Benefits of Vitamin Supplementation in Idiopathic Pulmonary Fibrosis
In patients with idiopathic pulmonary fibrosis, can supplementation with vitamins C, D, and E affect respiration, inflammation, and oxidative stress?
Restrictive Lung Disease
Cystic Fibrosis: Helping Teens, Young Adults Transition Into Making Care Decisions
How do adolescents and young adults with cystic fibrosis handle the transition to taking on their own treatment decisions, and what can be done to prepare for this transition?
Identifying Lung Impairment in Preschoolers With Primary Ciliary Dyskinesia
Can the Lung Clearance Index, which uses the multiple breath washout test, be used in preschool children to detect lung impairment from primary ciliary dyskinesia?
Dyspnea in Obesity Linked to Reduction in Lung Volumes, Higher BMIs
In patients with obesity, what relationships exist between dyspnea in daily living, lung function, and body composition?
Inhaled Therapy Gets Breakthrough Designation for Non-Cystic Fibrosis Bronchiectasis
The designation was supported by data from the multicenter, double-blind, placebo-controlled phase 3 PROMIS-I study.
Clinical Trial Compares Glassia, Prolastin for Alpha1-Antitrypsin Deficiency
A clinical trial compared the efficacy of 2 alpha1-proteinase inhibitors, Glassia and Prolastin, for the treatment of patients with alpha1-antitrypsin deficiency.
Sarcoidosis: the Clinical Value of Patient Self-Assessments
Can clinicians better manage sarcoidoisis by gathering patient self-assessment data at baseline, rather than focusing solely on traditional clinical measures?
Modified Lung Ultrasound for Evaluating Bronchopulmonary Dysplasia Severity
Researchers adapted the lung ultrasound score to evaluate bronchopulmonary dysplasia severity and short-term clinical outcomes in preterm infants.
ATS Guideline: Outpatient Management of Pediatric Post-Prematurity Respiratory Disease
How should clinicians handle the outpatient management of infants, children, and adolescents with post-prematurity respiratory disease? A summary of updated recommendations from the American Thoracic Society offers guidance.
Inhaled Hypertonic Saline vs Isotonic Saline for Children With Cystic Fibrosis
The SHIP + CT clinical trial compared the effect of isotonic vs inhaled hypertonic saline on lung structure in children with cystic fibrosis over 48 weeks.
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