Citrome Leslie
Department of Psychiatry and Behavioral Sciences, New York Medical College, Valhalla, NY, USA.
Patient Prefer Adherence. 2016 Aug 9;10:1529-37. doi: 10.2147/PPA.S45401. eCollection 2016.
When treating persons with schizophrenia, delaying time to relapse is a main goal. Antipsychotic medication has been the primary treatment approach, and there are a variety of different choices available. Lurasidone is a second-generation (atypical) antipsychotic agent that is approved for the treatment of schizophrenia and bipolar depression. Three long-term studies of lurasidone have examined time to relapse in persons with schizophrenia, including a classic placebo-controlled randomized withdrawal study and two 12-month active comparator studies (vs risperidone and vs quetiapine extended-release). Lurasidone 40-80 mg/d evidenced superiority over placebo (number needed to treat [NNT] vs placebo for relapse, 9). Lurasidone 40-160 mg/d was noninferior to quetiapine extended-release 200-800 mg/d on the outcome of relapse, and was superior on the outcome of avoidance of hospitalization (NNT 8) and the outcome of remission (NNT 7). Lurasidone demonstrated a lower risk for long-term weight gain than the active comparators. Demonstrated differences in tolerability profiles among the different choices of antipsychotics make it possible to attempt to match up an individual patient to the best choice for such patient based on past history of tolerability, comorbidities, and personal preferences, potentially improving adherence.
在治疗精神分裂症患者时,延迟复发时间是一个主要目标。抗精神病药物一直是主要的治疗方法,并且有多种不同选择。鲁拉西酮是一种第二代(非典型)抗精神病药物,已被批准用于治疗精神分裂症和双相抑郁症。三项关于鲁拉西酮的长期研究考察了精神分裂症患者的复发时间,包括一项经典的安慰剂对照随机撤药研究和两项为期12个月的活性对照研究(分别与利培酮和喹硫平缓释片对照)。鲁拉西酮40 - 80mg/天在复发方面显示出优于安慰剂(复发时治疗所需人数[NNT]与安慰剂相比为9)。鲁拉西酮40 - 160mg/天在复发结局上不劣于喹硫平缓释片200 - 800mg/天,在避免住院结局(NNT为8)和缓解结局(NNT为7)上更优。与活性对照药物相比,鲁拉西酮显示出较低的长期体重增加风险。不同抗精神病药物在耐受性方面已显示出差异,这使得有可能根据患者过去的耐受性病史、合并症和个人偏好,为个体患者匹配最佳选择,从而可能提高依从性。