Year in review 2015: Interstitial lung disease, pulmonary vascular disease, pulmonary function, sleep and ventilation, cystic fibrosis and paediatric lung disease

Jo, Helen; Corte, Tamera J.; Wort, Stephen J.; Eves, Neil D.; Piper, Amanda J.; Wainwright, Claire

doi:10.1111/resp.12749

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Neil D Eves1

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Cited by 4 publications

(2 citation statements)

References 107 publications

(126 reference statements)

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“…As highlighted in last year's review, 57 the forced oscillation technique (FOT) for the assessment of pulmonary function has grown in popularity especially in paediatric populations who have difficulty performing pulmonary function manoeuvres. 58 Ioan et al 59 investigated the utility of FOT for the diagnosis of vocal cord dysfunction (VCD) in children.…”

Section: Neil D Evesmentioning

confidence: 99%

Year in review 2016: Interstitial lung disease, pulmonary vascular disease, pulmonary function, paediatric lung disease, cystic fibrosis and sleep

et al. 2017

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Section: Neil D Evesmentioning

confidence: 99%

Year in review 2016: Interstitial lung disease, pulmonary vascular disease, pulmonary function, paediatric lung disease, cystic fibrosis and sleep

et al. 2017

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“…The prevalence in Europe is 0.737 per 10,000 and the incidence rate in Italy is estimated at 1/3,000 live births1 ) . It is associated with early airway inflammation with both functional and structural consequences2, 3 ) . Over the last 2–3 decades, the CF has evolved from an acute disease of childhood into a chronic disease of adulthood4 ) .…”

Section: Introductionmentioning

confidence: 99%

Functional evaluation of breath: spirometry and body plethysmography comparison in people with cystic fibrosis

Villafañe

Corbellini²,

Balestri

et al. 2017

J Phys Ther Sci

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[Purpose] The aim of the present study was to establish up-to-date data regarding the lung function of cystic fibrosis (CF) patients. [Subjects and Methods] Forty-eight patients of both genders, with a diagnosis of CF, were recruited. As a result our sample presented, according to the GOLD criteria, 23 patients with mild lung obstruction (FEV1%pred: 89.86), 16 patients with moderate lung obstruction (FEV1%pred: 56.1) and 9 patients with severe obstruction (FEV1%pred: 32.1). [Results] All patients presented normal total lung capacity followed by an important residual volume increase. [Conclusion] Our results were important to illustrate the CF patient’s lung functional status and to improve the health system strategy in treating such individuals.

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Idiopathic pulmonary fibrosis: current and future directions

2017

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Year in review 2015: Interstitial lung disease, pulmonary vascular disease, pulmonary function, sleep and ventilation, cystic fibrosis and paediatric lung disease

Cited by 4 publications

References 107 publications

Year in review 2016: Interstitial lung disease, pulmonary vascular disease, pulmonary function, paediatric lung disease, cystic fibrosis and sleep

Year in review 2016: Interstitial lung disease, pulmonary vascular disease, pulmonary function, paediatric lung disease, cystic fibrosis and sleep

Functional evaluation of breath: spirometry and body plethysmography comparison in people with cystic fibrosis

Idiopathic pulmonary fibrosis: current and future directions

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