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B R U C E E . H A S S E L Q U I S T , P H . D . , D A B R , D A B S N M
A S P I R U S W A U S A U H O S P I T A L
Implementation of the 2012 ACR CT QC Manual in a Community
Hospital Setting
Conflict of Interest Disclaimer
Employee of Aspirus Wausau Hospital
ACR Activities Reviewer for CT accreditation program (physics)
Reviewer for NM accreditation program (physics)
Member Medical Physics Guidelines Committee
No conflicts to disclose
Objectives
Review the major elements of the 2012 ACR QC manual
Compare the manual to current ACR accreditation program and phantom testing requirements and to the current technical standard
Highlight some interesting details of the new physicist testing recommendations
2012 ACR CT Quality Control Manual
Table of Contents Radiologist’s Section
Definitions of QA and QC
Responsibilities
Radiologic Technologist’s Section Daily QC
Weekly QC
Monthly QC
Medical Physicist’s Section Annual QC
http://www.acr.org/~/media/ACR%20No%20Index/Documents/Random/2012CTQCManual2.pdf
To be accredited by the ACR
“Effective 12/01/2013, all facilities applying foraccreditation must maintain a documented QC programand must comply with the minimum frequencies oftesting outlined in the 2012 ACR Computed TomographyQuality Control Manual.”
Page 4: 2012 ACR CT QC Manual
What’s Mandatory?
Should’s (177 instances!) Acceptance testing before 1st
patient scanned
Equipment evaluation dated within 1 year at renewal
Evaluation after major repairs, incl x-ray tube and detector assembly replacement
Refer to state and local regulations if more restrictive
Greater frequently for QC tests when being introduced or results inconsistent.
Records accessible from CT scanner location
Must’s (35 instances!) Maintain documented QC program
Comply with minimum testing frequencies
QMP oversees QC program
QMP monitors performance at installation and annually
Annual equipment evaluation submitted initially and at renewal
Evaluation dated within 14 months at renewal
Evaluation performed by a QMP
Annual QMP review of tech QC records (qtly preferred)
Quality Assurance is a comprehensive concept to ensure that:
1. Every imaging procedure is necessary and appropriate to the clinical problem at hand;
2. The combination of acquisition parameters used for each exam is appropriate to address the clinical question;
3. The images generated contain information critical to the solution of that problem;
4. The recorded information is correctly interpreted and made available in a timely fashion to the patient’s physician; and
5. The examination results in the lowest possible risk to the patient and is consistent with Objective 2 (above).
Quality Control is a series of distinct technical procedures
Four steps are involved:
1. Acceptance testing to detect defects in equipment that is newly installed
2. Establishment of baseline equipment performance
3. Detection and diagnosis of changes in equipment performance before they become apparent in images
4. Verification that the causes of deterioration in equipment performance have been corrected
(Supervising) Radiologist
“Radiologists must assume the primary responsibility for the quality of CT and for the implementation of an effective QA program at their site.”
Convene a CT QA or Protocol Review Committee Oversees QA program
Sets goals and directions
Determines policies
Assesses effectiveness of QA activities
Assist with development of CT QA Manual
Participate in “Interpretive Quality Assurance” aka peer review
Quality Assurance Committee
• Design and review all new or modified CT protocol settings to ensure that both image quality and radiation dose are appropriate
• Develop internal radiation dose thresholds during any new CT protocol design.
• Implement steps to ensure patient safety and to reduce future risk if an estimated dose value is above the applicable threshold for any routine clinical exam
• Review, at least annually, all protocols to ensure no unintended changes have been applied that may degrade image quality or unreasonably increase dose
• Establish a policy stating that the CT dose estimate interface option is not to be disabled and that the dose information is displayed during the exam prescription phase
“Good Practices” – Established by the Team
1. Technologists are provided access to adequate training and continuing education in CT that includes a focus on patient safety.
2. An orientation program has been provided for technologists based on a carefully established procedures manual.
3. A technologist has been selected as the primary QC technologist to perform the prescribed QC tests.
4. Appropriate test equipment and materials necessary for the technologist to perform the QC tests have been provided
5. Staffing and scheduling are arranged so that adequate time is available to carry out the QC tests and record and interpret the results.
