Vander Leek T K, Liu A H, Stefanski K, Blacker B, Bock S A
Department of Pediatrics, National Jewish Medical and Research Center, Denver, Colorado 80206, USA.
J Pediatr. 2000 Dec;137(6):749-55. doi: 10.1067/mpd.2000.109376.
To observe the nature and frequency of adverse reactions caused by accidental peanut exposure in young children with clinical peanut hypersensitivity and to determine the value of serum peanut-specific IgE levels during follow-up.
Eighty-three children with clinical peanut hypersensitivity diagnosed before their fourth birthdays were contacted yearly to track adverse peanut reactions. Serum peanut-specific IgE levels were determined in 51 of 83 subjects.
Fifty-eight percent (31/53) of subjects followed up for 5 years experienced adverse reactions from accidental peanut exposure. Regardless of the nature of their initial reaction, the majority with subsequent reactions (52%, 31/60) experienced potentially life-threatening symptoms. The group with isolated skin symptoms (11/51, 22%) had lower serum peanut-specific IgE levels than the group with respiratory and/or gastrointestinal symptoms (40/51, 78%) (median: 1.25 kU(A)/L vs 11. 65 kU(A)/L, P =.004, Wilcoxon rank sums test). Despite this, there was no threshold level below which only skin symptoms appeared to occur. Four selected subjects had negative double-blind placebo-controlled food challenge responses to peanuts during follow-up.
The majority of children with clinical peanut hypersensitivity followed up for 5 years will have adverse reactions from accidental peanut exposure. Symptoms experienced during subsequent adverse peanut reactions may not be consistent with symptoms reported during initial reactions. Therefore proper education regarding peanut avoidance and treatment of adverse reactions is necessary in all cases of clinical peanut hypersensitivity. Young children who are allergic to peanuts can lose clinical hypersensitivity.
观察临床花生过敏的幼儿因意外接触花生引起的不良反应的性质和频率,并确定随访期间血清花生特异性IgE水平的价值。
对83名4岁前被诊断为临床花生过敏的儿童每年进行随访,以追踪花生不良反应。在83名受试者中的51名中测定了血清花生特异性IgE水平。
随访5年的受试者中有58%(31/53)因意外接触花生出现不良反应。无论其初始反应的性质如何,大多数后续有反应的受试者(52%,31/60)出现了可能危及生命的症状。仅有皮肤症状的组(11/51,22%)血清花生特异性IgE水平低于有呼吸道和/或胃肠道症状的组(40/51,78%)(中位数:1.25 kU(A)/L对11.65 kU(A)/L,P = 0.004,Wilcoxon秩和检验)。尽管如此,并没有一个阈值水平,低于该水平似乎仅出现皮肤症状。4名选定的受试者在随访期间对花生的双盲安慰剂对照食物激发试验反应为阴性。
随访5年的大多数临床花生过敏儿童会因意外接触花生出现不良反应。后续花生不良反应期间出现的症状可能与初始反应期间报告的症状不一致。因此,在所有临床花生过敏病例中,关于避免花生和治疗不良反应的适当教育是必要的。对花生过敏的幼儿可能会失去临床过敏反应。