Pediatric Interstitial Lung Disease Tied to Novel Disorder with Genetic Causes
Researchers linked loss-of-function variants in the TMEM63B gene to a novel disorder causing interstitial lung disease in some pediatric patients.
Researchers linked loss-of-function variants in the TMEM63B gene to a novel disorder causing interstitial lung disease in some pediatric patients.
Researchers linked loss-of-function variants in the TMEM63B gene to a novel disorder causing interstitial lung disease in some pediatric patients.
Read MoreData from clinical trials investigating treatments for pulmonary hypertension and pulmonary fibrosis will be highlighted at ATS 2026.
Read MoreWhen comorbidity burden was assessed using the Rheumatic Disease Comorbidity Index (RDCI), higher scores were significantly associated with ILD development.
Read MoreInsmed will present four abstracts on treprostinil palmitil inhalation powder (TPIP), being evaluated as a once-daily therapy for the treatment of patients with PAH, PH-ILD, and other rare and serious pulmonary disorders.
Read MoreA new case report describes a novel approach for treating fibrosing mediastinitis using rituximab injections directly into mediastinal lymph nodes combined with pulmonary artery angioplasty.
Read MoreTreatment with an inhaled dry powder formulation of treprostinil was associated with improvements in cardiac effort for patients with pulmonary hypertension–interstitial lung disease (PH-ILD).
Read MoreA weekly 90-minute online group singing session delivered for 12 weeks over Zoom was associated with improved quality of life in patients with COPD or interstitial lung disease.
Read MoreThe AI-powered tool automatically assesses medical data for interstitial lung findings compatible with interstitial lung disease.
Read MorePatients receiving the drug also had slightly more side effects and needed more care from hospitals and family members.
Read MorePreclinical data reveals CAN10’s potential to target key proteins involved in systemic sclerosis-associated interstitial lung disease and idiopathic pulmonary fibrosis.
Read MoreResearchers have identified a potential treatment for the respiratory symptoms of long COVID by discovering an unknown cause of the condition within the lungs.
Read MoreThe Supplemental Oxygen Access Reform Act of 2024, designed to ease access to supplemental oxygen for Medicare beneficiaries, was introduced in the US House of Representatives by a bipartisan group of members of Congress.
Read MoreResearchers demonstrate how they can now study the most common genetic cause of pediatric interstitial lung disease using stem cells generated from each patient.
Read MoreAccording to Imvaria, the device’s manufacturer, the clearance signifies the first FDA authorization of a diagnostic tool of any type in lung fibrosis.
Read MoreHigher levels of omega-3 fatty acids were associated with better lung function and longer transplant-free survival in patients with pulmonary fibrosis, a new study finds.
Read MoreA new ATS clinical practice guideline recommends expanding antifibrotic treatment to all patients with systemic sclerosis associated with ILD, not just those with progressive disease.
Read MoreThe Pulmonary Fibrosis Foundation and Pulmonary Hypertension Association have developed a position statement that addresses gaps in the diagnosis and treatment of patients living with pulmonary hypertension related to interstitial lung disease.
Read MoreCHEST announced the recipients of quality improvement grants aimed at shortening the time to diagnosis for interstitial lung disease.
Read MoreTwo studies presented at CHEST 2023 validated the effectiveness of the Envisia Genomic Classifier in improving the detection of interstitial lung disease.
Read MoreThe Pulmonary Fibrosis Foundation announced that seven medical centers have joined the PFF Care Center Network as clinical associate members, a new membership option.
Read MoreThe Pulmonary Fibrosis Foundation announced Franck Rahaghi, MD, MHS, FCCP, as its incoming president, CEO, and chief medical officer, effective Sept 15.
Read MoreThe latest guideline from the American Thoracic Society reaffirms benefits for patients with COPD as well as pulmonary hypertension and interstitial lung disease.
Read MoreThe phase 2 clinical trial is expected to be a multi-center, randomized, double-blind, placebo-controlled study assessing the drug’s safety and effectiveness in treating approximately 90 pulmonary sarcoidosis patients.
Read MoreThe expansion of the clinical trial follows the clearance of an Investigational New Drug application by the US Food and Drug Administration, announced earlier this year.
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