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Autor(en) / Beteiligte
Titel
ORIGINAL ARTICLE: Features of Kawasaki disease at the extremes of age
Ist Teil von
  • Journal of paediatrics and child health, 2006-07, Vol.42 (7-8), p.423
Ort / Verlag
Oxford: Blackwell Publishing Ltd
Erscheinungsjahr
2006
Link zum Volltext
Quelle
Wiley Online Library Journals Frontfile Complete
Beschreibungen/Notizen
  • The diagnosis of Kawasaki disease (KD) in those outside the typical age range (6 months-4 years) is often delayed, potentially worsening prognosis. The features of KD in children ≤6 months and ≥5 years were compared with those presenting within the more typical age distribution. Korean children with complete diagnostic criteria for KD were grouped according to their age at presentation: Group A (≤6 months), Group B (7 months-4 years) and Group C (≥5 years). The clinical features, laboratory findings and outcome in each group were compared. Of 136 children presenting to a single centre between 1999 and 2003, 10 children were in Group A, 114 in Group B and 12 in Group C. The mean total fever duration was 8 days in Group C and 6.2 days in Group A (P = 0.03). All children in Group C had cervical lymphadenopathy, compared with 50% of Group A and 64% of Group B (P = 0.01). Coronary artery lesions were commoner in older children (Group C, 42%) compared with Group B (17%, P = 0.05). All children had an equivalent leukocytosis, but Group C had significantly higher neutrophil counts (P = 0.001). Group A had significantly lower mean haemoglobin (P = 0.003) and total protein (P = 0.002) at presentation and a more marked thrombocytosis 1 week after intravenous immunoglobulin therapy (P < 0.05). The clinical and laboratory phenotype of KD varies with age. Older children may have a more marked inflammatory response and worse outcome. Younger children who are treated appropriately may not have a chance to higher risk of coronary artery lesions.
Sprache
Englisch
Identifikatoren
ISSN: 1034-4810
eISSN: 1440-1754
DOI: 10.1111/j.1440-1754.2006.00898.x
Titel-ID: cdi_proquest_journals_208694165

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