Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/35538
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dc.contributor.authorSharifi, Vahid-
dc.contributor.authorBrazzale, Danny J-
dc.contributor.authorMcDonald, Christine F-
dc.contributor.authorHill, Catherine J-
dc.contributor.authorMichael, Chris-
dc.contributor.authorRuehland, Warren R-
dc.contributor.authorBerlowitz, David J-
dc.date2024-
dc.date.accessioned2024-10-21T03:53:53Z-
dc.date.available2024-10-21T03:53:53Z-
dc.date.issued2024-10-10-
dc.identifier.citationBMC Pulmonary Medicine 2024-10-10; 24(1)en_US
dc.identifier.issn1471-2466-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/35538-
dc.description.abstractPulmonary rehabilitation (PR) is widely recommended for short-term benefits in chronic respiratory diseases, yet long-term outcomes remain uncertain. This retrospective cohort study addresses this gap, comparing 20-year mortality rates between PR participants and matched controls, and hypothesizing that the short-term benefits of PR contribute to improved long-term survival. The 20-year mortality of stable chronic respiratory patients who participated in an outpatient PR program was compared with a matched control group based on the type of lung disease. Demographic and clinical variables, and the dates of deaths, were extracted and compared between two groups with two sample t-test and chi-square tests. Kaplan-Meier plots and Cox regression analyses were employed to evaluate survival differences. Between 2000 and 2002, 238 individuals enrolled in a pulmonary rehabilitation (PR) program (58% male, mean age ± SD: 69 ± 8 years, mean FEV1% predicted ± SD: 46 ± 21%). An equal number of people with comparable lung disease were selected as controls (88% COPD, 5% ILD). Controls had lower FEV1% predicted values (mean ± SD: 39 ± 17%, P < 0.001), smoked more (mean ± SD: 48 ± 35 pack-years, P = 0.032), and no differences in age, BMI, sex, and Index of Relative Socio-economic Advantage and Disadvantage (IRSAD). Median (IQR) follow-up time was 68 months (34-123), with 371 (78%) deaths. Univariable (HR = 1.71, p < 0.001) and multivariable (HR = 1.64, p < 0.001) Cox regression found higher mortality risk in controls. Subgroup analysis for COPD replicated these findings (HR = 1.70, P < 0.001). Despite some methodological limitations, our study suggests that clinically stable patients with chronic respiratory disease who undertake PR may have lower mortality than matched controls. Retrospectively registered.en_US
dc.language.isoeng-
dc.subjectAsthmaen_US
dc.subjectCOPDen_US
dc.subjectChronic respiratory diseaseen_US
dc.subjectILDen_US
dc.subjectMortalityen_US
dc.subjectPulmonary rehabilitationen_US
dc.subjectSpirometryen_US
dc.subjectSurvival analysisen_US
dc.titleEffect of pulmonary rehabilitation on all-cause mortality in patients with chronic respiratory disease: a retrospective cohort study in an Australian teaching hospital.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleBMC Pulmonary Medicineen_US
dc.identifier.affiliationRespiratory and Sleep Medicineen_US
dc.identifier.affiliationInstitute for Breathing and Sleepen_US
dc.identifier.affiliationFaculty of Medicine, Dentistry and Health Sciences, The University of Melbourne, Melbourne, VIC, Australia.en_US
dc.identifier.doi10.1186/s12890-024-03319-9en_US
dc.type.contentTexten_US
dc.identifier.pubmedid39390462-
dc.description.volume24-
dc.description.issue1-
dc.description.startpage501-
dc.subject.meshtermssecondaryPulmonary Disease, Chronic Obstructive/rehabilitation-
dc.subject.meshtermssecondaryPulmonary Disease, Chronic Obstructive/mortality-
dc.subject.meshtermssecondaryAustralia/epidemiology-
dc.subject.meshtermssecondaryLung Diseases, Interstitial/rehabilitation-
dc.subject.meshtermssecondaryLung Diseases, Interstitial/mortality-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
crisitem.author.deptRespiratory and Sleep Medicine-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptRespiratory and Sleep Medicine-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptPhysiotherapy-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptRespiratory and Sleep Medicine-
crisitem.author.deptPhysiotherapy-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
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