Morens D M, Sullivan-Bolyai J Z, Slater J E, Schonberger L B, Nelson D B
Am J Epidemiol. 1981 Sep;114(3):406-16. doi: 10.1093/oxfordjournals.aje.a113208.
Between December 1, 1976, and November 30, 1977, 454 cases of Reye syndrome were reported to the Centers for Disease Control by 43 states. Analysis of data about these cases revealed that Reye syndrome primarily affected white children under age 18 years, with a mean age of 7.7 years and bimodal incidence peaks in infancy and at age 6-7 years, was temporally and geographically associated with influenza B for about 75% of cases, but also occurred sporadically and not in association with influenza B activity. Although Reye syndrome was reported infrequently for non-white children aged one year or older, there was a high incidence in minority infants, and the case-fatality ratio in infants of all races was significantly higher than that of the older children. Favorable outcome was associated with prolonged interval between onset of prodromal illness and hospitalization, admission to hospital at a milder stage of illness, and treatment in hospitals with established pediatric training programs.
1976年12月1日至1977年11月30日期间,43个州向疾病控制中心报告了454例瑞氏综合征病例。对这些病例数据的分析显示,瑞氏综合征主要影响18岁以下的白人儿童,平均年龄为7.7岁,发病高峰呈双峰状,分别在婴儿期以及6至7岁时;在时间和地理上,约75%的病例与乙型流感有关,但也有散发病例,且与乙型流感活动无关。虽然一岁及以上非白人儿童中瑞氏综合征报告较少,但少数族裔婴儿发病率较高,所有种族婴儿的病死率显著高于大龄儿童。良好的预后与前驱疾病发作至住院的间隔时间延长、在疾病较轻阶段入院以及在设有成熟儿科培训项目的医院接受治疗有关。