Evidence map›Paper›PMID 24834364›Full record

ArticleMedicare & medicaid research review2013

Accounting for unobservable exposure time bias when using Medicare prescription drug data.

Elizabeth A Cook, Kathleen M Schneider, Elizabeth Chrischilles, John M Brooks

Abstract read
In one paragraph

Article in Medicare & medicaid research review, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

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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

4 authors.

Elizabeth A CookUniversity of Iowa College of Pharmacy-Department of Pharmacy Practice and Science.
Kathleen M SchneiderBuccaneer-A General Dynamics Company.
Elizabeth ChrischillesUniversity of Iowa College of Public Health-Department of Epidemiology.
John M BrooksUniversity of Iowa College of Pharmacy-Department of Pharmacy Practice and Science.

Funding

Comparative Effectiveness of Treatment Combinations Post MI in the ElderlyR01HS018381 · AHRQ · UNIVERSITY OF IOWA · PI SCHROEDER, MARY C. · 2010 to 2013
$1.6M
Interpreting IV Estimates with Treatment Effect Heterogeneity: ACE/ARBs & RaceRC4AG038635 · NIA · UNIVERSITY OF IOWA · PI BROOKS, JOHN M · 2010 to 2010
$1.5M
Should high-risk statin utilization rates be increased for complex AMI patients?R21HS019574 · AHRQ · UNIVERSITY OF IOWA · PI BROOKS, JOHN M · 2010 to 2010
$416k
AHRQ HHS R01 HS018381AHRQ HHS R21 HS019574NIA NIH HHS RC4 AG038635
6 · The paper itself

Abstract

objectiveTo describe the prevalence and correlates of unobservable medication exposure time, and to recommend approaches for minimizing bias, in studies using Medicare Part D data.. SAMPLE: 179,065 Medicare patients hospitalized for an AMI in 2007 or 2008.

methodsWe compared two methods for creating medication exposure observation periods using acute care discharge vs. post-acute care discharge dates. We examined options for increasing cohort sizes by requiring different thresholds for observable days, or by using as a covariate, in the observation period. We calculated the extent and health status correlates of unobserved Medicare Part D exposure time and examined its association with receipt of beta-blockers.

results39% of patients had unobservable time during the 30 day exposure assessment period following acute care; they were significantly older, had more comorbidity and longer acute care stays, had worse 1-year survival, and were significantly less likely to be classified as beta-blocker users. Using the alternative exposure assessment window, only 29% of the sample had unobservable time, and differences between groups were less pronounced. Significant gains in sample size can be obtained by restricting or controlling for the number of observable days required in the exposure assessment period.

conclusionsUnobservable exposure time is common among Medicare Part D beneficiaries, and they are often in worse health. To retain patients with unobservable exposure time, we recommend stratifying patients on receipt of post-acute facility-based care, calculating and using observable days as a covariate and, when appropriate, using the discharge date from contiguous post-acute facility care for beginning the exposure assessment period.

Indexed as

Adrenergic beta-AntagonistsBiasHospitalizationHumansMedicare Part DMyocardial InfarctionPatient DischargePrescription DrugsTime FactorsUnited StatesAdrenergic beta-AntagonistsPrescription DrugsAdministrative Data UsesEpidemiologyMedicarePharmacy

Identifiers

PMID24834364
PMCPMC4011646

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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.