WSLHD
Skip navigation
Please use this identifier to cite or link to this item: https://wslhd.intersearch.com.au/wslhdjspui/handle/1/9636
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSouthern, K. W.-
dc.contributor.authorAddy, C.-
dc.contributor.authorBell, S. C.-
dc.contributor.authorBevan, A.-
dc.contributor.authorBorawska, U.-
dc.contributor.authorBrown, C.-
dc.contributor.authorBurgel, P. R.-
dc.contributor.authorButton, B.-
dc.contributor.authorCastellani, C.-
dc.contributor.authorChansard, A.-
dc.contributor.authorChilvers, M. A.-
dc.contributor.authorDavies, G.-
dc.contributor.authorDavies, J. C.-
dc.contributor.authorDe Boeck, K.-
dc.contributor.authorDeclercq, D.-
dc.contributor.authorDoumit, M.-
dc.contributor.authorDrevinek, P.-
dc.contributor.authorFajac, I.-
dc.contributor.authorGartner, S.-
dc.contributor.authorGeorgiopoulos, A. M.-
dc.contributor.authorGursli, S.-
dc.contributor.authorGramegna, A.-
dc.contributor.authorHansen, C. M.-
dc.contributor.authorHug, M. J.-
dc.contributor.authorLammertyn, E.-
dc.contributor.authorLandau, E. E. C.-
dc.contributor.authorLangley, R.-
dc.contributor.authorMayer-Hamblett, N.-
dc.contributor.authorMiddleton, A.-
dc.contributor.authorMiddleton, Peter G.-
dc.contributor.authorMielus, M.-
dc.contributor.authorMorrison, L.-
dc.contributor.authorMunck, A.-
dc.contributor.authorPlant, B.-
dc.contributor.authorPloeger, M.-
dc.contributor.authorBertrand, D. P.-
dc.contributor.authorPressler, T.-
dc.contributor.authorQuon, B. S.-
dc.contributor.authorRadtke, T.-
dc.contributor.authorSaynor, Z. L.-
dc.contributor.authorShufer, I.-
dc.contributor.authorSmyth, A. R.-
dc.contributor.authorSmith, C.-
dc.contributor.authorvan Koningsbruggen-Rietschel, S.-
dc.date.accessioned2024-05-16T03:11:27Z-
dc.date.available2024-05-16T03:11:27Z-
dc.date.issued2024-
dc.identifier.urihttps://wslhd.intersearch.com.au/wslhdjspui/handle/1/9636-
dc.description.abstractThis is the second 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 establishing and maintaining health. The guidance is produced using an evidence-based framework and with wide stakeholder engagement, including people from the CF community. Authors provided a narrative description of their topic and statements, which were more directive. These statements were reviewed by a Delphi exercise, achieving good levels of agreement from a wide group for all statements. This guidance reinforces the importance of a multi-disciplinary CF team, but also describes developing models of care including virtual consultations. The framework for health is reinforced, including the need for a physically active lifestyle and the strict avoidance of all recreational inhalations, including e-cigarettes. Progress with cystic fibrosis transmembrane conductance regulator (CFTR) modulator therapy is reviewed, including emerging adverse events and advice for dose reduction and interruption. This paper contains guidance that is pertinent to all people with CF regardless of age and eligibility for and access to modulator therapy.-
dc.subjectCystic Fibrosis-
dc.subjectElectronic Nicotine Delivery Systems-
dc.subjectMutation-
dc.subjectCystic Fibrosis Transmembrane Conductance Regulator-
dc.subjectRespiratory System Agents-
dc.titleStandards for the care of people with cystic fibrosis; establishing and maintaining health-
dc.typeJournal Article-
dc.identifier.doiRespiratory and Sleep Medicine-
dc.identifier.journaltitleJournal of Cystic Fibrosis-
dc.identifier.departmentJournal of Cystic Fibrosis 23(1):12-28, 2024-
dc.contributor.wslhdMiddleton, Peter G.-
dc.type.studyortrialReview-
dc.identifier.pmid38129255-
dc.identifier.facilityWestmead-
Appears in Collections:Westmead Hospital 2019 - 2024

Files in This Item:
There are no files associated with this item.


Items in the repository are protected by copyright, with all rights reserved, unless otherwise indicated.