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Pulmonary Exacerbations in Adults With Cystic Fibrosis
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“As PEx are associated with declining lung function, reduced quality of life, and increased mortality [16]”
From Real-world safety and effectiveness of elexacaftor/tezacaftor/ivacaftor in people with cystic fibrosis: Interim results of a long-term registry-based study (2023) · cites this paper as [16]
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Elexacaftor–Tezacaftor–Ivacaftor for Cystic Fibrosis with a Single Phe508del Allele
Middleton, P. G., Mall, M. A., Dřevínek, P., Lands, L. C., McKone, E. F., Polineni, D., Ramsey, B. W., Taylor-Cousar, J. L., Tullis, E., Vermeulen, F., et al. (2019) · New England Journal of Medicine · doi:10.1056/nejmoa1908639 · Cited by 2,198
A CFTR Potentiator in Patients with Cystic Fibrosis and the G551D Mutation
Ramsey, B. W., Davies, J., McElvaney, N. G., Tullis, E., Bell, S. C., Dřevínek, P., Griese, M., McKone, E. F., Wainwright, C. E., Konstan, M. W., et al. (2011) · New England Journal of Medicine · doi:10.1056/nejmoa1105185 · Cited by 2,195
Rowbotham, N. J., Smith, S., Leighton, P. A., Rayner, O. C., Gathercole, K., Elliott, Z. C., Nash, E. F., Daniels, T., Duff, A. J. A., Collins, S., et al. (2018) · Thorax · doi:10.1136/thoraxjnl-2017-210473 · Cited by 252
Lechtzin, N., Mayer-Hamblett, N., West, N. E., Allgood, S., Wilhelm, E., Khan, U., Aitken, M. L., Ramsey, B. W., Boyle, M. P., Mogayzel, P. J., et al. (2017) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201610-2172oc · Cited by 127
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Research works printed but not linked: 62
- Bell, 2020, The future of cystic fibrosis care: a global perspective, Lancet Respir Med, 8, 65, 10.1016/S2213-2600(19)30337-6 · DOI
- Burgel, 2015, Future trends in cystic fibrosis demography in 34 European countries, Eur Respir J, 46, 133, 10.1183/09031936.00196314 · DOI
- Fuchs, 1994, Effect of aerosolized recombinant human DNase on exacerbations of respiratory symptoms and on pulmonary function in patients with cystic fibrosis. The Pulmozyme Study Group, N Engl J Med, 331, 637, 10.1056/NEJM199409083311003 · DOI
- Bilton D, Canny G, Conway S, et al. Pulmonary exacerbation: towards a definition for use in clinical trials. Report from the EuroCareCF Working Group on outcome parameters in clinical trials. J Cyst Fibros. 2011;10(suppl 2):S79-S81. · DOI
- Rabin, 2004, Pulmonary exacerbations in cystic fibrosis, Pediatr Pulmonol, 37, 400, 10.1002/ppul.20023 · DOI
- Rosenfeld, 2001, Defining a pulmonary exacerbation in cystic fibrosis, J Pediatr, 139, 359, 10.1067/mpd.2001.117288 · DOI
