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PMID: 17909372 Published · ppublish English Comparative Study Journal Article Research Support, N.I.H., Extramural

Increasing levels of restriction in pharmacoepidemiologic database studies of elderly and comparison with randomized trial results.

Medical care ·Vol. 45 ·No. 10 Supl 2 ·2007-10-00 ·Pages S131-42

Schneeweiss S, Patrick AR, Stürmer T, Brookhart MA, Avorn J, Maclure M, Rothman KJ, Glynn RJ

Abstract

The goal of restricting study populations is to make patients more homogeneous regarding potential confounding factors and treatment effects and thereby achieve less biased effect estimates. This article describes increasing levels of restrictions for use in pharmacoepidemiology and examines to what extent they change rate ratio estimates and reduce bias in a study of statin treatment and 1-year mortality. : The study cohort was drawn from a population of seniors age 65 years and older enrolled in both Medicare and the Pennsylvania Pharmaceutical Assistance Contract for the Elderly (PACE) between 1995 and 2002. We identified all users of statins during the study period and assessed the time until death within 1 year. The following progressive restrictions were applied: (1) study incident drug users only, (2) choose a comparison group most similar to the intervention group, (3) exclude patients with contraindications, (4) exclude patients with low adherence, and (5) restrict to specific high-risk/low-risk subgroups represented in randomized trails (RCTs). The basic cohort comprised 122,406 statin users, who were on average 78 years old and predominantly white (93%) and showed an unadjusted rate ratio of 0.32 for statin users. When all 5 restrictions were applied (N = 11,673), the unadjusted rate ratio had increased to 0.72. Multivariable Cox regression adjusted rate ratios increased from 0.62 [95% confidence interval (CI), 0.58-0.66] to 0.79 (95% CI, 0.60-1.03). However, after the first 3 restrictions the effect size changed little. The final estimate is similar to that obtained as a pooled estimate of 3 pravastatin RCTs in patients age 65 years and older. We argue that restrictions 1 through 4 compromised generalizability little. In our example of a large database study, restricting to incident drug users, similar comparison groups, patients without contraindication, and to adherent patients was a practical strategy, which limited the effect of confounding, as these approaches yield results closer to those seen in RCTs.

MeSH Terms
Aged Aged, 80 and over Confounding Factors, Epidemiologic Control Groups Female Humans Hydroxymethylglutaryl-CoA Reductase Inhibitors/therapeutic use Male Matched-Pair Analysis Mortality Multivariate Analysis Patient Compliance Patient Selection Pennsylvania/epidemiology Pharmacoepidemiology/statistics & numerical data Proportional Hazards Models Randomized Controlled Trials as Topic Reproducibility of Results Research Design Retrospective Studies Risk Adjustment United States/epidemiology
Chemicals
Hydroxymethylglutaryl-CoA Reductase Inhibitors
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Schneeweiss Sebastian
Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA. [email protected]
Patrick Amanda R
Stürmer Til
Brookhart M Alan
Avorn Jerry
Maclure Malcolm
Rothman Kenneth J
Glynn Robert J
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Article Info
Journal
Medical care
Abbr.
Med Care
ISSN
0025-7079
Published
2007-10-00
Pages
S131-42
Language
English
Region
United States
NLM ID
0230027
PMCID
PMC2905666
Subset
IM
Grants
NLM NIH HHS · R01 LM010213 · United States
NIA NIH HHS · R01 AG021950 · United States
AHRQ HHS · R01 HS010881 · United States
NIA NIH HHS · R01 AG021950-04 · United States
AHRQ HHS · 2-R01-HS10881 · United States
NIA NIH HHS · R01-AG023178 · United States
NIA NIH HHS · R01-AG021950 · United States
NIA NIH HHS · R01 AG023178 · United States
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