Brexpiprazole Augmentation in Treatment Resistant OCD: Safety and Efficacy in an Italian Sample.

4区 医学 Q2 Medicine
Psychiatria Danubina Pub Date : 2024-09-01
Vassilis Martiadis, Enrico Pessina, Azzurra Martini, Fabiola Raffone, Filippo Besana, Miriam Olivola, Carlo Ignazio Cattaneo
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引用次数: 0

Abstract

Obsessive-compulsive disorder (OCD) is a common and debilitating psychiatric disorder with an approximate incidence of 2.5% in the general population. Serotonin reuptake inhibitors (SRIs) are considered the first line of pharmacological treatment but up to 50% of patients fail to achieve clinical remission or response. Atypical antipsychotics are one of the most common augmentation strategies in OCD treatment resistant patients. Brexpiprazole, a novel atypical antipsychotic with dopamine partial agonism action, has never been studied in addition to SRIs treatment in OCD resistant patients. This study retrospectively investigated the safety and efficacy of a 12 week brexpiprazole augmentation trial in 34 OCD resistant patients. SRI treatment resistance was defined as failing to improve the YBOCS total score by more than 25% from the beginning of the SRI trial. Brexpiprazole augmentation response was defined as at least a 25% improvement in the YBOCS total score. At the end of the study, 17 patients (50.0%) met the response criteria of ≥25% improvement in YBOCS total score vs. baseline. No safety issues were raised throughout the observation period. A total of 19 patients (55.9%) reported adverse experiences, generally mild and not requiring medical intervention. This is the first study to examine the safety and efficacy of brexpiprazole augmentation in resistant OCD patients. Our findings show that brexpiprazole may be a promising and well-tolerated augmentation strategy for SRI-resistant OCD patients. However, further research in larger populations is needed to confirm these results and investigate the long-term safety and tolerability of brexpiprazole in OCD patients.

布雷克普拉唑增效治疗难治性强迫症:意大利样本的安全性和有效性
强迫症(OCD)是一种常见的使人衰弱的精神疾病,在普通人群中的发病率约为 2.5%。血清素再摄取抑制剂(SRIs)被认为是药物治疗的第一线,但多达50%的患者无法获得临床缓解或反应。非典型抗精神病药物是强迫症耐药患者最常用的增效策略之一。布雷哌唑是一种新型非典型抗精神病药物,具有多巴胺部分激动作用,但从未在强迫症耐药患者中进行过SRIs治疗的辅助研究。本研究回顾性地调查了在34名强迫症耐药患者中进行的为期12周的布来哌唑增强试验的安全性和有效性。SRI 治疗耐药的定义是,YBOCS 总分未能比 SRI 试验开始时提高 25% 以上。YBOCS总分至少提高25%即为布雷希拉唑增强反应。研究结束时,有17名患者(50.0%)达到了YBOCS总分与基线相比改善≥25%的应答标准。在整个观察期间,未出现任何安全问题。共有 19 名患者(55.9%)报告了不良反应,一般较轻,不需要医疗干预。这是第一项针对耐药性强迫症患者进行的布雷克哌唑增强治疗安全性和有效性的研究。我们的研究结果表明,对于SRI耐药的强迫症患者来说,布来哌唑可能是一种前景广阔且耐受性良好的增效策略。然而,还需要在更大的人群中开展进一步研究,以证实这些结果,并调查布来哌唑在强迫症患者中的长期安全性和耐受性。
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
Psychiatria Danubina
Psychiatria Danubina 医学-精神病学
CiteScore
3.00
自引率
0.00%
发文量
288
审稿时长
4-8 weeks
期刊介绍: Psychiatria Danubina is a peer-reviewed open access journal of the Psychiatric Danubian Association, aimed to publish original scientific contributions in psychiatry, psychological medicine and related science (neurosciences, biological, psychological, and social sciences as well as philosophy of science and medical ethics, history, organization and economics of mental health services).
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