Use este identificador para citar ou linkar para este item:
https://www.arca.fiocruz.br/handle/icict/9447
Tipo de documento
ArtigoDireito Autoral
Acesso restrito
Coleções
- IFF - Artigos de Periódicos [1284]
Metadata
Mostrar registro completo
PROFILE OF KAWASAKI DISEASE IN CHILDREN REFERRED TO TWO PEDIATRIC RHEUMATOLOGY SERVICES IN RIO DE JANEIRO, BRAZIL
Mucocutaneous Lymph Node Syndrome
Coronary Artery Disease
Antibiotic Prophylaxis
Autor(es)
Afiliação
Secretaria Municipal de Saúde. Rio de Janeiro, RJ, Brasil.
Secretaria Municipal de Saúde. Rio de Janeiro, RJ, Brasil.
Universidade Federal do Rio de Janeiro. Instituto de Puericultura e Pediatria Martagão Gesteira. Rio de Janeiro, RJ, Brasil. / Secretaria Municipal de Saúde. Rio de Janeiro, RJ, Brasil.
Universidade Federal do Rio de Janeiro. Rio de Janeiro, RJ, Brasil. / Universidade do Estado do Rio de Janeiro. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Fernandes Figueira. Departament of Pediatrics. Rio de Janeiro, RJ, Brasil.
Universidade Federal do Rio de Janeiro. Faculdade de Medicina. Rio de Janeiro, RJ, Brasil.
Secretaria Municipal de Saúde. Rio de Janeiro, RJ, Brasil.
Universidade Federal do Rio de Janeiro. Instituto de Puericultura e Pediatria Martagão Gesteira. Rio de Janeiro, RJ, Brasil. / Secretaria Municipal de Saúde. Rio de Janeiro, RJ, Brasil.
Universidade Federal do Rio de Janeiro. Rio de Janeiro, RJ, Brasil. / Universidade do Estado do Rio de Janeiro. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Fernandes Figueira. Departament of Pediatrics. Rio de Janeiro, RJ, Brasil.
Universidade Federal do Rio de Janeiro. Faculdade de Medicina. Rio de Janeiro, RJ, Brasil.
Resumo em Inglês
Objectives:To describe a population of children diagnosed with Kawasaki’s disease (KD) in pediatric rheumatology
centers of Rio de Janeiro, Brazil, defining the magnitude of the delay period in diagnosing KD and initiating treatment
due to confusion with common childhood febrile illnesses and the impact of this delay on the frequency of coronary
sequels. Methods:Data analysis from hospital records summarized in a dedicated form, including name, gender, age,
date of first recorded clinical signs, date of admission to the specialty service, information about symptoms, clinical
evolution, intravenous immunoglobulin (IVIG) use and coronary sequels. Results:Of 125 patients, 63% were males.
40% were under 2 years at diagnosis. Average lapse between earliest signs and KD diagnosis was 12 days (mean fever
duration, 14 d). Only 22.4% had a diagnosis of KD before entering the specialty service. For the remainder, initial hy-potheses included: bacterial (60%) and viral infections (12%), rheumatological diseases (4%) and adverse vaccination
reactions (1.6%). Hence, prevalent febrile illnesses of childhood were major confounding factors. For records (85.6%)
mentioning treatment, 46.7% reported IVIG treatment, beginning after day 10 in 23 cases (21.5%). 20 patients (16%)
presented coronary sequels, 9 of which were diagnosed late, including 3 given IVIG after day 10, and 6 given no IVIG.
We found no significant association between the frequency of coronary sequels and: a) sex; b) age; c) clinical criteria;
d) initiation of IVIG treatment (before or after day 10). Conclusions:Common febrile illnesses of childhood often
confound the diagnosis of KD.
Palavras-chave em inglês
VasculitisMucocutaneous Lymph Node Syndrome
Coronary Artery Disease
Antibiotic Prophylaxis
Compartilhar