Pulmonology Flashcards

1
Q

Clubbing definition

A

Bogginess and increased fluctuance of nailbed

Soft tissue expansion of distal phalanx

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2
Q

Respiratory causes of clubbing

A

Lung cancer

  • bronchial
  • mesothelioma

Chronic lung suppuration

  • empyema
  • bronchiectasis, CF

Fibrosis

  • Idiopathic pulmonary fibrosis
  • TB
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3
Q

Cardiac causes of clubbing

A

Infective endocarditis
Congenital cyanotic heart disease
Atrial myxoma

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4
Q

GI causes of clubbing

A
Cirrhosis 
Crohn's
ulcerative colitis
Coeliac
Cancer, GI lymphoma
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5
Q

Other causes of clubbing

A

Familial
thyroid acropachy
upper limb av malformations

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6
Q

Cyanosis definition

A

Blue discoloration of mucosal membranes or skin

Deoxygenated blood Hb>5g/dL

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7
Q

Classifying cyanosis

A

peripheral - cold with blue nails

central - blue tongue and lips

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8
Q

Respiratory causes of cyanosis

A

hypoventilation - copd msk
decreased diffusion of gases - pulmonary oedema and fibrosing alveolitis
V/Q mismatch - PE, AVM

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9
Q

Cardiac causes of cyanosis

A

Congenital - Fallot, transposition great vessels

Decreased CO
- Mitral stenosis, LV failure

Vascular

  • Raynauds
  • DVT
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10
Q

RBC causes of cyanosis

A

Low affinity Hb

may be hereditary or acquired

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11
Q

Anatomical classification of pneuonia

A

Bronchopneumonia
- patchy consolidation of both lobes

Lobar pneumonia

  • fibrosuppurative consolidation of a single lobe
  • Congestion → red → grey → resolution
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12
Q

Aetiological classification of pneumonia

A

Community acquired pneumonia

  • usually strep pneum or haemophilus
  • viruses 15%

Hospital acquired pneumonia

  • > 48 hours after hospital admission
  • gram negative enterobacteria eg Staph aureus
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13
Q

Aspiration pneumonia

A

High risk patients

  • stroke
  • bulbar palsy
  • low GCS
  • GORD
  • Parkinsons
  • achalasia

Mostly caused by anaerobes

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14
Q

Pathogens causing pneumonia in the immunocompromised

A

TB
Fungi
CMV
HSV

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15
Q

Pneumonia symptoms

A
Fever
Rigors
malaise and anorexia
Dyspnoea
Cough 
Purulent sputum
Haemoptysis 
Pleuritic pain
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16
Q

Signs of pneumonia

A

 ↑RR, ↑ HR
 Cyanosis
 Confusion

Consolidation
 ↓ expansion
 Dull percussion
 Bronchial breathing 
 ↓ air entry
 Crackles
 Pleural rub
 ↑VR
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17
Q

Investigations pneumonia

A

 Bloods: FBC, U+E, LFT, CRP, culture, ABG (if ↓SpO2)

 Urine: Ag tests (Pneumococcal, Legionella)

 Sputum: MC&S

 Imaging: CXR
 infiltrates, cavities, effusion

 Special
 Paired sera Abs for atypicals Mycoplasma, Chlamydia, Legionella
 Immunofluorescence (PCP) 
 BAL bronchiiolar lavage 
 Pleural tap
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18
Q

Assessing pneumonia severity

A

CURB-65 only used if Xray changes

Confusion < 8 AMTS
Urea > 7mM
Respiratory rate >30
Blood pressure <90/60
>65 years old 

Scores 0-1 = Home treatment
2 == Hospital treatment
3+ == Consider ITU

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19
Q

Management pneumonia

A
General protocol 
 Abx
 O2: PaO2≥8, SpO2 94-98%
 Fluids
 Analgesia
 Chest physio
 Consider ITU if shock, hypercapnoea, hypoxia
 F/up @ 6wks  ̄c CXR
 Check for underlying Ca
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20
Q

Antibiotics for CAP

A

Mild:
amoxicillin 500mg TDS PO for 5d
or clarithro 500mg BD PO for 7d

Mod
amoxicillin 500mg TDS
and clarithro 500mg BD PO/IV (clarithro alone if pen allergy) for 7d

Sev
Co-amoxiclav 1.2g TDS IV / cefuroxime 1.5g TDS IV
and clarithro 500mg BD IV for 7-10d
Add fluclox if staph suspected.

