Affiliation:
1. Department of Pharmaceutical Outcomes and Policy, College of Pharmacy University of Florida Gainesville Florida USA
2. Center for Medication Evaluation and Safety (CoDES) University of Florida Gainesville Florida USA
3. Faculty of Pharmacy HUTECH University Ho Chi Minh City Vietnam
4. Department of Epidemiology, College of Medicine and College of Public Health and Health Professions University of Florida Gainesville Florida USA
Abstract
AbstractBackgroundObservational designs can complement evidence from randomized controlled trials not only in situations when randomization is not feasible, but also by evaluating drug effects in real‐world, considering a broader spectrum of users and clinical scenarios. However, use of such real‐world scenarios captured in routinely collected clinical or administrative data also comes with specific challenges. Unlike in trials, medication use is not protocol based. Instead, exposure is determined by a multitude of factors involving patients, providers, healthcare access, and other policies. Accurate measurement of medication exposure relies on a similar broad set of factors which, if not understood and appropriately addressed, can lead to exposure misclassification and bias.AimTo describe core considerations for measurement of medication exposure in routinely collected healthcare data.MethodsWe describe the strengths and weaknesses of the two main types of routinely collected healthcare data (electronic health records and administrative claims) used in pharmacoepidemiologic research. We introduce key elements in those data sources and issues in the curation process that should be considered when developing exposure definitions. We present challenges in exposure measurement such as the appropriate determination of exposure time windows or the delineation of concomitant medication use versus switching of therapy, and related implications for bias.ResultsWe note that true exposure patterns are typically unknown when using routinely collected healthcare data and that an in‐depth understanding of healthcare delivery, patient and provider decision‐making, data documentation and governance, as well as pharmacology are needed to ensure unbiased approaches to measuring exposure.ConclusionsVarious assumptions are made with the goal that the chosen exposure definition can approximate true exposure. However, the possibility of exposure misclassification remains, and sensitivity analyses that can test the impact of such assumptions on the robustness of estimated medication effects are necessary to support causal inferences.
Subject
Pharmacology (medical),Epidemiology
Reference31 articles.
1. U.S. Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research (CDER) Center for Biologics Evaluation and Research (CBER).Guidance for Industry and FDA Staff: Best Practices for Conducting and Reporting Pharmacoepidemiologic Safety Studies Using Electronic Healthcare Data. Sliver Spring MD.2013.
2. Assessing Medicare Part D Claim Completeness Using Medication Self-Reports
3. Frequency and Magnitude of Co-payments Exceeding Prescription Drug Costs
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