한국 소아에서의 급성면역성혈소판감소성자반증 -대한소아혈액종양학회 다기관 공동연구-
- Author(s)
- Chuhl Joo Lyu; Heung Sik Kim; Soon Kyum Kim; Gwang Chul Lee; Don Hee Ahn; Im Joo Kang; Young Ho Lee; Hee Young Shin; Hyo Seop Ahn; Hae Lim Jeong; Hong Hoe Koo; Moon Kyu Kim; Hwang Min Kim; Chang Hyun Yang; 최은진; 이선민; 이건수; 정대철; 김학기; 김흥식; 김순겸; 이광철; 안돈희; 강임주; 이영호; 신희영; 안효섭; 정혜림; 구홍회; 김문규; 김황민; 유철주; 양창현; 하정옥; 서종진; 김태형; 김치관; 정철주; 최규철; 유경하; 유은선; 이순용; 김상우; 김순기; 국훈; 황태주; 황평한; 박경덕; 박현진; 김광남; 김기중; Eun Jin Choi; Sun Min Lee; Kun Soo Lee; Dae Chul Jeong; Hack Ki Kim; Jeong Ohk Ha; Jong Jin Seo; Thad T. Ghim; Chee Gwan Kim; Chul Joo Jeong; Kyu Chu Choi; Kyung Ha Yoo; Eun Seon Yoo; Soon Yong Lee; Sang Woo Kim; Soon Ki Kim; Hoon Kook; Tai Ju Hwang; Pyung Han Hwang; Kyung Duck Park; Hyun Jin Park; Kwang Nam Kim; Ki 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.
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