Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/34329
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dc.contributor.authorMunsif, Maitri-
dc.contributor.authorSweeney, Duncan J-
dc.contributor.authorLeong, Tracy L-
dc.contributor.authorStirling, Rob G-
dc.date2023-
dc.date.accessioned2023-12-01T02:13:38Z-
dc.date.available2023-12-01T02:13:38Z-
dc.date.issued2023-12-31-
dc.identifier.citationEuropean Respiratory Review : an Official Journal of the European Respiratory Society 2023-12-31; 32(170)en_US
dc.identifier.issn1600-0617-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/34329-
dc.description.abstractAutoimmune pulmonary alveolar proteinosis (aPAP) results from impaired macrophage-mediated clearance of alveolar surfactant lipoproteins. Whole lung lavage has been the first-line treatment but recent reports suggest the efficacy of granulocyte-macrophage colony-stimulating factor (GM-CSF). We aimed to review the efficacy and safety of nebulised GM-CSF in aPAP. We conducted a systematic review and meta-analysis searching Embase, CINAHL, MEDLINE and Cochrane Collaborative databases (1946-1 April 2022). Studies included patients aged >18 years with aPAP receiving nebulised GM-CSF treatment and a comparator cohort. Exclusion criteria included secondary or congenital pulmonary alveolar proteinosis, GM-CSF allergy, active infection or other serious medical conditions. The protocol was prospectively registered with PROSPERO (CRD42021231328). Outcomes assessed were St George's Respiratory Questionnaire (SGRQ), 6-min walk test (6MWT), gas exchange (diffusing capacity of the lung for carbon monoxide (D LCO) % predicted) and arterial-alveolar oxygen gradient. Six studies were identified for review and three for meta-analysis, revealing that SGRQ score (mean difference -8.09, 95% CI -11.88- -4.3, p<0.0001), functional capacity (6MWT) (mean difference 21.72 m, 95% CI -2.76-46.19 m, p=0.08), gas diffusion (D LCO % predicted) (mean difference 5.09%, 95% CI 2.05-8.13%, p=0.001) and arterial-alveolar oxygen gradient (mean difference -4.36 mmHg, 95% CI -7.19- -1.52 mmHg, p=0.003) all significantly improved in GM-CSF-treated patients with minor statistical heterogeneity (I2=0%). No serious trial-related adverse events were reported. Patients with aPAP treated with inhaled GM-CSF demonstrated significant improvements in symptoms, dyspnoea scores, lung function, gas exchange and radiology indices after treatment with nebulised GM-CSF of varying duration. There is an important need to review comparative effectiveness and patient choice in key clinical outcomes between the current standard of care, whole lung lavage, with the noninvasive treatment of nebulised GM-CSF in aPAP.en_US
dc.language.isoeng-
dc.titleNebulised granulocyte-macrophage colony-stimulating factor (GM-CSF) in autoimmune pulmonary alveolar proteinosis: a systematic review and meta-analysis.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleEuropean Respiratory Review : an Official Journal of the European Respiratory Societyen_US
dc.identifier.affiliationDepartment of Respiratory Medicine, Alfred Health, Melbourne, Australia.en_US
dc.identifier.affiliationRespiratory and Sleep Medicineen_US
dc.identifier.affiliationInstitute for Breathing and Sleepen_US
dc.identifier.affiliationCentral Clinical School, Faculty of Medicine, Nursing and Health Sciences, Monash University, Melbourne, Australia.en_US
dc.identifier.affiliationDepartment of Medicine, University of Melbourne, Melbourne, Australia.en_US
dc.identifier.doi10.1183/16000617.0080-2023en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0001-9877-5450en_US
dc.identifier.pubmedid37993127-
dc.description.volume32-
dc.description.issue170-
dc.subject.meshtermssecondaryPulmonary Alveolar Proteinosis/diagnosis-
dc.subject.meshtermssecondaryPulmonary Alveolar Proteinosis/drug therapy-
dc.subject.meshtermssecondaryGranulocyte-Macrophage Colony-Stimulating Factor/adverse effects-
dc.subject.meshtermssecondaryOxygen/therapeutic use-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.grantfulltextnone-
crisitem.author.deptRespiratory and Sleep Medicine-
crisitem.author.deptRespiratory and Sleep Medicine-
crisitem.author.deptInstitute for Breathing and Sleep-
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