RESP2 Flashcards

(55 cards)

1
Q
A
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2
Q

What are the types of primary lung cancer?

A
  1. Non small cell - adeno, squamous and large cell

adeno is most common

Non small cell is less aggressive

  1. Small cell - rarer and more aggressive
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3
Q

Management of lung cancer

A

Depends on histology

Small cell - poorly diferentiated

  • usually not appropriate for curative surgery b/c there’s spread at diagnosis.

Chemo is possible - but only extends life 3 months to 1.5 years

NON small cell - adeno/sq/large -

Curative resection is the aim

Radiotherapy is mostly palliative

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4
Q

What is bronchiectasis?

A

Morphologically - Permanent dilatation of bronchi and bronchioles

Clinically - Chronic cough, Recurrent or persistent bronchial infections AND often discoloured sputum production

Pathophys - small airway bronchiolitis –> protease production –> causes damage to large airways –> permanent dilatation

– MILD TO MODERATE OBSTRUCTIVE AIRWAYS DISEASE

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5
Q

What is a traction bronchiectasis?

A

In an area of lung fibrosis

Traction effect from fibrosis of adjacent bronchioles causes dilatation.

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6
Q

What are the risk factors for development/causes of bronchiectasis?

A
  1. Broncial obstruction - foreign bodies, impaction of mucous, atopic asthma, chronic bronchitis, tumour
  2. Congenital or hereditary conditions
    - cystic fibrosis - abnormally thick mucous

Immune deficiency states

Kartagener syndrome - situs inversitus, bronchiectasis, Sinusitis

  1. Necrotising or Supprative Pneumonia - often Staph species or Klebsiella, Mycobacterium Avium Complex, Aspergillus Fumigatus
  2. Mucocillary defects - Primary Cillary Dyskinesia
  3. Autoimmune conditions - Rheumatoid
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7
Q

Patient with symptoms of persistent chest infection, not responding to treatment and Pseudomonas Aeruginosa (or other gram negative) is found on culture. Which diagnosis must be excluded?

A

Bronchiectasis

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8
Q

Clinical Features of Bronchiectasis?

A

Dyspnoea, chronic cough, sputum, haemoptysis, malnutrition/LOW

Mild disease - symptoms with chest infections

Severe disease - recurrent febrile episodes with pneumonia, chronic COP (copious, offensive, purulent) sputum, LOW, LOA, Finger clubbing in 5%, haemoptysis

o/e

Finger clubbing 5%

central trachea

reduced chest expansion

Can have creps and rhonchi - bi basal creps common

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10
Q

When would you start antibiotics in an exacerbation of bronchiectasis?

A

MUST HAVE ALL THREE

  • Increased sputum volume
  • increase purulence
  • Increased COUGH
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11
Q

Patient presents with years of chronic cough and sputum production - discoloured sputum. Bibasal crepitations on examination. Diagnostic investigation?

A

HRCT

In cross section - Internal calibre of the bronchus is larger than the adjacent pulmonary vessel (Arterial branch) - Signet ring sign

IN longitudinal - Failure of bronchi to taper

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12
Q

Investigations in suspected bronchiectasis?

A

HRCT
Sputum test M/C/S and acid fast bacilli

FBE, LFT, UEC

Spirometry

Special diagnostic tests for associated conditions- eg sweat testing in kids for CF,

RF and ANA, Immunoglobulin concentrations (IgE, IgA, IgM, IgG)

Aspergillus serology

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13
Q

What is your management approach for a patient with bronchiectasis?

A

Management should be individualised in collaboration with a respiratory physician with a specific treatment plan.

  1. Prompt treatment of exacerbations.
  2. Avoid infections - sick kids, babysitting, sick contacts,
  3. Clear the airway of sputum - Chest physiotherapy
  4. Routine Vaccinations for Influenza and pneumococcal coverage
  5. Regular Review - annual in adults, 6 monthly in kids - at this time sputum culture/check for complications/disease progression and severity
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14
Q

Which subset of bronchiectasis is rapidly progressive

A

Likely those who are colonised by pseudomonas

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15
Q

Which antibiotics would you use for a bronchiectasis exac?

