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住院患者服用分劈药片的利弊 被引量:20

The Advantages and Disvantages of Split Tablets Given to In-patients
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摘要 目的 :探讨住院患者服用分劈药片的利弊。方法 :收集我院由药师分劈、住院患者常用的13种处方药片 ,每种10片 ,共260个分劈片 ,采用《美国药典》剂量单位一致性测试方法分析分劈药片的重量变异性。结果 :药片分劈后均未通过剂量单位一致性测试。药片分劈效果与外形有关 ,带有刻线的相对好一些。在分劈过程中都存在一定的剂量损耗。结论 :药片分劈导致高比率的重量变异 ,故为节省开支而分劈药片的做法仅适合于那些低毒和剂量 -反应效应曲线相对平坦的药物 ,对于那些毒性较大和剂量 OBJECTIVE:To analyse the advantages and disvantages of split tablets given to in-patients.METHODS:We collected13kinds of oral tablets(10tablets each kind and260pieces of the split tablet altogether),which were often splitted by pharmaceutists.We tested and analysed the weight variation of the split tablet on the basis of the dosage consistency metioned in the USP which is applied to the whole tablet.RESULTS:None of the13kinds of prescription drug passed the consistent testing after splitting.There was some relationship between the effect of the split tablet and its shape.It was relatively easy to break off the tablet with nick in half.The loss of dosage inevitably occurred during the process of splitting the tablet.CONCLUSION:Breaking off the tablet in half led to high ratio of weight variation.The modus operandi of splitting the tablet in half for saving expenses can only be applied to those drugs with low toxicities and relatively flat dose-effect curve.In the case of those drugs which bear high toxicities and steep dose-effect curve,carefulness should always be taken when applying such method.
出处 《中国药房》 CAS CSCD 2004年第8期509-510,共2页 China Pharmacy
关键词 分劈药片 重量变异 相对标准差 损耗率 split tablet weight variation relative standard deviation rate of loss
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参考文献3

  • 1Jay SC.Tablet splittind:Imperfest perhaps,but better than excessive dosing[J] .Journal of the American Pharmaceutical Association , 2002,42:160. 被引量:1
  • 2Jack MR,Josephp N,Fotios P.Weight variability of pharmacist .Dispensed split tablets[J] .Journal of the American Pharmaceutical Association, 2002,42: 200. 被引量:1
  • 3Jaja T,Clara KS,Roger LW,et al .Lack of medication dose uniformity in commonly split tablets[J] .Journal of the American Pharmaceutical Association, 2002,42:195. 被引量:1

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