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Thorax. 2019 Feb 5. pii: thoraxjnl-2018-212446. doi: 10.1136/thoraxjnl-2018-212446. [Epub ahead of print]

Interstitial lung abnormalities: erecting fences in the path towards advanced pulmonary fibrosis.

Abstract

Interstitial lung abnormalities, when present in members of undiagnosed family members recruited on the basis of familial interstitial pneumonia, or in undiagnosed research participants, have been associated with a syndrome that includes distinct sets of imaging abnormalities, restrictive physiological and exercise impairments, and an increased prevalence of histopathological findings, and genetic predictors, that have been noted in patients with idiopathic pulmonary fibrosis. Recent longitudinal studies have demonstrated that qualitative and quantitative assessments of interstitial abnormalities are associated with accelerated lung function decline, an increased rate of clinical diagnoses of interstitial lung disease and an increased rate of mortality. In this perspective, in addition to reviewing the prior information, four major efforts that could help the field of early pulmonary fibrosis detection move forward are discussed. These efforts include: (1) developing standards for characterising and reporting imaging findings from patients with existing CTs; (2) developing consensus statements on when undiagnosed and asymptomatic imaging abnormalities should be considered a disease; (3) identifying populations for which screening efforts might be beneficial; and (4) considering approaches to developing effective secondary prevention trials.

KEYWORDS:

ARDS; clinical epidemiology; idiopathic pulmonary fibrosis; imaging/CT MRI etc; interstitial fibrosis

PMID:
30723182
DOI:
10.1136/thoraxjnl-2018-212446
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Conflict of interest statement

Competing interests: GMH has been receiving funding from the National Institutes of Health and has performed consulting for the Gerson Lehrman Group, Medna, Genentech, Boehringer-Ingelheim and Mitsubishi Chemical.

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