Skip to main content

Main menu

  • Home
  • Content
    • Current
    • Ahead of print
    • Past Issues
    • JNM Supplement
    • SNMMI Annual Meeting Abstracts
    • Continuing Education
    • JNM Podcasts
  • Subscriptions
    • Subscribers
    • Institutional and Non-member
    • Rates
    • Journal Claims
    • Corporate & Special Sales
  • Authors
    • Submit to JNM
    • Information for Authors
    • Assignment of Copyright
    • AQARA requirements
  • Info
    • Reviewers
    • Permissions
    • Advertisers
  • About
    • About Us
    • Editorial Board
    • Contact Information
  • More
    • Alerts
    • Feedback
    • Help
    • SNMMI Journals
  • SNMMI
    • JNM
    • JNMT
    • SNMMI Journals
    • SNMMI

User menu

  • Subscribe
  • My alerts
  • Log in
  • Log out
  • My Cart

Search

  • Advanced search
Journal of Nuclear Medicine
  • SNMMI
    • JNM
    • JNMT
    • SNMMI Journals
    • SNMMI
  • Subscribe
  • My alerts
  • Log in
  • Log out
  • My Cart
Journal of Nuclear Medicine

Advanced Search

  • Home
  • Content
    • Current
    • Ahead of print
    • Past Issues
    • JNM Supplement
    • SNMMI Annual Meeting Abstracts
    • Continuing Education
    • JNM Podcasts
  • Subscriptions
    • Subscribers
    • Institutional and Non-member
    • Rates
    • Journal Claims
    • Corporate & Special Sales
  • Authors
    • Submit to JNM
    • Information for Authors
    • Assignment of Copyright
    • AQARA requirements
  • Info
    • Reviewers
    • Permissions
    • Advertisers
  • About
    • About Us
    • Editorial Board
    • Contact Information
  • More
    • Alerts
    • Feedback
    • Help
    • SNMMI Journals
  • View or Listen to JNM Podcast
  • Visit JNM on Facebook
  • Join JNM on LinkedIn
  • Follow JNM on Twitter
  • Subscribe to our RSS feeds
Research ArticlePerspective

Update on Appropriate Use Criteria for Amyloid PET Imaging: Dementia Experts, Mild Cognitive Impairment, and Education

Keith A. Johnson, Satoshi Minoshima, Nicolaas I. Bohnen, Kevin J. Donohoe, Norman L. Foster, Peter Herscovitch, Jason H. Karlawish, Christopher C. Rowe, Saima Hedrick, Virginia Pappas, Maria C. Carrillo and Dean M. Hartley
Journal of Nuclear Medicine July 2013, 54 (7) 1011-1013; DOI: https://doi.org/10.2967/jnumed.113.127068
Keith A. Johnson
1Departments of Radiology and Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Satoshi Minoshima
2Department of Radiology, University of Washington, Seattle, Washington
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Nicolaas I. Bohnen
3Departments of Radiology and Neurology, University of Michigan, and VA Ann Arbor Healthcare System, Ann Arbor, Michigan
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Kevin J. Donohoe
4Beth Israel Deaconess Medical Center, Boston, Massachusetts
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Norman L. Foster
5Department of Neurology, University of Utah, Salt Lake City, Utah
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Peter Herscovitch
6PET Department, NIH Clinical Center, National Institutes of Health, Bethesda, Maryland
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Jason H. Karlawish
7Department of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Christopher C. Rowe
8Department of Nuclear Medicine and Centre for PET, Austin Health, Victoria, Australia
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Saima Hedrick
9Society of Nuclear Medicine and Molecular Imaging, Reston, Virginia; and
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Virginia Pappas
9Society of Nuclear Medicine and Molecular Imaging, Reston, Virginia; and
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Maria C. Carrillo
10Division of Medical and Scientific Relations, Alzheimer’s Association, Chicago, Illinois
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Dean M. Hartley
10Division of Medical and Scientific Relations, Alzheimer’s Association, Chicago, Illinois
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Info & Metrics
  • PDF
Loading

