Respiratory Flashcards

1
Q

Aetiology Bronchiectasis

A
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2
Q

Complications of Bronchiectasis

A

Cor Pulmonale
Pneumonia
Empyema
Lung abscess
AA Amyloidosis
Cerebral abscess

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3
Q

Investigations for Bronchiectasis

A

-HRCT -> Confirms diagnosis
-Sweat chloride / immotile cilia function in young adults
- Eosinophil level (ABPA)
- Immunoglobulin levels - Sptum MCS
- PFT (FEV 1 affected in severe disease)
- ABG

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4
Q

Management Bronchiectasis

A
  • Treatment of infections
  • Long term azithromycin
  • Inhaled tobramycin
  • Bronchodilators / ICS if bronchial reactivity
  • Chest wall physio (postural drainage and PEEP)
  • Vaccination
  • Surgery for localised disease
  • Transplant
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5
Q

MRC Breathlessness Scale

A

0 - Only with strenuous exercise
1- When hurrying or walking uphill
2- When walking at own pace
3- Walking ~100m
4- When undressing / too breathless to leave house

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6
Q

Radiographic Types of Emphysema

A
  • Centrilobular (most common) involves proximal respiratory bronchioles in upper lobes
  • Panlobular involves secondary bronchioles predominately lower lobes (seen in A1ATD)
  • Paraseptal involves peripheral areas. Assoc with bullous emphysema / smoking
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7
Q

ECG findings COPD

A

1) Right ventricular hypertrophy ( Prominent R wave V1, TWI V1-2, RAD)
2) Multifocal atrial tachycardia

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8
Q

COPD and flying?

A

During flight equivalent Fi02 is ~15%

If patients Sats ate <95% supplemental oxygen will be needed.

If sats 88-95% then should have an altitude simulation test prior to flying.

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9
Q

Smoking Cessation

A
  • Ask
  • Assess motivation and nicotine dependance
  • Advise to quit
  • Assist with smoking cessation
    -Ensure follow up

Treatments:
- Non-pharmacological using QUIT helpline, hypnotherapy, counselling
- Varenicicline (Champix) which acts as partial nicotine agonist.
S/E: mood changes and suicidal thoughts
- Nicotine replacement therapy
- Bupropion
S/E: seizures

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10
Q

COPD Criteria Lung transplant?

A
  • FEV1 <25%
  • PaCO2 >55
  • Complications including cor pulmonate
  • Age <65yoa
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11
Q

Sleep apnoea exam

A

-Pharyngeal crowding
-Raised BMI
-Signs of pulmonary hypertension (loud p2, parasternal heave)
-Signs of acromegaly / hypothyroidism

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12
Q

Benefits of CPAP in OSA

A
  • Safe driving
  • Reduced sleepiness
  • Better QOL
  • Better cognition
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13
Q

Methotrexate and lungs

A
  • <5% of persons
  • No correlation between dose and severity of condition
  • Occur at any time during treatment
  • Resolves with withdrawal
  • May require steroids
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14
Q

Causes of idiopathic pulmonary hypertension

A
  • Idiopathic
  • Inherited (BMPR2)
  • Assoc Connective tissues disease
  • HIV
  • Cirrhosis / portal hypertension related
  • Chronic haemolytic anaemia
  • Shchistosomiasis
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15
Q

Clinical signs of Pulmonary Hypertension

A

Loud P2
Palpable P2
Large A wave
Larve V wave (if Concurrent tricuspid regurgitation)
Parasternal impulse

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16
Q

Pulmonary Hypertension

A

CXR -> Large pulmonary arteries with pruning in periphery +/- Right ventricular hypertrophy
PFT -> Isolated low DLCO
ECG -> Right heart strain, P Pulmonale
Bood Gas ->
VQ -> Rule out CTEPH
HRCT -> Rule out IPD
TTE
Six minute walk test -> <330 metres confers poor prognosis

17
Q

Clinical manifestations Sarcoid

A
  • Asymptomatic hilar adenopathy
  • Generalised symptoms: fever, lethargy, cough, dyspnoea
  • Pulmonary fibrosis (upper zone predominant)
  • Skin erythema nodosum
  • Polyarthralgia
  • Uveitis
  • Hypopituitarism
  • Cardiac conduction abnormalities (CHB and VT)
  • Facial nerve palsy or Peripheral neuropathy
  • Hypercalcaemia
18
Q

Clinical signs Sarcoidosis

A
  • Uveitis
  • Parotitis
  • Generalised lymphadenopathy
  • Lupus pernio
  • End inspiratory crackles
  • Erythema nodosum
  • Facial nerve palsy
  • Hepato / Splenomegaly
19
Q

Management of sarcoidosis

A

If evidence of detrimental end-organ involvement give prednisolone 1mg/Kg daily for 6 weeks then taper over 6 months.

