• 65 years old Male, smoker came with left-
  sided chest pain and increasing difficulty
  breathing since 2 weeks. He reports having
  fever and decreased appetite. He recalls being
  treated for tuberculosis when he was a child.
  He has a clear chest x-ray taken 15 years ago.
• On examination pallor present, trachea
  shifted to the right, chest expansion
  decreased on left side, dullness in the
  mammary, infra axillary areas, absent breath
  sounds in the same area.
• Pleural Effusion on the left side, secondary to
  TB with anemia
Clinical Features
Symptoms
• Chest pain (pleurisy)
• Breathlessness
• Symptoms associated with the actual cause of
  pleural effusion
  – Pnemonia
  – Renal disorder, Cardiac and liver disease
  – TB
  – Risk for thromboembolism
  – Exposure to asbestos (occupation)
Signs
• Trachea shifted to opposite side
• Bulge ?
• Chest movements decreased
• Stony dullness
• Absent breath sounds. Above
  effusion, crackles may be present.
• Decreased vocal resonance and fremitus on
  same side
• Traubes space percussion and tidal percussion
ETIOPATHOGENESIS OF PLEURAL
         EFFUSION
Normal Physiology
• Normally pleural space contains a thin layer of
  fluid.
• Fluid enters the pleural space from the capillaries
  in the parietal pleural and is removed by the
  lymphatics in the parietal pleura.
• Fluid can also enter the pleural space from the
  interstitial spaces of the lung via the visceral
  pleura or from the peritoneal cavity through the
  diaphragm.
PATHOGENESIS
• Pleural fluid accumulates when
  Formation increases
  Absorption decreases


• Pleural effusion can be
  Transudative
  Exudative
• Transudative effusion occurs commonly due to
  systemic factors which either increase the
  hydrostatic pressure or decrease the plasma
  oncotic pressure.
• Exudative effusion occurs due to local
  pathology in the lung or the pleura.
AETIOLOGY
• Transudative pleural effusion
  – Congestive cardiac failure
  – Cirrhosis
  – Pulmonary embolism
  – Nephrotic syndrome
  – Peritoneal dialysis
  – Myxoedema
Exudative Pleural Effusion
• Neoplastic diseases
   – Metastatic diseases
   – Mesothelioma
• Infectious diseases
   – Pneumonia
   – Tuberculosis
• Gastrointestinal diseases
   –   Pancreatic disease
   –   Esophageal perforation
   –   Intraabdominal abscess
   –   Diaphragmatic hernia
Exudative Pleural Effusion
• Collagen vascular diseases
    –   Rheumatoid arthritis
    –   SLE
    –   Drug-induced lupus
    –   Immunoblastic lymphadenopathy
    –   Sjogrens syndrome
    –   Wegener’s granulomatosis
    –   Churg-strauss syndrome
•   Asbestos exposure
•   Sarcoidosis
•   Uremia
•   Meigs’ syndrome
Investigations

Aaron John Mascarenhas
      080201022
Radiological examination
Types of Pleural Effusion on X-ray:
1. Free fluid in the pleural space
  a. Lamellar effusion
  b. Subpulmonary effusion
  c. Fissural effusion
2. Loculated effusion
3. Massive pleural effusion
Free fluid
1. First appears in the posterior CP angle (100-
   200ml fluid): Lateral film
2. Meniscus sign:
  –   Dense homogenous opacity
  –   Well defined concave upper edge
  –   Higher laterally than medially
  –   Obscures the diaphragmatic shadow
Atypical distribution of fluid
• Lamellar effusions:
  – Shallow collections between lung surface and visceral
    pleural
  – Represent interstial pulmonary fluid
• When large they form subpulmonary effusion
  –   Contour of diaphragm altered, apex shifted
  –   Blunting of CP angles and tracking into fissures
  –   Left: distance between gastric bubble and lung base
  –   Postural shifts in fluid
Loculated effusion
1. No change by gravitational methods
2. ?Extrapleural opacity, ?Peripheral lung lesion

Fissural effusion:
1. Lenticular, round or oval shadow
2. “Thickened” fissure
3. ‘Pseudo’ or ‘ Vanishing’ tumors?
