Evaluation of mean monocyte volume in septicemia caused by Salmonella species

Dilip Kumar1, Madhusoodanan Sudha1, Bansidhar Tarai1

  • 1Department of Microbiology, Institute of Lab Medicine, Max Super Speciality Hospital, New Delhi, India.

Abstract

Insights

Mean monocyte volume (MMV) is significantly elevated in Salmonella infection. This parameter can help predict Salmonella infections, offering a potential diagnostic aid in clinical settings.

Area of Science:

  • Hematology
  • Infectious Diseases
  • Immunology

Background:

  • Salmonella infections pose a significant global health burden.
  • Accurate and timely diagnosis of Salmonella is crucial for effective treatment.
  • Monocyte characteristics may offer insights into infectious processes.

Purpose of the Study:

  • To investigate the diagnostic utility of monocyte volume, conductivity, and scatter (VCS) parameters in Salmonella infection.
  • To determine if VCS parameters can differentiate Salmonella infections from other infections and normal states.

Main Methods:

  • Analysis of peripheral blood samples from 52 patients with confirmed Salmonella (S. typhi, S. paratyphi A) bloodstream infections.
  • Utilized a Beckman Coulter LH750 hematology analyzer to assess monocyte VCS parameters.
  • Compared monocyte VCS parameters between Salmonella-infected patients and two control groups (other infections, healthy subjects).

Main Results:

  • Mean monocyte volume (MMV) and standard deviation of MMV were significantly increased in Salmonella infection (P < 0.05) compared to both control groups.
  • Standard deviation of mean channel monocyte conductivity also showed significant increases in Salmonella infection.
  • A proposed cutoff value of 185 for MMV demonstrated 80% sensitivity and 73% specificity for predicting Salmonella infection.

Conclusions:

  • Mean monocyte volume (MMV) emerges as a valuable indicator for predicting Salmonella infection.
  • Monocyte VCS parameters, particularly MMV, show potential as a cost-effective diagnostic tool in clinical practice.
  • Further validation in diverse clinical settings is recommended to establish MMV as a reliable biomarker.

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