https://doi.org/10.4081/ecj.2026.15933
04 | Monocyte distribution width in early diagnosis of sepsis
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
Published: 15 July 2026
Background. Monocyte Distribution Width (MDW) measures the volumetric distribution width of monocytes, reflecting monocytic anisocytosis, and is detected using advanced hematological analyzers. Different studies have shown that an increased MDW value is associated with a higher risk of sepsis and that its combination with clinical parameters (such as qSOFA) and other biomarkers (CRP, PCT) can enhance diagnostic sensitivity and risk stratification capacity. Other advantages are its ease of measurement, its high negative predictive value (NPV) and the absence of correlations with demographic factors such as age, sex, or surgical conditions.
Sepsis is a complex and potentially life-threatening syndrome which can lead to death. Early diagnosis is crucial to improving prognosis and reducing hospital management costs.
Methods. We will set up a prospective study in ED of Policlinico Universitario A. Gemelli on the role of monocyte distribution width (MDW) as a diagnostic biomarker for sepsis, highlighting its advantages, limitations, and potential clinical applications.
We will enroll patients over 18 years who are able to give informed consent. Patients with a suspected clinical condition will be asked for CBC (containing MDW). A cutoff value of 20 will be used to indicate sepsis positivity, as supported by most studies.
Expected Results. The primary endpoint is based on evaluating the diagnostic performance of MDW, while the secondary endpoints involve comparison with other markers such as PCT and PSP. Finally, we may repeat MDW measurements to assess its utility in guiding antibiotic therapy management.
Downloads
-
CRediT authorship contribution
Supporting Agencies
Data Availability Statement
How to Cite

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
PAGEPress has chosen to apply the Creative Commons Attribution NonCommercial 4.0 International License (CC BY-NC 4.0) to all manuscripts to be published.




