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Cross infection with Pseudomonas aeruginosa is unusual
| The first 150 words of the full text of this article appear below. |
EDITOR
Mahadeva et al's paper provides valuable evidence of
benefit for paediatric and adult patients attending specialised cystic
fibrosis centres.1 Their conclusion, however, that the mean age at colonisation with Pseudomonas aeruginosa is
lower in patients who received paediatric and adult care in a centre (11.1 years; group A) than in patients who received adult but not
paediatric care in a centre (18.1 years; group B) cannot be accepted on
the basis of the data presented.
Early detection of infection with P aeruginosa is a major preoccupation for staff working in paediatric cystic fibrosis centres. Colonisation is associated with a rapid decline in pulmonary function, but it can often be delayed or prevented,2 and long term use of nebulised antibiotics improves the prognosis if it does occur.3
Mahadeva et al define colonisation using sputum culture. Most young
children with cystic fibrosis are unable to produce sputum so that
paediatricians have had
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