Abstract

Amyloid PET imaging is a novel diagnostic test that can detect in living humans one of the two defining pathologic lesions of Alzheimer disease, amyloid-β deposition in the brain. The Amyloid Imaging Task Force of the Alzheimer’s Association and Society for Nuclear Medicine and Molecular Imaging previously published appropriate use criteria for amyloid PET as an important tool for increasing the certainty of a diagnosis of Alzheimer disease in specific patient populations. Here, the task force further clarifies and expands 3 topics discussed in the original paper: first, defining dementia experts and their use of proper documentation to demonstrate the medical necessity of an amyloid PET scan; second, identifying a specific subset of individuals with mild cognitive impairment for whom an amyloid PET scan is appropriate; and finally, developing educational programs to increase awareness of the amyloid PET appropriate use criteria and providing instructions on how this test should be used in the clinical decision-making process.

  • amyloid PET
  • dementia
  • Alzheimer disease

Amyloid PET imaging is a breakthrough technology that can detect in living humans one of the defining pathologic lesions of Alzheimer disease, amyloid-β deposition in the brain. We, the Amyloid Imaging Task Force of the Alzheimer’s Association and Society for Nuclear Medicine and Molecular Imaging, convened to gather and evaluate published evidence and identify the circumstances under which amyloid PET would have important clinical utility. After nearly a year of evidence review and discussion, we concluded that the appropriate use of amyloid PET is limited to a subset of cognitively impaired patients, and then only under specific circumstances. Our appropriate use criteria (AUC) are described and supported in detail in a published report (1) but state in essence that amyloid PET is appropriately used only by a dementia expert as a single piece of information to support or oppose a clinical diagnosis of Alzheimer disease dementia or predementia in a patient in whom cognitive impairment has been objectively verified, in whom there is substantial uncertainty as to the underlying pathology, and for whom greater diagnostic certainty would change management.

We wish to supplement our recommendations on 3 specific issues as a result of discussions that have taken place since our report was published.

DEMENTIA EXPERTS AND DOCUMENTATION

Dementia Experts

We considered the role of the dementia expert to be critical and decisive to appropriately integrating imaging results with other clinical information. We carefully considered how to practically identify physicians with the requisite expertise. We concluded that clinical training and substantial clinical experience and practice in dementia care should be required. This level of expertise and familiarity is needed because amyloid PET is not a test for dementia or clinical Alzheimer disease but rather is an indicator of underlying pathology, which can be useful only when a particular clinical syndrome has been identified and other explanations have been adequately considered after a proper clinical evaluation. A high level of clinical experience with elderly patients and cognitive impairment is needed for the dementia expert to understand and properly apply the multifaceted consensus clinical criteria that define specific phases of Alzheimer disease dementia and predementia (1–4).

In response to particular interest expressed about our report since it appeared (1), we have reconvened and considered the specifications for a dementia expert in greater detail. There is no universally accepted definition of a dementia expert. Nevertheless, we concluded that a dementia expert for this purpose should be self-identified as a physician trained and board-certified in neurology, psychiatry, or geriatric medicine who devotes a substantial proportion (≥25%) of patient contact time to the evaluation and care of adults with acquired cognitive impairment or dementia, including probable or suspected Alzheimer disease, as confirmed by peer recognition. Physicians particularly likely to have these characteristics are those with fellowship training or board certification in the emerging fields of geriatric psychiatry, geriatric neurology, and behavioral neurology and psychiatry. Although at present these subspecialists are few, the growing elderly population requires a pool of experts with proficiency in the assessment of cognitive impairment and with expertise to properly and selectively integrate imaging technology into clinical decision making. Our definition of a dementia expert is likely to include physicians who can recognize the appropriate subset of patients, refer them to a qualified PET facility, and then apply and communicate the information obtained according to the AUC. The current level of expertise among these clinicians will be enhanced through ongoing educational programs that the Alzheimer’s Association, the Society of Nuclear Medicine and Molecular Imaging (SNMMI), and other professional organizations have already implemented.

