Resp Flashcards

1
Q

Pneumonia: Criteria for hospitalization

A

CURB-65

  • Confusion: abbrev MT 7mmol/L
  • RR > 30
  • BP < 90 systolic

Score 0-1 = home
Score 2 = hospital therapy
Score >2 = severe pneumonia and may require ICU.

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2
Q

Community acquire pneumonia: organisms & empirical treatment

A

Organisms:

  • Streptococcus pneum.
  • Haemophilus Influenza

Treatment for mild:

  • Oral amoxicillin 500mg/8hr OR
  • Clarithromycin 500mg/12hrs

Treatment for moderate:
- IV amoxicillin + clarirthromycin at doses
above.

Treatment of severe case:

  • Co-amoxiclav 1.2g/12hr IV or cefuroxime
    1. 5g/8hrs AND clarithromycin 500mg/12hr IV
  • Add flucloxacillin if Staph suspected.
  • Add vancomycin if MRSA suspected.
  • Treat for 10 days.
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3
Q

Hospital acquired pneumonia: Organisms and treatment

A

Organisms

  • Gram negative bacillus
  • Pneudomonas
  • Anaerobes

Treatment:

  • Aminoglycoside IV + pipericillin (anti-
    pseudo) IV. OR
  • 3rd generation cephalosporin IV.
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4
Q

Aspiration pneumonia: organisms + treatment

A

Organisms:

  • Streptococcus
  • Anaerobes

Treatment:
- Cefuroxime 1.5g/8hr IV + metronidazole 500mg/8h IV.

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5
Q

Differential diagnosis of lung nodule on chest XRY

A
  • Primary or secondary malignancy
  • Abscess
  • Granuloma
  • Carcinoid tumour
  • Pulmonary hamartoma
  • AV fistula
  • Cyst
  • Foreign body
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6
Q

Management of acute asthma attack: According to clinical oxford guidelines

A
  1. Assess the severity of attack
    • ABC’s
    • Can the patient talk/complete
      sentences.
    • Level of consciousness
    • Silent chest
  2. Immediate treatment
    • Sit patient up
    • High dose O2 in 100% non-
      rebreathing bag.
    • Salbutamol 5mg + ipratropium
      bromide 0.5mg nebulized with
      oxygen.
    • Prednisalone 40-50mg IV or
      hydrocortisone 100mg IV.
    • CXR to exclude pneumothorax
  3. Life threating features present
    • Call for senior help
    • Mg 1.2-2mg IV over 2 minutes.
    • Salbutamol 5mg every 15 min => ECG
  4. Patient improving
    • Decrease O2 to 40-60%
    • Pred 40-50mg/24hrs PO for 5 days
    • Neb salbutomol q4hr
    • Monitor peak flow + O2 sats
  5. Patient not improving
    • Continue 100% oxygen
    • Salbutamol every 15 min
    • Continue Ipratropium bromide 0.5mg
      q4-6hrs.
  6. Still not improving
    • Mg if not already given.
    • Consider aminophylline: 5mg/kg IV
      loading; 500ug/kg/hr
    • Adjust according to plasma levels.
    • OR IV Salbutamol 3-20ug/min
    • IPPV
    • ITU
  7. Once patient has improved
    • Wean off aminophylline over 24hrs
    • Switch to inhaled B2 agonist
    • Stop IV steroids; start oral
    • Monitor PEF
    • Look for cause.
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7
Q

Signs of severe asthma attack

A
  • Unable to complete sentences
  • RR > 25
  • Pulse > 110
  • PEF < 50% of predicted
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8
Q

Signs of life threatening attack

A
-  Peak expiratory flow < 33% of predicted 
   or best.
-  Silent chest.
-  Cyanosis
-  Decreased respiratory effort
-  Bradycardia or hypotension
-  Exhaustion, confusion, coma
-  ABG:  PaCO2 > 4.6, PO2 < 8kPa/60mmHg
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9
Q

Salbutamol:

