澳大利亚口服抗癌药物 10 年来的配药趋势。

IF 2.4 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Michael James Leach, Emily Griffin, Sinead Hickmott, Holly Atkinson, Louise Bettiol, Eli Ristevski
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引用次数: 0

摘要

目的:口服抗癌药物(OAMs)是一种易于使用但高风险的治疗方法。很少有研究调查了OAM分配的国家和次国家趋势。我们的目的是研究澳大利亚国家一级以及州/地区和药物类型/类别的OAM配药的10年趋势。方法:2014-2023年澳大利亚OAM分配和人口的汇总数据分别来自澳大利亚服务局和澳大利亚统计局。年度OAM分配率(每10万人口的数量)是按整体以及州/地区和药物类型/类别计算的。确定了2014年至2023年配药率的百分比变化(Δ)。在有效的情况下,进行Mann-Kendall趋势检验。结果:2014-2023年,澳大利亚每10万人口中任何一种OAM的配药数量从3 475增加到3 930 (+Δ13%),激素OAM从2 659减少到2 225 (-Δ16%),非激素OAM表现出显著的(p)。结论:2014-2023年澳大利亚非激素OAM配药数量增加,主要是PKIs。这可能反映了这些药物的可用性和处方者/患者对这些药物的需求不断增加,表明试点和扩大OAM依从性和安全性举措的范围。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Trends in the Dispensing of Oral Anti-Cancer Medications Across Australia Over 10 Years.

Purpose: Oral anti-cancer medications (OAMs) are easily administered yet high-risk treatments. Few studies have investigated national and subnational trends in OAM dispensing. We aimed to examine 10-year trends in Australia's OAM dispensing at the national level as well as by state/territory and medication type/class.

Methods: Aggregate data on Australia's OAM dispensing and population for 2014-2023 were sourced from Services Australia and the Australian Bureau of Statistics, respectively. Annual OAM dispensing rates (counts per 100 000 population) were calculated overall as well as by state/territory and medication type/class. Percentage change (Δ) in dispensing rates from 2014 to 2023 was determined. Where valid, Mann-Kendall trend tests were performed.

Results: Australia-wide from 2014 to 2023, dispensing counts per 100 000 population for any OAMs increased nonlinearly from 3 475 to 3 930 (+Δ13%), hormonal OAMs decreased nonlinearly from 2 659 to 2 225 (-Δ16%), and non-hormonal OAMs exhibited a significant (p < 0.05) near-linear upward trend from 816 to 1 705 (+Δ109%). This coincided with a significant upward trend in the number of unique non-hormonal OAMs dispensed Australia-wide (+Δ187%). Percentage changes in non-hormonal OAM dispensing rates were greatest for protein kinase inhibitor (PKI) dispensing Australia-wide (+Δ232%), with a significant, near-linear upward trend from 286 to 950, and non-hormonal OAM dispensing in South Australia (+Δ141%), with a significant, near-linear upward trend from 820 to 1972.

Conclusions: Australia's non-hormonal OAM dispensing increased over 2014-2023, mostly for PKIs. This likely reflects rising availability of and prescriber/patient demand for these medications, suggesting scope to pilot and expand OAM adherence and safety initiatives.

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来源期刊
CiteScore
4.80
自引率
7.70%
发文量
173
审稿时长
3 months
期刊介绍: The aim of Pharmacoepidemiology and Drug Safety is to provide an international forum for the communication and evaluation of data, methods and opinion in the discipline of pharmacoepidemiology. The Journal publishes peer-reviewed reports of original research, invited reviews and a variety of guest editorials and commentaries embracing scientific, medical, statistical, legal and economic aspects of pharmacoepidemiology and post-marketing surveillance of drug safety. Appropriate material in these categories may also be considered for publication as a Brief Report. Particular areas of interest include: design, analysis, results, and interpretation of studies looking at the benefit or safety of specific pharmaceuticals, biologics, or medical devices, including studies in pharmacovigilance, postmarketing surveillance, pharmacoeconomics, patient safety, molecular pharmacoepidemiology, or any other study within the broad field of pharmacoepidemiology; comparative effectiveness research relating to pharmaceuticals, biologics, and medical devices. Comparative effectiveness research is the generation and synthesis of evidence that compares the benefits and harms of alternative methods to prevent, diagnose, treat, and monitor a clinical condition, as these methods are truly used in the real world; methodologic contributions of relevance to pharmacoepidemiology, whether original contributions, reviews of existing methods, or tutorials for how to apply the methods of pharmacoepidemiology; assessments of harm versus benefit in drug therapy; patterns of drug utilization; relationships between pharmacoepidemiology and the formulation and interpretation of regulatory guidelines; evaluations of risk management plans and programmes relating to pharmaceuticals, biologics and medical devices.
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