Acr Practice Parameter For Contrast Mri Breast
Acr Practice Parameter For Contrast Mri Breast
and clinical
medical physicists in the United States. The College is a nonprofit professional society whose primary purposes are to advance the science of radiology,
improve radiologic services to the patient, study the socioeconomic aspects of the practice of radiology, and encourage continuing education for
radiologists, radiation oncologists, medical physicists, and persons practicing in allied professional fields.
The American College of Radiology will periodically define new practice parameters and technical standards for radiologic practice to help advance the
science of radiology and to improve the quality of service to patients throughout the United States. Existing practice parameters and technical standards
will be reviewed for revision or renewal, as appropriate, on their fifth anniversary or sooner, if indicated.
Each practice parameter and technical standard, representing a policy statement by the College, has undergone a thorough consensus process in which it has
been subjected to extensive review and approval. The practice parameters and technical standards recognize that the safe and effective use of diagnostic
and therapeutic radiology requires specific training, skills, and techniques, as described in each document. Reproduction or modification of the published
practice parameter and technical standard by those entities not providing these services is not authorized.
This document is an educational tool designed to assist practitioners in providing appropriate radiologic care for
patients. Practice Parameters and Technical Standards are not inflexible rules or requirements of practice and are
not intended, nor should they be used, to establish a legal standard of care1. For these reasons and those set forth
below, the American College of Radiology and our collaborating medical specialty societies caution against the
use of these documents in litigation in which the clinical decisions of a practitioner are called into question.
The ultimate judgment regarding the propriety of any specific procedure or course of action must be made by the
practitioner in light of all the circumstances presented. Thus, an approach that differs from the guidance in this
document, standing alone, does not necessarily imply that the approach was below the standard of care. To the
contrary, a conscientious practitioner may responsibly adopt a course of action different from that set forth in this
document when, in the reasonable judgment of the practitioner, such course of action is indicated by the condition
of the patient, limitations of available resources, or advances in knowledge or technology subsequent to
publication of this document. However, a practitioner who employs an approach substantially different from the
guidance in this document is advised to document in the patient record information sufficient to explain the
approach taken.
The practice of medicine involves not only the science, but also the art of dealing with the prevention, diagnosis,
alleviation, and treatment of disease. The variety and complexity of human conditions make it impossible to
always reach the most appropriate diagnosis or to predict with certainty a particular response to treatment.
Therefore, it should be recognized that adherence to the guidance in this document will not assure an accurate
diagnosis or a successful outcome. All that should be expected is that the practitioner will follow a reasonable
course of action based on current knowledge, available resources, and the needs of the patient to deliver effective
and safe medical care. The sole purpose of this document is to assist practitioners in achieving this objective.
1 Iowa Medical Society and Iowa Society of Anesthesiologists v. Iowa Board of Nursing, ___ N.W.2d ___ (Iowa 2013) Iowa Supreme Court refuses to find
that the ACR Technical Standard for Management of the Use of Radiation in Fluoroscopic Procedures (Revised 2008) sets a national standard for who may
perform fluoroscopic procedures in light of the standard’s stated purpose that ACR standards are educational tools and not intended to establish a legal
standard of care. See also, Stanley v. McCarver, 63 P.3d 1076 (Ariz. App. 2003) where in a concurring opinion the Court stated that “published standards or
guidelines of specialty medical organizations are useful in determining the duty owed or the standard of care applicable in a given situation” even though
ACR standards themselves do not establish the standard of care.
Magnetic resonance imaging (MRI) of the breast is a useful tool for the detection and characterization of breast
disease, assessment of local disease extent, evaluation of treatment response, and guidance for biopsy and
localization. MRI findings should be correlated with clinical history, physical examination findings, and the
results of mammography and any other prior breast imaging.
