Respiratory Flashcards

1
Q

Pneumonia

Aetiology (4)

A

Community acquired pneumonia: primary or secondary to underlying disease, Strep pneumoniae –> Haemophilus influenzae –> Mycoplasma pneumoniae –> viruses account for 15%
Hospital acquired (nosocomial, >48hr after admission): gram -ve or Staph aureus
Aspiration: stroke, reduced consciousness, oesophageal disease
Immunocompromised patients

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2
Q

Pneumonia

Signs + Symptoms (12)

A
Malaise 
Fever
Riggers
Dyspnoea
Cough and purulent sputum 
Haemoptysis 
Pleuritic chest pain 
Cyanosis 
Confusion (may be only sign in elderly) 
Hypotension 
Signs of consolidation: reduced expansion, dull percussion, increased vocal resonance, bronchial breathing 
Pleural rub
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3
Q

Pneumonia

Investigations (5)

A

CXR: lobar/multilobular infiltrates, pleural effusion
Assess saturation: O2 sats, ABG if severe, BP
Bloods: FBC, U&E, LFT, CRP, blood culture
Sputum: microscopy + culture
Legionella (sputum culture and urinary antigen) if severe

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4
Q

Pneumonia

Severity (8)

A
Confusion (abbreviated mental test <8) 
Ureal (>7mmol/l) 
Respiratory rate (>30/min) 
BP (<90 systolic or <60 diastolic) 
Age >65 

0-1: home with/without treatment
2: hospital therapy
3+: severe, consider ITU

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5
Q

Pneumonia

Treatment (7)

A

CURB 0-1: oral amoxicillin or clarithromycin or doxycycline
CURB 2: oral amoxicillin + clarithromycin or doxycycline (IV may be required)
CURB 3+: co-amoxiclav IV or cephalosporin IV and clarithromycin IV, add flucloxacillin +/- rifampicin if Staph suspected or vancomycin if MRSA suspected
Analgesia for pleurisy
O2 if sats <94%
IV fluids
VTE prophylaxis

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6
Q

Pneumonia

Complications (5)

A

Respiratory failure: aim sats 94-98%
Hypotension: due to dehydration and vasodilatation, give IV fluids
Pleural effusion: inflammation of pleura by adjacent pneumonia causing fluid exudation into pleural space
Empyema: pus in pleural space, suspect in patients with resolving pneumonia developing fever
Lung abscess
Septicaemia

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7
Q

Cystic Fibrosis

Aetiology (3)

A

Mutations in CFTR gene on chromosome 7
Cl- channel defect leads to defective chloride secretion and increased sodium absorption across airway epithelium
Autosomal recessive

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8
Q

Cystic Fibrosis

Signs + Symptoms (7)

A

In neonates: failure to thrive, meconium ileum, rectal prolapse
Cough
Wheeze
Recurrent infections
Cor pulmonale
Pancreatic insufficiency (diabetes, steatorrhoea)
Male infertility

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9
Q

Cystic Fibrosis

Investigations (5)

A
Sweat test: sodium + chloride >60mmol/l
Genetics screen 
Heel prick test (5 days old) 
CXR: hyperinflation, bronchiectasis 
Spirometry: obstructive pattern
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10
Q

Cystic Fibrosis

Treatment (7)

A

Regular chest physio
Antibiotics for acute infective exacerbations and prophylaxis
Mucolytics eg. DNase
Bronchodilators
Pancreatic enzyme replacement
Vitamine supplements (ADEK)
If advanced: non-invasive ventilation/transplant

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11
Q

Cystic Fibrosis

Common bacterial infections (2)

A

Pseudomonas aeruginosa in adulthood

Staph aureus + H.influenzae in children

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12
Q

Bronchiectasis

Definition (1)

A

Chronic infection of the bronchi and bronchioles leading to permanent dilation

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13
Q
Bronchiectasis
Main organisms (4)
A

H. influenzae
Strep pneumoniae
Staph aureus
Pseudomonas aeruginosa

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14
Q

Bronchiectasis

Aetiology (4)

A

Congenital: CF
Post infection: pneumonia, TB, HIV
Bronchial obstruction: tumour, foreign body
Allergic bronchopulmonary aspergillosis

