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"Pathogen Eradication" and "Emerging Pathogens": Difficult Definitions in Cystic Fibrosis.
Gilligan, Peter H; Downey, Damian G; Elborn, J Stuart; Flume, Patrick A; Funk, Sebastian; Gilpin, Deirdre; Kidd, Timothy J; McCaughan, John; Millar, B Cherie; Murphy, Philip G; Rendall, Jacqueline C; Tunney, Michael M; Moore, John E.
Afiliação
  • Gilligan PH; Pathology and Laboratory Medicine, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA Peter.Gilligan@unchealth.unc.edu.
  • Downey DG; Clinical Microbiology-Immunology Laboratories, UNC Health Care, Chapel Hill, North Carolina, USA.
  • Elborn JS; Northern Ireland Regional Adult CF Centre, Belfast Health and Social Trust, Belfast, Northern Ireland, United Kingdom.
  • Flume PA; Centre for Experimental Medicine, Queen's University, Belfast, Northern Ireland, United Kingdom.
  • Funk S; Centre for Experimental Medicine, Queen's University, Belfast, Northern Ireland, United Kingdom.
  • Gilpin D; Imperial College, London, United Kingdom.
  • Kidd TJ; Royal Brompton Hospital, London, United Kingdom.
  • McCaughan J; Department of Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.
  • Millar BC; Department of Pediatrics, Medical University of South Carolina, Charleston, South Carolina, USA.
  • Murphy PG; Centre for the Mathematical Modelling of Infectious Diseases, Department of Infectious Disease Epidemiology, The London School of Hygiene & Tropical Medicine, London, United Kingdom.
  • Rendall JC; School of Pharmacy, Queen's University, Belfast, United Kingdom.
  • Tunney MM; Centre for Experimental Medicine, Queen's University, Belfast, Northern Ireland, United Kingdom.
  • Moore JE; School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, Australia.
J Clin Microbiol ; 56(9)2018 09.
Article em En | MEDLINE | ID: mdl-29875191
Infection is a common complication of cystic fibrosis (CF) airway disease. Current treatment approaches include early intervention with the intent to eradicate pathogens in the hope of delaying the development of chronic infection and the chronic use of aerosolized antibiotics to suppress infection. The use of molecules that help restore CFTR (cystic fibrosis transmembrane conductance regulator) function, modulate pulmonary inflammation, or improve pulmonary clearance may also influence the microbial communities in the airways. As the pipeline of these new entities continues to expand, it is important to define when key pathogens are eradicated from the lungs of CF patients and, equally important, when new pathogens might emerge as a result of these novel therapies.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bactérias / Fibrose Cística / Antibacterianos Limite: Humans Idioma: En Revista: J Clin Microbiol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Bactérias / Fibrose Cística / Antibacterianos Limite: Humans Idioma: En Revista: J Clin Microbiol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos