Papachristos Apostolos, Kani Chara, Litsa Panagiota, Valsami Georgia, Souliotis Kyriakos, Saridi Maria, Markantonis Sophia
Faculty of Pharmacy, Laboratory of Biopharmaceutics-Pharmacokinetics, National and Kapodistrian University of Athens, Athens, Greece.
Consult Pharm. 2016 May;31(5):271-81. doi: 10.4140/TCP.n.2016.271.
Anemia in the elderly is often related to a higher prevalence of chronic diseases such as chronic kidney failure, arthritis, and malignancy. Erythropoiesis-stimulating agents (ESAs) have been used for years to effectively treat anemia and when used appropriately can substantially improve the health status and quality of life of older adults. Following the 2008 recession in Greece, the government introduced ESA price control restrictions, but no prescribing restrictions, in an effort to reduce drug expenditure.
ESA prescribing patterns and treatment costs were analyzed to determine inappropriate or appropriate use of these agents and related health care resources in Greece.
A retrospective register-based drug utilization study was carried out using data from prescriptions dispensed at the public pharmacy of the largest social insurance fund (IKA-ETAM), for patients receiving ESAs over a six-month period. For each patient, demographic data, ESA dosage regimen, treatment indication and cost, prescriber specialty, and prescription origin were recorded.
A total of 14,387 prescriptions from 6,074 patients (median age 74 years) were reviewed. A substantial number of patients (13.5%) were treated for off-label indications, for which the average cost per patient per indication was higher. ESA dosage/frequency of administration varied but was in accordance with recommendations. The percentage of patients who received innovator and biosimilar erythropoietin (EPO) was 88% and 12%, respectively.
For the optimization of ESA utilization and the reduction of treatment costs, strict ESA prescription monitoring, development of registries, and criteria for off-label indications and biosimilar use in naive patients under the umbrella of risk-sharing agreements should be proposed.
老年人贫血通常与慢性疾病(如慢性肾衰竭、关节炎和恶性肿瘤)的较高患病率相关。促红细胞生成素(ESA)多年来一直用于有效治疗贫血,适当使用时可显著改善老年人的健康状况和生活质量。2008年希腊经济衰退后,政府为降低药品支出,实施了ESA价格控制限制,但未实施处方限制。
分析希腊ESA的处方模式和治疗成本,以确定这些药物的使用是否不当或合理以及相关的医疗资源使用情况。
开展一项基于登记册的回顾性药物利用研究,使用来自最大社会保险基金(IKA - ETAM)公共药房在六个月期间发放的ESA处方数据。记录每位患者的人口统计学数据、ESA剂量方案、治疗适应症和费用、开处方者专业以及处方来源。
共审查了来自6074名患者(中位年龄74岁)的14387张处方。相当数量的患者(13.5%)接受了超适应症治疗,每个适应症每位患者的平均费用更高。ESA剂量/给药频率各不相同,但符合推荐标准。接受创新型和生物类似促红细胞生成素(EPO)的患者百分比分别为88%和12%。
为优化ESA使用并降低治疗成本,应建议在风险分担协议框架下,对ESA处方进行严格监测、建立登记册以及制定针对初治患者超适应症用药和生物类似药使用的标准。