  1. MOA
  2. SE
  3. Method of adminitration
  4. Dose used in asthma
A
  1. Relax bronchial smooth muscle within
    minutes - short acting.
  2. SE: tachyarrhythmias, decreased K+,
    tremor, anxiety.
  3. Aerosol, powder, nebulizer, PO or IV.
  4. Inhaled aerosol 100-200ug/6hrs
    Inhaled powder 200-400ug/6hrs
    Nebulized (supervised) 2.5-5mg/6hrs
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10
Q

Salmeterol: Dose/puff and regimen

A

Inhaled aerosol
Dose/puff = 25ug
Recommended = 50-100ug/12hrs

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11
Q

Corticosteroids in asthma

  1. MOA
  2. SE
  3. Doses used in acute vs. long term
A

1 Act over days to decrease bronchial
mucosal inflammation.

  1. Oral candidasis - rise mouth after use
    SE from oral - cushingoid
  2. Oral steroids
    Acute: prednisolong 40mg/24hr po
    Long term: 5-10mg/24hrs poInhaled beclometasone
    Dose/puff = 50ug, 100ug or 250ug
    Recommended = 100ug/12hrs up to
    1000ug/12hrs
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12
Q

Aminophylline

  1. MOA
  2. SE
  3. Indications
A
  1. Metabolized to theophylline
    Inhibits phosphodiesterase = increases
    cAMP = decreases bronchoconstriction
  2. Arrhythmias, GI upset, seizures
  3. Used as an adjunct if inhaled therapy is
    inadequate; given at night PO may
    prevent morning dips; used IV in acute
    severe asthma attacks.
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13
Q

Ipratropium bromide

  1. MOA
  2. SE
  3. Indications
  4. Dose
A
  1. Anticholinergic - decreases muscle spasm
  2. Not recommended in guidelines for
    asthma
    Used in severe asthma attacks
    More benefit in COPD
4.  Aerosol : Dose/puff = 20ug
                   Regimen 20-40ug/6hr
     Powder:  Dose/puff = 40ug
                   Regimen 40-80ug/6hrs
     Nebulized: Doss/puff = 250ug/mL
                     Regmen = 250-500ug/6hrs
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14
Q

Define asthma

A
  • Obstructive lung disease
  • Characterized by
    1. Airway hypersensitivity,
    2. Reversible airflow obstruction
    3. Inflammation of bronchi
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15
Q

Classification of asthma

A
  1. Intermittent
    • Day time asthma symptoms occur
      less than 2x per week.
    • < 2 nocturnal awakenings per month
    • Use SABA < 2/week
    • No interference with daily activity
    • FEV1 > 80% of predicted normal
    • Normal FEV1/FVC
  2. Mild persistent
    • Symptoms more than twice per week.
    • 3-4 nocturnal wakings per mo
    • SABA use for more than 2x week
    • Minor interference with activities
    • FEV1/FVC normal
    • > 2 exacerbations requiring steroids
      per year.
  3. Moderate persistent
    • Daily symptoms
    • Nocturnal wakings > 1x week
    • Need BA daily
    • Limitation in normal daily activities
    • FEV1 = 60-80%
    • FEV1/FVC < normal
  4. Severe persistent
    • Symptoms of asthma throughout day
    • Nocturnal waking every night
    • Use SABA several times a day
    • Extreme limitations to daily activity
    • FEV1 < 60% of predicted
    • FEV1/FVC < normal
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16
Q

Basic principals in managing asthma

A
  1. Lifestyle and triggers
  2. Education on proper technique
  3. Pharmcology
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17
Q

Step wise approach to managing asthma

A
Step 1
-  For intermittent asthma
-  SABA
-  If need SABA more than 2x / week = step 
   up.

Step 2
- Mild persistent asthma
- SABA + low dose glucocorticoid
(<800mcg/day).

