Evidence map›Paper›PMID 39086090›Full record

ArticleAmerican journal of epidemiology2025

Grace periods and exposure misclassification in self-controlled case-series studies of drug-drug interactions.

Hanxi Zhang, Warren B Bilker, Charles E Leonard, Sean Hennessy, Todd A Miano

Abstract read
In one paragraph

Article in American journal of epidemiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Hanxi ZhangCenter for Real-World Safety and Effectiveness of Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Warren B BilkerCenter for Real-World Safety and Effectiveness of Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Charles E LeonardCenter for Real-World Safety and Effectiveness of Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Sean HennessyCenter for Real-World Safety and Effectiveness of Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.
Todd A MianoCenter for Real-World Safety and Effectiveness of Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States.

Funding

Drug interactions involving psychoactive drugsR01AG060975 · NIA · UNIVERSITY OF PENNSYLVANIA · PI Charles Edward Leonard · 2019 to 2026
$3.9M
Drug-drug interactions and kidney disease in hospitalized patientsK08DK124658 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI MIANO, TODD ANTHONY · 2021 to 2025
$791k
NIA NIH HHS R01 AG060975NIDDK NIH HHS K08 DK124658NIH HHS R01 AG060975
6 · The paper itself

Abstract

The self-controlled case-series (SCCS) research design is increasingly used in pharmacoepidemiologic studies of drug-drug interactions (DDIs), with the target of inference being the incidence rate ratio (IRR) associated with concomitant exposure to the object plus precipitant drug vs the object drug alone. While day-level drug exposure can be inferred from dispensing claims, these inferences may be inaccurate, leading to biased IRRs. Grace periods (periods assuming continued treatment impact after days' supply exhaustion) are frequently used by researchers, but the impact of grace period decisions on bias from exposure misclassification remains unclear. Motivated by an SCCS study examining the potential DDI between clopidogrel (object) and warfarin (precipitant), we investigated bias due to precipitant or object exposure misclassification using simulations. We show that misclassified precipitant treatment always biases the estimated IRR toward the null, whereas misclassified object treatment may lead to bias in either direction or no bias, depending on the scenario. Further, including a grace period for each object dispensing may unintentionally increase the risk of misclassification bias. To minimize such bias, we recommend (1) avoiding the use of grace periods when specifying object drug exposure episodes and (2) including a washout period following each precipitant exposed period. This article is part of a Special Collection on Pharmacoepidemiology.

Indexed as

PharmacoepidemiologyTiclopidineWarfarinAnticoagulantsBiasClopidogrelDrug InteractionsHumansPlatelet Aggregation InhibitorsTime FactorsAnticoagulantsClopidogrelPlatelet Aggregation InhibitorsTiclopidineWarfarinbiasdrug–drug interactionexposure misclassificationgrace periodself-controlled case series

Identifiers

PMID39086090
PMCPMC11879552

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.