A. Current indications for breast MRI include, but are not limited to, the following:
1. Screening
a. High-risk patients – Clinical trials from the United States and Europe have demonstrated that
breast MRI can significantly improve the detection of cancer that is otherwise clinically,
mammographically, and sonographically occult [1-12]. Breast MRI is indicated in the
surveillance of women with greater than or equal to 20% lifetime risk of breast cancer (for
example, individuals with genetic predisposition to breast cancer as determined by either
gene testing or family pedigree, or individuals with a history of mantle radiation for Hodgkin
lymphoma ) [13]. High-risk patients may be referred for annual screening breast MRI in
addition to mammography, preferably after risk assessment and counseling either by
personnel trained in the assessment of hereditary breast cancer or by a referring physician
who has used a breast cancer risk assessment model. Although there is no direct evidence
that MRI reduces mortality, supplementing annual screening with MRI facilitates early
disease detection in high-risk patients [13].
c. Bilateral breast MRI for patients with a newly diagnosed breast malignancy can detect occult
malignancy in the contralateral breast in at least 3% to 5% of patients [15-20].Contralateral breast
MRI screening in the newly diagnosed cancer patient may reduce the incidence of metachronous
contralateral cancer [21].
d. For patients with breast augmentation While the integrity of silicone implants can be
determined by noncontrast breast MRI, the use of contrast may be indicated in the evaluation
of patients with silicone or saline implants and/or free injections with silicone, paraffin, or
polyacrylamide gel in whom mammography is difficult. Additionally, patients who have
undergone implant reconstruction following lumpectomy or mastectomy for breast cancer
may benefit from contrast-enhanced breast MRI screening (see 3a).
2. Extent of disease
a. Invasive carcinoma and ductal carcinoma in situ (DCIS) – Breast MRI may be useful to determine the
extent of disease and the presence of multifocality and multicentricity in patients with invasive
carcinoma and DCIS. Multiple clinical trials in the United States and Europe show that, on average,
MRI can detect occult disease in the ipsilateral breast (containing the index malignancy) in
approximately 15% of patients, with ranges reported from 12% to 27% and disease in the
contralateral breast in 4 3% to 5% of patients [15,16,22-29]. MRI determines disease extent more
accurately than mammography and physical examination in many patients. It remains to be shown
b. Invasion deep to fascia – MRI evaluation of breast carcinoma prior to surgical treatment may be
useful in both mastectomy and breast conservation candidates to define the relationship of the tumor
to the muscular fascia and identify any extension into the pectoralis major, serratus anterior, and/or
intercostal muscles [30,31].
c. Postlumpectomy with positive margins – Breast MRI may be useful for subsequent surgical planning
to identify occult multicentric or multifocal malignancy in the evaluation of patients whose
pathology specimens demonstrate close or positive margins [32].
d. Neoadjuvant chemotherapy – Breast MRI may be useful before, during, and/or after chemotherapy to
evaluate treatment response and the extent of residual disease prior to surgical treatment. If used for
this purpose, a pretreatment MRI is recommended [33-35] to facilitate assessment of
subsequent treatment response. MRI-compatible localization tissue markers should be placed prior to
neoadjuvant chemotherapy to indicate the location of the tumor in the event of complete response
[36,37].
a. Recurrence of breast cancer – Breast MRI may be useful in women with a prior history of breast
cancer and suspected recurrence when clinical, mammographic, and/or sonographic findings are
inconclusive [38].
b. Metastatic cancer when the primary is unknown and suspected to be of breast origin – MRI may be
useful in patients presenting with axillary or distant metastatic disease and no mammographic or
physical findings of primary breast carcinoma. Clinical trials demonstrate that breast MRI can locate
the primary tumor in over half of women presenting with metastatic axillary lymph adenopathy of
occult breast origin [39-42].
c. Lesion characterization – In rare cases, breast MRI may be indicated when other diagnostic imaging
examinations, such as ultrasound and mammography (with or without tomosynthesis), and physical
examination are inconclusive for the presence of breast cancer and biopsy cannot be performed (eg,
possible architectural distortion on only one mammographic view without a sonographic correlate)
[43-49]. MRI may also considered when the clinical suspicion is very high and mammography and
ultrasound are normal, such as bloody nipple discharge [50]. MRI should not precede or replace
diagnostic mammography and ultrasound to evaluate clinical signs or symptoms in the breast or to
evaluate lesions identified on screening mammography.
d. Postoperative tissue reconstruction – Breast MRI may be useful in the evaluation of suspected cancer
recurrence in patients with tissue transfer flaps. Breast MRI may also be helpful in differentiating
between recurrence and fat necrosis in patients with a history of breast cancer who have undergone
autologous fat grafting.
e. MRI-guided biopsy – MRI is indicated for guidance of interventional procedures such as vacuum-
assisted biopsy and preoperative wire localization for lesions that are occult on mammography or
sonography and demonstrable only with MRI.
