他汀类药物高、平均和低消费量的挪威县的他汀类药物处方方面——一项个人水平的处方数据库研究。

Ingeborg Hartz, Solveig Sakshaug, Kari Furu, Anders Engeland, Anne Elise Eggen, Inger Njølstad, Svetlana Skurtveit
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引用次数: 39

摘要

背景:先前的一项研究表明,他汀类药物用于一级预防的阈值和强度(脂质目标实现)的差异导致挪威他汀类药物总体消费量的地区差异。我们的目的是探讨个体患者中他汀类药物的使用流行率、剂量特征、选择和治疗连续性的差异如何为先前的结果增加新的信息。方法:数据从挪威处方数据库中检索。我们纳入了来自他汀类药物消费量高、平均和低的县的个人,他们在2004年至少有一个他汀类药物处方(N = 40143)。1年患病率,每日处方剂量(PDD),他汀类药物的选择,和治疗的连续性评估平均片剂每天。结果:高消费县各年龄组他汀类药物使用率均较高。79-87%的他汀类药物使用者配用了阿托伐他汀和辛伐他汀,高消费县的比例明显更高。估计的pdd高于DDD,高达阿托伐他汀DDD的两倍。高消费县辛伐他汀(25.9 mg)和阿托伐他汀(21.9 mg)的PDD最高,更多的用户服用的片剂在可用剂量的上限范围内。治疗的连续性在三个国家是相似的。结论:虽然年龄分布的差异似乎是他汀类药物消费差异的一个重要来源,但它不能解释挪威各县之间的总体差异。在PDD和他汀类药物选择方面,使用流行率和治疗强度的变化也会影响总消费量。本研究的结果似乎与先前的发现相一致,即他汀类药物在一级预防中的使用频率更高,在他汀类药物消费量最高的县,更多的他汀类药物使用者达到了血脂目标。
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Aspects of statin prescribing in Norwegian counties with high, average and low statin consumption - an individual-level prescription database study.

Background: A previous study has shown that variations in threshold and intensity (lipid goal attainment) of statins for primary prevention contribute to regional differences in overall consumption of statins in Norway. Our objective was to explore how differences in prevalences of use, dosing characteristics, choice of statin and continuity of therapy in individual patients adds new information to previous results.

Methods: Data were retrieved from The Norwegian Prescription Database. We included individuals from counties with high, average, and low statin consumption, who had at least one statin prescription dispensed during 2004 (N = 40 143).1-year prevalence, prescribed daily dose (PDD), statin of choice, and continuity of therapy assessed by mean number of tablets per day.

Results: The high-consumption county had higher prevalence of statin use in all age groups. Atorvastatin and simvastatin were dispensed in 79-87% of all statin users, and the proportion was significantly higher in the high-consumption county. The estimated PDDs were higher than the DDDs, up to twice the DDD for atorvastatin. The high-consumption county had the highest PDD for simvastatin (25.9 mg) and atorvastatin (21.9 mg), and more users received tablets in the upper range of available strengths. Continuity of therapy was similar in the three counties.

Conclusion: Although differences in age-distribution seems to be an important source of variation in statin consumption, it cannot account for the total variation between counties in Norway. Variations in prevalences of use, and treatment intensity in terms of PDD and choice of statin also affect the total consumption. The results in this study seems to correspond to previous findings of more frequent statin use in primary prevention, and more statin users achieving lipid goal in the highest consuming county.

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