Atyp
Chlamydia: tetracycline
PCP: Co-trimoxazole
Legionella: Clarithro + rifampicin

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21
Q

Antibiotics for HAP

A

 Mild / <5d: Co-amoxiclav 625mg PO TDS for 7d

 Severe / >5d: Tazocin ± vanc ± gent for 7d

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22
Q

Aspiration pneumonia antibiotics

A

 Co-amoxiclav 625mg PO TDS for 7d

As tend to be the anaerobes as causatives

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23
Q

Pneumonia vaccine

A

Pneumovax 23 valent

  • > 65
  • Chronic heart, liver, kindey, pancreas failure
  • Diabetes
  • Immunosuppression

revaccinate every 6 years

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24
Q

Complications of pneumonia

A
Respiratory failure 
Hypotension 
AF
Pleural effusion 
Empyema 
Lung abscess
Sepsis 
Pericarditis 
Jaundice
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25
Hypotension in pneumonia
 Cause: dehydration + septic vasodilatation Mx  If SBP<90 → 250ml fluid challenge over 15min  If no improvement: central line + IV fluids  If refractory: ITU for inotropes
26
Pleural effusion in pneumonia
Exudate - inflammatory Mx: - pleural tap - send for MCS, cytology and chemistry
27
Empyema of pneumonia
Pus in the pleural cavity Anaerobes, staph, gram -ve associated with anaerobes and aspiration a patient with resolving pneumonia develops recurring fever Pleural tap == turbid pH <7.2, low glucose, High LDH Mx; US guided drain and ABx
28
Lung abscess causes
often a complication of pneumonia - aspiration - bronchial obstruction - tumour, foreign body - Septic emboli - sepsis, IVDU, RH endocarditis - Pulmonary infarction - Subphrenic, hepatic abscess
29
Features of lung abscess
``` Swinging fever cough foul purulent sputum haemoptysis malaise, weight loss Pleuritic pain Clubbing Empyema ```
30
Investigations for lung abscess
 Blood: FBC, ESR, CRP, cultures  Sputum: micro, culture, cytology  CXR: cavity ̄c fluid level  Consider CT and bronchoscopy
31
Bronchiectasis pathophysiology
chronic infection of bronchi/bronchioles leads to permanent dilation Less efficient clearance leads to retained inflammatory secretions and microbes == airway damage and recurrent infection causative agents: - H.influenza - Pneumococcus - S aureus - Pseudomonas
32
Bronchiectasis causes
idiopathic = 50% Congenital - CF - Young's syndrome (azoospermia and bronchiectasis) Post infectious - Measles - pertussis - pneumonia - TB - bronchiolitis Immunodeficiency - hypogammaglobulinaemia
33
Symptoms bronchiectasis
Persistent cough and purulent sputum Haemoptysis Fever and weight loss
34
Bronchiectasis signs
clubbing coarse inspiratory crackles wheeze purulent sputum
35
complications of bronchiectasis
``` Pneumonia pleural effusion pneumothorax pulmonary HTN amyloidosis cerebral abscess ```
36
bronchiectasis investigations
Sputum: MCS Blood: Se Ig, Aspergillus precipitins, RF, α1-AT level Test Ig response to pneumococcal vaccine CXR: thickened bronchial walls (tramlines and rings) Spirometry: obstructive pattern HRCT chest  Dilated and thickened airways  Saccular dilatations in clusters ̄c pools of mucus Bronchoscopy + mucosal biopsy  Focal obstruction  PCD primary ciliary dyskinesia CF sweat test (pilocarpine iontopheresis)
37
Treatment bronchiectasis
 Chest physio: expectoration, drainage, pulm. rehab  Abx for exacerbations: e.g. cipro for 7-10d  Bronchodilators: nebulised β agonists  Treat underlying cause  CF: DNAase  ABPA: Steroids allergic bronchopulmonary aspergillosis  Immune deficiency: IVIg  Surgery may be indicated in severe localised disease
38
Cystic fibrosis pathogenesis
 Auto recessive, 1:2000 live Caucasian births  Mutation in CFTR gene on Chr 7 (commonly ∆F508)  → ↓ luminal Cl secretion and ↑ Na reabsorption → viscous secretions.  In sweat glands, ↓ Cl and Na reabsorption → salty sweat
39
Clinical features of CF
neonate - FTT - meconium ileus (even stickier than normal and causes obstruction) - rectal prolapse Children - nasal polyps and sinusitis resp: cough wheeze, infections, bronchiectasis, haemoptysis, pneumothorax, cor pulmonale GI: pancreatic insufficiency, diabetes, steatorrhoea, distal intestinal obstruction syndrome, gallstones, secondary biliary cirrhosis Male infertility, osteoporosis, vasculitis
40
Signs of CF
clubbing cyanosis bilateral coarse crepitations
41
Common respiratory infections in CF
