Can We Predict Individual Combined Benefit and Harm of Therapy? Warfarin Therapy for Atrial Fibrillation as a Test Case

PLoS One. 2016 Aug 11;11(8):e0160713. doi: 10.1371/journal.pone.0160713. eCollection 2016.

Abstract

Objectives: To construct and validate a prediction model for individual combined benefit and harm outcomes (stroke with no major bleeding, major bleeding with no stroke, neither event, or both) in patients with atrial fibrillation (AF) with and without warfarin therapy.

Methods: Using the Kaiser Permanente Colorado databases, we included patients newly diagnosed with AF between January 1, 2005 and December 31, 2012 for model construction and validation. The primary outcome was a prediction model of composite of stroke or major bleeding using polytomous logistic regression (PLR) modelling. The secondary outcome was a prediction model of all-cause mortality using the Cox regression modelling.

Results: We included 9074 patients with 4537 and 4537 warfarin users and non-users, respectively. In the derivation cohort (n = 4632), there were 136 strokes (2.94%), 280 major bleedings (6.04%) and 1194 deaths (25.78%) occurred. In the prediction models, warfarin use was not significantly associated with risk of stroke, but increased the risk of major bleeding and decreased the risk of death. Both the PLR and Cox models were robust, internally and externally validated, and with acceptable model performances.

Conclusions: In this study, we introduce a new methodology for predicting individual combined benefit and harm outcomes associated with warfarin therapy for patients with AF. Should this approach be validated in other patient populations, it has potential advantages over existing risk stratification approaches as a patient-physician aid for shared decision-making.

MeSH terms

  • Aged
  • Anticoagulants / therapeutic use*
  • Atrial Fibrillation / drug therapy*
  • Databases, Factual
  • Female
  • Humans
  • Male
  • Prognosis
  • Warfarin / therapeutic use*

Substances

  • Anticoagulants
  • Warfarin

Grants and funding

This work was supported by the Father Sean O'Sullivan Research Award to GL, the Research Institute of St. Joseph’s Healthcare Hamilton, and a doctoral award from the China Scholarship Council (CSC). DMW and TD received research funding from the Kaiser Permanente Pharmacy Department. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.