T1 & T2 Weighted Images PDF
Document Details
Uploaded by AdventurousKansasCity4372
Tags
Summary
This document explains T1 and T2 weighted images, important techniques in magnetic resonance imaging (MRI). It details how different parameters like TR (repetition time) and TE (echo time) affect image contrast, allowing visualisation of various tissues. The document highlights the importance of these parameters in medical diagnosis.
Full Transcript
T1 recovery/ weighted images - Fatty structures are seen brighter - White matter has myelin in it which is very fatty, will look paler than the grey matter - Fluid is seen dark - TR time around 400-650ms to allow recovery of structures excluding fluid - 300ms for pure fat -...
T1 recovery/ weighted images - Fatty structures are seen brighter - White matter has myelin in it which is very fatty, will look paler than the grey matter - Fluid is seen dark - TR time around 400-650ms to allow recovery of structures excluding fluid - 300ms for pure fat - 400ms for fatty structure - CSF, grey and white matter , we need to give TR long enough to allow contrast differentiation - This send another RF pulse, knowing these structures into the transverse plane and sends the fluid which has barely decayed or recovered another 90 degrees, out of transverse plane - We can take the image on echo time or TE of 15 ms which is right before fat decays again - TE time must be short because fat dephases fast - T1 recovery/ weighted= Short TE and short TR - Fat has a larger longitudinal magnetization resulting is faster T1 recovery T2 decay/ Weighted image - Fluid seen as bright - Golden standard - Cancers have fluid in them - Edema and inflammation also associated with cancers - Fluid needs to be in the transverse plane and in phase to see it as bright - Need to wait for fluid to recover and decay to flip but all structures will also be in the axis if we do this - This isn't what we want, TR cant control T2 - TE controls T2 weigthed images - Wait for fatty structures to decay, and we choose the TE time right before fluid dephasing - Fluid dephases at a 90TE and + - If we just want black and white, and ONLY see fluid: we increase TE time super high and a long TR because of high fluid recovery times (around 3000ms) - Called a "long drink" long TE - Depends on decay process Choose best sequence for pathology and then try to continue with the other sequences if possible with complicated patients - Ask to give patient something if they are agitated - Call radiologist to ask for prescription for something TR controls the image weighting - The TR controls how much T1 is weighed - Longer TR= more structures are brighter - Determines amount of T1 relaxation - The time between RF pulses TE - Time we wait to listen to the signal - Controls dephasing - Will never be more than TR - Time signal is taken Myographic effect - In spine: CSF surrounds chord - Do very bright T2 weighted image to only see the fluid bright, increase TE by a lot - For biliary system increase TE to almost 800ms Water has a higher energy than fat and doesn't absorb the RF pulses energy as easily - Causes slow T1 recovery - Water doesn't diphase or decay as easily also because the protons wont smack into each other as much as fat - Molecular tumbling is faster than the frequency which is why the recovery is slow Matrix of 256 X 192 - The second number in the matrix is what determines how many RF pulses (or TR's) that happen - In this example, 192 TR's - Gives you an idea of the scan time - If T1 takes 300ms to recover for each TR x 192 times, a T1 weighted image takes less time than the T2 which has 3000ms for each TR X 192 times - Scan time is ms per TR X matrix - Decreasing matrix will decrease time however will decrease spatial resolution - Matrix is dependant on resolution of images - High resolution = high matrix = small pixel - Used for looking at smaller structures - i.e in the IAC (external auditory cranial nerves), pituitary - = longer scan time Pulse sequences - Operator controlled - Series of RF PULSES signals and recovery periods - TR and TE are measured in ms Proton density images - Based on concentration of hydrogen in total - Some structures have more or less hydrogen - Bone minus marrow has hardly any hydrogen - Bone marrow gives signal (on a T1 particularly) because of the fat inside - Bones show up as bright on a T1 because of this - Tightly bound hydrogen nuclei