A

For non pseudom - same as CAP

Amox 1g TDS

or

Doxy 100mg bd

If recent Haemoph Inf or Moraxella

Augmentin DF (Amox and clavulanic acid 875 + 125 - one bd

If pseudo

Cipro 500mg bd

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16
Q

Which pathogens are associated with exacerbations of Bronchiectasis

A

Haemophillus influenzae

Strep Pneumo

Moraxella

Pseudomonas - if present - repeat the culutre and discuss with specialist - as this can be rapidly progressive

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17
Q

What are the clinical features of bronchiolitis?

A
  1. wheeze
  2. fever
  3. Cough
  4. Coryza
  5. tachypnoea
  6. +/- work of breathing/
  7. +/- feeding difficulties
  8. o/e widespread wheeze and crackles
  9. Infant under 12 months
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18
Q

Infectious agent in bronchiolitis

A

RSV

or rhino

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19
Q

Priniciples of management

A

Supportive

Support oxygenation and feeding

no ix or abx

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20
Q

Risk factors for more serious illness

A

Age less than 10 weeks at presentation

Chronic lung disease

Chronic neurological

Downs Syndrome

Indigenous ethnicity

Immune compromise

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21
Q

Admission criteria for bronchiolitis?

A

Moderate to severe work of breathing - RR, tracheal tug, nasal flaring, recessions

Oxygen saturations less than 94%

Feeding problems

Tachypnea RR

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22
Q

Further managment of Bronchiolitis?

A

O2 therapy only if sats persistently below 90%

Small frequent feeds

If clinically dehydrated - may need NG feeds or IV

Parental education (Handout from the RCH on bronchiolitis)

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23
Q

Complications of Bronchiolitis

A

Dehydration from feeding issues

Hypoxaemia

Bronchiolitis Obliterans (Can lead to permanent lung damage)

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24
Q

What are the clinical features of Bronchial Cancer?

A

1. Respiratory

Cough - over three weeks needs CXR

  • SOB - exertional - can be due to lobar collapse or underlying lung disease

Wheeze

Prolonged/unresolving chest infection

Chest pain - central dull if mediastinal mass or node invasion, peripheral sharp if pleural/chest wall invasion

  1. Local spread- PanCoast tumour - apical lung - Invasion symapthetic trunk - horners, Invasion of C8/T1 - and brachial plexus - pain in upper limb and wasting of small muscles of hand (+/- 2nd rib pain)
  2. Constitutional symptoms

LOA, LOW

  1. Metastatic symptoms

Brain -H/ache

Liver - LOA, LOW

Bone - #

Adrenal - usu asympto

25
Q

Investigations for broncial cancer?

A

CXR - can miss it sometimes ( A solitary nodule - granuloma, harmartoma, bronchial adenoma)

CT - if done for staging needs to include the abdomen

A LN less than 1cm is not considered enlarged but can still have cancer cells.

PET/CT - investigation of choice for staging

Fibreoptic bronchoscopy ( another type is fluorescence bronc can detect premalignant cells)

Endobronchial USS and biopsy, also u/s guided biopsy of supraclavicular lymph node can be done.

