Leonard H, Bower C, English D
TVW Telethon Institute for Child Health Research, West Perth, Western Australia.
Eur Child Adolesc Psychiatry. 1997;6 Suppl 1:8-10.
The Australian Paediatric Surveillance Unit and the Rett Syndrome Association of Australia (a parent support group) were the main sources of ascertainment of cases of Rett syndrome (RS) aged 18 years or less in Australia. Further information was obtained from questionnaires to paediatricians and families. Cases were categorised as classical, atypical, potential or non-verifiable, using internationally recognised criteria. Capture recapture methods were used to adjust prevalence measures for missing cases, and Kaplan Meier survival analysis to estimate cumulative incidence. A total of 134 cases of RS was identified, and of those over 5 years of age, 68% were classical and 32% were atypical. The adjusted prevalence was 0.72 per 10,000 females, and the cumulative incidence was 0.96 per 10,000 females to age 12 years. The prevalence was similar to that in Sweden and Scotland, but higher than in Texas. Comparing successive birth cohorts, there was evidence to suggest that RS is being diagnosed earlier and that more cases are being diagnosed as atypical.
澳大利亚儿科监测部门和澳大利亚瑞特综合征协会(一个家长支持组织)是澳大利亚18岁及以下瑞特综合征(RS)病例的主要确诊来源。通过向儿科医生和患儿家庭发放调查问卷获得了更多信息。按照国际公认的标准,病例被分为典型、非典型、疑似或无法确诊几类。采用捕获再捕获法对漏报病例的患病率测量值进行校正,并运用Kaplan Meier生存分析来估计累积发病率。共确诊134例瑞特综合征病例,其中5岁以上的病例中,68%为典型病例,32%为非典型病例。校正后的患病率为每10000名女性中有0.72例,到12岁时的累积发病率为每10000名女性中有0.96例。该患病率与瑞典和苏格兰的相似,但高于德克萨斯州。比较连续出生队列发现,有证据表明瑞特综合征的诊断时间更早,且更多病例被诊断为非典型。