Key result
Higher preprocedural hemoglobin-to-RDW ratio is linked to ~66% lower long-term mortality after TAVI.
Why the study?
Risk stratification after TAVI remains challenging, and evidence regarding the prognostic value of the hemoglobin-to-red cell distribution width ratio (HRR) in TAVI patients is limited.
Does a lower baseline hemoglobin-to-red cell distribution width ratio (HRR) predict increased long-term all-cause mortality in patients undergoing TAVI for severe aortic stenosis?
Observational (n=584)
No
Does a lower baseline hemoglobin-to-red cell distribution width ratio (HRR) predict increased long-term all-cause mortality in patients undergoing TAVI for severe aortic stenosis?
A low preprocedural hemoglobin-to-red cell distribution width ratio (HRR) is a strong, independent predictor of long-term mortality after TAVI, offering improved risk stratification beyond the standard STS score.
BACKGROUND Risk stratification after transcatheter aortic valve implantation (TAVI) remains challenging, particularly in elderly patients with substantial frailty and comorbidity burden. The hemoglobin-to-red cell distribution width ratio (HRR) has recently emerged as an integrated biomarker reflecting anemia, systemic inflammation, and nutritional status. However, evidence regarding its prognostic value in patients undergoing TAVI remains limited. METHODS This retrospective observational study included 584 consecutive patients who underwent TAVI for severe aortic stenosis between 2019 and 2023. Baseline HRR was calculated from preprocedural laboratory measurements. Patients were categorized into the low HRR group and the high HRR group according to a receiver operating characteristic–derived cut-off value (0.74). The primary endpoint was long-term all-cause mortality. Multivariable Cox regression analyses evaluated HRR as both a continuous and a categorical variable. Additional receiver operating characteristic, reclassification, and restricted cubic spline analyses were performed. RESULTS Patients in the low HRR group experienced significantly higher in-hospital, 30-day, one-year, and long-term all-cause mortality compared with those in the high HRR group (all P < 0.001). Kaplan-Meier survival analysis demonstrated significantly reduced long-term survival in the low HRR group (log-rank P < 0.001). HRR showed moderate discriminatory ability for one-year (AUC = 0.73) and long-term all-cause mortality (AUC = 0.70). HRR outperformed hemoglobin alone and improved risk discrimination and reclassification beyond the STS (Society of Thoracic Surgeons) score. In multivariable Cox regression analyses, HRR remained independently associated with long-term mortality when assessed as a continuous variable (HR = 0.09, 95% CI: 0.03–0.25, P < 0.001) and as a categorical variable (HR = 0.34, 95% CI: 0.24–0.49, P < 0.001), after adjustment for age, sex, STS score, and malignancy. CONCLUSIONS Preprocedural HRR is independently associated with long-term all-cause mortality after TAVI. HRR may provide complementary prognostic information when integrated into multiparametric risk assessment strategies for elderly patients undergoing TAVI.
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Kaplan et al. (2026) conducted an observational in Severe symptomatic aortic stenosis undergoing TAVI (n=584). Low hemoglobin-to-red cell distribution width ratio (HRR < 0.74) vs. High hemoglobin-to-red cell distribution width ratio (HRR ≥ 0.74) was evaluated on Long-term all-cause mortality (HR 0.34, 95% CI 0.24-0.49, p=<0.001). Preprocedural hemoglobin-to-red cell distribution width ratio evaluated as a categorical variable was independently associated with long-term all-cause mortality after TAVI (HR 0.34).
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