Questions and Answers ​in MRI
  • Home
  • Complete List of Questions
  • …Magnets & Scanners
    • Basic Electromagnetism >
      • What causes magnetism?
      • What is a Tesla?
      • Who was Tesla?
      • What is a Gauss?
      • How strong is 3.0T?
      • What is a gradient?
      • Aren't gradients coils?
      • What is susceptibility?
      • How to levitate a frog?
      • What is ferromagnetism?
      • Superparamagnetism?
    • Magnets - Part I >
      • Types of magnets?
      • Brands of scanners?
      • Which way does field point?
      • Which is the north pole?
      • Low v mid v high field?
      • Advantages to low-field?
      • Disadvantages?
      • What is homogeneity?
      • Why homogeneity?
      • Why shimming?
      • Passive shimming?
      • Active shimming?
    • Magnets - Part II >
      • Superconductivity?
      • Perpetual motion?
      • How to ramp?
      • Superconductive design?
      • Room Temp supercon?
      • Liquid helium use?
      • What is a quench?
      • Is field ever turned off?
      • Emergency stop button?
    • Gradients >
      • Gradient coils?
      • How do z-gradients work?
      • X- and Y- gradients?
      • Open scanner gradients?
      • Eddy current problems?
      • Active shielded gradients?
      • Active shield confusion?
      • What is pre-emphasis?
      • Gradient heating?
      • Gradient specifications?
      • Gradient linearity?
    • RF & Coils >
      • Many kinds of coils?
      • Radiofrequency waves?
      • Phase v frequency?
      • RF Coil function(s)?
      • RF-transmit coils?
      • LP vs CP (Quadrature)?
      • Multi-transmit RF?
      • Receive-only coils?
      • Array coils?
      • AIR Coils?
    • Site Planning >
      • MR system layout?
      • What are fringe fields?
      • How to reduce fringe?
      • Magnetic shielding?
      • Need for vibration testing?
      • What's that noise?
      • Why RF Shielding?
      • Wires/tubes thru wall?
  • ...Safety and Screening
    • Overview >
      • ACR Safety Zones?
      • MR safety screening?
      • Incomplete screening?
      • Passive v active implants?
      • Conditional implants?
      • Common safety issues?
      • Projectiles?
      • Metal detectors?
      • Pregnant patients?
      • Postop, ER & ICU patients?
      • Temperature monitoring?
      • Orbital foreign bodies?
      • Bullets and shrapnel?
    • Static Fields >
      • "Dangerous" metals?
      • "Safe" metals?
      • Magnetizing metal?
      • Object shape?
      • Forces on metal?
      • Most dangerous place?
      • Force/torque testing?
      • Static field bioeffects?
      • Dizziness/Vertigo?
      • Flickering lights?
      • Metallic taste?
    • RF Fields >
      • RF safety overview?
      • RF biological effects?
      • What is SAR?
      • SAR limits?
      • Operating modes?
      • How to reduce SAR?
      • RF burns?
      • Estimate implant heating?
      • SED vs SAR?
      • B1+rms vs SAR?
      • Personnel exposure?
      • Cell phones?
    • Gradient Fields >
      • Gradient safety overview
      • Acoustic noise?
      • Nerve stimulation?
      • Gradient vs RF heating?
    • Safety: Neurological >
      • Aneurysm coils/clips?
      • Shunts/drains?
      • Pressure monitors/bolts?
      • Deep brain stimulators?
      • Spinal cord stimulators?
      • Vagal nerve stimulators?
      • Cranial electrodes?
      • Carotid clamps?
      • Peripheral stimulators?
      • Epidural catheters?
    • Safety: Head & Neck >
      • Additional orbit safety?
      • Cochlear Implants?
      • Bone conduction implants?
      • Other ear implants?
      • Dental/facial implants?
      • ET tubes & airways?
    • Safety: Chest & Vascular >
      • Breast tissue expanders?
      • Breast biopsy markers?
      • Airway stents/valves/coils?
      • Respiratory stimulators?
      • Ports/vascular access?
      • Swan-Ganz catheters?
      • IVC filters?
      • Implanted infusion pumps?
      • Insulin pumps & CGMs?
      • Vascular stents/grafts?
      • Sternal wires/implants?
    • Safety: Cardiac >
      • Pacemaker dangers?
      • Pacemaker terminology?
      • New/'Safe" Pacemakers?
      • Old/Legacy Pacemakers?
      • Violating the conditions?
      • Epicardial pacers/leads?
      • Cardiac monitors?
      • Heart valves?
      • Miscellaneous CV devices?
    • Safety: Abdominal >
      • PIllCam and capsules?
      • Gastric pacemakers?
      • Other GI devices?
      • Contraceptive devices?
      • Foley catheters?
      • Incontinence devices?
      • Penile Implants?
      • Sacral nerve stimulators?
      • GU stents and other?
    • Safety: Orthopedic >
      • Orthopedic hardware?
      • External fixators?
      • Traction and halos?
      • Bone stimulators?
      • Magnetic rods?
  • …The NMR Phenomenon
    • Spin >
      • What is spin?
      • Why I = ½, 1, etc?
      • Proton = nucleus = spin?
      • Predict nuclear spin (I)?
      • Magnetic dipole moment?
