Respiratory

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Last updated 7:09 PM on 4/27/23
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1
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Briefly outline asthma- definition, symptoms
Heterogenous disease characterised by chronic airway inflammation

Reversible airflow limitation

SSx:
- wheeze
- breathlessness
- chest tightness
- cough
- worse at night
- triggered by allergen/exercise/cold air/aspirin/BB
- atopic features
2
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List 5 different phenotypes of asthma
Allergic

Non-allergic

Adult-onset

Asthma with persistent airflow limitation

Asthma with obesity
3
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Which clinical features make an asthma diagnosis LESS likely?
Dizziness, light-headedness or peripheral tingling

Productive cough in absence of wheeze/breathlessness

Normal examination when breathless

Voice disturbance

Smoking history (>20 pack years)

Cardiac disease

Normal PEF or FEV1 when symptomatic
4
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List the differential diagnoses of wheeze
Asthma

COPD

Obstruction e.g. foreign body

Anaphylaxis

Pulmonary oedema
5
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Outline the management of acute asthma
*O*xygen (high flow, aim for >92%

*S*albutamol

**H**ydrocortisone/prednisolone

**I**pratropium bromide

**T**heophylline

**!** Magnesium sulphate
6
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Define chronic bronchitis
Presence of chronic productive cough and sputum for at least 3 months in each of two successive years
7
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Define emphysema
Enlarged alveolar spaces and loss of alveolar walls
8
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Define COPD
Common, preventable and treatable disease

Characterised by persistent respiratory symptoms + airflow limitation

Due to airway and/or alveolar abnormalities caused by significant exposure to noxious particles or gases

Risk factors- over 35 yrs, smoke/ex-smoker
9
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How do you calculate pack years?
Number of packs (20) per day x years smoked

e.g. 1 pack a day for 30 yrs= 30
10
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Describe the pathophysiology of COPD
***Chronic bronchitis***

* hypertrophy of mucus secreting glands :. more mucus= sputum cough
* infiltration of bronchial walls with inflammatory cells :. airway narrowing

***Emphysema***

* loss of elastic recoil :. airflow limitation + air trapping
* bulla formation (air filled space after alveoli walls break down)
11
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Compare the inflammation in asthma and COPD
*ASTHMA:*
- triggered by sensitising agent
- CD4+ and t lymphocytes
- presence of eosinophils, macrophages + mast cells
- mostly REVERSIBLE

*COPD:*
- triggered by noxious agent
- CD8+ and T lymphocytes
- presence of macrophages + neutrophils
- mostly IRREVERSIBLE
12
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Describe the classic symptoms of COPD
Exertional breathlessness

Chronic cough

Regular sputum production

Frequent winter bronchitis

Wheeze
13
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Outline the clinical features of COPD
Tachypnoea

Use of accessory muscles

Hyperinflation

Reduced cricosternal distance (
14
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How is the severity of COPD assessed?
Using MRC dyspnoea scale

Ranges from grade 0 (only breathless with strenuous exercise) to grade 4 (too breathless to leave house or when dressing)

\
FEV1
15
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What is Dahl's sign?
Hyperpigmentation seen above knees/elbows in COPD patients
16
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List the smoking cessation drugs
Vareniciline (Champix)
- selective nicotine receptor partial agonist

Nicotine replacement therapy (patches, gums, spray, inhaler)

Bupropion (Zyban)
- atypical antidepressant
17
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Outline the pharmacological treatment of stable COPD
Flu vaccines

SABA (salbutamol, terbutaline)

Anti-cholinergics (ipratropium bromide, aclidinium)

LABA (salmeterol, indacterol)

ICS

Phosphodiesterase inhibitors (theophyllines, roflumilast)
18
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Outline the non-pharmacological treatment of stable COPD
Exercise training programmes

Long-term O2 therapy (>15 hrs a day)

