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Impact of clinical pharmacist interventions in reducing paediatric prescribing errors

机译:临床药剂师干预措施对减少儿科处方错误的影响

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Objective: To assess the impact of pharmacist intervention in reducing prescribing errors in paediatrics, and to analyse the clinical significance and reasons behind the errors detected. Methods: Cross-sectional epidemiological study analysing the activities of the paediatric pharmacist in a maternity and children's hospital with 180 paediatric beds, between January 2007 and December 2009. The following variables were analysed: impact of the pharmacist's recommendation on patient care, reason for the intervention, clinical significance, type of negative outcome associated with the medication, acceptance rate, medication involved, intervention detection date and observations. Results: A total of 1475 interventions in medical orders for 14 713 paediatric patients were recorded (40 (2.9%) extremely significant interventions and 155 (11.1%) very significant interventions). There were 1357 prescribing errors, 833 of which were dosing errors. 2.2% of the errors detected were potentially fatal (30 cases) and 14.3% (194 cases) were clinically serious. The main reason for interventions was detection of a dosage between 1.5 and 10 times higher than that recommended. The overall rate of acceptance of the pharmacist's suggestions was 94.3%. The pharmacist carried out an average of 0.019 interventions per patient day throughout the study period. Conclusion: Interventions by a clinical pharmacist had a major impact on reducing prescribing errors in the study period, thus improving the quality and safety of care provided.
机译:目的:评估药剂师干预对减少儿科处方错误的影响,并分析所发现错误的临床意义和原因。方法:横断面流行病学研究分析了2007年1月至2009年12月间拥有180张儿科床位的妇幼医院儿科药剂师的活动。分析了以下变量:药剂师建议对患者护理的影响,原因干预,临床意义,与药物相关的阴性结果类型,接受率,所用药物,干预检测日期和观察结果。结果:共记录了1475例针对14 713例儿科患者的医疗订单干预(40例(占2.9%)非常重要的干预措施和155例(占11.1%)非常重要的干预措施)。有1357个处方错误,其中833个是加药错误。检测到的错误中有2.2%具有潜在的致命危险(30例),有14.3%的错误(194例)是临床严重的。干预的主要原因是检测到的剂量比建议的剂量高1.5至10倍。药剂师建议的整体接受率为94.3%。在整个研究期间,该药剂师平均每位患者每天进行0.019次干预。结论:临床药剂师的干预对减少研究期间的处方错误有重大影响,从而提高了所提供护理的质量和安全性。

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