Evidence map›Paper›PMID 20473068›Full record

Trial reportJournal of clinical psychopharmacology2010

Efficacy and mood conversion rate of short-term fluoxetine monotherapy of bipolar II major depressive episode.

Jay D Amsterdam, Justine Shults

Abstract readClinical TrialComparative Study
In one paragraph

Trial report in Journal of clinical psychopharmacology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

15 citing papers in PubMed, 56 citations in OpenAlex.

  1. Trial
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  7. Article
  8. Article
  9. Bipolar II Disorder: Understudied and Underdiagnosed.Focus (American Psychiatric Publishing) · 2023
    Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Broadening the diagnosis of bipolar disorder: benefits vs. risks.World psychiatry : official journal of the World Psychiatric Association (WPA) · 2011
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Jay D AmsterdamDepression Research Unit, Department of Psychiatry, University of Pennsylvania School of Medicine, Philadelphia, PA, USA. jamsterd@mail.med.upenn.edu
Justine Shults
University of Pennsylvania · US

Funding

PREVENTION OF RECURRENCE IN DEPRESSION WITH DRUGS AND CTR01MH060998 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI DERUBEIS, ROBERT J · 2002 to 2011
$6.5M
Treatment of Bipolar Type II Major DepressionR01MH060353 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI DERUBEIS, ROBERT J · 2001 to 2011
$3.9M
1/2-Prevention of Relapse & Recurrence of Bipolar DepressionR01MH080097 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI DERUBEIS, ROBERT J · 2009 to 2013
$2.0M
Effect of Psychotherapy on Brain Serotonin ActivityR34MH077580 · NIMH · UNIVERSITY OF PENNSYLVANIA · PI AMSTERDAM, JAY D · 2008 to 2010
$638k
NIMH NIH HHS MH060353NIMH NIH HHS R01 MH060353NIMH NIH HHS R01 MH060998NIMH NIH HHS R01 MH080097NIMH NIH HHS R34 MH077580
6 · The paper itself

Abstract

objectiveAs part of a long-term, relapse-prevention study of antidepressant versus mood stabilizer monotherapy of bipolar II major depressive episode, we prospectively examined the efficacy and mood conversion rate of initial fluoxetine monotherapy. We hypothesized that there would be a statistically significant reduction in depressive symptoms without a clinically meaningful increase in mood conversion symptoms.

methodsPatients received open-label fluoxetine monotherapy 10 to 80 mg daily for up to 14 weeks. Primary outcome was change over time in Hamilton Depression Rating score, with secondary outcomes including the proportion of treatment responders and remitters, change over time in Young Mania Rating Scale (YMRS) score, and frequency of mood conversion episodes.

resultsOne hundred forty-eight patients had at least 1 post-baseline measurement. Mean Hamilton Depression Rating score decreased by 9.0 points (P < 0.0005). There were 88 responder patients (59.5%; 95% confidence interval [CI], 51.1%-67.4%) (P < 0.0005) and 86 remitter patients (58.1%; 95% CI, 49.7%-66.2%) (P < 0.0005). Mean time to remission was 64.4 days (95% CI, 59.1-69.7 days). Six patients (4.1%; 95% CI, 1.5%-8.6%) (P < 0.0005) had hypomania, and 29 patients (19.6%; 95% CI, 13.5%-26.9%) (P < 0.0005) had subsyndromal hypomania, which did not result in treatment discontinuation. Six patients (4.1%; 95% CI, 1.5%-8.6%) had a YMRS score of 8 or greater (P < 0.0005), and 4 patients (2.7%; 95% CI, 0.7%-6.8%) (P < 0.0005) had a YMRS score of 12 or greater at any study visit.

conclusionsAlthough design limitations constrain the interpretation of the current findings, fluoxetine monotherapy may be an effective short-term treatment of bipolar II major depressive episode with a relatively low rate of syndromal hypomanic episodes.

Indexed as

AdultAffectAgedAged, 80 and overBipolar DisorderFemaleFluoxetineFollow-Up StudiesHumansMajor Depressive DisorderMaleMiddle AgedProspective StudiesTime FactorsTreatment OutcomeYoung AdultFluoxetine

Identifiers

PMID20473068
PMCPMC2894607
OpenAlexW2030706521

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.