      • Gyromagnetic ratio (γ)?
      • "Spin" vs "Spin state"?
      • Energy splitting?
      • Fall to lowest state?
      • Quantum "reality"?
    • Precession >
      • Why precession?
      • Who was Larmor?
      • Energy for precession?
      • Chemical shift?
      • Net magnetization (M)?
      • Does M instantly appear?
      • Does M also precess?
      • Does precession = NMR?
    • Resonance >
      • MR vs MRI vs NMR?
      • Who discovered NMR?
      • How does B1 tip M?
      • Why at Larmor frequency?
      • What is flip angle?
      • Spins precess after 180°?
      • Phase coherence?
      • Release of RF energy?
      • Rotating frame?
      • Off-resonance?
      • Adiabatic excitation?
      • Adiabatic pulses?
    • Relaxation - Physics >
      • Bloch equations?
      • What is T1?
      • What is T2?
      • Relaxation rate vs time?
      • Why is T1 > T2?
      • T2 vs T2*?
      • Causes of Relaxation?
      • Dipole-dipole interactions?
      • Chemical Exchange?
      • Spin-Spin interactions?
      • Macromolecule effects?
      • Which H's produce signal?
      • "Invisible" protons?
      • Magnetization Transfer?
      • Bo effect on T1 & T2?
      • How to predict T1 & T2?
    • Relaxation - Clincial >
      • T1 bright? - fat
      • T1 bright? - other oils
      • T1 bright? - cholesterol
      • T1 bright? - calcifications
      • T1 bright? - meconium
      • T1 bright? - melanin
      • T1 bright? - protein/mucin
      • T1 bright? - myelin
      • Magic angle?
      • MT Imaging/Contrast?
  • …Pulse Sequences
    • MR Signals >
      • Origin of MR signal?
      • Free Induction Decay?
      • Gradient echo?
      • TR and TE?
      • Spin echo?
      • 90°-90° Hahn Echo?
      • Stimulated echoes?
      • STEs for imaging?
      • 4 or more RF-pulses?
      • Partial flip angles?
      • How is signal higher?
      • Optimal flip angle?
    • Spin Echo >
      • SE vs Multi-SE vs FSE?
      • Image contrast: TR/TE?
      • Opposite effects ↑T1 ↑T2?
      • Meaning of weighting?
      • Does SE correct for T2?
      • Effect of 180° on Mz?
      • Direction of 180° pulse?
    • Inversion Recovery >
      • What is IR?
      • Why use IR?
      • Phase-sensitive IR?
      • Why not PSIR always?
      • Choice of IR parameters?
      • TI to null a tissue?
      • STIR?
      • T1-FLAIR
      • T2-FLAIR?
      • IR-prepped sequences?
      • Double IR?
    • Gradient Echo >
      • GRE vs SE?
      • Multi-echo GRE?
      • Types of GRE sequences?
      • Commercial Acronyms?
      • Spoiling - what and how?
      • Spoiled-GRE parameters?
      • Spoiled for T1W only?
      • What is SSFP?
      • GRASS/FISP: how?
      • GRASS/FISP: parameters?
      • GRASS vs MPGR?
      • PSIF vs FISP?
      • True FISP/FIESTA?
      • FIESTA v FIESTA-C?
      • DESS?
      • MERGE/MEDIC?
      • GRASE?
      • MP-RAGE v MR2RAGE?
    • Susceptibility Imaging >
      • What is susceptibility (χ)?
      • What's wrong with GRE?
      • Making an SW image?
      • Phase of blood v Ca++?
      • Quantitative susceptibility?
    • Diffusion: Basic >
      • What is diffusion?
      • Iso-/Anisotropic diffusion?
      • "Apparent" diffusion?
      • Making a DW image?
      • What is the b-value?
      • b0 vs b50?
      • Trace vs ADC map?
      • Light/dark reversal?
      • T2 "shine through"?
      • Exponential ADC?
      • T2 "black-out"?
      • DWI bright causes?
    • Diffusion: Advanced >
      • Diffusion Tensor?
      • DTI (tensor imaging)?
      • Whole body DWI?
      • Readout-segmented DWI?
      • Small FOV DWI?
      • IVIM?
      • Diffusion Kurtosis?
    • Fat-Water Imaging >
      • Fat & Water properties?
      • F-W chemical shift?
      • In-phase/out-of-phase?
      • Best method?
      • Dixon method?
      • "Fat-sat" pulses?
      • Water excitation?
      • STIR?
      • SPIR?
      • SPAIR v SPIR?
      • SPIR/SPAIR v STIR?
  • …Making an Image
    • From Signals to Images >
      • Phase v frequency?
      • Angular frequency (ω)?
      • Signal squiggles?
      • Real v Imaginary?
      • Fourier Transform (FT)?
      • What are 2D- & 3D-FTs?
      • Who invented MRI?
      • How to locate signals?
    • Frequency Encoding >
      • Frequency encoding?
      • Receiver bandwidth?
      • Narrow bandwidth?
      • Slice-selective excitation?
      • SS gradient lobes?
      • Cross-talk?
      • Frequency encode all?
      • Mixing of slices?
      • Two slices at once?
      • Simultaneous Multi-Slice?
    • Phase Encoding >
      • Phase-encoding gradient?
      • Single PE step?
      • What is phase-encoding?
      • PE and FE together?
      • 2DFT reconstruction?
      • Choosing PE/FE direction?
    • Performing an MR Scan >
      • What are the steps?
      • Automatic prescan?
      • Routine shimming?
      • Coil tuning/matching?
      • Center frequency?
      • Transmitter gain?
      • Receiver gain?
      • Dummy cycles?
      • Where's my data?
      • MR Tech qualifications?