Early  S. aureus  H. influenza Late  P. aeruginosa: 85%  B. cepacia: 4%
42
Diagnosis CF
sweat test -- Na and Cl > 60mM genetic screening for common mutations Faecal elastase- tests pancreatic exocrine function immunoreactive trypsinogen test on heel prick
43
CF investigations
 Bloods: FBC, LFTs, clotting, ADEK levels, glucose TT  Sputum MCS  CXR: bronchiectasis  Abdo US: fatty liver, cirrhosis, pancreatitis  Spirometry: obstructive defect  Aspergillus serology / skin test (20% develop ABPA)
44
CF management
General  MDT: physician, GP, physio, dietician, specialist nurse ``` Chest  Physio: postural drainage, forced expiratory techniques  Abx: acute infections and prophylaxis  Mucloytics: DNAse  Bronchodilators  Vaccinate ``` GI  Pancreatic enzyme replacement: pancreatin (Creon)  ADEK supplements  Insulin  Ursodeoxycholic acid for impaired hepatic function  Stimulates bile secretion ``` Advanced Lung Disease  O2  Diuretics (Cor pulmonale)  NIV  Heart/lung transplantation ``` Other  Rx of complications: e.g. DM  Fertility and genetic counselling  DEXA osteoporosis screen
45
Pulmonary aspergillus infections diseases
``` Asthma - type 1 HS reaction to spores Allergic bronchopulmonary aspergillosis aspergilloma invasive aspergillosis extrinsic allergic alveolitis ```
46
ABPA cause
T1 and T3 reaction to aspergillus fumigatus | Bronchoconstriction leads to bronchiectasis
47
Symptoms of ABPA
wheeze productive cough dyspnoea
48
Investigations for ABPA
``` CXR: bronchiectasis Aspergillus in sputum (black on silver stain) Aspergillus skin test or IgE RAST +ve se precipitins ↑ IgE and ↑ eosinophils ```
49
Treatment of ABPA
pred 40mg/day + itraconazole for acute attacks pred maintenance 5-10mg/day bronchodilators for asthma
50
Lung cancer classification
Small cell lung cancer Non SCLC - adeno - large cell - squamous cell
51
Features of squamous cell carcinoma lung
35% lung cancer M>F smoking centrally located evidence of squamous differentiation - keratinisation locally invasive late mets via lymph nodes PTH releasing ==> increase calcium
52
Features of adenocarcinoma lung
``` 25% lung cancer females non smokers peripherally located glandular differentiation extrathoracic mets common and early 80% present with mets ```
53
Features of large cell carcinoma lung
10% lung cancer peripheral or central large poorly differentiated cells poor prognosis
54
small cell lung cancer features
20% lung cancer to do with smoking central location near bronchi histology == small poorly differentiated cells 80% present with advanced disease v chemosensitive BUT v poor prognosis Ectopic hormone secretion
55
Lung cancer symptoms
``` cough and haemoptysis dyspnoea chest pain recurrent pneumonia anorexia and weight loss hoarseness ```
56
Lung cancer signs
Chest  Consolidation  Collapse  Pleural effusion ``` General  Cachexia  Anaemia  Clubbing and HPOA (painful wrist swelling)  Supraclavicular and/or axillary LNs ``` ``` Metastasis  Bone tenderness  Hepatomegaly  Confusion, fits, focal neuro  Addison’s ```
57
complications of lung cancer
``` recurrent laryngeal nerve palsy phrenic nerve palsy SVC obstruction Horner's syndrome - pancoast tumour AF ```
58
Paraneoplsatic complications of lung cancer
Endo  ADH → SIADH ( euvolaemic ↓Na+)  ACTH → Cushing’s syndrome  Serotonin → carcinoid (flushing, diarrhoea)  PTHrP → 1O HPT (↑Ca2+, bone pain) – SCC Rheum  Dermatomyositis / polymyositis Neuro  Purkinje Cells (CDR2) → cerebellar degeneration  Peripheral neuropathy Derm  Acanthosis nigricans (hyperpigmented body folds)  Trousseau syndrome: thrombophlebitis migrans
59
Lung cancer investigations
Bloods Cytology Imaging ``` CXR  Coin lesion  Hilar enlargement  Consolidation, collapse  Effusion  Bony secondaries ``` Contrast-enhanced Volumetric CT  Staging: lower neck, chest, upper abdomen  Consider CT brain PET-CT: exclude distant mets Radionucleotide bone scan
60
Performance status analysis lung cancer
``` 0= Normal 1= symptomatic without significant decrease in activities 2= In bed or chair less than 50% day 3= In bed or chair more than 50% day 4= Bedridden ```
61
Lung cancer biopsy options
Percutaneous FNA bronchoscopy endoscopic bronchial US biopsy Mediastinoscopy
62
TNM staging lung cancer