Lung volume reduction surgery

Lung transplant
19
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Outline the complications of COPD
Respiratory failure
(PaO2
20
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List the investigations used to diagnosed COPD
O2 saturation

ABG

Sputum + blood cultures

CXR

ECG

Bloods- eosinophil count, U&E, CRP, theophylline, cardiac enzymes

CT/CTPA (rule out PE)
21
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List the differentials for COPD
Pneumonia

Pneumothorax

Malignancy

PE

HF/ACS
22
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Define pneumonia
Symptoms and signs consistent with an acute lower respiratory tract infection associated with new radiographic shadowing

British Thoracic Society
23
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Outline the symptoms of pneumonia
Fever

Shivers

Malaise

Dyspnoea

Cough

Sputum

Pleuritic pain

Haemoptysis
24
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Outline the signs of pneumonia
Pyrexia

Cyanosis

Confusion (elderly)

Tachypnoea/tachycardia

Consolidation (reduced expansion, dull percussion, increased fremitus, bronchial breathing)

Pleural rub (raspy breathing)
25
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List the lung defence mechanisms
Filtration in upper airways

Cough reflex

Mucociliary clearance

Alveolar macrophages

Humoral and cellular immunity

Oxidative metabolism of neutrophils
26
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Outline the different investigations for pneumonia
Diagnosis:
- CXR
- FBC/CRP

Severity:
- U&E
- FBC/CRP/LFT
- ABG

Target therapy:
- blood + sputum cultures
- Pneumococcal urinary antigen
- Legionella urinary antigen + sputum culture
- viral PCR
27
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What is CURB65?
A scoring system for pneumonia


Confusion
Urea (>7mmol/l)
Respiratory rate (>30/min)
Blood pressure (
28
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How does the CURB65 scoring affect the management of pneumonia?
0-1: treat at home

2: short admission, oral antibiotics

3: senior urgent review

4-5: critical care
29
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Outline the general management of pneumonia
O2 (aim for 94-98%)

Antibiotics

IV fluids, analgesia, DVT prophylaxis

Chest physio

Nutritional support

Smoking cessation
30
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Name the pathogen that causes Tb
Mycobacterium Tuberculosis
31
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Outline the risk factors of Tb
Immunosuppression e.g. HIV infection, silicosis (inhaling silica dust), substance abuse, severe kidney disease, low BMI, transplant, cancer, diabetes

Homelessness

Imprisonment
32
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Outline the presentation of Tb
Respiratory:
- cough
- sputum
- haemoptysis

Systemic:
- fever
- malaise
- loss of appetite
- night sweats
- weight loss
- lymphadenopathy
33
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Describe the pathogenesis of Tb
Inhaled particles deposited in alveoli →

invade and replicate in alveolar macrophages →

epithelial reaction to bacteria →

encapsulation of bacteria (tubercle) →

bacteria continue to replicate or become latent →

causes destruction and fibrosis of tissue
34
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Compare primary and post-primary Tb
*Primary:*
- Tb with no pre-existing immunity
- non-infectious
- high mortality in vulnerable (children, elderly)
- often outside lung
- HIV coinfection

*Post-primary:*
- with pre-existing immunity
- infectious
- forms cavities in lungs
- young adults
- immunocompetent immune system
35
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Outline the diagnosis of Tb
*Sputum*- PCR, culture

*CXR*- segmental/lobar consolidation, hilar or mediastinal lymphadenopathy, pleural effusion

*Inflammatory markers*- ESR, CRP

*Histology*- granuloma, caseation, histocytes, giant cells, lymphocytes
36
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Outline the treatment of Tb
4 antibiotics for 2-4 months intensive

Rifampicin
Isoniazid
Pyrazinamide
Ethambutol
37
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What is sarcoidosis? Who does it affect?
A multisystem granulomatous disorder of unknown cause

Highest prevalence in Northern Europe

Adults 20-40yrs

Caucasians

HLA-DRB1 + DBQ1 alleles
38
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Outline the clinical features of sarcoidosis
Fever

