Are you looking to master the routine brain MRI protocol?
The routine brain MRI protocol is essential for diagnosing neurological conditions, including tumors, strokes, multiple sclerosis, and other disorders affecting the brain structure and function.
This step-by-step guide is for MRI students and technologists who wish to improve their professional skills and master the routine brain MRI protocol.
What you will learn:
A routine brain MRI is one of the most requested protocols, so short scan time is often crucial. Most brain pathologies are identified by signal differences, making strong SNR essential. For smaller lesions, higher resolution is needed.
These sequences provide fast, high-quality images with excellent contrast and minimal artifacts, making them ideal for routine clinical diagnosis. They allow for multiple contrast weightings (T1, T2, FLAIR) that help assess brain structure and detect abnormalities.
Artifacts | Solution – How to Avoid It |
---|---|
Motion artifacts | Shorten the scan time to reduce the risk of patient movement. |
Susceptibility artifacts | Use spin echo instead of gradient echo sequences to reduce sensitivity to magnetic field inhomogeneities. |
Chemical shift artifacts | Increase the bandwidth to reduce the spatial displacement between fat and water signals. |
CSF flow artifacts | Use flow compensation gradients to correct for phase shifts caused by flowing CSF. Fast sequences like FLAIR also compensate for CSF pulsation. |
Truncation artifacts | Increase the resolution to capture more frequency information and reduce Gibbs ringing at tissue boundaries. |
Wrap-around artifacts | Activate fold-over suppression to prevent anatomy outside the field of view from overlapping. |
The brain is a complex organ responsible for controlling all body functions, processing sensory information, and enabling cognitive abilities. Due to its critical importance and susceptibility to various pathologies, the brain is one of the most frequently examined areas in MRI.
Brain MRI protocols are essential for diagnosing a wide range of neurological conditions, including tumors, strokes, multiple sclerosis, as well as psychiatric disorders that affect brain’s function.
In MRI, we always face a trade-off between 3 key metrics:
Improving one of these metric reduces the performance of the others. To decide what trade-offs to make, we must consider the needs of each clinical situation.
For routine brain MRIs, it’s generally true that:
Therefore, we typically 1) prioritize scan time, 2) maintain good SNR for clear contrast between tissues, and 3) optimize for resolution when finer details must be assessed.
The brain MRI study can help us diagnose a wide range of health conditions. The table below lists some of the most common conditions — and what pulse sequences that reveal them:
Common Brain Conditions | Clearly Seen on Sequence | Why This Sequence? |
---|---|---|
Anatomical structures and lesions: • Tumors • Subacute hemorrhage • Metastases • Bone marrow changes |
T1 TSE | Provides clear gray-white differentiation and baseline for contrast assessment. Detects T1 hyperintense findings like subacute hemorrhage and marrow pathology. Contrast-enhanced T1 improves tumor and metastasis visibility. |
Edema and fluid abnormalities: • Hydrocephalus • Cysts • Subacute stroke • Tumor-associated edema |
T2 TSE | Highlights water-rich tissues, making it ideal for detecting edema, inflammation, and CSF-related abnormalities. Helps assess fluid accumulation and tissue changes. |
White matter and ischemic lesions: • Multiple sclerosis (MS) • Small vessel disease • Chronic ischemia • Gliosis |
T2 FLAIR | Suppresses CSF signal while preserving sensitivity to pathological water, making white matter lesions highly visible. Ideal for detecting demyelination, chronic ischemia, and gliosis, especially near ventricles where bright CSF on T2 could obscure lesions. |
Acute ischemic changes: • Acute stroke • Cytotoxic edema • Early infarcts |
Diffusion-Weighted Imaging (DWI) | Detects restricted water molecule movement in acute ischemic tissue within minutes of onset, long before other sequences. Essential for rapid stroke diagnosis and treatment. |
The step-by-step guide below will show you how to set up and perform a routine brain MRI protocol in practice.
We will perform the protocol in 3 parts:
Lay the patient head-first and supine (on their back) with the head centered at the scanner's isocenter.