will create higher signals - Shows lots of signal because the many structures are all made of H, just different amounts - CSF is very rich in H , the other structures will look like different shades of gray - Good for white and grey matter in the brain, differentiate structures easily in the brain - Good for multiple sclerosis - We use a plane that shows us the white matter best - Always include a sagittal proton density for MS to see corpus collosum beautifully - The axial will show the brain best, there will also probably be an axial T2 T1 short TR and short TE (\ - flip angle for spin echo: 90 - Gradients - wire coils that are magnets themselves - T2 and PD will take a lot of time especially with the 180 echo time added - By applying gradient to the z magnet, we create an increase in magnet of main magnetic field and decreasing it in another direction - Can change processional frequency in some area of the body - Changes main magnetic field strength - Can activate z gradient to increase dephasing of slow dephasing protons and decrease dephasing of fast dephasing protons to create homogeneity - Additional magnetic field and can add or subtract from the main magnetic field **linearly** and **predictably** (we control this) Image weighting and contrast in gradient echo is determined by TR, TE and flip angle - gradient is added (T2\*) to dephase so that we can predict how to apply the gradient in the opposite direction to properly align the protons in phase - Predictably diphase it more and then slap down to put everything in phase Magnetic susceptibility artifacts - Metal will cause artifacts - T2\*(gradient echo) will show a larger artifact - for a brain bleed we want to use this magnetic susceptibility artifact shown - blood has iron Smaller flip angles creates smaller TR times, this speeds up the exam Even a 20 degree - make sure metal isn't present because it will show horribly in gradient echo pulsing - never use gradient echo for those with metal implant - instead call radiologist and ask to replace with a spin echo short TR: 300ms for a gradient echo flip angle for T2 weighted images is shorter \- fluid will recover faster with smaller flip angles Higher gradient used results in thicker slices The slices will precess at different frequencies with a gradient applied as the magnetization is altered which allows us to predictably excite a slice at a time \- resonance won't occur in the other slices at a specific frequency, only the slice at that frequency Gradients (vs spin echo) - scan time is shorter - T2\* or gradient echo sequence - doesn't have a 180 pulse, has bipolar gradients that spoil and reverse dephasing and rephasing process - because it is a gradient, it is a magnet which is inhomogeneous - spin echo T1 has better signal inhomogeneities but takes long - spin echo is in the 1000's ms, the gradient is in the 100's ms - smaller flip angles allow shorter scan time in T2\* - susceptible to metal artifact inhomogeneities but useful for a bleed - metal implants will not allow a good image - the z gradient will excite slices independently - x and y help us encode things Scan time: TR X phase encoding (second number of matrix) X \# of excitations For a SE (spin echo) T2: 256 X 192 Pe: 192 TR: 4000ms Scan time: 4000x192x1 = 768000ms or 768 seconds = 12 mins and 8 seconds For a GE (gradient echo) T2\*: Same parameters with... TR 300: 57.6s with is about 1 min Compensates for premature dephasing of nuclei in trasnverse plane \- from the inhomogeneous MF \- the rephasing is at different times until the 180 flip \- best signal to noise is at 90 degree pulse in transverse plane the gradients cause the loud noises, not the RF pulses for gradient echo pulse sequencing: \- short flip angle for T1 and PD to be able to see the fluid and allows for quicker recovery thus faster scan time , no more 180 degree pulse \- TR in the 100's instead of 1000's \- short TR allows fluid to be shown For gradient.... (incorporate flip control if necessary) T1 weighted \- larger flip angle (90-110) allows for fat to be seen -don't want water to recover fast \- to delay fluid, short TR still but a bit longer with gradients \- short TE \- flip angle and the TR controls for T1 T2 weighted \- long TR and small flip angle (10-15) -- want water to recover fast \- large TE \- just the TE controls T2 PD \- long TR, short flip and short TE \- anything offsetting the T1 and T2