EARLY BACTERIOLOGICAL, IMMUNOLOGICAL, AND CLINICAL COURSES OF YOUNG INFANTS WITH CYSTIC-FIBROSIS IDENTIFIED BY NEONATAL SCREENING

被引:109
作者
ABMAN, SH
OGLE, JW
HARBECK, RJ
BUTLERSIMON, N
HAMMOND, KB
ACCURSO, FJ
机构
[1] UNIV COLORADO, CHILDRENS HOSP, SCH MED, DEPT PEDIAT, DENVER, CO 80202 USA
[2] UNIV COLORADO, CHILDRENS HOSP, SCH MED, DEPT IMMUNOL, DENVER, CO 80202 USA
[3] NATL JEWISH CTR IMMUNOL & RESP DIS, DENVER, CO USA
关键词
D O I
10.1016/S0022-3476(05)80729-2
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
To understand better the events associated with the initiation of lung disease in young children with cystic fibrosis (CF), we prospectively performed a longitudinal study examining the early bacteriologic, immunologic, and clinical courses of 42 children with CF diagnosed after identification by neonatal screening. Serial evaluations included history and physical examination, chest radiographs, throat cultures for bacteria, and determinations of serum immunoglobulin levels and circulating immune complexes. At a mean follow-up age of 27 months, 19% of the children had serial throat cultures positive for Pseudomonas aeruginosa, the first positive culture was found of a mean age of 21 months. In three Infants the initial P. aeruginosa isolates were mucoid. As determined by typing with a DNA probe, serial P. aeruginosa isolates from each patient were identical over time but were genetically distinct from isolates recovered from other patients. Of 11 infants with P. aeruginosa, nine (82%) had previous isolates of Staphylococcus aureus or Haemophilus influenzae; all had received prior antibiotic therapy. In comparison with other infants with CF, children with P. aeruginosa grown on serial throat cultures more frequently had daily cough (p < 0.01), lower chest radiograph scores (p < 0.05), and elevated levels of circulating immune complexes (p < 0.01). None of the study infants had persistent hypogammaglobulinemia or hypergammaglobulinemia. We conclude that (1) S. aureus and H. influenzae remain the isolates most frequently recovered from infants with CF; (2) initial recovery of P. aeruginosa by throat culture is often preceded by the onset of chronic respiratory signs; (3) elevations of circulating immune complexes can occur early, often after the initial recovery of P. aeruginosa, and (4) early P. aeruginosa isolates are genetically distinct, demonstrating the lack of cross-colonization in this newborn population.
引用
收藏
页码:211 / 217
页数:7
相关论文
共 44 条
[1]   ROLE OF RESPIRATORY SYNCYTIAL VIRUS IN EARLY HOSPITALIZATIONS FOR RESPIRATORY-DISTRESS OF YOUNG INFANTS WITH CYSTIC-FIBROSIS [J].
ABMAN, SH ;
OGLE, JW ;
BUTLERSIMON, N ;
RUMACK, CM ;
ACCURSO, FJ .
JOURNAL OF PEDIATRICS, 1988, 113 (05) :826-830
[2]   SELECTIVE PRESSURE OF ANTISTAPHYLOCOCCAL CHEMOTHERAPEUTICS IN FAVOR OF PSEUDOMONAS-AERUGINOSA IN CYSTIC-FIBROSIS [J].
BAUERNFEIND, A ;
EMMINGER, G ;
HORL, G ;
LORBEER, B ;
PRZYKLENK, B ;
WEISSLEINPFISTER, C .
INFECTION, 1987, 15 (06) :469-470
[3]   LUNG IN CYSTIC-FIBROSIS - QUANTITATIVE STUDY INCLUDING PREVALENCE OF PATHOLOGIC FINDINGS AMONG DIFFERENT AGE-GROUPS [J].
BEDROSSIAN, CWM ;
GREENBERG, SD ;
SINGER, DB ;
HANSEN, JJ ;
ROSENBERG, HS .
HUMAN PATHOLOGY, 1976, 7 (02) :195-204
[4]  
BERGAN T, 1975, ACTA PATH MICRO IM B, V83, P553
[5]  
BRASFIELD D, 1979, PEDIATRICS, V63, P24
[6]   SERUM IGG ANTIBODIES IN PATIENTS WITH CYSTIC-FIBROSIS WITH EARLY PSEUDOMONAS-AERUGINOSA INFECTION [J].
BRETT, MM ;
GHONEIM, ATM ;
LITTLEWOOD, JM .
ARCHIVES OF DISEASE IN CHILDHOOD, 1987, 62 (04) :357-361
[7]  
CHARTRAND SA, 1988, RESPIRATORY INFECTIO, P276
[8]   PATHOGENESIS OF THE PSEUDOMONAS LUNG LESION IN CYSTIC-FIBROSIS [J].
FICK, RB .
CHEST, 1989, 96 (01) :158-164
[9]  
GIBSON LE, 1959, PEDIATRICS, V23, P545
[10]   GENOME FINGERPRINTING OF PSEUDOMONAS-AERUGINOSA INDICATES COLONIZATION OF CYSTIC-FIBROSIS SIBLINGS WITH CLOSELY RELATED STRAINS [J].
GROTHUES, D ;
KOOPMANN, U ;
VONDERHARDT, H ;
TUMMLER, B .
JOURNAL OF CLINICAL MICROBIOLOGY, 1988, 26 (10) :1973-1977