    • Image Quality Control >
      • Who regulates MRI?
      • Who accredits?
      • Mandatory accreditation?
      • Routine quality control?
      • MR phantoms?
      • Geometric accuracy?
      • Image uniformity?
      • Slice parameters?
      • Image resolution?
      • Signal-to-noise?
      • Ghosting?
  • …K-space & Rapid Imaging
    • K-space (Basic) >
      • What is k-space?
      • Parts of k-space?
      • What does "k" stand for?
      • Spatial frequencies?
      • Locations in k-space?
      • Data for k-space?
      • Why signal ↔ k-space?
      • Spin-warp imaging?
      • Big spot in middle?
      • K-space trajectories?
      • Radial sampling?
    • K-space (Advanced) >
      • K-space grid?
      • Negative frequencies?
      • Field-of-view (FOV)
      • Rectangular FOV?
      • Partial Fourier?
      • Phase symmetry?
      • Read symmetry?
      • Why not use both?
      • ZIP?
    • Rapid Imaging (FSE &EPI) >
      • What is FSE/TSE?
      • FSE parameters?
      • Bright Fat?
      • Other FSE differences?
      • Dual-echo FSE?
      • Driven equilibrium?
      • Reduced flip angle FSE?
      • Hyperechoes?
      • SPACE/CUBE/VISTA?
      • Echo-planar imaging?
      • HASTE/SS-FSE?
    • Parallel Imaging (PI) >
      • What is PI?
      • How is PI different?
      • PI coils and sequences?
      • Why and when to use?
      • Two types of PI?
      • SENSE/ASSET?
      • GRAPPA/ARC?
      • CAIPIRINHA?
      • Compressed sensing?
      • Noise in PI?
      • Artifacts in PI?
  • …Contrast Agents
    • Contrast Agents: Physics >
      • Why Gadolinium?
      • Paramagnetic relaxation?
      • What is relaxivity?
      • Why does Gd shorten T1?
      • Does Gd affect T2?
      • Gd & field strength?
      • Best T1-pulse sequence?
      • Triple dose and MT?
      • Dynamic CE imaging?
      • Gadolinium on CT?
    • Contrast Agents: Clinical >
      • So many Gd agents!
      • Important properties?
      • Ionic v non-ionic?
      • Intra-articular/thecal Gd?
      • Gd liver agents (Eovist)?
      • Mn agents (Teslascan)?
      • Feridex & Liver Agents?
      • Lymph node agents?
      • Ferumoxytol?
      • Blood pool (Ablavar)?
      • Bowel contrast agents?
    • Contrast Agents: Safety >
      • Gadolinium safety?
      • Allergic reactions?
      • Renal toxicity?
      • What is NSF?
      • NSF by agent?
      • Informed consent for Gd?
      • Gd protocol?
      • Is Gd safe in infants?
      • Reduced dose in infants?
      • Gd in breast milk?
      • Gd in pregnancy?
      • Gd accumulation?
      • Gd deposition disease?
  • …Cardiovascular and MRA
    • Flow effects in MRI >
      • Defining flow?
      • Expected velocities?
      • Laminar v turbulent?
      • Predicting MR of flow?
      • Time-of-flight effects?
      • Spin phase effects?
      • Flow void?
      • Why GRE ↑ flow signal?
      • Slow flow v thrombus?
      • Even-echo rephasing?
      • Flow-compensation?
      • Flow misregistration?
    • MR Angiography - I >
      • MRA methods?
      • Dark vs bright blood?
      • Time-of-Flight (TOF) MRA?
      • 2D vs 3D MRA?
      • MRA parameters?
      • Magnetization Transfer?
      • Ramped flip angle?
      • MOTSA?
      • Fat-suppressed MRA?
      • TOF MRA Artifacts?
      • Phase-contrast MRA?
      • What is VENC?
      • Measuring flow?
      • 4D Flow Imaging?
      • How accurate?
    • MR Angiography - II >
      • Gated 3D FSE MRA?
      • 3D FSE MRA parameters?
      • SSFP MRA?
      • Inflow-enhanced SSFP?
      • MRA with ASL?
      • Other MRA methods?
      • Contrast-enhanced MRA?
      • Timing the bolus?
      • View ordering in MRA?
      • Bolus chasing?
      • TRICKS or TWIST?
      • CE-MRA artifacts?
    • Cardiac I - Intro/Anatomy >
      • Cardiac protocols?
      • Patient prep?
      • EKG problems?
      • Magnet changes EKG?
      • Gating v triggering?
      • Gating parameters?
      • Heart navigators?
      • Dark blood/Double IR?
      • Why not single IR?
      • Triple IR?
      • Polar plots?
      • Coronary artery MRA?
    • Cardiac II - Function >
      • Beating heart movies?
      • Cine parameters?
      • Real-time cine?
      • Ventricular function?
      • Tagging/SPAMM?
      • Perfusion: why and how?
      • 1st pass perfusion?
      • Quantifying perfusion?
      • Dark rim artifact
    • Cardiac III - Viability >
      • Gd enhancement?
      • TI to null myocardium?
      • PS (phase-sensitive) IR?
      • Wideband LGE?
      • T1 mapping?
      • Iron/T2*-mapping?
      • Edema/T2-mapping?
      • Why/how stress test?
      • Stess drugs/agents?
      • Stress consent form?
  • …MR Artifacts
    • Tissue-related artifacts >
      • Chemical shift artifact?
      • Chemical shift in phase?
      • Reducing chemical shift?
      • Chemical Shift 2nd Kind?
      • In-phase/out-of phase?
      • IR bounce point?
      • Susceptibility artifact?
      • Metal suppression?
      • Dielectric effect?
