Effectiveness of Drugs in Routine Care: A Model for Sequential Monitoring of New Medicines Using Dronedarone as Example

• Published in: Clinical pharmacology and therapeutics Vol. 103; no. 3; p. 493
• Main Authors: Cars, T, Lindhagen, L, Malmström, R E, Neovius, M, Schwieler, J, Wettermark, B, Sundström, J
• Format: Journal Article
• Language: English
• Published: United States 01.03.2018
• Subjects: Aged; Aged, 80 and over; Anti-Arrhythmia Agents - therapeutic use; Atrial Fibrillation - drug therapy; Cohort Studies; Computer Systems; Databases, Factual; Dronedarone - therapeutic use; Drug Approval; Drug Monitoring - methods; Electronic Health Records; Female; Flecainide - therapeutic use; Humans; Male; Middle Aged; Product Surveillance, Postmarketing; Propensity Score; Sweden; Treatment Outcome; Sweden
• ISSN: 1532-6535
• DOI: 10.1002/cpt.751

Although there is no doubt about the scientific value of randomized controlled clinical trials, they are usually conducted in selected populations different from those treated in clinical practice. Therefore, it is important to optimize real-time postmarketing evaluation of the effectiveness, safety, and cost of new drugs. Using electronic health records and administrative health databases from a well-defined region with universal access to healthcare, we have built a framework for real-time sequential monitoring of the effectiveness of newly marketed drugs in routine care. We chose the antiarrhythmic agent dronedarone as the study drug and flecainide as the comparator drug for illustration of the model. We demonstrate that this model produces consistent results with increasing precision over time as data accumulates in the clinical systems. We believe that use of this model at the introduction of new drugs can provide complementary evidence, especially in settings of adaptive licensing of new drugs.