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15
Q

Bronchiectasis

Signs + Symptoms (4)

A

Persistent cough and sputum
Finger clubbing
Coarse inspiratory crepitations
Wheeze

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16
Q

Bronchiectasis

Complications (3)

A

Pneumonia
Pleural effusion
Pneumothorax

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17
Q

Bronchiectasis

Investigations (6)

A

Sputum culture
CXR: thickened bronchial walls
HRCT chest: assess extent and distribution of disease
Spirometry: obstructive pattern
Bronchoscopy: obtain samples, exclude obstruction
CF sweat test

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18
Q

Bronchiectasis

Treatment (5)

A
Postural drainage 
Chest physio 
Antibiotics 
Bronchodilators if asthma, COPD, CF, allergic bronchopulmonary aspergillosis 
Corticosteroids if ABPA
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19
Q

Pulmonary Aspergillus Infection

Effects of Aspergillus on the lung (5)

A

Asthma (type 1 hypersensitivity to fungal spores)
Allergic bronchopulmonary aspergillosis (causes bronchiectasis, give steroids)
Aspergilloma (fungus ball within pre-existing cavity)
Invasive aspergillosis
Extrinsic allergic alveoli’s

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20
Q
Lung Cancer
Risk factors (3)
A

Smoking
Asbestos
Radiation

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21
Q

Lung Cancer

Pathology (2)

A

Non-Small Cell Lung Cancer: squamous, adenocarcinoma, large cell undifferentiated
Small Cell Lung Cancer: endocrine

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22
Q

Lung Cancer

Signs + Symptoms (8)

A
Cough 
Haemoptysis 
Dyspnoea 
Chest pain 
Weight loss 
Anaemia 
Clubbing 
Metastatic signs (bone tenderness, hepatomegaly, confusion, fits)
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23
Q

Lung Cancer

Sites of metastatic spread (4)

A

Liver
Adrenal glands
Brain
Bone

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24
Q

Lung Cancer

Complications (3)