      • Dielectric Pads?
    • Motion-related artifacts >
      • Why discrete ghosts?
      • Motion artifact direction?
      • Reducing motion artifacts?
      • Saturation pulses?
      • Gating methods?
      • Respiratory comp?
      • Navigator echoes?
      • PROPELLER/BLADE?
    • Technique-related artifacts >
      • Partial volume effects?
      • Slice overlap?
      • Aliasing?
      • Wrap-around artifact?
      • Eliminate wrap-around?
      • Phase oversampling?
      • Frequency wrap-around?
      • Spiral/radial artifacts?
      • Gibbs artifact?
      • Nyquist (N/2) ghosts?
      • Zipper artifact?
      • Data artifacts?
      • Surface coil flare?
      • MRA Artifacts (TOF)?
      • MRA artifacts (CE)?
  • …Functional Imaging
    • Perfusion I: Intro & DSC >
      • Measuring perfusion?
      • Meaning of CBF, MTT etc?
      • DSC v DCE v ASL?
      • How to perform DSC?
      • Bolus Gd effect?
      • T1 effects on DSC?
      • DSC recirculation?
      • DSC curve analysis?
      • DSC signal v [Gd]
      • Arterial input (AIF)?
      • Quantitative DSC?
    • Perfusion II: DCE >
      • What is DCE?
      • How is DCE performed?
      • How is DCE analyzed?
      • Breast DCE?
      • DCE signal v [Gd]
      • DCE tissue parmeters?
      • Parameters to images?
      • K-trans = permeability?
      • Utility of DCE?
    • Perfusion III: ASL >
      • What is ASL?
      • ASL methods overview?
      • CASL?
      • PASL?
      • pCASL?
      • ASL parameters?
      • ASL artifacts?
      • Gadolinium and ASL?
      • Vascular color maps?
      • Quantifying flow?
    • Functional MRI/BOLD - I >
      • Who invented fMRI?
      • How does fMRI work?
      • BOLD contrast?
      • Why does BOLD ↑ signal?
      • Does BOLD=brain activity?
      • BOLD pulse sequences?
      • fMRI Paradigm design?
      • Why "on-off" comparison?
      • Motor paradigms?
      • Visual?
      • Language?
    • Functional MRI/BOLD - II >
      • Process/analyze fMRI?
      • Best fMRI software?
      • Data pre-processing?
      • Registration/normalization?
      • fMRI statistical analysis?
      • General Linear Model?
      • Activation "blobs"?
      • False activation?
      • Resting state fMRI?
      • Analyze RS-fMRI?
      • Network/Graphs?
      • fMRI at 7T?
      • Mind reading/Lie detector?
      • fMRI critique?
  • …MR Spectroscopy
    • MRS I - Basics >
      • MRI vs MRS?
      • Spectra vs images?
      • Chemical shift (δ)?
      • Measuring δ?
      • Backward δ scale?
      • Predicting δ?
      • Size/shapes of peaks?
      • Splitting of peaks?
      • Localization methods?
      • Single v multi-voxel?
      • PRESS?
      • STEAM?
      • ISIS?
      • CSI?
    • MRS II - Clinical ¹H MRS >
      • How-to: brain MRS?
      • Water suppression?
      • Fat suppression?
      • Normal brain spectra?
      • Choice of TR/TE/etc?
      • Hunter's angle?
      • Lactate inversion?
      • Metabolite mapping?
      • Metabolite quantitation?
      • Breast MRS?
      • Gd effect on MRS?
      • How-to: prostate MRS?
      • Prostate spectra?
      • Muscle ¹H-MRS?
      • Liver ¹H-MRS?
      • MRS artifacts?
    • MRS III - Multi-nuclear >
      • Other nuclei?
      • Why phosphorus?
      • How-to: ³¹P MRS
      • Normal ³¹P spectra?
      • Organ differences?
      • ³¹P measurements?
      • Decoupling?
      • NOE?
      • Carbon MRS?
      • Sodium imaging?
      • Xenon imaging?
  • ...Artificial Intelligence
    • AI Part I: Basics >
      • Artificial Intelligence (AI)?
      • What is a neural network?
      • Machine Learning (ML)?
      • Shallow v Deep ML?
      • Shallow networks?
      • Deep network types?
      • Data prep and fitting?
      • Back-Propagation?
      • DL 'Playground'?
    • AI Part 2: Advanced >
      • What is convolution?
      • Convolutional Network?
      • Softmax?
      • Upsampling?
      • Limitations/Problems of AI?
      • Is the Singularity near?
    • AI Part 3: Image processing >
      • AI in clinical MRI?
      • Super-resolution?
  • ...Tissue Properties Imaging
    • MRI of Hemorrhage >
      • Hematoma overview?
      • Types of Hemoglobin?
      • Hyperacute/Oxy-Hb?
      • Acute/Deoxy-Hb?
      • Subacute/Met-Hb?
      • Deoxy-Hb v Met-Hb?
      • Extracellular met-Hb?
      • Chronic hematomas?
      • Hemichromes?
      • Ferritin/Hemosiderin?
      • Subarachnoid blood?
      • Blood at lower fields?
    • T2 cartilage mapping
    • MR Elastography?
    • Synthetic MRI?
    • Amide Proton Transfer?
    • MR thermography?
    • Electric Properties Imaging?
  • Copyright/Legal
    • Copyright Issues
    • Legal Disclaimers
  • Forums/Blogs/Links
  • What's New
  • Self-test Quizzes - NEW!
    • Magnets & Scanners Quiz
    • Safety & Screening Quiz
    • NMR Phenomenon Quiz
    • Pulse Sequences Quiz
    • Making an Image Quiz
    • K-space & Rapid Quiz
    • Contrast & Blood Quiz
    • Cardiovascular & MRA Quiz
MRI Safety and Screening Quiz