26
What is Asbestos?
A group of naturally occuring fibres composed of **hydrated magnesium silicates** Once _inhaled_ they can block small airways and then proceed to _chronic inflammation and fibrosis_. (due to the bodys immune response)
27
Who is at risk of asbestos exposure?
Anyone who worked in the following industries **_in the past_** mining and milling of fiber cement textiles insulation ship building yard power stations
28
Which disorders arise from asbestos exposure?
The spectrum of disorders includes: 1. **Asbestosis** 2. **Pleural disease** (benign asbestos effusion, pleural plaques) 3. **Malignancies** (non small cell and small cell carcinoma of the lung as well as malignant mesothelioma) Primary lung Ca is 5 to 7 times higher in those with asbestosis and 1.5 times higher in those with pleural plaques
29
What is Asbestosis?
Pulmonary fibrosis caused by inhalation of asbestos fibres. Slow indolent course. Progressive Diffuse fibrosis. +/- pleural disease. Mostly people who were exposed in past years.
30
What is required for a histopathological dx of asbestosis?
**Uncoated or coated asbestos fibres (asbestos bodies)** in association with **Interstitial Pulmonary fibrosis** Similar to UIP (usual interstitial pneumonitis) Except - asbestos doesn't tend to have fibroblast foci and does have mild fibrosis of visceral pleura
31
Clinical features of Asbestosis?
Most will be **asymptomatic for 20-30** years after exposure **Chronic, progressive exertional dyspnoea** (often cough, wheeze and sputum are absent - unless smoker) o/e **fine bibasal end inspiratory crackles** **FInger clubbing 40%** cor pulmonale with **elevated JVP and peripheral oedema**
32
Investigations in asbestosis
1, **pulmonary function tests** - restrictive defect with reduced DLCO reduced pulmonary compliance, Reduced lung volumes 2. **HRCT** - parenchymal fibrosis, coarse _honeycombing_ in advanced disease - **pleural plaques** (these are differenitators from other types of fibrosis) 3**. Broncoalveolar lavage** - helps to differentiate from malignancy, infection, pneumonitis if other tests have not been sufficiently diagnostic
33
How is a diagnosis of Asbestosis made?
1. History of asbestos exposure 2. Evidence of lung fibrosis 3. Absence of other causes of diffuse parenchymal lung disease
34
What is the differential Dx of asbestosis?
Idiopathic pulmonary fibrosis Drug induced pneumonitis interstitial pneumonitis associated with rheumatoid arthritis or rheumatic disease Chronic hypersensitivity pneumonitis chronic pulmonary fibrosis and emphysema pleuropulmonary fibroelastosis
35
WHat is the management of Asbestosis?
NO cure 1. Smoking cessation 2. Vaccinations for influenza and pneumococcal disease. 3. Prompt treatment of respiratory infections 4. Supplemental oxygen if patient becomes hypoxaemic 5. Early detection of physiologic and radiologic abnormalities
36
What are the complications of asbestosis?
1. Pleural disease - eg pleural plaques or effusions 2. Malignancy - eg malignant mesothelioma or lung cancer 3. Respiratory failure in the context of progressive fibrosis
37
What are features of pleural disease in asbestosis?
1. Pleural involvement is a hallmark of asbestos related disease 2. Pleural effusions - benign asbestos related effusions 3. Pleural plaques and diffuse pleural thickening - benign but can cause pain and discomfort
38
What is Mesothelioma?
It is a rare neoplasm arising from the **mesothelial surface** of pleura, peritoneal cavity, tunica vaginalis, or pericardium **Malignant pleural mesothelioma is the most common type.** **Asbestos is the ONLY known risk factor** for malignant mesothelioma
39
How is smoking related to asbestos?
It appears that relative risk of lung cancer in smoking and asbestos exposure is mulitplicative - smoking and asbestos indepently increase risk of malignancy. Together they increase risk 59 fold
40
Chest xray findings in asbestos related disease?
- bilateral pleural calcifications and subdiaphragmatic calcifications - Pleural plaques alone are not a diagnosis of asbestosis (just asbestos exposure). Dx of asbestosis requires fibrosis and absence of other diffuse parenchymal lung disease Mesothelioma - often presents with an effusion on xr
41
How might a foreign body below the main bronchus present in a child?