- Ramsey, 1999, Intermittent administration of inhaled tobramycin in patients with cystic fibrosis, N Engl J Med, 340, 23, 10.1056/NEJM199901073400104 · DOI
- West, 2017, Standardized Treatment of Pulmonary Exacerbations (STOP) study: physician treatment practices and outcomes for individuals with cystic fibrosis with pulmonary exacerbations, J Cyst Fibros, 16, 600, 10.1016/j.jcf.2017.04.003 · DOI
- Wielpütz MO, Mall MA. Imaging modalities in cystic fibrosis: emerging role of MRI. Curr Opin Pulm Med. 2015;21(6):609-616. · DOI
- Sonneveld, 2015, Lung clearance index in cystic fibrosis subjects treated for pulmonary exacerbations, Eur Respir J, 46, 1055, 10.1183/09031936.00211914 · DOI
- Goss, 2007, Patient-reported outcomes in cystic fibrosis, Proc Am Thorac Soc, 4, 378, 10.1513/pats.200703-039BR · DOI
- Goss, 2009, Patient-reported respiratory symptoms in cystic fibrosis, J Cyst Fibros, 8, 245, 10.1016/j.jcf.2009.04.003 · DOI
- Ferkol, 2006, Cystic fibrosis pulmonary exacerbations, J Pediatr, 148, 259, 10.1016/j.jpeds.2005.10.019 · DOI
- Chmiel, 2014, Antibiotic management of lung infections in cystic fibrosis. II. Nontuberculous mycobacteria, anaerobic bacteria, and fungi, Ann Am Thorac Soc, 11, 1298, 10.1513/AnnalsATS.201405-203AS · DOI
- Ong, 1989, Infective respiratory exacerbations in young adults with cystic fibrosis: role of viruses and atypical microorganisms, Thorax, 44, 739, 10.1136/thx.44.9.739 · DOI
- van Ewijk, 2005, Viral respiratory infections in cystic fibrosis, J Cyst Fibros, 4, 31, 10.1016/j.jcf.2005.05.011 · DOI
- Aaron, 2004, Adult cystic fibrosis exacerbations and new strains of Pseudomonas aeruginosa, Am J Respir Crit Care Med, 169, 811, 10.1164/rccm.200309-1306OC · DOI
- Flight, 2014, Incidence and clinical impact of respiratory viruses in adults with cystic fibrosis, Thorax, 69, 247, 10.1136/thoraxjnl-2013-204000 · DOI
- Cosgriff, 2020, A multinational report to characterise SARS-CoV-2 infection in people with cystic fibrosis, J Cyst Fibros, 19, 355, 10.1016/j.jcf.2020.04.012 · DOI
- Smyth, 2014, European Cystic Fibrosis Society Standards of Care: best practice guidelines, J Cyst Fibros, 13, S23, 10.1016/j.jcf.2014.03.010 · DOI · Paper page
- Flume, 2009, Cystic fibrosis pulmonary guidelines, Am J Respir Crit Care Med, 180, 802, 10.1164/rccm.200812-1845PP · DOI
- Elphick, 2016, Single versus combination intravenous anti-pseudomonal antibiotic therapy for people with cystic fibrosis, Cochrane Database Syst Rev, 12, CD002007
- UK Cystic Fibrosis Trust Antibiotic Working Group. Antibiotic treatment for cystic fibrosis - 3rd edition. https://www.cysticfibrosis.org.uk/∼/media/documents/the-work-we-do/care/consensus-docs-with-new-address/anitbiotic-treatment.ashx?la=en. Accessed November 11, 2020.