Making an Image Quiz

  • Frequency and Phase Encoding
  • Scanning and Quality Control

Frequency and Phase Encoding

  1. What are the units for angular frequency (ω)?
    1. Hertz (Hz)
    2. Cycles per second (cps)
    3. Radians per cycle
    4. Radians per second

    Angular frequency (ω), also known as radial or circular frequency, measures angular displacement per unit time. Its units are therefore degrees (or radians) per second. Link to Q&A discussion

  2. Approximately how many degrees are in one radian?
    1. 30.0º
    2. 45.0º
    3. 57.3º
    4. 71.7º

    By definition, 2π radians span the arc of one circle, or 360º. So 1 radian = 360/2π ≈ 57.3º Link to Q&A discussion

  3. A 180º-pulse is sometimes expressed using radians as a
    1. π/2-pulse
    2. π-pulse
    3. 3π/2-pulse
    4. 2π-pulse

    A 180º-pulse is half a circle, or a π-pulse. Link to Q&A discussion

  4. As gradients are turned on and off, the angular frequency (ω) of a spin changes with time (t), expressed by the function ω(t). The area under the graph of ω(t) vs t between two time points (A and B) represents
    1. The spin’s accumulated phase shift between A and B
    2. The spin’s change in frequency between A and B
    3. The energy acquired by the spin between A and B
    4. The change in field strength experienced by the spin between A and B

    The area under the ω(t) vs t curve represents the accumulated phase of the spin during a certain interval. From a unit perspective, frequency is measured in radians or degrees per second while time is measured in seconds, so their product [ω(t) x t] will have units of radians (or degrees). Link to Q&A discussion

  5. The MR signal information received by the RF-coil can be classified as
    1. Frequency modulated
    2. Amplitude modulated
    3. Phase modulated
    4. Pulse modulated

    MR signal information, typically encoded over a range of 50-100kHz, arrives at the receiver amplitude-modulated on the RF carrier wave (e.g. at 64 MHz). The first step in signal process is called demodulation, which removes the carrier. Link to Q&A discussion

  6. The real and imaginary components during of an MR signal in the I and Q channels of a receiver are measured at a specific time point to be 3.0 and 4.0 au (arbitrary units) respectively. What is the actual magnitude of the signal?
    1. 3.5 au
    2. 5.0 au
    3. 7.0 au
    4. 12.0 au

    The magnitude (M) = [Re² + Im²]½ = [3² + 4²]½ [25]½ = 5.0 au. Link to Q&A discussion

  7. Concerning Fourier representation of the MR signal, which of the following statements is false?
    1. The Fourier expansion of a signal can be written in either trigonometric or exponential form.
    2. To represent any real signal exactly, an infinite number of frequency components must be included in its Fourier representation.
    3. The Fourier transformation converts a time-based signal into the frequency domain, but the change cannot be reversed.
    4. The Fourier series representation of an MR image is always cut short (truncated).

    All are true except for (c). Fourier transformation is the mathematical procedure connecting a time domain signal, s(t), and its frequency domain representation, S(ω). The inverse Fourier transform converts S(ω) back to s(t). Link to Q&A discussion

  8. The time domain signal, s(t), that corresponds to a uniform/rectangular band of frequencies in S(ω) is called a
    1. Double exponential
    2. Sinc function
    3. Gaussian
    4. Lorentzian

    The sinc function, sinc(t) = [sin t]/t, Fourier transforms into a uniform band of frequencies, such as those used to define a slice profile in conventional 2D MR imaging Link to Q&A discussion

  9. Which of the following scientists did not win the Nobel Prize for their work in NMR?
    1. Felix Bloch
    2. Raymond Damadian
    3. Paul Lauterbur
    4. Peter Mansfield

    Raymond Damadian did not win the Nobel Prize for his work and considered it a personal injustice. He placed full-page ads in several large world newspapers urging the Nobel committee to change their minds, which they never did. Link to Q&A discussion

  10. Which of the following is not a method for spatial localization of the MR signal?
    1. Frequency encoding
    2. Phase encoding
    3. Location of receiver coils
    4. Amplitude modulation

    Choice (d), amplitude modulation, refers to the shape of transmitted or received RF-pulses but is not by itself a method of spatial localization. Link to Q&A discussion

  11. Which of the following statements about frequency encoding is incorrect?
    1. It commonly used for in-plane localization for 2D imaging.
    2. It is commonly used for slice selection in 3D imaging.
    3. Each voxel actually contains a range of frequencies, not just a single frequency.
    4. For most applications a linear frequency encoding gradient is desired.