Erythema nodosum

Polyarthralgia

Bilateral hilar lymphadenopathy

Dry cough

Dyspnoea

Low exercise tolerance

Chest pain

Red eyes

Thirst, polyuria (hypercalcaemia)

Skin lesions
39
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How is sarcoidosis diagnosed?
Bloods: high ESR, lymphopenia, high Ca2+, high Ig,

Biopsy: non-caseating granuloma

Bone XR: 'punched out' lesions in distal phalanges
40
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Why do oxygen prescriptions need to be monitored?
Oxygen toxicity leads to free radicals

:. seizures + unconsciousness

Also results in constriction of pulmonary circulation
41
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What's the O2 saturation target for COPD patients?
88-92%
42
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What's the general O2 saturation target?
Above 94%
43
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Briefly outline the 4 ways O2 is administered
***Venturi mask:*** delivers fixed O2 concentration

5-10 L/min, 35-60% FIO2, type 1 resp failure

\
***Non-rebreather reservoir bag:*** critical/trauma patients, 70-80% FIO2, effecting for short term treatment

\
***Nasal cannulae:*** 2-5L/min, 24-50% FIO2, suitable for most patients with type 1 and 2 resp failure, comfortable
44
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What is humidified O2 and when is it prescribed?
Reduces dryness in upper airways

Should be humidified if O2 is being delivered for more than 24hrs
45
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How does the BTS classify acute asthma?
Life-threatening asthma mnemonic

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==**33, 92 CHEST:**==

\
PEFR **
Life-threatening asthma mnemonic

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==**33, 92 CHEST:**==

\
PEFR **<33%**
oxygen saturations **<92%**
**c**yanosis
**h**ypotension
**e**xhaustion
**s**ilent chest
**t**achycardia
46
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Define a pneumothorax
Air in the pleural space leading to lung collapse
47
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Outline the different types of pneumothoraxes
**Spontaneous:** primary (normal lung) or secondary to pre-existing lung disease

\
**Non-spontaneous:** traumatic or iatrogenic
48
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Diagnosis?
Diagnosis?
Large left pneumothorax
49
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Diagnosis?
Diagnosis?
knowt flashcard image
50
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Outline the causes of secondary pneumothorax
knowt flashcard image
51
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Outline the symptoms of pneumothorax
**Sudden** onset/ acute

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Pleuritic chest pain

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SOB

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Cough
52
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Outline the differentials of pneumothorax
==Respiratory==- __PE__, pneumonia, acute exacerbation of respiratory disease

\
%%Cardiovascular%%- __ACS, MI__, pericarditis, aortic dissection, aneurysm rupture, cardiac tamponade

\
Other- MSK, GORD, panic attack
53
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Outline the signs of pneumothorax
**Reduced** expansion

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**Hyper-resonant** percussion

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**Quiet** breath sounds

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Tachycardia
54
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Outline the management of a pneumothorax
A-E assessment

History and examination

\
\
A-E assessment

History and examination

\
\
55
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Where is the safe triangle?
Location used when aspirating pneumothorax

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Needle inserted right above rib to avoid neurovascular bundle

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Boundaries: latissimus dorsi, pec major, line superior to nipple + apex at axilla
Location used when aspirating pneumothorax

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Needle inserted right above rib to avoid neurovascular bundle

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Boundaries: latissimus dorsi, pec major, line superior to nipple + apex at axilla
56
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Describe tension pneumothorax
Increasing pressure in thoracic cavity

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Hole in visceral pleura is letting air in on inspiration

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On breathing out, air isn’t being let out :. one-way valve
Increasing pressure in thoracic cavity

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Hole in visceral pleura is letting air in on inspiration

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On breathing out, air isn’t being let out :. one-way valve
57
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Outline the clinical features of tension pneumothorax
Severe breathlessness

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Tachycardia

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Pulsus paradoxus (exaggerated fall in systolic pressure during inspiration >10mm/Hg)

