Da. Pegues et al., ACQUISITION OF PSEUDOMONAS-CEPACIA AT SUMMER CAMPS FOR PATIENTS WITH CYSTIC-FIBROSIS, The Journal of pediatrics, 124(5), 1994, pp. 694-702
To assess the risk of acquisition of Pseudomonas cepacia by person-to-
person transmission at cystic fibrosis summer camps, we conducted in 1
990 a study at three camps attended by patients with cystic fibrosis w
ho had P. cepacia infection and patients without P. cepacia infection
but who were considered susceptible to infection. We obtained sputum o
r throat cultures from campers on their arrival at, weekly during, at
the end of, and 14 to 30 days after camp. We compared the incidence of
sputum conversion of patients at camp with that of patients outside c
amp by culturing specimens from noncamper control subjects with cystic
fibrosis who were known not to be infected less than or equal to 2 we
eks before and 4 to 6 weeks after camp. We also determined the risk fa
ctors for P. cepacia acquisition by determining the relative risk of a
cquisition between campers who were exposed versus campers who were no
t exposed to campers known to be infected or to potential environmenta
l sources of P. cepacia at camp. The ribotype of P. cepacia isolates f
rom campers with sputum conversion was compared with that of isolates
from other campers and from an environmental source. The cumulative in
cidence of sputum conversion during the study period was 6.1% (11/181)
among campers compared with no incidence (0/92) among noncampers (p =
0.02, Fisher Exact Test). The incidence of sputum conversion at camp
varied according to the prevalence of campers with known infection (p
<0.001, chi-square test for trend). The rate of sputum conversion was
higher in the camp with longer duration (relative risk = 12.0; 95% con
fidence interval = 2.7 to 53.5). Ribotyping showed that P. cepacia iso
lates from all 11 campers with sputum conversion were identical or sim
ilar (1 to 2 band difference) to isolates of other P. cepacia-infected
campers including co-converters. These results suggest that P. cepaci
a can be acquired by patients with cystic fibrosis who are attending s
ummer camp for such patients, possibly through person-to-person transm
ission, and that the risk increases with the prevalence of P. cepacia-
infected campers and the duration of camp.