Step 3

  • Moderate persistent
  • SABA + inhaled corticosteroids
  • Add long acting B2 agonist
  • +/- leukotriene antagonist (montelukast)
  • +/- aminophylline
Step 4&5
- Severe persistent
- Inhaled glucocorticoids high dose (up to 
  2000mcg/day) + LABA
-  +/- leukotriene antagonist or 
   aminophylline
-  +/- Anti-IgE therapy = omalizumab } 
   consider for patients with allergies.

Step 6
- Below + oral steroids

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18
Q

Investigations for asthma

A
  • PFT: FEV1/FVC, PEFR
  • Bronchial provocation testing with
    histamine or metacholine.
  • Reversibility testing with B2 agonist }
    FEV1 should increase by 12%.
  • Diurinal varability
  • CXR for hyperinflation
  • CBC = eosinophilia
  • IgE = high
  • RAST test
  • Skin prick test
  • O2 sats = aim > 92%
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19
Q

Asthma: What indicates good control?

A
Well controlled
-  Less than 2 day time symptoms per 
   week.
-  No night time symptoms
-  Normal PEF

Partially controlled
- > 2 symptoms per week

Uncontrolled
- All of the above

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20
Q

Definition of COPD

A
- Characterized by irreversible airway 
  obstruction.
-  Two subtypes:  chronic bronchitis + 
   emphysema.
-  Characterized by a gradual decline in 
   FEV1 over years.
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21
Q

Chronic bronchitis:

  1. Definition
  2. Pathophys
  3. Signs & symptoms
  4. Chest XRY findings
  5. PFT
A
Chronic bronchitis
1. Productive cough on most days for at 
    least 3 consecutive months in 2 
    successive years.
    "Blue bloaters" - decrease alveolar 
     ventilation, hypoxic drive, low PaO2, 
     high PaCO2.
  1. Pathophys: obstruction due to narrowing of the airways lumen by mucosal thickening and excessive mucus production.
  2. Symptoms:
    • Chronic productive cough
    • Purulent sputum
    • Hemoptysis
    • Dyspnea
      Signs:
    • Cyanotic due to hypoexemia and
      hypercapnea.
    • RHF; cor pulmonale
    • Crackles; wheeze
    • Prolonged expiration
  3. Chest XRY: Normal AP diameter, increased bronchovascular markings, enlarged heart with cor pulmonale.
  4. PFT: Decrease FEV1/FVC, Normal TLC, normal Dco2.
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22
Q

Emphsema

  1. Definition & Pathophys
  2. Signs
  3. Symptoms
  4. Chest XRY findings
  5. PFT
A

Emphysema
1. Definition & pathophy:
- Dilation and destruction of air spaces
distal to the terminal bronchioles
without obvious fibrosis.

-  There is decreased elastic recoil => 
   causing air trapping and alveolar 
   collapse.

 -  Pink puffers - increased alveolar 
    ventilation, normal PaO2, normal/low 
    PaCO2.  Breathless but not 
   cyanosed.
  1. Symptoms
    • Dyspnea
    • Minimal cough
    • Tachypnea
    • Decreased exercise tolerance
  2. Signs
    • Pink skin
    • Accessory muscle use
    • Cachetic appearance due to anorexia &
      increased work of breathing.
    • Hyperinflation/barrel chest
    • Hyperressonant percussion note
    • Decreased breath sounds
    • Decreased diaphargmatic excursion.
  3. Chest XRY
    • Increased AP diameter
    • Flat hemidiaphragm = 6 ribs anteriorly
    • Decreased heart shadow
    • Bullae
    • Decreased vascular markings.
  4. PFTs
    • Decrease FEB1/FVC
    • Increase TLV = hyperinflation
    • Increase RV = gas trapping
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23
Q

Severity / Stages of COPD

A

FEV1 determines severity

  1. Stage I - Mild symptoms
    - FEV1/FVC < 70%
    - FEV1 > 80%
  2. Stage II - Moderate COPD
    - Symptoms on exertion
    - FEV1/FVC < 70%
    - FEV1 = 50-80%
  3. Stage III - Severe COPD
    - Symptoms on minimal
    exertion
    - FEV1/FVC < 70%
    - FEV1 30-50%
  4. Stage IV - Very severe COPD
    - Symptoms at rest
    - FEV1 < 30%
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24
Q

Treatment of COPD based on severity

A

Stage I - Mild

  • Stop smoking, influenza vaccine.
  • Inhaled ipratropium bromide preferred prn
  • Inhaled SABA prn

Stage II - Moderate

  • As above
  • Regular ipratropium bromide OR
  • Long acting B2 agonist

Stage III - Severe
- As above + add in inhaled steroids.

