board review pulm Flashcards

1
Q

differentiate flow volume loops for fixed obstruction, variable extra-thoracic and intrathoracic obstruction

A
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2
Q

obstruction: FEV1/FVC <70% or <LLN

A
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3
Q

PFT obstruction

A
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4
Q

bronchoprovocation

A

**Positive if decrease in FEV1 of more than 20%
at a concentration(PC 20) of less than
16mg/ml of methacholine or dose

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5
Q

dx of asthma

A
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6
Q

when is Ig E useful ina sthma

A

omalizumab

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7
Q

eosinophils in asthma

A

Eosinophilic inflammation
* Most commonly serum >/= 150 - 400/microL
* May benefit from mepolizumab/benralizumab etc

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8
Q

occupational asthma

A

15% of adult asthma
* High molecular weight substances: animal and plant allergens,
latex, grains, diisocyanates
* Once sensitized, may react to very low levels of exposure
* Diagnose: spirometry before and after workplace exposure, peak
flow
* Treatment: reduce exposure

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9
Q

asthma tx

A

Asthma treatment
* Remove/avoid environmental allergens
* Allergy shots
* Treat nasal symptoms
* Inhaled corticosteroids
* Inhaled bronchodilators
* Oral steroids
* Adjunctive immunomodulators
* IgE:
* Omalizumab
* Eosinophils:
* Mepolizumab
* Reslizomab
* Benralizumab
* Dupilumab

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10
Q

mild intermittent assthma

A

rescue

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11
Q

then

A

low dose ICS

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12
Q

then

A

higher dose ICS

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13
Q

then

A

add LABA

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14
Q

AERD/NERD

A

AERD/NERD
* Triad: asthma + nasal polyposis + chronic
rhinosinusitis
* + ASA sensitivity
*Intermittent symptoms following ingestion of ASA
or NSAID
*Aspirin desensitization can be used as a treatment
however and chronic use is felt to downregulate the
pathological inflammatory response
*Growing use of anti-IL-5 and anti-IgE therapy

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15
Q

ABPA

A

ABPA
*Immunologic response to inhaled aspergillus
* Other fungal organisms implicated in case reports
*Persistent eosinophilic inflammation
*Classically seen in asthma or cystic fibrosis * Reported in lung transplant, other bronchiectasis etc

dx criteria:
*Both
* Serum IgE specific to Aspergillus
* Elevated total IgE(typically >1000 iu/ml)

  • as well as Two of three of the following:
  • A. fumigatus specific IgG
  • Consistent radiograph
  • Total eosinophil count > 500 cells/microL * International Society for Human and Animal Mycology
    (ISHAM) working group diagnostic criteria for allergic
    bronchopulmonary aspergillosis
  • Treatment: steroids + antifungal (also omalizumab)
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16
Q

exercise-induced asthma

A
  • Pre-existing asthma exacerbated by exercise
  • Symptoms of cough, dyspnea and wheezing(typically following
    completion of exercise)
  • FEV1 drop by 10% or more post-exercise

peak flow meter before and after also works

17
Q

copd tx

18
Q

mild copd

19
Q

vocal cord dysfunction

20
Q

bronchiectasis

A

signet ring sign

21
Q

bronchiectasis cont’d

A

caused by anything that can damage airway - vicious cycle

Bronchiectasis
* Diagnosis
* Symptoms of cough, sputum production and DOE
* High resolution CT
* PFTs with airflow obstruction possibly reduced DLCO
* Treatment
* Bronchodilators
* Physiotherapy/airway clearance***
* Suppressive abx/po or inhaled
* Abx with acute exacerbations
* Steroids unstudied but used

22
Q

CF dx

A

Diagnosis
* Organ dysfunction consistent with CF in at least 1 organ
And
* Two abnormal CFTR mutations
* Sweat chloride >/= 60 mmol/L
* Abnormal nasal potential difference
* Infection/colonization with haemophilus influenzae, staph aureus, and
mucoid pseudomonas aeruginosa
* Pancreatic insufficiency (Exocrine in 85%)
* CFRD also common

