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A study involved 82 patients with Interstitial Lung Disease (ILD) found that nearly 30% had impaired diaphragm function. Patients with Connective Tissue Disease-ILD showed lower diaphragm displacement compared to those with Idiopathic Pulmonary Fibrosis (IPF). Diaphragmatic dysfunction was associated with moderate/severe dyspnea in both groups. Diaphragm thickness was linked to lung function only in Connective Tissue Disease-ILD, indicating its potential role in patient assessment.
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