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This episode is based on practice gaps in longitudinal COPD management. 1. Imprecise understanding of the diagnostic testing necessary to establish the diagnosis of COPD and the indication for empiric therapy. 2. Lack of clarity on the lab evaluation all COPD patients should have on diagnosis, and the criteria to guide selection of a first therapeutic agent. 3. Confusion about types of inhalers and the differences between them. 4. Insufficient understanding about indications to stop inhaled steroids in COPD patients. 5. Insufficient awareness of end-of-life issues that should be raised for all COPD patients. The Core IM team invites you to learn with them as they explore 5 Pearls on COPD.
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Pearl 1: Diagnosis and Empiric Therapy
- COPD label without spirometry is very common
- of patients are diagnosed empirically and do NOT receive spirometry
- You cannot without spirometry
- 鈥淗istory and physical examination are poor predictors of airway obstruction and its severity鈥 - from 2011 from ACP, ACCP, ATS, and ERS
- 1 in 3 .
- Despite not having obstruction on PFTs, 1 in 4!
- A note on defining airflow obstruction (AFO):
- Historically (and currently, by GOLD), defined as post-bronchodilator FEV1/FVC < 0.7 or by FEV1 < 80% of predicted.
- However, there are concerns that this can ignore normal, age-associated decreases in FEV1/FVC and lead to overdiagnosis.
- The are now recommending using the lower limit of normal (defined as the 5th percentile) to define AFO.
- Empiric initiation of maintenance inhalers for COPD generally shouldn鈥檛 be done
- However, in patients with radiographic evidence of emphysema/COPD and with symptoms consistent with the diagnosis, it鈥檚 probably ok to start maintenance inhalers so long as outpatient PFTs are ordered for confirmation
Pearl 2: The Initial Visit鈥揃lood Work and Initial Treatment Choices
- Blood work in COPD:
- 1) Every new diagnosis of COPD should be checked for
- 2) Every COPD patient should have a CBC with diff checked at least once to . Specifically, do not interpret eosinophils when they鈥檙e taking systemic steroids or have an acute infection.
- The idea behind this is that COPD patients with higher eosinophils may have an allergic or inflammatory phenotype that an ICS will directly treat and therefore reduce exacerbations.
- differ between studies and individual鈥檚 practice patterns, but there鈥檚 evidence that peripheral eosinophils predicts
- a patient's risk of exacerbation and
- More likely to .
- differ between studies and individual鈥檚 practice patterns, but there鈥檚 evidence that peripheral eosinophils predicts
- On the other hand, patients without high eosinophils don鈥檛 have an inflammatory phenotype and so are only getting the risk for immunosuppression and pneumonia with ICS use.
- is associated with an
- Data supports that if eos are , patients may have a higher rate of PNA and so at higher risk of harm from ICS use.
- The idea behind this is that COPD patients with higher eosinophils may have an allergic or inflammatory phenotype that an ICS will directly treat and therefore reduce exacerbations.
- Simplify inhalers by remembering that there are only 3 classes of medications:
- 1) Beta agonists
- Generally end with 鈥-辞濒鈥
- E.g. formoterol, salmeterol
- 2) Muscarinic antagonists
- Generally end with 鈥-颈耻尘鈥
- E.g. tiotropium, aclidinium, the umeclidinium
- 3) Inhaled corticosteroids
- Generally end with 鈥-辞苍别鈥
- E.g., fluticasone, beclomethasone
- 1) Beta agonists
- The most widely used staging/grouping schema (see infographic) is described by , which uses a combination of spirometry, symptom burden, and history of exacerbations over the last year to determine grade and group.
- COPD grade informs prognosis
- COPD group informs initial therapy.
- Memorization of specific cutoffs isn鈥檛 necessary, and can be looked up.
- The way you assess symptom burden matters.
- COPD is
- Consider using a standardized instrument to assess your patients- a significant number of symptomatic patients will otherwise.