Cited by 198Obsessive-Compulsive Spectrum DisordersSchizophrenia research and treatmentPsychoanalysis and Psychopathology Research

The DOI matches its Crossref record; 19 of the 19 references it cites were found in a registry or an index.

Risperidone augmentation in treatment-resistant obsessive–compulsive disorder: a double-blind, placebo-controlled study

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Hollander, Eric, Rossi, Nicolò Baldini, Sood, Erica, Pallanti, Stefano·2003·The International Journal of Neuropsychopharmacology

Abstract

This double-blind, placebo-controlled trial was performed to determine the efficacy and tolerability of 8 wk of risperidone augmentation of serotonin reuptake inhibitor (SRI) treatment in adult subjects with treatment-resistant obsessive-compulsive disorder (OCD) (failure of at least two SRI trials). Sixteen adult treatment-resistant OCD patients were randomly assigned to augmentation with 8 wk of either risperidone (n=10) (0.5-3.0 mg/d) or placebo (n=6) following at least 12 wk of SRI treatment. Four patients on risperidone (40%) and none (0%) on placebo were responders with both a Clinical Global Impression - Improvement (CGI-I) score of 1 or 2 and a Yale-Brown Obsessive-Compulsive Scale (Y-BOCS) decrease >/=25%. Risperidone was generally well tolerated: there were 3 dropouts, 1 on risperidone and 2 on placebo. Better Y-BOCS insight score at baseline significantly correlated with a greater CGI-I score at endpoint on risperidone augmentation. Risperidone may be an effective and well-tolerated augmentation strategy in treatment-resistant OCD subjects, but larger sample size studies are required to demonstrate this.

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  • Second-generation antipsychotic agents have shown benefit in OCD, either alone or as adjunctive therapy; high-dose olanzapine, quetiapine, and risperidone have all shown at least minimal clinical benefit relative to placebo.

    “Recently, second-generation antipsychotic agents have shown benefit, either alone or as adjunctive therapy. Specifically, high-dose olanzapine [522], quetiapine [523], and risperidone [524] have all shown at least minimal clinical benefit relative to placebo treatment [525].”

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Metadata

Authors
Hollander, E., Rossi, N. B., Sood, E., & Pallanti, S.
Affiliations
  • Icahn School of Medicine at Mount Sinai (US)
  • University of Pisa (IT)
  • University of Florence (IT)
Corresponding author
Hollander, Eric
Venue
The International Journal of Neuropsychopharmacology
Published
2003-12
Volume
6
Issue
4
Pages
397-401
ISSN
  • 1461-1457 (ISSN-L)
  • 1469-5111
OpenAlex
W1966161934
Cited by
197
References
19
Citations by year
2026: 2 · 2025: 5 · 2024: 5 · 2023: 3 · 2022: 3 · 2021: 3 · 2020: 3 · 2019: 7 · 2018: 8 · 2017: 7 · 2016: 5 · 2015: 16 · 2014: 10 · 2013: 7 · 2012: 10
FWCI
17.49
Type
journal article
Language
en
Open access
Locations
  • The International Journal of Neuropsychopharmacology (publishedVersion)
  • PubMed (publishedVersion)
  • INFM-OAR (INFN Catania) (submittedVersion, other-oa)
Funders
Janssen Pharmaceuticals
Topics
  • Social Sciences › Psychology › Clinical Psychology › Obsessive-Compulsive Spectrum Disorders
  • Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
  • Social Sciences › Psychology › Clinical Psychology › Psychoanalysis and Psychopathology Research
Keywords
risperidone, treatment-resistant OCD, augmentation therapy, serotonin reuptake inhibitors, antipsychotic augmentation, drug tolerability, treatment response, insight, Yale-Brown Obsessive Compulsive Scale, Clinical Global Impression Scale
MeSH terms
Adult, Ambulatory Care, Dose-Response Relationship, Drug, Double-Blind Method, Drug Administration Schedule, Drug Resistance, Drug Therapy, Combination, Female, Humans, Male, Middle Aged, Obsessive-Compulsive Disorder, Personality Inventory, Antipsychotic Agents, Treatment Outcome, Selective Serotonin Reuptake Inhibitors, Risperidone

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