An evaluation of children with Kawasaki disease in Istanbul: a retrospective follow-up study

BACKGROUND: Kawasaki disease (KD) is an acute, self-limiting vasculitis of unknown etiology. The incidence of KD is increasing world wide. However, the epidemiological data for KD in Turkey has not been well described. OBJECTIVE: To describe the demographic, clinical, and laboratory features of chil...

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Main Authors: Sinan Mahir Kayiran, Aygün Dindar, Berkan Gurakan
Format: Article
Language:English
Published: Elsevier España 2010-01-01
Series:Clinics
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1807-59322010001200007
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author Sinan Mahir Kayiran
Aygün Dindar
Berkan Gurakan
author_facet Sinan Mahir Kayiran
Aygün Dindar
Berkan Gurakan
author_sort Sinan Mahir Kayiran
collection DOAJ
description BACKGROUND: Kawasaki disease (KD) is an acute, self-limiting vasculitis of unknown etiology. The incidence of KD is increasing world wide. However, the epidemiological data for KD in Turkey has not been well described. OBJECTIVE: To describe the demographic, clinical, and laboratory features of children with KD who were diagnosed and managed in the American Hospital, Istanbul, Turkey. METHOD: Patients with KD were retrospectively identified from the hospital discharge records between 2002 and 2010. Atypical cases of KD were excluded. A standardized form was used to collect demographic data, clinical information, echocardiography and laboratory results. RESULTS: Thirty-five patients with KD, with a mean age of 2.5 + 1.9 years, were identified. Eighty-five point seven per cent of patients were under 5 years of age. A seasonal pattern favouring the winter months was noticed. In addition to fever and bilateral conjunctival injection, changes in the oral cavity and lips were the most commonly detected clinical signs in our cases. Coronary artery abnormalities were detected in nine patients. The majority of our patients had started treatment with intravenous immunoglobulin in the first 10 days of the onset of fever, and only one patient required systemic steroids for intravenous immunoglobulin-resistant KD. The coronary artery abnormalities resolved in all nine patients within 8 months. CONCLUSION: This study is the most comprehensive series of children from Turkey with KD included in Medline. As adult-onset ischemic heart disease may be due to KD in childhood, further prospective clinical investigations are needed to understand the epidemiology, management and long-term follow-up of the disease.
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spelling doaj.art-60c5505ee55e47f8902388941a2e27ad2022-12-22T01:22:54ZengElsevier EspañaClinics1807-59321980-53222010-01-0165121261126510.1590/S1807-59322010001200007An evaluation of children with Kawasaki disease in Istanbul: a retrospective follow-up studySinan Mahir KayiranAygün DindarBerkan GurakanBACKGROUND: Kawasaki disease (KD) is an acute, self-limiting vasculitis of unknown etiology. The incidence of KD is increasing world wide. However, the epidemiological data for KD in Turkey has not been well described. OBJECTIVE: To describe the demographic, clinical, and laboratory features of children with KD who were diagnosed and managed in the American Hospital, Istanbul, Turkey. METHOD: Patients with KD were retrospectively identified from the hospital discharge records between 2002 and 2010. Atypical cases of KD were excluded. A standardized form was used to collect demographic data, clinical information, echocardiography and laboratory results. RESULTS: Thirty-five patients with KD, with a mean age of 2.5 + 1.9 years, were identified. Eighty-five point seven per cent of patients were under 5 years of age. A seasonal pattern favouring the winter months was noticed. In addition to fever and bilateral conjunctival injection, changes in the oral cavity and lips were the most commonly detected clinical signs in our cases. Coronary artery abnormalities were detected in nine patients. The majority of our patients had started treatment with intravenous immunoglobulin in the first 10 days of the onset of fever, and only one patient required systemic steroids for intravenous immunoglobulin-resistant KD. The coronary artery abnormalities resolved in all nine patients within 8 months. CONCLUSION: This study is the most comprehensive series of children from Turkey with KD included in Medline. As adult-onset ischemic heart disease may be due to KD in childhood, further prospective clinical investigations are needed to understand the epidemiology, management and long-term follow-up of the disease.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1807-59322010001200007Kawasaki diseaseCoronary artery diseaseEchocardiographySteroids
spellingShingle Sinan Mahir Kayiran
Aygün Dindar
Berkan Gurakan
An evaluation of children with Kawasaki disease in Istanbul: a retrospective follow-up study
Clinics
Kawasaki disease
Coronary artery disease
Echocardiography
Steroids
title An evaluation of children with Kawasaki disease in Istanbul: a retrospective follow-up study
title_full An evaluation of children with Kawasaki disease in Istanbul: a retrospective follow-up study
title_fullStr An evaluation of children with Kawasaki disease in Istanbul: a retrospective follow-up study
title_full_unstemmed An evaluation of children with Kawasaki disease in Istanbul: a retrospective follow-up study
title_short An evaluation of children with Kawasaki disease in Istanbul: a retrospective follow-up study
title_sort evaluation of children with kawasaki disease in istanbul a retrospective follow up study
topic Kawasaki disease
Coronary artery disease
Echocardiography
Steroids
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1807-59322010001200007
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