B. Other Considerations
Routine screening breast MRI currently is not recommended for asymptomatic, average-risk women.
Breast MRI may yield findings that are not evident clinically or on mammography or ultrasound. The
findings may or may not be clinically significant. As with mammography or any other test, false-positive
results can be expected. The additional abnormalities detected on MRI may result in a follow-up
examination or recommendation for biopsy. Published results for MRI-directed biopsy are similar to
those for mammography [51,52].
3. Treatment planning
MRI findings in breast cancer patients may change their planned treatment. Caution should be exercised
in altering management based on MRI findings alone without biopsy confirmation. Additional biopsies
and/or correlation with other clinical and imaging information should be used together with clinical
judgment. There currently is no evidence that identification of additional ipsilateral or contralateral occult
malignancies improves patient outcomes.
MRI should not supplant careful problem-solving mammographic views or ultrasound in the diagnostic
setting. Because MRI will miss some cancers that mammography will detect, it should not be used as a
substitute for screening mammography. MRI should not be used in lieu of biopsy of a suspicious finding
identifiable by mammography, ultrasound, or clinical examination.
Recent preliminary studies have reported shortened or abbreviated MRI protocols to have similar
sensitivities and specificities compared to a full MRI protocol [53-57]. Such shortened MRI protocols
could make contrast-enhanced MRI more cost effective as a screening tool.
See the ACR Practice Parameter for Performing and Interpreting Magnetic Resonance Imaging (MRI), the ACR
Manual on Contrast Media, and the ACR Guidance Document on MR Safe Practices [57-60].
See the ACR Practice Parameter for Performing and Interpreting Magnetic Resonance Imaging (MRI) [59].
In addition, interpreting physicians should have knowledge and expertise in breast disease and breast imaging
diagnosis. Facilities performing breast MRI should have the capacity to perform mammographic correlation,
directed breast ultrasound, and MRI-guided intervention or create a referral arrangement with a cooperating
facility that can provide these services. If MRI-guided breast biopsy is performed, histopathologic results should
be available to the interpreting physician as well as the procedural physician.
Patients should undergo standard mammography in addition to breast MRI (unless patient consideration precludes
X-ray imaging), and the mammographic study images and report should be available for review. Additionally, an
attempt should be made to obtain prior breast MRI studies for comparison. If the patient has had recent
biopsy(ies) and/or excisional surgery, the histopathologic results should also be available for review.
The written or electronic request for MRI of the breast should provide sufficient information to demonstrate the
medical necessity of the examination and allow for its proper performance and interpretation.
The request for the examination must be originated by a physician or other appropriately licensed health care
provider. The accompanying clinical information should be provided by a physician or other appropriately
licensed health care provider familiar with the patient’s clinical problem or question and consistent with the stated
scope of practice requirements. (ACR Resolution 35, adopted in 2006 – revised in 2016, Resolution 12-b)
The physician responsible for the breast MRI should supervise patient selection and preparation. Patients should
be interviewed and screened for possible contraindications for MRI as discussed in section III. Patients suffering
from anxiety or claustrophobia may require sedation or additional assistance. Administration of anxiolysis or
moderate sedation may be needed to achieve a successful examination (see the ACR–SIR Practice Parameter for
Sedation/Analgesia) [63]. A recovery area is necessary, and appropriate personnel must be available to monitor
the patient following sedation. Sedation must be administered in accordance with institutional policy and state and
federal law by a physician or by a nurse with training in cardiopulmonary resuscitation.
Increased parenchymal enhancement has been observed normally during the secretory phase of the menstrual
cycle. This normal enhancement may give rise to false positive and false negative MRI scans. It is therefore
recommended that breast MRI scans be performed during the second week of the menstrual cycle for patients
undergoing screening examinations. This may not be warranted for women undergoing evaluation for breast
cancer treatment planning.
