What lab findings support the diagnosis of leptospirosis in a child with suspected infection?

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Laboratory Findings Supporting Leptospirosis Diagnosis in Children

In a child with suspected leptospirosis, obtain blood cultures (ideally within first 5 days), complete blood count with differential, comprehensive metabolic panel including liver and renal function tests, urinalysis, and serology (IgM ELISA), as these laboratory findings collectively support the diagnosis and guide management. 1

Hematologic Findings

Complete Blood Count Abnormalities

  • Thrombocytopenia (<150,000 cells/mm³) is a key finding, occurring in 65% of pediatric cases and showing significantly lower counts in severe disease with a declining trend as illness progresses. 2, 3
  • Leukocytosis (>11,000 cells/mm³) with polymorphonuclear predominance occurs significantly more in severe disease, particularly from day 4-5 of illness. 4, 2
  • Progressive decline in hemoglobin (<12.5 gm/dl) from day 1 to day 7 occurs in both mild and severe disease, with more pronounced anemia if significant hemorrhage is present. 4, 2
  • An elevated total band count (>1500/mm³) has the highest likelihood ratio (14.5) for detecting bacterial infection in the appropriate clinical context. 5

Biochemical Abnormalities

Hepatic Dysfunction

  • Markedly elevated bilirubin (often >580 μmol/L) with disproportionately mild transaminase elevation (AST <200 U/L) is a characteristic pattern that distinguishes leptospirosis from viral hepatitis. 4, 6
  • Jaundice occurs in 70% of pediatric cases and indicates severe disease (Weil's disease). 4, 3
  • Elevated transaminases occur in 56% of cases but remain relatively mild compared to the degree of hyperbilirubinemia. 3

Renal Dysfunction

  • Rapidly progressive acute kidney injury occurs in 79% of pediatric cases and is a hallmark of severe leptospirosis. 3, 6
  • Alterations in renal function tests (elevated creatinine and BUN) develop early and progress rapidly. 4

Urinalysis Findings

  • Proteinuria and hematuria on urinalysis are important laboratory findings that contribute to diagnosis and are included in Faine's diagnostic criteria. 1, 4

Microbiological Diagnosis

Blood Cultures

  • Blood cultures should be obtained before antibiotics if this causes no significant delay (<45 minutes), ideally within the first 5 days of illness when bacteremia is present. 1, 4
  • Three or more blood cultures should be taken at least 1 hour apart for optimal yield. 4
  • Culture can take weeks to months and does not contribute to early diagnosis but provides definitive confirmation. 7

Serological Testing

  • IgM ELISA with titers >1:320 (or >100 U/ml) is diagnostic of leptospirosis. 1, 4
  • IgM titers of 1:80 to 1:160 are consistent with early infection and should prompt repeat testing. 4
  • Convalescent serology with microscopic agglutination test (MAT) should be repeated >10 days after symptom onset, with a fourfold or greater increase in titer between acute and convalescent specimens confirming diagnosis. 1, 4
  • Faine's criteria using MAT ≥1:400 and/or PCR has 95.45% sensitivity but only 56.86% specificity. 1

Molecular Testing

  • Nucleic acid amplification testing (NAAT/PCR) can confirm diagnosis in the early phase before antibodies develop, with turnaround time of 1-2 hours. 1, 7
  • PCR is particularly valuable in the first week when serology is often negative. 7

Critical Pitfalls to Avoid

  • Do not wait for serological confirmation before starting antibiotics, as serology is often negative in the first week and each hour of delay increases mortality. 1, 7
  • Do not mistake leptospirosis for viral hepatitis in patients with fever and jaundice—the pattern of markedly elevated bilirubin with mild transaminase elevation is key. 1, 6
  • Do not rely on darkfield microscopy for direct observation of leptospires, as it is unreliable and not recommended. 7
  • Do not use urine for culture, as it is not suitable for leptospira isolation. 1
  • Recognize that afebrile presentations can occur in severe leptospirosis (<1% of cases), so do not exclude the diagnosis based solely on absence of fever in endemic areas with appropriate exposure history. 6

Diagnostic Algorithm

When evaluating a child with suspected leptospirosis based on exposure history (flood water, contaminated fresh water, animal contact within past 2-20 days) and clinical features (biphasic fever, severe myalgias, conjunctival suffusion): 1

  1. Immediately obtain: CBC with differential, comprehensive metabolic panel (liver and renal function), urinalysis, blood cultures (if <5 days of symptoms), and IgM ELISA. 1

  2. Start antibiotics immediately without waiting for laboratory confirmation if clinical suspicion is high. 1

  3. Interpret results in context: Thrombocytopenia + leukocytosis + proteinuria/hematuria + elevated bilirubin disproportionate to transaminases + acute kidney injury = highly suggestive pattern. 2, 3, 6

  4. Obtain convalescent serology >10 days after symptom onset to confirm diagnosis retrospectively. 1, 4

References

Guideline

Leptospirosis Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Research

Serial Changes in Complete Blood Counts in Patients with Leptospirosis: Our Experience.

Journal of clinical and diagnostic research : JCDR, 2017

Research

Outcome of leptospirosis in children.

The American journal of tropical medicine and hygiene, 1997

Guideline

Leptospirosis Classification and Treatment

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Laboratory diagnosis of leptospirosis: a challenge.

Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi, 2013

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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