Stage IV - Very severe
- Long term home oxygen.

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25
Q

Indications for home oxygen therapy

A
  • PaO2 < 7.2 kPa
  • Clinically stable non smoker
  • PaO2 7.3-8 and pulmonary HTN + cor
    pulm
  • Terminally ill patient
26
Q

Acute exacerbation of COPD

  1. Definition
  2. Management
A

Acute exacerbation of COPD
1. Increased breathlessness, increased
sputum production.

  1. Managment
    - ABC
    - O2 24-28%
    - Aim for: PaO2 > 8kPa with rise in PaCO2
    not greater than 1.5kPa.
    - Nebulized salbutamol 5mg/4hr +
    impratropium bromide 500ug/6hrs
    - Steroids: IV hydrocort 200mg +
    PO prednisolone 30-40mg
    Continue for 7-14 days
  • Antibiotics if infection suspected
    Amoxicillin 500mg/8hr PO
  • Physio: sputum expectoriation
  • Not responding: Repeat nebulizer
    Consider aminophylline
  • NR: Consider nasal PPV if RR > 30
  • NR: Consider intubation/ventilation if CO2
    rising.
27
Q

Bronchiectasis

  1. Definition
  2. Signs and symptoms
  3. Findings: PFT & Chest XRY
  4. Principals in treatment
A
  1. Definition
    - Irreversible dilatation of airways due to
    inflammation and destruction of airway
    walls from persistently infected mucus.
    - Usually medium to small sized airways
    effected.
  2. Signs and symptoms
    - Chronic cough
    - Purulent sputum
    - Hemoptysis massive
    - Recurrent pneumonia
    - Local crackles = inspir + expir
    - Wheeze
    - Clubbing
    - Difficult to differentiate from chronic
    bronchitis
  3. Findings on investigation
    - PFT: Obstructive pattern
    - XRY: Linear atelectasis, loss of volume,
    honeycomb structures
  4. Treatment
    - Vaccination: influenza & pneumovax
    - Antibiotics
    - Inhaled steroids
    - Oral steroids for acute exacerbations
    - Chest physio
    - Pulmonary resection if necessary
28
Q

Definitions

  1. Hypoexemic
  2. Hypercapnic
A
  1. Hypoxemic
    • PaO2 < 60mmHg
    • PaO2 < 8kPa
  2. Hypercapnic
    • PaCO2 > 50mmHg
    • PaCO2 > 6kPa
29
Q

Signs of hypoxemia

A
  • Dyspnea
  • Restlessness
  • Agitation
  • Confusion
  • Central cyanosis
  • Polycythemia
  • Pulmonary hypertension
  • Cor pulmonale
30
Q

Signs of hypercapnia

A
  • Headache
  • Dyspnea
  • Drowsiness
  • Asteixis / flapping tremor
  • Warm peripheries
  • Plethora
  • Raised ICP
  • Tachycardia
  • Bounding pulses
31
Q

Causes of hypoxemia

A
  1. Low FiO2 = high altitude
  2. Hypoventilation
  3. Shunting
  4. Low mixed venous O2 content
  5. V/Q mismatch
32
Q

Causes of hypercarbia

A
  1. High inspired CO2
  2. Low total ventilation
  3. High deadspace ventilation
  4. High CO2 production - fever, sepsis
33
Q

Target O2 sat in COPD patients

A

COPD patients: Goal SaO2 88-92%

Everyone else: Goal SaO2 94-98%

34
Q

Type I respiratory failure:

