Pulmonary Embolism

PE

·       DVT –> PE
·       Tx: LMWH –> Warfarin
Dx:

·       If the patient is likely to have PE, do spiral CT. If negative –> no further testing. If positive –> Tx.
·       If the patient is unlikely to have PE, do D-dimer. If negative (i.e., no further testing. If positive –> spiral CT.
·       If spiral CT is contraindicated (e.g., renal failure, morbid obesity, contrast allergy) or is inconclusive but not negative, do V/Q scan.
Tx 
PE
Sx
Heart effect
⤵️ BP
Pt go to
Tx
Asx
ø
ø
ø
HOME
LMWH → Warfarin
Sx
ø
ø
Ward
LMWH → Warfarin
Submassive
ø
ICU
LMWH → Warfarin
Massive
ICU
tPA

Lung Cancer

Solitary pulmonary nodules
Factors ⤴️ Malignant Probability
·       Large size (>2cm = 50% probability)
·       Advanced patient age
·       Female sex
·       Active or previous smoking hx
·       FHX / PMHx
·       Upper lobe location
·       Speculated radiographic appearance (irregular borders)
#
Site
Clx
Adecocarcinoma
 40-50%
Peripheral
·       Clubbing
·       Hypertrophic Osteoarthropathy
SqCC
 20-25%
Central
Hypercalcemia
Small cell
 10-15%
Central
·       Cushing
·       SIADH
·       Lambert-eaton
Large cell
 5-10%
Peripheral
Gynecomastia / Galactorrhea
DDxTB: Hemoptysis / Weight loss / LN
Pancoast Tumor
• Shoulder pain (most common)
• Horner syndrome (ipsilateral ptosis, miosis, enophthalmos & anhidrosis) from involvement of paravertebral sympathetic chain & inferior cervical ganglion
• C8-T2 neurological involvement
  o Weakness &/or atrophy of intrinsic hand muscles
  o Pain & paresthesias of 4th & 5th digits, medial arm & forearm
• Supraclavicular LN c
• Weight loss
Hypercalcemia of malignancy
Tumor type
Mechanism
Dx
PTHrP
·       SqCC
·       Renal & bladder cancer
·       Breast & ovarian
Mimics PTH
⤵️ PTH
⤴️ PTHrP
Bone metastasus
·       Breast
·       Multiple myeloma
⤴️ Osteolysis
⤵️ PTH & PTHrP
⤵️ Vit D
1,25 Vit D
·       Lymphoma
⤴️ Calcium Absorption
⤵️ PTH
⤴️ Vit D

Acute Respiratory Distress Syndrome

 Acute Respiratory Distress Syndrome
RF
Infection, trauma, massive transfusion, acute pancreatitis
Path
• Lung injury → fluid/cytokine leakage into alveoli
• Impaired gas exchange, decreased lung compliance, PHTN
Dx
·       New/worsening respiratory distress within 1 week of insult
·       lung opacities (pulmonary edema) not due to CHF/fluid overload
·       Hypoxemia with PaO2/FiO2 ratio ≤300
Tx
Mechanical ventilation (⤵️ TV, ⤴️ PEEP, permissive hypercapnia)

Mechanical ventilation 
·       low tidal volume, low plateau pressures, and titrating up
·       positive end-expiratory pressure (PEEP)
·       initial tidal volume to 8 mL/kg and reduce gradually to 6 mL/kg (low tidal volumes) 
·       want to achieve an inspiratory plateau airway pressure ≤ 30 cm H2O
·       titrate PEEP to prevent tidal alveolar collapse 
·       initial respiratory rate to approximate baseline minute ventilation (≤ 35/min)
·       oxygenation goal is a PaO2 of 55-80 mmHg
·       pH goal is 7.30-7.45

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)

