eMedicine Specialties > Rheumatology > Miscellaneous Inflammatory Arthritis
Kawasaki Disease: Follow-up
Updated: Aug 6, 2009
Follow-up
Further Inpatient Care
- Admit an affected patient to the hospital and administer intravenous gamma globulin. Consider aspirin and/or corticosteroids and observe until fever is controlled.
- Carefully monitor cardiovascular performance.
- Once the fever resolves, significant congestive heart failure or myocardial dysfunction is unlikely.
Further Outpatient Care
- Re-evaluate all patients within 1 week of hospital discharge.
- Schedule the patient for a repeat echocardiography 21-28 days after the onset of fever.
- Further echocardiograms are usually unnecessary if baseline and 3- to 4-week echocardiograms fail to reveal any evidence of coronary aneurysms.
- Patients with no cardiac changes on echocardiogram at any stage do not require activity restrictions or medications beyond 3 months after the initial illness.
- Ensure that a patient with coronary artery aneurysms or other cardiac abnormalities receives further care, as dictated by a cardiologist.
Transfer
- Transfer any patient with suspected Kawasaki disease to a facility that has skilled clinicians and a pediatric or adult cardiologist to evaluate the echocardiogram.
Complications
- Cardiovascular
- Once fever has resolved, significant heart failure or myocardial dysfunction is unlikely.
- Diffuse coronary artery ectasia and aneurysm formation, giant aneurysm (internal luminal diameter >8 mm)
- Myocardial infarction may occur.
- Myocarditis is common but rarely causes congestive heart failure.
- Valvulitis, usually mitral, occurs in only 1% of patients and rarely merits valve replacement.
- Pericarditis with small pericardial effusions occurs in 25% of patients who are acutely ill.
- Systemic artery aneurysms may occur.
- Rupture of coronary artery aneurysm with hemopericardium is possible.
- Other complications
- Extreme irritability, especially in younger infants
- Aseptic meningitis
- Arthritis
- Mild hepatic dysfunction, rarely jaundice
- Gallbladder hydrops (may be demonstrated on sonogram, but the condition usually resolves without surgical intervention)
- Diarrhea
- Pneumonitis
- Otitis media
- Erythema and induration at the site of BCG inoculation
- Peripheral extremity gangrene (extremely rare)
Patient Education
- The recurrence rate in Japan is 3% and approximately 1% in North America.
Miscellaneous
Medicolegal Pitfalls
- Failure to diagnose Kawasaki disease before 10 days of illness so that intravenous gamma globulin can be given to help prevent coronary artery aneurysms is a medicolegal pitfall.
- If the diagnosis cannot be confirmed but is suspected, quickly refer the patient to a center with experience in Kawasaki disease.
More on Kawasaki Disease |
| Overview: Kawasaki Disease |
| Differential Diagnoses & Workup: Kawasaki Disease |
| Treatment & Medication: Kawasaki Disease |
Follow-up: Kawasaki Disease |
| Multimedia: Kawasaki Disease |
| References |
| Further Reading |
| « Previous Page | Next Page » |
References
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Uehara R, Yashiro M, Nakamura Y, Yanagawa H. Clinical features of patients with Kawasaki disease whose parents had the same disease. Arch Pediatr Adolesc Med. Dec 2004;158(12):1166-9. [Medline].
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[Best Evidence] Inour Y, Okada Y, Shinohara M, Kobayashi T, Kobayashi T, Tomomasa T, et al. A multicenter prospective randomized trial of corticosteroids in primary therapy for Kawasaki disease: clinical course and coronary artery outcome. J Pediatr. Sep/2006;149(3):336-341. [Medline].
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Keywords
KD, Kawasaki syndrome, Kawasaki's syndrome, Kawasaki disease, Kawasaki's disease, mucocutaneous lymph node syndrome, infantile periarteritis nodosa, vasculitis, atypical KD, incomplete KD, atypical Kawasaki disease, incomplete Kawasaki disease, polymorphous rash, bilateral conjunctival injection, erythematous rash
Follow-up: Kawasaki Disease