Genetic Discovery for Primary Ciliary Dyskinesia
Researchers identified genetic-related structural defects that prevent cilia from clearing mucus in primary ciliary dyskinesia patients.
Researchers identified genetic-related structural defects that prevent cilia from clearing mucus in primary ciliary dyskinesia patients.
Researchers identified genetic-related structural defects that prevent cilia from clearing mucus in primary ciliary dyskinesia patients.
Read MoreA closer look at suction and airway secretion clearance therapy devices from ABM, Baxter, Neotech, Sentec, Seoil Pacific, and Synchrony Medical.
Read MoreCombining formoterol and methacholine significantly improves mucociliary clearance in animal models of cystic fibrosis, compared to using either drug alone.
Read MoreResearchers found that patients with both bronchiectasis and chronic rhinosinusitis are more likely to test positive for Pseudomonas aeruginosa (P aeruginosa).
Read MoreThe Quantitative Mucin Index (MUCQ) of the Lung analyzes sputum and other lung mucus samples to detect airway mucus abnormalities, assess disease risk, and track disease progression in patients over time.
Read MoreThe BiWaze Clear provides lung expansion, mucus mobilization, and aerosol therapy in a portable 10-minute session.
Read MoreThe BiWaze Cough’s assisted cough technology uses dual air pathways and positive airway pressure to help patients clear secretions and improve respiratory hygiene.
Read MoreThe Vest APX System utilizes high frequency chest wall oscillation to mobilize secretions and reduce pulmonary exacerbations for patients with chronic respiratory conditions.
Read MoreThe Volara Airway Clearance System combines oscillation and lung expansion therapy with aerosol...
Read MoreThe Synclara Cough System uses mechanical technology to help patients with weak coughs clear their airways and reduce infection risks.
Read MoreThe Comfort Cough II mechanical cough stimulator uses pressure synchronization and oscillatory vibration to assist patients with impaired respiratory function.
Read MoreThe AffloVest from Tactile Medical utilizes oscillating motors to mobilize lung secretions and improve patient treatment adherence.
Read MoreDevices like the Philips InCourage system help patients with COPD and cystic fibrosis manage mucus and reduce the risk of infections.
Read MoreThe Aerobika oscillating positive expiratory pressure (OPEP) device significantly lowers 30-day exacerbation rates and related medical expenses for patients with chronic respiratory conditions.
Read MoreThe IPV 1 features a unified connector and updated interface designed to improve clinical efficiency and patient safety.
Read MoreThe Sentec IPV-2C provides intrapulmonary percussive ventilation for neonatal and adult patients in hospital environments.
Read MoreThe VESTIGE study is the first study to show a reduction in lung mucus buildup in asthma patients treated with dupilumab/Dupixent.
Read MoreFunds from NIH will advance ALX1 as a potential treatment in cystic fibrosis and other chronic lung diseases.
Read MoreThe Simeox 200 is intended to promote and improve bronchial drainage by using high-frequency oscillatory vibrations and intermittent negative pressure.
Read MoreData shows that metered cryospray therapy with the investigational RejuvenAir System leads to airway remodeling and improved symptoms in chronic bronchitis patients.
Read MoreResearchers have developed enzyme-powered nanobots capable of navigating through mucus barriers—which typically keep out locally administered drug treatments.
Read MoreA closer look at suction and secretion clearance devices from ABM Respiratory, Neotech, Precision Medical, Seoil Pacific, and Tactile Medical.
Read MoreElectromed Inc has entered into a distribution agreement with Marathon Medical Corp, a medical supply distribution company and service-disabled veteran-owned small business (SDVOSB).
Read MoreScientists have engineered a living material resembling human phlegm, which will help them to better understand how a certain kind of infection develops on the lungs of patients with cystic fibrosis.
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