Tx - malignant cells in bronchial secretions Tis - Carcinoma in situ T0 - None evident T1- <3cm in lobar or more distal airway T2- >3cm and >2cm from carina or pleural involvement T3- <2cm from carina or involves chest wall or diaphragm T4 - Involves mediastinum or malignant effusion present N0- None involved N1- Peribronchial or ipsilateral hilum N2- Ipsilateral mediastinum N3- Contralateral mediastinum or supraclavicular
63
Lung cancer Mx overview
MDT involvement Use PSA score for chemo advise smoking cessation
64
NSCLC Mx
Surgical Resection  Rx of choice for peripheral lesions ̄c no metastatic spread = stage I/II (~25%)  Need good cardiorespiratory function  Wedge resection, lobectomy or pneumonectomy  ± adjuvant chemo Curative radiotherapy  If cardiorespiratory reserve is poor Chemo ± radio for more advanced disease  Platinum-based regimens  MAbs targeting EGFR (e.g. cetuximab) or TKI (e.g. erlotinib)
65
SCLC Mx
 Typically disseminated @ presentation |  May respond to chemo but invariably relapse
66
Lung cancer palliation
 Radio: bronchial obstruction, haemoptysis, bone or CNS mets  SVC obstruction: stenting + radio + dexamethasone  Endobronchial therapy: stenting, brachytherapy  Pleural drainage / pleurodesis  Analgesia
67
ARDS pahtogenesis
Lungs suddenly stop being able to supply rest of body with enough O2 May result from direct insult or secondary to a systemic illness Pulmonary oedema can arise from inflammatory mediators leading to increased capillary permeability and non cardiogenic pulmonary oedema
68
Clinical features of ARDS
Tachypnoea Cyanosis Bilateral fine crepitations SIRS - systemic inflammatory response syndrome
69
Diagnosing ARDS
Acute onset CXR shows bilateral infiltrates No evidence of congestive cardiac failure PaO2:FiO2 <200
70
Mx ARDS
admit to ICU for organ support and treatment of the underlying cause Ventilation Indications  PaO2<8KPa despite 60% FiO2  PaCO2>6KPa Method  6ml/kg + PEEP (e.g. 10cm H2O) SEs  VILI ventilation induced lung injury  VAP ventilation associated pneumonia  Weaning difficulty ``` Circulation  Invasive BP monitoring  Maintain CO and DO2 ̄c inotropes  E.g. norad or dobutamine  RF may require haemofiltration ``` Sepsis  Abx Other  Nutritional support: enteral (best), TPN
71
Causes ARDS
``` Pulmonary  Pneumonia  Aspiration  Inhalation injury  Contusion ``` ``` Systemic  Shock  Sepsis  Trauma  Haemorrhage and multiple transfusions  Pancreatitis  Acute liver failure  DIC  Obs: eclampsia, amniotic embolism  Drugs: aspirin, heroin ```
72
DDX ARDS
ARDS is caused by exudates any cause of transudates - DDx - nephrosis - cirrhosis - gastrosis - decreased lymphatic drainage due to cancer
73
Respiratory failure type 1
 PaO2 <8KPa and PaCO2 <6KPa  V/Q mismatch and diffusion failure
74
Respiratory failure type 2
 PaO2 <8KPa and PaCO2 >6KPa - alveolar hypoventilation +- V/Q mismatch
75
Alveolar hypoventilation
``` Obstructive  COPD  Asthma  Bronchiectasis  Bronchiolitis  Intra- and Extra-thoracic (Ca, LN, epiglottitis...) ``` ``` Restrictive  ↓ drive: CNS sedation, trauma, tumour  NM disease: cervical cord lesion, polio, GBS, MG  Chest: flail, kyphoscoliosis, obesity  Fluid and fibrosis ```
76
Clinical features respiratory failure Hypoxia
``` Acute  Dyspnoea  Agitation  Confusion  Cyanosis ``` Chronic  Polycythaemia  PHT  cor pulmonale
77
Clinical features respiratory failure hypercapnoea
``` headache flushing and peripheral vasodilation bounding pulse flap Confusion ==> coma ```
78
Mx type 1 respiratory failure
 Give O2 to maintain SpO2 94-98% |  Assisted ventilation if PaO2<8KPa despite 60% O2
79
Mx type 2 respiratory failure
 Controlled O2 therapy @ 24% O2 aiming for SpO2 88-92% and a PaO2 >8kPa  Check ABG after 20min  If PaCO2 steady or lower can ↑ FiO2 if necessary  If PaCO2 ↑>1.5KPa and pt. still hypoxic, consider NIV or respiratory stimulant (e.g. doxapram)
80
Principles of O2 therapy
 Critically ill pts. should receive high conc O2 immediately.  O2 should be prescribed to achieve target SpO2  94-98% for most patients  88-92% for those at risk or hypercapnic resp failure  In pts. at risk of hypercapnic resp failure:  Start O2 therapy at 24% and do an ABG – Blue Venturi @ 2-4L/min  Clinically: ↓ RR ̄c O2 may be useful sign  If PCO2 ≤6kPa: ↑ target SpO2 to 94-98%  If PCO2 >6kPa: maintain target SpO2
81
Oxygen delivery options
Nasal Prongs: 1-4L/min = 24-40% O2 Simple Face Mask Non-rebreathing Mask  Reservoir bag allows delivery of high concentrations of O2.  60-90% at 10-15L ``` Venturi Mask Provide precise O2 concentration at high flow rates  Yellow: 5%  White: 8%  Blue: 24%  Red: 40%  Green: 60% ```
