2000–2500 ms nulls CSF
DWI (EPI)3000–600060–100b = 0 and 1000 s/mm²
T2* / SWI600–80015–25Low flip angle; susceptibility-sensitive

Mistakes that cost repeats

  • Un-angled axials that make follow-up comparison unreliable.
  • A vertex gap from starting the stack a slice too low.
  • FLAIR with the wrong inversion time — CSF stays bright and the sequence becomes a noisy T2.
  • Leaving motion-intolerant sequences (DWI, FLAIR) until last, when the patient is least still.

Common questions

Why align brain axials to the AC–PC line?
Because comparability is diagnostic. Slices angled to the anterior–posterior commissure line reproduce the same anatomy across visits and scanners, so follow-up studies can be compared directly.
Why does DWI come early in a brain protocol?
Diffusion answers the most time-critical question — acute infarct — and tolerates motion least. If the exam ends early, DWI plus FLAIR already carries most of the clinical value.
What makes an epilepsy protocol different from a routine brain?
Angulation and resolution. Thin coronal T2 and FLAIR angled perpendicular to the long axis of the hippocampi, plus a volumetric T1, target mesial temporal sclerosis that a routine axial stack can miss.
Why is dynamic contrast used for pituitary imaging?
A microadenoma often enhances at a different rate than normal gland tissue. Imaging repeatedly during contrast arrival captures that difference, which a single post-contrast series can miss.

Try it in ScanFlo: Plan a routine brain axial stack aligned to AC–PC, then a second deliberately mis-angled by 15°, and scan both. Compare how the ventricles and basal ganglia change shape — that difference is why the alignment standard exists.

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