Granulocyte colony-stimulating factor combined with SOFA score for mortality prediction in patients with sepsis
2024

G-CSF and SOFA Score for Predicting Mortality in Sepsis Patients

Sample size: 171 publication 10 minutes Evidence: moderate

Author Information

Author(s): Fu Xiaomeng, Zhang Ye, Wang Junyu, Liu Yugeng, Wei Bing

Primary Institution: Beijing Chaoyang Hospital, Capital Medical University, Beijing, China

Hypothesis

Can granulocyte colony-stimulating factor (G-CSF) combined with the SOFA score predict mortality in sepsis patients?

Conclusion

G-CSF, SOFA, APACHE II, and SBP are independent predictors of mortality among patients with sepsis, with G-CSF and SOFA showing significant prognostic capability.

Supporting Evidence

  • G-CSF levels were significantly higher in non-survivors compared to survivors.
  • SOFA and APACHE II scores were identified as independent risk factors for mortality.
  • The combination of G-CSF and SOFA improved predictive accuracy for 28-day mortality.
  • Logistic regression analysis indicated G-CSF as an independent risk factor for mortality.
  • Receiver operating characteristic curve analysis showed G-CSF had a sensitivity of 81.1%.

Takeaway

Doctors can use a blood test for G-CSF and a scoring system called SOFA to help figure out if a patient with sepsis might not survive.

Methodology

The study included 171 sepsis patients, analyzed G-CSF levels, SOFA and APACHE II scores, and used logistic regression and ROC curve analysis.

Potential Biases

Potential bias due to the single-center study design and prior treatments affecting cytokine levels.

Limitations

The study is limited by its single-center design and the measurement of cytokines at only one time point.

Participant Demographics

Patients aged ≥18 with sepsis, including both genders, admitted to the emergency department.

Statistical Information

P-Value

0.017 for G-CSF, <0.001 for SOFA and APACHE II

Confidence Interval

95% CI for G-CSF: 1.000, 1.004; for SOFA: 1.282, 1.923; for APACHE II: 1.062, 1.242

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1097/MD.0000000000040926

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