The future of cystic fibrosis care: a global perspective

SC Bell, MA Mall, H Gutierrez, M Macek… - The Lancet …, 2020 - thelancet.com
Executive summary The past six decades have seen remarkable improvements in health
outcomes for people with cystic fibrosis, which was once a fatal disease of infants and young …

A systematic literature review on SME financing: Trends and future directions

P Rao, S Kumar, M Chavan, WM Lim - Journal of Small Business …, 2023 - Taylor & Francis
Small and medium-sized enterprises (SMEs) are a significant source of employment for
many people in developing and developed economies. However, one of the significant …

Efficacy and safety of elexacaftor plus tezacaftor plus ivacaftor versus tezacaftor plus ivacaftor in people with cystic fibrosis homozygous for F508del-CFTR: a 24-week …

S Sutharsan, EF McKone, DG Downey… - The Lancet …, 2022 - thelancet.com
Background Elexacaftor plus tezacaftor plus ivacaftor is a triple-combination cystic fibrosis
transmembrane conductance regulator (CFTR) modulator regimen shown to be generally …

[HTML][HTML] Impact of Pseudomonas aeruginosa Infection on Patients with Chronic Inflammatory Airway Diseases

M Garcia-Clemente, D de la Rosa, L Máiz… - Journal of clinical …, 2020 - mdpi.com
Pseudomonas aeruginosa (P. aeruginosa) is a ubiquitous and opportunistic microorganism
and is considered one of the most significant pathogens that produce chronic colonization …

[HTML][HTML] PROMISE: working with the CF community to understand emerging clinical and research needs for those treated with highly effective CFTR modulator therapy

DP Nichols, SH Donaldson, CA Frederick… - Journal of Cystic …, 2021 - Elsevier
Highly effective CFTR modulator drug therapy is increasingly available to those with cystic
fibrosis. Multiple observational research studies are now being conducted to better …

Long-Term Safety and Efficacy of Elexacaftor/Tezacaftor/Ivacaftor in Children Aged ⩾6 Years with Cystic Fibrosis and at Least One F508del Allele: A Phase 3, Open …

C Wainwright, SA McColley, P McNally… - American journal of …, 2023 - atsjournals.org
Rationale: A 24-week, phase 3, open-label study showed elexacaftor/tezacaftor/ivacaftor
(ELX/TEZ/IVA) was safe and efficacious in children aged 6–11 years with cystic fibrosis (CF) …

[HTML][HTML] Brazilian guidelines for the diagnosis and treatment of cystic fibrosis

RA Athanazio, LVRF Silva, AA Vergara… - Jornal Brasileiro de …, 2017 - SciELO Brasil
Cystic fibrosis (CF) is an autosomal recessive genetic disorder characterized by dysfunction
of the CFTR gene. It is a multisystem disease that most often affects White individuals. In …

[HTML][HTML] Diretrizes brasileiras de diagnóstico e tratamento da fibrose cística

RA Athanazio, LVRF Silva, AA Vergara… - Jornal brasileiro de …, 2017 - SciELO Brasil
RESUMO A fibrose cística (FC) é uma doença genética autossômica recessiva
caracterizada pela disfunção do gene CFTR. Trata-se de uma doença multissistêmica que …

Health-related quality of life in adolescents and adults with cystic fibrosis: physical and mental health predictors

JA Cronly, AJ Duff, KA Riekert, AP Fitzgerald… - Respiratory …, 2019 - rc.rcjournal.com
BACKGROUND: People with cystic fibrosis face substantial physical, psychological, and
social challenges as they move into adolescence and adulthood, which are likely to impact …

[HTML][HTML] Standards for the care of people with cystic fibrosis (CF); recognising and addressing CF health issues

PR Burgel, KW Southern, C Addy, A Battezzati… - Journal of Cystic …, 2024 - Elsevier
This is the third in a series of four papers updating the European Cystic Fibrosis Society
(ECFS) standards for the care of people with CF. This paper focuses on recognising and …