2017
DOI: 10.1080/24745332.2017.1359056
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Evaluation of patients with fibrotic interstitial lung disease: A Canadian Thoracic Society position statement

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Cited by 17 publications
(18 citation statements)
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“…Over the last decades, the diagnostic algorithm of ILD has evolved with an increased reliance on HRCT and MDD for a final diagnosis. [4][5][6][8][9][10][11][12][13][14][15]17 Nonetheless, a subset of patients remains with unclassifiable ILD for which SLB is still regarded as the gold standard for obtaining pathologic assessment and a final diagnosis. In this context, the decision regarding whether or not to undergo a SLB is tailored according to the individual risks of SLB and the potential benefit of obtaining a confident diagnosis guiding subsequent treatments.…”
Section: Discussionmentioning
confidence: 99%
“…Over the last decades, the diagnostic algorithm of ILD has evolved with an increased reliance on HRCT and MDD for a final diagnosis. [4][5][6][8][9][10][11][12][13][14][15]17 Nonetheless, a subset of patients remains with unclassifiable ILD for which SLB is still regarded as the gold standard for obtaining pathologic assessment and a final diagnosis. In this context, the decision regarding whether or not to undergo a SLB is tailored according to the individual risks of SLB and the potential benefit of obtaining a confident diagnosis guiding subsequent treatments.…”
Section: Discussionmentioning
confidence: 99%
“… 8 Our criteria were derived from literature describing long-term IPF outcomes, predisposing factors, and clinical course of AE-IPF, and risk of poor outcomes after surgical lung biopsy. 9 , 10 Because we could not identify clear criteria for >50% predicted mortality (level 2), we reiterated criteria for >80% predicted mortality (level 1). Level 3 criteria were validated in the sex, age, physiology model, predicting a relatively low probability of 1-year mortality.…”
Section: Pulmonary Fibrosismentioning
confidence: 99%
“…Deciding on the most appropriate pharmacotherapy for fibrotic ILD requires an accurate diagnosis. 2 Pirfenidone and nintedanib are approved in Canada for the treatment of IPF and both anti-fibrotic medications have been recommended for the management of IPF in recent international guidelines. 3 Pirfenidone is a nonspecific anti-fibrotic agent thought to act on multiple targets along the fibrotic cascade.…”
Section: Ild-targeted Pharmacotherapymentioning
confidence: 99%
“…Importantly, immunosuppressive medications have potential to cause harm in patients with IPF, 14 emphasizing the importance of establishing the correct diagnosis in patients with fibrotic ILD. 2 Referral to a tertiary care center for enrollment in clinical trials can be considered in selected cases of fibrotic ILD.…”
Section: Ild-targeted Pharmacotherapymentioning
confidence: 99%
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