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, Dragana Bugarski-Kirola, William T. Carpenter, John T. Csernansky, Pedro L. Dago, Dante M. Durand, Frederick J. Frese, Donald C. Goff, James M. Gold, Christine I. Hooker, Alex KopelowiczAntony Loebel, Susan R. McGurk, Lewis A. Opler, Amy E. Pinkham, Robert G. Stern

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

36 Scopus citations

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.

Original languageEnglish
Pages (from-to)19-33
Number of pages15
JournalSchizophrenia Bulletin
Volume42
Issue number1
DOIs
StatePublished - 1 Jan 2016
Externally publishedYes

Funding

FundersFunder number
BiolineRX
Department of Veteran
Feinstein Institute for Medical Research
NIH SBIR
NeuroCog Trials, Inc.
Otsuka
Sanofi/Aventis
Sunovion Pharma
Takeda Pharma
University of Texas South West Medical Center
Virtual Reality Functional Capacity Assessment Tool
National Institutes of Health
National Institute of Mental HealthP50MH103222
National Institute of Mental Health
AMGEN
Bristol-Myers Squibb
Eli Lilly and Company
Pfizer
Genentech
GlaxoSmithKline
Novartis
Roche
Teva Pharmaceutical Industries
AbbVie
F. Hoffmann-La Roche
Takeda Pharmaceuticals U.S.A.
Sunovion
INOVIO Pharmaceuticals
FORUM Pharmaceuticals
British Association for Chinese Studies
National Medical Research Council
Dainippon Sumitomo Pharma
Shire
H. Lundbeck A/S

    Keywords

    • cognitive assessment
    • neuropsychology
    • treatment

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