Pratt Nicole, Roughead Elizabeth
Quality Use of Medicines and Pharmacy Research Centre, School of Pharmacy and Medical Science, University of South Australia, Adelaide, Australia.
Curr Epidemiol Rep. 2018;5(4):357-369. doi: 10.1007/s40471-018-0176-6. Epub 2018 Sep 28.
The purpose of this review is to provide an overview of the published studies that have been used to generate evidence on the safety of medicine use when only medication dispensing data are available.
Medication dispensing databases are increasingly available for research on large populations, particularly in countries that provide universal coverage for medicines. These data are often used for drug utilisation studies to identify inappropriate medicine use at the population level that may be associated with known safety issues. Lack of coded diagnoses, to identify outcomes, and lack of data on confounders can limit use of these data in practice for medication safety assessment. To overcome these issues, studies have exploited the fact that symptoms of adverse effects of medications can be treated with other medications, for example antidepressants to treat depression or oxybutynin to treat urinary incontinence. The challenge of unmeasured confounding has been addressed by implementing self-controlled study designs that use within-person comparisons and provide inherent control for confounding. Prescription sequence symmetry analysis (SSA) is a within-person study design that has been demonstrated as a useful tool for safety signal generation in dispensing data.
Using medicine initiation as a proxy for the development of adverse events can help to generate evidence of the safety of medicines when only medication dispensing data are available. Careful consideration, however, should be given to the sensitivity and specificity of the proxy medicine for the adverse event and potential for time-varying confounding due to trends in medicine utilisation. Data-mining approaches using dispensing data have the potential to improve safety assessments; however, the challenge of unmeasured confounding with these methods remains to be investigated.
本综述旨在概述已发表的研究,这些研究用于在仅有配药数据可用时生成有关药物使用安全性的证据。
配药数据库越来越多地可用于对大量人群的研究,尤其是在提供药品全民覆盖的国家。这些数据通常用于药物利用研究,以识别在人群层面可能与已知安全问题相关的不适当用药情况。缺乏用于识别结果的编码诊断以及混杂因素的数据,可能会限制这些数据在药物安全性评估实际应用中的使用。为克服这些问题,研究利用了药物不良反应症状可用其他药物治疗的事实,例如用抗抑郁药治疗抑郁症或用奥昔布宁治疗尿失禁。通过实施自我对照研究设计来解决未测量混杂因素的挑战,该设计使用个体内部比较并提供对混杂因素的内在控制。处方序列对称性分析(SSA)是一种个体内部研究设计,已被证明是在配药数据中生成安全信号的有用工具。
当仅有配药数据可用时,将药物起始作为不良事件发生的替代指标有助于生成药物安全性的证据。然而,应仔细考虑替代药物对不良事件的敏感性和特异性以及由于药物利用趋势导致的随时间变化的混杂因素的可能性。使用配药数据的数据挖掘方法有可能改善安全性评估;然而,这些方法中未测量混杂因素的挑战仍有待研究。