Respiratory Flashcards

1
Q

Acute Asthma

A

Moderate: Can speak sentences, 75-50% PEFR, <110bpm, <25 RR.

Severe: Can’t speak full sentences, 33-50% PEFR, >110bpm, >25 RR.

Life threatening: <33% PEFR, O2<92%, cyanosis, silent chest and bradycardia.

Management:
Severe and life threatening need hospital admission, moderate if irresponsive.
Give O2 if hypoxaemic.
SABA- through and inhaler, unless LF in which case nebulised
Steroid- Give prednisone 40-50mg daily for 5 days since the attack minimum or until pt recovers.
Ipratropium bromide in severe/life threatening, or that which has not yet responded to therapy.
Magnesium sulphate may be used
After this consider ITU for ventilation and O2.

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2
Q

Acute asthma discharge criteria:

A

Stable on discharge medication for 12-24hrs
Correct inhaler technique
PEFR>75%

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3
Q

Acute bronchitis

A

Sore throat, cough, rhinnorhoea or wheeze. May also present with low grade fever.

Inflammation of the trachea and main bronchi, usually due to viral infection. Self resolving within 3wks.

Pneumonia is different as have at least wheeze, dyspnoea or sputum and has focal chest signs, as well as systemic features. Not the case in acute bronchitis.

Manage with rest, lots of fluid intake and analgaesia. Only consider Abx if systemically unwell or have existing co-morbidities. Doxycycline first line, in pregnant/children five amoxicillin.

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4
Q

Acute COPD exacerbation

A

Infective exacerbation usually due to H. Influenza (most common). May also be due to strep.pneumonia.

Get increase dyspnoea, increase wheeze, increase in sputum or may present hypoxic.

Treat with increased bronchodilator, consider nebulised also. Give 30mg prednisolone for at least 5 days. Usually give Abx with the exacerbation, although not recommended by NICE.

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5
Q

Acute respiratory distress syndrome

A

Increased alveolar capillary permeability, therefore increased fluid in the alveoli- can lead to non-cardiogenic pulmonary oedema.

Need urgent ITU admission for treatment of hypoxia, general organ support and treatment of underlying condition (Abx)

Features include dyspnoea, increased RR, low O2 sat, bilateral lung crackles.

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6
Q

Allergic bronchopulmonary aspergillosis

A

Allergic reaction to aspergillos spores.

Bronchoconstriction; cough, wheeze, dyspnoea
Bronchiectasis
Eosinophilia

Treat with glucocorticoids and may need itraconazole as second line

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7
Q

Alpha 1 anti trypsin deficiency

A

Genetic
Lungs- emphysema
Liver- cirrhosis, adults can develop hepatocellular carcinoma

Treat with no smoking. Supportive; bronchodilators, physio, IV A1AT, lung volume reduction surgery

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8
Q

Asbestos in lungs

A
Can cause;
Pleural plaques 
Pleural thickening
Asbestosis- low lobe fibrosis- dyspnoea and reduced exercise tolerance.
Mesothelioma- poor prognosis
Lung cancer
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9
Q

Aspiration pneumonia

A

Inhalation of a foreign object, depending on its acidity can lead to chemical pneumonitis

Main causes; strep pneumonia, staph aureus, h.influenza

Commonly affected at the right middle and lower lobes.

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10
Q
Asthma 
RF
Signs and symptoms 
Investigations 
Management (refer to drugs table) 
NB Step down review every 3 months
A

Chronic, reversible inflammation of the airways due to type 1 hypersensitivity reaction.

RF; FHx, maternal smoking/viral infection during pregnancy, not breastfed, exposed to smoking early on, occupation, LMBW, exposure to high levels of allergens (dust mites) etc

Signs + symptoms; wheeze, cough (worse at night), tight chest, dyspnoea. Also reduced FEV/FVC ratio, reduced PEFR. Atopy common

Investigations; fractions exhaled nitric oxide (used more as objective test), spirometry (including reversible spirometry), CXR.

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11
Q

Atelectasis

A

Alveolar collapse usually post op.

Should be considered if within 72hrs post op get dyspnoea/hypoxaemia.

