AI Article Synopsis

  • The study explores emulating a "target trial" using observational data to analyze the effectiveness of adding a disease-modifying anti-rheumatic drug (DMARD) to methotrexate for cardiovascular events in rheumatoid arthritis patients.
  • Researchers utilized electronic health records from Northwestern Medicine, following 659 RA patients over an average of 46 months, using logistic regression to assess cardiovascular risks.
  • The findings indicated no significant difference in major adverse cardiovascular events between using DMARD and not using it, aligning with existing randomized controlled trial meta-analyses, showcasing how observational studies can inform comparative effectiveness research.

Article Abstract

Background: Emulation of the "target trial" (TT), a hypothetical pragmatic randomized controlled trial (RCT), using observational data can be used to mitigate issues commonly encountered in comparative effectiveness research (CER) when randomized trials are not logistically, ethically, or financially feasible. However, cardiovascular (CV) health research has been slow to adopt TT emulation. Here, we demonstrate the design and analysis of a TT emulation using electronic health records to study the comparative effectiveness of the addition of a disease-modifying anti-rheumatic drug (DMARD) to a regimen of methotrexate on CV events among rheumatoid arthritis (RA) patients.

Methods: We used data from an electronic medical records-based cohort of RA patients from Northwestern Medicine to emulate the TT. Follow-up began 3 months after initial prescription of MTX (2000-2020) and included all available follow-up through June 30, 2020. Weighted pooled logistic regression was used to estimate differences in CVD risk and survival. Cloning was used to handle immortal time bias and weights to improve baseline and time-varying covariate imbalance.

Results: We identified 659 eligible people with RA with average follow-up of 46 months and 31 MACE events. The month 24 adjusted risk difference for MACE comparing initiation vs non-initiation of a DMARD was -1.47% (95% confidence interval [CI]: -4.74, 1.95%), and the marginal hazard ratio (HR) was 0.72 (95% CI: 0.71, 1.23). In analyses subject to immortal time bias, the HR was 0.62 (95% CI: 0.29-1.44).

Conclusion: In this sample, we did not observe evidence of differences in risk of MACE, a finding that is compatible with previously published meta-analyses of RCTs. Thoughtful application of the TT framework provides opportunities to conduct CER in observational data. Benchmarking results of observational analyses to previously published RCTs can lend credibility to interpretation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11178161PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0305467PLOS

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