Extract Pulmonary hypertension (PH) frequently develops among patients with interstitial lung disease (ILD) and leads to a markedly worsened prognosis (14% survival at 5 years) [1] and increased morbidity [2, 3]. Despite its high prevalence in ILD (10 - 20% at diagnosis [2]), there is no standardised screening tool for development of PH-ILD [2, 4]. Furthermore, it can be challenging to determine longitudinally whether worsening symptomatology in a patient with ILD is attributable to progression of underlying lung disease or to the development of a pulmonary vasculopathy.
European Respiratory Journal published a clinical update in Critical Care on 05 Mar 2026.
The item focuses on A normal BNP does not reliably exclude pulmonary hypertension in interstitial lung disease.
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