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Jointly sponsored by the Duke University School of Medicine and
Healthcare First

Release Date: April 30, 2007
Expiration Date: April 29, 2008
Estimated Time to complete: one (1) hour
This activity is supported by an educational grant from Shire
Pharmaceuticals Inc.

Agenda
Introduction-Moderator
Patient Case #1 "Abuse & Diversion"
Panel Views/Discussion
Final Views- Panelists
Patient Case #2 "Compliance"
Panel Views/Discussion
Final Views- Panelists
Closing-Moderator
Panel
George Bright, MD
David W. Goodman, MD
Andrew A. Nierenberg, MD
Timothy E. Wilens, MD
Peter Salgo, MD-moderator
Statement of Need
Attention deficit hyperactivity disorder (ADHD) is the most prominently
diagnosed and treated psychiatric disorder in children. Estimates
are that approximately 5% of the population are affected with
this disorder and is present in approximately 2 million children
in the US. Historically, clinicians have believed that the occurrence
of ADHD resolves after patients enter adulthood. Therefore, the
diagnosis and treatment of ADHD in adults remains an issue of
considerable concern. However, The National Co-morbidity Survey
actually showed that 4.4% of the adult population (roughly 9
million adults) in the U.S. has ADHD and that only 2 million
adults are treated on a monthly basis. Obviously, there is much
work to do since 7 million adults in the US remain undiagnosed
or untreated.
Despite the overwhelming evidence, the difficulty of diagnosing
and treating patients with ADHD continues and the landscape is
wrought with additional difficulties. In children, issues regarding
parental perceptions, treatments and their side effect profiles,
as well as the presence of comorbid conditions persist. In adults
and adolescents, issues regarding treatments and comorbid conditions
are also inherent. However, adolescents and adults are also plagued
by issues of substance abuse and diversion, compliance, and social
stigmas.
Effective management of ADHD can be greatly enhanced through the
education of clinicians in a Medical Case
Views activity format
featuring expert faculty views on challenging cases involving symptom
recognition, treatment selection, tolerability, and compliance
to provide better patient care.
Learning Objectives
At the conclusion of this activity, participants should be able
to:
- Review the clinical issues inherent with treating children, adults,
and adolescents with ADHD
- Identify the comorbid conditions that must be considered when
treating patients
- Recognize the limitations of commercially available agents for
treating ADHD
- Recognize how patient issues prohibit effective therapy through
the use of case studies
- Develop skills for altering therapeutic approaches for treating
patients with ADHD
Activity Medical Director
Scott H. Kollins, Ph.D.
Associate Professor
Director, Duke ADHD Program
Department of Psychiatry
Duke University Medical Center
Panel
George Bright, MD
Medical Director
Adolescent Health Center
Midlothian, VA
David W. Goodman, MD
Director
Adult Attention Deficit Disorder Center of Maryland;
Assistant Professor
Department of Psychiatry and Behavioral Sciences
Johns Hopkins University School of Medicine;
Director
Suburban Psychiatric Associates, LLC
Baltimore, Maryland
Andrew A. Nierenberg, MD
Medical Director, Bipolar Clinic and Research Program
Associate Director, Depression Clinical and Research Program
Massachusetts General Hospital
Director NIMH Bipolar Trials Network
Associate Professor, Harvard Medical School
Timothy E. Wilens, MD
Associate Professor of Psychiatry
Harvard Medical School;
Director of Substance Abuse Program
Pediatric Psychopharmacology Research Unit
Massachusetts General Hospital
Boston, Massachusetts
Moderator
Peter L. Salgo, MD
National Television Medical Correspondent;
Clinical Professor of Medicine and Anesthesiology
Columbia University College of Physicians and Surgeons
New York, New York
Target Audience
This educational activity is designed for psychiatrists, primary-care
physicians, and other health care professionals treating and
managing ADHD in adults.
Credit Designation
The Duke University School of Medicine designates this educational
activity for a maximum of 1 AMA PRA Category 1 Credit(s)TM. Physicians
should only claim credit commensurate with the extent of their
participation in the activity.
Accreditation
This activity has been planned and implemented in accordance with
the Essential Areas and Policies of the Accreditation Council
for Continuing Medical Education through the joint sponsorship
of the Duke University School of Medicine and Healthcare First.
