Trompeter R S, Lloyd B W, Hicks J, White R H, Cameron J S
Lancet. 1985 Feb 16;1(8425):368-70. doi: 10.1016/s0140-6736(85)91387-x.
A retrospective study was undertaken to assess the outcome of a cohort of 183 unselected children who presented with the nephrotic syndrome between 1963 and 1969. All subjects showed minimal glomerular changes in biopsy samples and were given conventional steroid therapy. Information was available on 152 children, now aged 14-32 years. Activity persisted longer in patients presenting at an early age. The outcome for most of the children was favourable. Only 10 patients (5.5%), all of whom presented with initial symptoms before their 6th birthday, continued to have steroid-responsive relapses in adult life. There were 11 deaths, of which 7 (4% of the series) were from avoidable complications of the disorder.
进行了一项回顾性研究,以评估1963年至1969年间出现肾病综合征的183名未经挑选儿童的队列结局。所有受试者的活检样本均显示肾小球变化极小,并接受了传统的类固醇治疗。现有152名儿童的信息,他们现在年龄在14至32岁之间。发病年龄较小的患者病情活动持续时间更长。大多数儿童的结局良好。只有10名患者(5.5%),他们均在6岁生日前出现初始症状,在成年后仍有类固醇反应性复发。有11例死亡,其中7例(占该系列的4%)死于该疾病可避免的并发症。