Treatment resistance in schizophrenia: a meta-analysis of prevalence and correlates

被引:14
|
作者
Diniz, Elton [1 ,2 ]
Fonseca, Lais [1 ,2 ]
Rocha, Deyvis [1 ,2 ]
Trevizol, Alisson [3 ,4 ]
Cerqueira, Raphael [1 ,2 ]
Ortiz, Bruno [1 ,2 ]
Brunoni, Andre R. [5 ,6 ]
Bressan, Rodrigo [1 ]
Correll, Christoph U. [7 ,8 ,9 ]
Gadelha, Ary [1 ,2 ,10 ]
机构
[1] Univ Fed Sao Paulo UNIFESP, Dept Psiquiatria, Lab Interdisciplinar Neurociencias Clin, Sao Paulo, SP, Brazil
[2] Univ Fed Sao Paulo, Dept Psiquiatria, Programa Esquizofrenia, Sao Paulo, SP, Brazil
[3] Ctr Addict & Mental Hlth, Toronto, ON, Canada
[4] Univ Toronto, Dept Psychiat, Toronto, ON, Canada
[5] Univ Sao Paulo, Fac Med, Serv Interdisciplinar Neuromodulacao, Inst Psiquiatria,Dept Psiquiatria, Sao Paulo, SP, Brazil
[6] Univ Sao Paulo, Inst Psiquiatria, Lab Neurociencias, Dept Psiquiatria, Sao Paulo, SP, Brazil
[7] Zucker Hillside Hosp, Dept Psychiat, New York, NY USA
[8] Hofstra Northwell, Donald & Barbara Zucker Sch Med, Dept Psychiat & Mol Med, Hempstead, NY USA
[9] Charite Univ Med Berlin, Dept Child & Adolescent Psychiat, Berlin, Germany
[10] Univ Fed Sao Paulo, Dept Psiquiatria, Lab Interdisciplinar Neurociencias Clin, Rua Pedro Toledo,669,3 Andar Fundos, BR-04039032 Sao Paulo, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Schizophrenia; clozapine; treatment-resistant; prevalence; meta-analysis; REAL-WORLD EFFECTIVENESS; 1ST-EPISODE SCHIZOPHRENIA; ANTIPSYCHOTIC TREATMENT; TREATMENT RESPONSE; CLOZAPINE USE; 1ST EPISODE; OPEN-LABEL; RISPERIDONE; PREDICTORS; OLANZAPINE;
D O I
10.47626/1516-4446-2023-3126
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: To define the prevalence and correlates of treatment-resistant schizophrenia (TRS) through a systematic review and meta-analysis.Methods: Following PRISMA criteria, an electronic search was performed in PubMed and EMBASE through May 17, 2022. All study designs that assessed a minimum of 20 schizophrenia-spectrum patients, providing data on TRS prevalence or allowing its calculation, were included. Estimates were produced using a random-effects model meta-analysis.Results: The TRS prevalence across 50 studies (n=29,390 subjects, mean age=38<middle dot>3 +/- 6<middle dot>2 years, males=64<middle dot>8 +/- 12<middle dot>1%, mean illness duration=14<middle dot>3 +/- 5<middle dot>3 years) was 36.7% (95%CI=33.1-40.5%; I2=97.3%, p<0.0001). The prevalence ranged from 22% (95%CI=18.4-25.8%) in first-episode to 39.5% (95%CI=32.2-47.0%) in multiple-episode samples (Q=18.27, p<0.0001). Primary treatment resistance was 23.6% (95%CI=20<middle dot>5-26<middle dot>8%) vs. 9.3% (95%CI=6<middle dot>8-12<middle dot>2) for later-onset/secondary (>= 6 months after initial treatment response). Longer illness duration and recruitment from long-term hospitals or clozapine clinics were associated with higher prevalence estimates. In meta-regression analyses, older age and poor functioning predicted greater TRS. When including only studies with lower bias risk, the TRS prevalence was 28.4%.Conclusions: Different study designs and recruitment strategies accounted for most of the observed heterogeneity in TRS prevalence rates. The results point to early-onset and later-onset TRS as two separate disease pathways requiring clinical attention.
引用
收藏
页码:448 / 458
页数:11
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