Evidence map›Paper›PMID 27056606›Full record

Trial reportThe American journal of psychiatry2016

Pharmacotherapy Relapse Prevention in Body Dysmorphic Disorder: A Double-Blind, Placebo-Controlled Trial.

Katharine A Phillips, Aparna Keshaviah, Darin D Dougherty, Robert L Stout, William Menard, Sabine Wilhelm

Open access · bronzeAbstract readClinical Trial, Phase IClinical Trial, Phase IIComparative Study
In one paragraph

Trial report in The American journal of psychiatry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
9.9field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 72 citations in OpenAlex.

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  5. Body dysmorphic disorder.Nature reviews. Disease primers · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Katharine A PhillipsFrom Rhode Island Hospital, Butler Hospital, and the Department of Psychiatry and Human Behavior, Alpert Medical School, Brown University, Providence, R.I.; Massachusetts General Hospital, and the Department of Psychiatry, Harvard Medical School, Boston; and Decision Sciences Institute, Pawtucket, R.I.
Aparna KeshaviahFrom Rhode Island Hospital, Butler Hospital, and the Department of Psychiatry and Human Behavior, Alpert Medical School, Brown University, Providence, R.I.; Massachusetts General Hospital, and the Department of Psychiatry, Harvard Medical School, Boston; and Decision Sciences Institute, Pawtucket, R.I.
Darin D DoughertyFrom Rhode Island Hospital, Butler Hospital, and the Department of Psychiatry and Human Behavior, Alpert Medical School, Brown University, Providence, R.I.; Massachusetts General Hospital, and the Department of Psychiatry, Harvard Medical School, Boston; and Decision Sciences Institute, Pawtucket, R.I.
Robert L StoutFrom Rhode Island Hospital, Butler Hospital, and the Department of Psychiatry and Human Behavior, Alpert Medical School, Brown University, Providence, R.I.; Massachusetts General Hospital, and the Department of Psychiatry, Harvard Medical School, Boston; and Decision Sciences Institute, Pawtucket, R.I.
William MenardFrom Rhode Island Hospital, Butler Hospital, and the Department of Psychiatry and Human Behavior, Alpert Medical School, Brown University, Providence, R.I.; Massachusetts General Hospital, and the Department of Psychiatry, Harvard Medical School, Boston; and Decision Sciences Institute, Pawtucket, R.I.
Sabine WilhelmFrom Rhode Island Hospital, Butler Hospital, and the Department of Psychiatry and Human Behavior, Alpert Medical School, Brown University, Providence, R.I.; Massachusetts General Hospital, and the Department of Psychiatry, Harvard Medical School, Boston; and Decision Sciences Institute, Pawtucket, R.I.
Butler Hospital · US

Funding

Pharmacotherapy Relapse Prevention in BDDR01MH072917 · NIMH · BUTLER HOSPITAL (PROVIDENCE, RI) · PI PHILLIPS, KATHARINE ANNE · 2005 to 2009
$1.5M
Pharmacotherapy Relapse Prevention in Body Dysmorphic DisorderR01MH072854 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI WILHELM, SABINE · 2005 to 2009
$1.5M
NIMH NIH HHS R01 MH072854NIMH NIH HHS R01 MH072917
6 · The paper itself

Abstract

objectiveBody dysmorphic disorder is common, distressing, and often severely impairing. Serotonin reuptake inhibitors appear efficacious, but the few existing pharmacotherapy studies were short term (≤4 months), and no relapse prevention studies or continuation phase studies have been conducted to the authors' knowledge. The authors report results from the first relapse prevention study in body dysmorphic disorder.

methodAdults (N=100) with DSM-IV body dysmorphic disorder received open-label escitalopram for 14 weeks (phase 1); 58 responders were then randomized to double-blind continuation treatment with escitalopram versus switch to placebo for 6 months (phase 2). Reliable and valid outcome measures were utilized.

resultsIn phase 1, 67.0% of treated subjects and 81.1% of subjects who completed phase 1 responded to escitalopram. Body dysmorphic disorder severity (in both the intent-to-treat and the completer groups) and insight, depressive symptoms, psychosocial functioning, and quality of life significantly improved from baseline to end of phase 1. In phase 2, time to relapse was significantly longer with escitalopram than with placebo treatment (hazard ratio=2.72, 95% CI=1.01-8.57). Phase 2 relapse proportions were 18% for escitalopram and 40% for placebo. Among escitalopram-treated subjects, body dysmorphic disorder severity significantly decreased over time during the continuation phase, with 35.7% of subjects showing further improvement. There were no significant group differences in body dysmorphic disorder severity or insight, depressive symptoms, psychosocial functioning, or quality of life.

conclusionsContinuation-phase escitalopram delayed time to relapse, and fewer escitalopram-treated subjects relapsed than did placebo-treated subjects. Body dysmorphic disorder severity significantly improved during 6 additional months of escitalopram treatment following acute response; more than one-third of escitalopram-treated subjects experienced further improvement.

Indexed as

AdultBody Dysmorphic DisordersCitalopramComorbidityDepressive DisorderDouble-Blind MethodFemaleHumansMaleMiddle AgedQuality of LifeSecondary PreventionSocial AdjustmentCitalopram

Identifiers

PMID27056606
PMCPMC5009005
OpenAlexW2332936953

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.