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脾切除术在免疫性(特发性)血小板减少性紫癜中的作用。

Role of splenectomy in immune (idiopathic) thrombocytopenic purpura.

作者信息

Bell W R

机构信息

Department of Medicine, The Johns Hopkins University School of Medicine, The Johns Hopkins Medical Institutions, Baltimore, MD 21287-4928, USA.

出版信息

Blood Rev. 2002 Mar;16(1):39-41. doi: 10.1054/blre.2001.0180.

Abstract

Idiopathic thrombocytopenic purpura (ITP) is an immune disorder, which causes an acute or chronic thrombocytopenia, and may result in potentially life-threatening hemorrhage. Splenectomy is one of the treatment options that needs to be weighed in the treatment of ITP, particularly in cases that have shown response failure to medical modalities such as prednisone, i.v.Ig, or anti-D globulin therapy. Although most studies demonstrate good early response following splenectomy, the long-term outcome is less favorable. Furthermore, other negative factors, such as rendering the patient ineligible for anti-D globulin or oral tolerance therapy and vulnerable to possible life-threatening sepsis, must be weighed prior to splenectomy.

摘要

特发性血小板减少性紫癜(ITP)是一种免疫性疾病,可导致急性或慢性血小板减少,并可能引发危及生命的出血。脾切除术是ITP治疗中需要权衡的治疗选择之一,尤其是在对泼尼松、静脉注射免疫球蛋白或抗-D球蛋白治疗等药物治疗无反应的情况下。尽管大多数研究表明脾切除术后早期反应良好,但长期预后并不理想。此外,在进行脾切除术之前,必须权衡其他负面因素,如使患者不符合抗-D球蛋白或口服耐受治疗的条件,以及易患可能危及生命的败血症。

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