    All are correct except (b). Frequency encoding is commonly used for slice selection in 2D imaging, but phase encoding is typically used for slice selection in 3D. Link to Q&A discussion

  12. What is a typical total receiver bandwidth for a 1.5T MR scanner?
    1. 1 kHz
    2. 50 kHz
    3. 250 kHz
    4. 500 kHz

    Receiver bandwidth is an operator-selectable parameter, chosen by the technologist before the scan begins. Available values for total receiver BW range from about 5-100 kHz with 50kHz being typical. Link to Q&A discussion

  13. What is the width of a pixel in the frequency encoding direction if the field-of-view is 25.6 cm and 512 frequency-encoding steps are used?
    1. 0.5 mm
    2. 1.0 mm
    3. 2.0 mm
    4. 5.0 mm

    Pixel width = FOVf ÷ # frequency encode steps = 256 mm ÷ 512 = 0.5 mm. Link to Q&A discussion

  14. If 256 complex measurements of a digitized MR signal are sampled in a period of 5.12 ms, what is the dwell time?
    1. 5 μs
    2. 10 μs
    3. 20 μs
    4. 200 μs

    The dwell time is the interval between digitized samples. So if 256 samples were obtained over a 5.12 ms period, the dwell time would be 5.12 ms/256 = 20 μs. Link to Q&A discussion

  15. What is the total receiver bandwidth if the interval between digitized samples (dwell time) is 25 μs?
    1. 2,500 Hz
    2. 25,000 Hz
    3. 40,000 Hz
    4. 50,000 Hz

    Total receiver BW is the same as the digitization rate of the MR signal. In equation form, BW = 1/td = 1/(25 μs) = 40,000 Hz. Link to Q&A discussion

  16. In clinical MR imaging at 1.5T, what frequency range would be typical for setting the receiver to “narrow bandwidth”?
    1. 1 – 5 kHz
    2. 5 – 20 kHz
    3. 50 – 52 kHz
    4. 100 – 101 kHz

    A typical range for narrow receiver bandwidth would be choice (b), 5 – 20 kHz. Link to Q&A discussion

  17. Which of the following statements about narrow bandwidth is incorrect?
    1. Narrow BW implies reduced sampling time.
    2. Narrow BW increases signal-to-noise.
    3. Narrow BW accentuates chemical shift artifacts.
    4. Narrow BW accentuates susceptibility artifacts.

    Option (a) is false. Bandwidth is inversely proportional to sampling time. A synonym for "narrow bandwidth" is therefore "extended sampling time". Link to Q&A discussion

  18. Which of the following statements about transmitter bandwidth is true?
    1. It is automatically determined once receiver bandwidth is specified.
    2. Transmitter BW per se is not directly adjusted by the technologist when specifying scan parameters.
    3. Typical values for transmit BW are 50-100 kHz.
    4. Most modern RF-pulses for 2D slice-select are sinc-shaped.

    The transmit bandwidth is not usually user-adjustable, so choice (b) is true. Typical values are 1000-2000 Hz and are independent of receiver bandwidth. Simple sinc pulses are no longer used for slice select, being supplanted by more sophisticated designs using the SLR algorithm. Link to Q&A discussion

  19. Cross-talk can be reduced by all of the following methods except:
    1. Increasing gaps between slices
    2. Increasing the strength of the slice-select gradient
    3. Performing slice interleaving
    4. Improving the RF slice profile

    Increasing the strength of the slice-select gradient will only serve to produce thinner slices, not improve cross-talk. Link to Q&A discussion

  20. The earliest commercial version of simultaneous slice excitation (offered by GE in the 1990s) applicable to single-channel RF coils was called
    1. Phase Offset MultiPlanar (POMP)
    2. MultiBand (MB)
    3. Simultaneous Multi-Slice (SMS)
    4. HyperBand (HB)

    The historical precursor to modern MB/SMS methods was POMP (Phase Offset MultiPlanar) imaging. The POMP technique used a composite RF-pulse to simultaneously excite two slices, each of which were phase-encoded over only one-half of the total field-of-view (FOV). Phase alternation allowed the two slices to be separately reconstructed without overlap. Unlike SMS, POMP does not utilize parallel imaging technology and is hence applicable to single-channel RF coils. Link to Q&A discussion

  21. Which of the following statements about MultiBand/Simultaneous Multi-Slice imaging is false?
    1. Use of parallel imaging arrays is required.
    2. Acceleration factors of 2-4 are typical.
    3. The slices must be widely spaced apart (2-3 cm).
    4. The technique imposes a significant penalty in terms of signal-to-noise.