“Good Practices” – Established by the Team
6. A qualified medical physicist will review the technologist’s test results at least every 3 months or more frequently if consistency has not yet been achieved.
7. A qualified individual has been designated to oversee the safety program for employees, patients, and other individuals in the surrounding area.
8. Established protocols will be followed
9. Corrective action procedures will be followed when images of poor quality are presented for interpretation
“Good Practices” – Established by the Team
10. Radiologists will participate in the Radiology Department’s practice improvement program
11. Documentation of current qualifications will be provided by all interpreting radiologists in accordance with ACR Accreditation and local rules.
CT QA Procedures Manual
1. Who is responsible for QC?
2. What are your QC procedures?
3. Where are the records of all QC tests, service reports, etc?
4. How are your CT operators trained?
5. How is your scanner maintained?
6. What CT protocols are in place? Contrast? Positioning?
7. Do you have minutes from your CT QA committee?
8. What are your policies for pregnant patients and staff?
9. What are your procedures for disinfecting equipment?
Technologist QC
Effective 12/01/2013, all facilities applying for accreditation must maintain a documented QC program and must comply with the minimum frequencies of testing outlined in the 2012 ACR Computed Tomography Quality Control Manual.
Daily Water CT# and standard deviation
Artifact evaluation
Weekly Wet laser printer QC
Monthly Visual checklist
Dry laser QC
Display monitor QC
(See also current ACR CT accreditation requirements document.)
Daily QC
The QMP should assist with setting up QC protocols and determining pass / fail criteria.
Should acquire a set of standard artifact-free images for comparison with daily QC. Must use daily QC scan protocols to acquire these images.
Test Procedure
Water CT Number and StandardDeviation (noise)
Axial and Helical scansROI in center of image at center of scan as well as at leading or trailing edge of fan beamCT# CriteriaWater: 0 ± 5 HU(“must”)ACR Phan: 0 ± 7 HU(“must”)
Artifact Evaluation Axial scanThinnest available axial imagesacross the full z-axis extent; 2 (LS16) or 3 (VCT) scans, if necessaryRecommend periodic use of larger uniform phantom (manufacturer’s or 32 cm dosimetry phantom)
Weekly QC
To be performed if film is used for primary interpretation.
Test Procedure
Wet Laser Printer QC
Film SMPTE pattern 6 on 1 in all 6 frames. Monitor OD’s in upper left image for 0%, 10%, 40% & 90% gray level patches.Evaluate film for artifacts.Should be done for each sending modality, e.g. CT and MRI.Target OD’s and control limits are provided in manual.
Monthly QC
Laser printer QC to be performed if film is used for primary interpretation. Backup printers may be tested prior to clinical use as well as when initiating QC program.
Display monitors should be recalibrated at least annually.
All QC records should be reviewed and signed by QMP as part of equipment evaluation. Retain records for 5 yr.
Test Procedure
Visual Checklist See QC manual for recommended list of items to check.
Dry Laser Printer QC (same as for WetLaser Printers)
Film SMPTE pattern 6 on 1 in all 6 frames. Monitor OD’s in upper left image for 0%, 10%, 40% & 90% gray level patches.Evaluate film for artifacts.Should be done for each sending modality, e.g. CT and MRI.Target OD’s and control limits are provided in manual.
Display Monitor QC
Display SMPTE (or TG18-QC) on acquisition monitor.Evaluate 5% & 95% patches and other gray level patches.
Automatic QC Procedures
Automatic analysis SW may be used but must be approved by QMP.
Automatic QC procedures may be used in place of these tests if the Qualified Medical Physicist has critically reviewed them and approved this substitution (in writing).
It is not recommended that an automatic QC process be considered as a replacement for the artifact analysis portion of daily QC.
Physicist (QMP)
Our role Establish continuous QC program for facility
Review QC program results annually
Equipment evaluations at acceptance and annually
“Communicating test results and recommending corrective action are areas that can be improved in the practices of most QMPs.”
Required tests
Missing tests Relegate to acceptance?
Annual Physics QC
Effective 12/01/2013, all facilities applying for accreditation must maintain a documented QC program and must comply with the minimum frequencies of testing outlined in the 2012 ACR Computed Tomography Quality Control Manual.