Use a dedicated head coil to ensure high-resolution imaging. This coil provides strong signal reception and full coverage of the brain.
✅ Correct Patient Positioning:
Once the patient is in place, review your scanner’s hardware settings.
In this guide, we will use the following settings:
Scanner Setting | Value | Why This Value |
---|---|---|
Magnetic field strength | 1.5 T | Enables high Signal-to-Noise Ratio, which gives superior image quality. |
Maximum gradient strength | 45 mT/m | Enables faster acquisitions while preserving high image quality. |
This hardware setup is widely used in clinical practice. It balances acquisition time, image quality, and patient comfort.
Before we can perform any MRI protocol, we must always capture initial localizer images of the patient. These images act as a guide for planning the detailed scans we will perform next.
We should always capture localizers in three planes:
Once acquired, upload the initial localizer images into the three viewports.
Then, scroll through each of the image stacks to locate a central slice that clearly shows the anatomy of the brain.
✅ Correct Setup of Localizer Images for Routine Brain MRI:
When all preparations are ready, we can start planning and acquiring the protocol sequences.
Let’s go through the pulse sequences that a standard brain MRI protocol includes, why we perform them, and how to set them up.
We mainly use fast or turbo spin echo sequences for this study. These sequences provide fast, high-quality images with excellent contrast and minimal artifacts, making them ideal for routine clinical diagnosis.
Turbo Spin Echo also let us create multiple types of contrasts, including T2, T1, and inversion recovery for fat suppression.
This helps us assess the brain's structure, detect abnormalities, and identify common pathologies like tumors, strokes, and demyelination.
In the sections below, we go through how to plan and set up each sequence.
✅ Correct Planning:
Planning Instructions:
Parameters for Axial T2 TSE:
Parameter | Recommended Values | Why These Values |
---|---|---|
Echo Time (TE) | 100–120 ms | Longer TE is required for T2 contrast. |
Repetition Time (TR) | 4,000–6,000 ms | Longer TR is required for T2 contrast. |
Field-of-View (FOV) | 210 x 250 mm | Large enough to cover and fit the shape of the brain while avoiding wrap-around artifacts. |
Matrix | 384 x 288 | Medium matrix size to get sufficient resolution and detail, while maintaining short scan time and high SNR. |
Foldover Direction (Phase) | Anterior-to-Posterior (AP) | To reduce pulsation artifacts from the carotid arteries and optimize the field-of-view for the brain's shape. |
Slice Thickness | 6 mm | Medium thickness to get good resolution, without sacrificing scan time or SNR. |
Slice Gap | 1 mm | ~20% of slice thickness to provide continuity between slices and avoid cross-talk. |
Number of Slices | 20-23 | Enough slices to fully cover the brain region. |
NEX / Averages | 1-2 | To get enough SNR, while keeping scan time short. |
Turbo Factor / ETL | 16-24 | Higher turbo factor to enhance T2 contrast and reduce scan time. |
Bandwidth | 100,000 Hz | High enough to avoid chemical shift artifacts, without reducing SNR. |
Fold-over Suppression | Yes | To avoid aliasing or wrap-around artifacts. |
✅ Correct Planning:
Planning Instructions:
Parameters for Axial T2 FLAIR:
Parameter | Recommended Values | Why These Values |
---|---|---|
Echo Time (TE) | 100–120 ms | Longer TE is required for T2 contrast. |
Repetition Time (TR) | 4,000–6,000 ms | Longer TR is required for T2 contrast. |
Inversion Time (TI) | 1,800–2,500 ms | High enough TI to match the cerebrospinal fluid’s null point and suppress its signal in 1.5T. |
Field-of-View (FOV) | 210 x 250 mm | Large enough to cover and fit the shape of the brain while avoiding wrap-around artifacts. |
Matrix | 384 x 288 | Medium matrix size to get sufficient resolution and detail, while maintaining short scan time and high SNR. |
