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必须考虑多项举措,以最大限度地提高仿制药可用性的处方效率:来自阿布扎比的案例历史。

Imperative to consider multiple initiatives to maximize prescribing efficiency from generic availability: case history from Abu Dhabi.

机构信息

Drugs and Medical Products Regulation, Health Authority - Abu Dhabi, PO Box 5674, Abu Dhabi, United Arab Emirates.

出版信息

Expert Rev Pharmacoecon Outcomes Res. 2012 Feb;12(1):115-24. doi: 10.1586/erp.11.90.

Abstract

INTRODUCTION

Pharmaceutical expenditure has risen rapidly in Abu Dhabi, resulting in policies surrounding generics. However, various circumstances will reduce potential savings, including pharmacists still being free to dispense either originator or branded generics and be fully reimbursed.

OBJECTIVES

To research the changes in utilization patterns of proton pump inhibitors (PPIs) and lipid-lowering drugs before and after combined reforms on generics; and subsequently, calculate potential savings based on 'best practices' among Western European countries.

METHODS

An uncontrolled before-and-after observational study of utilization and expenditure of PPIs, statins and ezetimibe between 2004 and 2010, as well as up to 12 months before the first generic policy, to 1 year after the second generic policy, was carried out. Utilization was converted to defined daily doses (DDDs; 2011 DDDs) and DDDs/1000 inhabitants per day. Expenditure/DDD was calculated for omeprazole and simvastatin.

RESULTS

PPI utilization rose by 6.5-fold from 2004 to 2010, principally driven by increased utilization of patent-protected PPIs, although more recently stabilization in esomperazole utilization has occurred. Similar changes were seen for statins. Introduction of best practices would reduce PPI expenditure in 2010 by 32.8 million United Arab Emirates dirham (AED; €6.26 million) and statins by over 27 million AED (€5.15 million).

CONCLUSION

Limited demand-side measures led to increased utilization of patent-protected products in Abu Dhabi following the generic reforms. Successful measures will release considerable resources.

摘要

简介

阿布扎比的药品支出迅速增长,因此出台了一些有关仿制药的政策。但是,各种情况会减少潜在的节省,包括药剂师仍然可以自由配给原研药或品牌仿制药并获得全额报销。

目的

研究在仿制药综合改革前后质子泵抑制剂(PPIs)和降脂药的使用模式变化;随后,根据西欧国家的“最佳实践”计算潜在节省。

方法

对 2004 年至 2010 年间 PPIs、他汀类药物和依折麦布的使用和支出进行了一项非对照的前后观察性研究,以及在第一个仿制药政策之前的 12 个月至第二个仿制药政策之后的 1 年。使用量转换为定义日剂量(DDD;2011 DDD)和每千居民每日 DDD。计算奥美拉唑和辛伐他汀的支出/DDD。

结果

PPIs 的使用量从 2004 年到 2010 年增加了 6.5 倍,主要是由于受专利保护的 PPIs 的使用增加,尽管最近埃索美拉唑的使用趋于稳定。他汀类药物也出现了类似的变化。采用最佳实践将使 2010 年的 PPI 支出减少 3280 万阿联酋迪拉姆(626 万欧元),他汀类药物支出减少 2700 多万阿联酋迪拉姆(515 万欧元)。

结论

在仿制药改革后,阿布扎比的有限需求方措施导致受专利保护产品的使用增加。成功的措施将释放大量资源。

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