TY - JOUR
T1 - Treatment resistant schizophrenia and response to antipsychotics
T2 - A review
AU - Suzuki, Takefumi
AU - Remington, Gary
AU - Mulsant, Benoit H.
AU - Rajji, Tarek K.
AU - Uchida, Hiroyuki
AU - Graff-Guerrero, Ariel
AU - Mamo, David C.
N1 - Funding Information:
Dr. Mulsant currently receives research support from the Canadian Institutes of Health Research, the US National Institute of Health (NIH), Bristol-Myers Squibb (medications for a NIH-funded clinical trial), and Wyeth (medications for a NIH-funded clinical trial). Over the past three years, he has also received research support (medications for a NIH-funded clinical trial) from Eli Lilly and Pfizer and travel support from Roche.
Funding Information:
Dr. Suzuki has received fellowship grants from the Japanese Society of Clinical Neuropsychopharmacology, Government of Canada Post-Doctoral Research Fellowships, Kanae Foundation and Mochida Memorial Foundation, manuscript fees from Dainippon Sumitomo Pharma and speakers' honoraria from Eli Lilly.
Funding Information:
Dr. Remington currently receives support from the following Canadian Institutes of Health Research: Schizophrenia Society of Ontario, and the Canadian Diabetes Association. He has also received research support from Novartis Canada, Medicure Inc. and Neurocrine in the last 2 years. In addition, he has received consultant fees from CanAm Bioresearch Inc., Roche, Neurocrine and Medicure Inc., and speaker's fees from Novartis.
Funding Information:
Dr. Rajji has received research support from the Brain and Behavior Research Foundation (previously known as NARSAD), the Canadian Foundation for Innovation, the Canadian Institutes of Health Research, the Ontario Ministry of Health and Long-Term Care, the Ontario Ministry of Research and Innovation, and the US Department of Veterans Affairs.
PY - 2011/12
Y1 - 2011/12
N2 - Background: There remains a lack of agreement regarding criteria for treatment-resistant schizophrenia (TRS) and definition of response. Method: A literature search was conducted to identify clinical studies of antipsychotics in TRS using PubMed, EMBASE and PsycINFO (last search 31 July 2011). Psychopharmacological studies with the number of participants of ≥ 40 were evaluated in terms of definitions for TRS and subsequent treatment response. Results: Thirty-three studies of antipsychotics in TRS were reviewed. TRS has been defined mainly by severity in symptoms. Many studies based TRS with at least 2 failed adequate antipsychotic trials (at chlorpromazine equivalent doses of ≥ 1000. mg/day for ≥ 6. weeks), but some studies adopted prospective treatment arm to be certain of sample refractoriness. Treatment response has been defined by a relative change in the representative scales (most commonly ≥ 20% decrease in the Positive and Negative Syndrome Scale), but it sometimes included the absolute criteria such as post-treatment score of ≤ 35 in the Brief Psychiatric Rating Scale or Clinical Global Impression-severity score of ≤ 3 (mild or less severe). Social functioning has not been a primary outcome measure in past pivotal trials, and other important domains of the illness such as cognition and subjective perspectives have not been incorporated into definitions of treatment resistance or response. However, adopting various assessment scales can be time-consuming and complicated, with an additional possibility of disagreement among raters. Conclusion: Defining outcomes in schizophrenia is a challenging task. It is imperative that the field agrees on how this population is better defined and what constitutes treatment response.
AB - Background: There remains a lack of agreement regarding criteria for treatment-resistant schizophrenia (TRS) and definition of response. Method: A literature search was conducted to identify clinical studies of antipsychotics in TRS using PubMed, EMBASE and PsycINFO (last search 31 July 2011). Psychopharmacological studies with the number of participants of ≥ 40 were evaluated in terms of definitions for TRS and subsequent treatment response. Results: Thirty-three studies of antipsychotics in TRS were reviewed. TRS has been defined mainly by severity in symptoms. Many studies based TRS with at least 2 failed adequate antipsychotic trials (at chlorpromazine equivalent doses of ≥ 1000. mg/day for ≥ 6. weeks), but some studies adopted prospective treatment arm to be certain of sample refractoriness. Treatment response has been defined by a relative change in the representative scales (most commonly ≥ 20% decrease in the Positive and Negative Syndrome Scale), but it sometimes included the absolute criteria such as post-treatment score of ≤ 35 in the Brief Psychiatric Rating Scale or Clinical Global Impression-severity score of ≤ 3 (mild or less severe). Social functioning has not been a primary outcome measure in past pivotal trials, and other important domains of the illness such as cognition and subjective perspectives have not been incorporated into definitions of treatment resistance or response. However, adopting various assessment scales can be time-consuming and complicated, with an additional possibility of disagreement among raters. Conclusion: Defining outcomes in schizophrenia is a challenging task. It is imperative that the field agrees on how this population is better defined and what constitutes treatment response.
KW - Definition
KW - Response
KW - Treatment-resistant schizophrenia
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U2 - 10.1016/j.schres.2011.09.016
DO - 10.1016/j.schres.2011.09.016
M3 - Review article
C2 - 22000940
AN - SCOPUS:81955161935
SN - 0920-9964
VL - 133
SP - 54
EP - 62
JO - Schizophrenia Research
JF - Schizophrenia Research
IS - 1-3
ER -