Review of clinical protocols
Scout / alignment light accuracy
Image thickness
Table travel accuracy
Radiation beam width
Low-contrast performance
Spatial resolution
CT number accuracy
Artifact evaluation
CT number uniformity
Dosimetry
Display monitor performance
Review of Clinical Protocols
Recommendations provided in QC manual.
Team should design and review all new or modified protocol settings
Institute a regular review process of all protocols At least 6 protocols (ped / adult: head &
abd; high res chest; brain perfusion, if used)
Review appropriate use of dose reduction methods
Review clinical scans for: Image quality
Dose
Centering
Scout / Alignment Light Accuracy
1. Align phantom with laser and do axial scan.
2. Scout phantom and scan at marker.
Scan location relative to alignment light or scout prescription should be accurate to within 2 mm.
ACR CTAP Phantom Module 1 or similar (see AAPM Rpt #39)
Image Thickness
Perform axial scans of the phantom for each reconstructed image thickness used clinically.
Image thickness should be within 1.5 mm of nominal thickness.
Good practice mandates helical scans (SSP’s) at acceptance
.
0.625 mm
2.5 mm
10 m
m
5 mm
1.25
mm
ACR CTAP Phantom Module 1 or similar
Table Travel Accuracy
Check known distance and accuracy of return to initial position after travel to max distance.
Translation accuracy should be within 2 mm.
ACR CTAP Phantom or any phantom with 2 sets of external fiducial markers of known separation (see AAPM Rpt #39)
Radiation Beam Width
Scan strip at isocenterusing each unique NxTproduct (beam collimation) available. Measure FWHM of beam profile.
Compare to manufacturer’s standards or ACR criteria of within the greater of 3 mm or 30% of the nominal beam collimation.
Note: 120 kVp, 200 mAs works well with GAF Chromic film.
Low-Contrast Performance
Establish correlation to ACR phantom for alternate phantoms.
Equivalent to ACR accreditation LCR test protocol, analysis and criteria.
Additionally, 6 mm targets must be visualized for adult head and abdomen.
Corrective action is immediate.
ACR CTAP Phantom Module 2 or any phantom with low contrast objects of known contrast.
Scan Protocol CNR (ACR)
Adult Head 1.0
Pediatric Head 1.0
Adult Abdomen 1.0
Pediatric Abdomen 0.5
Spatial Resolution
Evaluate HCR for relevant clinical exams, e.g. adult abdomen and high-resolution chest.
Corrective action is immediate.
Scan Protocol Limiting Resolution
Adult Abdomen 6 lp/cmHigh-Resolution Chest 8 lp/cm
ACR CTAP Phantom Module 4 or any phantom with high contrast objects of known resolution.
CT Number Accuracy
Scan phantom using all 4 ACR clinical protocols. Evaluate CT # in at least three target materials for all 4 scans.
Scan water (or water equivalent) phantom at all clinical kVp’s.
Use ACR accreditation criteria for ACR phantom.
80 kVp 100 kVp
120 kVp 140 kVp
ACR CTAP Phantom Module 1 or similar phantom with water, air and 1 other material
Artifact Evaluation
Same test as for daily technologist QC.
Perform axial scan(s) using the thinnest available axial slices, spanning the z-axis extent of the detector array. For a GE VCT this could include:
0.625 mm, 16i (10 mm)
1.25 mm, 16i (20 mm)
2.5 mm, 16i (40 mm) Water phantom provided by CT manufacturer or ACR CTAP Phantom Module 3.
2.5 mm 16i (40 mm beam collimation) W/L: 20/0
CT Number Uniformity
ACR recommends using technologist artifact QC protocol.
Analysis and criteria are the same as for the ACR accreditation program.
Water phantom provided by CT manufacturer or ACR CTAP Phantom Module 3.
Dosimetry
Equivalent to ACR accreditation dosimetrymeasurement protocol, analysis and criteria.
Additionally, compare measured CTDIvol to the values reported by the scanner. Agreement should be within 20%. Be sure to note if scanner display value based on phantom other than the one use for measurement. Year-to-year variation should be no more than 5%.
16 cm (head) and 32 cm (body) CTDI dosimetry phantoms
In head holder for adult head;On table for pediatric head and abdomen protocols.
On table for adult abdomen protocol.