82
Chronic asthma definition
Episodic reversible airway obstruction due to bronchial hyperreactivity to a variety of stimuli
83
Chronic asthma pathophysiology
Acute - Mast cell - Ag interaction and histamine release - Bronchoconstriction, mucous plugs and mucosal swelling Chronic - Th2 cells release IL 3,4,5 gives mast cell eosinophil and B cell recruitment - Airway remodelling
84
Causes of asthma
Atopy  T1 hypersensitivity to variety of antigens  Dust mites, pollen, food, animals, fungus ``` Stress  Cold air  Viral URTI  Exercise  Emotion ``` Toxins  Smoking, pollution, factory  Drugs: NSAIDS, β-B
85
Asthma symptoms
Cough and sputum often at night Wheeze dyspnoea diurnal variation with morning dipping (worse)
86
Asthma signs
``` tachypnoea tachycardia widespread polyphonic wheeze hyperinflated chest decreased air entry signs of steroid use ```
87
Asthma associated diseases
GORD Churg strauss ABPA
88
Investigations asthma
Bloods  FBC (eosinophila)  ↑IgE  Aspergillus serology CXR: hyperinflation Spirometry  Obstructive pattern ̄c FEV1:FVC < 0.75  ≥15% improvement in FEV1 ̄c β-agonist PEFR monitoring / diary  Diurnal variation >20%  Morning dipping Atopy: skin-prick, RAST
89
Mx asthma general measures
TAME Technique - inhaler use Avoidance - known irritants Monitor - peak flow diary (2-4x/day) Educate- specialist nurse, crisis plan, emphasise importance of treatment
90
Drug ladder for asthma 2016 bts guidelines
SABA PRN ``` 1- low dose ICS 2-Add LABA to low dose ICS 3- Consider increased dose Consider adding theophylline, LAMA, Leukotriene agonist 4- Refer to specialist Consider increased dose Consider 4th drug 5- Refer to specialist Add daily oral steroid ```
91
Acute severe asthma info
Acute breathlessness and wheeze ask: - precipitant - usual treatment - previous attacks and itu - best pefr
92
Acute asthma investigations
``` PEFR ABG - PaO2 usually normal or slightly low - PaCO2 usually low - If PaCO2 high send to ITU for ventilation FBC UE CRP Blood cultures ```
93
Assessing asthma attack severity
``` Severe: any one of  PEFR <50%  RR>25  HR >110  Can’t complete sentence in one breath ``` ``` Life Threatening: any one of  PEFR <33%  SpO2 <92%, PCO2 >4.6kPa, PaO2 <8kPa  Cyanosis  Hypotension  Exhaustion, confusion  Silent chest, poor respiratory effort  Tachy-/brady-/arrhythmias ```
94
DDX acute asthma
Pneumothorax Acute exacerbation COPD Pulmonary oedema
95
Admission and discharge of asthma attack
admit if life threatening admit if severe and not responding to treatment Discharge if PEFR> 75% 1hr after initial treatment Discharge if stable on meds for 24 hours Discharge if PEFR>75% with diurnal variability <20%
96
Discharge plan for asthma attack
TAME po steroids for 5 days GP appointment within 1 week Respiratory clinic within 1 month
97
Mx acute asthma attack
1. sit up 2. 100% O2 non rebreathe mask 94-98% 3. Nebulised salbutamol 5mg and ipratropium (anti muscarinic) 4. Hydrocortisone 100mg IV or pred 50mg po or both 5. Write no sedation on drug chart Life threatening - ITU, MGSO4 2g IV infusion over 20 min nebulised salbutamol every 15 minutes and monitor ECG
98
Acute asthma not improving further treatment
``` Nebulised salbutamol every 15 mins Continue ipratropium 0.5mg every 4-6 hrs MGSO4 IVI 2mg over 20 mins Salbutamol IVI3-20ug/min Consider aminophylline ITU for invasive ventilation ```
99
Monitoring following asthma attack
PEFR every 15-30 mins - pre and post B agonist SpO2 keep >92% ABG if initial PaCO2 normal or increased
100
COPD definition
Airway obstruction FEV1<80% FEV1:FVC < 0.70 Chronic bronchitis == cough and sputum production on most days for 3mo of 2 successive years Emphysema == histological diagnosis of enlarged airway spaces distal to terminal bronchioles with destruction of alveolar walls
101
COPD causes
Smoking | a1Anti trypsin deficiency
102
COPD symptoms
Cough and sputum Dyspnoea Wheeze Weight loss
103
COPD signs
``` Tachypnoea prolonged expiratory phase Hyperinflated lungs - decreased cricosternal distance normally 3cm - loss of cardiac dullness - displaced liver edge wheeze early inspiratory crackles cyanosis cor pulmonale - raised jvp - oedema - loud P2 signs of steroid use ```
104
Pink puffers emphysema
Increased alveolar ventilation ==> breathless but not cyanosed Normal PaO2 Normal or low PaCO2 Progresses to ==> Type 1 respiratory failure
