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Bacteremia in private pediatric practice

Pediatrics
|August 1, 1980
PubMed

Insights

Capillary white blood cell (WBC) counts can help identify infants with unexplained fever who may have bacteremia. Specific WBC criteria effectively distinguish high-risk infants needing blood cultures from those likely to recover without antibiotics.

Area of Science:

  • Pediatric Infectious Diseases
  • Clinical Pathology
  • Hematology

Background:

  • Unexplained febrile illness in infants and toddlers poses diagnostic challenges.
  • Distinguishing bacteremia is crucial for timely antibiotic intervention and preventing complications.
  • Office-based diagnostic tools are needed to guide further testing like blood cultures.

Purpose of the Study:

  • To evaluate the utility of capillary white blood cell (WBC) count and differential in identifying bacteremia in febrile infants and toddlers.
  • To determine specific WBC criteria predictive of bacteremia in this age group.
  • To assess the ability of these criteria to differentiate infants who require blood cultures from those who do not.

Main Methods:

  • Retrospective analysis of 146 infants (3-24 months) with unexplained febrile illness.
  • Capillary WBC count and differential performed in office practice.
  • Four criteria evaluated: WBC count ≥15,000/cu mm, segmented neutrophils ≥10,000/cu mm, band cells ≥500/cu mm, and total polymorphonuclear leukocytes ≥10,500/cu mm.

Main Results:

  • Bacteremia was confirmed in 8 out of 146 infants.
  • Seven of the 8 bacteremic infants met three or four of the defined WBC criteria.
  • Only 10 (7.2%) of the 138 non-bacteremic infants met the same criteria (P < .001).

Conclusions:

  • Capillary WBC count and differential are valuable tools for risk stratification in febrile infants.
  • The established WBC criteria help identify infants with a higher likelihood of bacteremia.
  • This approach can guide decisions regarding blood cultures and early bacteriologic diagnosis, potentially avoiding unnecessary antibiotic treatment in low-risk infants.

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