Dodge J A, Lewis P A, Stanton M, Wilsher J
Dept of Child Health, University of Wales Swansea, Singleton Hospital, Sketty Road, Swansea SA2 8QA, UK.
Eur Respir J. 2007 Mar;29(3):522-6. doi: 10.1183/09031936.00099506. Epub 2006 Dec 20.
Data up to 1995 on the survival of 3-yr cohorts of patients with cystic fibrosis (CF) born in the UK in the period 1968-1992 have previously been published. The present study reports survival data up to the end of 2003 together with a 2003 population estimate. All subjects with CF born in the UK in the period 1968-1992 were identified up to 1997 by active enquiry through recognised CF clinics and other hospital consultants. Information from the death certification authorities up to the end of 2003 was added. Death certificates that could not be matched with UK Cystic Fibrosis Survey records were investigated and the data reconciled. The observed survival up to 2003 of CF patients born in 1978 was 55% for males and 49% for females. For 1988 and 1992 the data were 91 and 88%, and 97 and 96%, respectively. The estimated 2003 mid-year CF population was 8,284. The continuing improvement in survival of cystic fibrosis patients in successive cohorts means that the previous prediction of median survival of >50 yrs of age for individuals born in 2000 continues to look realistic, even in the absence of proven effective therapy aimed at correcting the basic cystic fibrosis defect.
此前已发表过关于1968 - 1992年期间在英国出生的囊性纤维化(CF)患者3年队列生存率的数据,截止到1995年。本研究报告了截至2003年底的生存数据以及2003年的人口估计数。通过认可的CF诊所和其他医院顾问进行积极查询,在1997年前识别出了所有1968 - 1992年期间在英国出生的CF患者。添加了截至2003年底死亡证明机构提供的信息。对无法与英国囊性纤维化调查记录匹配的死亡证明进行了调查并核对数据。1978年出生的CF患者截至2003年的观察生存率,男性为55%,女性为49%。1988年和1992年出生患者的数据分别为91%和88%,以及97%和96%。2003年年中CF患者估计人数为8284人。囊性纤维化患者连续队列的生存率持续提高,这意味着之前预测2000年出生个体的中位生存期超过50岁仍然看起来是现实的,即使在没有旨在纠正基本囊性纤维化缺陷的经证实有效疗法的情况下。