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Distended jugular veins

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Tracheal deviation (AWAY)

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Ipsilateral reduced/absent breath sounds
58
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Outline the emergency management of a tension pneumothorax
No CXR

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Needle decompression

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Large bore cannula in MCL 2nd ICS
59
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Advice to prevent recurrence of pneumothorax
No diving

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Stop smoking

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No aeroplane travel for 2-6 weeks

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Pregnancy can increase risk

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Return immediately if SOB
60
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Epidemiology of PE
knowt flashcard image
61
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Outline the risk factors for VTE- major and non major
knowt flashcard image
62
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Outline the clinical features of a minor PE
**Symptoms:**

* May be asymptomatic
* SOB
* Pleuritic chest pain
* Haemoptysis

\
**Signs:**

* Tachypnoea
* Low grade fever
* Sinus tachycardia or new AF
* Hypoxia
* Localised pleural rub
* DVT
63
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Outline the clinical features of a massive PE
Hypotension

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Collapse

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Cardiac arrest

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Sudden death

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Hypoxia

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Acute right heart strain

* loud P2, wide splitting of 2nd heart sound, gallop rhythm, tricuspid regurgitation

\
RHF

* low cardiac output, raised JVP, low BP
64
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Outline the diagnostic tests for PE
knowt flashcard image
65
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Describe the Well’s score for PE
knowt flashcard image
66
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How does a PE present on a CXR?
Usually normal

\
May be signs of:

* pulmonary hypertension (enlarged vessels)
* pleural effusions
* Westermark’s sign- focal hyperlucency
* Hampton’s hump- wedge-shaped infarcts
Usually normal

\
May be signs of:

* pulmonary hypertension (enlarged vessels)
* pleural effusions
* Westermark’s sign- focal hyperlucency
* Hampton’s hump- wedge-shaped infarcts
67
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How does PE present on an ECG?
Non-specific ST and T wave abnormalities

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Sinus tachycardia

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New AF

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Right axis deviation

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RBB

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S1Q3T3 (large S wave in lead I, Q wave in III, inverted T in III- classic cor pulmonale presentation)
Non-specific ST and T wave abnormalities

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Sinus tachycardia

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New AF

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Right axis deviation

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RBB

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S1Q3T3 (large S wave in lead I, Q wave in III, inverted T in III- classic cor pulmonale presentation)
68
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When is a V/Q scan indicated in suspected PE?
Only used if:

* normal CXR
* no concurrent symptomatic CVD
* inconsistent with clinical suspicion
Only used if:

* normal CXR
* no concurrent symptomatic CVD
* inconsistent with clinical suspicion
69
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How is PE managed in pregnancy?
Well’s score and D-dimer unhelpful

\

1. Start LMWH (continue for 6 wks postnatal)
2. CXR (with lead protection for foetus)
3. ECG
4. Bilateral leg ultrasound
5. Half-dose VQ scan
70
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Outline the general management of PE
LMWH or fondaparinux or UFH

\
If major PE:

* open pulmonary embolectomy (surgical removal)
* IVC filter (traps fragmented thromboemboli on way to pulmonary circulation)
LMWH or fondaparinux or UFH

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If major PE:

* open pulmonary embolectomy (surgical removal)
* IVC filter (traps fragmented thromboemboli on way to pulmonary circulation)
71
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Briefly outline the features of the different types of lung cancer
Small cell lung cancer (SCLC)- 10%

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Non small cell lung cancer (NSCLC)

* Squamous cell carcinoma 20-30%
* adenocarcinoma 40-50%
* large cell carcinoma 10-15%
Small cell lung cancer (SCLC)- 10%

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Non small cell lung cancer (NSCLC)

