Amy Visit 2: A 16-Year-Old Girl With Depression and Hypersomnia
| Title: | Amy Visit 2: A 16-Year-Old Girl With Depression and Hypersomnia |
| Topic: | Psychiatry |
| Relevant Terms: | Adolescent, Major Depressive Disorder, Mood Disorders |
| Primary Audience: | Family Physicians, Pediatricians, Psychiatrists |
| Launch Date: | 26-May-11 |
| Credits: | 0.5 AMA PRA Category 1 Credit™ |
| Expiration Date: | The accreditation for this activity has expired. |
| Curriculum Name: | Diagnosis and Treatment of Adolescent Depression |
Learning Objectives
Upon completion of the activity, participants should be able to:
- Employ evidence-based strategies in the selection and use of antidepressants when treating depression in special populations
- Implement individualized treatment plans for patients with depression that maximize outcomes
Faculty
TARGET AUDIENCE
This activity has been developed for clinicians specializing in psychiatry. There are no prerequisites. All health care providers interested in psychopharmacology, especially primary care physicians, nurses, psychologists, and pharmacists, are welcome for advanced study.DISCLAIMER
Information and opinion offered by the speakers represent their viewpoints. Conclusions drawn by the audience should be derived from careful consideration of all available scientific information. Because this course is meant to educate physicians with what is currently in use and what may be available in the future, there may be "off-label" use discussed in the presentations. Speakers have been requested to inform the audience when off-label use is being discussed.
DISCLOSURE POLICY STATEMENT
Stephen M. Stahl, MD, PhD
Grant/Research: AstraZeneca, BioMarin, Dainippon Sumitomo, Forest, GenOmind, Lilly, Merck, Novartis, Pamlab, Pfizer, PGxHealth/Clinical Data, Schering-Plough, Sepracor, Servier, Shire, and Torrent.
Consultant/Advisor: Advent, Alkermes, Allergan, Arena, AstraZeneca, BioMarin, Boehringer Ingelheim, Bristol-Myers Squibb, Cypress Bioscience, Dainippon Sumitomo, Eisai, Forest, GenOmind, Janssen Division of Ortho-McNeil-Janssen, Jazz, Labopharm, Lilly, Lundbeck, Meiji, Merck, Neuronetics, Novartis, Orexigen, Otsuka America, Pamlab, Pfizer, PGxHealth/Clinical Data, Rexahn, Royalty, Schering-Plough, Servier, Shire, and VIVUS.
Speakers Bureau: Dainippon Sumitomo, Lilly, Merck, Pamlab, Sepracor, and Sunovion.
Thomas Schwartz, MD
Grant/Research: Cephalon, Inc.; Cyberonics; Forest Laboratories, Inc.; Forest Pharmaceuticals, Inc.
Consultant/Advisor: Pamlab, L.L.C.
Speakers Bureau: AstraZeneca Pharmaceuticals LP (divested); Pfizer Inc (divested); Wyeth Pharmaceuticals (divested)
Ronnie G. Swift, MD
Nothing to disclose.
Adam M. Brenner, MD
Nothing to disclose.
Planning Committee Members
Richard Vanderpool, CCMEP
Sr. Continuing Education Coordinator
University of Texas Southwestern Medical Center
Nothing to disclose.
Rory Daly, MPH
Associate Director, Program Development
Neuroscience Education Institute
Nothing to disclose.
Steve Smith
President and COO
Neuroscience Education Institute
Nothing to disclose.
CREDIT DESIGNATION
The University of Texas Southwestern Medical Center designates this enduring material for a maximum of 0.5 AMA PRA Category 1 Credit™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
ACCREDITATION STATEMENT
The University of Texas Southwestern Medical Center is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.
HOW TO RECEIVE CREDIT
By reviewing the course content and successfully completing the posttest and evaluation, physicians are entitled to receive 0.5 AMA PRA Category 1 Credit™. Statements of credit will be available to print from your user history page.
- Read the learning objectives and faculty disclosures.
- Participate in the activity.
- Complete the posttest and activity evaluation.
- Physicians who successfully complete the posttest and evaluation will receive CME credit. You must score 70% or higher on the posttest to receive credit for this activity.
- All other participants who successfully complete the posttest and evaluation will receive a certificate of participation.
COURSE VIEWING REQUIREMENTS
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PC
Internet Explorer (v6 or greater) or Firefox |
MAC
Safari |
Release Date: May 25, 2011
Expiration Date: May 24, 2012
COMMERCIAL SUPPORT
This activity is being supported by an educational grant from Pfizer Inc.



