Impact of clozapine once-daily versus multiple-daily dosing regimen on relapse in patients with treatment-resistant schizophrenia: A 1-year retrospective cohort study.

IF 3.5 3区 医学 Q2 NEUROSCIENCES Psychopharmacology Pub Date : 2024-08-06 DOI:10.1007/s00213-024-06658-x
Masaru Tsukahara, Ryuhei So, Kohei Kitagawa, Yuji Yada, Masafumi Kodama, Shinichiro Nakajima, Yoshiki Kishi, Norihito Yamada, Hiroyoshi Takeuchi
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Abstract

Rationale: Clozapine, the standard treatment for treatment-resistant schizophrenia (TRS), is generally recommended in a multiple-daily dosing regimen. However, it is commonly administered once daily in clinical practice. Few studies have compared the longitudinal clinical outcomes of these two dosing regimens.

Objective: To investigate the effect of once-daily versus multiple-daily dosing regimens of clozapine on relapse in patients with TRS.

Methods: This retrospective cohort study included patients with TRS who commenced treatment with clozapine during hospitalization and were discharged between April 2012 and January 2022 from a tertiary psychiatric hospital in Japan. Relapse, defined as a psychiatric exacerbation requiring re-hospitalization within the first-year post-discharge, was analyzed. Multivariable Cox proportional hazards regression analysis compared the relapse risk between once-daily and multiple-daily dosing regimens. A subgroup analysis was conducted to examine the potential interactions between dosing regimen and dose category (low versus high dose).

Results: Among 179 patients, 107 (59.8%) received clozapine once daily. No significant difference in the relapse risk was observed between once-daily and multiple-daily dosing regimens (adjusted hazard ratio [aHR]: 1.16; 95% confidence interval [CI]: 0.68-1.99; p = 0.58). However, in patients receiving high doses of clozapine (> 300 mg/day), multiple-daily dosing increased the relapse risk compared to once-daily dosing (aHR: 2.23; 95% CI: 1.00-4.97; p = 0.049).

Conclusions: Once-daily clozapine dosing may not be associated with an increased relapse risk. The increased relapse risk in high-dose multiple-daily dosing may be confounded by unmeasured non-adherence. Further randomized controlled trials are required to validate these findings.

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每日一次氯氮平与每日多次氯氮平给药方案对耐药精神分裂症患者复发的影响:为期一年的回顾性队列研究。
理由氯氮平是治疗耐药性精神分裂症(TRS)的标准疗法,一般建议每天多次给药。但在临床实践中,氯氮平通常每天给药一次。很少有研究对这两种给药方案的纵向临床疗效进行比较:研究氯氮平每日一次与每日多次给药方案对 TRS 患者复发的影响:这项回顾性队列研究纳入了日本一家三级精神病医院2012年4月至2022年1月期间住院期间开始接受氯氮平治疗并出院的TRS患者。研究分析了复发情况,复发的定义是出院后第一年内需要再次住院治疗的精神症状加重。多变量考克斯比例危险回归分析比较了每日一次和每日多次给药方案的复发风险。还进行了亚组分析,以研究给药方案与剂量类别(低剂量与高剂量)之间的潜在相互作用:在179名患者中,107人(59.8%)每天服用一次氯氮平。每日一次和每日多次给药方案的复发风险无明显差异(调整后危险比 [aHR]:1.16;95% 置信区间 [CI]:0.68-1.99; p = 0.58).然而,在接受大剂量氯氮平(> 300 毫克/天)的患者中,与每日一次给药相比,每日多次给药会增加复发风险(aHR:2.23;95% CI:1.00-4.97;p = 0.049):结论:每天服用一次氯氮平可能与复发风险增加无关。结论:每日一次氯氮平用药可能与复发风险增加无关,每日多次大剂量用药导致的复发风险增加可能与未测量的不依从性有关。需要进一步的随机对照试验来验证这些发现。
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来源期刊
Psychopharmacology
Psychopharmacology 医学-精神病学
CiteScore
7.10
自引率
5.90%
发文量
257
审稿时长
2-4 weeks
期刊介绍: Official Journal of the European Behavioural Pharmacology Society (EBPS) Psychopharmacology is an international journal that covers the broad topic of elucidating mechanisms by which drugs affect behavior. The scope of the journal encompasses the following fields: Human Psychopharmacology: Experimental This section includes manuscripts describing the effects of drugs on mood, behavior, cognition and physiology in humans. The journal encourages submissions that involve brain imaging, genetics, neuroendocrinology, and developmental topics. Usually manuscripts in this section describe studies conducted under controlled conditions, but occasionally descriptive or observational studies are also considered. Human Psychopharmacology: Clinical and Translational This section comprises studies addressing the broad intersection of drugs and psychiatric illness. This includes not only clinical trials and studies of drug usage and metabolism, drug surveillance, and pharmacoepidemiology, but also work utilizing the entire range of clinically relevant methodologies, including neuroimaging, pharmacogenetics, cognitive science, biomarkers, and others. Work directed toward the translation of preclinical to clinical knowledge is especially encouraged. The key feature of submissions to this section is that they involve a focus on clinical aspects. Preclinical psychopharmacology: Behavioral and Neural This section considers reports on the effects of compounds with defined chemical structures on any aspect of behavior, in particular when correlated with neurochemical effects, in species other than humans. Manuscripts containing neuroscientific techniques in combination with behavior are welcome. We encourage reports of studies that provide insight into the mechanisms of drug action, at the behavioral and molecular levels. Preclinical Psychopharmacology: Translational This section considers manuscripts that enhance the confidence in a central mechanism that could be of therapeutic value for psychiatric or neurological patients, using disease-relevant preclinical models and tests, or that report on preclinical manipulations and challenges that have the potential to be translated to the clinic. Studies aiming at the refinement of preclinical models based upon clinical findings (back-translation) will also be considered. The journal particularly encourages submissions that integrate measures of target tissue exposure, activity on the molecular target and/or modulation of the targeted biochemical pathways. Preclinical Psychopharmacology: Molecular, Genetic and Epigenetic This section focuses on the molecular and cellular actions of neuropharmacological agents / drugs, and the identification / validation of drug targets affecting the CNS in health and disease. We particularly encourage studies that provide insight into the mechanisms of drug action at the molecular level. Manuscripts containing evidence for genetic or epigenetic effects on neurochemistry or behavior are welcome.
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