- Hurley, 2015, Intravenous antibiotics for pulmonary exacerbations in people with cystic fibrosis, Cochrane Database Syst Rev, 7, CD009730
- Bullington, 2019, 1078. Expectations and attitudes toward antimicrobial stewardship among cystic fibrosis care providers, Open Forum Infect Dis, 6, S382, 10.1093/ofid/ofz360.942 · DOI
- Lechtzin, 2006, Outcomes of adults with cystic fibrosis infected with antibiotic-resistant Pseudomonas aeruginosa, Respiration, 73, 27, 10.1159/000087686 · DOI
- Waters, 2019, Reconciling antimicrobial susceptibility testing and clinical response in antimicrobial treatment of chronic cystic fibrosis lung infections, Clin Infect Dis, 69, 1812, 10.1093/cid/ciz364 · DOI
- Zemanick, 2020, Antimicrobial Resistance International Working Group in Cystic Fibrosis. Antimicrobial resistance in cystic fibrosis: a Delphi approach to defining best practices, J Cyst Fibros, 19, 370, 10.1016/j.jcf.2019.10.006 · DOI
- Einarsson, 2017, WS03.1 Longitudinal airway microbiota profiling in cystic fibrosis patients enrolled in the CFMATTERS clinical trial, J Cyst Fibros, 16, S4, 10.1016/S1569-1993(17)30168-6 · DOI
- Aaron, 2005, Combination antibiotic susceptibility testing to treat exacerbations of cystic fibrosis associated with multiresistant bacteria: a randomised, double-blind, controlled clinical trial, Lancet, 366, 463, 10.1016/S0140-6736(05)67060-2 · DOI
- Tümmler, 2019, Emerging therapies against infections with Pseudomonas aeruginosa, F1000 Research, 8, F1000, 10.12688/f1000research.19509.1 · DOI
- Wagener, 2013, Oral, inhaled, and intravenous antibiotic choice for treating pulmonary exacerbations in cystic fibrosis, Pediatr Pulmonol, 48, 666, 10.1002/ppul.22652 · DOI
- Sanders, 2017, Standardized Treatment of Pulmonary Exacerbations (STOP) study: observations at the initiation of intravenous antibiotics for cystic fibrosis pulmonary exacerbations, J Cyst Fibros, 16, 592, 10.1016/j.jcf.2017.04.005 · DOI
- Briggs, 2012, Oral antimicrobial use in outpatient cystic fibrosis pulmonary exacerbation management: a single-center experience, Clin Respir J, 6, 56, 10.1111/j.1752-699X.2011.00246.x · DOI
- Stanojevic, 2017, Effect of pulmonary exacerbations treated with oral antibiotics on clinical outcomes in cystic fibrosis, Thorax, 72, 327, 10.1136/thoraxjnl-2016-208450 · DOI
- Smith, 2018, Inhaled antibiotics for pulmonary exacerbations in cystic fibrosis, Cochrane Database Syst Rev, 10, CD008319
- Abbott, 2019, Duration of intravenous antibiotic therapy in people with cystic fibrosis, Cochrane Database Syst Rev, 9, CD006682
- Schechter, 2017, Treatment setting and outcomes of cystic fibrosis pulmonary exacerbations, Ann Am Thorac Soc, 15, 225, 10.1513/AnnalsATS.201702-111OC · DOI
- Vandevanter, 2016, Probability of IV antibiotic retreatment within thirty days is associated with duration and location of IV antibiotic treatment for pulmonary exacerbation in cystic fibrosis, J Cyst Fibro, 15, 783, 10.1016/j.jcf.2016.04.005 · DOI
- Sanders, 2017, Poor recovery from cystic fibrosis pulmonary exacerbations is associated with poor long-term outcomes, Pediatric Pulmonol, 52, 1268, 10.1002/ppul.23765 · DOI · Paper page
- Parkins, 2012, Incidence and risk factors for pulmonary exacerbation treatment failures in patients with cystic fibrosis chronically infected with Pseudomonas aeruginosa, Chest, 141, 485, 10.1378/chest.11-0917 · DOI
- Burgel, 2017, A first step to STOP cystic fibrosis exacerbations, J Cyst Fibro, 16, 529, 10.1016/j.jcf.2017.08.006 · DOI