Could be asymptomatic Could have persistent wheeze, cough, dyspnoea Could present with **recurrent pneumonia** might have asymetric chest wall movements and/or tracheal deviation on examination ( or could be normal) Ix - CXRay - inspiratory and expiratory films may give better visualisation
42
How would you manage a TOTAL obstruction of main bronchus by foreign body
1. Open airway and under direct vision (pref with laryngoscope) look in mouth for a foreign body - if present remove with magills forceps 2. Place child prone with head down 3. Administer 5 intrascapular back blows 4. Turn child over and apply five chest thrusts 5. Check in the mouth if foreign body has appeared 6. continue alternating back blows and chest thrusts 7. Call ambulance for urgent transfer
43
If PARTIAL obstruction of main bronchus or FB lower than main bronchus
Sit child upright in position they feel most comfortable arrange for urgent transfer to hospital for removal of foreign body in operating theatre
44
How would you prevent foreign body inhalation?
No child less that 15 months should be offered pop corn, raw apples, hard lollies or raw carrot. Children under 4 should not be offered peanuts Avoid toys with small parts until age of 3 Children should be offered one piece of food at a time and encouraged to sit quietly while eating
45
What symptoms arise from laryngeal or tracheal pathology?
1. Stridor 2. Barking cough 3. Hoarseness 4. Respiratory distress - increased effort and reduced efficacy
46
What is the severity of upper airway obstruction indicated by?
1. At rest or only with activity? (Rest - severe) 2. Respiratory effort - Work of breathing 3. Respiratory efficacy - cyanosis and Sp02 Not how 'loud' the stridor is
47
What causes stridor
Turbulent flow in the upper airway
48
DDx of stridor
Croup Laryngomalacia Epiglottitis Bacterial Tracheiits Foreign body inhalation Angioedema Trauma to throat Tonsillitis with peritonsilar abcess
49
Basic Mx for someone with stridor
Avoid overhandling/examination of the throat Keep calm - child, parent and staff, sit upright, dont separate child from parents arms Assess severity and monitor progression Ascertain and treat cause nebulised adrenaline if in doubt early referral to ED if indicated
50
How does laryngomalacia present?
Its caused by laxity of the supraglottic structures 99% mild or moderate - Commences 4-6 weeks after birth and lasts for up to two years Inspiratory stridor worse when supine, during URTI, when feeding Improves when prone Otherwise healthy Severe - FTT, feeding issues, apnoea, cor pulmonale - needs referral to otolaryngology for endoscopic evaluation Management - medical - acid suppression, high calorie diet , posture repositioning Surgical review for severe cases
51
How would you differentiate croup, bacterial tracheitis and epiglotitis?
BT and EPI - toxic, high fever BT - exp and insp stridor EPI - drooling, sitting up in tripod position, no Hib croup - responds to pred, and adrenaline Croup - insp
53
Treatment of acute bronchitis?
1. Educate patient on the self limiting nature of illness - explain that cough lasts 2-3 weeks and 90% have cough resolution by 4 weeks. 2. Prescribe paracetamol for fever (sympto mx) 3. Prescribe NSAID for pain (sympto mx) 4. SAFETY NETTING Review if new-onset fever, difficulty breathing, symptoms last greater than 3 to 4 weeks, or bloody sputum 5. If cough persists for more than 8 weeks, need to investigate for causes of chronic cough
54
Definition of acute bronchitis?
SELF LIMITING lower respiratory tract infection involving the large airways, WITHOUT EVIDENCE OF PNEUMONIA, that occurs in the ABSENCE OF COPD
55
Definition of chronic bronchitis?
Subset of COPD Cough lasts for more than 3 months in 2 consecutive years
56
How would you differentiate an acute bronchitis from its differentials
Pneumonia - would have **SIGNS OF SEVERE INFECTION** tachycardia, tachypnoea, rigors, hypoxia, audible crackles + bronhcial breath sounds, percussive dullness etc Acute bronchitis **can't happen in a person with COPD** So this will be a well, fit person with minimal past history and no signs of severity except for a productive cough with sputum **_cough with coloured or purulent sputum does not BY ITSELF need a chest xray or antibiotics_** **_Education, symptomatic mx and safety netting_**
57
What are the common causes of an acute bronchitis?
90% is viral Influenza A and B Parainfluenza Respiratory Syncitial virus Corona virus types 1 to 3 Rhinovirus Bacteria are uncommon - bordetella pertussis, mycoplasma pneumoniae