Epidemiology of Pseudomonas aeruginosa in cystic fibrosis in British Columbia, Canada.

Pseudomonas aeruginosa is the most common respiratory pathogen in patients with cystic fibrosis (CF), but the predominant mechanism by which it is acquired is controversial. To determine the frequency of patient-to-patient spread, we evaluated P. aeruginosa isolates from 174 patients treated at the...

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Published in:American Journal of Respiratory & Critical Care Medicine Vol. 166; no. 7; pp. 988 - 994
Main Authors: Speert, David P, Campbell, Maureen E, Henry, Deborah A, Milner, Ruth, Taha, Fatma, Gravelle, Anna, Davidson, A George F, Wong, Lawrence T K, Mahenthiralingam, Eshwar
Format: research Journal Article
Published: Oxford University Press / USA 2002 Oct 1
Online Access:View this record in EBSCOhost
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      dt: 2002 Oct 1
      vid: 166
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      pub: Oxford University Press / USA
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        10.1164/rccm.2203011
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        atl: Epidemiology of Pseudomonas aeruginosa in cystic fibrosis in British Columbia, Canada.
      aug:
        au:
          Speert, David P
          Campbell, Maureen E
          Henry, Deborah A
          Milner, Ruth
          Taha, Fatma
          Gravelle, Anna
          Davidson, A George F
          Wong, Lawrence T K
          Mahenthiralingam, Eshwar
        affil: Division of Infectious and Immunological Diseases, Department of Pediatrics, University of British Columbia, Vancouver, British Columbia, Canada
      sug:
        subj:
          Cystic Fibrosis Epidemiology
          Cystic Fibrosis Microbiology
          Pseudomonas
          Infant
          Cross Infection Microbiology
          Pseudomonas Infections Epidemiology
          Pseudomonas Infections Microbiology
          Electrophoresis, Gel, Pulsed-Field
          Human
          Child Welfare
          Pseudomonas Infections Transmission
          Disease Outbreaks
          Child
          British Columbia
          Cross Infection Epidemiology
          Child, Preschool
          Adult
          Adolescence
          Cross Infection Transmission
          Family Health
          Validation Studies
          Comparative Studies
          Evaluation Research
          Multicenter Studies
          Center for Epidemiological Studies Depression Scale
          Scales
          Infant: 1-23 months
          Child: 6-12 years
          Child, Preschool: 2-5 years
          Adult: 19-44 years
          Adolescent: 13-18 years
      ab: Pseudomonas aeruginosa is the most common respiratory pathogen in patients with cystic fibrosis (CF), but the predominant mechanism by which it is acquired is controversial. To determine the frequency of patient-to-patient spread, we evaluated P. aeruginosa isolates from 174 patients treated at the CF clinics in Vancouver, BC, Canada, since 1981. Multiple isolates were obtained from each patient and genetically typed by random amplified polymorphic DNA and pulsed field gel electrophoresis analyses. A total of 157 genetic types of P. aeruginosa was identified, 123 of which were unique to individual patients. A total of 34 types was shared by more than one patient; epidemiologic evidence linked these individuals only in the cases of 10 sibships and 1 pair of unrelated patients. We conclude that there is an extremely low risk in Vancouver for patients with CF to acquire P. aeruginosa from other patients. It appears that prolonged close contact, such as occurs between siblings, is necessary for patient-to-patient spread. The major source of acquisition of P. aeruginosa in CF appears to be from the environment. Considering these observations, we do not recommend segregation of patients with CF on the basis of their colonization status with P. aeruginosa.
      pubtype: Academic Journal
      doctype:
        research
        Journal Article
      ougenre: Article
    language: English
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