Methodological guidance for the use of real-world data to measure exposure and utilization patterns of osteoporosis medications

IF 2.1 Q3 ENDOCRINOLOGY & METABOLISM Bone Reports Pub Date : 2023-12-04 DOI:10.1016/j.bonr.2023.101730
Kaleen N. Hayes , Suzanne M. Cadarette , Andrea M. Burden
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Abstract

Observational studies of osteoporosis medications can provide critical real-world evidence (RWE) that fills knowledge gaps left by clinical trials. However, careful consideration of study design is needed to yield reliable estimates of association. In particular, obtaining valid measurements of exposure to osteoporosis medications from real-world data (RWD) sources is complicated due to different medication classes, formulations, and routes of administration, each with different pharmacology. Extended half-lives of bisphosphonates and extended dosing of denosumab and zoledronic acid require particular attention. In addition, prescribing patterns and medication taking behavior often result in gaps in therapy, switching, and concomitant use of osteoporosis therapies. In this review, we present important considerations and provide specialized guidance for measuring osteoporosis drug exposures in RWD. First, we compare different sources of RWD used for osteoporosis drug studies and provide guidance on identifying osteoporosis medication use in these data sources. Next, we provide an overview of osteoporosis pharmacology and how it can influence decisions on exposure measurement within RWD. Finally, we present considerations for the measurement of osteoporosis medication exposure, adherence, switching, long-term exposures, and drug holidays using RWD. Ultimately, a thorough understanding of the differences in RWD sources and the pharmacology of osteoporosis medications is essential to obtain valid estimates of the relationship between osteoporosis medications and outcomes, such as fractures, but also to improve the critical appraisal of published studies.

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使用真实世界数据评估骨质疏松症药物接触和使用模式的方法指南
骨质疏松症药物的观察性研究可以提供关键的真实世界证据(RWE),填补临床试验留下的知识空白。然而,要获得可靠的关联性估计值,需要对研究设计进行仔细考虑。特别是,由于药物类别、剂型和给药途径不同,每种药物的药理作用也不尽相同,因此从真实世界数据(RWD)来源中获取骨质疏松症药物暴露的有效测量值非常复杂。双膦酸盐的延长半衰期以及地诺单抗和唑来膦酸的延长给药时间需要特别注意。此外,处方模式和服药行为往往会导致治疗间隙、转换和同时使用骨质疏松症疗法。在本综述中,我们提出了一些重要的注意事项,并为测量 RWD 中的骨质疏松症药物暴露提供了专门指导。首先,我们比较了用于骨质疏松症药物研究的不同 RWD 来源,并就如何识别这些数据来源中的骨质疏松症药物使用情况提供了指导。接下来,我们将概述骨质疏松症药理学,以及它如何影响 RWD 中暴露测量的决策。最后,我们介绍了使用 RWD 测量骨质疏松症药物暴露、依从性、转换、长期暴露和药物假期的注意事项。归根结底,透彻了解 RWD 来源和骨质疏松症药物药理学的差异对于获得骨质疏松症药物与骨折等结果之间关系的有效估计至关重要,同时也有助于改进对已发表研究的批判性评估。
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来源期刊
Bone Reports
Bone Reports Medicine-Orthopedics and Sports Medicine
CiteScore
4.30
自引率
4.00%
发文量
444
审稿时长
57 days
期刊介绍: Bone Reports is an interdisciplinary forum for the rapid publication of Original Research Articles and Case Reports across basic, translational and clinical aspects of bone and mineral metabolism. The journal publishes papers that are scientifically sound, with the peer review process focused principally on verifying sound methodologies, and correct data analysis and interpretation. We welcome studies either replicating or failing to replicate a previous study, and null findings. We fulfil a critical and current need to enhance research by publishing reproducibility studies and null findings.
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