This complimentary CME educational activity is designed for all healthcare providers (HCPs) involved in developing, delivering, consulting, and monitoring care for patients with moderate, moderately severe, and severe AD who are cared for both in the outpatient, assisted living, and skilled nursing facility.
This constituency of HCPs shall include the following audience:
Primary care physicians
Geriatric NPs
PAs
Neurologists
Geriatricians
Geropsychiatrists
Geriatric nurse practitioners
Clinical and consulting pharmacists
Clinical nurses
Case managers
Other clinical providers for AD
Registration
Participation in this iQ&A interactive Medical Intelligence Zone for Alzheimer’s Disese is complimentary, and clinicians are invited to view this CME-certified program and/or share this invitation with other colleagues, departmental staff members, and healthcare professionals.
Grantor Support
Supported by an educational grant from Eisai, Inc.
Accreditation Statement
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 University of Massachusetts Medical School Office of Continuing Medical Education (UMMS-OCME) and CMEducation Resources, LLC. The UMMS-OCME is accredited by the ACCME to provide continuing medical education for physicians.
Credit Designation Statement
The University of Massachusetts Medical School designates this enduring material for a maximum of 4.0 AMA PRA Category 1 Credits(s)™. Physicians should claim only credit commensurate with the extent of their participation in the activity.
Policy on Faculty & Provider Disclosure
It is the policy of the University of Massachusetts Medical School to ensure fair balance, independence, objectivity and scientific rigor in all activities. All faculty participating in CME activities sponsored by the University of Massachusetts Medical School are required to present evidence-based data, identify and reference off-label product use and disclose all relevant financial relationships with those supporting the activity or others whose products or services are discussed. Faculty disclosure will be provided in the activity materials.
Policy on Faculty & Provider Disclosure
It is the policy of the University of Massachusetts Medical School to ensure fair balance, independence, objectivity and scientific rigor in all activities. All faculty participating in CME activities sponsored by the University of Massachusetts Medical School are required to present evidence-based data, identify and reference off-label product use and disclose all relevant financial relationships with those supporting the activity or others whose products or services are discussed. Faculty disclosure will be provided in the activity materials.
Program Faculty and Disclosure
David H. Cribbs, Ph.D.
Professor & Associate Director
Institute for Memory Impairments and Neurological Disorders
Department of Neurology
University of California, Irvine
Irvine, CA
Research Support: Boehringer-Ingelheim
Jeffrey Cummings, MD
Professor of Neurotherapeutics and Drug Development
Cleveland Clinic Lerner College of Medicine
Director, Cleveland Clinic Lou Ruvo Center for Brain Health
Las Vegas, NV
Martin Farlow, MD
Professor of Neurology
Vice-Chairman of Research
Department of Neurology
Indiana University School of Medicine
Indianapolis, IN
Consultant: Accera, Inc.; Adamas Pharmaceuticals, Inc.; Adlyfe Inc.; Astellas Pharma US, Inc.; AstraZeneca Pharmaceuticals LP; CoMentis, Inc.; Eisai Inc.; Eli Lilly and Company; GlaxoSmithKline Inc.; Medivation, Inc.; Merck & Co., Inc.; Novartis Pharmaceuticals Corporation; Noven Pharmaceuticals, Inc.; Octapharma AG; QR Pharma; sanofi-aventis; Schering-Plough Corporation; and Toyama Chemical Co., Ltd.
Grant/Research Support: Bristol-Myers Squibb Company; Elan Corporation, plc; Eli Lilly and Company; Novartis Pharmaceuticals Corporation; Octapharma AG; Pfizer Inc; and Sonexa Therapeutics, Inc.
Speakers Bureau: Eisai Inc.; Forest Pharmaceuticals, Inc.; Pfizer Inc; and Novartis Pharmaceuticals Corporation.