Restrictive Diseases

Interstitial Lung Disease
Causes
• Vasculitis (eg, granulomatosis with polyangiitis)
• Infections (eg, fungal, tuberculosis, viral pneumonia)
• Occupational & environmental agents (eg, silicosis, Common hypersensitivity pneumonitis)
• Connective tissue disease (eg, systemic lupus erythematous, scleroderma)
• Idiopathic pulmonary fibrosis, interstitial pneumonia
• Cryptogenic organizing pneumonia
S/S
• Progressive exertional dyspnea or persistent dry cough
• Pulmonary findings due to other underlying conditions (eg, silicosis, connective tissue disease)
• 50% of patients with significant smoking history
• Lung examination with fine crackles during mid-late inspiration, possible digital clubbing
Dx
CXR: reticular or nodular opacities
High-resolution chest CT: fibrosis, honeycombing, or traction bronchiectasis
PFTs: or ⤴️ FEV1/FVC ratio, ⤵️ DLCO,
• Resting arterial blood gas can be normal or show mild hypoxemia
• Exertion usually causes significant hypoxemia due to V/Q mismatch
Sarcoidosis
#
 African Americans
S/S
Pulmonary: hilar LN I Interstitial infiltrates
Skin
·       Papular, nodular, or plaque-like lesions
·       Erythema nodosum
Ophtha:
·       Anterior/posterior uveitis
·       Keratoconjunctivitis sicca
Hema: Peripheral LN I HSM
MSK: Acute polyarthritis (especially ankles)
CVS:
·       AV block
·       Dilated or restrictive cardiomyopathy
CNS:
·       7th CN Palsy
·       Central DI
Imaginc
Hilar LN 
Labs
·       ⤴️ Ca / ⤴️ Ca in urin
·       ⤴️ ACE level
Bx
Noncaseating granuloma
Tx
Steroids 
Obesity Hypoventilation Syndrome
Dx criteria
·       BMI ≥30
·       Awake daytime hypercapnia (PaCO2 >45)
·       No altemate cause of hypoventilation
Work-up
·       ABG on room air (hypercapnia, normal A-a gradient)
·       No intrinsic pulmonary disease on chest x-ray
·       Restrictive pattern on PFTs
·       Normal TSH
·       Polysomnography
Tx
·       Noctumal positive-pressure ventilation as first-line therapy
·       Weight loss (bariatric surgery in select cases)
·       Avoidance of sedative medications
·       Respiratory stimulants (Acetazolamide) as last resort
Asbestosis
RF
·       Prolonged Asbestos exposure (Shipyard, mining)
·       Sx develop ≥20 years after initial exposure
S/S
·       DRY COUGH 
·       Progressive SOB,
·       Basilar fine crackles,
·       Clubbing
·       ⤴️ Risk for Lung cancer & Mesothelioma
Dx
·       Pleural plaques on chest imaging
·       Imaging, PFT & histology consistent w/ pulmonary fibrosis

Sleep Apnea

 Sleep Apnea
features
·       Central vs. Obstructive: both when u wake up, no more apnea
·       What’s Central SA? no respiratory effort deriving from decreased CNS drive
PEx
·       In general, the physical examination is normal in patients with OSA, aside from the presence of obesity (body mass index: >30 kg/m2), an enlarged neck circumference (men: >43 cm [17 in]; women: >37 cm [15 in]), and hypertension.
·       ⤴️ Mallampati score:  difficult tracheal intubation
·       Narrowing of the lateral airway walls: Independent predictor of the presence of obstructive sleep apnea in men but not women
·       Enlarged -kissing- tonsils
·       Systemic arterial hypertension
·       CHF
·       pHypertension
S/S
Pt is not sleeping well, thus not refreshed from sleeping.
·       chronic fatigue: similar to narcolepsy
·       morning headache: specific to Central SA
·       loud snoring w/ periods of apnea: specific to OSA
·       PEx: hypertension
Dx
Sleep studies (Polysomnography)
·       ddx b/w Central vs. Obstructive
·       in central: no respiratory drive
CBC: polycythemia (2˚ to chronic hypoxia –> ⤴️ EPO)
Tx
Pediatrics:
·       Weight reduction & adenotonsillectomy are the first line of management in appropriately selected children.
Adults:
·       Non-medical: weight loss / ⤵️ Alcohol intake / Smoking
·       OSA: CPAP / Surgery: obstruction correction
·       If central sleep apnea: BiPAP
Conservative
·       body positions during sleep (avoid supine position)
·       smoking cessation
·       Avoiding alcohol
Pharmacotherapy
·       no much role
·       you can use modafinil as a stimulant
Mechanical
·       Nasal CPAP: Standard treatment option
·       BiPAP
Surgical
·       Uvulopalatopharyngoplasty
·       Craniofacial reconstruction with advancement of tongue or maxillomandibular bones
·       Tracheostomy
Complications
·       pulmonary HTN → HF
·       Systemic HTN
·       Arrhythmia –> cause of death

