Bronchiectasis Flashcards

1
Q

Bronchiectasis - definition

A

Bronchiectasis is the permanent dilation of bronchi due to the destruction of the elastic and muscular components of the bronchial wall. It is often caused as a consequence of recurrent and/or severe infections secondary to an underlying disorder.

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2
Q

Bronchiectasis - aetiology

A
  • Post-infectious: viruses (i.e., measles, influenza, pertussis), Mycobacteria or severe bacterial pneumonia
  • Immunodeficiency: Immunoglobulin deficiency, HIV
  • Genetic: CF, ciliary dyskinesia +/- Kartagener’s syndrome, A1ATd, Ehlers-Danlos, Marfan’s
  • Aspiration or inhalation injury
  • Connective tissue disorders: RA, Sjogren’s
  • Inflammatory bowel diseases: UC, Crohn’s

(all of these are risk factors)

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3
Q

Pathophys

A
  1. Persistent airway inflammation
  2. Bronchial wall oedema and increased mucus
  3. Neutrophils, T lymphocytes, +other are recruited
  4. Release inflammatory cytokines, proteases, and reactive oxygen mediators
  5. Progressive destruction of the airways
  6. Decreased ability to clear secretions
  7. Microbes collect, further inflammation and dilation
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4
Q

Clinical features

A
  • Cough - may be a/w large amounts of purulent sputum and, less commonly, haemoptysis
  • dyspnoea
  • fever +/- fatigue, malaise
  • crackles, high-pitched inspiratory squeaks and rhonchi
  • wheeze
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5
Q

Investigations

A
  • spirometry: may be normal or obstructive
  • sputum culture
  • CXR
  • Post-bronchodilator spirometry
  • gold standard: High-resolution CT (HRCT)
  • PFTs: reduced FEV1, elevated RV/TLC

consider testing for CF, serum A1AT etc

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6
Q

CXR - findings

A
  • May be normal
  • Ring opacities – dilated end of bronchi
  • Tram-tracks - dilated airways seen in a horizontal orientation
  • Fluid-filled cysts or bronchocoeles
  • may show obscured hemidiaphragm, tubular or ovoid opacities
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7
Q

HRCT - findings

A
  • Signet ring sign – resembles a signet (or pearl) ring, which is an opacity representing a dilated bronchus in cross section and a smaller adjacent opacity representing its pulmonary artery
  • Tram-tracks – dilated airways seen in a horizontal orientation
  • Lack of tapering of airways, varicose constrictions
  • Mucus impaction, cysts
  • Mosaicism
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8
Q

Bronchiectasis - Management

A
  • conservative: check BMI (encourage weight loss if needed), smoking cessation, pulmonary rehabilitation (exercise, health education, breathing techniques)
  • physio: airway clearance therapy includes postural drainage, percussion, vibration. The primary goal is bronchopulmonary hygiene.
  • treatment of infection – 10-14 day course of Abx
  • Influenza/pneumococcal vaccine
  • Test sputum culture for unusual/colonising organisms
  • Consider checking vitamin D levels
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9
Q

Which antibiotic is prescribed for Pseudomonas aeruginosa?

A
  • Only orally active antimicrobial is Ciprofloxacin

- IV options include Tazocin (Piperacillin and Tazobactam), Ceftazidime

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10
Q

Exacerbation - features

A
  • worsening cough
  • change in sputum colour and an increase in sputum volume
  • increasing breathlessness
  • haemoptysis may become massive (>250 mL/day), which warrants hospital admission
  • may have persistent pleuritic chest pain
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11
Q

Criteria for hospital admission (general)

A

Any signs suggesting a more serious illness or condition (such as cardiorespiratory failure or sepsis):

  • Cyanosis
  • Confusion
  • RR> 25
  • Marked breathlessness, rapid respiration, or laboured breathing.
  • Peripheral oedema
  • T of 38°C or more.
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12
Q

Exacerbation - management

A
  • Preview previous sputum culture results and most recent course of antibiotics given
  • Send more sputum for culture
  • Choose Abx (in line with local guidance)
     Amoxicillin/clarithromycin/doxycycline oral
     Ciprofloxacin if pseudomonas aeruginosa
  • Total course 10-14 days
  • May need to consider outpatient IV antibiotics
  • Chest physiotherapy
  • Prescribe a SABA (such as salbutamol) if necessary
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