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Table 1.

Baseline characteristics of the full cohort, stratified by hemoglobin groups.

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Table 2.

Index admission interventions and discharge medications in the full cohort, stratified by hemoglobin group.

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Fig 1.

Covariate balance before and after adjustment.

Standardized mean differences (SMDs) are shown for each covariate in the original unmatched cohort (blue circles), after Mahalanobis distance matching (MDM; green squares), and after entropy balancing (EBAL; orange triangles). Vertical dashed lines mark SMD thresholds of 0.1 (red) and 0.2 (orange). CKD, chronic kidney disease; COPD, chronic obstructive pulmonary disease; AF, atrial fibrillation; IHD, ischemic heart disease; PVD, peripheral vascular disease; HTN, hypertension.

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Table 3.

Clinical outcomes in the matched cohort (Mahalanobis distance matching, 3:3:1), stratified by hemoglobin group.

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Fig 2.

Kaplan–Meier survival curves for patients in the matched cohort (Mahalanobis distance matching, 3:3:1), stratified by hemoglobin group.

The overall log-rank test showed a significant difference between groups (p = 0.027). In Cox proportional hazards analysis (reference = normocythemia), anemia was associated with higher mortality (HR 1.30, 95% CI 1.03–1.63, p = 0.026), whereas polycythemia was not (HR 0.90, 95% CI 0.64–1.27, p = 0.533). Post-hoc pairwise log-rank tests with Bonferroni correction were not statistically significant (anemia vs. normocythemia p = 0.073; anemia vs. polycythemia p = 0.109; normocythemia vs. polycythemia p = 1.000). Numbers at risk are displayed below the x-axis.

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Fig 3.

Kaplan–Meier survival curves from the sensitivity analysis using entropy balancing (EBAL), stratified by hemoglobin group.

The overall weighted log-rank test was significant (p < 0.001). In weighted Cox proportional hazards analysis (reference = normocythemia), anemia was associated with higher mortality (HR 1.76, 95% CI 1.61–1.92, p < 0.001), whereas polycythemia was not (HR 1.14, 95% CI 0.83–1.57, p = 0.410). Post-hoc weighted log-rank tests with Bonferroni correction showed significant differences between anemia and normocythemia (p < 0.001) and between anemia and polycythemia (p = 0.015), but not between normocythemia and polycythemia (p = 0.931). Numbers at risk are not displayed because weighting alters group counts.

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