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한국 소아에서의 급성면역성혈소판감소성자반증 -대한소아혈액종양학회 다기관 공동연구-

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Author(s)
Chuhl Joo LyuHeung Sik KimSoon Kyum KimGwang Chul LeeDon Hee AhnIm Joo KangYoung Ho LeeHee Young ShinHyo Seop AhnHae Lim JeongHong Hoe KooMoon Kyu KimHwang Min KimChang Hyun Yang최은진이선민이건수정대철김학기김흥식김순겸이광철안돈희강임주이영호신희영안효섭정혜림구홍회김문규김황민유철주양창현하정옥서종진김태형김치관정철주최규철유경하유은선이순용김상우김순기국훈황태주황평한박경덕박현진김광남김기중Eun Jin ChoiSun Min LeeKun Soo LeeDae Chul JeongHack Ki KimJeong Ohk HaJong Jin SeoThad T. GhimChee Gwan KimChul Joo JeongKyu Chu ChoiKyung Ha YooEun Seon YooSoon Yong LeeSang Woo KimSoon Ki KimHoon KookTai Ju HwangPyung Han HwangKyung Duck ParkHyun Jin ParkKwang Nam KimKi Joong Kim
Keimyung Author(s)
Kim, Heung Sik
Department
Dept. of Pediatrics (소아청소년학)
Journal Title
대한소아혈액종양학회지
Issued Date
2003
Volume
10
Issue
1
Abstract
Purpose: Childhood acute immune thrombocytopenic purpura (ITP) is a benign hematologic disease. Therapy does not affect the natural history of the illness. We evaluated the clinical and laboratory findings, treatment and prognosis of childhood acute ITP in Korea through a retrospective multicenter study.
Methods: We analyzed retrospectively the data of 1,829 children with acute ITP through survey of 33 hospitals among 43 hospitals in Korea from Sep. 1992 to Aug. 2001.
Results: Male to female ratio was 1.3:1 and the median age at the diagnosis of ITP was 2.9 (0.1∼17) years. Median duration of follow up was 6 months. One hundred and forty nine cases of the total 1,829 patients (8.1%) received no treatment. The initial median platelet count of the non-treated group was 42,500/mm3. Among the 861 cases who were followed up over 6 months, 315 cases (36.6%) progressed into chronic ITP. Associated with this high rate of chronicity of childhood acute ITP patients in Korea, we must consider the fact that acute ITP patients with fast improvement in the first episode tend not to follow up. Considering that fact, the rate of chronicity becomes 17.2% of the 1,829 acute ITP patients. The treated group used many kinds of treatment methods. Intravenous immunoglobulins (IVIG) with or without prednisolone (PD) (67.5%) were the most commonly used regimens. In the group treated with IVIG alone, the platelet count began to rise above 50,000/mm3 at 2.6 days, 100,000/mm3 at 3.7 days and 150,000/mm3 at 4.9 days. Four hundred and twenty two cases of the 1,686 (25.0%) cases followed up after first episode of ITP relapsed. The relapse rate was significantly higher in older patients and in girls than in younger patients and in boys (P<0.05). The chronicity of ITP statistically increased with age (P<0.05) and that was the only valuable factor.
Conclusion: Despite the fact that childhood acute ITP is a pretty common disaese, there is no agreement on the best treatment method for this disease. The establishment of Korean treatment guideline of childhood acute ITP, based on an analysis of multicenters, seems to be needed.
Alternative Title
Childhood Acute Immune Thrombocytopenic Purpura in Korea -Multicenter Study of Korean Society of Pediatric Hematology/Oncology-
Keimyung Author(s)(Kor)
김흥식
Publisher
School of Medicine
Citation
Chuhl Joo Lyu et al. (2003). 한국 소아에서의 급성면역성혈소판감소성자반증 -대한소아혈액종양학회 다기관 공동연구-. 대한소아혈액종양학회지, 10(1), 14–21.
Type
Article
ISSN
1225-6978
URI
https://kumel.medlib.dsmc.or.kr/handle/2015.oak/39207
Appears in Collections:
1. School of Medicine (의과대학) > Dept. of Pediatrics (소아청소년학)
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