01 Feb Extreme restriction design as a method for reducing confounding by indication in pharmacoepidemiologic research
Extreme restriction design as a method for reducing confounding by indication in pharmacoepidemiologic research
What is the issue?
- Confounding by indication is a concern in observational pharmacoepidemiologic studies, including those that use active comparator, new user (ACNU) designs.
- Here, we present a method of restriction to an indication, which we call “extreme restriction,” to reduce confounding in such studies.
How was the study conducted?
- As a case study, we evaluated the effect of proton pump inhibitors (PPIs) on hospitalization for community‐acquired pneumonia (HCAP). PPI use has been associated with increased HCAP risk, but this association likely results from confounding by indication due to gastroesophageal reflux disease (GERD).
- Using the UK’s Clinical Practice Research Datalink, we compared the risk of HCAP within 180 days between PPI users and histamine‐2 receptor antagonist (H2RA) users in an ACNU cohort using Cox proportional hazard models with a time‐fixed exposure definition adjusted for high‐dimensional propensity score deciles.
- We then performed the same analysis on an “extremely‐restricted” cohort of incident nonsteroidal anti‐inflammatory drug (NSAID) users, some of whom received PPIs for prophylaxis. Because PPIs were given as prophylaxis in this population, confounding due to GERD should be limited.
- We compared effect estimates between ACNU and restricted cohorts to evaluate confounding in both analyses.
What did the study find?
- In the ACNU cohort, PPIs were associated with an increased risk of HCAP (hazard ratio [HR]: 1.25; 95% confidence interval [CI]: 1.05, 1.47), but this association was not present in the restricted cohort (HR: 1.06; 95% CI: 0.75, 1.49).
- Restriction to a single indication for treatment may reduce confounding by indication in studies conducted in distributed data networks and other large databases.
- Restriction of the study population to patients with a single indication (ie, “extreme restriction”) may reduce confounding by indication in pharmacoepidemiologic studies that use large databases.
- Large distributed health networks such as the Canadian Network for Observational Drug Effects Studies and other organizations with data on very large populations are well suited for analysis of more restricted and internally valid study populations.
Secrest MH, Platt RW, Dormuth CR, Chateau D, Targownik L, Nie R, Doyle CM, Dell’Aniello S, Filion KB. Extreme restriction design as a method for reducing confounding by indication in pharmacoepidemiologic research. Pharmacoepidemiol Drug Saf. 2020 Jan;29 Suppl 1:26-34.