Welcome to NGC. Skip directly to: Search Box, Navigation, Content.


Brief Summary

GUIDELINE TITLE

Management of adults with major depression.

BIBLIOGRAPHIC SOURCE(S)

  • Michigan Quality Improvement Consortium. Management of adults with major depression. Southfield (MI): Michigan Quality Improvement Consortium; 2008 May. 1 p.

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: Michigan Quality Improvement Consortium. Management of adults with major depression. Southfield (MI): Michigan Quality Improvement Consortium; 2008 Jan. 1 p.

BRIEF SUMMARY CONTENT

 
RECOMMENDATIONS
 EVIDENCE SUPPORTING THE RECOMMENDATIONS
 IDENTIFYING INFORMATION AND AVAILABILITY
 DISCLAIMER

 Go to the Complete Summary

RECOMMENDATIONS

MAJOR RECOMMENDATIONS

The level of evidence grades (A-D) are provided for the most significant recommendations and are defined at the end of the "Major Recommendations" field.

Detection and Diagnosis

Assess if Diagnostic and Statistic Manual of Mental Disorders, Fourth Edition, Text Revision (DSM-IV-TR) criteria for major depression are met [A]:

Must have a total of five symptoms for at least two weeks. One of the symptoms must be depressed mood or loss of interest:

  • Depressed mood
  • Markedly diminished interest or pleasure in all or almost all activities
  • Significant weight loss or gain (>5% body weight), or increase or decrease in appetite
  • Insomnia/hypersomnia
  • Psychomotor agitation or retardation
  • Fatigue/loss of energy
  • Feeling of worthlessness or inappropriate guilt
  • Diminished concentration or indecisiveness
  • Recurrent thoughts of death or suicide (Recognition may be increased with the use of a validated screening tool, e.g., Patient Health Questionnaire [PHQ-9], Harvard Department of Psychiatry National Depression Screening Day Scale [HANDS], Center for Epidemiologic Studies - Depression Scale [CES-D] Revised, Zung [see "Availability of Companion Documents" field], Primary Care Evaluation of Mental Disorders [PRIME-MD])

Assess whether patients have symptoms suggesting bipolar disorder [C]

Eligible Population

Adults 18 years or older with high risk for major depressive disorder including prenatal and postpartum populations

Frequency

  • At each evaluation where the patient's high-risk status, symptoms, or signs raise suspicion of current or uncontrolled depression
  • At the first prenatal care visit through end of first post-partum year

Screening for Suicide Risk

Assess risk of suicide by direct questioning about suicidal ideation and, if present, suicidal planning, potential means, and personal/family history of suicidal attempts. [D]

Eligible Population

Individuals diagnosed with significant mood symptoms, particularly those meeting criteria for major depression

Frequency

At each encounter addressing depression until patient is treated to remission, is stable and has not expressed suicidal thinking in previous visits.

Management of Patients Who Are Prescribed Antidepressant Medication

  • Initiate antidepressant medication following manufacturer's recommended doses. [A]
  • Referral to, and coordination with, Behavioral Health Specialist when [D]:
    • Identified or suspected risk of suicide
    • Additional counseling as desired
    • Primary physician not comfortable managing patient's depression
    • Diagnosis is uncertain or complicated by other psychiatric factors
    • Complex social situation
    • Management is complex, response to medication at therapeutic dosage is not optimal, or considering prescribing multiple agents
    • Psychotherapy and/or hospitalization required
  • Monitor medication frequently and adjust to a therapeutic level as assessed by clinical data not to exceed the highest recommended dose. [D] Medication should not be abruptly discontinued.
  • If no response after 2 to 3 weeks on therapeutic dosage increase dosage as tolerated and begin new observation period. If no response after 2 to 3 weeks on maximal dosage then switch antidepressant. If partial response after 2 to 3 weeks on maximal dosage then switch antidepressant or augment with additional agent.
  • For patients with recurrent major depression, continue medication for at least one year or longer at effective dosage. [B]

Eligible Population

Individuals diagnosed with significant mood symptoms, particularly those meeting criteria for major depression

Frequency

Medications for at least 9 to 12 months after acute symptoms resolve [A]