Pass/Fail Criteria and Reference Levels
Pass/FailCriteria
ReferenceLevels
Examination CTDIvol (mGy) CTDIvol (mGy)
Adult Head 80 75
Adult Abdomen 30 25
Pediatric Head (1 y.o.) 40 (new) 35 (new)
Pediatric Abdomen (5 y.o. /40 lb) 20 (was 25) 15 (was 20)
Effective July 1, 2013
Display Monitor Performance
Observe:1) 5%/95% patches2) Line pair patterns3) Black-white transitions4) Loss of bit depth5) Geometric distortion
Measure:1) Min and max brightness (0%, 100%)2) Response curve (GSDF)3) Center / edge brightness uniformity
SMPTE pattern or equivalent (e.g. TG18‐QC)
Min (0%) ≤ 1.2 cd/m2
Max (100%) ≥ 90 cd/m2Luminance nonuniformity should be no more than 15% for FPDs
GSDF should be visually consistent year‐to‐year. (see also TG18 report)
Automatic QC Software
Automatic analysis SW may be used but must be verified.
CT Scanner Acceptance Testing Perform all tests independent of
manufacturer’s QC SW
Must compare results to SW if it is to be used during annual testing
Must verify SW if it was not evaluated during acceptance testing
Annual Performance Evaluation Manufacturer’s automatic QC SW may
be used if previously verified by QMP
Additional Physics Tests
These tests are not mentioned in the QC manual but could be done at acceptance.
Some manufacturer’s provide specifications and CTDI adjustment factors that apply to these measurements. Comparison can also be made to console CTDI display values.
Image Noise
CTDI Accuracy
Output Reproducibility
Output kVp dependence
mR/mAs Linearity
Output Beam Thickness Dependence
EKG mA Modulation
Slice Sensitivity Profile
Beam Angulation Accuracy
Scatter
Slice Sensitivity Profile
SSP measurements are recommended as part of acceptance testing in the slice thickness section of the ACR QC manual.
ACR CTAP Phantom Module 3 or any phantom with a small high contrast object (0.28 mm for ACR) in a uniform background.
0200400600800
10001200
1 3 5
Max
in R
OI
Distance (mm)
Slice Sensitivity Profile
1.25 mm slice
Collimation (mm)
Slice Thickness
(mm)
Recon Interval
(mm)Meas FWHM
(mm)Manuf. Spec.
(mm)
20 1.25 0.125 1.09 1.17
20 2.5 0.25 2.26 2.40
20 5.0 0.5 4.98 5.48
20 (Plus mode) 1.25 0.125 1.34 1.46
40 (Plus mode) 1.25 0.125 1.38 1.50
2012 ACR-AAPM CT Medical Physics Technical Standard
Limited protocol review
Image localization from SPR
Alignment light accuracy
Table incrementation accuracy
Reconstructed image thickness
Radiation beam width
Image qualityHCR, LCR, Uniformity, Noise, Artifact
CT number accuracy
Dosimetry (CTDIvol, patient dose)
Acquisition workstation display
Safety evaluation, scatter at AT
Review of clinical protocols
Scout/alignment light accuracy
Table travel accuracy
Image thickness
Radiation beam width
Spatial resolution
Low-contrast performance
CT number uniformity
Artifact evaluation
CT number accuracy
Dosimetry
Display monitor performance
2012 ACR CT QC Manual
Minnesota Rules 4732.1100
Accuracy of scout localization view
Table backlash & Table indexing
Accuracy of distance measurements
CT # uniformity and artifacts
CT # calibration and noise
CT dose index
CT # dependence on slice thickness
Hard copy output & visual display
Review of clinical protocols
Scout/alignment light accuracy
Table travel accuracy
Image thickness
Radiation beam width
Spatial resolution
Low-contrast performance
CT number uniformity
Artifact evaluation
CT number accuracy
Dosimetry
Display monitor performance
2012 ACR CT QC Manual
How are we doing?
Modified annual equipment evaluation protocols
Convened CT QA committee
Modified our technologist QC program and associated forms – not implemented at WI sites
Revised policies & procedures at MI sites
Created draft site specific CT QA manual
Implementing ACR NRDR/DIR program in Wausau
Installing and implementing Dose Check SW
Continuing to review protocols (esp. pediatric)
QC phantom images analyzed monthly by QMP