Literature DB >> 26976053

The lag-time approach improved drug-outcome association estimates in presence of protopathic bias.

Andrea Arfè1, Giovanni Corrao2.   

Abstract

OBJECTIVES: Protopathic bias is a systematic error which occurs when measured exposure status may be affected by the latent onset of the target outcome. In this article, we aimed to discuss the benefits and drawbacks of the lag-time approach to address this type of bias. STUDY DESIGN AND
SETTING: The lag-time approach consists in excluding from exposure assessment the period immediately preceding the outcome detection date. With the help of simple causal diagrams, we illustrate the rationale and limitations of such strategy. The lag-time approach was illustrated in a case-crossover study, based on the health care utilization databases of the Italian Lombardy Region, on the real-world effectiveness of some respiratory drugs (exposure) in preventing asthma exacerbations (outcome).
RESULTS: A total of 7,300 of patients who were admitted to an emergency department (ED) for asthma during 2010-2012 (cases) were included. Use (vs. nonuse) of short-acting beta-agonists (SABAs, an asthma reliever medication) during the 90 days before the ED admission date was associated with an increased risk of the outcome [odds ratio (OR): 1.95; 95% confidence interval (CI): 1.72, 2.22]. This paradoxical finding may be explained by protopathic bias, as SABA use prior the ED admission may be affected by preceding respiratory distress. Indeed, when a 120-day period preceding the ED admission was ignored from drug exposure assessment (lag time), SABAs were found to be associated with a reduced risk of the outcome (OR: 0.81; 95% CI: 0.84, 0.92), as expected.
CONCLUSIONS: The lag-time approach can be a useful strategy to circumvent protopathic bias in observational studies.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Asthma exacerbations; Health care utilization database; Lag-time approach; Observational studies; Protophatic bias; Respiratory drugs

Mesh:

Substances:

Year:  2016        PMID: 26976053     DOI: 10.1016/j.jclinepi.2016.03.003

Source DB:  PubMed          Journal:  J Clin Epidemiol        ISSN: 0895-4356            Impact factor:   6.437


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