Steroids sparing agents MTX, AZA

20
Q

Physiotherapy treatment for Cystic Fibrosis

A

Postural drainage
Positive End Expiratory devices
Percussion
Deep breathing exercises
Pulmonary Rehabilitation

21
Q

Clinical signs Cystic Fibrosis

A

Prolonged Forced Expiratory Time >6 seconds
Barrell chest
Clubbing
Wheeze, local crackles
Muscle wasting
Faecal loaded colon
Right heart failure secondary to pulmonary HTN

22
Q

CF investigations

A

Sputum MCS
CXR
FBC -> May be anaemic
Fat soluble Vitamins (ADEK) due to concurrent pancreatic insufficiency
Spirometry: FEV1 <40% confers poor prognosis

23
Q

Cystic Fibrosis management

A
  • Ivacaftor / Tezacaftor
  • Chest Physiotherapy **Very important
  • Tune ups for IV antibiotics according to sputum MCS
  • Azithromycin as anti-inflammatory
  • Bronchodilators
  • Home oxygen
  • DNAse mucolytic
  • Lung transplant
  • ** Pancreatic enzyme replacement
  • Regular aperients to avoid constipation
24
Q

Tuberculosis Treatment

A

Active TB:
- 2 months RIPE
- 4 months RI
* Ensure smear negative at conclusion of treatment

Latent TB:
- Treat in high risk groups
> HIV
> Less than 35yo
> Contact with smear positive patient
> Health care worker
> About to receive immunosuppressive drugs
- Isoniazid 9 months
- 3 Months RI
- Rifampicin 4 months

25
Q

Most common indications lung transplant

A

Pulmonary Hypertension
COPD
Eisenmengers
Cystic fibrosis

26
Q

Indications and Contraindications for Lung Transplant

27
Q

Bronchiolitis Obliterans

A

Chronic damage and obstruction of small airways seen in chronic rejection post transplant.

Manifest as gradual development of dyspnoea, fatigue and cough.

Accompanied slow decline in FEV1

Treat: agressive immunosuppresion steroids / ATG

28
Q

Acute Lung Rejection

A

Fever, breathlessness, pulmonary infiltrates, declining FEV1

Diagnose on Bronchoscopy and transbronchial biopsy

Treatment: High dose steroids

29
Q

Causes of Clubbing

A

Bronchiectasis
Cystic fibrosis
Bronchogenic Carcinoma
Interstitial lung disease
Cyanotic congenital heart disease
Infective endocarditis
Inflammatory bowel disease
Primary biliary Cirrhosis
Hypothyroidism

30
Q

Causes of tracheal deviation

A

Upper lobe fibrosis (towards side deviation)
Mediastinal lesion (Retrosternal goitre)
Tension pneumothorax
Pneumonectomy (towards deviation)
Large Pleural effusion (away)

31
Q

Stooped Posture

A

May indicate Ankylosing Spondylitis -> Upper lobe fibrosis

32
Q

Bronchial breath sound

A

Harsh blowing quality, inspiration equal to expiration with pause between respiration.

Causes: lobar pneumonia, above pleural effusion, localised fibrosis.

33
Q

Wheeze

A

Expiratory wheeze: Asthma or COPD
Fixed inspiratory wheeze: Bronchogenic carcinoma

34
Q

Crackles

A

Late or Paninspiratory Crackles
Fine: Fibrosis
Medium: Pulmonary Oedema
Coarse: Bronchiectasis

Early inspiratory coarse crackles: COPD

35
Q

Cavitating Lung lesion

A

TB
Carcinoma (Especially squamous cell)
Aspergilloma
Lung Abscess