105
Blue bloaters chronic bronchitis
decreased alveolar ventilation ==> cyanosed but not breathless Decreased PaO2 Increased PaCO2 - now reliant on hypoxic respiratory drive Progresses to ==> type 2 respiratory failure and cor pulmonale
106
mMRC dyspnoea score
1. dyspnoea only on vigorous exertion 2. SOB on hurrying or walking up steps 3. Walks slowly or has to stop for breath 4. Stops for breath after <100m/ few mins 5. Too breathless to leave house or SOB on dressing
107
COPD complications
``` Acute exacerbation +- infection Polycythaemia pneumothorax == ruptured bullae cor pulmonale lung carcinoma ```
108
Investigations for COPD
 BMI Bloods: FBC (polycythaemia), α1-AT level, ABG ``` CXR  Hyperinflation (> 6 ribs anteriorly)  Prominent pulmonary arteries  Peripheral oligaemia  Bullae ``` ECG:  R atrial hypertrophy: P pulmonale  RVH, RAD Spirometry: FEV1 <80%, FEV1:FVC <0.70, ↑TLC, ↑RV Echo: PHT
109
General management chronic COPD
Assess severity based on FEV1 % General measures - Stop smoking MDT and nicotine - pulmonary rehabilitation - Treat nutrition - flu and pneumococcal vaccine - review 1-2 yrs - air travel risky if FEV1 <50%
110
Pharmacological management COPD
Mucolytics - chronic productive cough SABA and SAMA PRN Exacerbations = LABA or LAMA if FEV>50% LABA + ICS <50% FEV1 Persistent exacerbations or breathlessness - LABA+LAMA+ICS - theophylline may be considered - consider home nebs LTOT - aim to keep PaO2>8 for >15 hours /day increases survival 50% - know criteria for home oxygen (7.3-8 with PHT, polycythaemia, cor pulmonale, nocturnal hypoxaemia)
111
What surgery used for COPD
used for recurrent pneumothoraces used for isolated bullous disease used for lung volume reduction
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Acute exacerbation of COPD causes and history
Viral URTI and can be bacterial ask about smoking status exercise capacity current treatment previous exacerbations present with - dyspnoea - cough and sputum - wheeze
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Investigations for acute COPD
``` PEFR Bloods Sputum culture CXR- infection, pneumothorax ECG ```
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DDX COPD exacerbation
pneumothorax asthma PE Pulmonary oedema
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When to discharge COPD exacerbation
``` done spirometry establish optimal maintenance GP and specialist therapy Prevention using home steroids and oral ABx Pneumococcal and flu vaccine Home assessment ```
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Management COPD exacerbation
1. sit up 2. 24% O2 via venturi mask 88-92% 3. Vary fiO2 and sats target according to ABG - aim for paO2 >8 and an increase in PCO2 of <1.5kPa Nebulised bronchodilators - air driven - salbutamol 5mg/4hr - ipratropium 0.5mg/6hr Steroids - hydrocortisone 200mg IV - Prednisolone 40mg PO for 7-14 days ABx - if evidence of infection - doxycyline 200mg PO stat then 100mg OD PO for 5 days IF no response - repeat nebs and consider aminophylline IV - consider NIV if pH< 7.35 and or RR>30 - consider invasive ventilation if pH<7.26
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PE causes
usually arise from DVTs in proximal leg rarely right ventricle post MI septic emboli in right sided endocarditis
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PE risk factors
SPASMODICAL ``` Sex- F Pregnancy Age Surgery Malignancy Oestrogen - COCP/HRT DVT/PE previous history Immobility Colossal size Antiphopholipid Abs Lupus anti-coagulant ```
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Symptoms of PE
Dyspnoea Pleuritic chest pain Haemoptysis Syncope
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Signs of PE
``` Fever cyanosis tachycardia tachypnoea RHF- hypotension, raised JVP, loud P2 Evidence of cause DVT ```
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Investigations PE
 Bloods: FBC, U+E, clotting, D-dimers  ABG: normal or ↓PaO2 and ↓PaCO2, ↑pH  CXR: normal or oligaemia, linear atelectasis  ECG: sinus tachycardia, RBBB, right ventricular strain (inverted T in V1-V4)  S1, Q3, T3 is rare  Doppler US: thigh and pelvis (+ve in 60%)  CTPA + venous phase of legs and pelvis  85-95% sensitivity  V/Q scan no longer used
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Diagnosis of PE
first assess patient using WELLS score if high risk go straight to CTPA if low risk to D-Dimer - negative - excludes PE - positive - CTPA
