Predictive 5-year survivorship model of cystic fibrosis

被引:552
作者
Liou, TG
Adler, FR
FitzSimmons, SC
Cahill, BC
Hibbs, JR
Marshall, BC
机构
[1] Univ Utah, Hlth Sci Ctr, Dept Internal Med, Div Resp Crit Care & Occupat Pulm Med, Salt Lake City, UT 84132 USA
[2] Univ Utah, Hlth Sci Ctr, Lung Transplantat Program, Salt Lake City, UT 84132 USA
[3] Univ Utah, Intermt Cyst Fibrosis Ctr, Salt Lake City, UT 84132 USA
[4] Univ Utah, Dept Math, Salt Lake City, UT 84132 USA
[5] Univ Utah, Dept Biol, Salt Lake City, UT 84132 USA
[6] Cyst Fibrosis Fdn, Bethesda, MD USA
[7] New York State Dept Hlth, Albany, NY USA
[8] Salt Lake Vet Adm Med Ctr, Salt Lake City, UT USA
关键词
cystic fibrosis; logistic models; models; theoretical; multivariate analysis; proportional hazards models; survival analysis;
D O I
10.1093/aje/153.4.345
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
The objective of this study was to create a 5-year survivorship model to identify key clinical features of cystic fibrosis. Such a model could help researchers and clinicians to evaluate therapies, improve the design of prospective studies, monitor practice patterns, counsel individual patients, and determine the best candidates for lung transplantation. The authors used information from the Cystic Fibrosis Foundation Patient Registry (CFFPR), which has collected longitudinal data on approximately 90% of cystic fibrosis patients diagnosed in the United States since 1986. They developed multivariate logistic regression models by using data on 5,820 patients randomly selected from 11,630 in the CFFPR in 1993. Models were tested for goodness of fit and were validated for the remaining 5,810 patients for 1993. The validated 5-year survivorship model included age, forced expiratory volume in 1 second as a percentage of predicted normal, gender, weight-for-age z score, pancreatic sufficiency, diabetes mellitus, Staphylococcus aureus infection, Burkerholderia cepacia infection, and annual number of acute pulmonary exacerbations. The model provides insights into the complex nature of cystic fibrosis and supplies a rigorous tool for clinical practice and research.
引用
收藏
页码:345 / 352
页数:8
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