  • Treatment:
  • Airway clearance: chest PT, vest, exercise, flutter device
  • Mucolytics: recombinant DNase,hypertonic saline
  • Bronchodilators, antimicrobials, anti-inflammatory
  • Disease modifying agents
  • Improve production, intracellular processing and/or function of CFTR protein
  • Trikafta: ivacaftor + texacaftor + elexacaftor*****
  • Approved for delta F508 homozygotes
23
Q

pulm htn

A

WHO groups 1 – 5. * Group 1 (PAH) - idiopathic, hereditary (BMPR2 mutations), HIV, meds/illicit drugs, connective tissue disease, congenital heart disease
* Group 2 – 2/2 left heart disease/elevated wedge
* Group 3 – 2/2 pulmonary disease and or chronic hypoxic vasoconstriction
* Group 4 – chronic thromboembolic pulmonary hypertension
* Group 5 – misc…chronic hemolytic anemia, sarcoidosis, CKD, fibrosing
mediastinitis
* Defined as an increase in mean pulmonary arterial pressure
(mPAP) at rest as assessed by right heart catheterization
(RHC)
* mPAP > 20 mm Hg (normal10-12 mm Hg) with a normal wedge
* PVR > 2 Wood units
* PAOP </= 15 (except group 2)

24
Q

phtn dx

A
  • PE: Loud P2, TR, RV heave
  • PFTs: Isolated decrease in DLCO
  • Screen: Echo
  • Diagnosis: Right heart catheterization
  • Vasodilator reactivity (iNO or IV epoprostinol) * Decrease in mPAP by >10 mmHg, mPAP <40 mmHg and CO remains
    stable or improves
  • Predicts potential long-term response to oral calcium channel blocker
  • Predicts overall better prognosis
25
pHTN tx
Pulmonary HTN Treatment * Calcium channel blockers IF reactive in cath lab * nifedipine, amlodipine, and diltiazem * Phosphodiesterase type 5 inhibitors * Sildenafil, Tadalafil * Endothelin Receptor Antagonists * Bosentan, Ambrisentan, Macitentan * Cyclic GMP Stimulator - CTEPH * Riociguat * Inhaled Treprostinil-Group 3 PH-ILD * Tyvaso * Prostanoids * Epoprostenol, Iloprost, Treprostinil * Oxygen, diuretics, pulmonary rehab, anticoagulation (some Group 1, Group 4) * Transplant
26
massive PE
* Severity * Massive - hemodynamic instability * SBP < 90 or drop by 40 mmHg or pressor requirement even after fluids * Lasting > 15 minutes * Sub-massive – none of the above * High risk, Intermediate risk, low risk of mortality – PESI score
27
indications for thrombolysis in massive PE
* Thrombolysis * Massive PE(sbp < 90 or 40 mmHg < baseline or pressors) * PERT team to make multidisciplinary decision * High risk factors * HR >120 * CT with dilated RV or reflux of contrast * TTE with dilated RV/RV pressure overload/RV systolic dysfunction * Elevated BNP * Clot in transit * Significant hypoxia requiring supplemental oxygen * Poor cardiac/respiratory reserve * sPESI > 0 * To give or not to give lytics…. * Massive PE(high risk)-> give lytics * Hemodynamically unstable. Could be BP 89/60, could be on 2 pressors, could be cardiac arrest * Submassive PE * Intermediate risk-> no one knows * No hemodynamic instability, but….. * RV dysfunction on echo or CT * Elevated BNP * Elevated trop * Tachycardic etc * Low risk-> don’t give lytics * None of the above
28
absolute contraindications to lytics
Absolute contraindications to fibrinolytic therapy * Prior ICH or known lesion * Suspected aortic dissection * Active bleeding * Significant head trauma Relative contraindications to fibrinolytic therapy * Poorly controlled HTN * Hx ischemic stroke * Noncompressible vascular puncture * Bleeding within 4 weeks * Recent CPR
29
cor pulmonale
RV dilatation, hypertrophy or failure in Group 3 PH. * Some may include group 1(PAH) * Classically chronic hypoxic respiratory failure with chronic pulmonary vasoconstriction * Treat the underlying caus
30
hepatopulmonary syndrome
Hepatopulmonary Syndrome * Hepatopulmonary syndrome (HPS) * abnormal arterial oxygenation caused by intrapulmonary vascular dilatations * setting of liver disease, portal hypertension, or congenital portosystemic shunts * Orthodeoxia and platypnea * Shunt on TTE bubble study(CT rarely show AVM/shunt) * Liver transplant
31
hemoptysis imaging
* Imaging/procedures * If stable CTA-bronchial circulation otherwise CXR, potential DSA, bronchoscopy
32
management of hemoptysis
* Assess and secure airway * Consider mainstem intubation * If known, place bleeding side down** * Bronchoscopy * Bronchial blocker, potential diagnostic and therapeutic utility * IR * Thoracic or cardiac surgery * Treat underlying cause * Abx * FFP, platelets, DDAVP, specific anticoag reversal etc