Yaprak I, Cağlayan S, Kansoy S, Ozdoğru E, Bakiler A R, Aydinlioğlu H
Department of Pediatrics, SSK Tepecik Teaching Hospital, Izmir.
Turk J Pediatr. 1994 Jan-Mar;36(1):43-7.
Chronic idiopathic thrombocytopenic purpura is an autoimmune disease characterized by antibody-mediated destruction of platelets. To maintain the platelets above the symptomatic level, we administered anti-D (100 micrograms for 5 consecutive days) in 19 children with idiopathic thrombocytopenic purpura (ITP). Four patients did not respond to treatment. Fifteen responded with an increase in the average platelet number to 76,000/microL on the 7th postinjection day. Within 45 days, however, platelets dropped to 27,000/microL. Three months after this study, two patients from the study group were re-administered anti-D in daily injections for 5 consecutive days, as was done previously. Monthly administration of anti-D in two patients maintained platelets above 30,000/microL for periods of five and six months. We concluded that monthly administration of anti-D after five consecutive daily injections can maintain platelet levels above the symptomatic level and may provide a corticosteroid-free safe interval of nearly five months.
慢性特发性血小板减少性紫癜是一种自身免疫性疾病,其特征为抗体介导的血小板破坏。为使血小板维持在症状水平以上,我们对19例特发性血小板减少性紫癜(ITP)患儿给予抗-D(100微克,连续5天)治疗。4例患者治疗无效。15例患者有反应,注射后第7天平均血小板数增至76,000/微升。然而,在45天内,血小板降至27,000/微升。本研究3个月后,研究组的2例患者按先前方法再次连续5天每日注射抗-D。2例患者每月注射抗-D使血小板在5个月和6个月期间维持在30,000/微升以上。我们得出结论,连续5天每日注射后每月给予抗-D可使血小板水平维持在症状水平以上,并可能提供近5个月无皮质类固醇的安全间隔期。