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What laboratory investigations are recommended to support the diagnosis of Kawasaki Disease?
Answer
Guideline-Aligned (High Confidence)
Generated by iatroX. Developer: Dr Kola Tytler MBBS CertHE MBA MRCGP (General Practitioner).
Last reviewed: 16 August 2025
Laboratory investigations recommended to support the diagnosis of Kawasaki Disease include:
- Full blood count (FBC) to detect leukocytosis with neutrophilia and thrombocytosis, which typically develops in the subacute phase.
- Inflammatory markers such as C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR) are usually elevated, reflecting systemic inflammation.
- Elevated liver enzymes and hypoalbuminaemia may be present, supporting systemic involvement.
- Urinalysis may show sterile pyuria, which can be a supportive finding.
- Additional tests such as serum sodium (often low) and elevated brain natriuretic peptide (BNP) or N-terminal pro-BNP can assist in assessing cardiac involvement.
- Blood cultures and other infection screens are important to exclude alternative diagnoses.
These investigations are primarily supportive, as Kawasaki Disease remains a clinical diagnosis based on characteristic signs and symptoms. Recent literature also highlights emerging biomarkers such as noncoding RNAs that may improve diagnostic accuracy in the future, but these are not yet standard in clinical practice (Dimitriades et al., 2014; Zhong et al., 2022; Ahn, 2024) 1.
Key References
- NG143 - Fever in under 5s: assessment and initial management
- CKS - Parvovirus B19 infection
- CKS - Feverish children - risk assessment and management
- NG95 - Lyme disease
- CKS - Giant cell arteritis
- (Dimitriades et al., 2014): Kawasaki disease: pathophysiology, clinical manifestations, and management.
- (Zhong et al., 2022): Diagnostic significance of noncoding RNAs in kawasaki disease: A systematic review and meta-analysis.
- (Ahn, 2024): Overview of childhood vasculitis.
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