symptoms sufficient to meet the criteria for major depression or Hamilton




Critically Appraised Topic

Evidence-Based Medicine.

Date:  1/17/2006

Theme:  Therapy 
 

Question:  In a 45 year old woman with first time major depressive episode and wary of taking medication, does combination of medication and psychotherapy reduce the duration of treatment with medication or otherwise improve response to therapy (less depressive symptoms)? 
 

Clinical Bottom Line

We found an evidence based summary which presented the results of two systematic reviews and two subsequent RCTs.  Overall the evidence supports the combined use of  pharmacotherapy and psychotherapy over the use of either alone in the treatment of Depression. 
 

 
 
 

Search strategies:

 

Cochrane Database

Depression and Psychotherapy

Most interestingly yielded full protocol for systematic Cochrane review but not yet complete.
     
Clinical Evidence   Great summary with references to 2 systematic reviews and 2 subsequent RCT’s.

http://www.clinicalevidence.com/ceweb/conditions/meh/1003/1003_I14.jsp

     
TRIP+    
     
PubMed    
     
PubMed Clinical Queries    
     

 
 
 

Articles:

1:  Browne G, Steiner M, Roberts J, Gafni A, Byrne C, Dunn E, Bell B, Mills M, Chalklin L, Wallik D, Kraemer J. Sertraline and/or interpersonal psychotherapy for patients with dysthymic disorder in primary care: 6-month comparison with longitudinal 2-year follow-up of effectiveness and costs. J Affect Disord. 2002 Apr;68(2-3):317-30.

 
 
 
 
 
 

BACKGROUND: There is little information on the long-term effects and costs of a combination of Sertraline and interpersonal psychotherapy (IPT) for the treatment of dysthymia in primary care. METHODS: In a single-blind, randomized clinical trial, 707 adults (18-74 years of age inclusive) with DSM-IV dysthymic disorder, with or without past and/or current major Depression, as an acute or chronic episode, in a community-based primary care practice in Ontario, Canada, were randomized to treatment with either Sertraline alone (50-200 mg), or IPT alone (10 sessions), or Sertraline plus IPT combined. In the acute treatment phase (first 6 months) all groups received full active treatment. This was followed by an additional 18-month naturalistic follow-up phase. Subjects were assessed for effectiveness of treatment in reducing depressive symptoms using the Montgomery Asberg Depression Rating Scale (MADRS) at 6 months and twice again during the 18-month follow-up by blind independent observers. Treatment costs and subjects' use of other health and social services were also investigated. RESULTS: At 6 months, 586 subjects completed the MADRS questionnaire. There was a significant difference (P=0.025) in mean MADRS scores: 14.3 (Group I); 14.9 (Group II); 16.8 (Group III), using analysis of covariance. Response (40% improvement) rates were 60.2% for Sertraline alone, 46.6% for IPT alone, and 57.5% for Sertraline augmented by IPT (P=0.02). At 2 years, 525 subjects were retained for follow-up. There was no statistically significant difference between Sertraline alone and Sertraline plus IPT in symptom reduction. However, both were more effective than IPT alone in reducing depressive symptoms (P=0.03). There was a statistically significant difference between groups in costs for use of health and social services. The IPT treatment groups had the lower costs for use of health and social services. CONCLUSIONS: Sertraline or Sertraline plus IPT was more effective than IPT alone after 6 months. Over the long term (2 years), all three treatments provide reasonably effective treatment for reducing symptoms of dysthymia, but Sertraline or combining Sertraline with IPT is more effective than IPT alone. Of these two more effective treatments, subjects in the Sertraline plus IPT group had less health and social service costs by $480 per person over 2 years. These findings underscore the effects of combining pharmacotherapy and psychotherapy and the economic value of this more comprehensive treatment of dysthymia in primary care.

 
 

Critical Appraisal:

 

Validity Was it randomized?

Was randomization concealed?

Yes.

Yes.  Box with sealed envelopes.

Was the follow up sufficiently long and complete? Yes.  6 months and 2 years.

707 -> 586 @ 6mos (82% retention)

Was the data analyzed on an intention to treat basis? Yes.
Was there adequate blinding of subjects and researchers? Single blinding of the outcomes assessor.
Were there similar baseline characteristics in each group? Don’t know.

At six months, they were not similar.

Groups treated equally other than intervention? No. The sertraline group received different counseling at 6 months.

 
 

Clinical Importance What is the magnitude of treatment effect (e.g. what is the relative risk reduction, absolute risk reduction, NNT)?

Response defined as a 40% improvement rate in MADRS.

 
 
RRR = (CER - EER)/CER = (59.7 – 59.5)/59.7

ARR = CER – EER =

NNT = 1/AAR.

The response rates between the two groups were similar (and in fact, perhaps slightly favoring the control group).  No NNT was calculated.