We recognized, on the one hand, that because of the current shortage of dementia experts, the overall availability of amyloid PET will likely be narrow. On the other hand, the AUC indicate that amyloid PET is relevant only in a subset of cognitively impaired individuals in whom diagnosis remains uncertain after a complete evaluation. This is the subset of patients who are already likely to be referred to a dementia expert. Most initial work-up and management of suspected dementia is now in the hands of primary care providers and will undoubtedly remain there. However, this activity represents only a small fraction of a typical primary provider’s practice; consequently, these providers often lack the experience or motivation to develop expertise in evaluating atypical and uncertain cases relevant to amyloid PET. For the appropriate use of amyloid PET, the expertise of the provider ordering the study and using the results to guide patient care is as critical as the technical quality and interpretation of the PET data. Dementia experts recognize that amyloid PET data must be carefully integrated with clinical data from detailed cognitive assessment and knowledgeable informant reporting. To the extent that proficiency with these integrative skills is not available in primary care practices, the inappropriate use of amyloid PET will be more likely to occur.

We concluded that the number of dementia experts would increase to serve the demand for amyloid PET referral if indeed amyloid PET can enable more effective management. We expect that interest in developing the requisite expertise will occur naturally as the technology is used in practice over time. Thus, we concluded that any initial constraint on amyloid PET due to the limited availability of the dementia expert will gradually resolve and that requiring a dementia expert to order the scan is justified now to maximize the potential that it will be used only under appropriate circumstances. After the medical community acquires greater experience in using amyloid PET, and training and expertise in cognitive evaluations increase, these limitations might be reconsidered.

Documentation for Amyloid PET

We developed a checklist to ensure appropriate use of amyloid PET, to standardize referral by dementia experts, and to ensure that patients considered for this study have undergone a standard clinical evaluation and treatment of comorbidities before the scan is ordered. The dementia expert should collect and share with the PET physician the following information, which should be maintained in the patient medical record for extraction and review:

  • □ Age and date of onset of symptoms;

  • □ Identification of clinical syndrome (mild cognitive impairment, or MCI; dementia);

  • □ Clinical evidence of persistent or progressive cognitive decline;

  • □ Structured objective assessment of mental status such as the Mini-Mental State Examination, Montreal Cognitive Assessment, or a similar measure;

  • □ Known comorbidities;

  • □ List of prescribed medications and rationale for use of psychoactive medications, if any;

  • □ Results of neuropsychologic testing performed;

  • □ Results of structural brain imaging (such as MR imaging or CT) performed;

  • □ Relevant laboratory tests, which should include complete blood count, chemistry profile, B12, and thyroid hormone;

  • □ Reasons that the cause of cognitive impairment remains uncertain after completion of a standard clinical evaluation and treatment of comorbidities;

  • □ Treatment and care plan based on amyloid PET findings.

We recommend that the dementia expert and PET physician be required to document this information in the medical record of each patient. Third-party payers should consider this information fully sufficient to demonstrate the medical necessity of amyloid PET, and this information could be submitted to payers on request. This information also could be the basis for sponsorship of a voluntary registry for independent assessment of appropriate use and for targeting of educational efforts.

MCI

The recent SNMMI/Alzheimer’s Association AUC emphasize that amyloid PET for patients with persistent or progressive unexplained MCI may be appropriate under limited and specific circumstances. These guidelines emphasize that “not all patients with MCI would be appropriate for amyloid PET. Rather, amyloid PET would be appropriate only in those [MCI] individuals who the dementia expert has concluded would benefit from greater certainty of the underlying pathology and whose clinical management would change as a result of this greater certainty” (1). The above checklist will be applied to this patient group for the purpose of limiting referrals for amyloid PET to appropriate patients. Amyloid PET is indicated only for those who, according to the dementia expert, carry a diagnosis of MCI that conforms to established consensus criteria as discussed above (indication 1 in the AUC document (1–4)). We considered that the scope of use of amyloid PET would be substantially limited by 2 prerequisites imposed by the AUC, the requirement for etiologic uncertainty and the requirement for a change in patient management.

