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A Clinico-Epidemiological Study of Childhood Acute and Chronic Idiopathic Thrombocytopenic Purpura / 대한소아혈액종양학회지
Korean Journal of Pediatric Hematology-Oncology ; : 1-10, 2005.
Article in Korean | WPRIM | ID: wpr-220873
ABSTRACT

PURPOSE:

Childhood idiopathic thrombocytopenic purpura (ITP) is an acute, self-limited disease of several weeks, but 10~20% of cases may have chronic courses. This study was aimed to evaluate factors that might predict the progression to chronic ITP.

METHODS:

Ninty-four patients with ITP were divided into acute and chronic on the basis of disease duration of 6 months. Clinical and laboratory characteristics were compared between the two groups. Response to intravenous immunoglobulin (IVIg) of either 400 mg/kg for 5 days or IVIg 1, 000 mg/kg for 2 days and progression to chronic ITP was compared.

RESULTS:

67 cases (71.3%) were acute and 19 (28.7%) were chronic ITP. Sex, preceding viral infection history, clinical manifestations were not significantly different, but acute ITP was more prevalent in less than 1 year of age (P=.001). The initial WBC count was higher in acute than in chronic ITP (9, 600/microL vs. 7, 600/microL) (P .05). The relapse rate and progression to chronic ITP were not different.

CONCLUSION:

The intial WBC counts, AST, MPV, the changes of hemoglobin level and MPV after IVIg infusion could be useful predictors of developing chronic ITP in children.
Subject(s)

Full text: Available Index: WPRIM (Western Pacific) Main subject: Recurrence / Blood Platelets / Immunoglobulins / Purpura, Thrombocytopenic, Idiopathic / Immunoglobulins, Intravenous Type of study: Prognostic study Limits: Child / Humans Language: Korean Journal: Korean Journal of Pediatric Hematology-Oncology Year: 2005 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Recurrence / Blood Platelets / Immunoglobulins / Purpura, Thrombocytopenic, Idiopathic / Immunoglobulins, Intravenous Type of study: Prognostic study Limits: Child / Humans Language: Korean Journal: Korean Journal of Pediatric Hematology-Oncology Year: 2005 Type: Article