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静脉注射免疫球蛋白与大剂量甲基强的松龙治疗儿童急性特发性血小板减少性紫癜的随机对照研究

A randomized and comparative study of intravenous immunoglobulin and mega dose methylprednisolone treatments in children with acute idiopathic thrombocytopenic purpura.

作者信息

Erduran Erol, Aslan Yakup, Gedik Yusuf, Orhan Fazil

机构信息

Department of Pediatrics, Karadeniz Technical University, Faculty of Medicine, Trabzon, Turkey.

出版信息

Turk J Pediatr. 2003 Oct-Dec;45(4):295-300.

Abstract

The most common cause of mortality in childhood acute idiopathic thrombocytopenic purpura (ITP) is intracranial hemorrhage (ICH), which occurs in about 0.1% of children with platelet counts below 20,000/microl. Forty-two children (1-13 years) with ITP and platelet counts < or = 20,000/microl were randomly divided into two groups. Twenty patients received mega-dose methylprednisolone (MDMP) in a dosage of 30 mg/kg/d for three days and 20 mg/kg/d for four days. Twenty-two patients received intravenous immunoglobulin (IVIG) in a dosage of 1 g/kg/d two days. Platelet counts of the patients were determined at diagnosis, at 2, 4, 7, 14, 30, 60, 90, 120, 150, and 180 days and at three-month intervals after the 6th month. The mean platelet counts of both groups gradually increased and peaked on the 7th day (p > 0.05). There were no significant differences between the mean platelet counts of patients, in the two groups on treatment days 0, 2, 4, 7, and 14. The mean time for achievement of platelet counts above 20,000/microg in the MDMP group and the IVIG group was 4.1 and 2.9 days (p < 0.05) and above 50,000/microl was 5.0 and 5.2 days (p > 0.05), respectively. The percentages of patients with platelet counts above 20,000/microl at the 2nd day of the treatment were 50% in the MDMP group, and 86% in the IVIG group (p < 0.05). No significant differences were observed in the mean platelet counts of the two groups treatment days 30, 60, 90, 120 and 180 (p > 0.05). Chronic ITP developed in five patients (25%) in the MDMP group, and in four patients (18%) in the IVIG group (p > 0.05). Intravenous immunoglobulin (IVIG) (1 g/kg/d for 2 days) and MDMP treatments (30 mg/kg/d for 3 days, 20 mg/kg/d for 4 days, perorally) are equally effective in the treatment of acute ITP. Because of its nonbiologic source, lower cost, fewer side effects and oral use, we prefer oral preparations of MDMP in the treatment of childhood ITP.

摘要

儿童急性特发性血小板减少性紫癜(ITP)最常见的死亡原因是颅内出血(ICH),在血小板计数低于20,000/微升的儿童中发生率约为0.1%。42例年龄在1至13岁、血小板计数≤20,000/微升的ITP患儿被随机分为两组。20例患者接受大剂量甲基强的松龙(MDMP)治疗,剂量为30毫克/千克/天,持续3天,之后20毫克/千克/天,持续4天。22例患者接受静脉注射免疫球蛋白(IVIG)治疗,剂量为1克/千克/天,持续2天。在诊断时、第2、4、7、14、30、60、90、120、150和180天以及第6个月后的三个月间隔时测定患者的血小板计数。两组的平均血小板计数均逐渐升高,并在第7天达到峰值(p>0.05)。在治疗第0、2、4、7和14天时,两组患者的平均血小板计数无显著差异。MDMP组和IVIG组血小板计数达到20,000/微克以上的平均时间分别为4.1天和2.9天(p<0.05),达到50,000/微升以上的平均时间分别为5.0天和5.2天(p>0.05)。治疗第2天时血小板计数高于20,000/微升的患者百分比,MDMP组为50%,IVIG组为86%(p<0.05)。在治疗第30、60、90、120和180天时,两组的平均血小板计数无显著差异(p>0.05)。MDMP组有5例患者(25%)发展为慢性ITP,IVIG组有4例患者(18%)发展为慢性ITP(p>0.05)。静脉注射免疫球蛋白(IVIG)(1克/千克/天,持续2天)和MDMP治疗(30毫克/千克/天,持续3天,之后20毫克/千克/天,口服)在治疗急性ITP方面同样有效。由于MDMP的非生物来源、成本较低、副作用较少且可口服,我们在儿童ITP治疗中更倾向于使用MDMP口服制剂。

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