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Current Concepts in Interstitial Lung Abnormalities

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That brings us here to interstitial lung abnormality

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and progressive pulmonary fibrosis.

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These are two interrelated ideas.

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They're not actual diagnoses, they're more like ideas.

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And I know that might be confusing.

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We'll go into it in just a bit.

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So let's talk about interstitial lung abnormalities.

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So what the heck are interstitial lung abnormalities?

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There's, there's a definition here, so I'll just,

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here's a definition, bottom line,

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but again, it's more of an idea.

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So I talked about this before.

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It's these cases of mild reticulation,

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usually in the lung basis, usually in the lung periphery,

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where you're not sure if it's just from a previous one-time

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event, like a bad aspiration

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or bad infection causing some reticulation

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or if it's the earliest finding of a progressive subtype

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of pulmonary fibrosis.

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So it's that dichotic decision point.

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'cause on one hand,

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if it's just scarring, you don't do anything.

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A patient just lives their life.

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They have plenty of lung parenchyma for them to, to be able

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to ventilate normally and they're gonna be fine.

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If it's early fibrosis, you wanna treat that patient.

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And we have antifibrotic medications

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and we know that antifibrotics can slow the progression

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of pulmonary fibrosis

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and obviously they wanna see,

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they wanna maybe be put on a pulmonary rehab

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and just followed closely to decrease their risk factors

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for pulmonary fibrosis progression.

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So it, it sounds so simple,

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but at this point I think it's like the holy grail

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of interstitial lung disease is, is there a way

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to differentiate these two groups?

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And at this point there isn't when it's very mild like this.

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The way interstitial lung abnormal body is defined in this

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guideline that was actually just recently published this

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year, is that you wanna have non-dependent lung

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abnormalities, which can be comprised

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of ground glass opacity, reticulation,

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architectural distortion, traction,

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bronchi have even honeycombing involving at least 5%

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of a lung zone if it starts approaching 5%

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of the total lung.

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So lung zone, right? It's like superior, mid inferior.

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So 5% of a third of a lung zone, right?

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So it's like a one third of,

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of 5%, whatever the heck that is.

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So less than 2%, more than 1% of the total lung.

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You get these interstitial changes

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or glast abnormality, we start

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to think about interstitial lung abnormality.

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If it's greater than that, then we start to actually think,

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oh this might be a real interstitial lung disease.

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This patient needs a, a more aggressive workup

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and more maybe aggressive follow up.

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But bottom line, this is how ILAs are defined.

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But even with these definitions, they're

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so worded in such a way

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where there's not a lot of specificity.

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I think just to remember these interstitial lung

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abnormalities, it's an idea, it's not a diagnosis.

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And you kind of know when you're coming across a case

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of ILA, even

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before you think about the definition itself, it used to be

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that we only considered low risk patients

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to have interstitial lung

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abnormality and high risk

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patients. We didn't. We just said,

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Well high risk patients, you have ILD.

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But now either in low

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or high risk patients, we understand

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that interstitial lung abnormalities exist.

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So cases where it's just mild scarring

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or it's early interstitial lung disease,

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interstitial lung abnormality,

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in most cases we bilateral with some exception.

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So if you're very, very high risk for development

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of interstitial lung disease, maybe, I dunno,

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some genetic abnormality

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or connective tissue disease,

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maybe even a unilateral interstitial changes will

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make you invoke this.

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But most cases can be bilateral. What's not ILA?

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Things that we know don't progress to pulmonary fibrosis.

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So dependent lung alais, some osteophyte fibrosis,

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if it's a focal

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or unilateral abnormality, it's just like scar.

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We're not gonna call that interstitial lung abnormality.

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Uh, things like central lo nodularity or

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or non emphysema cyst, we're not like a,

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like those post-infectious

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or post-inflammatory pneumatic seal.

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So not diffuse cystic lung disease, like one or two cysts.

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They don't progress into fibrosis.

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So we're not gonna call it ILA findings

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of acute things like heart failure or aspiration.

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Obviously these are not ILAs.

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We also wanna differentiate ILA interstitial lung

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abnormality from early interstitial lung disease.

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So the patient's symptomatic, if the patient is abnormal,

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pulmonary function testing has clear fibrosis greater than

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5% of a total lung volume.

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So not just like one to 2% of the total lung volume, right?

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So 5% of a lung zone,

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but there's more of this abnormality

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relative to the total lung volume.

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We start thinking about ILD

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or if we see obviously progression

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or a defined fibrotic ILD pattern on ct.

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So U-I-P-N-S-I-P fibrotic,

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hp certainly we're not gonna call it ILA

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'cause now our suspicion

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that this is early pulmonary fibrosis is quite high

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and we're gonna treat it that way.

Report

Faculty

Jonathan H. Chung, MD

Professor of Radiology and Division Chief of Cardiothoracic Imaging

UCSD - University of California San Diego

Tags

Syndromes

Non-infectious Inflammatory

Lungs

Idiopathic

Drug related

Chest CT

Chest

CT