Etiologic Uncertainty

Sources of etiologic uncertainty—which may arise in any patient being evaluated for MCI or Alzheimer disease dementia—are well known to the dementia expert. They are typically clinical issues that can be evaluated with established methods and usually do not ultimately interfere with proper diagnosis and management. For example, uncertainty may arise when the clinical onset of the syndrome is atypical or sudden, when the illness may be etiologically mixed because of vascular pathology or evidence of possible Lewy pathology, or when potentially confounding circumstances are involved, such as depression, substance abuse, medication effects, and cardiovascular, endocrine, or other medical disorders. Occasionally, however, the dementia expert is confronted by complexities such as these and cannot determine the likelihood that amyloid-β pathology is ultimately responsible for the impairment. In these relatively unusual but important cases, substantial uncertainty then remains as to the cause of the syndrome, and further patient care is severely constrained or compromised. The treating physician must then adopt a wait-and-see approach that is unsatisfying, potentially misguided, at times wasteful, and potentially harmful.

Change in Patient Management

Because disease-modifying treatments for Alzheimer disease have not yet been established, the dementia expert is stymied by a limited range of management alternatives. Nevertheless, important choices are made by the treating physician, the patient, and caregivers on the basis of the presence or absence of detectable amyloid-β. Once the cause of deficits is properly assessed, a more confident diagnosis frequently helps anticipate future needs, including closer monitoring for progression and safety, periodic functional assessments for retirement planning, and allocation of financial and family resources. For management decisions such as these, we concluded that amyloid PET could be appropriately used “when knowledge of the presence or absence of [amyloid-β] pathology is expected to increase diagnostic certainty and alter management” (1).

EDUCATION

We are committed to assisting professional organizations in creating educational materials to ensure appropriate use of amyloid PET, in increasing awareness of the criteria among physicians and patients, and in providing instructions on how to incorporate amyloid PET findings into clinical decision making. To ensure appropriate use of amyloid PET, several educational activities are currently ongoing through the Alzheimer’s Association and the SNMMI.

National Meetings

The SNMMI has established a session devoted to amyloid PET and related technology at its annual mid-winter meetings. In addition, the SNMMI added several sessions, including a “Read with the Expert” session for amyloid PET, to its 2013 annual meeting in Vancouver and will be doing the same at subsequent annual meetings.

Local Meetings

The SNMMI continues to organize numerous regional meetings to provide information on amyloid PET for both physicians and technologists.

Educational Materials

The SNMMI is developing educational materials for Maintenance of Certificate modules for physicians. The SNMMI in collaboration with the European Association of Nuclear Medicine is developing a procedure guideline to ensure high-quality imaging techniques for amyloid PET. The Alzheimer’s Association is developing educational materials that will be shared with the organization’s national distribution of chapters for guiding patients, caregivers, and physicians on seeking a dementia specialist and the appropriate uses of amyloid PET.

Educational Outreach

The Outreach Committee at the SNMMI has organized sessions at professional societies advocating appropriate use of amyloid PET. Such a session will be included at the 2013 annual meetings of the American Academy of Neurology and the American Association of Geriatric Psychiatry. Similar sessions are planned for the annual meetings of the American Academy of Family Physicians and the American Psychiatric Association. An online education program is being developed to include didactic materials for neurologists, geriatricians, and psychiatrists. The Alzheimer’s Association has developed talking points that are used in nationwide presentations to patients, caregivers, and physicians to educate these individuals on the appropriate uses of amyloid PET. These outreach efforts will continue to ensure appropriate use of amyloid PET for the patients who most benefit from this imaging procedure.

DISCLOSURE

No potential conflict of interest relevant to this article was reported.

Footnotes

  • Published online Jun. 10, 2013.

  • This article is being published jointly in The Journal of Nuclear Medicine and Alzheimer’s & Dementia.

  • © 2013 by the Society of Nuclear Medicine and Molecular Imaging, Inc.

