scholarly journals Cystic fibrosis adults' perception and management of the risk of infection withBurkholderia cepaciacomplex

2006 ◽  
Vol 8 (4) ◽  
pp. 395-415 ◽  
Author(s):  
Karen Lowton ◽  
Jonathan Gabe
1981 ◽  
Vol 2 (8) ◽  
pp. 251-251

L. J. Janchar of Marion, Ohio, wrote: "In PEDIATRICS IN REVIEW, July 1980 (p 29), in regard to the article `Mist Tent for Cystic Fibrosis' you state that " mist therapy increases the risk of `water-bug' infection (Pseudomonas, Serratia, etc)..."I have often heard this comment but I have seen no literature in regard to evidence supporting this statement. Could you please furnish me with references in regard to the risk of infection secondary to mist therapy?" Dr Rapkin (author of the abstract) replied: "In July 1967, Dr Hugh Moffet and colleagues in a series of three articles described the association of infection and inhalation therapy. The titles of the articles are revealing: "Bacteria recovered from distilled water and inhalation therapy equipment"; `Survival and dissemination of bacteria in nebulizers and incubators'; `Colonization of infants exposed to bacterially contaminated mists' (Am J Dis Child 114:7, 13, 21, 1967). Previously Hoffman and Finberg (J Pediatr 46:626, 1955) had made the association between water and infection. Much subsequent data have been accumulated and the bibliography is long and detailed. The conclusions have been the same as Moffet's: mist therapy and use of inhalationtherapy apparatus poses an additional risk which must be carefully weighed against the benefit of the therapy to the patient.


2015 ◽  
Vol 14 (6) ◽  
pp. 741-747 ◽  
Author(s):  
Pieter C. Goeminne ◽  
Tim S. Nawrot ◽  
Kris De Boeck ◽  
Ben Nemery ◽  
Lieven J. Dupont

2020 ◽  
Vol 46 (2) ◽  
pp. e20190226-e20190226 ◽  
Author(s):  
Lauren Alexander ◽  
Jane Carson ◽  
John McCaughan ◽  
John Edmund Moore ◽  
Beverley Cherie Millar

2018 ◽  
Vol 22 (4) ◽  
pp. 631-645 ◽  
Author(s):  
Fiona Moola

While cross-respiratory infection guidelines reduce the risk of infection, this may have deleterious impacts on the socialization skills of young people living with cystic fibrosis (CF). The purpose of this study was to explore the experience of social isolation among young Canadians with CF, as well as how they navigate these complex contamination restrictions. The thematic analytic qualitative research tradition was adopted and social theories of risk provided theoretical grounding. The youth described a pressing sense of social isolation in their everyday lives. Although most of the youth ‘obeyed’ the cross-contamination guidelines, some demonstrated a more carefree attitude. Social media was employed across the group as a tool to reduce isolation. In accordance with the sociology of risk, youth with CF demonstrate sophisticated decision-making abilities, navigating exceedingly difficult choices to preserve an always-precarious future. While necessary, cross-contamination guidelines might further marginalize an already isolated group of children and youth.


2011 ◽  
Vol 10 ◽  
pp. S88
Author(s):  
L. Reynolds ◽  
G. Latchford ◽  
A. Duff ◽  
M. Denton ◽  
T. Lee ◽  
...  

JAMA ◽  
1966 ◽  
Vol 195 (12) ◽  
pp. 993-1000 ◽  
Author(s):  
R. J. Grand
Keyword(s):  

Author(s):  
J. V. Briggman ◽  
J. Bigelow ◽  
H. Bank ◽  
S. S. Spicer

The prevalence of strands shown by freeze-fracture in the zonula occludens of junctional complexes is thought to correspond closely with the transepi-thelial electrical resistance and with the tightness of the junction and its obstruction to paracellular flow.1 The complexity of the network of junc¬tional complex strands does not appear invariably related to the degree of tightness of the junction, however, as rabbit ileal junctions have a complex network of strands and are permeable to lanthanum. In human eccrine sweat glands the extent of paracellular relative to transcellular flow remains unknown, both for secretion of the isotonic precursor fluid by the coil and for resorption of a hypertonic solution by the duct. The studies reported here undertook, therefore, to determine with the freeze-fracture technique the complexity of the network of ridges in the junctional complexes between cells in the secretory coil and the sweat ducts. Glands from a patient with cystic fibrosis were also examined because an alteration in junctional strands could underlie the decreased Na+ resorption by sweat ducts in this disease. Freeze-fracture replicas were prepared by standard procedures on isolated coil and duct segments of human sweat glands. Junctional complexes between clear cells, between dark cells and between clear and dark cells on the main lumen, and between clear cells on intercellular canaliculi of the coil con¬tained abundant anastomosing closely spaced strands averaging 6.4 + 0.7 (mean + SE) and 9.0 +0.5 (Fig. 1) per complex, respectively. Thus, the junctions in the intercellular canaliculi of the coil appeared comparable in complexity to those of tight epithlia. Occasional junctions exhibited, in addition, 2 to 5 widely spaced anastomosing strands in a very close network basal to the compact network. The fewer junctional complexes observed thus far between the superficial duct cells consisted on the average of 6 strands arranged in a close network and 1 to 4 underlying strands that lay widely separated from one another (Fig. 2). The duct epitelium would, thus, be judged slightly more "leaky" than the coil. Infrequent junctional complexes observed to date in the secretory coil segment of a cystic fibrosis specimen disclosed rela¬tively few closely crowded strands.


1999 ◽  
Vol 37 (4) ◽  
pp. 291-293 ◽  
Author(s):  
B. Cimon ◽  
J. Carrere ◽  
J. P. Chazalette ◽  
J. F. Vinatier ◽  
D. Chabasse ◽  
...  

2001 ◽  
Vol 120 (5) ◽  
pp. A137-A137
Author(s):  
D CHILDS ◽  
D CROMBIE ◽  
V PRATHA ◽  
Z SELLERS ◽  
D HOGAN ◽  
...  

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