- Gold, 2019, Correspondence between lung function and symptom measures from the Cystic Fibrosis Respiratory Symptom Diary–Chronic Respiratory Infection Symptom Score (CFRSD-CRISS), J Cyst Fibro, 18, 886, 10.1016/j.jcf.2019.05.009 · DOI
- Sequeiros, 2009, Home intravenous antibiotic treatment for acute pulmonary exacerbations in cystic fibrosis—is it good for the patient?, Ann Thorac Med, 4, 111, 10.4103/1817-1737.53346 · DOI
- Heltshe, 2018, Study design considerations for the Standardized Treatment of Pulmonary Exacerbations 2 (STOP2): a trial to compare intravenous antibiotic treatment durations in CF, Contemporary Clinical Trials, 64, 35, 10.1016/j.cct.2017.11.012 · DOI
- West, 2018, Unmet needs in cystic fibrosis: the next steps in improving outcomes, Expert Rev Respir Med, 12, 585, 10.1080/17476348.2018.1483723 · DOI
- Skolnik, 2018, Recent advances in the understanding and management of cystic fibrosis pulmonary exacerbations, F1000Research, 7, F1000, 10.12688/f1000research.13926.1 · DOI
- Hurt, 2014, Inhaled interventions in cystic fibrosis: mucoactive and antibiotic therapies, Respiration, 88, 441, 10.1159/000369533 · DOI
- Nevitt, 2018, Inhaled mannitol for cystic fibrosis, Cochrane Database Syst Rev, 2, CD008649
- Wark, 2018, Nebulised hypertonic saline for cystic fibrosis, Cochrane Database Syst Rev, 9, CD001506
- Yang, 2018, Dornase alfa for cystic fibrosis, Cochrane Database Syst Rev, 9, CD001127
- Nevitt, 2018, Inhaled mannitol for cystic fibrosis, Cochrane Database Syst Rev, 2, CD008649
- Dentice, 2016, A randomised trial of hypertonic saline during hospitalisation for exacerbation of cystic fibrosis, Thorax, 71, 141, 10.1136/thoraxjnl-2014-206716 · DOI
- Ward, 2019, Exercise is commonly used as a substitute for traditional airway clearance techniques by adults with cystic fibrosis in Australia: a survey, J Physiother, 65, 43
- Holland, 2003, Non-invasive ventilation assists chest physiotherapy in adults with acute exacerbations of cystic fibrosis, Thorax, 58, 880, 10.1136/thorax.58.10.880 · DOI
- Dwyer, 2015, Non-invasive ventilation used as an adjunct to airway clearance treatments improves lung function during an acute exacerbation of cystic fibrosis: a randomised trial, J Physiother, 61, 142
- Dovey, 2007, Oral corticosteroid therapy in cystic fibrosis patients hospitalized for pulmonary exacerbation: a pilot study, Chest, 132, 1212, 10.1378/chest.07-0843 · DOI
- Heltshe, 2016, Short-term and long-term response to pulmonary exacerbation treatment in cystic fibrosis, Thorax, 71, 223, 10.1136/thoraxjnl-2014-206750 · DOI
- Archangelidi, 2019, Non-invasive ventilation and clinical outcomes in cystic fibrosis: findings from the UK CF registry, J Cyst Fibro, 18, 665, 10.1016/j.jcf.2018.11.006 · DOI
- O’driscoll, 2008, BTS guideline for emergency oxygen use in adult patients, Thorax, 63, vi1
- Milross, 2019, Non-invasive ventilation versus oxygen therapy in cystic fibrosis: a 12-month randomized trial, Respirology, 24, 1191, 10.1111/resp.13604 · DOI
- van Gool, 2013, Understanding the costs of care for cystic fibrosis: an analysis by age and health state, Value Health, 16, 345, 10.1016/j.jval.2012.12.003 · DOI
Cited by
Sorted by citations
Bower, J. K., Volkova, N., Ahluwalia, N., Sahota, G., Xuan, F., Chin, A., Weinstock, T. G., Ostrenga, J., & Elbert, A. (2023) · Journal of Cystic Fibrosis · doi:10.1016/j.jcf.2023.03.002 · Cited by 140
Metadata
- Authors
- Stanford, G. E., Dave, K., & Simmonds, N. J.
- Venue
- Chest
- Publisher
- Elsevier BV
- Published
- 2021-01
- Volume
- 159
- Issue
- 1
- Pages
- 93-102
- ISSN
- 0012-3692
- PMC
- PMC7502225
- Cited by
- 70
- References
- 4
- Language
- en
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