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ArticleDigestive diseases and sciences2025

Neutrophil-to-Lymphocyte Ratio Differentiates Infections from Sterile Inflammation in First Week of Acute Pancreatitis.

Gauri Kumbhar, Reuben Thomas Kurien, A J Joseph, Ebby George Simon, Amit Kumar Dutta, Ashish Goel, David Whitcomb, Sudipta DharChowdhury

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Article in Digestive diseases and sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

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1citing papers in PubMed, 1 pooled it
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Gauri KumbharDepartment of Gastroenterology, Christian Medical College, Vellore, Tamil Nadu, India.
Reuben Thomas KurienDepartment of Gastroenterology, Christian Medical College, Vellore, Tamil Nadu, India.
A J JosephDepartment of Gastroenterology, Christian Medical College, Vellore, Tamil Nadu, India.
Ebby George SimonDepartment of Gastroenterology, Christian Medical College, Vellore, Tamil Nadu, India.
Amit Kumar DuttaDepartment of Gastroenterology, Christian Medical College, Vellore, Tamil Nadu, India.
Ashish GoelDepartment of Hepatology, Christian Medical College, Vellore, Tamil Nadu, India.
David WhitcombDepartment of Gastroenterology, Christian Medical College, Vellore, Tamil Nadu, India.
Sudipta DharChowdhuryDepartment of Gastroenterology, Christian Medical College, Vellore, Tamil Nadu, India. sudiptadharchowdhury@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDifferentiating infections from sterile inflammation is crucial in early AP management.

aimThis study aimed to assess the capability of Neutrophil-to-Lymphocyte Ratio (NLR) and procalcitonin to differentiate between sterile inflammation and infections in the first week of AP and to analyze the source, microbiological profile, and impact of infections in AP.

methodsConsecutive patients presenting within 5 days of symptom onset were included. Microbiological profiles and serious adverse events (SAEs: in-hospital mortality or discharge in critical state) were analyzed. Blood count obtained at fever onset was used for calculating the NLR. The ability of NLR and procalcitonin to differentiate infections from sterile inflammation in the first week was assessed.

resultsOf 505 AP patients, 150 developed fevers. 48 (32%) had sterile inflammation, while 102 (68%) had infections. Most patients (n = 98, 65.3%) developed fever during the first week of illness (sterile inflammation (n = 43) and infections (n = 55)). NLR demonstrated good accuracy in differentiating infections from sterile inflammation in the first week (AUROC 0.70, p = 0.001), outperforming procalcitonin (AUROC 0.54, p = 0.58). Within infections (n = 102), 44 (43.1%) had infected pancreatic necrosis, 68 (66.7%) had extra-pancreatic infections, and 10 (9.8%) had both. Lower respiratory tract infection was the most common extra-pancreatic infection. Of 54 patients with culture-positive infections, 36 (66.7%) had grown multidrug-resistant (MDR) organisms. Fungal isolates were identified in 5 patients. Patients with infections had higher SAE incidence (21.6% vs. 4.2%, p = 0.007) than those with inflammation. The SAE incidence was higher with MDR infections than those without MDR (37.5% vs. 9.3%, p < 0.01).

conclusionsInfections in AP occur early in the course of illness. NLR could serve as a reliable biomarker to distinguish infections from sterile inflammation in the early course of AP, aiding timely management. Patients with MDR infections have higher serious adverse outcomes.

Indexed as

InflammationLymphocytesNeutrophilsPancreatitisAcute DiseaseAdultAgedBiomarkersDiagnosis, DifferentialFemaleHumansLymphocyte CountMaleMiddle AgedProcalcitoninBiomarkersProcalcitoninAcute pancreatitisInfectionsMicrobiological profileNeutrophil-to-lymphocyte ratio

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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.