Lang J M, Amaral D, Audhuy B, Barats J C, Boilletot A, Oberling F
Service d'Onco-Hématologie, Centre Hospitalier Universitaire de Hautepierre, Strasbourg, France.
Nouv Rev Fr Hematol (1978). 1987;29(5):285-7.
A total of twenty-six patients with idiopathic thrombocytopenic purpura ITP refractory to corticosteroids were alternately allocated to undergo splenectomy alone (N = 12) or to receive a 5 day course of high dose immunoglobulin G i.v. immediately followed by splenectomy (N = 14). Although there were less initial failures after splenectomy in patients receiving IgG, the proportion of sustained complete remission at 1 and 2 years was identical in both groups. It is concluded that high dose IgG infusions do not improve the results of splenectomy in refractory ITP.
共有26例对皮质类固醇难治的特发性血小板减少性紫癜(ITP)患者被交替分配接受单纯脾切除术(n = 12)或先接受5天高剂量静脉注射免疫球蛋白G疗程,随后立即进行脾切除术(n = 14)。虽然接受免疫球蛋白G的患者脾切除术后初始失败较少,但两组在1年和2年时持续完全缓解的比例相同。结论是,高剂量免疫球蛋白G输注并不能改善难治性ITP患者脾切除术的效果。