Resp Flashcards

(46 cards)

1
Q

Pancoast tumour

A

Ptosis
Miosis
Wasting of 1st webbed space

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2
Q

Clubbing

A

Interstitial lung disease
Malignancy (bronchogenic carcinoma AND mesothelioma)
Suppurative lung disease (bronchiectasis, abscess, empyema, CF)

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3
Q

Consolidation Examination features

A

Percussion: dull
Breath sounds: bronchial or reduced
Vocal resonance: hyper resonant
Mediastinal shift: none

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4
Q

Collapse (or lobectomy/pneumonectomy) Examination features

A

Percussion: dull
Breath sounds: reduced or absent
Vocal resonance: reduced or absent
Mediastinal shift: towards

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5
Q

Effusion (or raised hemidiaphragm due to phrenic nerve palsy) Examination features

A

Percussion: stony dull
Breath sounds: reduced or absent
Vocal resonance: reduced or absent
Mediastinal shift: away if big

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6
Q

Pneumothorax Examination features

A

Percussion: hyper resonant
Breath sounds: reduced or absent
Vocal resonance: reduced of absent
Mediastinal shift: away if tension

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7
Q

Hoover’s sign

A

intercostal indrawing = hyperinflation

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8
Q

Wheeze causes

A

Small airway obstruction = asthma or COPD

Obstruction from object or tumour ==> monophonic and probably collapse further down

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9
Q

Creps causes

A

Secretions (if normal get them to cough and should disappear, if not pneumonia)
Pus (cystic fibrosis, bronchiectasis)
Oedema
ILD

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10
Q

ILD

see extra notes

A

Idiopathic:
Extrinsic allergic alveolitis: bird fancier’s lung; farmer’s lung
Inhaled irritant: asbestosis; silicosis; coal worker’s pneumoconosis
Systemic disease: SLE; RA; sarcoid; systemic sclerosis
Iatrogenic: methotrexate, amiodarone, radiotherapy

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11
Q

Horner’s syndrome

A

Central lesion: stroke/tumour
T1 root lesion: neurofibroma
Brachial plexus lesion: pancoast tumour, cervical rib, trauma (at birth = Klumpke’s)
Neck lesion: tumour, carotid artery aneurysm

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12
Q

Fine creps causes

A

Pulmonary oedema

ILD

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13
Q

Coarse creps causes

A

Bonchiectasis
CF
Bibasal pneumonia

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14
Q

Pleural effusion classification

A

Transdate (<30g/L) = reduced oncotic pressure
E.g. LVF, volume overload, hypoalbuminaemia, Meig’s syndrome
Exudate (>30g/L) = infection (pneumonia, TB); infarction (PE); inflammation (RA, SLE); malignancy (bronchogenic, mesothelioma)

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15
Q

Pneumonia CURB-65

A
Confusion (< or equal 8)
Urea >7mM
RR >30
BP <90/60
> or equal 65

0-1 –> home Rx
2 –> hospital Rx
3 or > –> consider ITU

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16
Q

Pneumonia Empiric Rx

A

CAP:
Mild - amoxi 500mg TDS for 5 d OR clari 500mg BD 7 d
Moderate - amoxi AND clari 500mg BD for 7 d
Severe - clari 500mg BD IV AND co-amoxi 1.2g TDS IV / cefuroxime 1.5g TDS IV 7-10 d; (add fluclox if staph suspected)
Atypical typically treated with clari:
chlamydia - tetracycline (clari)
PCP - co-trimoxazole
Legionella - clarithromycin + rifampicin

HAP:
mild/<5days/aspiration: co-amoxi 625mg TDS PO for 7 days
Severe: tazocin +/- vanc +/- gent for 7 days

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17
Q

SIRS

A
> or equal 2 of:
Temp >38 or <36
HR >90
RR >20 or PaCo2 <4.6
WCC >12 or <4
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18
Q

Klebsiella features

A

Cavating pneumonia esp upper lobes

Treated with cefotaxime

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19
Q

Mycoplasma features

A

Dry cough
reticular-nodular shadowing
Flu-like prodrome
Treated with clari

Legionella looks similar but bibasal consolidation and hyponatraemia / deranged LFTs. Also treated with clari and both can be investigated via serology

20
Q

Chlam. pneum features

A

pharyngitis, otitis –> pneumonia

treated with clari and Ix serology

21
Q

Chlam. psittaci features

A
dry cough
horder's spots - rose spots
splenomegaly
epistaxis
meningo-encephalitis
treated with clari and Ix serology
22
Q

PCP features

A
Dry cough
Exertional dyspnoea
Bilateral creps
CXR: normal or bilateral perihilar
interstitial shadowing

Ix: BAL, sputum and biopsy
Rx: high dose co-trimoxazole

23
Q

Bronchiectasis causes

A

idiopathic (50%)
Congenital - CF, Kartagener’s (situs inversus), Young’s syndrome
Post-infectious - Measles, pertussis, pneumonia, TB
Immunodeficiency - Bruton’s, CVID
Yellow nail syndrome

24
Q

Bronchiectasis signs

A

O/E: Clubbing, coarse creps and wheeze, purulent sputum
CXR - thickened bronchial walls (tramlines and rings)
Spirometry: obstructive pattern

