Lord R V, Coleman M J, Milliken S T
Department of Surgery, St Vincent's Hospital, Sydney, New South Wales, Australia.
Arch Surg. 1998 Feb;133(2):205-10. doi: 10.1001/archsurg.133.2.205.
To determine the effectiveness and safety of splenectomy for patients with human immunodeficiency virus (HIV)-related immune thrombocytopenia, using the results of splenectomy for patients with non-HIV immune thrombocytopenic purpura as a control group for comparison.
Retrospective study.
Tertiary care university hospital.
Fourteen patients who underwent splenectomy for symptomatic, medically refractory HIV-related immune thrombocytopenia at this hospital from 1988 to 1997. During the same period, 20 patients had splenectomy for treatment of non-HIV immune thrombocytopenic purpura.
Splenectomy.
Platelet response, need for postsplenectomy medical therapy, progression of HIV disease, and complications.
All patients with HIV-related thrombocytopenia had a complete early platelet response to splenectomy, with an elevation of the platelet count to greater than 100X10(9)/L. After a median follow-up of 26.5 months, all but 1 patient had a sustained complete remission with no need for medical therapy for thrombocytopenia. Splenectomy was more effective in the HIV-related thrombocytopenia group than in the non-HIV immune thrombocytopenic purpura group, with significantly higher platelet counts at 1 week and 1 month after splenectomy in the HIV group (t test, P=.02 and P=.009, respectively). There were significantly fewer patients needing medical therapy for thrombocytopenia after splenectomy in the HIV group (chi2 test, P=.02). There were no remarkable short- or long-term complications in the patients with HIV infection, including no overwhelming postsplenectomy infections. Three patients have died, and 2 patients have developed AIDS since operation.
Splenectomy is effective treatment for patients with symptomatic HIV-related thrombocytopenia that is resistant to medical therapy. The effectiveness of this treatment suggests that the predominant mechanism of thrombocytopenia in HIV-infected patients is increased destruction of platelets because of platelet-associated immunoproteins.
以非HIV免疫性血小板减少性紫癜患者的脾切除结果作为对照组进行比较,确定脾切除术治疗人类免疫缺陷病毒(HIV)相关免疫性血小板减少症患者的有效性和安全性。
回顾性研究。
三级医疗大学医院。
1988年至1997年期间在本院因有症状、药物治疗无效的HIV相关免疫性血小板减少症接受脾切除术的14例患者。同期,20例患者因非HIV免疫性血小板减少性紫癜接受脾切除术。
脾切除术。
血小板反应、脾切除术后药物治疗需求、HIV疾病进展及并发症。
所有HIV相关血小板减少症患者脾切除术后早期血小板均完全反应,血小板计数升高至大于100×10⁹/L。中位随访26.5个月后,除1例患者外,其余患者均持续完全缓解,无需进行血小板减少症的药物治疗。脾切除术对HIV相关血小板减少症组的疗效优于非HIV免疫性血小板减少性紫癜组,HIV组脾切除术后1周和1个月时血小板计数显著更高(t检验,P分别为0.02和0.009)。HIV组脾切除术后因血小板减少症需要药物治疗的患者明显更少(χ²检验,P = 0.02)。HIV感染患者无明显短期或长期并发症,包括无脾切除术后暴发性感染。3例患者死亡,2例患者术后发生艾滋病。
脾切除术是治疗有症状、药物治疗抵抗的HIV相关血小板减少症患者的有效方法。该治疗方法的有效性表明,HIV感染患者血小板减少的主要机制是血小板相关免疫蛋白导致的血小板破坏增加。