* Squamous cell carcinoma 20-30%
* adenocarcinoma 40-50%
* large cell carcinoma 10-15%
72
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Outline the staging and diagnostic investigations of lung cancer
* staging CT of chest and upper abdomen
* blood tests
* bronchoscopy
* CT guided biopsy
* PET scan
* MRI scan for Pancoast tumours
* bone scan
* brain CT/MRI
73
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Describe the TNM staging of lung cancer
knowt flashcard image
74
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List the treatment options for lung cancer

1. ==Surgical== (for localised tumours that have not metastasised)

\
2. ==Radical Radiotherapy== (useful in squamous cell carcinoma where surgery is not possible)

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3. ==Palliative Radiotherapy== (to relieve symptoms)

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4. ==Chemotherapy or immunotherapy==

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5. ==Adjuvant/neo-adjuvant chemotherapy== (chemo given __after surgery__ to reduce recurrence OR chemo given __before surgery__ to ensure cancer is well controlled)

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6. Other ==palliative measures== and counselling

\

\
75
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List the paraneoplastic syndromes of SCLC
knowt flashcard image
76
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Outline the paraneoplastic features of squamous cell carcinoma

1. PTH- related protein secretion causing hypercalcaemia
2. clubbing
3. hypertrophic pulmonary osteoarthropathy (HPOA)


1. proliferative periostitis affecting long bones
4. hyperthyroidism due to ectopic TSH
77
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Outline the paraneoplastic features of adenocarcinoma

1. gynaecomastia
2. hypertrophic pulmonary osteoarthropathy (HPOA)
78
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Define Type 1 RF
A partial pressure of oxygen below 8 kPa
79
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Define Type 2 RF
A partial pressure of O2 below 8 kPa

\
AND PaCO2 greater than 6.5 kPa
80
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Describe the mechanisms of hypoxia
**Hypoventilation** (asthma, COPD, motor neurone disease, obesity)

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**Diffusion abnormality** (pulmonary fibrosis, sarcoidosis, COPD)

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**V/Q mismatch** (lobar pneumonia, asthma, PE, pneumothorax)

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**Right to left cardiac shunt** (patent truncus arteriosus)

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**Low inspired O2** (high altitude, air-flight)
**Hypoventilation** (asthma, COPD, motor neurone disease, obesity)

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**Diffusion abnormality** (pulmonary fibrosis, sarcoidosis, COPD)

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**V/Q mismatch** (lobar pneumonia, asthma, PE, pneumothorax)

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**Right to left cardiac shunt** (patent truncus arteriosus)

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**Low inspired O2** (high altitude, air-flight)
81
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Describe LTOT
knowt flashcard image
82
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Describe CPAP
knowt flashcard image
83
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Define Obstructive Sleep Apnoea
Repetitive episodes of partial or complete upper airway obstruction during sleep
Repetitive episodes of partial or complete upper airway obstruction during sleep
84
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Outline the details needed in a sleep history for OSA
knowt flashcard image
85
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How is the severity of OSA assessed?
AHI

\
RDI

\
Epworth Sleepiness Scale (OSA= score >10/24)
AHI

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RDI

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Epworth Sleepiness Scale (OSA= score >10/24)
86
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Outline the treatment options for OSA
Weight loss

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CPAP (for moderate-severe OSA)

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Avoiding alcohol and sedatives

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Non-supine sleep

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Tonsillectomy

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Mandibular advancement splints

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Maxillofacial splints

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Treat underlying cause e.g. Cushing’s
Weight loss

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CPAP (for moderate-severe OSA)

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Avoiding alcohol and sedatives

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Non-supine sleep

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Tonsillectomy

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Mandibular advancement splints

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Maxillofacial splints

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Treat underlying cause e.g. Cushing’s
87
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Briefly outline the steps in asthma management (adults)

1. Newly diagnosed→ SABA
2. Not controlled or more symptoms→ SABA + low dose ICS
3. SABA + low dose ICS + LTRA
4. SABA + low dose ICS + LABA
5. SABA +/- LTRA


1. switch ICS/LABA for maintenance and reliever therapy (includes ICS)
6. SABA +/- LTRA + medium dose ICS MART
7. SABA +/- LTRA plus one of


