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Kawasaki disease: Clinico-laboratory spectrum and outcome in a cohort of children treated at a tertiary care hospital in Islamabad, Pakistan.
Sakina, Seema; Owais, Syeda Sobya; Khan, Ejaz Ahmed; Sheikh, Abdul Malik.
Afiliação
  • Sakina S; Seema Sakina, MBBS. Post Graduate Resident, Department of Pediatrics, Shifa International Hospital and Shifa Tameer-e-Millat University, H-8/4, Islamabad, Pakistan.
  • Owais SS; Syeda Sobya Owais, MD. Associate Consultant Pediatrician, Emergency Department, Shifa International Hospital and Shifa Tameer-e-Millat University, H-8/4, Islamabad, Pakistan.
  • Khan EA; Ejaz Ahmed Khan, MD. Chief of Pediatrics, Shifa International Hospital and Shifa Tameer-e-Millat University, H-8/4, Islamabad, Pakistan.
  • Sheikh AM; Abdul Malik Sheikh, FCPS. Associate Consultant Pediatric Cardiologist. Shifa International Hospital and Shifa Tameer-e-Millat University, H-8/4, Islamabad, Pakistan.
Pak J Med Sci ; 36(2): 260-264, 2020.
Article em En | MEDLINE | ID: mdl-32063971
ABSTRACT

OBJECTIVE:

To describe the demographics; clinical, laboratory, echocardiographic findings; treatment and outcome in a cohort of children with Kawasaki disease in a tertiary care hospital.

METHODS:

This is a descriptive, observational, retrospective cohort study conducted at Shifa International Hospital, Islamabad, from January 2013-June 2019. Children who met the criteria for Kawasaki disease according to the American Heart Association and American Academy of Pediatrics guidelines were included.

RESULTS:

A total of 25 children who met the criteria of Kawasaki disease were included. Their mean age was 43 months (4-150 months). Majority (76%) were males. Eighteen (72%) had complete Kawasaki disease and 7 (28%) had incomplete Kawasaki disease. Fever (> five days) was present in 20 (80%) patients. Eight patients (32%) had echocardiographic changes, out of which two patients (25%) had complete Kawasaki disease and six patients (75%) had incomplete Kawasaki disease. Intravenous immunoglobulin was given to all patients. Fifteen children (60%) received intravenous immunoglobulin within 10 days of fever. None required a second dose. All patients received high dose aspirin at diagnosis which was reduced to antiplatelet dose after resolution of fever for ≥48hrs. Eighteen patients (72%) came for regular follow up. Follow up at 6 months showed complete resolution of echocardiographic changes in six patients (75%), 1 (12.5%) was lost to follow up and one (12.5%) child had persistent coronary artery dilatation.

CONCLUSION:

Complete KD was present in 72% of our cohort of children. Coronary artery abnormalities were present in one third of these children, at younger age and more common in those with incomplete KD but recovered in most.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline / Observational_studies / Risk_factors_studies Idioma: En Revista: Pak J Med Sci Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline / Observational_studies / Risk_factors_studies Idioma: En Revista: Pak J Med Sci Ano de publicação: 2020 Tipo de documento: Article