Q141 ★ ·
DNB/MD 2025/1Kawasaki Disease (KD) & Coronary Aneurysms
Examiner's Intent: KD is a near-universal, guaranteed high-yield topic given both its clinical importance and its direct comparative relationship to MIS-C (Section 3, Q47) — examiners expect precise AHA diagnostic criteria (complete versus incomplete), a clear understanding of the echocardiographic coronary surveillance schedule, and knowledge of the IVIG-resistance management escalation pathway.
AHA Guidelines — Complete Kawasaki Disease
Diagnosed based on fever for ≥5 days combined with at least 4 of the following 5 principal clinical features:
| # | Feature | Details |
|---|
| 1 | Bilateral, non-exudative conjunctival injection | — |
| 2 | Oral mucosal changes | Erythematous, cracked lips; “strawberry tongue” (prominent erythematous papillae); diffuse oral/pharyngeal erythema |
| 3 | Polymorphous rash | Variable in morphology, typically truncal |
| 4 | Extremity changes | Acute: erythema/edema of hands and feet. Subacute (2–3 weeks): periungual desquamation — a useful retrospective clue |
| 5 | Cervical lymphadenopathy | Typically unilateral, ≥1 node ≥1.5 cm — the least consistently present feature |
Incomplete Kawasaki Disease
In a child with fever ≥5 days and only 2–3 principal criteria (particularly relevant in infants, who carry disproportionately elevated coronary complication risk), the AHA algorithm incorporates:
- Supplemental laboratory criteria — elevated CRP/ESR plus supportive findings: anemia, thrombocytosis after day 7, hypoalbuminemia, elevated ALT, leukocytosis, sterile pyuria
- Echocardiographic findings — coronary artery abnormalities are themselves sufficient supportive evidence to diagnose incomplete KD and initiate treatment
[Diagram: AHA incomplete-KD algorithm flowchart: fever ≥5 days + 2-3 criteria → CRP/ESR → supplemental labs / echo → diagnosis pathway]
Echocardiographic Screening for Coronary Artery Aneurysms
| Timing | Purpose |
|---|
| At diagnosis | Baseline assessment |
| ~1–2 weeks after treatment initiation | Early surveillance |
| ~4–6 weeks after illness onset | Later surveillance (extended further if coronary abnormalities confirmed) |
Coronary findings are graded using standardized z-score-based (body-surface-area-adjusted) classification: no involvement → small → medium → large/giant aneurysm — directly determining follow-up intensity and antithrombotic strategy.
IVIG Resistance and Escalation Therapy
Standard initial treatment: IVIG 2 g/kg single infusion + aspirin.
- Second dose of IVIG (2 g/kg) — first escalation step for IVIG-resistant disease
- Methylprednisolone/corticosteroids — escalation step, or upfront in high-risk children (validated risk-scoring systems)
- Infliximab (anti-TNF-alpha) — for refractory disease despite IVIG + steroid escalation
Long-Term Management
Stratified by aneurysm size: low-dose aspirin alone for small aneurysms → combined antiplatelet + anticoagulant therapy for large/giant aneurysms (elevated thrombosis risk), with periodic cardiology follow-up, stress testing, and consideration of interventional/surgical revascularization for significant coronary stenosis.