Primary (AL) Amyloidosis in Plasma Cell Disorders
TEST_code
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CME Activity Information |
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Release Date: |
July 31, 2006 |
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Most Recent Review: |
July 31, 2006* |
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Most Recent Update: |
July 31, 2006 |
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Date Credit Expires: |
July 31, 2008 |
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Time to Complete: |
1 hour |
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Medium: |
Internet Online |
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*Click here
to learn more about our review process. |
Instructions for Participation
- Read the following information before beginning the educational activity
and click the "Take this course" link at the bottom of the page
- Study the educational activity
- Complete the CME quiz and evaluation
- After successful completion of the CME quiz and evaluation, you will receive
the credit or participation certificate
*The CME quiz and evaluation must be completed by July 31, 2008, in order
to receive the credit or participation certificate.
Target Audience
Physicians who wish to advance their current knowledge of clinical cancer medicine
regarding lymphomas and are involved in providing patient care in a cancer care
environment.
Learning Objectives
After completing this course, the reader should be able to:
- Describe the pathogenesis of AL amyloidosis.
- Identify other disorders often associated with AL amyloidosis.
- Discuss the importance of the prompt diagnosis and treatment of AL amyloidosis
and any underlying plasma cell disorder.
- Identify presenting signs and symptoms that should lead to the suspicion
of AL amyloidosis.
Accreditation and Credit Designation
This activity has been planned and implemented in accordance
with the Essential Areas and policies of the Accreditation Council for Continuing
Medical Education (ACCME) through the joint sponsorship of the National Institutes
of Health Foundation for Advance Education in the Sciences (NIH/FAES) and The
Oncologist. The NIH/FAES is accredited by the ACCME to provide continuing
medical education for physicians.
The NIH/FAES designates this educational activity for a maximum of 1.00 AMA
PRA Category 1 Credit™. Physicians should only claim credit commensurate
with the extent of their participation in the activity.
Disclosure Policy
In compliance with the Standards of the ACCME, it is the policy of the NIH/FAES
to ensure balance, independence, objectivity, and scientific rigor in all of its
educational activities and to include information free of commercial bias and
based on the best evidence available. All individuals in a position to influence
the content of this activity have disclosed relevant financial interests or relationships
of their own, their spouse/partner, or their worksite, with manufacturers or providers
of commercial products, services, technology, or programs; and disclosed relationships
with current non-governmental supporters of the activity. The faculty and planners
have indicated that they have no relevant commercial relationships. For a list
of the faculty and planners, please visit the Editorial Board online at http://cme.theoncologist.com/misc/edboard.shtml.
All information is submitted and reviewed and found to be scientifically rigorous,
based on the best available evidence, fair and balanced, and free of commercial
bias. All the recommendations involving clinical medicine in this CME activity
are based on evidence that is accepted within the profession of medicine as
adequate justification for their indications and contraindications in the care
of patients. All scientific research referred to, reported or used in CME in
support or justification of a patient care recommendation conforms to the generally
accepted standards of experimental design, data collection and analysis.
Any potential conflicts of interests are resolved via The Oncologist's
anonymous peer review process: http://theoncologist.alphamedpress.org/misc/ifora.shtml.
All manuscripts are reviewed by the Editorial Board with ad hoc assistance from
two or more external experts in the field. All final publication decisions are
made by the Editorial Board. The acceptance of a manuscript is based on its
originality and importance to the field as assessed by the Editors.
Author Disclosure(s)
Antonia M. S. Müller, M.D.
Credentials: Department of Hematology/Oncology, University
Medical Center Freiburg, Freiburg, Germany.
Disclosures: The author has indicated no relevant commercial
relationships.
Annette Geibel, M.D.
Credentials: Department of Cardiology/Angiology, University
Medical Center Freiburg, Freiburg, Germany.
Disclosures: The author has indicated no relevant commercial
relationships.
Hartmut P. H. Neumann, M.D.
Credentials: Department of Nephrology, University Medical
Center Freiburg, Freiburg, Germany.
Disclosures: The author has indicated no relevant commercial
relationships.
Alexander Kühnemund, M.D.
Credentials: Department of Hematology/Oncology, University
Medical Center Freiburg, Freiburg, Germany.
Disclosures: The author has indicated no relevant commercial
relationships.
Annette Schmitt-Gräff, M.D.
Credentials: Pathology Department, University Medical Center
Freiburg, Freiburg, Germany.
Disclosures: The author has indicated no relevant commercial
relationships.
Joachim Böhm, M.D.
Credentials: Pathology Department, University Medical Center
Freiburg, Freiburg, Germany.
Disclosures: The author has indicated no relevant commercial
relationships.
Monika Engelhardt, M.D.
Credentials: Department of Hematology/Oncology, University
Medical Center Freiburg, Freiburg, Germany. Telephone: 49-761-270-3401;
Fax: 49-761-270-3318; E-mail: mgrossbard{at}chpnet.org.
Disclosures: The author has indicated no relevant commercial
relationships.
Commercial Support
Non-governmental supporters of this activity: AstraZeneca, Bristol-Myers
Squibb Oncology, and sanofi-aventis
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