Cystic fibrosis: A system for assessing and predicting progression

被引:25
作者
Cleveland, RH
Neish, AS
Zurakowski, D
Nichols, DP
Wohl, MEB
Colin, AA
机构
[1] Harvard Univ, Childrens Hosp, Sch Med, Dept Radiol, Boston, MA 02115 USA
[2] Harvard Univ, Childrens Hosp, Sch Med, Dept Res Comp & Biostat, Boston, MA 02115 USA
[3] Univ Chicago, Chicago, IL 60611 USA
[4] SPSS Inc, Chicago, IL 60611 USA
[5] Harvard Univ, Childrens Hosp, Sch Med, Dept Pediat,Div Pulm Med, Boston, MA 02115 USA
关键词
D O I
10.2214/ajr.170.4.9530060
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
OBJECTIVE. This study presents a radiography-based database scoring changes over time in a large population of patients with cystic fibrosis. The purpose of this database is to provide comparison for groups of patients undergoing experimental treatment to assess effect of the treatment. The data may also be used to compare individuals with their age-matched cohorts with cystic fibrosis. MATERIALS AND METHODS. From 230 patients, 3038 chest radiographs were scored using the Brasfield system. The scores from radiographs from all the patients were individually plotted for age, and a single age-based severity curve was created. The age-based severity curve was compared with similar curves derived from pulmonary function studies of a subset of the same patient population. RESULTS. We found high inter-and intraobserver reliability. The difference between the observers averaged 1.3 Brasfield points, the scale of which ranges up to 25 points. The age-based severity curve was presented as mean Brasfield scores versus age (birth to >30 years) plotted with 95% confidence limits; the curve was also plotted in percentiles. The rate of decline of this curve was similar to the decline of pulmonary function studies in this patient population. CONCLUSION. The age-based curve, a structural anatomic parameter, differs from pulmonary function studies, which are functional. Thus the age-based severity curve provides an additional, independent basis for comparison between groups and individuals. It may be used for the initial assessment of lung disease and for gauging and predicting the rate of decline. The curve may be used as a long-range outcome criterion to evaluate new treatments in groups of patients with cystic fibrosis.
引用
收藏
页码:1067 / 1072
页数:6
相关论文
共 30 条
[1]   RADIOLOGIC ASSESSMENT OF PULMONARY ARTERIAL-PRESSURE AND BLOOD-VOLUME IN CHRONIC, DIFFUSE, INTERSTITIAL PULMONARY-DISEASES [J].
AUSTIN, JHM ;
YOUNT, BG ;
THOMAS, HM ;
ENSON, Y .
INVESTIGATIVE RADIOLOGY, 1979, 14 (01) :9-17
[2]   PULMONARY-FUNCTION IN INFANTS WITH CYSTIC-FIBROSIS - THE EFFECT OF ANTIBIOTIC-TREATMENT [J].
BEARDSMORE, CS ;
THOMPSON, JR ;
WILLIAMS, A ;
MCARDLE, EK ;
GREGORY, GA ;
WEAVER, LT ;
SIMPSON, H .
ARCHIVES OF DISEASE IN CHILDHOOD, 1994, 71 (02) :133-137
[3]   CYSTIC-FIBROSIS - SCORING SYSTEM WITH THIN-SECTION CT [J].
BHALLA, M ;
TURCIOS, N ;
APONTE, V ;
JENKINS, M ;
LEITMAN, BS ;
MCCAULEY, DI ;
NAIDICH, DP .
RADIOLOGY, 1991, 179 (03) :783-788
[4]   EVALUATION OF SCORING SYSTEM OF THE CHEST RADIOGRAPH IN CYSTIC-FIBROSIS - A COLLABORATIVE STUDY [J].
BRASFIELD, D ;
HICKS, G ;
SOONG, S ;
PETERS, J ;
TILLER, R .
AMERICAN JOURNAL OF ROENTGENOLOGY, 1980, 134 (06) :1195-1198
[5]  
COREY M, 1976, AM REV RESPIR DIS, V114, P1085
[6]  
Fleiss J. L., 1981, STAT METHODS RATES P, P598
[7]   EFFECT OF AEROSOLIZED RECOMBINANT HUMAN DNASE ON EXACERBATIONS OF RESPIRATORY SYMPTOMS AND ON PULMONARY-FUNCTION IN PATIENTS WITH CYSTIC-FIBROSIS [J].
FUCHS, HJ ;
BOROWITZ, DS ;
CHRISTIANSEN, DH ;
MORRIS, EM ;
NASH, ML ;
RAMSEY, BW ;
ROSENSTEIN, BJ ;
SMITH, AL ;
WOHL, ME .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (10) :637-642
[8]   A CYSTIC-FIBROSIS MUTATION ASSOCIATED WITH MILD LUNG-DISEASE [J].
GAN, KH ;
VEEZE, HJ ;
VANDENOUWELAND, AMW ;
HALLEY, DJJ ;
SCHEFFER, H ;
VANDERHOUT, A ;
OVERBEEK, SE ;
DEJONGSTE, JC ;
BAKKER, W ;
HEIJERMAN, HGM .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (02) :95-99
[9]  
HAMOSH A, 1993, NEW ENGL J MED, V329, P1308
[10]  
International Labour Office, 1980, GUID US ILO INT CLAS