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12
Q

Bilateral hilar lymphadenopathy

A

Common causes:
Sarcoidosis
TB

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13
Q

Bronchiectasis

A

Permanent dilation of the bronchi (larger than corresponding artery), due to infection/inflammation. (Pseudomonas, CF)
Gold standard diagnosis is CTPA.

Management:
Physio training of sputum clearance 
Postural drainage
Abx for exacerbation
Immunisations
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14
Q

CXR

A

Cavitation; TB, abscess, RA, PE

Lobar lung collapse; lung cancer, asthma, inhaled foreign body. On CXR will see tracheal deviation and mediastinal shift towards collapse, hemidiaphragm elevation

Metastasis; renal (cannon ball mets), breast, colorectal, prostate and bladder.

‘White out lung’; consolidation, pleural effusion, pulmonary oedema, collapse or pneumonectomy. Look at tracheal deviation. Towards the white- pneumonectomy, lung collapse. Central- consolidation, oedema, mesothelioma. Away from the white- pleural effusion

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15
Q

Clubbing causes

A

Cardiac; congenital cyanotic conditions (Tetrology of fallout), bacterial endocarditis and atrial myxoma.

Respiratory; lung cancer, CF, TB.

Gastro; Crohns, coeliacs, liver cirrhosis.

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16
Q
COPD
Causes 
Features
Investigations
Management
A

Chronic bronchitis or emphysema
Main causes are smoking!!! And also A1AT deficiency.

Features; cough (sputum usually), dyspnoea (especially on exertion), wheeze. May get RSHF in extreme cases.

Investigations: Spirometry post bronchodilator, CXR (barrel chest, bullae), FBC (exclude secondary polycythaemia), BMI.

Some pts may require long term oxygen therapy (15hrs/day). Consider if FEV1<30%, cyanosis, polcythaemia, O2 sats<92%. If a person is still smoking don’t offer LTOT.

Management of COPD:
SMOKING CESSATION 
PULMONARY REHAB 
Annual influenza vaccine
One off strep vaccine 

Give SABA
If they have features of asthma/responsive to steroids (eosinophilia, previous asthma, atopy etc)- give ICS+LABA.
If not then LABA+LAMA

If still breathless then ICS+LAMA+LABA

17
Q

Churg-Strauss syndrome

Eosinophillic granulomatosis with polyangitis

A
Asthma 
Eosinophilia 
Dyspnoea 
Sinusitis 
pANCA (small vessel vasculitis)
18
Q

Wegeners syndrome

Granulomatosis with polyangitis

A

cANCA
Affecting URT- epistaxis, sinusitis, LRT- dyspnoea, haemoptysis and the kidneys- GN.
Also may have saddle nose deformity

Treat with steroids, cyclophosphamide, plasma exchange

19
Q

Extrinsic allergic alveolitis

A

Inhalation of an allergen causing a type III hypersensitivity reaction.

Bird fanciers lungs (avian protein from bird dropping)
Farmers lungs
Malt workers lungs

Acute:
Dyspnoea
Cough (dry)
Fever

Chronic:
Lethargy 
Weight loss 
Dyspnoea 
Productive cough 

Treat by avoiding precipitating factors and glucocorticoids.

NB no eosinophilia. Fibrosis in mid/upper lobes of the lungs.

20
Q

Idiopathic lung fibrosis

A

Lung fibrosis due to an unknown cause.

Dyspnoea, dry cough, clubbing.

Treat with pulmonary rehab, meds not effective, poor prognosis.

21
Q

Lung cancer
Types
Management

A
Types: 
Non-small cell: 
Adenocarcinoma- gynaecomastia
Squamous cell- PTHrP (hyperCa), clubbing
Large cell

Small cell:
ACTH- Cushing’s syndrome, ADH- hypoNa, Lambert-Eaton syndrome- destruction of NMJ therefore MS like symptoms.

Non small cell management:
Usually can treat with surgery, unless metastatic, poor general health of vocal chord paralysis. Can also do palliative radiotherapy, poor response to chemo.

