首页> 美国卫生研究院文献>Journal of Clinical Medicine >Paliperidone Palmitate Every Three Months (PP3M) 2-Year Treatment Compliance Effectiveness and Satisfaction Compared with Paliperidone Palmitate-Monthly (PP1M) in People with Severe Schizophrenia
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Paliperidone Palmitate Every Three Months (PP3M) 2-Year Treatment Compliance Effectiveness and Satisfaction Compared with Paliperidone Palmitate-Monthly (PP1M) in People with Severe Schizophrenia

机译:Paliperidone棕榈酸盐每三个月(PP3M)2年治疗合规性有效性和满意度与严重精神分裂症的人的人们(PP1M)相比

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摘要

Paliperidone palmitate every three months (PP3M) is expected to facilitate patient’s treatment compliance and satisfaction. The objective here was to compare PP3M treatment compliance and satisfaction, effectiveness and tolerability, with paliperidone palmitate-monthly (PP1M) in patients with severe schizophrenia. A 24-month prospective, open-label study of patients with severe schizophrenia treated with PP3M after at least 2 years of stabilization with PP1M (n = 84) was carried out. Treatment satisfaction was assessed with the Treatment Satisfaction Questionnaire for Medication (TSQM) and with a Visual Analogue Scale (VAS). Effectiveness was measured with psychiatric hospital admissions and the Clinical Global Impression-Severity (CGI-S) scale. Tolerability assessments included laboratory tests, weight and adverse effects. Reasons for treatment discontinuation were recorded. CGI-S significantly improved after 24 months. Three patients changed back to PP1M due to adverse effects, and four were hospitalized. There were neither abandoning nor significant changes in weight or biological parameters, and lower incidence of side effects, with PP3M treatment. TSQM and VAS scales increased. No differences were found related to doses. Apart from somewhat improvement in treatment adherence, effectiveness, and tolerability, patients with severe schizophrenia lengthy treated with PP1M showed more satisfaction with PP3M, even those who needed high doses to get clinical stabilization.
机译:预计每三个月棕榈酸棕榈酸棕榈酸术(PP3M)将促进患者的治疗遵守性和满意度。这里的目的是将PP3M治疗依从性和满足,有效性和耐受性与严重精神分裂症的患者进行比较,帕利酮棕榈酸酯 - 月(PP1M)。进行了24个月的前瞻性,在用PP1M(n = 84)稳定至少2年后,用PP3M治疗严重精神分裂症患者的患者的前瞻性开放标签研究。用治疗满意度调查问卷(TSQM)和视觉模拟量表(VAS)评估治疗满意度。用精神病院入院和临床全球印象 - 严重程度(CGI-S)衡量了有效性。可耐受性评估包括实验室测试,重量和不良反应。记录了治疗中断的原因。 24个月后CGI-S显着改善。由于不良反应,三名患者因不良反映而变回PP1M,四个都住院了。 PP3M治疗既没有放弃也没有放弃或重量或生物参数的重量或生物参数发生率降低。 TSQM和VAS尺度增加。没有发现差异与剂量有关。除了治疗依恋,有效性和耐受性的情况下,患有PP1M的严重精神分裂症的患者均为PP3M延长,甚至是那些需要高剂量以获得临床稳定的人也更满意。

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