A

Recurrent laryngeal nerve palsy
Phrenic nerve palsy
SVC obstruction

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25
Lung Cancer | Investigations (6)
Cytology: sputum and pleural fluid CXR: hilar enlargement, consolidation, collapse, pleural effusion Fine needle aspiration or biopsy of peripheral lesions/superficial lymph nodes CT: staging PET: staging Bronchoscopy: to give histology and assess operability
26
Lung Cancer | Staging (11)
T1: <3cm T2: >3cm T3: close to carina or involving chest wall/diaphragm T4: involves carina, mediastinum, heart, great vessels, trachea, oesophagus N0: no nodes N1: peribronchial and/or ipsilateral hilum N2: ipsilateral mediastinum N3: contralateral M0: none M1a: in other lung M1b: distant metastases
27
Lung Cancer | Treatment (3)
NSCLC: stage 1/2 surgery, curative radio if respiratory reserve is poor, chemo +/- radio if advanced SCLC: chemo but relapse rate high and mortality high Palliation: radio for bronchial/SVC obstruction or haemoptysis
28
Lung Cancer | Prognosis (2)
NSCLC: 50% 2 year survival without spread, 10% with spread SCLC: survive 3 months if untreated, 1-1.5 years if treated
29
Acute Respiratory Distress Syndrome | Definition (2)
May be due to direct lung injury or secondary to severe systemic illness Lung damage and release of inflammatory mediators cause increase in capillary permeability and pulmonary oedema, often associated with multi organ failure
30
Acute Respiratory Distress Syndrome | Aetiology (4)
Pulmonary: pneumonia, injury, inhalation Shock Haemorrhage Septicaemia
31
``` Acute Respiratory Distress Syndrome Risk Factors (6) ```
``` Sepsis Hypovolaemic shock Trauma Burns and smoke inhalation Diabetic ketoacidosis Pneumonia ```
32
Acute Respiratory Distress Syndrome | Signs + Symptoms (5)
``` Cyanosis Tachypnoea Tachycardia Peripheral vasoldilatation Bilateral inspiratory crackles ```
33
Acute Respiratory Distress Syndrome | Investigations (3)
Bloods: FBC, U+E, LFT, amylase, clotting, CRP, blood cultures ABG CXR: bilateral pulmonary infiltrates
34
Acute Respiratory Distress Syndrome | Treatment (5)
Admit to ITU Respiratory support: CPAP/mechanical ventilation Circulatory support: inotropes (eg. dobutamine), vasodilators, transfusion Sepsis: identity organism and treat accordingly Steroids for subacute
35
Asthma | Definition (1)
Recurrent episodes of dyspnoea, cough and wheeze caused by reversible airway obstruction
36
Asthma | Pathology (3)
Bronchial muscle contraction, triggered by a variety of stimuli Mucosal swelling/inflammation, caused by mast cel and basophil degranulation resulting in release of inflammatory mediators Increased mucus production
37
Asthma | Symptoms (6)
Intermittent dyspnoea, wheeze, cough (often nocturnal) and sputum Precipitants: cold air, exercise, allergens (home dust mite, pollen, fur), smoking, B-blockers Diurnal variation Disturbed sleep Acid reflux Other atopic disease eg. eczema, hay fever
38
Asthma | Signs (7)
Tachypnoea Wheeze Hyperinflated chest Hyperresonant percussion Severe attack: inability to complete sentences, pulse >110bpm, RR >25 Life-threatening attack: silent chest, confusion, exhaustion, cyanosis, bradycardia Near fatal: high PaCO2
39
Asthma | Investigations for chronic (4)
PEF monitoring Spirometry: obstructive defect (low FV1/FVC) CXR: hyperinflation Skin prick test may help identify allergens
40
Asthma | Investigations for attack (5)
``` PEF Sputum culture Bloods: FBC, U&E, CRP, cultures ABG CXR: to exclude infection/pneumothorax ```
41
``` Asthma Chronic treatment (5) ```
Step 1: SABA as required (unless using MART), consider starting low-dose ICS Step 2: regular preventer (low-dose ICS) + SABA as required Step 3: initial add-on therapy (add inhaled LABA to low-dose ICS- fixed dose or MART) + SABA as required Step 4: additional controller therapies (increase ICS to medium dose or add LTRA), if no response to LABA then stop + SABA as required Step 5: specialist therapies (high dose ICS + oral steroids)
42
Asthma | Treatment of attack (4)