    MB uses coil encoding together with either gradient- or RF-encoding to resolve data along the slice-select (z)-axis. Because modern coil arrays typically have only a few coil elements in the z-direction, coil sensitivity differences along that axis are rather poor. Accordingly the simultaneously excited slices must be spaced widely apart (typically at least 25−30 mm). Unlike standard parallel imaging acceleration techniques, MB/SMS acceleration results in little to no penalty in signal-to-noise. (Option d is false). This is because neither the echo train length, number of phase-encoding steps, nor number of k-space samples has been reduced as occurs in conventional parallel imaging acceleration methods. Link to Q&A discussion

  22. What is the approximate in-plane pixel dimensions of a 25 x 25 cm FOV image acquired using 192 phase-encoding steps and 512 samples in the frequency direction
    1. 1.3 x 0.5 mm
    2. 2.6 x 0.5 mm
    3. 1.3 x 5.0 mm
    4. 2.6 x 5.0 mm

    The pixel width in the phase encode direction is 250 mm ÷ 192 ≈ 1.3 mm, while that in the frequency encode direction is 250 ÷ 512 ≈ 0.5 mm. Link to Q&A discussion

  23. Concerning 2D Fourier Transform imaging, which statement is false
    1. The number of unique echo signals equals the number of phase-encoding steps.
    2. The phase shifts between successive echoes are multiples of 180º.
    3. For low-amplitude phase-encodings the MR signal is strong but provides little information about spatial detail.
    4. For high-amplitude phase-encodings the MR signal is weak and provides little information about image contrast.

    Choice (b) is false. The phase shifts between the rows are not simple multiples of 180°, but vary from echo to echo depending on the size of the phase-encoding step. The number of echo signals acquired equals the number of phase encode steps, which is usually 192 or 256. For low order phase-encodings, the MR signal is strong. The frequency projection approximates the general shape of the object but lacks edge definition. The higher order phase encode steps have smaller MR signals but provide more information about spatial detail, such as the location of edges. Link to Q&A discussion

  24. Why is the phase-encode direction often chosen along the shortest anatomic dimension?
    1. This reduces wrap-around artifact.
    2. This reduces flow-related artifact.
    3. This reduces artifacts from gross patient motion.
    4. It is a requirement for parallel imaging.

    Wrap-around (also called aliasing) occurs when the size of the body part imaged exceeds the defined field-of-view (FOV) in the phase-encode direction. This causes anatomy outside the FOV to be folded in over the main part of the image. To avoid wrap-around the phase-encoding direction is usually chosen to be along the shortest anatomic dimension. Flow-related and other motion artifacts may be moved around by changing the phase-encode direction, but the best direction is based on the location and types of these artifacts, which may or may not be best along the shortest dimension. For parallel imaging there may be some restrictions on possible phase-encode directions allowed, but setting phase-encode along the shortest axis is not necessarily required. Link to Q&A discussion

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Scanning and Quality Control

  1. Which steps in setting up an MR scan are in the proper chronological order?
    1. Set landmark → Perform prescan → Acquire localizer → Position slices
    2. Acquire localizer → Position slices → Set landmark → Perform prescan
    3. Set landmark → Acquire localizer → Position slices → Perform prescan
    4. Perform prescan → Acquire localizer → Set landmark → Position slices

    Choice (c) shows the correct order. Link to Q&A discussion

  2. Which process in the list below is not a part of automatic prescan?
    1. Specific Absorption Rate (SAR) estimation
    2. Quick shimming
    3. Center frequency adjustment
    4. Transmitter gain adjustment
    5. Receiver gain adjustment

    Specific Absorption Rate (SAR) is estimated by the scanner based on the patient’s body weight, pulse sequence, and pulse sequence parameters selected. This occurs before automatic prescan, allowing the operator to adjust parameters to keep SAR within established limits. Automatic prescan is essentially the last step before the actual scan begins. Link to Q&A discussion

  3. In which of the following situations is manual shimming (in addition to prescan quick shimming) nearly always required?
    1. Diffusion-weighted imaging
    2. MR Spectroscopy
    3. Fast-spin echo imaging
    4. Dixon fat-water imaging

    Very detailed high-order shimming is mandatory for spectroscopy. Although spectroscopy shimming can be automated, the settings always require review and often tweaking by the MR technologist. Link to Q&A discussion

  4. In which of the following situations is center frequency adjustment most critical?
    1. When using spatial saturation pulses
    2. When using flow saturation pulses
    3. When using arterial spin labeling pulses
    4. When using fat saturation pulses

    The center frequency may be set on water protons, fat protons, or some average of the two. Accurate center frequency setting is particularly important when spectral fat saturation pulses are employed to make sure the fat peak is adequately suppressed. Link to Q&A discussion

  5. What artifact will occur if the receiver attenuator value is set too low during prescan?
    1. Data clipping
    2. Wrap around
    3. Ghosts
    4. Diffuse noise

    If the attenuator value is set too low (i.e., receiver gain is set too high), then the signal will overload the analog-to-digital converter, and data clipping will occur. Since the largest peaks of the MR signal typically are the low order phase-encode steps at the center of k-space, data clipping interferes with image contrast. The result is an image with an "eerie" appearance Link to Q&A discussion

