Evidence map›Paper›PMID 25514063›Full record

Trial reportJournal of clinical psychopharmacology2015

Complexity of illness and adjunctive benzodiazepine use in outpatients with bipolar I or II disorder: results from the Bipolar CHOICE study.

William V Bobo, Noreen A Reilly-Harrington, Terence A Ketter, Benjamin D Brody, Gustavo Kinrys, David E Kemp, Richard C Shelton, Susan L McElroy, Louisa G Sylvia, James H Kocsis and 13 more

Open access · greenAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Journal of clinical psychopharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
0.6field-weighted citation impact, top 33% 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

9 citing papers in PubMed, 2 syntheses or guidelines pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Treatment of Bipolar Depression with Deep TMS: Results from a Double-Blind, Randomized, Parallel Group, Sham-Controlled Clinical Trial.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2017
    Trial
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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

23 authors at 11 institutions in 1 country.

William V BoboFrom the *Department of Psychiatry and Psychology, Mayo Clinic, Rochester, MN; †Department of Psychiatry, The Massachusetts General Hospital, Boston, MA; ‡Department of Psychiatry and Behavioral Sciences and the Bipolar Disorders Clinic, Stanford University School of Medicine, Stanford, CA; §Department of Psychiatry, Weill Cornell Medical College of Cornell University, New York, NY; ∥Department of Psychiatry, University Hospitals Case Medical Center, Case Western Reserve University School of Medicine, Cleveland, OH; ¶Department of Psychiatry, University of Alabama-Birmingham School of Medicine, Birmingham, AL; #Lindner Center of HOPE, Mason, Ohio and Department of Psychiatry and Behavioral Neuroscience, University of Cincinnati College of Medicine, Cincinnati, OH; **Department of Psychiatry and Depression Center, The University of Michigan, Ann Arbor, MI; ††Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA; ‡‡Department of Psychiatry, University of Texas Health Science Center at San Antonio, San Antonio, TX; §§Department of Psychiatry, University of New Mexico, Health Sciences Center, Albuquerque, NM; ∥∥Department of Psychiatry, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA; and ¶¶Department of Psychiatry, Upstate Medical University, State University of New York, Syracuse, NY.
Noreen A Reilly-Harrington
Terence A Ketter
Benjamin D Brody
Gustavo Kinrys
David E Kemp
Richard C Shelton
Susan L McElroy
Louisa G Sylvia
James H Kocsis
Melvin G McInnis
Edward S Friedman
Vivek Singh
Mauricio Tohen
Charles L Bowden
Thilo Deckersbach
Joseph R Calabrese
Michael E Thase
Andrew A Nierenberg
Dustin J Rabideau
David A Schoenfeld
Stephen V Faraone
Masoud Kamali
University of Pittsburgh · USMassachusetts General Hospital · USUniversity Hospitals Case Medical Center · USMayo Clinic in Arizona · USThe University of Texas Health Science Center at San Antonio · USUniversity of Alabama at Birmingham · USUniversity of New Mexico · USCornell University · USLindner Center of HOPE · USStanford University · USUniversity of Michigan–Ann Arbor · US

Funding

Comparative Effectiveness Study for Bipolar DisorderR01HS019371 · AHRQ · MASSACHUSETTS GENERAL HOSPITAL · PI NIERENBERG, ANDREW A · 2010 to 2010
$9.8M
AHRQ HHS 1R01HS019371-01AHRQ HHS R01 HS019371
6 · The paper itself

Abstract

Benzodiazepines are widely prescribed for patients with bipolar disorders in clinical practice, but very little is known about the subtypes of patients with bipolar disorder or aspects of bipolar illness that contribute most to benzodiazepine use. We examined the prevalence of and factors associated with benzodiazepine use among 482 patients with bipolar I or II disorder enrolled in the Bipolar CHOICE study. Eighty-one subjects were prescribed benzodiazepines at study entry and were considered benzodiazepine users. Stepwise logistic regression was used to model baseline benzodiazepine use versus nonuse, using entry and exit criteria of P < 0.1. In bivariate analyses, benzodiazepine users were prescribed a significantly higher number of other psychotropic medications and were more likely to be prescribed lamotrigine or antidepressants as compared with benzodiazepine nonusers. Benzodiazepine users were more likely to have a diagnosis of bipolar I disorder and comorbid anxiety disorder, but not comorbid alcohol or substance use disorders. Benzodiazepine users also had experienced more anxiety and depressive symptoms and suicidality, but not irritability or manic symptoms, than did benzodiazepine nonusers. In the multivariate model, anxiety symptom level (regardless of diagnosis), lamotrigine use, number of concomitant psychotropic medications, college education, and high household income predicted benzodiazepine use. Benzodiazepine use in patients with bipolar disorders is associated with greater illness complexity as indicated by a higher number of concomitant psychotropic medications and higher anxiety symptom burden, regardless of a comorbid anxiety disorder diagnosis. Demographic factors were also important determinants of benzodiazepine use, which may be related to access to care and insurance coverage for benzodiazepines.

Indexed as

Severity of Illness IndexAdultAntidepressive AgentsBenzodiazepinesBipolar DisorderCohort StudiesCross-Sectional StudiesFemaleHumansMaleMiddle AgedOutpatientsAntidepressive AgentsBenzodiazepines

Identifiers

PMID25514063
PMCPMC6557444
OpenAlexW1984843840

What OpenQuestion holds

Textmetadata
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.