Overview
Ready for a Closeup: Differentiating Inadequate Response and Emotional Blunting During Treatment for Major Depressive Disorder
Cinemeducation
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Major depressive disorder (MDD) can have a significant impact on your patients’ lives. However, MDD is not just about feeling “down.” It’s a life-threatening condition that is a leading cause of suicide. Fortunately, there are a variety of effective therapies; however, many patients may experience an inadequate response to treatment and others may have experience anhedonia or reduced emotional responsiveness (ie, emotional blunting) associated with both selective serotonin reuptake inhibitors/serotonin-norepinephrine reuptake inhibitors (SSRIs/SNRIs). Do you have questions about the symptoms of emotional blunting or differentiating emotional blunting from inadequate treatment response? What about assessing the effectiveness of different therapies? Access this innovative “cinemeducation” format in which representative patient and clinician dialogues come to life to model best practices. Find out how to use measurement-based care for tracking symptoms of depression; assess and manage treatment-related emotional blunting; and involve patients in shared decision making. Enhance your clinical practices and help your patients find the light again.
This activity is intended for psychiatrists, primary care providers, and other members of the
multidisciplinary team managing patients with depression.
multidisciplinary team managing patients with depression.
Major depressive disorder (MDD) is a common condition with a wide range of symptoms. Research has shown that medication alone or in combination with other therapeutic modalities is effective in improving depression. However, many patients do not receive adequate care and, despite the availability of a wide array of antidepressants to treat depression, up to 50% of patients with MDD fail to respond to an initial course of antidepressant therapy and more than 75% experience relapse. This failure to achieve and maintain remission compromises patients’ quality of life and ability to function, as well as other health outcomes including cardiovascular and metabolic diseases, which people with depression have a 40% higher risk of developing. To combat these trends, clinicians and patients must collaboratively establish treatment goals considerate of cognitive, physical, and emotional endpoints. In addition, when tailoring treatment to individual patients, it is important to consider the potential for patients to suffer from a reduced ability to experience and anticipate pleasure (anhedonia) and from reduced emotional responsiveness – either positive or negative (ie, emotional blunting)—both of which are common in patients with MDD. It is particularly noteworthy that emotional blunting, beyond being a symptom of MDD, has also been linked to some antidepressant treatments; evidence indicates that approximately 50% of MDD patients treated with selective serotonin reuptake inhibitors/serotonin-noradrenaline reuptake inhibitors (SSRIs/SNRIs) suffer emotional blunting. Therefore, it is vital that clinicians are able to determine to what extent emotional blunting is a residual symptom of depression or an adverse event stemming from antidepressant treatment.
Upon completion of this activity, learners will be able to:
• Describe the burden of emotional blunting in patients with MDD
• Review the latest research exploring how and to what extent different therapies may affect emotional blunting in patients with MDD
• Individualize treatment strategies for patients with MDD taking in to account the possible effects of emotional blunting in patient response to therapy
• Employ measurement-based care (MBC) and shared-decision making to assess emotional blunting as part of evaluation of patient response to treatment
• Describe the burden of emotional blunting in patients with MDD
• Review the latest research exploring how and to what extent different therapies may affect emotional blunting in patients with MDD
• Individualize treatment strategies for patients with MDD taking in to account the possible effects of emotional blunting in patient response to therapy
• Employ measurement-based care (MBC) and shared-decision making to assess emotional blunting as part of evaluation of patient response to treatment
Provided by the Academy for Continued Healthcare Learning (ACHL).
Supported by an educational grant from Takeda Pharmaceuticals U.S.A., Inc.
Professor of Psychiatry and Pharmacology
University of Toronto
Chairman and Executive Director
Brain and Cognition Discovery Foundation
Toronto, ON
Anita Clayton, MD (Faculty)
Wilford W. Spradlin Professor and Chair
Department of Psychiatry and Neurobehavioral Sciences
Professor of Clinical Obstetrics and Gynecology
University of Virginia School of Medicine
Charlottesville, VA
The Academy for Continued Healthcare Learning (ACHL) requires that the faculty participating in an accredited continuing education activity disclose all affiliations or other financial relationships within 24 months (1) with the manufacturers of any commercial product(s) and/or provider(s) of commercial services discussed in an educational presentation and (2) with all ineligible companies. All relevant financial relationships have been mitigated prior to this activity.
The following financial relationships have been provided:
Roger McIntyre, MD, FRCPC, (Chair)
Consultant (Occasional): AbbVie, Alkermes, Bausch Health, Eisai, Intra-Cellular, Janssen, Kris, Lundbeck
Neurocrine, NewBridge Pharmaceuticals, Novo Nordisk, Otsuka, Pfizer Inc., Purdue, Sanofi, Sunovion, Takeda
Grant/Research Support recipient: CIHR/GACD/Chinese National Natural Research Foundation and Milken Institute
Speaker Bureau: AbbVie, Alkermes, Atai Life Science, Bausch Health, Eisai, Intra-Cellular, Janssen, Kris, Lundbeck, Neurocrine, NewBridge Pharmaceuticals, Novo Nordisk, Otsuka, Pfizer Inc., Purdue, Sanofi, Sunovion, Takeda, Viatris
Anita Clayton, MD, (Faculty)
Advisory Board/Consultant: AbbVie, Inc., Biogen, Brii Biosciences, Fabre-Kramer, Initiator Pharma, Janssen Research & Development, LLC, Lundbeck, MindCure, Ovoca Bio plc, Praxis Precision Medicines, PureTech Health, Reunion Neuroscience, Inc. (formerly Field Trip Health), S1 Biopharma, Sage Therapeutics, Sertsei Pharmaceuticals, Inc., Takeda Pharmaceuticals, Vella Bioscience, Inc., WCG MedAvante-ProPhase
Grant/Research Support recipient: Dare Bioscience, Janssen Pharmaceuticals, Otsuka, Relmada Therapeutics, Inc., Sage Therapeutics Inc.
Royalties/Copyright: Ballantine Books/Random House, Changes in Sexual Functioning Questionnaire, Guilford Publications
Discussion of Off-Label, Investigational, or Experimental Drug/Device Use: None
ACHL staff members and others involved with the planning, development, and review of the content for this activity have no relevant affiliations or financial relationships to disclose.
The content for this activity was developed independently of any ineligible company. All materials are included with permission. The opinions expressed are those of the faculty and are not to be construed as those of the publisher or grantor(s).
This educational activity was planned and produced in accordance with the ACCME Standards for Integrity and Independence in Accredited Continuing Education. Recommendations involving clinical medicine in a continuing medical education (CME/CE) activity must be 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/CE in support or justification of a patient care recommendation must conform to the generally accepted standards of experimental design, data collection, and analysis.
This CME/CE activity might describe the off-label, investigational, or experimental use of medications and/or devices that may exceed their FDA-approved labeling. Physicians should consult the current manufacturers’ prescribing information for these products. ACHL requires the speaker to disclose that a product is not labeled for the use under discussion.
This activity will take approximately 60 minutes to complete. To receive credit, learners are required to complete the pretest, view the online activity, and complete the posttest and evaluation. To receive credit, 75% must be achieved on the posttest. A certificate will be immediately available. There is no fee to participate in the activity or for the generation of the certificate.
For questions, contact Michelle Forcier mforcier@achlcme.org
The Academy for Continued Healthcare Learning designates this enduring material for a maximum of 1.0 AMA PRA Category 1 Credit™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
Physician assistants, nurse practitioners, and nurses may participate in this educational activity and earn a certificate of completion as AAPA, AANP, and ANCC accept AMA PRA Category 1 Credits™ through their reciprocity agreements.