Consideration of Polypharmacology in Relation to Effective Weight Reduction: A Patient on Antipsychotic Medication

To Receive a Certificate for This Activity

1 Read the CME information on this page.
2 Review information on the contributor biographies.
3 Go to the course presentations and review the material.
4 Complete the CME posttest.
5 Complete the evaluation and registration forms. A link to your certificate will be emailed to you within 24 hours of satisfactory completion of these documents.


CME Information


Course Overview

Several antidepressant and antipsychotic medications are associated with weight gain and changes in the lipid profile. Healthcare professionals need to become familiar with the medications that are most associated with weight gain and dyslipidemia, as well as learn how to monitor patients on these antidepressants and antipsychotic medications.

Educational Objectives

At the conclusion of this activity, the participant should be able to:

  • Understand the weight gain and metabolic derangements related to treatment with certain antidepressants and antipsychotic medications

  • Describe the standard approach to evaluation and monitoring weight and metabolic changes in the setting of antidepressant and antipsychotic medical therapy

  • Describe the eligibility criteria for pharmacotherapy and surgical therapy for obesity

Target Audience

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This CME activity is designed to meet the educational needs of cardiologists, endocrinologists, primary care physicians, and other physicians caring for patients at risk for cardiovascular disease.

Method of Participation

This clinical case is in text format accompanied by references linked to PubMed.

To receive a maximum of 0.5 AMA PRA Category 1 Credit(s)™ you should:

  • View the presentations in this CME activity and evaluate the content presented

  • Complete and submit the posttest, CME registration and activity evaluation forms

The estimated time to complete this activity, including review of the materials, is 0.5 hour(s).

Accreditation/Credit Designation

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Baylor College of Medicine is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.

Baylor College of Medicine designates this educational activity for a maximum of 0.5 AMA PRA Category 1 Credit(s)™.  Physicians should only claim credit commensurate with the extent of their participation in the activity.    

ACCME accredited providers may issue credit to both U.S. and international physicians for any activity that has been designated for AMA PRA Category 1 Credit(s)™ in accordance with PRA requirements.

Term of Approval

December 2007 through December 2008. Original release date: December 2007

Peer Review

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In October 2007, this continuing medical education activity was reviewed by Venkateshwar R. Polsani, MD, Clinical Endocrinology and Atherosclerosis Fellow, Center for Cardiovascular Disease Prevention and Division of Endocrinology, Baylor College of Medicine, Houston, Texas. In order to ensure the continued scientific relevance of this enduring material it will be reviewed again December 2008.

Disclosure: Nothing to disclose.

Program Director

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Christie M. Ballantyne, MD
Professor of Medicine
Associate Chief and Clinical Director, Section of Atherosclerosis and
Lipoprotein Research
Department of Medicine
Baylor College of Medicine
Houston, Texas

Director, Center for Cardiovascular Disease Prevention
Methodist DeBakey Heart Center
Co-Director, Lipid Metabolism and Atherosclerosis Clinic
The Methodist Hospital
Houston, Texas

Disclosure: non-public support of research – AstraZeneca, GlaxoSmithKline, KOS, Merck, Merck/Schering-Plough, Novartis, Pfizer, Sankyo, sanofi-aventis, Schering, Takeda; speakers bureau member – AstraZeneca, Merck, Merck/Schering-Plough, Pfizer, Reliant, Schering; advisory committee member – AstraZeneca, KOS, Merck/Schering-Plough, Reliant, sanofi-aventis, Schering; consultant – AstraZeneca, GlaxoSmithKline, Merck, Merck/Schering-Plough, Pfizer, Reliant, sanofi-aventis, Schering; honorarium recipient – AstraZeneca, GlaxoSmithKline, KOS, Merck, Merck/Schering-Plough, Pfizer, Reliant, sanofi-aventis, Schering.

Disclaimer

This CME activity is designed for use by healthcare professionals for educational purposes only. Information and opinion offered by the contributors represent their viewpoints. Conclusions drawn by the participant should be derived from careful consideration of all available scientific information. Prescription information and use of medical devices should be undertaken only after confirmation of information by consulting the FDA-approved uses and information.

Baylor College of Medicine makes every effort to have accurate information presented, no warranty, expressed or implied, is offered. The participant should use his/her clinical judgment, knowledge, experience, and diagnostic decision-making before applying any information, whether provided here or by others, for any professional use.

Links are provided to other Internet sites solely for the convenience of users. Once you link to another site, you are subject to the site's terms and conditions of use including copyright and licensing restrictions.

Disclosure

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The Office of Continuing Medical Education (OCME) makes every effort to develop CME activities that are scientifically based, accurate, current, and objectively presented. In accordance with the Accreditation Council for Continuing Medical Education Standards for Commercial Support, Baylor College of Medicine (BCM) has implemented a mechanism requiring everyone in a position to control the content of an educational activity (e.g., directors, planning committee members, contributors, peer reviewers) to disclose any relevant financial relationships with commercial interests (drug/device companies) and manage/resolve any conflicts of interest prior to the activity. Individuals must disclose to participants the existence or non-existence of financial relationships: l) at the time of the activity or within 12 months prior; and 2) of their spouses/partners.

Baylor College of Medicine does not view the existence of interests or relationships with commercial entities as implying bias or decreasing the value of a presentation. It is up to the participants to determine whether the interests or relationships influence the presenter with regard to exposition or conclusions.

If at any time during this activity you feel that there has been commercial or promotional bias, please inform us by using the commercial bias comments box in the evaluation form. Please answer the questions about balance in the CME activity evaluation candidly.

The following individual(s) has/have reported financial or other relationship(s) with commercial entities whose products/services may relate to the educational content of this activity:

Christie M. Ballantyne, MD, Activity Director: non-public support of research – AstraZeneca, GlaxoSmithKline, KOS, Merck, Schering, Novartis, Pfizer, Sankyo, sanofi-aventis, Merck/Schering-Plough, Takeda; speakers bureau member – AstraZeneca, Merck, Schering, Pfizer, Reliant, Merck/Schering-Plough; advisory committee member – AstraZeneca, KOS, Reliant, Schering, sanofi-aventis, Merck/Schering-Plough; consultant – AstraZeneca, GlaxoSmithKline, Merck, Pfizer, Reliant, Schering, sanofi-aventis, Merck/Schering-Plough; honorarium recipient - AstraZeneca, GlaxoSmithKline, KOS, Merck, Pfizer, Reliant, Schering, Merck/Schering-Plough, sanofi-aventis.

Vijay Nambi, MD, Contributor: speakers bureau member - American Heart Association; honorarium recipient – National Lipid Association.

The following individual(s) has/have reported no financial or other relationships with commercial entities whose products/services may relate to the educational content of this activity:

Venkateshwar R. Polsani, MD, Peer Reviewer: nothing to disclose.

Madhuri M. Vasudevan, MD, MPH, Contributor: nothing to disclose.

Some drugs/devices identified during this activity may have United States Food and Drug Administration (FDA) clearance for specific purposes only or for use in restricted research settings. The FDA has stated that it is the responsibility of the individual physician to determine the FDA status of each drug or device that he/she wishes to use in clinical practice and to use the products in compliance with the applicable law.

Baylor College of Medicine requires that all contributors disclose an unlabeled use or investigational use (not yet approved for any purpose) of pharmaceutical and medical device products, and provide adequate scientific and clinical justification for such use. Physicians are urged to fully review all the available data on products or procedures before using them to treat patients.

Acknowledgement of Support

This CME activity is supported by an educational grant from sanofi-aventis.

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