Obstructive Diseases

 COPD
Features
·       Both emphysema and chronic bronchitis are manifestations of COPD.
·       Pulmonary function tests show obstructive physiology (reduced FEVI/FVC, increased RV and TLC)
·       DLCO is normal in chronic bronchitis and decreased in emphysema.
S/S
SOB – Productive Cough
Dx
Clx –> PFT
Tx
Stable pt:
1˚ Ipratropium
  Albuterol (may precipitate HF through ⤴️ HF)
3˚ Theophyline
Stop smoking
-Home O2 (Start if: PaO2 <55 / O2 <88%)
-Vaccine: Pneumococcus q5 ys / Flu q1y
Exacerbation 🚨
·       Get: O2 Saturation + ABG + CXR
·       Give O2
·       Ipratropium + Albuterol TOGETHER
·       Systemic Corticosteroids (PO = IV)
·       ABx
If pt is on theophylline → check levels & DON’T D/C!

 Acute Exacerbation of COPD
S/S
·       ⤴️ SOB
·       ⤴️ Cough (more frequent or severe)
·       Sputum (change in color or volume)
Dx
CXR: Hyperinflation
ABG: Hypoxia, C02 retention (chronic &/or acute)
Tx
·       Oxygen (target Sp02 of 88%-92%)
·       Inhaled bronchodilators
·       Systemic GCS
·       Abx if? ≥2 cardinal sx
·       oseltamivir if? evidence of influenza
·       Non-invasive positive pressure ventilation if ventilatory failure
·       Tracheal intubation if NPPV failed or contraindicated
 Asthma
Features
Reversible AW obstruction
S/S
Acute AW obstruction w/ SOB & Wheezing
Dx
·       Clx → PFT (Gold standard)
·       CXR:
Acute Exacerbation
Tx
·       1˚ O2 / SABA / ipratropium?
·       2˚ IV methylprednisone
·       3˚ (no improvement w/i 1 h) Mg
·       non-invasive positive pressure
·       If iminent resp failure → ICU + Intubation
·       If pt has /⤴️ PaCO2
·       Muscle fatigue
·       ⤵️  Breath sounds
·       Hypoxia
·       AMS
Chronic Tx

 Bronchiectasis
Pathology
·       Recurrent infections + Impaired clearance
·       That leads to bacterial overgrowth & Nø infiltration → tissue damage & AW structural changes
Causes/RF
·       AW obstruction (Cancer)
·       Aotuimmune (RA, Sjögren),
·       Chronic infection (Aspergillosis, mycobacteria)
·       Immunodeficiency (Hypo-Ig)
·       Congenital (Cystic Fibrosis, alpha1-antitrypsin deficiency)
S/S
·       chronic daily cough
·       a lot of pus produced
·       Rx Rhinosinusitis, SOB, hemoptysis
·       Crackles, wheezing
Dx
·       High Resolution CT scan of the chest (needed for initial diagnosis)
·       Immunoglobulin quantification
·       CF testing, sputum culture (bacteria, fungi & mycobacteria)

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