Evidence map›Paper›PMID 26362273›Full record

ArticleSchizophrenia bulletin2016

Report on ISCTM Consensus Meeting on Clinical Assessment of Response to Treatment of Cognitive Impairment in Schizophrenia.

Richard S E Keefe, George M Haig, Stephen R Marder, Philip D Harvey, Eduardo Dunayevich, Alice Medalia, Michael Davidson, Ilise Lombardo, Christopher R Bowie, Robert W Buchanan and 15 more

Open access · bronzeAbstract readConsensus Statement
In one paragraph

Article in Schizophrenia bulletin, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 2 pooled it
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

23 citing papers in PubMed, 2 syntheses or guidelines pooled it, 44 citations in OpenAlex.

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  13. Targeting Serotonin 5-HTCNS drugs · 2020
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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

25 authors at 17 institutions in 5 countries.

Richard S E KeefeDepartment of Psychiatry, Duke University Medical Center, Durham, NC; richard.keefe@duke.edu.
George M HaigDepartment of Neuroscience Clinical Development, Abbvie, North Chicago, IL;
Stephen R MarderSemel Institute for Neuroscience at UCLA, and VA Desert Pacific Mental Illness Research, Education, and Clinical Center, Los Angeles, CA ;
Philip D HarveyDepartment of Psychiatry and Behavioral Sciences, University of Miami School of Medicine, Miami, FL;
Eduardo DunayevichClinical Development, Takeda, Los Angeles, CA;
Alice MedaliaDepartment of Psychiatry, Columbia University, New York, NY;
Michael DavidsonDepartment of Psychiatry, The Chaim Sheba Medical Center, Tel Hashomer, Israel;
Ilise LombardoClinical Research, FORUM Pharmaceuticals, Waltham, MA;
Christopher R BowieDepartment of Psychology, Queen's University, Kingston, Ontario, Canada;
Robert W BuchananDepartment of Psychiatry, Maryland Psychiatric Research Center, University of Maryland School of Medicine, Baltimore, MD;
Dragana Bugarski-KirolaDepartment of Psychiatry, F. Hoffmann-La Roche Ltd., Basel, Switzerland;
William T CarpenterDepartment of Psychiatry, Maryland Psychiatric Research Center, University of Maryland School of Medicine, Baltimore, MD;
John T CsernanskyDepartment of Psychiatry, Northwestern University Feinberg School of Medicine, Evanston, IL;
Pedro L DagoDepartment of Psychiatry, Northwestern University Feinberg School of Medicine, Evanston, IL;
Dante M DurandDepartment of Psychiatry and Behavioral Sciences, University of Miami School of Medicine, Miami, FL;
Frederick J FreseDepartment of Psychiatry, Northeast Ohio Medical University, Rootstown, OH;
Donald C GoffDepartment of Psychiatry, Nathan Kline Institute, and New York University School of Medicine New York, NY;
James M GoldDepartment of Psychiatry, Maryland Psychiatric Research Center, University of Maryland School of Medicine, Baltimore, MD;
Christine I HookerHarvard University;
Alex KopelowiczPsychiatry and Behavioral Sciences, David Geffen School of Medicine at UCLA, Los Angeles, CA;
Antony LoebelGlobal Clinical Development, Sunovion, Ft. Lee, NJ;
Susan R McGurkCenter for Psychiatric Rehabilitation, Boston University, Boston, MA;
Lewis A OplerDepartment of Psychiatry, Columbia University, New York, NY;
Amy E PinkhamSchool of Behavioral and Brain Sciences, The University of Texas at Dallas, Richardson, TX;
Robert G SternEssex County Hospital Center, Cedar Grove, NJ.
University of Maryland, Baltimore · USColumbia University · USNorthwestern University · USUniversity of Miami · USAbbVie (United States) · USBoston University · USHarvard University Press · USNathan Kline Institute for Psychiatric Research · USNortheast Ohio Medical University · USQueen's University · CARoche (Switzerland) · CHSheba Medical Center · ILTakeda (Japan) · JPThe University of Texas at Dallas · USThomas Cole Historic House · USUniversity of California, Los Angeles · USVion Pharmaceuticals (United States) · US

Funding

The Effects of Kynurenine Aminotransferase Inhibition in People with SchizophreniaP50MH103222 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE · PI SCHWARCZ, ROBERT · 2014 to 2023
$25.2M
NIMH NIH HHS P50 MH103222
6 · The paper itself

Abstract

If treatments for cognitive impairment are to be utilized successfully, clinicians must be able to determine whether they are effective and which patients should receive them. In order to develop consensus on these issues, the International Society for CNS Clinical Trials and Methodology (ISCTM) held a meeting of experts on March 20, 2014, in Washington, DC. Consensus was reached on several important issues. Cognitive impairment and functional disability were viewed as equally important treatment targets. The group supported the notion that sufficient data are not available to exclude patients from available treatments on the basis of age, severity of cognitive impairment, severity of positive symptoms, or the potential to benefit functionally from treatment. The group reached consensus that cognitive remediation is likely to provide substantial benefits in combination with procognitive medications, although a substantial minority believed that medications can be administered without nonpharmacological therapy. There was little consensus on the best methods for assessing cognitive change in clinical practice. Some participants supported the view that performance-based measures are essential for measurement of cognitive change; others pointed to their cost and time requirements as evidence of impracticality. Interview-based measures of cognitive and functional change were viewed as more practical, but lacking validity without informant involvement or frequent contact from clinicians. The lack of consensus on assessment methods was viewed as attributable to differences in experience and education among key stakeholders and significant gaps in available empirical data. Research on the reliability, validity, sensitivity, and practicality of competing methods will facilitate consensus.

Indexed as

Schizophrenic PsychologyAntipsychotic AgentsCognition DisordersHumansNeuropsychological TestsNootropic AgentsPatient SelectionPsychiatric RehabilitationSchizophreniaSeverity of Illness IndexAntipsychotic AgentsNootropic Agentscognitive assessmentneuropsychologytreatment

Identifiers

PMID26362273
PMCPMC4681562
OpenAlexW1949836637

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.