  1. Definition
  2. Cause
  3. Treatment
A
  1. Definition:
    - Hypoxia: PaO2 < 8kPa
    - Normal or low PaCO2
  2. Cause
    - V/Q mismatch: asthma, COPD,
    pulmonary edema, PE
    - Shunt: alvelar collapse, intracardiac
    shunt, intrapulmonary shut = AVM
    - Low inspired O2: High altitude
  3. Treatment
    - Reverse pathology / underlying cause
    - Maintain oxygenation
    - Increase FiO2 Supplementing O2 won’t
    work if shunting is the problem

    - PEEF/CPAP: to recruit alveoli
35
Q

Type II respiratory failure

  1. Definition
  2. Cause
  3. Treatment
A
  1. Definition
    - PaCO2 increased = hypercapnia
    - PaO2 decreased = hypoxia
  2. Causes:
    - Increased CO2 production: fever, sepsis
    - Alveolar hypoventilation: COPD, asthma,
    chest wall disorder, CF.
    - Hypoventilation: Central = stroke
    Drugs = opiates, benzo
    NMJ = GB, MG, fatigue
  3. Treatment
    - Find and fix cause
    - Same as above - maintain oxygenation,
    mechanical ventilation if necessary.
36
Q

Differential diagnosis of hemoptysis

A
Resp causes:
-  Infectious: TB, lung abscess
-  Airway disease:  COPD, chronic 
   bronchitis, bronchiectasis.
-  Pulm vasc disease:  PHTN, vasculitis, 
   PE
-  Parencymal disease:  pneumonia, 
   wegener's, goodpastures
-  Malignancy

Cardiac causes:

  • MI
  • CHF
  • MS

Hem:

  • Anemia
  • Coagulopathy
37
Q

Definition of finger clubbing

A

Loss of the angle between the nail and nail fold. The nail fold feels boggy.

38
Q

Causes of finger clubbing

A

Respiratory causes:
- Lung ca, mesothelioma
- Chronic lung infection: bronchiectasis,
TB, empyema, abscess, cystic fibrosis.

GI:

  • IBD (especially Crohn’s)
  • Malabsorption = celiac
  • GI lymphoma
  • Cirrhosis

Cardiac:

  • Cyanotic heart disease
  • Endocarditis
  • Atrial myxoma
  • Aneurysms

Other:

  • Thyroid acropachy
  • Esophageal Ca.
39
Q

Normal values:pH, PaO2, PaCO2, HCO3

A

pH: 7.35-7.45
PaCO2: 4.7-6kPa ; 35-45mmHg
PaO2: >10.6kPa ; 75-100mmHg
HCO3: 24mEq/L

40
Q

Anion gap: Formula and when to calculate

A

If there is a metabolic acidosis - calculate the anion and osmolar gap.

AG: Na - [(CL + HCO3)] = 10-15 mmol/L

If the anion gap is increased - is the change in the AG the same as the change in bicarbonate? If no = mixed picture.

Osmolar gap = measure - calculated osmolarity = (2[Na] + glucose + urea) = normal 10

41
Q

Differential diagnosis of respiratory acidosis

A

**Characterized by increased PCO2 secondary to hypoventilation **

Resp center depression
-  Stroke
-  Drugs: opiates, sedatives, anesthesia
-  Raised ICP
-  Encephalitis
-  Central apnea
-  Supplemental O2 in CO2 retainers 
   (COPD)

Neuromuscular disorders

  • MG
  • GB
  • Poliomyositis
  • Muscular dystrophies
  • ALS
Lung disease
-  Airway obstruction: asthma, COPD, 
   foreign body
-  Parenchymal disease: pneumonia, 
  pneumothorax, pulm edema, ARDS

Other:
- Inadequate mechanical ventilation

42
Q

Differential diagnosis of respiratory alkalosis

A

Characterized by decreased PaCO2 secondary to hyperventilation

Hypoxemia

  • Pneumonia, PE, edema
  • Severe anemia
  • Heart failure
  • High altitude

Resp center stimulation

  • CNS disorders
  • Hepatic failure
  • Drugs: stimulants, ASA, catecholamines
  • Pregnancy
  • Anxiety
  • Pain

