4CPS-344 Prescription auditing of the 3 monthly formulation of paliperidone palmitate in adult patients with schizophrenia

S. Nobili, N. Rossetti, S. Davies, L. Gambitta, E. Calzavara, E. Magni, S. Vimercati
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Abstract

Background and importance The 3 monthly formulation of paliperidone palmitate (3MPP) was introduced to the Italian market in 2017 for the treatment of schizophrenia in adult patients. 3MPP is a useful treatment option for patients who are adequately treated with the 1 monthly formulation of paliperidone palmitate (PP) but who may benefit from longer dosing intervals. Aim and objectives To assess the appropriateness of 3MPP prescriptions and the effectiveness of treatment in our centre. Material and methods This was an observational retrospective study of patients with a 3MPP prescription between January 2018 and July 2020. The variables used to evaluate appropriateness were the number of switches from PP to 3MPP, dosage and administration time. Effectiveness was evaluated by recording treatment interruptions, dose variations and switch back to PP. Data were extracted from an administrative database and collected in Excel. Results 38 patients were included, 23 men (60.5%), with a mean age of 50±14 years. The dosages of 3MPP were: 175 mg in 5 patients (13.2%), 263 mg in 6 (15.8%), 350 mg in 18 (47.4%) and 525 mg in 9 (23.7%). In 30 patients (78.9%), the 3MPP prescription was appropriate. The number of switches was 35/38 (92.1%): 3 patients received a first prescription of 3MPP without a previous prescription of antipsychotic depot drugs from our centre. An appropriate dosage was selected in 33/35 patients (94.3%): 1 patient switched from PP 100 mg to 3MPP 263 mg and another from PP 150 mg to 3MPP 263 mg. An appropriate administration time was selected in 35/38 patients (92.1%): 1 patient took the drug every 4 months and two patients received only one administration of 3MPP. In total, six patients interrupted treatment (3 in 2019; 3 in 2020). Dose variation of 3MPP during treatment occurred in 2 patients: 1 switched from 3MPP 350 mg to 525 mg and the other from 3MPP 263 mg to 350 mg. Two patients returned to treatment with PP. Conclusion and relevance Most of the 3MPP prescriptions were appropriate. This treatment has been shown to be effective in this setting where clinical diagnosis and therapeutic choice are not simple and medication adherence is a clinical challenge. The intervention of the pharmacist by auditing prescriptions is important to further increase appropriate treatments in these patients. References and/or acknowledgements Conflict of interest No conflict of interest
成人精神分裂症患者3个月服用棕榈酸帕利哌酮的处方审核
背景和重要性帕利哌酮棕榈酸酯(3MPP)于2017年被引入意大利市场,用于治疗成人精神分裂症患者。3MPP是一个有用的治疗选择,患者充分治疗1个月的配方棕榈酸帕利哌酮(PP),但谁可能受益于较长的给药间隔。目的和目的评价我院3MPP处方的适宜性和治疗效果。材料和方法本研究是一项观察性回顾性研究,研究对象为2018年1月至2020年7月期间服用3MPP处方的患者。用于评估适宜性的变量是从PP到3MPP的切换次数、剂量和给药时间。通过记录治疗中断、剂量变化和切换回PP来评估有效性。数据从管理数据库中提取并在Excel中收集。结果纳入38例患者,其中男性23例(60.5%),平均年龄50±14岁。3MPP的剂量为:175 mg 5例(13.2%),263 mg 6例(15.8%),350 mg 18例(47.4%),525 mg 9例(23.7%)。在30例(78.9%)患者中,3MPP处方是合适的。切换次数为35/38(92.1%):3例患者首次使用3MPP处方,既往未使用本中心抗精神病药物储备。33/35例患者(94.3%)选择了合适的剂量:1例患者从PP 100 mg切换到3MPP 263 mg,另1例患者从PP 150 mg切换到3MPP 263 mg。38例患者中有35例(92.1%)选择了合适的给药时间:1例患者每4个月服药一次,2例患者仅服用一次3MPP。共有6名患者中断治疗(2019年为3名;2020年3个)。2例患者在治疗期间出现3MPP剂量变化:1例从3MPP 350 mg切换到525 mg,另1例从3MPP 263 mg切换到350 mg。结论及相关性大多数3MPP处方是合适的。在这种情况下,临床诊断和治疗选择并不简单,药物依从性是一项临床挑战,这种治疗已被证明是有效的。药师通过审核处方的干预对于进一步增加对这些患者的适当治疗是重要的。参考文献和/或致谢利益冲突无利益冲突
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