Pleural Space Flashcards

1
Q

The clinical importance of the pleural space in pleural effusion

A

-Pleural space: negative pressure
-As pleural fluid collects in the space, the pressure changes and becomes positive
-Changes again when fluid is drained out of lung; pressure change can cause cough and chest pain/ tightness

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2
Q

What can accumulate in the pleural space?

A

-Air: PTX
-Proteinaceous fluid: exudative pleural effusion
-Protein deficient fluid: transudative pleural effusion
-Blood: haemothorax
-Chyle (fluid from lymphatic system): Chylothorax
-Fluid and air: hydropneumothorax
-Pus: empyema
-Tumour: primary or secondary (benign or malignant)
-Asbestos fibres: pleural plaque disease

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3
Q

Physiology of pleural fluid accumulation

A
  • Increased interstitial fluid in lung (LVSD, CAP, PTE)
  • Increased intravascular pressure in the pleura (LVSD, SVCO, RVF)
  • Increased permeability of the capillaries in the pleura (Inflammation)
  • Increased pleural fluid protein level
  • Decreased pleural pressure (Lung atelectasis)
  • Increased fluid in peritoneal cavity (ascites, PD)
  • Disruption of the thoracic duct (iatrogenic, haem malignancy)
  • Disruption of thoracic blood vessels (iatrogenic, trauma)
  • Obstruction of lymphatics draining parietal pleura (malignancy)
  • Elevation of systemic vascular pressures SVCO, RVF)
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4
Q

Exudate vs transudate

A

-Exudate: high protein content (>30g/L)
-Transudate: low protein content (<30g/L)- organ failure, usually bilateral and smaller
-More specifically the Light’s criteria however misclassify 25% transudates as exudates

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5
Q

Describe the Light’s criteria

A

Exudate diagnosed if 2 of:
-Pleural to serum protein ratio >0.5
-Pleural to serum LDH ratio >0.6
-Pleural LDH >2/3 upper limit normal (>145)
IN THE RIGHT CLINICAL CONTEXT

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6
Q

Common causes of exudate pleural effusion

A

-Parapneumonic (pneumonia= increased vocal resonance, bronchial breathing, crackles).
-Malignancy

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7
Q

Less common causes of exudate pleural effusion

A

-Tuberculosis
-PE/infarction
-Rheumatoid arthritis
-SLE
-Pancreatitis
-Benign asbestos
effusion
-Post MI/CABG

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8
Q

Very rare causes of exudate pleural effusion

A

-Yellow nail syndrome
-Drugs (amiodarone, methotrexate)

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9
Q

Common causes of transudate pleural effusion

A

-Heart failure
-Liver failure

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10
Q

Less common causes of transudate pleural effusion

A

-Hypalbuminaemia
-Nephrotic syndrome
-Peritoneal dialysis

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11
Q

Very rare causes of transudate pleural effusion

A

-Hypothyroidism
-Constrictive pericarditis
-Meigs syndrome

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12
Q

Investigations of pleural effusions

A
  • Imaging: CXR, USS, CT (PET/MRI experimentally), ECG if chest pain
    -Bloods: FBC, UE, LFT, albumin/calcium, CRP +/- coag screen. Blood cultures if pyrexial, sputum microscopy and culture if productive cough, ABG if low O2
  • Pleural aspiration (60ml syringe, green needle, USS): 50ml under USS, ensure not on anticoag, platelet and clotting normal prior
    =If a patient is hypoxic or extremely breathless, then it is sometimes appropriate to
    perform a therapeutic aspiration of around 1L of fluid at the outset
  • Appearance/Odour, clarity (srous, haemoserous, heavily blood-stained, purulent, chylous, brown)
    – Biochemistry: total protein, glucose, LDH, pH (10ml)
    – Microbiology: bacteriology (Blood culture bottles),
    AAFB/mycobacterial culture (20ml-60mls)
    – Pathology: cytology (60% sensitivity) 60-200ml, look for inflammatory and malignant cells
  • Repeat aspiration?
  • Medical thoracoscopy vs VATS