  6. What is the purpose of dummy cycles during prescan?
    1. To adjust RF-voltage to achieve a perfect 90º-pulse
    2. To allow warm-up of the transmit and receive circuitry
    3. To optimally match coil impedance with that of the patient
    4. To allow steady state longitudinal and transverse magnetization to be established

    Once RF-excitation begins, the longitudinal and transverse magnetizations need time to reach their steady-state values. During prescan the scanner plays out several cycles of the sequence without recording a signal. These are called dummy cycles, disabled, or discarded acquisitions (DDA). The precise number of dummy cycles depends on the TR and the sequence chosen. Only once the system is near equilibrium does data collection begin. Link to Q&A discussion

  7. To sell an MR scanner in the United States, a company must receive what kind of premarket clearance from the Food and Drug Administration?
    1. 401(k)
    2. 501(k)
    3. 1099
    4. 457(b)

    In the United States the Food and Drug Administration (FDA) has statutory authority to regulate the sale and use of MRI equipment. MRI scanners are considered Class II devices, meaning that they have the potential for human harm and require pre-market 501(k) clearance prior to marketing. The FDA has issued guidance documents with non-binding (but strongly suggested) criteria — including those related to hardware, software, performance, site planning, and safety — to attain this premarket approval. The other numbers are all IRS forms and investment accounts unrelated to MRI Link to Q&A discussion

  8. Which of the following organizations does not offer MRI accreditation in the United States?
    1. American College of Radiology (ACR)
    2. Centers for Medicare & Medicaid Services (CMS)
    3. RadSite
    4. The Joint Commission (TJC)

    In the US there are four MRI accrediting organizations that are currently sanctioned by the Centers for Medicare & Medicaid Services (CMS) – the American College of Radiology (ACR), the Intersocietal Accreditation Commission (IAC), The Joint Commission (TJC), and RadSite. Link to Q&A discussion

  9. Which of the following quality control measurements must be performed at least weekly on an MR scanner?
    1. Center frequency
    2. Magnetic field homogeneity
    3. Slice thickness accuracy
    4. Monitor resolution

    Daily QC activities include visual inspection of all scanner hardware, the function of safety and communication devices, and general assessment of image quality including identification of artifacts. On at least a weekly basis, a special MR phantom is placed in the scanner and various measurements are made and recorded. Such measurements include landmark accuracy (table position), center frequency, image uniformity, transmitter gain or attenuation, geometric distortion, spatial resolution, artifact evaluation, and signal-to-noise ratio. Other more sophisticated testing should be performed semiannually or yearly by a medical physicist. Link to Q&A discussion

  10. The most common cause of geometric errors is
    1. Warping of the MR phantom
    2. Abnormal RF-coil impedance
    3. Miscalibration of one or more imaging gradients
    4. Center frequency drift

    The most common cause of geometric errors is miscalibration of one or more imaging gradients. Gradients tend to drift over time and require periodic re-calibration by service engineers. Occasionally the problem is caused by Bo inhomogeneity due to improper shim adjustments or an occult ferromagnetic object lodged in the scanner bore. Link to Q&A discussion

  11. Detailed procedures and standards for the two most commonly used methods of measuring signal-to-noise in a phantom come from which organization?
    1. The National Electrical Manufacturers Association (NEMA)
    2. The International Electrotechnical Commission (IEC)
    3. The International Commission on Non-Ionizing Radiation Protection (ICNIRP)
    4. The American Society for Testing and Materials (ASTM International)

    The National Electrical Manufacturers Association (NEMA) provides detailed methods and standards for evaluating all types of electrical devices. Those relating specifically to MRI quality include how to measure signal-to-noise (MS 1, 6, & 9), geometric distortion (MS 2 & 12), and uniformity (MS 3). Link to Q&A discussion

  12. When complex-valued MR signal data is converted into a magnitude image, the noise statistics are best described using a
    1. Gaussian (normal) distribution
    2. Poisson distribution
    3. Gamma distribution
    4. Rician distribution

    Because region-of-interest (ROI) measurements are typically made on magnitude-reconstructed images, some correction to the statistics must take place. Recall that "raw" MR data is a complex number with real and imaginary parts. When converted to a magnitude only image, the pixel values corresponding to noise are no longer Gaussian, but skewed into a so-called Rician distribution. Link to Q&A discussion

  13. The section of an MR phantom consisting of closely spaced lines or holes containing material with strong difference in signal intensity from the background is used to measure
    1. Low-contrast object detectability
    2. Geometric distortion
    3. High-contrast spatial resolution
    4. Image uniformity

    The high-contrast portion of MR phantoms contains closely spaced lines, edges, or holes containing material with strong differences in signal intensity from background. Low-contrast resolution refers to the ability to identify small holes in the phantom with only slightly different relaxation times from background. Link to Q&A discussion

  14. The section of an MR phantom consisting of triangular ramps or wedges oriented at a known angle is used to measure
    1. Slice thickness
    2. Slice position
    3. Linear accuracy
    4. Low-contrast resolution

    The most common method to estimate slice thickness is to use a phantom containing triangular ramps or wedges whose surfaces are oriented at a known angle (θ) to the plane of the slice. When a slice passes through the ramp, it produces a stretched "shadow" image whose full width half maximum (FWHM) can be estimated. Link to Q&A discussion

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