Other cause:
- Mechanical hyperventilation

43
Q

Causes of anion gap metabolic acidosis

A
MUDPILES
Methanol
Uremia
DKA/starvation/alcoholic
Paraldehyde
Isopropyl alcohol/Iron/INH
Lactic acidosis
Ethylene glycol
Salicylates
44
Q

Causes of non-anion gap metabolic acidosis

A
HARDUP
Hyperailmentation
Acetazolamide
RTA**
Ureteroenteric fistual
Pancreaticoduodenal fistula increased
45
Q

Causes of metabolic alkalosis

A
  • Vomiting = loss GI H+
  • Exogenous alkali syndrome
  • Milk alkali syndrome
  • Diuretics = contraction alkalosis
  • Post hypercapnea
  • Hyperaldosterisms
  • Hypokalemia
46
Q

Interstitial lung disease

  1. Pathophy
  2. Causes of ILD by lung field effects
A
  1. Pathophy
    - Inflammatory process in the alveoli that
    results in thickening, destruction and
    fibrosis.
    - Restrictive lung disease
    - Decreased lung compliance & lung
    volumes.
  2. Upper lung disease
    • Farmers lung
    • Ankylosing spondylitis
    • Sarcoidosis
    • Silicosis
    • TB
    • Neurofibromatosis
     Lower lung disease
     -  Asbestosis
     -  Drugs: nitrofurantoin, amiodarone, 
        chemo
     -  Rhematological disease
     - Scleroderma
47
Q

Interstitial lung disease: Cause based on known and unknown etiology

A

Unknown etiology

  • Idiopathic pulmonary fibrosis
  • Sarcoidosis
  • Histocytosis X
ILD associated with known systemic disease
Rheumatological
-  Scleroderma
-  Rhematoid arthritis
-  SLE
-  Mixed CTD

Enviro/occupational

  • Farmers lung
  • Bird lung
  • Air conditioners
  • Silicosis
  • Asbestosis
  • Coal workers pneumoconiosis
  • Berylliosis

Drugs

  • Nitrofurantoi
  • Methotrexate
  • amiodarone
  • Chemotherapy
  • Ampetamines
  • Radiation

Pulm vasclitis

  • Wegeners
  • Churg strauss
  • Hypersensitivity reaction

Inherited disorders

  • Neurofibromatosis
  • Tuberous sclerosis
  • Gauchers disease
48
Q

Clinical features of interstitial lung disease

A
  • Dyspnea on exertion
  • Non productive cough
  • Abnormal breath sounds
  • Fine end inspiratory crepitations PF
  • Weight loss
  • Arthralagia (depending on type)
  • Restrictive pattern on PFTs
  • Decreased DL due to loss of SA for gas
    exchange.
49
Q

Pleural effusions:

  1. Lights criteria: transudate vs exudate
  2. Cause of transudate
  3. Cause of exudate
A
1.  Lights criteria
Transudate:  Protein [P/S] < 0.5
                   LDH [P/S] < 0.6
                   Pleural LDH < 2/3 upper limit 
                   of N serum LDH

Exudate Protein [P/S] > 0.5
LDH [P/S] > 0.6
Pleural LDH > 2/3 upper limit
of N serum LDH

  1. Cause of transudate
    - CHF
    - Cirrhosis
    - Nephrotic syndrome
    - Pulmonary embolism
    - Hypothryoidism
  2. Causes of exudate
    - Infectious: pneumonia, parapneumonic
    effusion, empyema.
    - Malignancy
    - Inflammatory: collagen vascular disorder,
    RA, SLE, pulmonary embolism
    - Intra-abdo: Meigs syndrome,
    pancreatitis, esophageal rupture.
    - Trauma
50
Q

Pleural fluid analysis: Protein, glucose, pH, cytology

A

Protein content

  • < 30g/L = transudate
  • > 30g/L = exudate
  • Between 25-35g/L use Lights criteria

Glucose content
- < 3.3 mmol/L = malignancy, TB, RA

pH < 7.2 = infection or malignancy, requires drainage.

