Cystic Fibrosis and Abnormal Lung Function
Changes in lung function are of critical importance to patients with cystic fibrosis (CF), as lung function is a key indicator of disease progression and treatment effectiveness.
Changes in lung function are of critical importance to patients with cystic fibrosis (CF), as lung function is a key indicator of disease progression and treatment effectiveness.
Changes in lung function are of critical importance to patients with cystic fibrosis (CF), as lung function is a key indicator of disease progression and treatment effectiveness.
Read MoreBaxter unveiled its next-generation Vest APX System, featuring patient-centered improvements for those with chronic lung conditions.
Read MoreIn RT’s May-June 2023 issue, we cover the potential of vaping devices as smoking cessation aids; best practices for bubble CPAP use; plethysmography in the PFT lab; and infection control for intubated patients.
Read MoreThis article will present notable insights from a roundtable of pulmonologists who discuss potential solutions to improve treatment strategies for non-cystic fibrosis bronchiectasis patients.
Read MoreIn RT’s October-November 2022 issue, we cover proper tracheostomy care techniques; endotracheal suctioning in the NICU/PICU; accurate interpretation of arterial blood gases; and inhaled nitric oxide delivery.
Read MoreSuction? PEP? Percussion? Oscillation? Cough assist? With an array of airway clearance therapy options available for respiratory therapists, how do RTs choose the right method for the job?
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