lectures 29-30 (COPD treatment) Flashcards

exam 3

1
Q

COPD diagnosis

A

symptoms support diagnosis, but spirometry is required for diagnosis
- dyspnea
- cough +/- sputum production
- wheezing
- chest tightness
- fatigue
- activity limitation

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2
Q

spirometry

A

FEV1: amount of air that can be forcefully exhaled in one second
FVC: maximum amount of air that is exhaled after taking a deep breath
- COPD dx is consistent with FEV1/FVC < 0.7 (or 70%)

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3
Q

goals of therapy

A

reduce symptoms
- relieve symptoms
- improve exercise tolerance
- improve health status

reduce risk
- prevent disease progression
- prevent and treat exacerbations
- reduce mortality

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4
Q

assessment of COPD

A

COPD assessment test (CAT)
modified medical research council (mMRC)
- collection of both CAT and mMRC essential for most accurate pharmacologic medication selection

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5
Q

SABAs

A

albuterol
- ProAir
- Proventil
- Ventolin
levalbuterol (xopenex)

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6
Q

LABAs

A

arformoterol (brovana)
formoterol (perforomist)
olodaterol (striverdi)
salmeterol (serevent)

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7
Q

SAMAs

A

ipratropium (atrovent)

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8
Q

LAMAs

A

tiotropoum (spiriva)
umeclidinium (incruse)

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9
Q

muscarinic antagonist side effects

A

dry mouth
uRTI
cough
bitter taste
blurred vision

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10
Q

group A

A

criteria:
- mMRC 0-1, CAT <10
- 0-1 moderate exacerbations not leading to hospital admission
treatment:
- bronchodilator
- improvement in
breathlessness
- can be long acting or short acting (long acting preference)

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11
Q

group B

A

criteria:
- mMRC >2, CAT >10
- 0-1 moderate exacerbations (not leading to hospital admission)
treatment:
- LABA + LAMA
- tiotropium/olodaterol (stiolto)
- umeclidinium/vilanterol (anoro)

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12
Q

group E

A

criteria:
- >2 moderate exacerbations
OR
- >1 leading to hospitalization
- consider LABA+LAMA+ICS if blood eos >300
treatment:
- tiotropium/olodaterol (stiolto)
- umeclidinium/vilanterol (anoro)
- dual long-acting bronchodilator therapy > monotherapy for reducing exacerbation risk
- use of ICS/LABA not encouraged –> escalation to LABA/LAMA/ICS if there is an indication for ICS therapy
- effect of ICS on exacerbation prevention likely only if blood eos. >300

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13
Q

GOLD guideline changes

A

group A:
- a bronchodilator
- mMRC 0-1, CAT <10
- 0 or 1 moderate exacerbations not leading to hospital admission

group B:
- LABA or LAMA
- mMRC >2, CAT >10
- 0 or 1 moderate exacerbations not leading to hospital admission

group C:
- LAMA
- mMRC 0-1, CAT <10
- >2 moderate exacerbations or >1 leading to hospitalization

group D:
- LAMA or LAMA+LABA or ICS+LABA
- mMRC >2, CAT >10
- >2 moderate exacerbations or >1 leading to hospitalization

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14
Q

role of ICS in COPD

A

strongly favors use:
- history of hospitalization(s) or exacerbation(s) in COPD
- >2 moderate exacerbations of COPD per year
- blood eosinophils >300
- history of or concomitant asthma

favors use:
- 1 moderate exacerbation of COPD per year
- blood eosinophils 100 to < 300

against use:
- repeated pneumonia events
- blood eosinophils <100
- history of mycobacterial infection

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15
Q

follow-up treatment for dyspnea

A

LABA or LAMA –> LABA + LAMA
- consider switching inhaler device or molecules
- implement or escalate non-pharmacological treatment(s)
- consider adding ensifentrine
- investigate and treat other causes of dyspnea

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16
Q

follow-up treatment for exacerbations

A

LABA or LAMA –> LABA + LAMA or LABA + LAMA + ICS –> rofumilast (FEV < 50% and chronic bronchitis), azithromycin (preferred in former smokers), dupilumab (chronic bronchitis)

17
Q

PDE-4i

A

roflumilast (daliresp)
- dosing: 250mg PO daily x 4 weeks, then increase to 500mg PO daily
- 4 week 250mg period intended to increase tolerability; not considered a therapeutic dose
- cautioned use in those with moderate to severe liver impairment
- most common side effects: diarrhea, weight loss, nausea, decreased appetite, HA, insomnia

18
Q

IL-4 receptor antagonist

A

dupilumab (dupixent)
- dosing: 300mg SC every other week
- hypersensitivity reactions: skin rash, erythema (usually in the first hour of admin. but can appear 1 month after initiation)
- dermatologic reactions: alopecia, psoriasis (delayed; can appear anywhere from first month of therapy to >1 year after initiation