Evidence map›Paper›PMID 42553353›Full record

ArticleCureus2026

Diagnostic Accuracy of Immature Granulocyte Count for Early Sepsis Detection: A Comparative Evaluation With C-Reactive Protein and Procalcitonin.

Rekha Taver, Viswadeep Gupta, Prachi Saxena, Juhi Sharma, Adarshika Yadav, Abhijeet Humne

Abstract read
In one paragraph

Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Rekha TaverDepartment of Pathology, Veerangana Avanti Bai Lodhi Autonomous State Medical College, Etah, IND.
Viswadeep GuptaDepartment of General Surgery, Veerangana Avanti Bai Lodhi Autonomous State Medical College, Etah, IND.
Prachi SaxenaDepartment of Pathology, Autonomous State Medical College, Pilibhit, IND.
Juhi SharmaDepartment of Pathology, Geetanjali Institute of Medical Sciences, Jaipur, IND.
Adarshika YadavDepartment of Orthodontics, Career Post Graduate Institute of Dental Science and Hospital, Lucknow, IND.
Abhijeet HumneDepartment of Oral and Maxillofacial Surgery, Babu Banarasi Das College of Dental Sciences, Lucknow, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionSepsis is a life-threatening condition characterized by a dysregulated host response to infection, resulting in organ dysfunction and high mortality rates among critically ill patients. Early recognition is essential for prompt therapeutic intervention; however, nonspecific clinical presentation often delays diagnosis. Conventional biomarkers, such as C-reactive protein (CRP) and procalcitonin (PCT), are frequently used, but their diagnostic performance varies. Immature granulocyte (IG) parameters obtained from routine hematological analyses have recently gained attention as potential early indicators of sepsis. This study aimed to evaluate the diagnostic accuracy of immature granulocyte count (IG#) and immature granulocyte percentage (IG%) for early sepsis detection and compare their performance with that of CRP and PCT in critically ill patients. MATERIALS AND

methodsThis retrospective observational study included 178 critically ill patients admitted to the intensive care unit of a single institution. Laboratory investigations performed within 24 hours of admission included complete blood count with IG parameters, CRP, PCT, lactate, and other biochemical markers. Patients were monitored for the development of sepsis and subsequently categorized into sepsis and non-sepsis groups. The diagnostic performance was assessed using receiver operating characteristic (ROC) curve analysis.

resultsOf the 178 patients, 72 developed sepsis during the observation period. Patients with sepsis demonstrated significantly elevated IG#, IG%, PCT, CRP, lactate, white blood cell count, neutrophil percentage, serum creatinine, and bilirubin levels compared with patients without sepsis. ROC curve analysis revealed good diagnostic performance for IG%, followed by IG# and PCT, whereas CRP demonstrated a comparatively lower discriminatory ability. The combination of IG% and PCT achieved the best overall diagnostic performance, indicating improved accuracy in identifying patients at risk of developing sepsis. Elevated immature granulocyte parameters were strongly associated with sepsis and reflected early activation of the bone marrow response to infection.

conclusionImmature granulocyte parameters, particularly IG%, are reliable and readily available biomarkers for early sepsis detection. Their diagnostic performance is comparable to that of established markers and may be enhanced when combined with procalcitonin. Routine assessment of immature granulocytes may facilitate the early recognition of sepsis and support timely clinical decision-making in critically ill patients.

Indexed as

c-reactive proteinimmature granulocytesprocalcitoninretrospectivesepsis

Identifiers

PMID42553353
PMCPMC13433898

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.