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首页> 外文期刊>Progress in Neuro-Psychopharmacology & Biological Psychiatry: An International Research, Review and News Journal >Safety and tolerability of deltoid and gluteal injections of paliperidone palmitate in schizophrenia.
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Safety and tolerability of deltoid and gluteal injections of paliperidone palmitate in schizophrenia.

机译:帕潘立酮棕榈酸酯的三角肌和臀肌注射在精神分裂症中的安全性和耐受性。

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摘要

Paliperidone palmitate is an investigational, injectable atypical antipsychotic. The safety and tolerability of initiating treatment with paliperidone palmitate via deltoid versus gluteal injections given once monthly, and of switching injection sites, in adults with stable schizophrenia were assessed. In this crossover trial, stable outpatients (N=252) were randomly assigned 1:1:1 to 3 dose groups (paliperidone palmitate 50, 75, or 100 mg eq.) and 2 treatment sequences (blinded to dose): deltoid muscle (period 1 [13 weeks]) followed by gluteal muscle (period 2 [12 weeks]) or the reverse. The intent-to-treat analysis set had 249 patients: mean age=43 (SD: 12.8) years; 57% men, 81% white, baseline mean Positive and Negative Syndrome Scale (PANSS) total score=56 (SD: 11.5). A total of 170 (68%) patients completed the study, with a similar proportion completing each treatment sequence. The incidence of systemic treatment-emergent adverse events (TEAEs) was similar between the 2 injection sites across doses during period 1 (deltoid [D]: 61% to 67%; gluteus [G]: 58% to 65%), and during the last 8 weeks of the 2 study periods (DG: 32% to 45% [period 1], 29% to 42% [period 2]; GD: 31% to 40% [period 1], 30% to 41% [period 2]). During the first treatment week, median plasma paliperidone concentrations were higher with treatment initiation in the deltoid muscle compared with the gluteal muscle. At apparent steady state, there was little difference in plasma paliperidone concentrations between the deltoid and gluteus sites for a given dose. Local tolerability was slightly better with gluteal injections. Patient preference for injection sites differed between geographical regions, e.g. patients from the US preferred deltoid to gluteal sites. The most common (>or=5% overall) TEAEs were: (period 1) insomnia, anxiety, headache, and agitation; and (period 2) insomnia, psychotic disorder, weight increased, and tachycardia. Paliperidone palmitate treatment was tolerated, irrespective of injection site, and thus could offer the choice of administration into either the deltoid or gluteal muscle to meet patient and physician preference.
机译:帕潘立酮棕榈酸酯是一种可研究的,可注射的非典型抗精神病药。评估了在稳定的精神分裂症患者中,每月一次通过三角肌和臀肌注射帕潘立酮棕榈酸酯开始治疗的安全性和耐受性,以及切换注射部位的安全性和耐受性。在这项交叉试验中,将稳定的门诊患者(N = 252)随机分配为1:1:1的3个剂量组(棕榈酸帕潘立酮50、75或100 mg当量)和2个治疗顺序(按剂量盲法):三角肌(周期1 [13周]),然后是臀肌(周期2 [12周]),或相反。意向治疗分析组有249例患者:平均年龄= 43(SD:12.8)岁; 57%的男性,81%的白人,基线平均阳性和阴性综合征量表(PANSS)总分= 56(标准差:11.5)。共有170位患者(68%)完成了研究,完成每个治疗序列的比例相似。在第1阶段中,不同剂量的2个注射部位之间的全身治疗紧急不良事件(TEAE)的发生率相似(三角肌[D]:61%至67%;臀肌[G]:58%至65%),而在此期间2个研究阶段的最后8周(DG:32%至45%[时段1],29%至42%[时段2]; GD:31%至40%[时段1],30%至41%[期2])。在第一个治疗周期间,与臀肌相比,三角肌中开始治疗时血浆中帕潘立酮的中位数浓度较高。在明显的稳态下,给定剂量的三角肌和臀肌部位血浆帕潘立酮浓度几乎没有差异。臀肌注射局部耐受性稍好。患者对注射部位的偏好在不同的地理区域之间有所不同,例如来自美国的患者首选三角肌而不是臀位。最常见的TEAE(总数≥5%)是:(第1阶段)失眠,焦虑,头痛和躁动。 (第二阶段)失眠,精神病,体重增加和心动过速。帕潘立酮棕榈酸酯治疗不受任何注射部位的影响,因此可以选择对三角肌或臀肌的给药方式,以满足患者和医生的喜好。

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