 
 

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    symptoms sufficient to meet the criteria for major depression or Hamilton

    Critically Appraised Topic

    Evidence-Based Medicine.

    Date:  1/17/2006

    Theme:  Therapy 
     

    Question:  In a 45 year old woman with first time major depressive episode and wary of taking medication, does combination of medication and psychotherapy reduce the duration of treatment with medication or otherwise improve response to therapy (less depressive symptoms)? 
     

    Clinical Bottom Line

    We found an evidence based summary which presented the results of two systematic reviews and two subsequent RCTs.  Overall the evidence supports the combined use of  pharmacotherapy and psychotherapy over the use of either alone in the treatment of Depression. 
     

     
     
     

    Search strategies:

     

    Cochrane Database

    Depression and Psychotherapy

    Most interestingly yielded full protocol for systematic Cochrane review but not yet complete.
         
    Clinical Evidence   Great summary with references to 2 systematic reviews and 2 subsequent RCT’s.

    http://www.clinicalevidence.com/ceweb/conditions/meh/1003/1003_I14.jsp

         
    TRIP+    
         
    PubMed    
         
    PubMed Clinical Queries    
         

     
     
     

    Articles:

    1:  Browne G, Steiner M, Roberts J, Gafni A, Byrne C, Dunn E, Bell B, Mills M, Chalklin L, Wallik D, Kraemer J. Sertraline and/or interpersonal psychotherapy for patients with dysthymic disorder in primary care: 6-month comparison with longitudinal 2-year follow-up of effectiveness and costs. J Affect Disord. 2002 Apr;68(2-3):317-30.

     
     
     
     
     
     

    BACKGROUND: There is little information on the long-term effects and costs of a combination of Sertraline and interpersonal psychotherapy (IPT) for the treatment of dysthymia in primary care. METHODS: In a single-blind, randomized clinical trial, 707 adults (18-74 years of age inclusive) with DSM-IV dysthymic disorder, with or without past and/or current major Depression, as an acute or chronic episode, in a community-based primary care practice in Ontario, Canada, were randomized to treatment with either Sertraline alone (50-200 mg), or IPT alone (10 sessions), or Sertraline plus IPT combined. In the acute treatment phase (first 6 months) all groups received full active treatment. This was followed by an additional 18-month naturalistic follow-up phase. Subjects were assessed for effectiveness of treatment in reducing depressive symptoms using the Montgomery Asberg Depression Rating Scale (MADRS) at 6 months and twice again during the 18-month follow-up by blind independent observers. Treatment costs and subjects' use of other health and social services were also investigated. RESULTS: At 6 months, 586 subjects completed the MADRS questionnaire. There was a significant difference (P=0.025) in mean MADRS scores: 14.3 (Group I); 14.9 (Group II); 16.8 (Group III), using analysis of covariance. Response (40% improvement) rates were 60.2% for Sertraline alone, 46.6% for IPT alone, and 57.5% for Sertraline augmented by IPT (P=0.02). At 2 years, 525 subjects were retained for follow-up. There was no statistically significant difference between Sertraline alone and Sertraline plus IPT in symptom reduction. However, both were more effective than IPT alone in reducing depressive symptoms (P=0.03). There was a statistically significant difference between groups in costs for use of health and social services. The IPT treatment groups had the lower costs for use of health and social services. CONCLUSIONS: Sertraline or Sertraline plus IPT was more effective than IPT alone after 6 months. Over the long term (2 years), all three treatments provide reasonably effective treatment for reducing symptoms of dysthymia, but Sertraline or combining Sertraline with IPT is more effective than IPT alone. Of these two more effective treatments, subjects in the Sertraline plus IPT group had less health and social service costs by $480 per person over 2 years. These findings underscore the effects of combining pharmacotherapy and psychotherapy and the economic value of this more comprehensive treatment of dysthymia in primary care.

     
     

    Critical Appraisal:

     

    Validity Was it randomized?

    Was randomization concealed?

    Yes.

    Yes.  Box with sealed envelopes.

    Was the follow up sufficiently long and complete? Yes.  6 months and 2 years.

    707 -> 586 @ 6mos (82% retention)

    Was the data analyzed on an intention to treat basis? Yes.
    Was there adequate blinding of subjects and researchers? Single blinding of the outcomes assessor.
    Were there similar baseline characteristics in each group? Don’t know.

    At six months, they were not similar.

    Groups treated equally other than intervention? No. The sertraline group received different counseling at 6 months.

     
     

    Clinical Importance What is the magnitude of treatment effect (e.g. what is the relative risk reduction, absolute risk reduction, NNT)?

    Response defined as a 40% improvement rate in MADRS.

     
     
    RRR = (CER - EER)/CER = (59.7 – 59.5)/59.7

    ARR = CER – EER =

    NNT = 1/AAR.

    The response rates between the two groups were similar (and in fact, perhaps slightly favoring the control group).  No NNT was calculated.