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Moderation of antidepressant and placebo outcomes by baseline severity in late-life depression: A systematic review and meta-analysis.
Locher, Cosima; Kossowsky, Joe; Gaab, Jens; Kirsch, Irving; Bain, Paul; Krummenacher, Peter.
Affiliation
  • Locher C; Department of Clinical Psychology and Psychotherapy, University of Basel, Basel, Switzerland. Electronic address: cosima.locher@unibas.ch.
  • Kossowsky J; Department of Clinical Psychology and Psychotherapy, University of Basel, Basel, Switzerland; Department of Anesthesiology, Perioperative and Pain Medicine, Boston Children's Hospital, Harvard Medical School, Boston, USA; Program in Placebo Studies and the Therapeutic Encounter, Beth Israel Deacones
  • Gaab J; Department of Clinical Psychology and Psychotherapy, University of Basel, Basel, Switzerland.
  • Kirsch I; Program in Placebo Studies and the Therapeutic Encounter, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, USA.
  • Bain P; Countway Library of Medicine, Harvard Medical School, Boston, USA.
  • Krummenacher P; Department of Clinical Psychology and Psychotherapy, University of Basel, Basel, Switzerland; Collegium Helveticum, University of Zurich and ETH Zurich, Zurich, Switzerland.
J Affect Disord ; 181: 50-60, 2015 Aug 01.
Article in En | MEDLINE | ID: mdl-25917293
ABSTRACT

BACKGROUND:

Baseline severity is a crucial moderator of trial outcomes in adult depression, with the advantage of antidepressants over placebo increasing as severity increases. However, this relationship has not been examined in late-life depression.

METHODS:

PubMed, Embase, Web of Science, PsycINFO, and Cochrane were searched for studies published through September 2014. Randomized, acute phase, and double-blind studies comparing an antidepressant group with a placebo group in depressed elderly patients were included.

RESULTS:

Nineteen studies met all inclusion criteria. Within-group effect sizes revealed significant improvement in antidepressant groups (g=1.35, p<.000), as well as in placebo groups (g=.96, p<.000). Change in depressive symptoms assessed by Hamilton Depression Rating Scale (HDRS) was moderated by baseline severity in antidepressant groups (Z=2.67, p=.008) and placebo groups (Z=4.46, p<.000). However, this would be expected as a result of regression toward the mean, and mean differences between groups did not increase (r=.19, p=.469) as a function of baseline severity.

LIMITATIONS:

Limited to published data and information was only analyzed at the level of treatment groups.

CONCLUSION:

Baseline severity was not associated with an antidepressant-placebo difference and placebo responses are large in the treatment of depressed elderly people. We propose a stepwise approach, i.e., to initially offer elderly depressed patients psychosocial interventions and only consider antidepressants if patients do not respond.
Subject(s)
Key words

Full text: 1 Database: MEDLINE Main subject: Placebo Effect / Depression / Late Onset Disorders / Antidepressive Agents Type of study: Clinical_trials / Systematic_reviews Limits: Humans Language: En Year: 2015 Type: Article

Full text: 1 Database: MEDLINE Main subject: Placebo Effect / Depression / Late Onset Disorders / Antidepressive Agents Type of study: Clinical_trials / Systematic_reviews Limits: Humans Language: En Year: 2015 Type: Article