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Background: There is limited evidence on the outcomes of clozapine deprescribing in remitted treatment-resistant schizophrenia (TRS) patients. We present a series of TRS patients in remission who underwent progressive reductions in their maintenance clozapine dose.
Study Design: This was a retrospective chart review of patients treated with clozapine from March 20, 2014 to March 20, 2024, at the Centre for Addiction and Mental Health, Toronto, Canada. We included patients who met criteria for TRS, were in remission on clozapine, and underwent progressive reduction > 25% in their maintenance dose.
Study Results: Of the 9 cases included, 4 (44.4%) maintained remission following progressive dose reductions. Two patients (22.2%) relapsed and were hospitalized, while 3 (33.3%) relapsed and required an increase in clozapine dose. Of those who relapsed, 3 had subtherapeutic clozapine levels and one had stopped clozapine before relapse. Overall dose reductions ranged from 100% (complete discontinuation with sustained remission) to 25% (with subsequent dose increase after relapse). The average rate of clozapine reduction was slow across cases, with a median of 25 mg every 12 weeks. Although not statistically significant, patients who maintained remission had slower tapering rates, ranging from 25 mg every 5 weeks to 25 mg every 2 years.
Conclusions: Reducing the clozapine maintenance dose in remitted TRS patients carried a substantial risk of relapse. The risk may be lower when dose reductions are guided by clozapine levels and implemented gradually over several months to years. Larger samples are needed to identify predictors of relapse in TRS patients undergoing clozapine deprescribing.
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http://dx.doi.org/10.1093/schbul/sbaf139 | DOI Listing |
J Clin Epidemiol
September 2025
TRS National Resource Center for Rare Disorders, Sunnaas Hospital, Bjørnemyrveien 11, 1453, Bjørnemyr, Norway.
WHAT IS THIS PAPER ABOUT?: Important decisions about healthcare are made in guideline meetings. It is therefore important to involve people who will be affected by the decision. This can include patients, healthcare workers and policy makers.
View Article and Find Full Text PDFDisabil Rehabil
September 2025
TRS National Resource Centre for Rare Disorders, Department of Innovation and Research, Sunnaas Rehabilitation Hospital, Nesodden, Norway.
Purpose: Stickler syndrome is a rare, hereditary connective tissue disorder characterized by visual, auditory, and musculoskeletal complications. Research on quality of life remains limited. This study aimed to: (i) explore existing literature on psychosocial aspects, pain, fatigue, and quality of life in individuals with Stickler syndrome, (ii) describe the impact of health complaints on daily living, contacts with healthcare- and social service systems and quality of life in a cohort of adults with Stickler syndrome.
View Article and Find Full Text PDFJ Clin Psychiatry
August 2025
Department of Psychiatry, Kasturba Medical College, Manipal Academy of Higher Education, Manipal, India; Department of Clinical Psychopharmacology and Neurotoxicology, National Institute of Mental Health and Neurosciences, Bangalore, India.
Schizophrenia is a major mental illness with a median lifetime prevalence, across studies, of 0.5%. Across definitions of treatment resistance, about 37% of schizophrenia patients do not respond to treatment, and about 24% are treatment resistant from the first-episode, itself.
View Article and Find Full Text PDFBackground: 22q11.2 deletion syndrome is associated with schizophrenia, seizures, and often experience intolerance to antipsychotics. Periventricular nodular heterotopia (PNH) is a neuronal migration disorder that can also be observed in individuals with 22q11.
View Article and Find Full Text PDFMol Psychiatry
August 2025
Engineering Research Center of Molecular and Neuro Imaging of the Ministry of Education, School of Life Science and Technology, Xidian University, Xian, 710126, China.
Negative symptoms in treatment-resistant schizophrenia (TRS) are notably persistent and minimally affected by antipsychotics, the transcutaneous auricular vagus nerve stimulation (taVNS) is a promising treatment approach. However, clinical trials are scarce, and further efficacy data are needed. We conducted a double-blind, sham-controlled, randomized clinical trial to determine the efficacy and safety of taVNS as an add-on treatment for patients with TRS with predominantly negative symptoms and to investigate potential biomarkers of efficacy.
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