25
Bronchiectasis Rx
chest physio Abx for exacerbations - e.g. cipro for 7-10 days bronchodilators (nebulised B agonists) From CF - GI dysfunction give Creon to replace pancreatic enzymes, insulin and UDCA for bile stimulation
26
Lung cancer complications
``` Local  Recurrent laryngeal N. palsy  Phrenic N. palsy  SVC obstruction  Horner’s (Pancoast’s tumour)  AF ``` Paraneoplastic 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
27
DDx of pulmonary oedema
``` Tranusdates: ↑ capillary hydrostatic pressure  CCF  Iatrogenic fluid overload  Renal failure  Relative ↑ in negative pressure pulmonary oedema ↓ capillary oncotic pressure  Liver failure  Nephrotic syndrome  Malnutrition, malabsorption, protein-losing enteropathy ↑ interstitial pressure  ↓lymphatic drainage: e.g. Ca ``` Exudates  ARDS (admit to ITU for organ support and treat underlying cause)
28
Indications for ventilation in ARDS
 PaO2<8KPa despite 60% FiO2  PaCO2>6KPa Method  6ml/kg + PEEP (e.g. 10cm H2O)
29
Type 1 resp failure
PaO2 <8kPa and PaCO2 <6kPA; caused by V/Q mismatch which can be vascular (PE, pulmonary shunt); asthma; pneumothorax; atelectasis as well as fluid and fibrosis
30
Type 2 resp failure
PaO2 <8kPa and PaCO2 >6kPA; caused by alveolar hypoventilation from obstructive (COPD, asthma, bronciectasis) or restrictive (GBS, fluid and fibrosis) causes
31
A-a gradient
 PAO2= (95 x FiO2) – (PaCO2/0.8) |  ↑ (PAO2-PaO2) suggests lung pathology
32
O2 therapy
In pts. at risk of hypercapnic resp failure:  Start O2 therapy at 24% and do an ABG – Blue Venturi @ 2-4L/min
33
O2 therapy mechanism
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% ```
34
mMRC dyspnoea score (COPD)
1. Dyspnoea only on vigorous exertion 2. SOB on hurrying or walking up stairs 3. Walks slowly or has to stop for breath 4. Stops for breath after <100m / few min 5. Too breathless to leave house or SOB on dressing
35
COPD Severity
Spirometry should show FEV1:FVC <0.7 for COPD and usually FEV1 <80% ``` Assess Severity  Mild: FEV1 >80% (but FEV/FVC <0.7 and symptomatic)  Mod: FEV1 50-79%  Severe: FEV1 30-49%  Very Severe: FEV1 < 30% ```
36
PE score system
For PE assess probability from Well's score If low probability perform D-dimer (if negative excludes PE, if positive do CTPA) If high probability perform CTPA NB. -ve D-dimer has 95% NPV for PE NB review management of PE
37
Pleural effusion classification
 Effusion protein < 25g/L = transudate  Effusion protein >35g/L = exudate  Between 25-35g/L: apply Light’s Criteria ``` Light’s Criteria  An exudate has one of:  Effusion : serum protein ratio >0.5  Effusion : serum LDH ratio >0.6  Effusion LDH is 0.6 x ULN ```
38
Pleural effusion Ix
Diagnostic Tap  Percuss upper boarder and go 1-2 spaces below  Infiltrate down to pleura with lignocaine.  Aspirate with 21G needle Send for:  Chemistry: protein, LDH, pH, glucose, amylase  Bacteriology: MCS, auramine stain, TB culture  Cytology  Immunology: SF, ANA, complement
39
Sarcoidosis features
``` GRANULOMA General (FLAWS) Respiratory - dry cough SOB, chest pain Arthralgia Neurological (Bell's palsy) Urine (renal stones from hypercalcaemia) Low hormones (amenorrhoea) Ophthalmological (uveitis, Sjogren's) Myocardial (restrictive cardiomyopathy) Abdominal (hepatosplenomegaly + cholestatic LFT) Skin (erythema nodosum/lupus pernio) ```
40
Stages of sarcoid
 Stage 1: BHL  Stage 2: BHL + peripheral infiltrates  Stage 3: Peripheral infiltrates alone  Stage 4: Progressive mid-zone fibrosis with bullae
41
Granulomatous Disease Differential
 Infections: TB, leprosy, syphilis, crypto, schisto  AI: PBC  Vasculitis: GCA, PAN, Wegener’s, Takayasu’s  Idiopathic: Crohns, Sarcoid  Interstitial lung: EAA, silicosis
42
Sarcoidosis Rx
Acute sarcoidosis  Usually resolves spontaneously  Bed rest and NSAIDs Chronic sarcoidosis  Steroids: pred 40mg/d for 4-6wks  Additional immunosuppression: methotrexate, ciclosporin, cyclophosphamide
43
ILD causes by location
``` Upper Zone: A PENT  Aspergillosis : ABPA  Pneumoconiosis: Coal, Silica  Extrinsic allergic alveolitis  Negative, sero-arthropathy  TB ``` Lower Zone: STAIR  Sarcoidosis (mid zone)  Toxins: BANS ME (bleomycin, amiodarone, nitrofurantoin, sulfasalazine, methotrextrate)  Asbestosis  Idiopathic pulmonary fibrosis  Rheum: RA, SLE, Scleroderma, Sjogren’s, PM/DM
44
Quitting smoking advice
Referral to NHS stop smoking service Nicotine gum/patches Varenicline (C/I depression) Bupropion (C/I epilepsy)
45
Obstructive sleep apnoea
Daytime Features: morning headache, somnolence, reduced memory, irritability, depression ``` Polysomnography is diagnostic Rx: weight loss, avoid smoking and EtOH CPAP during sleep surgery to relieve obstruction (tonsillectomy or uvulopalatpharyngoplasty) ```
46
COPD X-ray
``` Hyperinflation (>6 ant ribs) Decreased cricosternal distnace Flat hemidiaphragms Large central pulmonary arteries Decreased peripheral markings Bullae ```