Pulmonary Hypertension in Patients with Chronic Fibrosing Idiopathic Interstitial Pneumonias
Marius M. Hoeper; Juergen Behr; Matthias Held; Ekkehard Grünig; Carmine Dario Vizza; Anton Vonk Noordegraaf; Tobias Lange; Martin Claussen · 2015 · PLoS ONE
WASTE classifies this as Negative / Null Result Report · AI classification, approximate
The study found no significant effect — useful as a negative control or null benchmark for your own design.
Abstract
BACKGROUND: Pulmonary hypertension (PH) is a common finding in patients with chronic fibrosing idiopathic interstitial pneumonias (IIP). Little is known about the response to pulmonary vasodilator therapy in this patient population. COMPERA is an international registry that prospectively captures data from patients with various forms of PH receiving pulmonary vasodilator therapies. METHODS: We retrieved data from COMPERA to compare patient characteristics, treatment patterns, response to therapy and survival in newly diagnosed patients with idiopathic pulmonary arterial hypertension (IPAH) and
Abstract by Marius M. Hoeper; Juergen Behr; Matthias Held; Ekkehard Grünig; Carmine Dario Vizza; Anton Vonk Noordegraaf; Tobias Lange; Martin Claussen, PLoS ONE (2015) — licensed CC BY 4.0.
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Metadata source: OpenAlex · DOI 10.1371/journal.pone.0141911