Predictors of diagnosis and survival in idiopathic pulmonary fibrosis and connective tissue disease-related usual interstitial pneumonia
Teng Moua; Ana Carro Martínez; Misbah Baqir; Robert Vassallo; Andrew H. Limper; Jay H. Ryu · 2014 · Respiratory Research
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: Although usual interstitial pneumonia (UIP) appears to portend better survival when associated with connective tissue disease (CTD-UIP), little is known about the presenting clinical, radiologic, and pathologic features that differentiate pathologically confirmed UIP with CTD from idiopathic pulmonary fibrosis (IPF). In patients with atypical radiologic and clinical features, what specific findings predict underlying IPF vs. CTD-UIP diagnosis and their respective long term survival? METHODS: A large retrospective cohort analysis was done of consecutive patients seen from 1995 throu
Abstract by Teng Moua; Ana Carro Martínez; Misbah Baqir; Robert Vassallo; Andrew H. Limper; Jay H. Ryu, Respiratory Research (2014) — licensed CC BY 4.0.
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Metadata source: OpenAlex · DOI 10.1186/s12931-014-0154-6