Respiratory Flashcards
Assessment of asthma control*
- Daytime symptoms >2x/ week
- Night waking
- Reliever use >2x/week
- Activity limitation
- Well controlled: none above
- Partly controlled: 1-2
- Poor controlled: 3-4
Step ladder for Asthma - GINA*
1 - symptoms <2/month
(Preferred: As needed low dose ICS-formoterol)
2 - symptoms >2/month, but less than daily
(Preferred: Daily low dose inhaled ICS/ As-needed low dose ICS-formoterol)
3 - symptoms most day/ waking with asthma >=1/week
(Preferred: Low dose ICS-LABA)
4 - symptoms most days/ waking with asthma >=1/week/ low lung function
(Preferred: Medium dose ICS-LABA)
5 - uncontrolled symptoms/ exacerbation
(Preferred: High dose ICS-LABA; Refer for specialist assessment of contributory factors +- add-on therapy eg: tiotropium, anti-IgE
Adjusting treatment for asthma*
> Step up
Assess the following before consider stepping up treatment:
i. Incorrect inhaler technique
ii. Poor adherence to medications
iii. Modifiable risk factors
iv. Symptoms due to co-morbid conditions
- Sustained step up (at least 2 - 3 months)-> persistent symptoms and/or exacerbations despite 2-3 months of controller treatment
- Short term step up (for 1 - 2 weeks) with written asthma action plan e.g. for during viral infection or allergen exposure
- Day-to-day adjustment by patient for those with mild asthma and on low dose ICS-formoterol as maintenance and reliever
> Step down
Indication: good asthma control for 3 months
Step down: reduce dosage of ICS by 25-50% at 2-3 month interval but never stop ICS unless the diagnosis is in doubt
Assessing the severity of acute asthma attack*
○ Severe attack § Unable to complete sentences in one breath § Respiratory rate >25/min § Pulse rate >110 beats/min § PEF 33-50%
○ Life-threatening attack § PEF <33% § Silent chest, cyanosis § Arrhythmia or hypotension § Exhaustion, confusion or coma § ABG: Normal/high PaCO2 >4.6kPa PaO2 <8Pa, or SaO2 <92%
Approach to acute exacerbation of Asthma
- Assess severity of attack
- Immediate treatment
- Supplemental O2 to maintain 94-98%
- Salbutamol 5mg nebulized with O2
- If severe + ipratropium 0.5mg/6h to nebulizers
- Hydrocortisone 100mg IV/ Prednisolone 40-50mg PO - Reassess every 15min
- If PEF <75% repeat Salbutamol nebulizer every 15-30min. Add ipratropium if not already given
- Monitor ECG; watch for arrhythmias - -> If not improving
- Refer ICU +- IV salbutamol
- > If improving
- Continue nebulized salbutamol every 4-6 hours
- Prednisolone 40-50mg PO OD for 5-7 days
What is FEV1, FVC and their normal value
- FEV1: the volume exhaled in the first second after deep inspiration and forced expiration (Normal: >80% predicted)
- FVC: the total volume of air that the patient can forcibly exhale in one breath (Normal: >80% predicted)
GOLD classification
COPD severity
- 1: Mild (FEV1 >= 80%)
- 2: Moderate (50-80)
- 3: Severe (30-50)
- 4: Very severe (<30)
MMRC Scale*
Grade of dyspnea
- 0: No except on strenous exercise
- 1: SOB hurrying on level/ walking up slight hill
- 2: Walk slower than same age/ stop for breath when walking at own pace on the level
- 3: Stop for breath after walking about 100m/ few minutes on the level
- 4: Too breathless to leave the house/ dressing
How to diagnose COPD
- Spirometry (FEV1/ FVC <70%, both pre and post bronchodilator)
X-ray sign for COPD**
- Hyperinflation
- Flat hemidiaphragm
- Large central pulmonary artery
- Decrease peripheral vascular marking
HRCT finding for COPD
- Bronchial wall thickening
- Scarring
- Air space enlargement
Medication for acute COPD attack
- Nebulized bronchodilator: Salbutamol 5mg/4h and ipratropium 500mcg/6h
- Controlled oxygen therapy if SaO2 <88% or PaO2 <7 kPa
- Steroids: IV hydrocortisone 200mg and oral prednisolone 30mg OD (continue for 7-14 days)
- Antibiotics: if evidence of infection, eg: amoxicillin 500mg/8h PO
- IV Aminophylline: if no response to nebulizer and steroids
Causes of Bronchiectasis***
> Congenital
- cystic fibrosis
- primary ciliary dyskinesia
> Acquired
- TB
- pneumonia
- bronchial obstruction (tumor, foreign body)
Signs of bronchiectasis*
- Clubbing
- Coarse inspiratory crepitation
- Wheeze
Investigation for bronchiectasis***
> Initial Ix
- CXR (tram-line, cystic lesion)
- Spirometry (variable, may show obstructive pattern)
> To diagnosed bronchiectasis
- HRCT (signet ring appearance)
> To find the cause
- Mantoux test
- Sweat test
- FBC
- Sputum culture
- Bronchoscopy (locate site of hemoptysis, exclude obstruction)
Management for bronchiectasis***
- Airway clearance technique and mucolytic
- Antibiotics
- Bronchodilators (eg: nebulized salbutamol)
- Corticosteroid (eg: prednisolone)
- Surgery (indicated in local disease or to control severe hemoptysis)
History directing to asthma diagnosis
- Wheeze, SOB
- Diurnal variation
- Response to exercise, cold air, allergen
- Symptoms after aspirin, B-blocker
- History/ Family Hx of atopy/ asthma
Light’s criteria
> Transudate
- Fluid/Serum protein <=0.5
- Fluid/Serum LDH <=0.6
> Exudate
- Fluid/Serum protein >0.5
- Fluid/Serum LDH >0.6
Definition of bronchiectasis**
- Irreversible abnormal dilatation of the bronchial tree
- Divide macroscopically into: cylindrical, varicose, cystic
- Main organism: H. influenzae, Strep. pneumoniae, Staph. aureus
Complications of bronchiectasis*
- Recurrent pneumonia
- Empyema
- Lung abscess
- Progressive respiratory failure
- Cor pulmonale
Physical signs expected in COPD**
> General
- Breathlessness
- Cachexia
- Malnourished
- Evidence of respiratory distress
> Respiratory
- Reduced chest expansion
- Reduced breath sound
- Loss of cardiac dullness, downward displacement of liver - hyperinflated lungs
- Coarse crepitation - sign of pneumonia
> Cardiovascular
- Raised JVP
- Right displacement of apex beat
- Parasternal heave
- Peripheral edema, hepatomegaly
Examination finding for pneumothorax**
○ Inspection
- Respiratory distress
○ General examination
- Raised JVP
- Distended neck veins
- Tracheal deviation away
○ Respiratory examination
- Reduced chest expansion
- Hyper-resonance
- Absent breath sound
CXR features of pneumothorax**
- Exaggerated radiolucency
- Loss of vascular marking
- Contralateral shift of the trachea and mediastinum
- Flattening of the ipsilateral diaphragm