Adolescent schizophrenia

  • 文章类型: Journal Article
    在39%的精神分裂症患者中,精神病症状的发作发生在19岁之前。青少年精神分裂症的批准治疗选择有限。Brexpiprazole于2022年获得美国食品和药物管理局(FDA)批准用于治疗青少年精神分裂症。
    将成人数据外推至青少年,并使用药物模型结合公开的长期安全性数据,FDA批准了宝立哌唑治疗青少年精神分裂症。这些都在这里进行了综述。
    D2受体部分激动剂抗精神病药物在精神病治疗的早期阶段是优选的。在青少年精神分裂症中批准brexpiprazole提供了另一种选择。Brexpiprazole是FDA根据成人数据外推批准的,没有在青少年中进行对照试验。这减少了年轻人的安慰剂暴露。先前批准用于成人精神分裂症的两种药物(阿塞那平和齐拉西酮)在青少年精神分裂症研究中未能与安慰剂分开;这在一定程度上破坏了外推过程。对于布立哌唑,青少年数据的匮乏使其沦为二线代理。需要更多的研究来描述其在青少年精神分裂症管理中的相对作用。
    UNASSIGNED: The onset of psychotic symptoms occurs prior to age 19 in 39% of the patients with schizophrenia. There are limited approved treatment options for adolescents with schizophrenia. Brexpiprazole was approved by the United States Food and Drug Administration (FDA) for treatment of schizophrenia in adolescents in 2022.
    UNASSIGNED: Extrapolation of adult data to youth and use of pharmacologic modeling coupled with open long-term safety data were used by the FDA to approve brexpiprazole for adolescent schizophrenia. They were all reviewed herein.
    UNASSIGNED: D2 receptor partial agonist antipsychotic agents are preferred in the early phase of treatment of psychotic disorders. Approval of brexpiprazole in adolescent schizophrenia provides an additional option. Brexpiprazole was approved by the FDA on the basis of extrapolation of adult data without controlled trials in adolescents. This reduces placebo exposure in young people. Two previous agents (asenapine and ziprasidone) approved for adult schizophrenia failed to separate from placebo in adolescent schizophrenia studies; this partially undermines the process of extrapolation. For brexpiprazole, the paucity of data in adolescents relegates it to a second-line agent. More research on brexpiprazole is needed to delineate its relative role in the management of adolescent schizophrenia.
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  • 文章类型: Review
    精神分裂症通常始于青春期的前驱症状。在39%的患者中,精神病症状的发作发生在19岁之前。本文综述了近十年来药物治疗精神病的研究进展。
    了解如何在精神分裂症早期开出抗精神病药,需要了解疾病的病理生理学。综述了目前多巴胺假说的结构。利培酮,帕潘立酮,奥氮平,喹硫平,阿立哌唑和阿立哌唑在2012年之前已成为既定治疗方法.自2012年以来,鲁拉西酮(2017年)和布立哌唑(2022年)也已获得批准。Lurasidone基于安慰剂对照研究获得批准,但在公开安全性试验的基础上,已获批准.在比较试验中,阿立哌唑的耐受性较好,较少引起高催乳素血症和代谢异常.
    抗精神病药可以引起大脑的适应性变化,使患者容易出现迟发性运动障碍和超敏性精神病等未来问题。当精神分裂症的病理生理学,和现有的抗精神病药物的药理学清楚的理解包括在循证分析,使用部分激动剂,不太可能引起大脑的适应性变化,并且不太可能引起代谢和催乳素副作用,成为首选代理商。
    UNASSIGNED: Schizophrenia usually begins with prodromal symptoms in adolescence. In 39% of patients, onset of psychotic symptoms occurs prior to age 19. Advances in the treatment of psychosis with medications over the last decade are reviewed in this paper.
