Interactive Transcript
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While the primary focus
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of looking at the lungs on lung cancer screening CT exams is
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to identify early evidence of lung cancer.
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There are many abnormalities that can be seen in the lungs
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that are associated with cigarette smoking, as well
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as the usual findings
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that we can see on any chest CT that we're interpreting.
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Patients undergoing lung cancer screening cts are often at
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increased risk for both interstitial
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and obstructive lung disease.
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Sometimes these diseases are already known
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and recognized clinically and sometimes they're not.
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In COPD, we have emphysema small a, a wall thickening as
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commonly seen in patients with chronic bronchitis
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or chronic asthma, mucus plugging and bronchiectasis.
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And in interstitial lung disease,
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the most common findings related
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to cigarette smoking are respiratory bronchiolitis
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and langer hand cell histiocytosis.
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But we're also now picking up early interstitial lung
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disease or interstitial lung abnormalities on
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screening cts as well.
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If we look to the American College
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of Radiology's Lung Cancer Screening Registry for
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how frequently we see these findings
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and the first 1.7 million screens in the lung cancer
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screening registry, 2.2%
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of patients had interstitial lung disease other than
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pulmonary fibrosis, things like respiratory bronchitis
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or laying or hand cell histiocytosis,
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and half a percent of patients had frank pulmonary fibrosis.
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So that's nearly 3%
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of patients having interstitial lung disease.
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Emphysema that is moderate
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or severe occurred in 1% of all the screening cts
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and represented 6% of all the abnormalities.
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I put a caveat on the way emphysema is reported into the
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lung cancer screening registry.
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Many people expect
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to see emphysema on lung cancer screening cts due
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to the Association of Heavy Smoking history with
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emphysema, as well as with lung cancer,
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which is the primary reason we're doing the
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screening CT exam.
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So the majority of people don't report emphysema
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as an S modifier finding as they consider expected.
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We strongly encourage people to report emphysema as moderate
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or severe using the S modifier,
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but for mild emphysema, it's perfectly fine
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to mention in the report.
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I will say that increasingly early evidence of various forms
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of small airway disease
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and emphysema, as well as even small areas
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of mucus plugging are being recognized to be associated
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with increased morbidity and mortality.
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So as I'm thinking about this more looking into the future,
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it's not just important enough
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to mention those findings in the body of the report.
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It's gonna become increasingly important to recognize
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and report early evidence of obstructive disease, emphysema,
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mucus plugging, and so on in the impression as well,
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particularly the first time it's detected.
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If we look to the ACRs, a quick guide
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for incidental findings, we have a section for lung and
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Pleural abnormalities.
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Much of this language here is intended
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to help primary care physicians
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or nurse coordinators of nurse navigators
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and lung cancer screening programs understand how
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to translate what we say as radiologists into actionable
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or not actionable next steps for a patient
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or to answer patient's questions
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as they get their reports electronically.
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Very commonly now through the patient portals, a little bit
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of mild subsegmental, aacts
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or scar, not really an actual finding, emphysema
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and bronchial wall thickening wall expected should still be
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considered for evaluation by the PCP to maximize
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any treatments for COPD that the patient may be appropriate
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for and to consider pulmonary function tests
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and potentially a pulmonary medicine consultation.
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Advances in treatment are really accelerating in the space
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of obstructive lung disease.
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If fibrotic interstitial lung diseases identified such
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as IPF pulmonary fibrosis,
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a pulmonary medicine consultation is strongly recommended
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as antifibrotic therapies are now becoming the standard
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of care and we recognize the increased association
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of fibrotic lung disease with unrecognized
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and undiagnosed connective tissue disease more
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and more when we see bronchiectasis, ground glass opacity,
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cystic lung disease and diffuse nodule disease.
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Yes, the pulmonary medicine physician can certainly do an
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assessment for signs and symptoms of the disease
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and undergo a referral for pulmonary medicine consultation
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and pulmonary function testing evaluation.
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We don't see a lot
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of unexpected plural findings on lung cancer screening
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disease such as a fusion thickening or mass.
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We usually recommend significant findings in these areas
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to the PCP or consider pulmonary function testing
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with pulmonary medicine consultation,
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particularly when there are pulmonary symptoms,
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and we apply the same criteria we would when
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interpreting NHS ct.
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I think it's important to understand
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that we know a lot more about COPD than we ever used to,
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but we still know so very little
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and have a lot more to learn.
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COPD is characterized by persistent airflow limitation
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that's usually progressive
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and associated with an enhanced chronic inflammatory
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response in the airways and the lung to noxious particles
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or gas symptoms include shortness of breath, cough,
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wheezing, decreased activity, and weight loss.
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The severity of COPD is rated on what's known
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as the gold scale for the global initiative
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for chronic obstructive lung disease.
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Risk factors for COPD include smoking,
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and that's one of the most common risk factors for COPD,
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but at least one in six individuals
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who do not smoke have COPD.
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This is usually related
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to environmental exposures like chemicals, dust fumes,
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outdoor air pollution.
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Cooking in poorly ventilated kitchens is a manifestation
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of indoor air pollution and in some cases secondhand smoke.
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It can also be seen in genetic conditions such
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as alpha one antitrypsin deficiency.
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The gold score, as I mentioned, is used
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to classify the severity of COPD.
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So if you see the gold score in a reason for exam,
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a patient's having shortness of breath with a gold score
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of 1, 2, 3, 4, you can understand its significance.
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Gold 1, 2, 3, and four described as mild, moderate, severe,
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and very severe obstructive pulmonary disease based on the
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FEV 1% predicted with relatively preserved fev one
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of an 80%
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or greater being considered mild by the gold score,
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and a less than 30% predicted FEV
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one considered very severe.
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COPD is underdiagnosed in the US and around the world.
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Just in this three year timeframe from 2007 to 2010, eight
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and a half million adults were diagnosed with COPD,
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but more than 18 million had evidence
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of impaired lung function on pulmonary function testing.
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So we know that we are under diagnosing COPD
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and that has long-term implications for patient morbidity,
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lung function, and mortality.
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So one thing we can do
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with our lung cancer screening cts is report early evidence.
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The prevalence of COPD ranges across the United States
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and is more common in areas with higher tobacco use.
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So it's expected that the states
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that have higher tobacco use,
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higher cigarette smoking have higher rates of COPD.
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In general, COPD is extremely costly based on all
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the treatments in the outpatient space, ER visits,
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home health office-based care
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and inpatient admissions, as well as prescription drugs
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that are increasingly being developed
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and changed to treat COPD.