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Sources and magnitude of error in preparing morphine infusions for nurse-patient controlled analgesia in a UK paediatric hospital

机译:在英国一家儿科医院中为护理人员控制的镇痛准备吗啡输注液的误差来源和严重程度

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Background Administering nurse/patient controlled analgesia (N/PCA) to children requires complex dose calculations and multiple manipulations to prepare morphine solutions in 50 mL syringes for administration by continuous infusion with additional boluses. Objective To investigate current practice and accuracy during preparation of morphine N/PCA infusions in hospital theatres and wards at a UK children's hospital. Methods Direct observation of infusion preparation methods and morphine concentration quantification using UV-Vis spectrophotometry. The British Pharmacopoeia specification for morphine sulphate injection drug content (+/- 7.5 %) was used as a reference limit. Results Preparation of 153 morphine infusions for 128 paediatric patients was observed. Differences in preparation method were identified, with selection of inappropriate syringe size noted. Lack of appreciation of the existence of a volume overage (i.e. volume in excess of the nominal volume) in morphine ampoules was identified. Final volume of the infusion was greater than the target (50 mL) in 33.3 % of preparations. Of 78 infusions analysed, 61.5 % had a morphine concentration outside 92.5-107.5 % of label strength. Ten infusions deviated by more than 20 %, with one by 100 %. Conclusions Variation in morphine infusion preparation method was identified. Lack of appreciation of the volume overage in ampoules, volumetric accuracy of different syringe sizes and ability to perform large dilutions of small volumes were sources of inaccuracy in infusion concentration, resulting in patients receiving morphine doses higher or lower than prescribed.
机译:背景对儿童进行护士/患者自控镇痛(N / PCA)要求复杂的剂量计算和多种操作,以在50 mL注射器中制备吗啡溶液,以便通过连续输注额外的大剂量给药。目的探讨英国儿童医院在医院剧院和病房中制备吗啡N / PCA输注时的现行做法和准确性。方法直接观察输液制备方法,并采用紫外可见分光光度法对吗啡浓度进行定量。硫酸吗啡注射药物含量(+/- 7.5%)的英国药典规范被用作参考限值。结果观察到128例儿科患者制备了153剂吗啡。确定了制备方法的差异,并指出了选择不合适的注射器尺寸。发现缺乏对吗啡安瓿中存在容量超支(即,超出标称容量的容量)的欣赏。在33.3%的制剂中,最终输注体积大于目标值(50 mL)。在分析的78次输注中,有61.5%的吗啡浓度超出标签强度的92.5-107.5%。 10次​​输注的偏差超过20%,其中1次的偏差为100%。结论确定了吗啡输注方法的差异。缺乏对安瓿中过量药物的认识,不同注射器尺寸的体积准确性以及对小体积进行大稀释的能力是输注浓度不准确的根源,导致患者接受的吗啡剂量高于或低于处方剂量。

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