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[儿童重型获得性再生障碍性贫血的治疗结果]

[Results of treatment for severe acquired aplastic anemia in children].

作者信息

Ochocka M, Karwacki M, Matysiak M, Armata J, Dłuzniewska A, Bogusławska-Jaworska J, Pejcz J, Kowalczyk J, Skomra S, Radwańska U

机构信息

Klinika Hematologii i Chorób Rozrostowych Dzieci Akademii Medycznej w Warszawie.

出版信息

Pediatr Pol. 1995 Mar;70(3):205-11.

PMID:8657487
Abstract

The authors evaluated results of treatment of 106 children with acquired aplastic anemia. The patients were divided into 3 groups depending on the severity of their disease. Thirty-nine patients were classified as very severe, 30 as severe and 37 as non-severe according to the modified Camitta criteria. Among them, 47 children were treated with oxymetholone and prednisolone. In this group 32 died. Antilymphocyte globulin (ALG) was given to 48 patients and 20 received cyclosporin A (CsA). The results obtained by these two methods are nearly the same and 5 year survival was 61% and 59% respectively. Bone marrow was transplanted in only one child, who is still in complete remission. Statistical analysis showed a steady increase in incidence of aplastic anemia in the years 1987-1989, which might coincide with the Czarnobyl explosion. However, further research is required to prove this point.

摘要

作者评估了106例获得性再生障碍性贫血患儿的治疗结果。根据疾病严重程度,将患者分为3组。按照改良的卡米塔标准,39例患者被归类为极重度,30例为重度,37例为非重度。其中,47例儿童接受了羟甲烯龙和泼尼松龙治疗。该组中有32例死亡。48例患者接受了抗淋巴细胞球蛋白(ALG)治疗,20例接受了环孢素A(CsA)治疗。这两种方法获得的结果几乎相同,5年生存率分别为61%和59%。仅1例儿童接受了骨髓移植,该患儿仍处于完全缓解状态。统计分析显示,1987 - 1989年再生障碍性贫血的发病率稳步上升,这可能与切尔诺贝利核爆炸事件相符。然而,需要进一步研究来证实这一点。

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