Immediate treatment: nebulised salbutamol, IV hydrocortisone +/- oral prednisolone, start O2 if sats <92% If life-threatening: salbutamol nebulisers every 15 minutes, add ipratropium to nebulisers, single dose IV magnesium sulfate If no improvement: consider ventilatory support and intensification of medical therapy eg. aminophylline, IV salbutamol (ITU) If improving within 15-30 mins: nebulised salbutamol every 4 hours, prednisolone oral for 5-7 days
43
COPD | Definition (2)
Progressive disorder characterised by airway obstruction with little/no reversibility FEV1 <80%
44
COPD | Pathology (1)
Chronic bronchitis (clinical diagnosis- cough + sputum) + emphysema (histological diagnosis- enlarged air spaces distal to terminal bronchioles with destruction of alveolar walls)
45
``` COPD Pink puffers (5) ```
``` Increased alveolar ventilation Near normal PaO2 Normal/low PaCO2 Breathless but not cyanosed May progress to type 1 respiratory failure ```
46
``` COPD Blue bloaters (5) ```
``` Reduced alveolar ventilation Low PaO2 High PaCO2 Cyanosed but not breathless May develop cor pulmonale ```
47
COPD | Signs + symptoms (6)
``` Cough + sputum Dyspnoea + tachypnoea Wheeze Use of accessory muscles of respiration Reduced expansion Resonant percussion ```
48
COPD | Complications (5)
``` Acute exacerbations +/- infection Respiratory failure Cor pulmonale Pneumothorax Lung cancer ```
49
COPD | Investigations (5)
CXR: hyperinflation, flat hemidiaphragms, bullae ECG: cor pulmonale ABG: low PaO2 +/- hypercapnia Spirometry: obstructive pattern (FEV1 <80% of predicted) Trial of steroids
50
COPD | Severity (4)
Stage 1 mild: FEV1 >80% of predicted Stage 2 moderate: FEV1 50-79% of predicted Stage 3 severe: FEV1 30-49% of predicted Stage 4 very severe: FEV1 <30% of predicted
51
COPD | Treatment of stable COPD (5)
General: stop smoking, pulmonary rehav, vaccinate against influenza, SAMA (ipratropium)/SABA Mild/moderate: LAMA (tiotropium) Severe: LABA + corticosteroids (eg. Symbicort- budesonide + formoterol) or tiotropium If still symptomatic: tiotropium + ICS + LABA, refer to specialist, consider steroid trial, home nebulisers, theophylline, long term O2 therapy Indications for specialist referral: rapid FEV1 decline, cor pulmonale, assessment for oral corticosteroids/nebulisers/home O2
52
COPD | Treatment of acute exacerbation (6)
Nebulised bronchodilators (salbutamol, ipratropium) O2 therapy IV hydrocortisone + oral prednisolone Antibiotics if infection: amoxicillin, clarithromcyin, doxycycline If no response to nebulisers + steroids, consider IV aminophylline If no response: non-invasive ventilation --> intubation + ventilation
53
Pulmonary Embolism | Aetiology (2)
Venous thrombosis in pelvis/legs pass through veins and right side of heart before lodging in the pulmonary circulation Right ventricular thrombus (post MI)
54
``` Pulmonary Embolism Risk factors (7) ```
``` Recent surgery Thrombophilia Leg fracture Prolonged bed rest/reduced mobility Malignancy Pregnancy, post-partum, OCP, HRT Previous PE ```
55
Pulmonary Embolism | Signs + symptoms (8)
``` Acute breathlessness Pleuritic chest pain Haemoptysis Dizziness/syncope Cyanosis Tachypnoea + tachycardia Hypotension Raised JVP ```
56
Pulmonary Embolism | Investigations (6)
Bloods: FBC, U&E, baseline clotting, D-dimer (high sensitivity but low specificity) CXR: may be normal or show dilated pulmonary artery CTPA: 1st line imaging ABG: low PaO2, low PaCO2 V/Q scan: rarely done ECG: normal, tachycardia, right bundle branch block, SIQIIITIII pattern (deep S waves in I, pathological Q waves in III, inverted T waves in III)
57
Pulmonary Embolism | Treatment (7)
Oxygen Morphine IV unfractionated heparin or SC LMWH If systolic <90 start colloid infusion but if remains low consider IV noradrenaline If systolic >90 start warfarin If PE is massive then thrombolyse (alteplase) Stop heparin when INR >2 and continue warfarin for minimum 3 months
58
Pneumothorax | Aetiology (4)
Spontaneous primary: weight of lung inducing apical blebs that rupture Spontaneous secondary: pre-existing disease, eg. CF, COPD Traumatic non-iatrogenic: penetrating or blunt injury Traumatic iatrogenic: pleural aspiration/biopsy, subclavian vein cannulation
59
Pneumothorax | Pathology (1)
