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| MRI
Accreditation Checklist: Prepare for Success |
| United
Healthcare’s decision to require MRI accreditation
after March 1, 2008, initiated a trend among payers
that is likely to gain steam. It has also sent hospitals
and freestanding imaging centers scrambling to secure
MRI accreditation from the American College of Radiology,
which has accredited over to 5,000 MRI units since beginning
its MRI program in 1996.
The accreditation process is no cause for panic. A
majority of applicants passed on their first attempt,
and most of those that did not went on to attain accreditation.
So the odds of undergoing a successful accreditation
are in your favor. But before initiating the accreditation
process, it is important to designate a champion who
will accept responsibility for this task and then to
give that person the time and support to accomplish
it. The following guidelines will help ensure success.
- Construct a timeline. Your site’s champion
should begin by studying the information on the ACR
website and constructing a timeline identifying
the anticipated needs for critical stages. Remember
that even after you submit your application it may
take the ACR up to two months to process it and award
accreditation. You may also want to leave at least
a two-month cushion in the unlikely event that you
fail a portion of the process and need to appeal or
resubmit. Presuming a site desires accreditation as
of December 1, 2007, it would be wise to submit the
application no later than the beginning of October.
This also means the application has to be started
no earlier than the middle of August since there is
only a 45 day window once the application file is
opened (once you pay the fee and the accreditation
materials are sent to you).
- Get the help you need. Parts of the application
refer to peer review and to the date of your system’s
most recent technical review (physics test). Take
questions on peer review to the physicians at your
site responsible for clinical interpretation. The
MRI scientist or medical physicist who conducts your
annual MRI performance testing and assists with your
local quality control (QC) program can address the
issues on instrument testing. The ACR will not accept
an application without proof of an MRI scientist’s
or medical physicist’s report on your system
dated within twelve months of submission.
- Initiate a QC program if you do not have one. Most
new sites (and a number of previously accredited sites)
have not maintained their QC programs properly and
have not had their systems tested. The first step
is to find an MRI scientist or a medical physicist
with MRI experience to help you get on track. (See
sidebar on how to hire an MR scientist or medical
physicist.) QC is considered a nuisance by some imaging
center personnel, but the alternative is worse. I
have tested over 1,000 MRI units in the past twenty
years and have encountered problems in about 80% of
those systems, including bad head and body coils,
poor homogeneity, faulty gradient amplifiers, intermittent
RF systems, and monitors that don’t meet specifications.
Independent annual testing and on-site quality control
can help to identify issues before they become catastrophic.
- When your application is accepted, get busy! You
have 45 days to complete you submission. The first
thing you should do on receipt of your packet and
MRAP number is order the ACR MRI phantom from the
manufacturer. Phantoms are subject to periodic shortages
due to the requirements of the manufacturing process.
The paperwork is self-explanatory, but the project
leader should distribute appropriate parts to the
appropriate people with a deadline.
- The most common source of failure is the selection
of clinical cases for review. Each applicant must
submit an exam of the brain, C-spine, L-spine, and
knee. These should demonstrate your standard scan
techniques and do not have to include pathology. Be
advised that the ACR
has requirements for in-plane resolution and slice
thickness In the knee, for instance, slice thickness
must be less than or equal to 4mm and in-plane resolution
is less than or equal to 0.75mm. Remember that in-plane
resolution is the field of view (FOV) divided by the
acquisition matrix (for example, if you use a 16cm
FOV you will have to use phase and frequency matrices
exceeding 213 to meet this requirement). If you submit
a 5mm-thick knee exam or if it has a resolution greater
than 0.75mm, you will fail the clinical portion of
the review. Be sure to have the physician selecting
the clinical exams verify that all meet or exceed
the ACR requirements.
- Phantom studies represent another common failure
point. The ACR phantom is a plastic cylinder filled
with water, salt, and a bit of nickel chloride, with
“head” and “chin” engraved
on it to ensure proper orientation in the head coil.
A pad will minimize vibration and also help in leveling.