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PE prevention
Risk assess all patients TED stockings Prophylactic LMWH Avoid COCP/HRT if at high risk
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PE management
- Sit up - 100% O2 via non rebreath mask - Analgesia - Morphine +- metoclopramide if distressed Critically ill with massive PE == - Alteplase 50mg bolus stat - surgical or interventional embolectomy LMWH - enoxaparin 1.5mg/kg/24 hr subcut If SBP<90 give 500ml colloid If SBP> 90 start warfarin and confirm diagnosis IF low BP still give inotropes Ongoing use TED and continue LMWH target INR 2-3
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Pneumothorax definition
Accumulation of air in the pleural space with secondary lung collapse
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Pneumothorax classification
Closed - intact chest wall and air leaks from lung into cavity Open - Defect in the chest wall allows communication between pleural cavity and outside world Tension - air enters pleural cavity through one way valve and cannot escape ==> mediastinal compression
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Causes of pneumothorax
spontaneous primary -- young thin men with ruptured subpleural bullae - smokers secondary - COPD - marfans, ehlers danlos - pulmonrary fibrosis, sarcoidosis Trauma - penetrating wound - rib fractures Iatrogenic - subclavian CVP line - NIV - liver biopsy - transbronchial biopsy
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Pneumothorax symptoms
sudden onset dyspnoea pleuritic chest pain TENSION== respiratory distress and cardiac arrest
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pneumothorax signs
Chest - decreased expansion - resonant percussion - decreased breath sounds TENSION - increased jvp - medastinal shift - raised HR - decreased BP Crepitus - surgical emphysema
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Pneumothorax investigations
ABG US CXR (expiratory film may be helpful)  Translucency + collapse (2cm rim = 50% vol loss)  Mediastinal shift (away from PTX)  Surgical emphysema  Cause: rib #s, pulmonary disease (e.g. bullae)
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Management tension pneumothorax
ABCDE and resus No CXR Large bore venflon cannula into 2nd ICS mid clavicular line thoracocentesis Insert intrapleural chest drain in to safe triangle
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Management traumatic chest drain
ABCDE resus Analgesia - morphine 3 sided wet dressing if sucking Insert chest drain safe triangle
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Management primary pneumothorax
SOB and greater than 2cm from hilum -yes = aspirate first then failing that chest drain -no consider discharge
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Management of secondary pneumothorax
SOB and >50 years and greater than 2cm from hilum - yes = chest drain and admit - if 1-2cm = aspirate first then chest drain then admit and monitor - no admit for 24 hours with oxygen therapy
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Pleural effusion classification
effusion protein < 25g/L = transudate | effusion protein >35g/L = exudate
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Causes of pleural effusion | Exudate
``` Exudates: ↑ capillary permeability Infection: pneumonia, TB Neoplasm: bronchial, lymphoma, mesothelioma Inflammation: RA, SLE Infarction ``` ``` Transudates: ↑ capillary hydrostatic or ↓ oncotic pressure CCF Renal failure ↓ albumin: nephrosis, liver failure, enteropathy Hypothyroidism Meig’s Syndrome Right pleural effusion Ascites Ovarian fibroma ```
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Symptoms pleural effusion
Asymptomatic dyspnoea Pleuritic chest pain
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Signs pleural effusion
Chest Tracheal deviation away from effusion ↓ expansion Stony dull percussion ↓ air entry Bronchial breathing just above effusion ↓VR ``` Associated disease Ca: cachexia, clubbing, HPOA, LNs, radiation burn, radiation tattoo Chronic liver disease Cardiac failure RA, SLE Hypothyroidism ```
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Pleural effusion investigations
Blood: FBC, U+E, LFT, TFT, Ca, ESR ``` CXR Blunt costophrenic angles Dense shadow ̄c meniscus Mediastinal shift away Cause: coin lesion, cardiomegaly ``` US: facilitates tapping Volumetric CT