Breach of visceral/parietal pleura with entry of air, lung collapses due to elastic recoil
60
Pneumothorax | Signs + symptoms (7)
``` Asymptomatic if small Acute breathlessness Pleuritic chest pain Reduced breath sounds Tracheal deviation (non tension to affected side, tension away from affected side) Reduced expansion Hyperresonant percussion ```
61
Pneumothorax | Treatment (3)
Tension: chest drain 2nd intercostal space Chest drain if any trauma For others try aspirating before chest drain
62
Pleural Effusion | Definition (3)
Fluid in the pleural space Transudates <30g/l protein conc. Exudates >30g/l protein conc.
63
Pleural Effusion | Aetiology (2)
Transudates: increased venous pressure (cardiac failure, fluid overload), hypoproteinaemia (cirrhosis, nephrotic syndrome) Exudates: increased leakiness of pleural capillaries secondary to infection, inflammation or malignancy (pneumonia, TB, RA, SLE)
64
Pleural Effusion | Signs + symptoms (8)
``` May be asymptomatic Dyspnoea Pleuritic chest pain Reduced expansion Stony dull percussion note Reduced breath sounds Reduced vocal resonance If large, tracheal deviation away from effusion ```
65
Pleural Effusion | Investigations (4)
CXR: effusions visible Ultrasound: identifies pleural fluid Diagnostic aspiration Pleural biopsy if aspiration inconclusive
66
Pleural Effusion | Treatment (3)
Drainage if symptomatic Pleurodesis for recurrent effusions Surgery for persistent collections and increasing pleural thickness
67
``` Sarcoidosis Definition (1) ```
Multisystem granulomatous disorder of unknown cause
68
``` Sarcoidosis Risk factors (3) ```
Age 20-40 Women Afro-Caribbean affected more frequently and severely
69
Sarcoidosis | Signs + symptoms (7)
``` Often asymptomatic Acute sarcoidosis often presents with erythema nodosum +/- polyarthralgia and resolves spontaneously Dry cough Progressive dyspnoea Chest pain Lymphadenopathy Hepatmegaly + splenomegaly ```
70
``` Sarcoidosis Investigations (6) ```
Bloods: high ESR, high LFT, high serum ACE, high Ca, high immunoglobulins 24h urine: high Ca CXR: bilateral hilar lymphadenopathy --> pulmonary infiltrates --> pulmonary fibrosis --> bulla formation ECG: arrhythmias or bundle branch block Bronchoalveolar lavage: high lymphocytes CT/MRI: to assess severity of pulmonary disease
71
``` Sarcoidosis Treatment (2) ```
Acute sarcoidosis: bed rest, NSAIDs | Indications for corticosteroids: uveitis, hypercalcaemia, neuro/cardiac involvement
72
Interstitial Lung Disease | Definition (2)
A number of conditions that primarily affect the lung parenchyma Characterised by chronic inflammation and/or progressive interstitial fibrosis
73
Interstitial Lung Disease | Signs + symptoms (2)
Dyspnoea on exertion | Non productive paroxysmal cough
74
Interstitial Lung Disease | Investigations (3)
CXR HRCT Spirometry: restrictive patten
75
Interstitial Lung Disease | Classification (3)
Those with known cause: occupational (asbestosis), drugs (nitrofuratnoin, sulfasalazine), hypersensitivity reactions (extrinsic allergic alveolitis), infections, GORD Those associated with systemic disorders: sarcoidosis, RA, SLE, systemic sclerosis, Sjogren's, ulcerative colitis Idiopathic: idiopathic pulmonary fibrosis
76
Extrinsic Allergic Alveolitis | Aetiology (2)
Proteins in bird droppings | Farmer's lung (Micropolyspora faeni)
77
Extrinsic Allergic Alveolitis | Signs + symptoms (2)
Post-exposure: fever, rigors, dry cough, dyspnoea, crackles | Chronic: increased dyspnoea, weight loss, type 1 respiratory failure, cor pulmonale
78
``` Extrinsic Allergic Alveolitis Acute investigations (4) ```
Bloods: FBC (neutrophilia), increased ESR ABG CXR: upper-zone consolidation, hilar lymphadenopathy Spirometry: reversible restrictive pattern
79
``` Extrinsic Allergic Alveolitis Chronic Investigations (4) ```
Bloods CXR: upper zone fibrosis Spirometry: persistent restrictive pattern Bronchoalveolar lavage: increased lymphocytes and mast cells
80
Extrinsic Allergic Alveolitis | Treatment (2)
Acute: remove allergen, give O2, oral prednisolone Chronic: avoid allergen or wear protective equipment, long term steroids
81
Industrial Lung Disease | Silicosis (4)
