Interactive Transcript
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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.