Foldover Direction (Phase) | Anterior-to-Posterior (AP) | To reduce pulsation artifacts from the carotid arteries and optimize the field-of-view for the brain's shape. |
Slice Thickness | 6 mm | Medium thickness to get good resolution, without sacrificing scan time or SNR. |
Slice Gap | 1 mm | ~20% of slice thickness to provide continuity between slices and avoid cross-talk. |
Number of Slices | 20-23 | Enough slices to fully cover the brain region. |
NEX / Averages | 1-2 | To get enough SNR, while keeping scan time short. |
Turbo Factor / ETL | 16-24 | Higher turbo factor to enhance T2 contrast and reduce scan time. |
Bandwidth | 100,000 Hz | High enough to avoid chemical shift artifacts, without reducing SNR. |
Fold-over Suppression | Yes | To avoid aliasing or wrap-around artifacts. |
Fat Suppression | Spectral | To suppress fat signal from orbital and scalp, which enhances lesion visibility. |
✅ Correct Planning:
Planning Instructions:
Parameters for Axial T1 TSE:
Parameter | Recommended Values | Why These Values |
---|---|---|
Echo Time (TE) | 10–20 ms | Shorter TE is required for T1 contrast. |
Repetition Time (TR) | 400–600 ms | Shorter TR is required for T1 contrast. |
Field-of-View (FOV) | 210 x 250 mm | Large enough to cover and fit the shape of the brain while avoiding wrap-around artifacts. |
Matrix | 384 x 288 | Medium matrix size to get sufficient resolution and detail, while maintaining short scan time and high SNR. |
Foldover Direction (Phase) | Anterior-to-Posterior (AP) | To reduce pulsation artifacts from the carotid arteries and optimize the field-of-view for the brain's shape. |
Slice Thickness | 6 mm | Medium thickness to get good resolution, without sacrificing scan time or SNR. |
Slice Gap | 1 mm | ~20% of slice thickness to provide continuity between slices and avoid cross-talk. |
Number of Slices | 20-23 | Enough slices to fully cover the brain region. |
NEX / Averages | 1-2 | To get enough SNR, while keeping scan time short. |
Turbo Factor / ETL | 3-5 | Lower turbo factor to minimize T2-weighting and get a purer T1 contrast. |
Bandwidth | 100,000 Hz | High enough to avoid chemical shift artifacts, without reducing SNR. |
Fold-over Suppression | Yes | To avoid aliasing or wrap-around artifacts. |
✅ Correct Planning:
Planning Instructions:
Parameters for Sagittal T1 TSE:
Parameter | Recommended Values | Why These Values |
---|---|---|
Echo Time (TE) | 10–20 ms | Shorter TE is required for T1 contrast. |
Repetition Time (TR) | 400–600 ms | Shorter TR is required for T1 contrast. |
Field-of-View (FOV) | 220 x 240 mm | Large enough to cover the brain while avoiding wrap-around artifacts. |
Matrix | 320 x 224 | Medium matrix size to get sufficient resolution and detail, while maintaining short scan time and high SNR. |
Foldover Direction (Phase) | Anterior-to-Posterior (AP) | To contain swallowing and respiratory motion artifacts away from critical central brain structures. |
Slice Thickness | 6 mm | Medium thickness to get good resolution, without sacrificing scan time or SNR. |
Slice Gap | 1 mm | ~20% of slice thickness to provide continuity between slices and avoid cross-talk. |
Number of Slices | 20-23 | Enough slices to fully cover the brain region. |
NEX / Averages | 1-2 | To get enough SNR, while keeping scan time short. |
Turbo Factor / ETL | 3-5 | Lower turbo factor to minimize T2-weighting and get a purer T1 contrast. |
Bandwidth | 100,000 Hz | High enough to avoid chemical shift artifacts, without reducing SNR. |
Fold-over Suppression | Yes | To avoid aliasing or wrap-around artifacts. |
✅ Correct Planning:
Planning Instructions:
Parameters for Coronal T1 TSE:
Parameter | Recommended Values | Why These Values |
---|---|---|
Echo Time (TE) | 10–20 ms | Shorter TE is required for T1 contrast. |
Repetition Time (TR) | 400–600 ms | Shorter TR is required for T1 contrast. |
Field-of-View (FOV) | 220 x 200 mm | Large enough to cover the brain while avoiding wrap-around artifacts. |
