TY - JOUR
T1 - Drug-Induced Acute Myocardial Infarction
T2 - Identifying 'Prime Suspects' from Electronic Healthcare Records-Based Surveillance System
AU - Coloma, Preciosa M.
AU - Schuemie, Martijn J.
AU - Trifirò, Gianluca
AU - Furlong, Laura
AU - van Mulligen, Erik
AU - Bauer-Mehren, Anna
AU - Avillach, Paul
AU - Kors, Jan
AU - Sanz, Ferran
AU - Mestres, Jordi
AU - Oliveira, José Luis
AU - Boyer, Scott
AU - Helgee, Ernst Ahlberg
AU - Molokhia, Mariam
AU - Matthews, Justin
AU - Prieto-Merino, David
AU - Gini, Rosa
AU - Herings, Ron
AU - Mazzaglia, Giampiero
AU - Picelli, Gino
AU - Scotti, Lorenza
AU - Pedersen, Lars
AU - van der Lei, Johan
AU - Sturkenboom, Miriam
N1 - Funding Information:
M. Sturkenboom is running the IPCI research group that occasionally performs studies for pharmaceutical companies (including AstraZeneca, Pfizer, Lilly, Boehringer) and has been consultant to Pfizer, Consumer Health, Novartis, Servier, Celgene, and Lundbeck on issues not related to the study. R. Herings is scientific director of the PHARMO Institute which performs studies for many pharmaceutical companies on issues not related to the study. S. Boyer and E. Helgee are employees of Astra Zeneca. M.J. Schuemie has, since completion of this research, accepted a full-time position at Janssen R&D. G. Mazzaglia has, since completion of this research, started working for the European Medicines Agency (EMA). M. Molokhia has received support from the National Institute for Health Research (NIHR) Biomedical Research Centre at Guy’s and St Thomas’ NHS Foundation Trust and King’s College London. None of the other authors have any conflict of interest to declare.
PY - 2013/8/28
Y1 - 2013/8/28
N2 - Background:Drug-related adverse events remain an important cause of morbidity and mortality and impose huge burden on healthcare costs. Routinely collected electronic healthcare data give a good snapshot of how drugs are being used in 'real-world' settings.Objective:To describe a strategy that identifies potentially drug-induced acute myocardial infarction (AMI) from a large international healthcare data network.Methods:Post-marketing safety surveillance was conducted in seven population-based healthcare databases in three countries (Denmark, Italy, and the Netherlands) using anonymised demographic, clinical, and prescription/dispensing data representing 21,171,291 individuals with 154,474,063 person-years of follow-up in the period 1996-2010. Primary care physicians' medical records and administrative claims containing reimbursements for filled prescriptions, laboratory tests, and hospitalisations were evaluated using a three-tier triage system of detection, filtering, and substantiation that generated a list of drugs potentially associated with AMI. Outcome of interest was statistically significant increased risk of AMI during drug exposure that has not been previously described in current literature and is biologically plausible.Results:Overall, 163 drugs were identified to be associated with increased risk of AMI during preliminary screening. Of these, 124 drugs were eliminated after adjustment for possible bias and confounding. With subsequent application of criteria for novelty and biological plausibility, association with AMI remained for nine drugs ('prime suspects'): azithromycin; erythromycin; roxithromycin; metoclopramide; cisapride; domperidone; betamethasone; fluconazole; and megestrol acetate.Limitations:Although global health status, co-morbidities, and time-invariant factors were adjusted for, residual confounding cannot be ruled out.Conclusion:A strategy to identify potentially drug-induced AMI from electronic healthcare data has been proposed that takes into account not only statistical association, but also public health relevance, novelty, and biological plausibility. Although this strategy needs to be further evaluated using other healthcare data sources, the list of 'prime suspects' makes a good starting point for further clinical, laboratory, and epidemiologic investigation.
AB - Background:Drug-related adverse events remain an important cause of morbidity and mortality and impose huge burden on healthcare costs. Routinely collected electronic healthcare data give a good snapshot of how drugs are being used in 'real-world' settings.Objective:To describe a strategy that identifies potentially drug-induced acute myocardial infarction (AMI) from a large international healthcare data network.Methods:Post-marketing safety surveillance was conducted in seven population-based healthcare databases in three countries (Denmark, Italy, and the Netherlands) using anonymised demographic, clinical, and prescription/dispensing data representing 21,171,291 individuals with 154,474,063 person-years of follow-up in the period 1996-2010. Primary care physicians' medical records and administrative claims containing reimbursements for filled prescriptions, laboratory tests, and hospitalisations were evaluated using a three-tier triage system of detection, filtering, and substantiation that generated a list of drugs potentially associated with AMI. Outcome of interest was statistically significant increased risk of AMI during drug exposure that has not been previously described in current literature and is biologically plausible.Results:Overall, 163 drugs were identified to be associated with increased risk of AMI during preliminary screening. Of these, 124 drugs were eliminated after adjustment for possible bias and confounding. With subsequent application of criteria for novelty and biological plausibility, association with AMI remained for nine drugs ('prime suspects'): azithromycin; erythromycin; roxithromycin; metoclopramide; cisapride; domperidone; betamethasone; fluconazole; and megestrol acetate.Limitations:Although global health status, co-morbidities, and time-invariant factors were adjusted for, residual confounding cannot be ruled out.Conclusion:A strategy to identify potentially drug-induced AMI from electronic healthcare data has been proposed that takes into account not only statistical association, but also public health relevance, novelty, and biological plausibility. Although this strategy needs to be further evaluated using other healthcare data sources, the list of 'prime suspects' makes a good starting point for further clinical, laboratory, and epidemiologic investigation.
UR - http://www.scopus.com/inward/record.url?scp=84883144641&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0072148
DO - 10.1371/journal.pone.0072148
M3 - Article
SN - 1932-6203
VL - 8
JO - PLoS ONE
JF - PLoS ONE
IS - 8
M1 - e72148
ER -