    UNASSIGNED: Understanding how to prescribe antipsychotics early in schizophrenia requires an understanding of the pathophysiology of the disease. The current structure of the dopamine hypothesis is reviewed. Risperidone, paliperidone, olanzapine, quetiapine, and aripiprazole have become established treatments prior to 2012. Since 2012, lurasidone (2017) and brexpiprazole (2022) have also been approved. Lurasidone was approved based on placebo-controlled studies, but brexpiprazole has been approved on the bases of open safety trials. In comparative trials, aripiprazole was better tolerated and less likely to cause hyperprolactinemia and metabolic abnormalities.
    UNASSIGNED: Antipsychotics can induce adaptive changes in the brain that predispose patients to future problems such as tardive dyskinesia and supersensitivity psychosis. When pathophysiology of schizophrenia, and a clear understanding of the pharmacology of existing antipsychotics are included in the evidence-based analysis, use of partial agonists, which are less likely to induce adaptive changes in the brain and less likely to induce metabolic and prolactin side effects, become the preferred agents.
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  • 文章类型: Journal Article
    UNASSIGNED:目前将精神分裂症概念化为神经发育障碍,应该在重组精神卫生保健系统方面导致创新的公共卫生政策,特别是在从青春期到成年的过渡中,为了减少个人,熟悉的,社会成本和负担。该项目的目的是在意大利精神分裂症专家小组中进行一项调查,分享有关青少年精神分裂症的循证信息,并探索以下四个宏观领域专业人员的共识程度:早期诊断;药物治疗;医疗保健系统的组织和从青少年到成年的过渡过程;和社会心理干预措施。
    UNASSIGNED:共识过程由基于Web的两步Delphi方法组成,发生在2021年6月至11月之间。这项调查是由四名精神科医生和四名儿童神经精神科医生组成的小组制定的,被确定为关键意见领袖(KOL)。KOL确定了21项陈述,涉及70个项目,主要需要澄清早发性精神分裂症(EOS)。该调查已分发给86名精神病学和儿童神经精神病学专家。
    UNASSIGNED:结果显示,专家组在青少年精神分裂症的护理和管理模式的所有调查领域都达成了共识。德尔福调查的67个项目(95.7%)最终达成了共识,对2个项目达成了否定共识,对1个项目没有达成共识。
    未经评估:总的来说,结果表明,获得的科学知识与临床实践之间存在显着差距。在这种情况下,应该有必要在多个层面规划具体举措,编辑临床决策建议,以及促进政治和组织层面的变革,还涉及科学社会,病人,和家庭协会,克服拖延实施进程的障碍。
    UNASSIGNED: The current conceptualization of schizophrenia as neurodevelopmental disorder should lead to innovative public health policies in terms of a reorganization of the mental health care systems, particularly in the transition from adolescence to adulthood, to reduce personal, familiar, and social costs and burdens. The purpose of the project was to perform a survey among a panel of Italian schizophrenia experts, to share evidence-based information on adolescent schizophrenia and explore the degree of consensus among professionals in the following four macro-areas: early diagnosis; pharmacological treatment; health care system organization and transition process from adolescent to adulthood; and psychosocial interventions.
    UNASSIGNED: The consensus process consisted of a two-step web-based Delphi method, which took place between June and November 2021. The survey was developed by a panel of four psychiatrists and four child neuropsychiatrists, identified as key opinion leaders (KOLs). The KOLs identified 21 statements involving a total of 70 items with a major need of clarification on early-onset schizophrenia (EOS). The survey was distributed to 86 specialists in psychiatry and child neuropsychiatry.
    UNASSIGNED: The results revealed a large agreement among the expert group on all the investigated areas of adolescent schizophrenia patterns of care and management. Consensus was ultimately reached for 67 items of the Delphi survey (95.7%), while negative consensus was reached for 2 items and no consensus was reached for 1 item.
    UNASSIGNED: Overall, results showed a significant gap between the acquired scientific knowledge and clinical practice. In this scenario, it should be necessary to plan specific initiatives at a multiple level, to edit recommendations on clinical decision-making, as well as to prompt changes at the political and organizational levels, also involving scientific societies, patients, and family associations, to overcome the barriers that delay the implementation process.
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