Results 31 to 40 of about 1,819,303 (176)
The quality of home spirometry in school children with asthma [PDF]
Handheld electronic spirometers provide the opportunity for more comprehensive monitoring of lung function at home than has hitherto been available. The aim of this study was to assess the quality of spirometric data collected at home by 90 asthmatic schoolchildren aged 7-14 years.After training, children carried out twice daily recordings at home for ...
D C, Wensley, M, Silverman
openaire +2 more sources
Quantifying variation in home spirometry in people with cystic fibrosis during baseline health, and associations with clinical outcomes [PDF]
Lindsay J Caverly +2 more
exaly +2 more sources
Spirometry reference equations for central European populations from school age to old age. [PDF]
Spirometry reference values are important for the interpretation of spirometry results. Reference values should be updated regularly, derived from a population as similar to the population for which they are to be used and span across all ages.
Rochat, Mascha K +44 more
core +1 more source
People with cystic fibrosis experience bronchopulmonary exacerbations, leading to lung damage, lung function decline, increased mortality, and a poor health-related quality of life.
Carsten Schwarz +5 more
doaj +1 more source
Background Fibrotic interstitial lung disease (ILD) is often associated with poor outcomes, but has few predictors of progression. Daily home spirometry has been proposed to provide important information about the clinical course of idiopathic pulmonary ...
Tobias Veit +15 more
doaj +1 more source
BackgroundDaily home-based spirometry in idiopathic pulmonary fibrosis (IPF) has been shown to be feasible and clinically informative. The patientMpower app facilitates home-based spirometry along with home-based monitoring of IPF-related symptoms.
Edwards, Colin +4 more
doaj +1 more source
Clinical trial simulations in pulmonary fibrosis: patient-focused insights and adaptations
Background Patient recruitment and retention are a challenge when conducting clinical trials in patients with pulmonary fibrosis, including idiopathic pulmonary fibrosis and other interstitial lung diseases. This study aimed to understand and address the
Steve Jones +10 more
doaj +1 more source
View Score: An early warning score to detect possible complications among COVID-19 patients
Introduction: Understanding pulmonary function at various phases after coronavirus disease 2019 (COVID-19) infection is critical for determining the exact pathophysiological mechanism of COVID-19.
Meenakshi Bhakare +7 more
doaj +1 more source
Home spirometry for idiopathic pulmonary fibrosis: ready for prime time? [PDF]
Home spirometry in IPF can be used to shorten clinical trials and may enable patient self-management in the future http://ow.ly ...
Toby M. Maher, Maher, TM
core +1 more source
Distinct Systemic Sclerosis Phenotypes Related to Ethnicity: An Opportunity to Personalize Care?
Objective The objective is to describe and compare demographic, clinical, and serological characteristics of patients with systemic sclerosis (SSc) according to ethnic background. Methods Participants enrolled in the Canadian Scleroderma Research Group cohort who self‐identified to a single ethnicity group were included.
Danick Goulet +11 more
wiley +1 more source