Caused by inhalation of silica particles Associated jobs: metal mining, pottery/ceramic manufacture Signs + symptoms: progressive dyspnoea, increased incidence of TB Investigations: CXR, spirometry (restrictive defect)
82
Industrial Lung Disease | Asbestosis (2)
Types of asbestos: chrysotile (white), crocidolite (blue), amosite (brown) Signs + symptoms: progressive dyspnoea, clubbing, crackles
83
``` Industrial Lung Disease Malignant mesothelioma (5) ```
Definition: tumour of mesothelial cells that usually occurs int he pleura Aetiology: asbestos Signs + symptoms: chest pain, dyspnoea, weight loss, clubbing Investigations: CXR/CT show pleural thickening/effusion, thoracoscopy allows histological diagnosis Treatment: pemetrexed + cisplatin chemo but prognosis is poor
84
Idiopathic Pulmonary Fibrosis | Definition (2)
A type of idiopathic interstitial pneumonia | Commonest cause of interstitial lung disease
85
Idiopathic Pulmonary Fibrosis | Signs + symptoms (7)
``` Dry cough Exertional dyspnoea Malaise Weight loss Cyanosis Clubbing Crepitations ```
86
Idiopathic Pulmonary Fibrosis | Investigations (6)
``` Bloods: high CRP, high immunoglobulins ABG: low PaO2, if severe high PaCO2 CXR: reduced lung volume CT Spirometry: restrictive pattern Bronchoalveolar lavage: high lymphocytes (good prognosis), high neutrophils (poor prognosis) ```
87
Idiopathic Pulmonary Fibrosis | Treatment (2)
Best supportive care: oxygen, pulmonary rehabilitation, opiates Lung transplant
88
Pulmonary Hypertension | Definition (2)
Normal pulmonary arterial pressure 12-16mmHg | Hypertension >25mmHg
89
Pulmonary Hypertension | Pathology (3)
Walls of pulmonary arteries become thickened and stiff, and can't expand as well Can lead to right heart failure Commonly due to heart/lung condition
90
Pulmonary Hypertension | Signs + symptoms (4)
Dyspnoea Chest pain Palpitations Oedema/ascites
91
Pulmonary Hypertension | Investigations (6)
Echo Right heart catheterisation Bloods: BNP CXR: enlarged right ventricle/pulmonary arteries, emphysema, fibrosis V/Q scan: check for blood clots as this may be the cause or can be a complication
92
Pulmonary Hypertension | Treatment (5)
``` Treat underlying condition Anticoagulation: warfarin Oxygen Diuretics: to treat oedema due to heart failure Digoxin: slows down heart rate ```
93
Cor Pulmonale | Definition (1)
Right heart failure caused by chronic pulmonary arterial hypertension
94
Cor Pulmonale | Aetiology (3)
Lung disease: COPD, bronchiectasis, pulmonary fibrosis, severe asthma Pulmonary vascular disease: pulmonary emboli, pulmonary hypertension, acute respiratory distress syndrome Thoracic cage abnormality: scoliosis, kyphosis
95
Cor Pulmonale | Signs + symptoms (8)
``` Dyspnoea Fatigue Syncope Cyanosis Tachycardia Elevated JVP RV heave Pansystolic murmur (tricuspid regurgitation) ```
96
Cor Pulmonale | Investigations (4)
FBC: high Hb and haematocrit (secondary polycythaemia) ABG: hypoxia CXR: enlarged right atrium and ventricle, prominent pulmonary arteries ECG: P pulmonale, right axis deviation
97
Cor Pulmonale | Treatment (4)
Treat underlying cause Treat respiratory failure: oxygen Treat cardiac failure Consider heart-lung transplant in young patients as prognosis is poor
98
Sleep Apnoea | Definition (1)
Intermittent closure/collapse of the pharyngeal airway, causing apnoeic episodes during sleep
99
Sleep Apnoea | Signs + symptoms (5)
``` Loud snoring Daytime somnolence Poor sleep quality Morning headache Reduced cognitive performance ```
100
``` Sleep Apnoea Risk factors (3) ```
Obesity Alcohol Enlarged tonsils
101
Sleep Apnoea | Complications (2)
Pulmonary hypertension | Type II respiratory failure
102
Sleep Apnoea | Investigations (3)
Overnight pulse oximetry Polysomnography (O2sats, air flow, ECG, EMG chest + abdo movement) Epworth sleep survey
103
Sleep Apnoea | Treatment (4)
Weight reduction Avoid tobacco and alcohol CPAP for moderate-severe disease Surgery to relieve pharyngeal obstruction (eg. tonsillectomy)
104
Sleep Apnoea | Severity based on Epworth Sleep Survey (3)
0-10 normal 11-15 excessive daytime sleepiness 16-24 severe daytime sleepiness