Gahr Maximilian, Kölle Markus A, Schönfeldt-Lecuona Carlos, Lepping Peter, Freudenmann Roland W
Department of Psychiatry and Psychotherapy, University of Ulm, Ulm, Germany.
Drug Des Devel Ther. 2011 Mar 11;5:125-46. doi: 10.2147/DDDT.S17266.
Paliperidone (9-hydroxy-risperidone), the active metabolite of risperidone, was approved for treating schizophrenia worldwide in 2006 as paliperidone extended-release (PER), and became the first second-generation antipsychotic specifically licensed for treating schizoaffective disorder in 2009. However, at the same time, its comparatively high cost gave rise to concerns about the cost-effectiveness of PER as compared with its precursor, risperidone. This paper reviews the existing knowledge of the pharmacology, kinetics, efficacy, tolerability, and fields of application of PER, and compares PER with risperidone in order to determine whether it has a place in antipsychotic therapy. An independent assessment of all relevant publications on PER published until July 2010 was undertaken. PER has a unique pharmacological profile, including single dosing, predominantly renal excretion, low drug-drug interaction risk, and differs from risperidone in terms of mode of action and pharmacokinetics. High-level evidence suggests that PER is efficacious and safe in schizophrenia, schizoaffective disorder, and acute manic episodes. There is a striking lack of published head-to-head comparisons between PER and risperidone, irrespective of indication. Low-level evidence shows a lower risk for hyperprolactinemia and higher patient satisfaction with PER than with risperidone. PER adds to the still limited arsenal of second-generation antipsychotics. In the absence of direct comparisons with risperidone, it remains difficult to come to a final verdict on the potential additional therapeutic benefits of PER which would justify its substantially higher costs as compared with risperidone. However, in terms of pharmacology, the available evidence cautiously suggests a place for PER in modern antipsychotic therapy.
帕利哌酮(9-羟基利培酮)是利培酮的活性代谢产物,于2006年作为帕利哌酮缓释片(PER)在全球获批用于治疗精神分裂症,并于2009年成为首个专门获批用于治疗分裂情感性障碍的第二代抗精神病药物。然而,与此同时,其相对较高的成本引发了人们对帕利哌酮缓释片与它的前体药物利培酮相比成本效益的担忧。本文回顾了关于帕利哌酮缓释片的药理学、动力学、疗效、耐受性及应用领域的现有知识,并将帕利哌酮缓释片与利培酮进行比较,以确定其在抗精神病治疗中是否有一席之地。对截至2010年7月发表的所有关于帕利哌酮缓释片的相关出版物进行了独立评估。帕利哌酮缓释片具有独特的药理学特征,包括单次给药、主要经肾脏排泄、药物相互作用风险低,并且在作用方式和药代动力学方面与利培酮不同。高级别证据表明,帕利哌酮缓释片在治疗精神分裂症、分裂情感性障碍及急性躁狂发作时有效且安全。无论适应证如何,帕利哌酮缓释片与利培酮之间均缺乏已发表的直接对比研究。低级别证据显示,与利培酮相比,帕利哌酮缓释片导致高催乳素血症的风险更低,患者满意度更高。帕利哌酮缓释片为第二代抗精神病药物这一仍较有限的药物库增添了品种。由于缺乏与利培酮的直接对比,目前仍难以最终判定帕利哌酮缓释片潜在的额外治疗益处是否足以证明其成本远高于利培酮是合理的。然而,从药理学角度来看,现有证据谨慎地表明帕利哌酮缓释片在现代抗精神病治疗中占有一席之地。