Small cell management:
Usually present at metastatic state therefore radio/chemotherapy. Unless early diagnosis then consider surgery.

22
Q

Lung cancer
Features
Investigations
Referral

A

Features; dyspnoea, haemoptysis, persistent cough, weight loss, chest pain, hoarseness of voice.

Investigate with CXR first. Diagnostic by CT.

Referral via 2ww if >40yrs with unexplained persistent haemoptysis or if CXR suggestive of lung cancer.

23
Q

Lung fibrosis

A

Upper lobe:
Extrinsic allergic alveolitis
Sarcoidosis
TB

Lower lobe:
Idiopathic LF
SLE
Drugs

24
Q

Obstructive sleep apnoea

A

RF: obesity, HF, large tonsils, Marfans syndrome, large tongue-acromegaly, hypoT,

Leads to- HTN, daytime sleepiness, compensated resp acidosis.

Assess usually with questionnaire, also monitoring sleep with pulse oximetry.

Treat with weight loss, CPAP (continuous positive airway pressure), meds not effective.

25
Q

Dissociation curves

A

Shifts to right if increased O2 delivery.
In the cases of raised CO2, raised H+, raised 2,3 BPG, raised temperature.

Opposite for shifting to the left

26
Q

Oxygen saturation

A

Aim for 94-98%
COPD- 88-92% (Venturi mask)
COVID- 92-94%

27
Q

Pleural effusion

A

Dyspnoea +/- dry cough, chest pain. Dull percussion, reduced BS

Transudate:
<30g/L protein 
HF (common) 
Hypoalbuminameia 
HypoT 
Exudate:
>30g/L protein 
Infection
Connective tissue disorder 
PE
Neoplasia 

Investigate with aspiration to determine if transudate or exudate.
Treat the cause, if recurrent then may need pleurodesis, recurrent aspiration or indwelling pleural catheter.

28
Q

Pneumonia:
Features
CURB65

A

Inflammation of the alveoli usually secondary to a bacterial infection. Causing dyspnoea, chest pain, productive cough, fever, reduced O2 sats.

Commonly s.pneumonia, h.influenza in COPD, staph.aureus, can also be pneumocystis jiroveci in HIV.

CURB65
Confusion (8/10)
Urea>7mM
Resp rate>30
BP<90/<60
>65yrs

In community use CRB65. If >2 then hospital admission

29
Q

Pneumonia
Investigations
Management

A

CXR- shows consolidation, FBC shows neutrophilia in bacterial infection, urea high and CRP increased, sputum cultures may be collected.

Give O2 if <92%

Mild CAP- 5 day amoxicillin (macrolide if allergy)
Moderate/severe CAP- 7-10 day amoxicillin +macrolide

30
Q

Pneumothorax

A

Sudden onset chest pain, dyspnoea, tachycardia and tachypnoea.

RF include lung condition, connective tissue disorder, ventilation.

Management:
Primary- if <2cm and asymptomatic then discharge.
If <2cm but symptomatic then aspirate.
If >2cm then chest drain.
Avoid smoking to decrease recurrence.

Secondary- if >50yrs old >2cm +/- symptoms chest drain.
If <2cm then aspirate

Iatrogenic pneumothorax are less likely to recur and will usually resolve with observation.

31
Q

RA manifestations in the lungs

A

Pleural effusion
Pulmonary fibrosis
Pleurisy
Infections (immunosuppressed)

32
Q

Sarcoidosis

A

Multisystem disorder of unknown aetiology causing caseous granulomas.

Presents with erythema nodusum, bilateral hilar lymphadenopathy, dyspnoea, non-productive cough, malaise, weight loss, hyperCa

Spirometry may show restrictive pattern

Manage with steroids

33
Q

Silicosis

A

Inhalation of silicone dioxide, can predispose to developing TB.

34
Q

NRT- nicotine replacement therapy

A

Offer to those who are wanting to reduce smoking. Offered supply upto two weeks after their target date.

Don’t offer repeat if not committed.
Side effects: headaches, nausea, flu like symptoms.

Pregnant women should be tested to see if they smoke. First line CBT, motivational interview and self help. Can offer NRT but some contraindicated.