Although many sites report difficulties in leveling,
your physics expert should be able to provide appropriate
advice. ACR offers an excellent guide to phantom
setup and evaluation, invaluable for any technologist
new to the ACR program. It shows what each of the
images should look like and how the ACR reviewer will
examine them. If your images don’t look like
those in the guide you might want to find out why
before sending them in. Your submission must contain
five phantom studies. These are described in MRI_Site_Scanning_Data_Form.pdf
and site_scanning_instructions_phantom.pdf on
the ACR website. The first is a sagittal slice through
the center that is used for head-foot distance accuracy
and for locating the remaining studies. There is an
11-slice T1-weighted series that is used to check
geometric distortion, ghosting, resolution, slice
thickness, landmark accuracy, image intensity uniformity,
and low density contrast detectability. The T2-weighted
ACR series also examines slice thickness, landmark
accuracy, imaging intensity uniformity, and low-density
contrast detectability. ACR also requires applicants
to submit phantom studies using the site’s standard
brain T1- and T2-weighted protocols. These are modified
to use 11 slices of 5mm thickness skip 5mm. Reviewers
also consider these exams for slice thickness, resolution,
and low-density contrast detectability.
- The ACR requires that the clinical exams selected
for review must be dated within plus or minus one
week of the date on which the phantom studies were
done.
- Many 8-channel head coils fail portions of the technical
testing if you do not use image-correction software.
Make sure to employ the normal artifact correction
software provided by your vendor (eg, SCIC, Prescan
Normalize, CLEAR, etc.) that you use on your clinical
exams if your site uses an 8-channel head coil . If
you have any questions about this, discuss it with
your physics expert and your vendor’s applications
specialist.
- Check your work carefully, especially the clinical
exams. Double-check that the clinical exams you are
submitting meet the ACR requirements for resolution
and slice thickness. Examine each of your five phantom
series according to the test criteria using the instructions
detailed in the ACR phantom guide. Questions? Ask
your physics expert, or arrange to have him or her
do this for you. There is scant likelihood your submission
will be rejected if you verify that your clinical
and your phantom studies meet requirements.
- Sell your staff on the importance of QC. Besides
needing it to achieve and maintain accreditation,
a QC program can help spot changes in system performance
before catastrophic failure or substantial loss of
image quality. This can minimize loss of scan time
by alerting service to correct the problem promptly.
Annual testing and QC can identify problems with system
components that may not get regular vendor testing.
Some examples include poorly performing specialty
coils, monitors that do not meet specifications, substandard
magnet homogeneity, geometric distortion, mis-calibrated
laser cameras, and ghosting artifacts.
If you approach the process seriously, it is probable
that you will get a letter from the ACR noting your
successful accreditation for a period of three years.
Plan a party, congratulate your champion for his or
her efforts, and proudly post your new ACR certificate.
But if you receive a notice of failure, take a deep
breath. Read the letter carefully to understand the
reasons accreditation was not granted. This is likely
to be in only one of the two review areas, clinical
or technical. If the failure is due to a clinical issue,
discuss the results with your physicians. If one or
more of your submitted studies do not meet ACR resolution
and/or slice thickness minimums, you will have to change
your protocols, resubmit the new studies, and pay the
extra fee for resubmission. If the failure is due to
the reviewer’s general rejection of your protocols
and your physicians believe your methods are adequate,
appeal the rejection. Have your physicians author a
letter to the ACR explaining why their protocols should
be allowed. A second reviewer can be requested to guarantee
objectivity in the appeal process. If you win your appeal,
you receive accreditation. In the event of a loss, you
have the choice to change your protocols and resubmit.
If the failure was of a technical nature contact your
physics expert. He or she can help explain the reasons
for rejection and assist in a strategy to correct the
problems. If the rejection is due to legitimate problems,
correct them and resubmit (extra fee for resubmission).
If the rejection is not consistent with the information
you have submitted, appeal the findings and ask for
a second review. Have your physics expert assist you
in authoring a letter that points out the reasons why
the rejection does not appear to follow ACR analysis
and why your data supports passing. If the appeal is
granted, toast your success. If it is rejected, rescan
the phantom studies, check your results, and resubmit.