Schedule at least 3 follow-up visits in first 12 weeks, one of which can be telephonic [D]

Definitions:

Levels of Evidence for the Most Significant Recommendations

  1. Randomized controlled trials
  2. Controlled trials, no randomization
  3. Observational studies
  4. Opinion of expert panel

CLINICAL ALGORITHM(S)

None provided

EVIDENCE SUPPORTING THE RECOMMENDATIONS

TYPE OF EVIDENCE SUPPORTING THE RECOMMENDATIONS

IDENTIFYING INFORMATION AND AVAILABILITY

BIBLIOGRAPHIC SOURCE(S)

  • Michigan Quality Improvement Consortium. Management of adults with major depression. Southfield (MI): Michigan Quality Improvement Consortium; 2008 May. 1 p.

ADAPTATION

DATE RELEASED

2004 Jan (revised 2008 May)

GUIDELINE DEVELOPER(S)

Michigan Quality Improvement Consortium - Professional Association

SOURCE(S) OF FUNDING

Michigan Quality Improvement Consortium

GUIDELINE COMMITTEE

Michigan Quality Improvement Consortium Medical Directors' Committee

COMPOSITION OF GROUP THAT AUTHORED THE GUIDELINE

Physician representatives from participating Michigan Quality Improvement Consortium health plans, Michigan State Medical Society, Michigan Osteopathic Association, Michigan Association of Health Plans, Michigan Department of Community Health and Michigan Peer Review Organization

FINANCIAL DISCLOSURES/CONFLICTS OF INTEREST

Standard disclosure is requested from all individuals participating in the Michigan Quality Improvement Consortium (MQIC) guideline development process, including those parties who are solicited for guideline feedback (e.g., health plans, medical specialty societies). Additionally, members of the MQIC Medical Directors' Committee are asked to disclose all commercial relationships as well.

GUIDELINE STATUS

This is the current release of the guideline.

This guideline updates a previous version: Michigan Quality Improvement Consortium. Management of adults with major depression. Southfield (MI): Michigan Quality Improvement Consortium; 2008 Jan. 1 p.

GUIDELINE AVAILABILITY

AVAILABILITY OF COMPANION DOCUMENTS

PATIENT RESOURCES

None available

NGC STATUS

This NGC summary was completed by ECRI on December 10, 2004. The information was verified by the guideline developer on January 21, 2005. This summary was updated by ECRI on August 15, 2005, following the U.S. Food and Drug Administration advisory on antidepressant medications. This NGC summary was updated by ECRI on October 12, 2006. The updated information was verified by the guideline developer on November 3, 2006. This summary was updated by ECRI Institute on November 9, 2007, following the U.S. Food and Drug Administration advisory on Antidepressant drugs. This summary was updated by ECRI Institute on April 14, 2008. The updated information was verified by the guideline developer on April 18, 2008. This summary was updated by ECRI Institute on July 28, 2008. The updated information was verified by the guideline developer on July 29, 2008.

COPYRIGHT STATEMENT

This NGC summary is based on the original guideline, which may be reproduced with the citation developed by the Michigan Quality Improvement Consortium.

DISCLAIMER

NGC DISCLAIMER

The National Guideline Clearinghouse™ (NGC) does not develop, produce, approve, or endorse the guidelines represented on this site.

All guidelines summarized by NGC and hosted on our site are produced under the auspices of medical specialty societies, relevant professional associations, public or private organizations, other government agencies, health care organizations or plans, and similar entities.

Guidelines represented on the NGC Web site are submitted by guideline developers, and are screened solely to determine that they meet the NGC Inclusion Criteria which may be found at http://www.guideline.gov/about/inclusion.aspx .

NGC, AHRQ, and its contractor ECRI Institute make no warranties concerning the content or clinical efficacy or effectiveness of the clinical practice guidelines and related materials represented on this site. Moreover, the views and opinions of developers or authors of guidelines represented on this site do not necessarily state or reflect those of NGC, AHRQ, or its contractor ECRI Institute, and inclusion or hosting of guidelines in NGC may not be used for advertising or commercial endorsement purposes.

Readers with questions regarding guideline content are directed to contact the guideline developer.


 

 

   
DHHS Logo