B. Facility Requirements
Appropriate emergency equipment with medications must be immediately available to treat adverse reactions
associated with administered medications. The equipment and medications should be monitored for inventory and
drug expiration dates on a regular basis. The equipment, medications, and other emergency support must also be
appropriate for the range of ages and sizes in the patient population.
VI. DOCUMENTATION
Reporting should be in accordance with the ACR Practice Parameter for Communication of Diagnostic Imaging
Findings [64]. The report should follow the guidelines for terminology, including descriptions of lesion features
and location, as published in the ACR BI-RADS® Lexicon for Breast MRI. Analysis of abnormalities on breast
MRI ought to consider both morphologic and kinetic features of the abnormality. The BI-RADS assessment
category should be included in the conclusion of the report [65].
The MRI equipment specifications and performance must meet all state and federal requirements. The
requirements include, but are not limited to, specifications of maximum static magnetic field strength, maximum
rate of change of magnetic field strength (dB/dT), maximum radiofrequency power deposition (specific
absorption rate), and maximum acoustic noise levels [65,66].
Technical Guidelines
1. Resolution, contrast, and field strength – The selection of field strength is a major technical decision. A
1.5T magnet has traditionally been considered a minimum technical recommendation because of the
relationship between field strength and resolution. However, improvements in other components of the
scanning process have resulted in improved scan quality at lower field strengths. High spatial and temporal
2. Scan time – A precontrast scan is obtained. Scan time in relation to contrast injection is extremely
important for lesion characterization. Kinetic information should be reported and based on enhancement
data determined at specified intervals separated by 4 minutes or less. Imaging sites should have
adequately short temporal resolution for accurate capture of lesion kinetics. Computer-aided detection
(CAD) software is commonly used at image interpretation to manage large datasets and highlight kinetic
information.
3. Contrast – Gadolinium contrast enhancement is required for the evaluation of breast parenchyma but is
not necessary in the evaluation of implant integrity in asymptomatic average-risk patients. Gadolinium
contrast should be administered as a bolus with a standard dose of 0.1 mmol/kg followed by a saline flush
of at least 10 ml.
4. Scan time – A precontrast scan is obtained. Scan time in relation to contrast injection is extremely
important for lesion characterization. Kinetic information should be reported and based on enhancement
data determined at specified intervals separated by 4 minutes or less. Imaging sites should have
adequately short temporal resolution for accurate capture of lesion kinetics. Computer-aided detection
(CAD) software is commonly used at image interpretation to manage large datasets and highlight kinetic
information.
Policies and procedures related to quality, patient education, infection control, and safety should be developed and
implemented in accordance with the ACR Policy on Quality Control and Improvement, Safety, Infection Control,
and Patient Education appearing under the heading Position Statement on QC & Improvement, Safety, Infection
Control, and Patient Education on the ACR website (https://www.acr.org/Clinical-Resources/Practice-
Parameters-and-Technical-Standards).
Equipment monitoring should be in accordance with the ACR–AAPM Technical Standard for Diagnostic Medical
Physics Performance Monitoring of Magnetic Resonance Imaging (MRI) Equipment, including testing of the
breast coil(s) by a Qualified Medical Physicist or Qualified Medical Scientist [67].
Examinations should be systematically reviewed and evaluated as part of the overall quality improvement
program at the facility. Monitoring should evaluate the accuracy of interpretation as well as the appropriateness of
indications for the examinations. Complications and adverse events or activities that may have the potential for
sentinel events must be monitored, analyzed, reported, and periodically reviewed to identify opportunities to
improve patient care. These data should be collected in a manner that complies with statutory and regulatory peer-
review procedures in order to ensure the confidentiality of the peer-review process.
ACKNOWLEDGEMENTS
This practice parameter was revised according to the process described under the heading The Process for
Developing ACR Practice Parameters and Technical Standards on the ACR website
(https://www.acr.org/Clinical-Resources/Practice-Parameters-and-Technical-Standards) by the Committee
Practice Parameters – Breast Imaging of the ACR Commission on Breast Imaging.
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*Practice parameters and technical standards are published annually with an effective date of October 1 in the
year in which amended, revised, or approved by the ACR Council. For practice parameters and technical
standards published before 1999, the effective date was January 1 following the year in which the practice
parameter or technical standard was amended, revised, or approved by the ACR Council.