Wang Sheng-Min, Han Changsu, Lee Soo-Jung, Patkar Ashwin A, Masand Prakash S, Pae Chi-Un
*Department of Psychiatry, The Catholic University of Korea, College of Medicine; †Department of Psychiatry, Korea University College of Medicine, Seoul, Republic of Korea; ‡Department of Psychiatry and Behavioural Sciences, Duke University Medical Center, Durham, NC; and § Global Medical Education, New York, NY.
Clin Neuropharmacol. 2013 Nov-Dec;36(6):223-38. doi: 10.1097/WNF.0b013e3182aa38c4.
Schizophrenia is a serious, chronic, and devastating mental illness with a substantial impact on psychological, physical, social, and economical areas of an individual and society. To treat such critical mental illness, a number of first-generation (typical) and second-generation (atypical) antipsychotics are currently available in the market. Despite such treatment options, most of patients with schizophrenia have a poor treatment outcome and become treatment resistant, causing continual deterioration on positive, negative, and cognitive symptoms, resulting in impairment of socio-occupational functioning. Hence, additional novel antipsychotics with better efficacy, safety, and tolerability profiles are needed to enable clinicians to diversify treatment options to improve treatment of schizophrenia. Recently, the 3 antipsychotics, including iloperidone (2009), asenapine (2009), and lurasidone (2010), have been approved by the US Food and Drug Administration. Two other atypical antipsychotics, including sertindole and blonanserin, are approved and used outside the United States for treatment of schizophrenia. Sertindole, after it has been voluntarily suspended by the manufacturer in 1998 due to its potential risk in causing cardiovascular-related death, was relaunched to the European market in 2005. More recently, blonanserin was approved in Japan (2008) and in Korea (2009) for the management of schizophrenia. Individual antipsychotic may have differential pros and cons compared with other antipsychotic in terms of efficacy, safety, tolerability, restoration of functional capacity, and economic aspect reflecting relapse prevention. The purpose of this review was to provide distinctive clinical characteristics and up-to-date of clinical trial data of the 5 novel atypical antipsychotics for the management of schizophrenia, which may deliver clinicians better understanding in the use of such atypical antipsychotics for the treatment of schizophrenia in clinical practice.
精神分裂症是一种严重、慢性且具有毁灭性的精神疾病,对个人和社会的心理、身体、社会和经济领域都有重大影响。为了治疗这种严重的精神疾病,目前市场上有多种第一代(传统型)和第二代(非典型)抗精神病药物。尽管有这些治疗选择,但大多数精神分裂症患者的治疗效果不佳且产生耐药性,导致阳性、阴性和认知症状持续恶化,进而损害社会职业功能。因此,需要更多具有更好疗效、安全性和耐受性的新型抗精神病药物,以使临床医生能够多样化治疗选择,从而改善精神分裂症的治疗。最近,包括伊潘立酮(2009年)、阿立哌唑(2009年)和鲁拉西酮(2010年)在内的3种抗精神病药物已获得美国食品药品监督管理局的批准。另外两种非典型抗精神病药物,包括舍吲哚和布南色林,在美国以外地区被批准用于治疗精神分裂症。舍吲哚曾因有导致心血管相关死亡的潜在风险,于1998年被制造商自愿撤市,2005年重新进入欧洲市场。最近,布南色林于2008年在日本、2009年在韩国被批准用于治疗精神分裂症。与其他抗精神病药物相比,每种抗精神病药物在疗效、安全性、耐受性、功能恢复能力以及反映预防复发的经济方面可能都有不同的优缺点。本综述的目的是提供这5种用于治疗精神分裂症的新型非典型抗精神病药物独特的临床特征和最新临床试验数据,这可能有助于临床医生在临床实践中更好地理解如何使用这些非典型抗精神病药物来治疗精神分裂症。