Key result
Slowly declining hemoglobin trajectories are linked to ~72% lower 30-day mortality versus rapid decline.
Why the study?
The utility of early Hb trajectories as a dynamic biomarker for prognostic assessment in aneurysmal subarachnoid hemorrhage was unclear.
Do early 7-day hemoglobin trajectories predict 30-day and 180-day mortality and unfavorable neurological outcomes better than static hemoglobin measurements in patients with aneurysmal subarachnoid hemorrhage?
Cohort (n=665)
Do early 7-day hemoglobin trajectories predict 30-day and 180-day mortality and unfavorable neurological outcomes better than static hemoglobin measurements in patients with aneurysmal subarachnoid hemorrhage?
Longitudinal hemoglobin trajectory assessment over the first 7 days of ICU admission outperforms static hemoglobin measurements in predicting mortality and neurological outcomes after aneurysmal subarachnoid hemorrhage.
Answers are grounded in this paper and cite their sources.
Hb trajectories may refine aSAH prognosis; extends static measures but leaves open prospective validation.
Objective This study aimed to identify early Hb trajectories in aneurysmal subarachnoid hemorrhage (aSAH) and evaluate Hb as a dynamic biomarker for prognostic assessment. Methods We included 665 patients with aSAH. Group-based trajectory modeling classified Hb patterns during the first 7 days of intensive care unit admission. Associations with 30-day and 180-day mortality and unfavorable neurological outcomes (modified Rankin Scale score ≥ 3) were analyzed. Predictive performance was compared with static Hb measurements, and machine-learning models were developed to identify the poorest-prognosis trajectory. Results Three trajectories were identified: Class 1 ( n = 357, 53.68 %), slow decline from a lower baseline; Class 2 ( n = 214, 32.18 %), rapid decline from an intermediate baseline; and Class 3 ( n = 94, 14.14 %), slow decline from an intermediate baseline. Compared with Class 2, Class 1 and Class 3 had lower 30-day mortality ( HR 0.28, 95 % CI 0.19–0.41; HR 0.42, 95 % CI 0.24–0.75) and unfavorable neurological outcomes ( OR 0.46, 95 % CI 0.29–0.71; OR 0.13, 95 % CI 0.06–0.25). The trajectory model outperformed Day 1 Hb and Hb tertiles ( AUC 0.759 vs 0.721 and 0.720; DeLong P < 0.05). XGBoost had the highest AUC (0.832) among the machine-learning models. Conclusion Longitudinal Hb assessment may support dynamic prognostic assessment and trajectory-based risk stratification, highlighting Hb as a longitudinal biomarker in aSAH.
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Pan et al. (2026) conducted a cohort in Aneurysmal subarachnoid hemorrhage (aSAH) (n=665). Early hemoglobin trajectories (Class 1: slow decline from lower baseline; Class 3: slow decline from intermediate baseline) vs. Class 2 hemoglobin trajectory (rapid decline from an intermediate baseline) and static hemoglobin measurements was evaluated on 30-day mortality (HR 0.28, 95% CI 0.19-0.41). Slowly declining 7-day Hb trajectories (Classes 1 and 3) predicted lower 30-day mortality vs rapid decline.
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