1. high dose ICS
2. LAMA or theophylline
3. seek specialist advice

\
88
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Describe bronchiectasis and its causes
Permanent __dilatation of the airways__ secondary to chronic infection or inflammation

\
**Causes:**

* post-infective e.g. Tb, measles, pertussis, pneumonia
* CF
* bronchial obstruction e.g. lung cancer, foreign body
* immune deficiency e.g. selective IgA, hypogammaglobulinemia

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ECG showing tramlines (bronchial wall thickening), prominent in left lower zone
Permanent __dilatation of the airways__ secondary to chronic infection or inflammation

\
**Causes:**

* post-infective e.g. Tb, measles, pertussis, pneumonia
* CF
* bronchial obstruction e.g. lung cancer, foreign body
* immune deficiency e.g. selective IgA, hypogammaglobulinemia 

\
ECG showing tramlines (bronchial wall thickening), prominent in left lower zone
89
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List the causes of upper zone fibrosis
Fine inspiratory crackles on auscultation

\
==**CHART**==

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**C**oal worker’s pneumoconiosis

**H**istiocytosis/ hypersensitivity pneumonitis

**A**nkylosing spondylitis

**R**adiotherapy

**T**b

**S**ilicosis/ sarcoidosis
90
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List the causes of lower zone fibrosis
==**I Don’t Care Actually**==

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**I**PF

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**D**rug-induced e.g. amiodarone, methotrexate

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**C**onnective tissue disorders e.g. systemic lupus erythematous (SLE)

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**A**sbestosis
91
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List 3 consequences of OSA
Daytime somnolence

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Compensated respiratory acidosis

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Hypertension
92
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Name the most likely causative agent of an infective exacerbation of COPD
Haemophilus influenzae
93
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Outline the inhaler technique guideline recommended by the BTS

1. Remove cap and shake

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2. Breathe out gently

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3. Put mouthpiece in mouth and as you begin to breathe in, which should be slow and deep, press canister down and continue to inhale steadily and deeply

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4. Hold breath for 10 seconds, or as long as is comfortable

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5. For a second dose wait for approximately 30 seconds before repeating steps 1-4

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Only use the device for the number of doses on the label, then start a new inhaler.
94
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Briefly outline the management of low-severity CAP
==**Amoxicillin**== first-line

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If penicillin allergic, then use macrolide (erythromycin) or tetracycline

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**5 day course** of antibiotics

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Repeat CXR at 6wks
95
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Briefly outline the management of moderate and high-severity CAP
==**Dual antibiotic therapy**== with amoxicillin and a macrolide

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**7-10 day course**

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NICE recommend considering beta-lactamase stable penicillin such as **co-amoxiclav, ceftriaxone or piperacillin with tazobactam and a macrolide** in high-severity CAP

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Repeat CXR at 6wks
96
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List the indications for a chest drain insertion
(Tube inserted into pleural cavity which creates a one-way valve, allowing movement of air or liquid out)

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* pleural effusion
* pneumothorax not suitable for conservative management or aspiration (therapeutic and diagnostic)
* empyema
* haemothorax
* haemopneumothorax
* chylothorax (accumulation of lymph from GIT in lungs)
97
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List the contraindications of a chest drain insertion
* **INR > 1.3** (greater risk of bleeding and complications)
* platelet count
98
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Outline the staging of COPD

1. Mild: FEV1 >80%
2. Moderate: FEV1 50-79%
3. Severe: FEV1 30-49%
4. Very severe: FEV1
99
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Outline the LTOT criteria for COPD patients
lungS POP

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Secondary polycythaemia

Peripheral oedema

Oxygen 7.3-8

Pulmonary hypertension
100
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Describe bronchiectasis and what its most common organism is
==**Permanent dilatation of airways**== secondary to chronic infection

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Commonly caused by **Haemophilus influenzae**