Observational studyScientific reports2026
Distinct 72-hour fluid balance trajectories are associated with 28-day mortality in a multicenter cohort of sepsis patients.
Observational study in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
2 citing papers in PubMed.
- Influence of adrenergic drugs and volume loading on mean systemic filling pressure in non-septic and septic sheep.Frontiers in medicine · 2026Article
- Early relative glycemic stress trajectories identify a high-risk metabolic phenotype in critically ill patients with atherosclerotic cardiovascular disease: a dual-cohort study.Frontiers in endocrinology · 2026Article
Corrections and comments
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Authors and funding
5 authors.
Funding
Abstract
Fluid management in sepsis is controversial, and while persistent positive fluid balance is linked to adverse outcomes, the prognostic value of the temporal patterns (trajectories) of cumulative fluid balance (CFB) during the first 72 h after sepsis diagnosis remains unclear. This study aimed to identify distinct subphenotypes based on 72-hour CFB trajectories in adult sepsis patients and evaluate their independent association with 28-day mortality. This multicenter retrospective cohort study utilized three large-scale critical care databases (MIMIC-IV, MIMIC-III-CareVue, and eICU). We included adult patients meeting Sepsis-3 criteria with an ICU stay of over 72 h. Group-Based Trajectory Modeling (GBTM) identified five distinct 72-hour CFB (mL/kg) subphenotypes in the MIMIC-IV development cohort (n = 16,069). Trajectories were validated in the MIMIC-III (n = 2,162) and eICU (n = 13,805) cohorts. We used Kaplan-Meier analysis and multivariable Cox proportional hazards models, including Inverse Probability of Treatment Weighting (IPTW), to assess the association with 28-day mortality, adjusting for baseline confounders. GBTM identified five reproducible CFB subphenotypes, notably a “Persistent Negative Balance” (Class 1), a “High, Rapid Decline” (Class 4), and a “Persistently High Balance” (Class 5). Class 5 patients exhibited the highest illness severity (e.g., highest SOFA scores). Kaplan-Meier analysis showed significant differences in 28-day survival (P < 0.001), with Class 1 and Class 4 having the best survival and Class 5 the worst. In the MIMIC-IV cohort, compared to the highest-risk Class 5 (reference) after full multivariable adjustment, all other trajectories were associated with significantly lower 28-day mortality: Class 1 (HR: 0.50, 95% CI: 0.44–0.56) and Class 4 (HR: 0.51, 95% CI: 0.46–0.57). These protective findings were consistent across all validation cohorts. Sepsis patients exhibit five distinct, reproducible CFB trajectories strongly associated with 28-day mortality, independent of baseline severity. The finding that the “High, Rapid Decline” (Class 4) trajectory shares an excellent prognosis with the “Persistent Negative” (Class 1) trajectory challenges static fluid assessments. The ability to predict the high-risk Class 5 phenotype early using machine learning (AUC ≈ 0.81) provides a potential pathway toward individualized fluid stewardship.
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