Cell types
-  Neutrophilia = infection
-  Lymphocytes = TB, lymphoma, 
   malignancy
-  RBC = trauma, cancer, lymphoma
51
Q

Classification of pleura effusion: simple vs complication

A

Simple effusion:
pH > 7.2, LDH < 1/2 serum, glucose > 2.2

Complicated
pH < 7.2, LDH > 1/2 serum, glucose < 2.2, positive gram stain = needs drainage

52
Q

Differential diagnosis of solitary pulmonary nodule

A

Nodule is defined as being < 3cm
Mass > 3cm

  • Infectious granuloma
  • Abscess
  • Aspergilloma
  • Hamartoma
  • Bronchiogenic cyst
  • Fibroma
  • AVM
  • Rheumatoid nodule
  • Sarcoidosis
  • Primary lung ca
  • Secondary lung ca
  • Pulmonary carcinoid
53
Q

Features of benign vs. malignant pulmonary nodule

A

Benign pulmonary nodule

  • < 3cm, round, regular
  • Smooth
  • Calcified pattern
  • Doubles in > 2 years

Malignant pulmonary nodule

  • > 3cm, irregular, spiculated
  • Ill defined or noticed
  • NOT calcified
  • Doubles in < 1 month or < 2 years.
54
Q

Paraneoplastic syndrome associated with small cell carcinoma of lung “oat cell”

A
  • ACTH = cushing
  • SIADH
  • Eaton Lambert
55
Q

Paraneoplastic syndrome associated with NSC lung cancer

A

Squamous cell carcinoma

PTH-related peptide = hypercalcemia + hypophosphatemia

56
Q

Pleural effusions: amount of fluid required before it can be detected clinically

A

500mL

57
Q

Signs and symptoms of PE

A

Symptoms:

  • Acute breathlessness
  • Pleuritic chest pain
  • Hemoptysis
  • Dizziness
  • Collapse

Signs:

  • Pyrexia
  • Tachycardia
  • Tachpnea
  • Hypotension
  • Raised JVP
  • Pleural rub
  • Pleural effusion
58
Q

Wells score for investigating a suspected DVT

A

Risk factors

  • Active cancer (1)
  • Paralysis/immobility (1)
  • Major surgery (1)

Clinical signs

  • Tenderness along leg (1)
  • Entire leg swollen (1)
  • Calf circumference > 3cm (1)
  • Pitting edema (1)
  • Collateral superficial veins visible (1)

Other:
- Alternative as likely or more likely than
DVT (-2)

59
Q

Investigation of PE

A
  • CXR
  • ABG: decreased PaO2 and PaCO2
  • ECG: S1Q3T3 pattern
  • D-dimers: High sen, low spec
    Can exclude PE if normal in
    low risk patient.
  • CTPA: Sen & spec; First line
  • V/Q scan: If CXR normal and no lung
    disease.
  • Bilateral venograms
60
Q

Management of Pulmonary Embolus

A
  • Give 100% oxygen
  • Morphine 10mg for pain relief
  • If critically ill with passive PE consider
    immediate thrombolysis (50mg Alteplase)
  • IV access
  • SC LMWH: Dalteparin 200U/kg o.d
    Enoxaparin 1mg/kg bid
    No lab monitoring
    Avoid in renal failure
  • UF Heparin IV: 10,000U bolus
    Then 18U/kg/h guided by
    aPTT
  • Systolic BP: > 90 = Warfarin 10mg od
    < 90 = 500mL colloid
    Dobutamine 2.5-
    10ug/kg/min
  • Continue warfarin and heparin for 5 days
    or until INR 2-3.
61
Q

Duration of anti-coagulation following PE

A
  • If reversible cause = 3-6 mo
  • PE unprovoked = 6mo to indefinite
  • Ongoing risk present = indefinite