Rosthøj S, Nielsen S M, Pedersen F K
Aalborg Sygehus Nord, børneafdelingen.
Ugeskr Laeger. 1998 Mar 9;160(11):1640-4.
Forty three children with newly diagnosed idiopathic thrombocytopenic purpura (ITP), platelet count (pl.c.) below 20 x 10(9)/l, and either clinically significant bleeding or failure to show a spontaneous platelet rise within three days of admission were randomly allocated to treatment with intravenous infusions of either immunoglobulin (IVIG) 1 g/kg or methylprednisolone (MPPT) 30 mg/kg on two consecutive days. Prompt induction of partial remission with pl.c. > 50 x 10(9)/l after 72 hours was seen in 21/23 given IVIG versus 10/20 given MPPT (exact p = 0.003); mean pl.c.s after 72 hours were 188 versus 77 x 10(9)/l (2p < 0.001). Poor responders were then given the alternative infusions in addition. After six days, complete remission with pl.c. > 150 x 10(9)/l was achieved in 16/23 versus 10/20 (p = 0.16). During six months follow-up, there were no significant differences regarding relapse rates or chronic course. Eleven children with relapse were crossed over to the alternative treatment arm: the estimated treatment effect in pl.c. after 72 hours was 134 x 10(9)/l in favour of IVIG. These results indicate that IVIG infusions may be preferable to high-dose corticosteroids as initial treatment for children with ITP.
43名新诊断为特发性血小板减少性紫癜(ITP)的儿童,血小板计数(pl.c.)低于20×10⁹/L,且有临床显著出血或入院三天内未出现血小板自发升高,被随机分配接受连续两天静脉输注免疫球蛋白(IVIG)1g/kg或甲泼尼龙(MPPT)30mg/kg治疗。接受IVIG治疗的23例中有21例在72小时后血小板计数迅速诱导部分缓解,pl.c.>50×10⁹/L,而接受MPPT治疗的20例中有10例(确切p = 0.003);72小时后的平均血小板计数分别为188×10⁹/L和77×10⁹/L(2p<0.001)。反应不佳者随后加用另一种输注治疗。六天后,23例中有16例达到完全缓解,pl.c.>150×10⁹/L,而20例中有10例(p = 0.16)。在六个月的随访期间,复发率或慢性病程方面无显著差异。11例复发儿童转而接受另一种治疗:72小时后血小板计数的估计治疗效果为IVIG优于MPPT,差值为134×10⁹/L。这些结果表明,对于ITP儿童,IVIG输注作为初始治疗可能优于大剂量皮质类固醇。