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Diagnostic tap pleural effusion
Percuss upper boarder and go 1-2 spaces below Infiltrate down to pleura ̄c lignocaine. Aspirate ̄c 21G needle Send for: Chemistry: protein, LDH, pH, glucose, amylase Bacteriology: MCS, auramine stain, TB culture Cytology Immunology: SF, ANA, complement
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Pleural effusion management
Treat underlying cause Drainage if symptomatic Chemical pleurodesis (attach pleurae together) if recurrent malignant effusion Persistent effusions may require surgery
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Sarcoidosis definition
Multisystem granulomatous disorder of unknown cause
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Clinical features sarcoidosis
granulomas 20-40% cases present incidentally on CXR General - fever - anorexia and weight loss - fatigue - lymphadenopathy Respiratory - upper: otitis and sinusitis - lower: dry cough SOB chest pain and reduced lung function Arthralgia Neurological - bells palsy, meningitis Urine - renal stones due to calcium Low hormones - amenorrhoea Ophthalmological - uveitis sjogrens syndrome Myocardial - restrictive cardiomyopathy due t granulomas and fibrosis pericardial effusion Abdominal - hepatomegaly and cholestatic lfts splenomegaly Skin - lupus pernio raised dusky purple patches on nose cheek and fingers
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Investigations sarcoidosis
``` Bloods ↑ESR ↑Ca Lymphopenia ↑seACE ↑Ig ↑LFTs ``` CXR, CT, MRI Tuberculin skin test Negative in 2/3 Lung function tests Restrictive pattern ̄c ↓FVC ↓ transfer factor Tissue Biopsy Lung, LNs, skin nodules, liver Diagnostic: non-caseating granulomas Ophthalmology assessment
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Treatment sarcoidosis
Acute: - usually resolves spontaneously - bed rest and NSAIDS chronic - steroids - immunosuppression, ciclosporin and MTX
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Granulomatous disease DDX
Infections: TB, leprosy, syphilis, crypto, schisto AI: PBC primary biliary cirrhosis Vasculitis: GCA, PAN, Wegener’s, Takayasu’s Idiopathic: Crohns, Sarcoid Interstitial lung: EAA extrinsic allergic alveolitis , silicosis
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Pulmonary hypertension definition
PA pressure >25mmHg
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Pulmonary HTN causes
Cardiac- Left heart failure - mitral stenosis - mitral regurgitation - L-R shunt - LV failure Left lung parenchyma disease - chronic hypoxia = global vasoconstriction and vascular changes - COPD - Asthma - bronchiectasis - CF Pulmonary vascular disease - idiopathic pulmonary hypertension - sickle cell disease - SLE - PE Hypoventilation - myaesthenia gravis - nm disease - scoliosis - osa
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Investigations pulmonary htn
ECG P pulmonale RVH RAD Echo Velocity of tricuspid regurgitation jet Right atrial or ventricular enlargement Ventricular dysfunction Valve disease ``` Right heart catheterisation: gold standard Mean pulmonary artery pressure Pulmonary vascular resistance CO Vasoreactivity testing to guide Rx ```
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OSA definition
intermittent closure/ collapse of pharyngeal airway leads to apnoeic episodes throughout the day
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OSA risk factors
``` Obesity Male Smoker EtOH Idiopathic pulmonary fibrosis Structural airway pathology: e.g. micrognathia NM disease: e.g. MND ```
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Investigations OSA
O2 sats | polysomnography is diagnostic
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Treatment OSA
stop smoking lose weight NIV at night
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Features OSA
``` apnoeic episodes morning headache somnolescense loss of memory and attention Irritability and depression ``` Pulmonary HTN type 2 respiratory failure
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Smoking cessation
ask and advise give both pharmacological support and psychological drugs - verenicline - partial nicotine receptor agonoist makes you ill while smoking so encourages cessation can also use bupropion - normally used for SAD and depression