Pleural Effusion

 Pleural Effusion
Features
Excessive fluid in the pleural space
S/S
·       SOB
·       dullness to percussion
·       decreased breath sounds on the effusion
·       decreased tactile fremitus
DDx
Exudate
Transudate
Light Criteria
P/S protein ratio >0.5
OR
P/S LDH ratio >0.6
Not exudative
Path
Inflammation
Hydrostatic or oncotic pressure
?
·       Infection (pneumonia)
·       Malignancy
·       Rheumatologic disease (SLE / RA)
·       CHF
·       Cirrhosis (hepatic hydrothorax)
·       Nephrotic syn
Tx
Depends on the u/c:  If pt has PNA → give ABx
Procedural
·       Therapeutic thoracentesis →  if massive effusion and its affecting the patient’s breathing
·       Tube Thoracostomy → in complicated parapneumonic effusions or empyema

Parapneumonic effusions
Uncomplicated
Complicated
Cause
 Sterile exudate in pleural space
Bacterial invasion of pleural space
Fluid Analysis
• pH ≥7.2
• Glucose ≥60
• WBC ≤50,000
• pH <7.2
• Glucose <60
• WBC >50,000
Gram stain & Cx
 
Tx
 Abx
Abx + drainage
Transudate
Exudate
Protein (pleural/serum)
<0.5
>0.5
LDH (pleural/serum)
<0.6
>0.6
OR
Pleural LDH < two-thirds upper limit of normal serum LDH
Pleural LDH > two-thirds upper limit of normal serum LDH
Common causes
• Hypoalbuminemia (cirrhosis, nephrotic syndrome)
• Congestive heart failure
• Infection (parapneumonic, TB, fungal, empyema)
• Malignancy
• PE
– Pleural fluid in a chylothorax, which occurs from disruption of the thoracic duct, has elevated levels (>110 mg/dL) of triglycerides.
– Hemothorax rarely occurs without a history of trauma and reveals grossly bloody fluid on drainage with elevated hematocrit on
analysis. Fever does not typically occur.
– A malignant effusion occurs when a primary neoplastic process results in the collection of exudative fluid containing malignant cells in
the pleural space. Leukocyte counts are usually and cytology demonstrates malignant cells.
– Uncomplicated parapneumonic pleural effusions, which can progress to empyema, have pH >7.2, slightly decreased to normal glucose,
and cell count Streptococcus pneumoniae is the most common cause in children; however, bacterial Gram stain and
culture are negative in parapneumonic effusions.
– Mycobacterium tuberculosis effusions typically present with chronic, rather than acute, symptoms. Although pleural fluid may show
low glucose and pH, leukocyte counts are with a lymphocytic predominance.

Physical Examinations and PFTs

Physical examinations and PFTs

Pulmonary auscultation examination findings
Breath sounds
Tactile Fremitus
Percussion
Mediastinal Shift
Normal Lung
·       Bronchial breathing centrally
·       Vesicular breathing peripherally
Resonance
ø
Consolidation (pneumonia)
⤴️
⤴️
dull
ø
Pleural Effusion
⤵️
⤵️
dull
Away from effusion
Pneumothorax
⤵️
⤵️
hyperresonance
Away from PTX
Emphysema
⤵️
⤵️
hyperresonance
ø
Atelectasis
⤵️
⤵️
dull
Toward atelectasis


PFT
#
Measures
🆎 in?
FVC
The difference between the volume of air in the lungs after maximal inspiration and after maximal expiration.
(Air in lung: maximal inspiration – maximal expiration)
COPD
FEV1
The maximum volume of air that can be forcefully expired within 1 second after maximal inspiration
COPD
RV
Residual volume in lung
⤴️ COPD
TLC
Total lung capacity
⤴️ COPD
VC
Vital capacity is the maximum amount of air a person can expel from the lungs after a maximum inhalation. 
⤵️  ILD + COPD
COPD
Restrictive
FEV1
⤵️
/ ⤵️
FVC
⤵️
FEV1/FVC
⤵️
/ ⤴️
VC
⤵️
⤵️
RV
⤴️
⤵️
TLC
⤴️
⤵️
Compliance
⤵️
Normal Spirometry
Obstructive
Restrictive
⤵️ DLCO
·       Anemia
·       PE
·       pHTN
 Emphysema
·       Interstitial lung disease
·       Sarcoidosis
·       Asbestosis
·       HF
DLCO
·        Chronic bronchitis
·       Asthma
·       MSK deformity
·       NM Disoder
⤴️ DLCO
·       Polycythemia
·       Pulmonary hemorrhage
 Morbid Obesity
Morbid Obesity