Also look for?
1. Positioning?
2. Breast shadows?
3. Rib: Erosions, #
4. Trachea: Shift, Paratracheal shadows
5. Cardiac shadow
6. Lung fields: Cavity, “cotton wool” infiltrates,
   Cannon ball mets
7. Hilum: Lymphadenopathy
8. Air-fluid level
9. Pleura: Masses, thickening.
Massive Pleural effusion
1. White out lung(WOL) + Contralateral
   Mediastinal shift

D/D:
1. Collapse (WOL + Ipsilateral Mediastinal Shift)
2. Consolidation (WOL + Central trachea)
Ultrasonography
• Detects even 5ml of fluid in excess on normal
• Differentiation of pleural thickening from
  loculated pleural effusion
• Associated abnormalities
Pleural aspiration and Analysis
Transudative or Exudative?
LIGHT’S CRITERIA:
1. Pleural fluid protein/Serum Protein >0.5
2. Pleural fluid LDH/Serum LDH >0.6
3. Pleural fluid LDH > 2/3rd the upper limit of
   serum LDH
Tuberculous effusion
1. “Amber” coloured to sero-sanguineous
2. >10%eosinophils; <5%: Mesothelial cells
3. Centrifuged deposits:
     – AFB +ve: <10% immunocompetent host
     – Culture +ve: 25%
4.   ADA elevated (>40U/L)
5.   Others: LDH, Soluble IL-2 receptors, IFN-γ
6.   Detection of Mycobacteria DNA by PCR
7.   Nucleic acid amplification assays
8.   Pleural biopsy: Non-caseating granulomas > 80%
MANAGEMENT OF PLEURAL EFFUSION
MEDICAL MANAGEMNT
Treatment of underlying cause
Therapeutic aspiration is necessary in order to
 relieve dyspnoea
Precautions:
  Removing more than 1L in one episode in inadvisable
  Can result in re-expansion pulmonary oedema
  Should never be aspirated to dryness before the exact
   etiology is determined
THORACOCENTESIS
INDICATIONS
  Diagnostic
  therapeutic

POSITION
  Sitting position, leaning forward over a support
SITE
  Below the scapula, posteriorly through the seventh
   intercostal space
PROCEDURE
 Informed consent
 Clean the are with povidine
  iodine
 Local anesthesia
 Insert the needle and flexible
  catheter over the needle
 Aspirate pleural fluid
COMPLICATIONS
  Iatrogenic pneumothorax
  Infection
  Dry tap or bloody tap
  Re-expansion pulmonary oedema
  Pain and respiratory distress
Surgical Management
  of Pleural Effusion
Effusion due to Heart Failure
• Most common cause of pleural effusion
• a diagnostic thoracentesis is done if:
    – the effusions are not bilateral and comparable in size
    – the patient is febrile
    – the patient has pleuritic chest pain to verify that the effusion is
       transudative
• Otherwise the patient's heart failure is treated
• If the effusion persists despite therapy, a diagnostic thoracentesis should
  be done
• A pleural fluid N-terminal pro-brain natriuretic peptide (NT-proBNP)
  >1500 pg/mL is diagnostic of an effusion secondary to congestive heart
  failure
Parapneumonic Effusions
• most common cause of exudative pleural effusion (bacterial
  pneumonias, lung abscess, bronchiectasis)
• The presence of free pleural fluid can be demonstrated with a lateral
  decubitus radiograph, CT of the chest, or ultrasound
• If the free fluid separates the lung from the chest wall by >10 mm, a
  therapeutic thoracentesis should be performed
• A procedure more invasive than thoracentesis is needed if the
  following factors are present:
    – Loculated pleural fluid
    – Pleural fluid pH <7.20
    – Pleural fluid glucose <3.3 mmol/L (<60 mg/dL)
    – Positive Gram stain or culture of the pleural fluid
    – Presence of gross pus in the pleural space
Parapneumonic Effusion
• If the fluid recurs after the initial therapeutic thoracentesis and if
  any of these characteristics are present - a repeat thoracentesis

• If the fluid cannot be completely removed with the therapeutic
  thoracentesis,
    – insert a chest tube and instill a fibrinolytic agent (e.g., tissue
       plasminogen activator, 10 mg)
    – perform a thoracoscopy with the breakdown of adhesions
    – Decortication (if these measures are ineffective)
Malignant Pleural Effusions
• 2nd most common type of exudative pleural effusion (lung carcinoma,
  breast carcinoma, & lymphoma)
• Diagnosis: cytology of the pleural fluid
• If cytology is negative, thoracoscopy is done if malignancy is suspected
• Pleural abrasion should be performed to effect a pleurodesis
• Pleural abrasion: a scourer is used to scrape off the surface of parietal
  pleura
• An alternative to thoracoscopy : CT- or ultrasound-guided needle
  biopsy of pleural thickening or nodules
• Patients with a malignant pleural effusion are treated symptomatically
• Dyspnea if present and is relieved with a therapeutic thoracentesis,
  one of the following procedures should be considered:
    – insertion of a small indwelling catheter or
    – tube thoracostomy with the instillation of a sclerosing agent such as
       doxycycline, 500 mg
Chylothorax
• Occurs when thoracic duct is disrupted and chyle
  accumulates in the pleural space.
• Thoracentesis shows milky fluid, and biochemical
  analysis reveals a triglyceride level that exceeds
  1.2 mmol/L (110 mg/dL)
• Treatment: insertion of a chest tube plus the
  administration of octreotide
• If these measures fail, a pleuroperitoneal shunt
  should be placed
• An alternative treatment is ligation of the thoracic
  duct
Hemothorax
• Diagnostic thoracentesis shows bloody pleural fluid,
• Hematocrit :if >1/2 of that in the peripheral blood, the
  patient is considered to have a hemothorax
• Treatment: tube thoracostomy ( helps quantify
  bleeding)
• If the bleeding emanates from a laceration of the
  pleura, apposition of the two pleural surfaces is likely
  to stop the bleeding.
• If the pleural hemorrhage exceeds 200 mL/h, perform
  thoracoscopy or thoracotomy

Pleural effusion

  • 1.
    • 65 yearsold Male, smoker came with left- sided chest pain and increasing difficulty breathing since 2 weeks. He reports having fever and decreased appetite. He recalls being treated for tuberculosis when he was a child. He has a clear chest x-ray taken 15 years ago. • On examination pallor present, trachea shifted to the right, chest expansion decreased on left side, dullness in the mammary, infra axillary areas, absent breath sounds in the same area.
  • 2.
    • Pleural Effusionon the left side, secondary to TB with anemia
  • 3.
    Clinical Features Symptoms • Chestpain (pleurisy) • Breathlessness • Symptoms associated with the actual cause of pleural effusion – Pnemonia – Renal disorder, Cardiac and liver disease – TB – Risk for thromboembolism – Exposure to asbestos (occupation)
  • 4.
    Signs • Trachea shiftedto opposite side • Bulge ? • Chest movements decreased • Stony dullness • Absent breath sounds. Above effusion, crackles may be present. • Decreased vocal resonance and fremitus on same side • Traubes space percussion and tidal percussion
  • 5.
  • 6.
    Normal Physiology • Normallypleural space contains a thin layer of fluid. • Fluid enters the pleural space from the capillaries in the parietal pleural and is removed by the lymphatics in the parietal pleura. • Fluid can also enter the pleural space from the interstitial spaces of the lung via the visceral pleura or from the peritoneal cavity through the diaphragm.
  • 7.
    PATHOGENESIS • Pleural fluidaccumulates when Formation increases Absorption decreases • Pleural effusion can be Transudative Exudative
  • 8.
    • Transudative effusionoccurs commonly due to systemic factors which either increase the hydrostatic pressure or decrease the plasma oncotic pressure. • Exudative effusion occurs due to local pathology in the lung or the pleura.
  • 9.
    AETIOLOGY • Transudative pleuraleffusion – Congestive cardiac failure – Cirrhosis – Pulmonary embolism – Nephrotic syndrome – Peritoneal dialysis – Myxoedema
  • 10.
    Exudative Pleural Effusion •Neoplastic diseases – Metastatic diseases – Mesothelioma • Infectious diseases – Pneumonia – Tuberculosis • Gastrointestinal diseases – Pancreatic disease – Esophageal perforation – Intraabdominal abscess – Diaphragmatic hernia
  • 11.
    Exudative Pleural Effusion •Collagen vascular diseases – Rheumatoid arthritis – SLE – Drug-induced lupus – Immunoblastic lymphadenopathy – Sjogrens syndrome – Wegener’s granulomatosis – Churg-strauss syndrome • Asbestos exposure • Sarcoidosis • Uremia • Meigs’ syndrome
  • 12.
  • 13.
    Radiological examination Types ofPleural Effusion on X-ray: 1. Free fluid in the pleural space a. Lamellar effusion b. Subpulmonary effusion c. Fissural effusion 2. Loculated effusion 3. Massive pleural effusion
  • 14.
    Free fluid 1. Firstappears in the posterior CP angle (100- 200ml fluid): Lateral film 2. Meniscus sign: – Dense homogenous opacity – Well defined concave upper edge – Higher laterally than medially – Obscures the diaphragmatic shadow
  • 15.
    Atypical distribution offluid • Lamellar effusions: – Shallow collections between lung surface and visceral pleural – Represent interstial pulmonary fluid • When large they form subpulmonary effusion – Contour of diaphragm altered, apex shifted – Blunting of CP angles and tracking into fissures – Left: distance between gastric bubble and lung base – Postural shifts in fluid
  • 16.
    Loculated effusion 1. Nochange by gravitational methods 2. ?Extrapleural opacity, ?Peripheral lung lesion Fissural effusion: 1. Lenticular, round or oval shadow 2. “Thickened” fissure 3. ‘Pseudo’ or ‘ Vanishing’ tumors?
  • 17.
    Also look for? 1.Positioning? 2. Breast shadows? 3. Rib: Erosions, # 4. Trachea: Shift, Paratracheal shadows 5. Cardiac shadow 6. Lung fields: Cavity, “cotton wool” infiltrates, Cannon ball mets 7. Hilum: Lymphadenopathy 8. Air-fluid level 9. Pleura: Masses, thickening.
  • 18.
    Massive Pleural effusion 1.White out lung(WOL) + Contralateral Mediastinal shift D/D: 1. Collapse (WOL + Ipsilateral Mediastinal Shift) 2. Consolidation (WOL + Central trachea)
  • 19.
    Ultrasonography • Detects even5ml of fluid in excess on normal • Differentiation of pleural thickening from loculated pleural effusion • Associated abnormalities
  • 20.
    Pleural aspiration andAnalysis Transudative or Exudative? LIGHT’S CRITERIA: 1. Pleural fluid protein/Serum Protein >0.5 2. Pleural fluid LDH/Serum LDH >0.6 3. Pleural fluid LDH > 2/3rd the upper limit of serum LDH
  • 22.
    Tuberculous effusion 1. “Amber”coloured to sero-sanguineous 2. >10%eosinophils; <5%: Mesothelial cells 3. Centrifuged deposits: – AFB +ve: <10% immunocompetent host – Culture +ve: 25% 4. ADA elevated (>40U/L) 5. Others: LDH, Soluble IL-2 receptors, IFN-γ 6. Detection of Mycobacteria DNA by PCR 7. Nucleic acid amplification assays 8. Pleural biopsy: Non-caseating granulomas > 80%
  • 23.
    MANAGEMENT OF PLEURALEFFUSION MEDICAL MANAGEMNT Treatment of underlying cause Therapeutic aspiration is necessary in order to relieve dyspnoea Precautions: Removing more than 1L in one episode in inadvisable Can result in re-expansion pulmonary oedema Should never be aspirated to dryness before the exact etiology is determined
  • 24.
