Distribution of disease in cystic fibrosis - Correlation with pulmonary function

被引:15
作者
Gurney, JW [1 ]
Habbe, TG [1 ]
Hicklin, J [1 ]
机构
[1] INDIANA UNIV HOSP, DEPT RADIOL, INDIANAPOLIS, IN 46202 USA
关键词
age distribution; cystic fibrosis; pulmonary function tests; radiographic image interpretation;
D O I
10.1378/chest.112.2.357
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Study objective: We hypothesized that the radiographic distribution of disease is important in determining pulmonary function, with the lower lung zones of more importance than the upper lung zones. To test this hypothesis, we retrospectively studied patients with cystic fibrosis, a disease with a known proclivity for the upper lung zones. Subjects ana methods: Two hundred seventy-six chest radiographs obtained at 2- to 3-year intervals from 51 patients were scored by two radiologists using a 100-point visual severity scale. The distribution of disease was assessed by dividing the lungs into four equal horizontal zones and scoring each zone for the severity of disease. There were 146 concurrent chest radiographs and pulmonary function tests from which multiple linear regression was used to correlate these zonal scores with FEV1/FVC percent predicted. Results: There was excellent interobserver agreement, intraclass correlation coefficients >0.?. The distribution of disease became predominant in the upper lung zones as the patients aged. Although the median score in the upper lung zones was nearly twice that of the lower lung zones, the lower lung zones were nearly three times (partial F ratio; 6.9 lower zone score vs 2.4 upper lung zone score) as important in determining pulmonary function. Conclusion: The regional distribution of disease is important in determining pulmonary function. Sparing of the lower lung zones is important in preserving pulmonary function.
引用
收藏
页码:357 / 362
页数:6
相关论文
共 52 条
[1]   QUANTITATIVE ASSESSMENT OF REGIONAL VENTILATION AND PERFUSION IN CHILDREN WITH CYSTIC-FIBROSIS [J].
ALDERSON, PO ;
SECKERWA.RH ;
STROMINGER, DB ;
MCALISTER, WH ;
HILL, RL ;
MARKHAM, J .
RADIOLOGY, 1974, 111 (01) :151-156
[2]   CT IN SILICOSIS - CORRELATION WITH PLAIN FILMS AND PULMONARY-FUNCTION TESTS [J].
BERGIN, CJ ;
MULLER, NL ;
VEDAL, S ;
CHANYEUNG, M .
AMERICAN JOURNAL OF ROENTGENOLOGY, 1986, 146 (03) :477-483
[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]  
BRASFIELD D, 1979, PEDIATRICS, V63, P24
[5]   STRUCTURE AND FUNCTION IN SARCOIDOSIS [J].
CARRINGTON, CB ;
GAENSLER, EA ;
MIKUS, JP ;
SCHACHTER, AW ;
BURKE, GW ;
GOFF, AM .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1976, 278 (SEP9) :265-283
[6]   REPEATABILITY AND METHOD COMPARISON [J].
CHINN, S .
THORAX, 1991, 46 (06) :454-456
[7]   HIGH-RESOLUTION CT IN SIMPLE COAL-WORKERS PNEUMOCONIOSIS - LACK OF CORRELATION WITH PULMONARY-FUNCTION TESTS AND ARTERIAL BLOOD-GAS VALUES [J].
COLLINS, LC ;
WILLING, S ;
BRETZ, R ;
HARTY, M ;
LANE, E ;
ANDERSON, WH .
CHEST, 1993, 104 (04) :1156-1162
[8]   PATHO-PHYSIOLOGY OF PULMONARY-DISEASE IN CYSTIC-FIBROSIS [J].
DAVIS, PB .
SEMINARS IN RESPIRATORY MEDICINE, 1985, 6 (04) :261-270
[9]  
DISANTAGNESE PA, 1953, PEDIATRICS, V12, P178
[10]  
EVANS I, 1987, EUR J NUCL MED, V12, P620