It would be useful to organise a CT with contrast (chest, abdomen and pelvis if malignancy is suspected, or CT
thorax with pleural (venous)-phase contrast if pleural infection is suspected)

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13
Q

Pleural effusion on CXR

A

This demonstrates opacification in the left mid and lower zones.
This is due to a left pleural effusion – the opacification is very dense (completely obscuring both the left heart
border and the left hemi-diaphragm), there is a meniscus at the superior lateral edge and the trachea is
deviated away (tracheal deviation towards the opacification would be more in keeping with lung/lobar
collapse). The presence of a pleural effusion should be confirmed by pleural ultrasound

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14
Q

Added diagnostic information of USS

A

-Echogenic fluid
-Septations
-Pleural thickening
-Pleural/ diaphragmatic nodularity

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15
Q

Likely cause of frank pus effusion

A

Empyema

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16
Q

Likely cause of blood-stained effusion

A

-Malignancy
-Pulmonary infraction
-Post cardiac injury syndrome
-Infection
-TB

17
Q

Likely cause of frank blood effusion

A

Haemothorax

18
Q

Likely cause of milky effusion

A

Chylothorax (due to thoracic duct disruption)

19
Q

Likely cause of food particle effusion

A

Oesophageal rupture

20
Q

Likely cause of bile stained effusion

A

Biliary fistula (biliothorax)

21
Q

Pleural fluid characteristic tests

A

-pH (low in pleural infection, RhA, malignancy)
-Protein
-LDH (high malignancy, infection, inflammation)
-Glucose (very low in empyema, RhA)
-Triglycerides (chylothorax: >1.24mmol/L)
-Cholesterol (>5.18mmol/l in pseudochylothorax)
-Haematocrit (blood-stained vs frank blood)
-Amylase (oesophageal rupture, pancreatitis)

22
Q

Low pleural fluid glucose results differentials

A

parapneumonic effusion/empyema, RA, TB, malignancy,
oesophageal rupture

23
Q

Management of parapneumonic effusion

A

Simple parapneumonic effusion indicates a reactive process (no bacterial infection within the pleural space
itself) whereas complicated parapneumonic effusion indicates infection within the pleural space and empyema
indicates pus in the pleural space. ‘Pleural infection’ is now the preferred term that encompasses both
empyema and complicated parapneumonic effusion (especially as there might not be a pneumonia present).
pH is the most useful (pus on aspiration or a pH of ≤7.2 are two of the indications for urgent intercostal tube
drainage of an empyema/effusion). pH of >7.2 but <7.4 indicates intermediate risk of pleural infection
(decision to place intercostal drain depends on other factors). It would also be important to ensure that the
patient is on appropriate antibiotic therapy! CT imaging in pleural infection may show an enhancing pleural
margin or gas locules in the fluid. Operative management by the Thoracic surgeons is sometimes required -
either video-assisted thoracoscopic surgery (VATS) or open thoracotomy. Intrapleural fibrinolytic therapy is
sometimes used if the collection of fluid doesn’t fully drain via the ICD

24
Q

Management of malignant pleural effusion

A

Mesothelioma (also consider invasion of the chest wall/ribs/brachial plexus, or PE).
As well as mesothelioma (by far the most common primary pleural malignancy), lung cancer, breast cancer, GI
and GU cancers, and lymphoma are the most common malignancies affecting the pleura.
Other tests for diagnosing malignant pleural effusion include medical thoracoscopy or CT-guided pleural biopsy
(both done under local anaesthetic) or VATS thoracoscopy (under general anaesthetic).
Procedures to prevent recurrence of a malignant pleural effusion include talc slurry pleurodesis (instillation of
talc via an intercostal drain), talc poudrage done during medical/surgical thoracoscopy or insertion of an
indwelling pleural catheter +/- talc pleurodesis

25
Q

Resources

A

British Thoracic Society Pleural Disease Guideline (2023) https://thorax.bmj.com/content/78/Suppl_3/s1
Cochrane Review of intrapleural fibrinolytic therapy (2019)
https://www.cochranelibrary.com/cdsr/doi/10.1002/14651858.CD002312.pub4/full?cookiesEnabled