Literature DB >> 24996790

Recent advances in the management of cystic fibrosis.

Jane C Davies1, Anne-Marie Ebdon2, Christopher Orchard3.   

Abstract

Cystic fibrosis is a disease that still causes a reduced life expectancy. The treatment burden remains high for affected individuals with often a combination of multiple oral and inhaled medications, as well as physiotherapy, required on a daily basis. In this article, we look at an overview of the pathogenesis, how this might lead to treatment options and look at some of the available new therapies, all in the aim of increasing life expectancy and reducing treatment burden. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.

Entities:  

Keywords:  Cystic Fibrosis; Therapeutics

Mesh:

Substances:

Year:  2014        PMID: 24996790     DOI: 10.1136/archdischild-2013-304400

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  9 in total

Review 1.  CFTR and lung homeostasis.

Authors:  James F Collawn; Sadis Matalon
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2014-11-07       Impact factor: 5.464

Review 2.  Standard (head-down tilt) versus modified (without head-down tilt) postural drainage in infants and young children with cystic fibrosis.

Authors:  Diana A Freitas; Gabriela Ss Chaves; Thayla A Santino; Cibele Td Ribeiro; Fernando Al Dias; Ricardo O Guerra; Karla Mpp Mendonça
Journal:  Cochrane Database Syst Rev       Date:  2018-03-09

3.  Nodular glomerulosclerosis in a patient with cystic fibrosis, but not diabetes mellitus: A paediatric case.

Authors:  A D Lalayiannis; C Thompson; R Malcomson; D V Milford
Journal:  Respir Med Case Rep       Date:  2016-07-14

Review 4.  Cystic fibrosis lung environment and Pseudomonas aeruginosa infection.

Authors:  Anjali Y Bhagirath; Yanqi Li; Deepti Somayajula; Maryam Dadashi; Sara Badr; Kangmin Duan
Journal:  BMC Pulm Med       Date:  2016-12-05       Impact factor: 3.317

5.  The metabolic footprint of the airway bacterial community in cystic fibrosis.

Authors:  Vaishnavi Narayanamurthy; John M Sweetnam; Darcy R Denner; Lena W Chen; Edward T Naureckas; Bharathi Laxman; Steven R White
Journal:  Microbiome       Date:  2017-06-30       Impact factor: 14.650

Review 6.  Factoring in the Complexity of the Cystic Fibrosis Lung to Understand Aspergillus fumigatus and Pseudomonas aeruginosa Interactions.

Authors:  Emily Beswick; Jorge Amich; Sara Gago
Journal:  Pathogens       Date:  2020-08-06

7.  Comparison of Vancomycin Pharmacokinetics in Cystic Fibrosis Patients Pre and Post-lung Transplant.

Authors:  Shannon White; Colleen Sakon; Linda Fitzgerald; Charissa Kam; Erin McDade; Alanna Wong
Journal:  Clin Med Insights Circ Respir Pulm Med       Date:  2020-06-15

8.  Host cystathionine-γ lyase derived hydrogen sulfide protects against Pseudomonas aeruginosa sepsis.

Authors:  Georgios Renieris; Dionysia-Eirini Droggiti; Konstantina Katrini; Panagiotis Koufargyris; Theologia Gkavogianni; Eleni Karakike; Nikolaos Antonakos; Georgia Damoraki; Athanasios Karageorgos; Labros Sabracos; Antonia Katsouda; Elisa Jentho; Sebastian Weis; Rui Wang; Michael Bauer; Csaba Szabo; Kalliopi Platoni; Vasilios Kouloulias; Andreas Papapetropoulos; Evangelos J Giamarellos-Bourboulis
Journal:  PLoS Pathog       Date:  2021-03-26       Impact factor: 6.823

9.  Respiratory microbiota resistance and resilience to pulmonary exacerbation and subsequent antimicrobial intervention.

Authors:  Leah Cuthbertson; Geraint B Rogers; Alan W Walker; Anna Oliver; Laura E Green; Thomas W V Daniels; Mary P Carroll; Julian Parkhill; Kenneth D Bruce; Christopher J van der Gast
Journal:  ISME J       Date:  2015-11-10       Impact factor: 10.302

  9 in total

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