Matrix | 320 x 224 | Medium matrix size to get sufficient resolution and detail, while maintaining short scan time and high SNR. |
Foldover Direction (Phase) | Right-to-Left (RL) | To keep field-of-view small and minimize left-right wrap-around artifacts. |
Slice Thickness | 6 mm | Medium thickness to get good resolution, without sacrificing scan time or SNR. |
Slice Gap | 1 mm | ~20% of slice thickness to provide continuity between slices and avoid cross-talk. |
Number of Slices | 23-26 | Enough slices to fully cover the brain region. |
NEX / Averages | 1-2 | To get enough SNR, while keeping scan time short. |
Turbo Factor / ETL | 3-5 | Lower turbo factor to minimize T2-weighting and get a purer T1 contrast. |
Bandwidth | 100,000 Hz | High enough to avoid chemical shift artifacts, without reducing SNR. |
Fold-over Suppression | Yes | To avoid aliasing or wrap-around artifacts. |
✅ Correct Planning:
Planning Instructions:
Parameters for Axial DWI:
Parameter | Recommended Values | Why These Values |
---|---|---|
Echo Time (TE) | 70–100 ms | Longer TE is required for diffusion contrast, allowing signal loss from moving water molecules. |
Repetition Time (TR) | 4,000–6,000 ms | Longer TR prevents T1-weighting and ensures pure diffusion contrast. |
Field-of-View (FOV) | 210 x 250 mm | Large enough to cover and fit the shape of the brain while avoiding wrap-around artifacts. |
Matrix | 64 x 100 | Low matrix since DWI detects water mobility rather than fine anatomical details. |
Foldover Direction (Phase) | Anterior-to-Posterior (AP) | To contain geometric distortions to the AP direction rather than the diagnostically critical left-right axis. |
Slice Thickness | 6 mm | Medium thickness to get good resolution, without sacrificing scan time or SNR. |
Slice Gap | 1 mm | ~20% of slice thickness to provide continuity between slices and avoid cross-talk. |
Number of Slices | 14-18 | To cover key brain regions while minimizing susceptibility artifacts from air-filled sinuses and mouth areas. |
NEX / Averages | 1-2 | To get enough SNR while keeping scan time short. |
Turbo Factor / ETL | N/A | DWI uses echo-planar imaging instead of turbo/fast spin echo acquisition methods. |
Bandwidth | 250,000 Hz | To minimize susceptibility-induced geometric distortions common in echo-planar imaging sequences. |
Fold-over Suppression | Yes | To avoid aliasing or wrap-around artifacts. |
B-value | 0 and 1,000 s/mm² | These standard b-values provide optimal contrast between normal tissue (b=0) and restricted diffusion (b=1000) for detecting acute stroke. |
The table below lists the 6 common brain artifacts, and what techniques you can use to avoid them:
Artifacts | Solution – How to Avoid It |
---|---|
Motion artifacts | Shorten the scan time to reduce the risk of patient movement. |
Susceptibility artifacts | Use spin echo instead of gradient echo sequences to reduce sensitivity to magnetic field inhomogeneities. |
Chemical shift artifacts | Increase the bandwidth to reduce the spatial displacement between fat and water signals. |
CSF flow artifacts | Use flow compensation gradients to correct for phase shifts caused by flowing CSF. Fast sequences like FLAIR are also used to compensate for CSF pulsation effects. |
Truncation artifacts | Increase the resolution to capture more frequency information and reduce Gibbs ringing at tissue boundaries. |
Wrap-around artifacts | Activate fold-over suppression to prevent anatomy outside the field of view from overlapping. |
Finally, we will review the images to ensure all the anatomical information we need is clear.
These key structures must be clearly visible in a brain MRI:
Below, we will go through all the different image contrasts and explain their specific role in imaging the brain.
T2-weighted imaging makes fluids appear bright. This contrast is ideal for detecting tissues and abnormalities associated with high water content.
In brain MRI, T2 sequences are excellent for evaluating hydrocephalus, cysts, and edema. They clearly show the ventricles and cerebrospinal fluid spaces, making them useful for assessing size and configuration of these structures.
✅ Axial T2 of the Brain – Correct Image:
The axial T2 sequence provides a horizontal view of the brain, which lets us:
T2 FLAIR (Fluid Attenuated Inversion Recovery) is a special type of T2-weighted sequence that suppresses the signal from a specific tissue – in this case the cerebrospinal fluid (CSF) – making it appear dark instead of bright. This contrast is ideal for detecting lesions adjacent to CSF spaces.
In brain MRI, FLAIR sequences are crucial for evaluating multiple sclerosis, small vessel disease, and chronic ischemia. They are particularly effective at highlighting white matter lesions near the ventricles.
✅ Axial T2 FLAIR of the Brain – Correct Image:
The axial T2 FLAIR sequence provides a view similar to T2, but with CSF suppression, which lets us:
T1-weighted imaging makes fat appear bright and fluid dark. This contrast is ideal for anatomical detail and fat-containing structures.
In brain MRI, T1 sequences are essential for evaluating structural anatomy, tumors, metastases, and sub-acute hemorrhage. They provide excellent contrast between gray and white matter, and serve as the baseline for post-contrast studies.
✅ Axial T1 of the Brain – Correct Image:
The axial T1 sequence provides a horizontal view, showing:
✅ Sagittal T1 of the Brain – Correct Image:
The sagittal T1 sequence provides a side view of the brain, which lets us:
✅ Coronal T1 of the Brain – Correct Image:
The coronal T1 sequence provides a front-to-back view, useful for:
Diffusion-weighted imaging is sensitive to the movement of water molecules in tissue. In normal brain tissue, water diffuses freely, but in damaged areas (like in acute stroke), water movement is restricted.
In brain MRI, DWI sequences are critical for evaluating acute stroke and cytotoxic edema. They can detect ischemic changes within minutes of onset, making them invaluable for early stroke diagnosis.
The DWI sequence generates 3 different types of images from a single acquisition, each providing unique diagnostic information:
The b=0 Image is acquired at the beginning of the diffusion sequence with no diffusion gradients applied. It’s essentially a T2-weighted image that shows baseline tissue contrast before diffusion weighting.
In clinical practice, this image is sometimes informally referred to as a "susceptibility image" because it clearly displays susceptibility artifacts caused by magnetic field inhomogeneities. These artifacts appear as signal distortions near air-tissue interfaces or metal implants.
The b=0 image serves three important purposes:
By comparing the b=0 image with the true diffusion image, radiologists can better distinguish between actual diffusion restrictions and artifacts.
✅ Correct Image Example:
The True Diffusion Image (b=1000) shows areas of restricted water diffusion as bright signal intensity. It detects acute ischemic changes where water movement is restricted due to cytotoxic edema.
This is the primary image for identifying acute stroke, showing the infarct core as a hyperintense (bright) region within minutes of symptom onset.
✅ Correct Image Example:
The ADC (Apparent Diffusion Coefficient) Map quantifies the degree of water diffusion, where restricted diffusion appears dark.
The map verifies whether bright areas on the DWI are truly due to restricted water movement (as in acute stroke), or simply because the tissue naturally appears bright on T2-weighted images (called "T2 shine-through"). This distinction is crucial for accurate diagnosis.
Specifically, this map is crucial to differentiate acute ischemia vs sub-acute or chronic ones. Acute stroke appears dark on ADC maps, while chronic lesions typically show normal or increased diffusion.
✅ Correct Image Example:
When these three DWI images are evaluated together, they provide comprehensive information about water diffusion in brain tissue.
This enables accurate diagnosis of acute ischemia, and lets us differentiate it from other pathologies that appear similar on standard sequences.
When reviewing brain MRI images, always check for:
By following this protocol and carefully reviewing the images, you can ensure an excellent diagnostic evaluation of the brain.