REFERENCES

  1. 1.↵
    1. Johnson KA,
    2. Minoshima S,
    3. Bohnen NI,
    4. et al
    . Appropriate use criteria for amyloid PET: a report of the Amyloid Imaging Task Force, the Society of Nuclear Medicine and Molecular Imaging, and the Alzheimer’s Association. Dual publication in: Alzheimers Dement. 2013;9:e-1-16 and J Nucl Med. 2013;54:476–490.
  2. 2.
    1. McKhann GM,
    2. Knopman DS,
    3. Chertkow H,
    4. et al
    . The diagnosis of dementia due to Alzheimer’s disease: recommendations from the National Institute on Aging–Alzheimer’s Association workgroups on diagnostic guidelines for Alzheimer’s disease. Alzheimers Dement. 2011;7:263–269.
    OpenUrlCrossRefPubMed
  3. 3.
    1. Albert MS,
    2. DeKosky ST,
    3. Dickson D,
    4. et al
    . The diagnosis of mild cognitive impairment due to Alzheimer’s disease: recommendations from the National Institute on Aging–Alzheimer’s Association workgroups on diagnostic guidelines for Alzheimer’s disease. Alzheimers Dement. 2011;7:270–279.
    OpenUrlCrossRefPubMed
  4. 4.↵
    1. Dubois B,
    2. Feldman HH,
    3. Jacova C,
    4. et al
    . Revising the definition of Alzheimer’s disease: a new lexicon. Lancet Neurol. 2010;9:1118–1127.
    OpenUrlCrossRefPubMed
  • Received for publication May 31, 2013.
  • Accepted for publication May 31, 2013.
PreviousNext
Back to top

In this issue

Journal of Nuclear Medicine: 54 (7)
Journal of Nuclear Medicine
Vol. 54, Issue 7
July 1, 2013
  • Table of Contents
  • Table of Contents (PDF)
  • About the Cover
  • Index by author
Print
Download PDF
Article Alerts
Sign In to Email Alerts with your Email Address
Email Article

Thank you for your interest in spreading the word on Journal of Nuclear Medicine.

NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address.

Enter multiple addresses on separate lines or separate them with commas.
Update on Appropriate Use Criteria for Amyloid PET Imaging: Dementia Experts, Mild Cognitive Impairment, and Education
(Your Name) has sent you a message from Journal of Nuclear Medicine
(Your Name) thought you would like to see the Journal of Nuclear Medicine web site.
Citation Tools
Update on Appropriate Use Criteria for Amyloid PET Imaging: Dementia Experts, Mild Cognitive Impairment, and Education
Keith A. Johnson, Satoshi Minoshima, Nicolaas I. Bohnen, Kevin J. Donohoe, Norman L. Foster, Peter Herscovitch, Jason H. Karlawish, Christopher C. Rowe, Saima Hedrick, Virginia Pappas, Maria C. Carrillo, Dean M. Hartley
Journal of Nuclear Medicine Jul 2013, 54 (7) 1011-1013; DOI: 10.2967/jnumed.113.127068

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Share
Update on Appropriate Use Criteria for Amyloid PET Imaging: Dementia Experts, Mild Cognitive Impairment, and Education
Keith A. Johnson, Satoshi Minoshima, Nicolaas I. Bohnen, Kevin J. Donohoe, Norman L. Foster, Peter Herscovitch, Jason H. Karlawish, Christopher C. Rowe, Saima Hedrick, Virginia Pappas, Maria C. Carrillo, Dean M. Hartley
Journal of Nuclear Medicine Jul 2013, 54 (7) 1011-1013; DOI: 10.2967/jnumed.113.127068
Twitter logo Facebook logo LinkedIn logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One
Bookmark this article

Jump to section

  • Article
    • Abstract
    • DEMENTIA EXPERTS AND DOCUMENTATION
    • MCI
    • EDUCATION
    • DISCLOSURE
    • Footnotes
    • REFERENCES
  • Info & Metrics
  • PDF

Related Articles

  • This Month in JNM
  • PubMed
  • Google Scholar

Cited By...

  • Updated Appropriate Use Criteria for Amyloid and Tau PET: A Report from the Alzheimers Association and Society for Nuclear Medicine and Molecular Imaging Workgroup
  • Concordance between amyloid-PET quantification and real-world visual reads: results from IDEAS
  • The RSNA QIBA Profile for Amyloid PET as an Imaging Biomarker for Cerebral Amyloid Quantification
  • First Tau PET Tracer Approved: Toward Accurate In Vivo Diagnosis of Alzheimer Disease
  • Clinical Use and Utility of Amyloid Imaging
  • SNMMI Procedure Standard/EANM Practice Guideline for Amyloid PET Imaging of the Brain 1.0
  • Google Scholar

Similar Articles

Keywords

  • amyloid PET
  • dementia
  • Alzheimer disease
SNMMI

© 2025 SNMMI

Powered by HighWire