    THORACOCENTESIS INDICATIONS Diagnostic therapeutic POSITION Sitting position, leaning forward over a support SITE  Below the scapula, posteriorly through the seventh intercostal space
  • 25.
    PROCEDURE Informed consent Clean the are with povidine iodine Local anesthesia Insert the needle and flexible catheter over the needle Aspirate pleural fluid
  • 26.
    COMPLICATIONS Iatrogenicpneumothorax Infection Dry tap or bloody tap Re-expansion pulmonary oedema Pain and respiratory distress
  • 27.
    Surgical Management of Pleural Effusion
  • 28.
    Effusion due toHeart Failure • Most common cause of pleural effusion • a diagnostic thoracentesis is done if: – the effusions are not bilateral and comparable in size – the patient is febrile – the patient has pleuritic chest pain to verify that the effusion is transudative • Otherwise the patient's heart failure is treated • If the effusion persists despite therapy, a diagnostic thoracentesis should be done • A pleural fluid N-terminal pro-brain natriuretic peptide (NT-proBNP) >1500 pg/mL is diagnostic of an effusion secondary to congestive heart failure
  • 29.
    Parapneumonic Effusions • mostcommon cause of exudative pleural effusion (bacterial pneumonias, lung abscess, bronchiectasis) • The presence of free pleural fluid can be demonstrated with a lateral decubitus radiograph, CT of the chest, or ultrasound • If the free fluid separates the lung from the chest wall by >10 mm, a therapeutic thoracentesis should be performed • A procedure more invasive than thoracentesis is needed if the following factors are present: – Loculated pleural fluid – Pleural fluid pH <7.20 – Pleural fluid glucose <3.3 mmol/L (<60 mg/dL) – Positive Gram stain or culture of the pleural fluid – Presence of gross pus in the pleural space
  • 30.
    Parapneumonic Effusion • Ifthe fluid recurs after the initial therapeutic thoracentesis and if any of these characteristics are present - a repeat thoracentesis • If the fluid cannot be completely removed with the therapeutic thoracentesis, – insert a chest tube and instill a fibrinolytic agent (e.g., tissue plasminogen activator, 10 mg) – perform a thoracoscopy with the breakdown of adhesions – Decortication (if these measures are ineffective)
  • 31.
    Malignant Pleural Effusions •2nd most common type of exudative pleural effusion (lung carcinoma, breast carcinoma, & lymphoma) • Diagnosis: cytology of the pleural fluid • If cytology is negative, thoracoscopy is done if malignancy is suspected • Pleural abrasion should be performed to effect a pleurodesis • Pleural abrasion: a scourer is used to scrape off the surface of parietal pleura • An alternative to thoracoscopy : CT- or ultrasound-guided needle biopsy of pleural thickening or nodules • Patients with a malignant pleural effusion are treated symptomatically • Dyspnea if present and is relieved with a therapeutic thoracentesis, one of the following procedures should be considered: – insertion of a small indwelling catheter or – tube thoracostomy with the instillation of a sclerosing agent such as doxycycline, 500 mg
  • 32.
    Chylothorax • Occurs whenthoracic duct is disrupted and chyle accumulates in the pleural space. • Thoracentesis shows milky fluid, and biochemical analysis reveals a triglyceride level that exceeds 1.2 mmol/L (110 mg/dL) • Treatment: insertion of a chest tube plus the administration of octreotide • If these measures fail, a pleuroperitoneal shunt should be placed • An alternative treatment is ligation of the thoracic duct
  • 33.
    Hemothorax • Diagnostic thoracentesisshows bloody pleural fluid, • Hematocrit :if >1/2 of that in the peripheral blood, the patient is considered to have a hemothorax • Treatment: tube thoracostomy ( helps quantify bleeding) • If the bleeding emanates from a laceration of the pleura, apposition of the two pleural surfaces is likely to stop the bleeding. • If the pleural hemorrhage exceeds 200 mL/h, perform thoracoscopy or thoracotomy