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Prognostic value of baseline plasma D-dimer levels in sepsis: a prospective cohort study
Xiaoxiao Qu1, Shishi Wang1, Xuanmei Ye1
1Department of Clinical Laboratory, The Second Affiliated Hospital & Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, 325000, Zhejiang, China.
Insights
Plasma D-dimer levels at admission predict 30-day mortality and septic shock in sepsis patients. Higher D-dimer indicates increased risk, aiding early sepsis management and risk stratification.
Area of Science:
- Critical Care Medicine
- Hematology
- Biomarkers
Background:
- Plasma D-dimer, a fibrin degradation product, indicates coagulation activation and is often elevated in critically ill patients.
- The prognostic value of D-dimer for short-term outcomes in sepsis is not well-established.
Purpose of the Study:
- To investigate the prognostic significance of plasma D-dimer levels for short-term outcomes in adult ICU patients with sepsis.
- To determine if D-dimer can serve as an early biomarker for risk stratification in sepsis management.
Main Methods:
- A prospective cohort study included 175 adult ICU patients diagnosed with sepsis (Sepsis-3 criteria).
- Plasma D-dimer levels were measured at ICU admission and daily for five days.
- Outcomes assessed were 30-day all-cause mortality and in-hospital septic shock, analyzed using Cox regression and Kaplan-Meier analysis.
Main Results:
- Elevated admission D-dimer levels were significantly associated with increased risks of 30-day mortality and septic shock.
- Each 1 μg/mL increase in D-dimer correlated with a 6% higher mortality risk (HR=1.06) and an 8% higher septic shock risk (HR=1.08).
- Patients in the highest D-dimer quartile exhibited the worst outcomes, with a significant interaction observed between D-dimer and serum amyloid A (SAA) for mortality.
Conclusions:
- Baseline plasma D-dimer levels independently predict 30-day mortality and septic shock in sepsis patients.
- D-dimer shows potential as a valuable early biomarker for risk stratification in sepsis management.
- Further research may explore D-dimer's role in guiding therapeutic interventions for sepsis.
Background:
Plasma D-dimer, a fibrin degradation product, reflects coagulation activation and is often elevated in critically ill patients. Its prognostic significance in sepsis, particularly for short-term outcomes, remains unclear.
Methods:
In this prospective cohort study, we enrolled 175 adult ICU patients with sepsis (Sepsis-3 criteria) from March 2024 to February 2025. Plasma D-dimer levels were measured at ICU admission and daily for five days. D-dimer levels were categorized into quartiles. The primary outcome was 30-day all-cause mortality; secondary outcome was in-hospital septic shock. Associations were analyzed using Cox regression, Kaplan-Meier analysis, and subgroup analysis.
Results:
Elevated admission D-dimer levels were significantly associated with increased risks of 30-day mortality and septic shock. Each 1 μg/mL increase in D-dimer was linked to a 6 % higher mortality risk (HR = 1.06; 95 % CI: 1.02-1.11; P = 0.008) and an 8 % higher septic shock risk (HR = 1.08; 95 % CI: 1.03-1.12; P < 0.001), after adjusting for confounders. Patients in the highest quartile had the worst outcomes. A significant interaction with serum amyloid A (SAA) was observed for mortality (P = 0.043), but not for septic shock.
Conclusion:
Baseline plasma D-dimer levels independently predict 30-day mortality and septic shock in sepsis. D-dimer may serve as a valuable early biomarker for risk stratification in sepsis management.
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