ACR accreditation is granted for a period of three years.
During this time sites are required to conduct weekly
QC, visual checklist, and film densitometry. Annual
performance testing is also mandatory. The records of
these studies must be available at the site in the event
ACR personnel make an unannounced visit, and this does
happen, so be prepared. Work with your physics expert
to ensure your staff members are conducting exams properly
and that they understand the reasons for these efforts.
Teach the attitude that such programs demonstrate your
excellence and will help to find any problems as early
as possible.
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Robert
A. Bell, PhD
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Submit Your Application
Online
ACR offers two mechanisms for first-time
application, the standard paper forms or online. The
online method is very convenient. When you open an
account, you can begin by filling in the information
that you have at the time, and log back in to add
more or edit your entries. There is no cost for either
method until you actually submit the application.
Download and print a copy of the online application
overview to guide you through the collection of required
information.
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by

How
To Hire an MRI Physics Expert
The
job of an MR scientist or MR physicist is to provide
a thorough independent review of your MRI equipment
and to identify issues that may need attention from
service or from staff. Just as you want clinical interpretations
done by a highly experienced reader, look for MRI
experience in your physics expert.
-
How
many MRI units of your vendor and model has the
physicist tested?
-
Can
he or she operate your MRI without assistance from
your technologists? Would you trust your car to
a mechanic who couldn’t drive it? I recognize
that new software versions may necessitate some
initial assistance but this should not take more
than about one hour.
-
If
he or she requires vendor service to be present
for the testing, does the contract specify that
all extra service charges will be paid by the physics
expert? Also, if the physics expert is just rubber-stamping
the vendor’s QC, is it really an independent
evaluation?
-
Does
your physicist’s contract specify testing
all sixteen separate areas that must be addressed
in the annual MRI performance review per the physics
section of the ACR QC Manual? In particular, check
for (1) SNR for each and every specialty coil that
you use clinically (must include model and serial
number for each coil), (2) system homogeneity (describe
method as well as data and note how results compare
to vendor specs), (3) system monitor luminance (the
tester must have a calibrated luminance meter),
and (4) SNR, image intensity uniformity, and ghosting
ratio for all volume specialty coils (should include
description of setup and method as well as raw test
data).
-
Does
your contract specify that the physics expert will
provide suggested action limits for your QC program?
Will the physics expert assess the QC measurements
that you have taken over the past year?
The
ACR has informed me it will reject physics reports
that do not address all of their specified criteria.
Make sure your contract obligates the physics expert
to return and complete any missing tests without additional
charge should ACR reject the report.
After
Accreditation:
QC Goes On
Earning an MRI accreditation from the ACR is not something
that can be shelved for three years The ACR requires
accredited sites to:
-
Maintain a weekly QC program, consisting of three
sections. Results must be recorded and be available
to your physics expert for review during the annual
MRI performance testing. You will also have to demonstrate
compliance with this requirement to become recertified.
-
Perform
weekly phantom studies and assess results against
action limits (only takes about 10 minutes; see
weekly_mri_equip_qc.pdf). Action limits should be
set up initially by your physics expert as a part
of the annual ACR MRI performance testing. Make
sure to list these at the top of your QC form (space
is provided) so weekly measurements can be compared
against them. If the measured value is outside the
action limits you may want to contact service.
-
Perform
weekly reviews of the condition of your MRI system
and environment (see Visual_Checklist.pdf). This
takes about 5 minutes.
-
Print the SMPTE test pattern once a week (if you
print film) and assess optical densities for the
0%, 10%, 40%, and 100% grayscale levels using a
transmission densitometer (see Laser_Control_Chart.pdf).
Those sites participating in the Mammography MSQA
program will be familiar with this testing. If you
do not film at your site, you can opt out of this
requirement by signing an attestation (see Laser_Attestation.pdf).
This may also be possible if you make no films for
patient treatment (e.g., only for legal, etc.)
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Robert Bell, PhD, is president of R.A. Bell and Associates,
in Encinitas, Calif, a consulting company specializing in
MRI science and operations. He welcomes your questions and
comments (858-759-0150).

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