Premium
The feasibility of using multiple databases to study rare outcomes: the potential effect of long‐acting beta agonists with inhaled corticosteroid therapy on asthma mortality
Author(s) -
Johannes Catherine B.,
McQuay Lisa J.,
Midkiff Kirk D.,
Calingaert Brian,
Andrews Elizabeth B.,
Tennis Patricia,
Brown Jeffrey S.,
Camargo, Jr. Carlos A.,
DiSantostefano Rachael L.,
Rothman Kenneth J.,
Stürmer Til,
Lanes Stephan,
Davis Kourtney J.
Publication year - 2017
Publication title -
pharmacoepidemiology and drug safety
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.023
H-Index - 96
eISSN - 1099-1557
pISSN - 1053-8569
DOI - 10.1002/pds.4151
Subject(s) - medicine , asthma , corticosteroid , b2 receptor , inhaled corticosteroids , beta (programming language) , pharmacoepidemiology , intensive care medicine , anesthesia , pharmacology , bradykinin , receptor , computer science , medical prescription , programming language
Purpose Long‐acting beta agonists (LABAs) when used without concomitant inhaled corticosteroids (ICS) increase the risk of asthma‐related deaths, but the effect on asthma‐related death of LABA used in combination with ICS therapy is unknown. To address this question, we explored the feasibility of conducting an observational study using multiple US health care data sources. Methods Retrospective cohort study to evaluate the likelihood of getting an upper 95% confidence limit ≤1.4 for the asthma mortality rate ratio and ≤0.40 per 10 000 person‐years for the mortality rate difference, assuming no effect of new use of combined LABA + ICS (versus non‐LABA maintenance therapy) on asthma mortality. Ten research institutions executed centrally distributed analytic code based on a standard protocol using an extracted (2000–2010) persistent asthma cohort (asthma diagnosis and ≥4 asthma medications in 12 months). Pooled results were analyzed by the coordinating center. Asthma deaths were ascertained by linkage with the National Death Index. Results In a cohort of 994 627 persistent asthma patients (2.4 million person‐years; 278 asthma deaths), probabilities of the upper 95% confidence limit for effect estimates being less than targeted values, assuming a null relation, were about 0.05. Modifications in cohort and exposure definitions increased exposed person‐time and outcome events, but study size remained insufficient to attain study goals. Conclusions Even with 10 data sources and a 10‐year study period, the rarity of asthma deaths among patients using certain medications made it infeasible to study the association between combined LABA + ICS and asthma mortality with our targeted level of study precision. Copyright © 2016 John Wiley & Sons, Ltd.