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Improving the prediction of long-term readmission and mortality using a novel biomarker panel
Jeremiah R Brown1,2, Devin M Parker1, Meagan E Stabler1
1Department of Epidemiology, Dartmouth Geisel School of Medicine, Hanover, New Hampshire, USA.
Insights
Cardiac biomarkers significantly improve 5-year prediction of readmission or mortality after coronary artery bypass graft (CABG) surgery. This enhances risk assessment for patients undergoing CABG.
Area of Science:
- Cardiology
- Biomarker research
- Surgical outcomes
Background:
- Short-term prediction models for coronary artery bypass graft (CABG) surgery outcomes exist.
- Long-term prediction using biomarkers after CABG is less understood.
- Cardiac biomarkers are linked to short-term adverse events.
Purpose of the Study:
- To investigate if cardiac biomarkers improve 5-year prediction of readmission or mortality after CABG.
- To assess the added predictive value of a biomarker panel to existing clinical models.
Main Methods:
- Analyzed plasma biomarkers from 1149 patients post-CABG.
- Compared a clinical model (STS ASCERT) alone versus with a biomarker panel.
- Evaluated model discrimination using area under the receiver operating characteristic (AUROC) curves.
Main Results:
- 40% of patients experienced readmission or death within 5 years.
- The clinical model had an AUROC of 0.69.
- The biomarker-augmented model achieved a significantly improved AUROC of 0.74 (p <.0001).
- Increased predicted risk by biomarkers correlated with higher hazard ratios (2.2-7.9).
Conclusions:
- A panel of biomarkers significantly enhances the prediction of long-term readmission or mortality risk post-CABG.
- Biomarkers aid clinical teams in better assessing long-term patient risk.
- This can lead to improved patient management strategies after CABG surgery.
Objective:
Several short-term readmission and mortality prediction models have been developed using clinical risk factors or biomarkers among patients undergoing coronary artery bypass graft (CABG) surgery. The use of biomarkers for long-term prediction of readmission and mortality is less well understood. Given the established association of cardiac biomarkers with short-term adverse outcomes, we hypothesized that 5-year prediction of readmission or mortality may be significantly improved using cardiac biomarkers.
Materials And Methods:
Plasma biomarkers from 1149 patients discharged alive after isolated CABG surgery from eight medical centers were measured in a cohort from the Northern New England Cardiovascular Disease Study Group between 2004 and 2007. We assessed the added predictive value of a biomarker panel with a clinical model against the clinical model alone and compared the model discrimination using the area under the receiver operating characteristic (AUROC) curves.
Results:
In our cohort, 461 (40%) patients were readmitted or died within 5 years. Long-term outcomes were predicted by applying the STS ASCERT clinical model with an AUROC of 0.69. The biomarker panel with the clinical model resulted in a significantly improved AUROC of 0.74 (p value <.0001). Across 5 years, the hazard ratio for patients in the second to fifth quintile predicted probabilities from the biomarker augmented STS ASCERT model ranged from 2.2 to 7.9 (p values <.001).
Conclusions:
We report that a panel of biomarkers significantly improved prediction of long-term readmission or mortality risk following CABG surgery. Our findings suggest biomarkers help clinical care teams better assess the long-term risk of readmission or mortality.
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