Salzman Carl, Jeste Dilip V, Meyer Roger E, Cohen-Mansfield Jiska, Cummings Jeffrey, Grossberg George T, Jarvik Lissy, Kraemer Helena C, Lebowitz Barry D, Maslow Katie, Pollock Bruce G, Raskind Murray, Schultz Susan K, Wang Philip, Zito Julie M, Zubenko George S
Department of Psychiatry, Harvard Medical School, Boston, Mass 02115, USA.
J Clin Psychiatry. 2008 Jun;69(6):889-98. doi: 10.4088/jcp.v69n0602.
Atypical antipsychotic drugs have been used off label in clinical practice for treatment of serious dementia-associated agitation and aggression. Following reports of cerebrovascular adverse events associated with the use of atypical antipsychotics in elderly patients with dementia, the U.S. Food and Drug Administration (FDA) issued black box warnings for several atypical antipsychotics titled "Cerebrovascular Adverse Events, Including Stroke, in Elderly Patients With Dementia." Subsequently, the FDA initiated a metaanalysis of safety data from 17 registration trials across 6 antipsychotic drugs (5 atypical antipsychotics and haloperidol). In 2005, the FDA issued a black box warning regarding increased risk of mortality associated with the use of atypical antipsychotic drugs in this patient population.
Geriatric mental health experts participating in a 2006 consensus conference (Bethesda, Md., June 28-29) reviewed evidence on the safety and efficacy of antipsychotics, as well as nonpharmacologic approaches, in treating dementia-related symptoms of agitation and aggression. EVIDENCE/CONSENSUS PROCESS: The participants concluded that, while problems in clinical trial designs may have been one of the contributors to the failure to find a signal of drug efficacy, the findings related to drug safety should be taken seriously by clinicians in assessing the potential risks and benefits of treatment in a frail population, and in advising families about treatment. Information provided to patients and family members should be documented in the patient's chart. Drugs should be used only when nonpharmacologic approaches have failed to adequately control behavioral disruption. Participants also agreed that there is a need for an FDA-approved medication for the treatment of severe, persistent, or recurrent dementia-related symptoms of agitation and aggression (even in the absence of psychosis) that are unresponsive to nonpharmacologic intervention.
This article outlines methodological enhancements to better evaluate treatment approaches in future registration trials and provides an algorithm for improving the treatment of these patients in nursing home and non-nursing home settings.
非典型抗精神病药物已在临床实践中被用于治疗严重的痴呆相关激越和攻击行为,但未按照药品说明书用药。在有报道称老年痴呆患者使用非典型抗精神病药物会出现脑血管不良事件后,美国食品药品监督管理局(FDA)针对几种非典型抗精神病药物发布了黑框警告,标题为“老年痴呆患者的脑血管不良事件,包括中风”。随后,FDA对6种抗精神病药物(5种非典型抗精神病药物和氟哌啶醇)的17项注册试验的安全数据进行了荟萃分析。2005年,FDA发布了黑框警告,指出在该患者群体中使用非典型抗精神病药物会增加死亡风险。
参加2006年共识会议(6月28 - 29日,马里兰州贝塞斯达)的老年心理健康专家审查了抗精神病药物以及非药物方法在治疗痴呆相关激越和攻击行为症状方面的安全性和有效性证据。
证据/共识过程:参与者得出结论,虽然临床试验设计中的问题可能是未能发现药物疗效信号的原因之一,但临床医生在评估体弱人群治疗的潜在风险和益处以及向家属提供治疗建议时,应认真对待与药物安全性相关的研究结果。提供给患者及其家属的信息应记录在患者病历中。仅在非药物方法未能充分控制行为紊乱时才应使用药物。参与者还一致认为,需要一种经FDA批准的药物来治疗严重、持续或复发的痴呆相关激越和攻击行为症状(即使没有精神病症状),且这些症状对非药物干预无反应。
本文概述了方法学上的改进措施,以便在未来的注册试验中更好地评估治疗方法,并提供了一种算法,用于改善在养老院和非养老院环境中对这些患者的治疗。