Gumbs Pearl D, Verschuren W M Monique, Souverein Patrick C, Mantel-Teeuwisse Aukje K, de Wit G Ardine, de Boer Anthonius, Klungel Olaf H
Division of Pharmacoepidemiology and Pharmacotherapy, Utrecht Institute for Pharmaceutical Sciences (UIPS), Utrecht University, Utrecht, The Netherlands.
Br J Clin Pharmacol. 2007 Nov;64(5):680-5. doi: 10.1111/j.1365-2125.2007.02958.x. Epub 2007 Sep 13.
To assess the potential annual savings due to generic and therapeutic substitution of statin therapy for the general Dutch population, taking the patients medical history into account.
We conducted a population-based costing study using the PHARMO Record Linkage System (RLS). PHARMO RLS contains drug dispensing records from a representative sample of pharmacies located in more than 50 regions in the Netherlands. We selected all statin users in the database since 2003. The cost-savings of generic substitution of statin therapy for all simvastatin and pravastatin users, and of therapeutic substitution of statin therapy for other statin users were calculated. Substituting current users and new users of statins were considered separately. Therapeutic substitution was based on the medical history of the individual patient. Patients were only substituted if there was an appropriate substitute available. The appropriateness of substitution was based on drug-drug interactions between statins and possible comedication and the availability of an equipotent alternative.
Substituting (generic and therapeutic) statin therapy for all current users would lead to potential annual savings of approximately 87 million euros. Substituting (generic and therapeutic) all starters on statin therapy would lead to potential annual savings of around 51 million euros. In the case of generic substitution only, the potential annual savings for all current simvastatin and pravastatin users would be 2.4 million euros and for the new users about 1.8 million euros.
From an economic point of view, society could gain a lot from substituting statin therapy, especially from therapeutic substitution.
考虑患者病史,评估荷兰普通人群因他汀类药物的仿制药替代和治疗性替代而可能实现的年度节约。
我们使用PHARMO记录链接系统(RLS)进行了一项基于人群的成本核算研究。PHARMO RLS包含来自荷兰50多个地区代表性药房样本的药品配药记录。我们选取了自2003年以来数据库中的所有他汀类药物使用者。计算了所有辛伐他汀和普伐他汀使用者他汀类药物治疗的仿制药替代成本节约,以及其他他汀类药物使用者他汀类药物治疗的治疗性替代成本节约。分别考虑了他汀类药物现有使用者和新使用者的替代情况。治疗性替代基于个体患者的病史。只有在有合适替代药物时才对患者进行替代。替代的适宜性基于他汀类药物与可能的合并用药之间的药物相互作用以及等效替代药物的可用性。
对所有现有使用者进行(仿制药和治疗性)他汀类药物替代将导致每年约8700万欧元的潜在节约。对所有开始使用他汀类药物治疗的患者进行(仿制药和治疗性)替代将导致每年约5100万欧元的潜在节约。仅考虑仿制药替代的情况下,所有现有辛伐他汀和普伐他汀使用者的年度潜在节约为240万欧元,新使用者约为180万欧元。
从经济角度来看,他汀类药物治疗的替代,尤其是治疗性替代,可为社会带来诸多益处。