Lindell-Osuagwu L, Hakkarainen M, Sepponen K, Vainio K, Naaranlahti T, Kokki H
School of Pharmacy, University of Eastern Finland, Kuopio, Finland.
J Clin Pharm Ther. 2014 Apr;39(2):144-53. doi: 10.1111/jcpt.12119. Epub 2013 Dec 16.
The European Paediatric Regulation aims to reduce off-label use of medicines in paediatric pharmacotherapy. Prescribing for off-label use and unauthorized medicines was common in the paediatric wards of the Kuopio University Hospital in 2001. To evaluate the possible impact of the Regulation on the prevalence and the frequency on such prescribing, we repeated the study in 2011 as it was conducted 10 years earlier.
In this prospective study, the prescriptions for patients below 18 years of age were reviewed during a 2-week period in each of the three wards; neonatal intensive care unit, general paediatric ward and paediatric surgical ward in April and May 2011. The medicine's authorizing status of all prescriptions was determined according to the approved summary of product characteristics valid during the study in Finland. Data concerning unauthorized medicines were also recorded and classified.
Out of the entire study population of 123 patients, 119 received a total of 1054 prescriptions in 2011. The proportion of patients with at least one prescription for off-label use or for an unauthorized medicine was significantly higher, 79% (n = 97) in 2011, compared to 58% in 2001 (P < 0·001). For newborns, significantly more prescriptions were for off-label use in 2011 than in 2001 (51% vs. 22%; P < 0·001). The proportion of prescriptions for unauthorized medicines was significantly higher in children below 2 years of age than in older children in both years (21% vs. 5% in 2011 and 24% vs. 3% in 2001, P < 0·001).
The prescribing for off-label use and unauthorized medicines was more prevalent in 2011 than in 2001. This indicates that the recent legislation has had only minor or no impact on the authorizing status of medicines commonly used in paediatric inpatients in specialized care.
欧洲儿科用药法规旨在减少儿科药物治疗中的超说明书用药情况。2001年,在库奥皮奥大学医院的儿科病房,超说明书用药和使用未经批准药物的处方很常见。为评估该法规对这类处方的发生率和频率可能产生的影响,我们于2011年重复了这项10年前开展的研究。
在这项前瞻性研究中,于2011年4月和5月,在三个病房(新生儿重症监护病房、普通儿科病房和儿科外科病房)对18岁以下患者的处方进行了为期2周的审查。根据芬兰研究期间有效的批准产品特性摘要确定所有处方药物的批准状态。还记录并分类了有关未经批准药物的数据。
在2011年的123名研究对象中,119人共接受了1054张处方。2011年,至少有一张超说明书用药或使用未经批准药物处方的患者比例显著高于2001年,分别为79%(n = 97)和58%(P < 0.001)。对于新生儿,2011年超说明书用药的处方明显多于2001年(51% 对 22%;P < 0.001)。在这两年中,2岁以下儿童使用未经批准药物的处方比例均显著高于大龄儿童(2011年为21% 对 5%,2001年为24% 对 3%,P < 0.001)。
2011年超说明书用药和使用未经批准药物的处方比2001年更为普遍。这表明,近期的立法对专科护理中儿科住院患者常用药物的批准状态影响甚微或没有影响。