Honoraria: Accera, Inc.; Adamas Pharmaceuticals, Inc.; Adlyfe Inc.; Astellas Pharma US, Inc.; AstraZeneca Pharmaceuticals LP; CoMentis, Inc.; Eisai Inc.; Eli Lilly and Company; Forest Pharmaceuticals, Inc.; GlaxoSmithKline Inc.; Medivation, Inc.; Merck & Co., Inc.; Novartis Pharmaceuticals Corporation; Noven Pharmaceuticals, Inc.; Octapharma AG; Pfizer Inc; QR Pharma; sanofi-aventis; Schering-Plough Corporation; and Toyama Chemical Co., Ltd
Steven H. Ferris, PhD
Friedman Professor and Director
Alzheimer's Disease Center
Center of Excellence on Brain Aging
New York University Langone School of Medicine
New York, NY
Adam S. Fleisher, MD, MAS
Associate Director of Brain Imaging
Banner Alzheimer's Institute
Medical Director, Alzheimer's Disease Cooperative Study
Associate Professor, Department of Neurosciences
University of California, San Diego
Nothing to disclose
James E. Galvin, MD, MPH
Professor of Neurology and Psychiatry
Director of Clinical Operations, Center of Excellence on Brain Aging
Director, Pearl Barlow Center for Memory Evaluation and Treatment
New York University Langone School of Medicine
New York, NY
Clinical Trial Investigator: Novartis, Eli Lilly, Elan, Wyeth, and Bristol-Meyer-Squibb
Consultant: Novartis, Forest, Pfizer, Eisai and Medivation
Irving Gomolin MDCM, FACP, FRCPC
Chief, Division of Geriatric Medicine
Chief, Division of Clinical Pharmacology
Winthrop University Hospital
Mineola, NY
Nothing to disclose
Robert C. Green, MD, MPH
Fellow in Genetics/Professor of Neurology, Genetics, and Epidemiology
Division of Genetics, Department of Medicine
Brigham and Women’s Hospital
Harvard Medical School
Boston, MA
Nothing to disclose
Michael D. Greicius, MD, MPH
Medical Director, Stanford Memory Clinic
Stanford Hospitals & Clinics
Assistant Professor of Neurology
Stanford University School of Medicine
Stanford, CA
Patient Safety Monitoring Panel: Forest
John Olichney, MD
Associate Professor of Neurology
Center for Mind and Brain
UC Davis School of Medicine
Sacramento, CA
Nothing to disclose
Lon Schneider, MD, MS
Professor of Psychiatry, Neurology, and Gerontology
Keck School of Medicine
University of Southern California
Director, California Alzheimer's Disease Center
Do-director, Clinical Core
University of Southern California Alzheimer's Disease Research Center
Los Angeles, CA
Grant funding, contracts, and/or consulting: Lilly, Myriad, Lundbeck, Elan, Johnson and Johnson, Pfizer, Transition.
Thomas Wisniewski MD
Professor of Neurology, Pathology and Psychiatry
New York University School of Medicine
Dept. of Neurology, Psychiatry and Pathology
New York, NY
Nothing to disclose
Program Managers and Web Editor Disclosure Program Manager Gideon Bosker, MD has nothing to disclose.
Program Reviewer Denise Leary has nothing to disclose.
Educational Objectives
Upon completion of this activity, participants will be able to:
Detail the epidemiology and burden of Alzheimer’s disease, with a focus on special considerations and challenges that apply to patients with moderate and severe AD.
Understand the role of dysregulation of cholinergic transmission as one of the key underpinnings for deterioration of cognitive and related symptoms in AD, and the implications for therapeutic interventions based on associated disruptions in neurotransmission.
Stage patients with moderate or severe AD; and, be more skilled at pharmacologic management of patients with advancing disease.
Deploy agents in the current pharmacologic armamentarium for moderate and severe AD, including both those options that stimulate the cholinergic system, and that work through NMDA receptors.
Deploy agents indicated and approved for treatment of moderate and severe AD, what dosage options are available for cholinesterase inhibitors, based on evidence derived from clinical trials demonstrate; and, better understand the relationships among dosage of ChEIs, cognitive improvement, and global function.
Treat patients with moderate, moderately severe, and severe AD based on national guidelines and consensus-based recommendations for managing this patient population.
Manage patients with moderate and severe AD when cholinergic stimulation is deployed as the foundation strategy for management; and better skilled at evaluating dosage options and available formulations in order to select evidence- and trial-based solutions that optimize both cognitive and global function outcomes in patients with AD.
Manage patients in the outpatient, assisted living, and chronic care setting will become better able to apply expert-based guidelines for agents indicated for treatment of moderate or severe AD.
Hardware and Software Requirements:
To participate in this program, viewers must have a PC or Macintosh computer that has active, ongoing internet access for the duration of the program, as well as a compatible Flash-viewer. An email address is required for registration, and a printer is required to print out the CME certificate..
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