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首页> 外文期刊>International clinical psychopharmacology >Relationship between plasma concentration levels of risperidone and clinical effects in the treatment of delirium.
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Relationship between plasma concentration levels of risperidone and clinical effects in the treatment of delirium.

机译:利培酮的血浆浓度水平与of妄治疗的临床效果之间的关系。

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摘要

The present study aimed to examine the relationship between plasma concentration levels of risperidone and clinical effects in the treatment of delirium. We conducted a prospective, open-label, flexible-dose study of risperidone oral solution. Ten patients with delirium were assessed using Delirium Rating Scales. Plasma concentration levels of risperidone were measured 30 min after the first administration of a 0.5 mg dose. Two patients with high plasma levels had adverse effects and one patient with the lowest plasma level did not achieve remission; the remaining seven patients achieved remission without any adverse effects. A highly significant negative correlation was observed in these responders without adverse effects between the plasma levels and durations of treatment until remission (r=-0.861, P=0.0095). The plasma concentration level of risperidone at 30 min after the first 0.5 mg dose may be a favourable response predictor in the treatment of delirium. Further studies in larger samples are needed to verify this preliminary finding.
机译:本研究旨在检查血浆利培酮浓度水平与clinical妄治疗的临床效果之间的关系。我们进行了利培酮口服溶液的前瞻性,开放标签,灵活剂量研究。使用Deli妄评定量表评估十名with妄患者。首次给予0.5 mg剂量后30分钟测量利培酮的血浆浓度水平。两名血浆水平高的患者有不良反应,而血浆水平最低的一名患者未达到缓解。其余7例患者均获得缓解,无任何不良反应。在这些反应者中观察到高度显着的负相关性,血浆水平和直至缓解的治疗持续时间之间无不良影响(r = -0.861,P = 0.0095)。最初0.5 mg剂量后30分钟时利培酮的血浆浓度水平可能是治疗ir妄的有利反应指标。需要对更大的样本进行进一步的研究以验证这一初步发现。

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