Risperidone ISM®: review and update of its usefulness in all phases of schizophrenia.

IF 3.4 3区 医学 Q2 PHARMACOLOGY & PHARMACY Therapeutic Advances in Psychopharmacology Pub Date : 2024-10-04 eCollection Date: 2024-01-01 DOI:10.1177/20451253241280046
Thomas Messer, Miquel Bernardo, Lourdes Anta, Javier Martínez-González
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Abstract

One of the most important challenges in the management of patients with schizophrenia is to ensure adherence to antipsychotic treatment. The contribution of long-acting injectables (LAI) is undeniable in this matter, but there are still some unmet medical needs not covered by these drugs (e.g. quick onset of action for patients with acute exacerbation of schizophrenia). This article summarises the pharmacokinetics, efficacy and safety of Risperidone ISM (in situ microparticles). The aim of this review is to provide information about the potential uses of this new LAI formulation of risperidone for the treatment of schizophrenia, contextualising and diving into the published evidence. Risperidone ISM shows a rapid release which allows achieving within 12 h risperidone active moiety levels similar to those observed in the steady-state for oral risperidone treatment, achieving a mean average concentration of 38.63 ng/mL. The plasma concentration of active moiety achieved by Risperidone ISM comes with a predictable dopamine D2 receptor occupancy above 65% throughout the 28-day dosing period, which is accepted as a threshold for the efficacy of the antipsychotic treatment. This can be associated with the positive efficacy findings throughout its clinical development. In the short term, it provides an early and progressive reduction of symptoms in adult patients with acute exacerbation of schizophrenia without the need for loading doses or oral risperidone supplementation, which could contribute to reinforcing the therapeutic alliance between the patient and the psychiatrist. In addition, long-term treatment was effective, safe and well tolerated regardless of the initial disease severity or whether patients were previously treated with Risperidone ISM during an acute exacerbation or switched from stable doses of oral risperidone. Improvement and maintenance of personal and social functioning and health-related quality of life were observed in each setting, respectively. All these findings endorse Risperidone ISM as a useful and valuable treatment for the acute and maintenance management of patients with schizophrenia.

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利培酮 ISM®:回顾并更新其在精神分裂症各阶段的实用性。
精神分裂症患者治疗过程中最重要的挑战之一就是确保患者坚持接受抗精神病治疗。长效注射剂(LAI)在这方面的贡献毋庸置疑,但仍有一些医疗需求尚未得到满足(例如,精神分裂症急性加重患者的快速起效)。本文总结了利培酮 ISM(原位微粒)的药代动力学、疗效和安全性。本综述旨在提供有关利培酮这种新型LAI制剂在治疗精神分裂症方面的潜在用途的信息,并对已发表的证据进行背景分析和深入研究。利培酮 ISM 具有快速释放的特点,可在 12 小时内达到与口服利培酮治疗稳态时相似的利培酮活性分子水平,平均浓度为 38.63 纳克/毫升。在整个 28 天的用药期间,利培酮 ISM 所达到的血浆活性分子浓度可预测地高于 65% 的多巴胺 D2 受体占有率,而这一占有率被认为是抗精神病药物疗效的临界值。这与该药物在整个临床开发过程中取得的积极疗效有关。在短期内,该药可使精神分裂症急性加重的成年患者的症状早期逐渐减轻,而无需服用负荷剂量或补充口服利培酮,这有助于加强患者与精神科医生之间的治疗联盟。此外,无论患者最初的病情严重程度如何,也无论患者之前是在急性加重期接受利培酮ISM治疗,还是从稳定剂量的口服利培酮转为利培酮治疗,长期治疗都是有效、安全和耐受性良好的。在每种情况下,患者的个人和社会功能以及与健康相关的生活质量都分别得到了改善和维持。所有这些研究结果都表明,利培酮ISM是精神分裂症患者急性期和维持期治疗的一种有用且有价值的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.90
自引率
2.40%
发文量
35
审稿时长
10 weeks
期刊介绍: Therapeutic Advances in Psychopharmacology delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies across all areas of psychopharmacology. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in psychopharmacology, providing a forum in print and online for publishing the highest quality articles in this area.
期刊最新文献
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