THE AGE AT ONSET OF CHRONIC PSEUDOMONAS-AERUGINOSA COLONIZATION IN CYSTIC-FIBROSIS - PROGNOSTIC-SIGNIFICANCE

被引:32
作者
AEBI, C
BRACHER, R
LIECHTIGALLATI, S
TSCHAPPELER, H
RUDEBERG, A
KRAEMER, R
机构
[1] UNIV BERN,INSELSPITAL,DEPT PAEDIAT,CH-3010 BERN,SWITZERLAND
[2] UNIV BERN,DEPT CLIN PHARMACOL,GENET MOLEC LAB,CH-3012 BERN,SWITZERLAND
[3] UNIV BERN,INSELSPITAL,DIV PAEDIAT RADIOL,CH-3010 BERN,SWITZERLAND
关键词
CYSTIC FIBROSIS; PSEUDOMONAS AERUGINOSA; LUNG INVOLVEMENT; SURVIVAL; PROGNOSIS;
D O I
10.1007/BF02191510
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
To evaluate the prognostic significance of the age at onset of chronic Pseudomonas aeruginosa colonization (OPCP) with respect to pulmonary disease progression in patients with cystic fibrosis (CF), a retrospective long-term analysis using annual chest radiographs was performed on 54 CF patients. Thirty-seven patients (68%) were chronically colonized before the age of 12 years (group 1), 17 patients (32%) thereafter (group 2). These two groups did not significantly differ in terms of mean duration of follow up (16.2 +/- 5.9 years), sex, CF genotypes, colonization with other respiratory pathogens, supportive medical treatment and death rate during the study period. Chest radiographs were evaluated according to the Chrispin-Norman score, increasing scores representing increasing severity of respiratory disease. Ln both groups, progression of score means was not accelerated up to 6 years after OCPC (Scores at OCPC set 0; mean score +/- SEM 6 years prior to OCPC - 5.6 +/- 2.0; 10 years after OCPC + 3.6 +/- 0.7 points). Patients chronically colonized prior to age 12 years (group 1) scored significantly higher between age 2 and 11 years (maximum difference at age 8 years [mean +/- SEM]: 9.4 +/- 0.7 vs. 4.3 +/- 1.3 points; P = 0.002) as compared to group 2. After age ii years, mean scores were similar in both groups, since in group 2 scores increased rapidly after age s years. We conclude that OCPC did not cause an immediate acceleration of CF lung disease judged by serial chest radiographs. Rapid progression in group 2 (OCPC after age 12 years) was independent of OCPC since it occurred earlier. These data indicate that OCPC may be a marker rather than the cause of respiratory disease progression.
引用
收藏
页码:S69 / S73
页数:5
相关论文
共 23 条
[11]   PULMONARY-FUNCTION AND CLINICAL COURSE IN PATIENTS WITH CYSTIC-FIBROSIS AFTER PULMONARY COLONIZATION WITH PSEUDOMONAS-AERUGINOSA [J].
KEREM, E ;
COREY, M ;
GOLD, R ;
LEVISON, H .
JOURNAL OF PEDIATRICS, 1990, 116 (05) :714-719
[12]   RISK-FACTORS FOR PSEUDOMONAS-AERUGINOSA COLONIZATION IN CYSTIC-FIBROSIS PATIENTS [J].
KEREM, E ;
COREY, M ;
STEIN, R ;
GOLD, R ;
LEVISON, H .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 1990, 9 (07) :494-498
[13]   RELATIVE UNDERWEIGHT IN CYSTIC-FIBROSIS AND ITS PROGNOSTIC VALUE [J].
KRAEMER, R ;
RUDEBERG, A ;
HADORN, B ;
ROSSI, E .
ACTA PAEDIATRICA SCANDINAVICA, 1978, 67 (01) :33-37
[14]  
KRAEMER R, 1979, HELV PAEDIATR ACTA, V34, P417
[15]  
KULCZYCKI LL, 1988, ANN ALLERGY, V60, P423
[16]  
LIECHTIGALLATI S, 1990, CLIN GENET, V37, P442
[17]   GENOTYPE PHENOTYPE ASSOCIATION IN CYSTIC-FIBROSIS - ANALYSES OF THE DELTA-F508, R553X, AND 3905INST MUTATIONS [J].
LIECHTIGALLATI, S ;
BONSALL, I ;
MALIK, N ;
SCHNEIDER, V ;
KRAEMER, LG ;
RUEDEBERG, A ;
MOSER, H ;
KRAEMER, R .
PEDIATRIC RESEARCH, 1992, 32 (02) :175-178
[18]   INTERACTION OF STEROIDAL HORMONES WITH MUCUS GLYCOPROTEINS [J].
MARTIN, GP ;
MARRIOTT, C ;
KELLAWAY, IW .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1978, 30 :P10-P10
[19]  
NIEMAN RB, 1993, AM REV RESPIR DIS, V147, pA28
[20]   MANAGEMENT OF PSEUDOMONAS-AURUGINOSA LUNG INFECTION IN DANISH CYSTIC-FIBROSIS PATIENTS [J].
PEDERSEN, SS ;
JENSEN, T ;
HOIBY, N ;
KOCH, C ;
FLENSBORG, EW .
ACTA PAEDIATRICA SCANDINAVICA, 1987, 76 (06) :955-961