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Factors associated with development of coronary artery aneurysms after Kawasaki disease are similar for those treated promptly and those with delayed or no treatment.
Downie, Mallory L; Manlhiot, Cedric; Collins, Tanveer H; Chahal, Nita; Yeung, Rae S M; McCrindle, Brian W.
Afiliação
  • Downie ML; Labatt Family Heart Centre, University of Toronto, The Hospital for Sick Children, 555 University Avenue, Toronto M5G 1X8, Canada. Electronic address: mallory.downie@sickkids.ca.
  • Manlhiot C; Labatt Family Heart Centre, University of Toronto, The Hospital for Sick Children, 555 University Avenue, Toronto M5G 1X8, Canada.
  • Collins TH; Labatt Family Heart Centre, University of Toronto, The Hospital for Sick Children, 555 University Avenue, Toronto M5G 1X8, Canada.
  • Chahal N; Labatt Family Heart Centre, University of Toronto, The Hospital for Sick Children, 555 University Avenue, Toronto M5G 1X8, Canada.
  • Yeung RSM; Division of Rheumatology, Department of Paediatrics, University of Toronto, The Hospital for Sick Children, 555 University Avenue, Toronto M5G 1X8, Canada.
  • McCrindle BW; Labatt Family Heart Centre, University of Toronto, The Hospital for Sick Children, 555 University Avenue, Toronto M5G 1X8, Canada. Electronic address: brian.mccrindle@sickkids.ca.
Int J Cardiol ; 236: 157-161, 2017 Jun 01.
Article em En | MEDLINE | ID: mdl-28089146
BACKGROUND: While the risk is reduced, patients may develop coronary artery (CA) aneurysms after Kawasaki disease (KD) despite receiving intravenous immunoglobulin (IVIG) within 10days of symptom onset. Risk factors for CA aneurysms may differ compared to those patients with delayed or no treatment. METHODS: Patients diagnosed with KD between 1990 and 2013 were included. Patients with maximum coronary artery z-scores>5 were classified as having CA aneurysms. Separate multivariable regression models were used to determine factors associated with CA aneurysms for those with versus without prompt treatment. RESULTS: Of 1358 patients included, 83% (n=1126) were treated with IVIG within 10days and 5% (n=53) developed CA aneurysms. Patients who had delayed (>10days) or no IVIG treatment were at increased odds of developing CA aneurysms (OR: 3.1,95% CI: 1.9-5.1, p<0.001). For patients with prompt treatment with IVIG, factors associated with increased odds of CA aneurysms were: longer duration of fever prior to treatment (OR: 1.2/day, p=0.04), age<1year (OR: 3.9, p=0.001), higher pre-IVIG white blood cell count (OR: 1.05/×109/L, p=0.007), lower hemoglobin (OR: 1.4/g/L, p=0.004) and non-response to initial IVIG treatment (OR: 2.5, p<0.001). For patients with delayed or no treatment, factors associated with increased odds of CA aneurysms were: males (OR: 5.4, p=0.009), age<1year (OR: 29.9, p<0.001), and higher platelet count (OR: 1.4/100×1012/L, p=0.001). Delayed treatment with IVIG did not reduce the risk of CA aneurysms (OR: 1.9, p=0.28), and total duration of fever was not associated with CA aneurysms for this group (OR: 1.04/day, p=0.16). CONCLUSIONS: Factors associated with the development of CA aneurysms are generally similar for those treated promptly versus those with delayed or no treatment. For those with delayed diagnosis, treatment with IVIG does not appear to be effective to prevent CA aneurysms.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aneurisma Coronário / Imunoglobulinas Intravenosas / Síndrome de Linfonodos Mucocutâneos Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Int J Cardiol Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aneurisma Coronário / Imunoglobulinas Intravenosas / Síndrome de Linfonodos Mucocutâneos Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Int J Cardiol Ano de publicação: 2017 Tipo de documento: Article