ISOLATION AND TREATMENT OF CYSTIC-FIBROSIS PATIENTS WITH LUNG INFECTIONS CAUSED BY PSEUDOMONAS-(BURKHOLDERIA)-CEPACIA AND MULTIRESISTANT PSEUDOMONAS-AERUGINOSA
N. Hoiby, ISOLATION AND TREATMENT OF CYSTIC-FIBROSIS PATIENTS WITH LUNG INFECTIONS CAUSED BY PSEUDOMONAS-(BURKHOLDERIA)-CEPACIA AND MULTIRESISTANT PSEUDOMONAS-AERUGINOSA, Netherlands journal of medicine, 46(6), 1995, pp. 280-287
Cross-infection with Pseudomonas aeruginosa and Pseudomonas cepacia ha
s been shown sometimes to occur between cystic fibrosis (CF) patients
in some CF centres, in some summer camps and during some social contac
ts between CF patients. Cohort isolation and improved hygienic precaut
ions, however, have successfully been employed in some CF centres resu
lting in a decrease or elimination of cross-infection. Chronic P. aeru
ginosa infection is in most CF patients preceded by a period of interm
ittent colonization. Early aggressive chemotherapy (oral ciprofloxacin
and nebulized colistin for 3 weeks) every time P. aeruginosa is detec
ted in sputum has significantly decreased the incidence of new chronic
infection in CF patients. Chronic P. aeruginosa infection can be trea
ted by ''maintenance chemotherapy'' (= chronic suppressive chemotherap
y). The principle is to restore lung function repeatedly by regular 2-
week courses of intensive intravenous treatment every 3 months in the
CF centre and adding daily inhalations of colistin between the courses
, and sometimes also by giving oral ciprofloxacin during these interva
ls to unstable patients. Eradication of P. cepacia infection is virtua
lly never obtained by antibiotic treatment with, e.g., ceftazidime and
tobramycin or co-trimoxazole. Chronic suppression with doxycyclin or
co-trimoxazole may give rise to some improvement in the clinical sympt
oms.