The Duke University School of Medicine is accredited by the ACCME
to provide continuing medical education for physicians.
Disclosure Summary
The following speakers and/or planning committee members have indicated
they have no relationship(s) with industry to disclose relative
to the content of this CME activity: Peter Salgo, MD
George Bright, MD, receives honoraria as a PI for Cephelon and
Rickets. He receives honoraria as a consultant for Forrest. He
receives honoraria from Shire as a speaker and advisory board member.
David Goodman, MD, receives honoraria as
a PI for Alza/Ortho-McNeil Pharmaceuticals, Cephalon, Johnson & Johnson,
New River Pharmaceuticals and Shire US. He receives honoraria
as a consultant for Alza/Ortho-McNeil Pharmaceuticals, Shire
US. He receives honoraria as a speaker for Alza/Ortho-McNeil
Pharmaceuticals, Forest Laboratories, GlaxoSmithKline, Novartis,
Shire US, and Wyeth.
Scott Kollins, MD, receives grants as a PI for New River Pharmaceuticals,
Pfizer, Psychogenics Inc., Shire US. He receives honoraria as a
consultant for Abbott Laboratories, Athenagen Inc., Eli Lilly and
Company, Shire US. He receives honoraria as an advisory board member
for Cephalon, Shire US.
Andrew Nierenberg, MD, receives honoraria as a PI for Eli Lilly
and Company, Janssen, Pfizer, Wyeth-Ayerst, Forest Laboratories,
Cyberonics Inc., Bristol-Myers Squibb Company, GlaxoSmithKline.
He receives honoraria as a speaker from Eli Lilly and Company,
Janssen, Wyeth-Ayerst, Forest Laboratories, Cyberonics Inc., Bristol-Myers
Squibb Company, GlaxoSmithKline.
Timothy Wilens, MD, receives honoraria as a PI for Abbott Laboratories,
Alza/Ortho-McNeil Pharmaceuticals, Cephalon, Eli Lilly and Company,
Glaxo-SKB, Janssen, NIDA, NIMH, NICMH, NeuroSearch, Novartis, Pfizer,
Saegis Pharmaceuticals, Sanofi-Synthelabo, Shire US; . He receives
honoraria as a consultant for Abbott Laboratories, Alza/Ortho-McNeil
Pharmaceuticals, Cephalon, Eli Lilly and Company, Glaxo-SKB, Janssen,
NeuroSearch, Novartis, Pfizer, Saegis Pharmaceuticals, Sanofi-Synthelabo,
Shire US; He receives honoraria as a speaker Abbott Laboratories,
Alza/Ortho-McNeil Pharmaceuticals, Cephalon, Eli Lilly and Company,
Glaxo-SmithKline, Janssen, NeuroSearch, Novartis, Pfizer, Saegis
Pharmaceuticals, Sanofi-Synthelabo, Shire US.
Disclaimer
The information provided at this CME activity is for continuing
education purposes only and is not meant to substitute for the
independent medical judgment of a physician relative to diagnosis
and treatment options of a specific patient’s medical condition.
How to Receive Credit
To receive credit participates must review the materials on accreditation
information, target audience, learning objectives, and disclosure
information; complete the entire self-assessment and evaluation/claim
form and mail form to: Duke Office of CME
3100 Tower Boulevard, Suite 1300
Durham, NC 27707
Questions about the Video:
Healthcare First
9 Davison Avenue
Jamesburg, NJ 08831
Telephone: 732.521.2213
Questions about CME Credit:
Duke Office of Continuing Medical Education
Telephone: 919.401.1200
Email: cme@mc.duke.edu
Unapproved Use Disclosure
Duke School of Medicine requires CME faculty (speakers) to disclose
to the attendees: 1) when products or procedures being discussed
are off-label, unlabeled, experimental, and/or investigational
(not FDA approved); and 2) any limitations on the information
that is presented, such as data that are preliminary or that
represent ongoing research, interim analyses, and/or unsupported
opinion. Faculty may discuss information about pharmaceutical
agents that is outside of U.S. Food and Drug Administration approved
labeling. This information is intended solely for continuing
medical education and is not intended to promote off-label use
of these medications. If you have questions, contact the medical
affairs department of the manufacturer for the most recent prescribing
information.
Copyright 2007 Duke University School of Medicine
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