Pleural Effusiion By Haider Abdulkareem Radhi

1. By
Haider Abdulkareem Radhi

2. Background
A pleural effusion is collection of fluid
abnormally present in the pleural space,
usually resulting from excess fluid
production and/or decreased lymphatic
absorption. It is the most common
manifestation of pleural disease, and its
etiologies range in spectrum from
cardiopulmonary disorders and/or systemic
inflammatory conditions to malignancy

3. Etiology
The normal pleural space contains
approximately 10 mL of fluid, representing
the balance between (1) hydrostatic and
oncotic forces in the visceral and parietal
pleural capillaries and (2) persistent
lymphatic drainage. Pleural effusions may
result from disruption of this natural balance.

4. Presence of a pleural effusion indicate an
underlying disease process that may be
pulmonary or nonpulmonary in origin and,
furthermore, that may be acute or chronic.
Although the etiologic spectrum of pleural
effusion can be extensive, most pleural
effusions are caused by congestive heart
failure, pneumonia, malignancy, or
pulmonary embolism.

5. Mechanisms
* Altered permeability of the pleural membranes (eg,
inflammation, malignancy, pulmonary embolism)
* Reduction in intravascular oncotic pressure (eg,
hypoalbuminemia due to nephrotic syndrome or cirrhosis)
* Increased capillary permeability or vascular disruption (eg,
trauma, malignancy, inflammation, infection, pulmonary
infarction, drug hypersensitivity, uremia, pancreatitis)
* Increased capillary hydrostatic pressure in the systemic
and/or pulmonary circulation (eg, congestive heart failure,
superior vena cava syndrome)
* Reduction of pressure in the pleural space (ie, due to an
inability of the lung to fully expand during inspiration); this is
known as "trapped lung" (eg, extensive atelectasis due to an
obstructed bronchus or contraction from fibrosis leading to
restrictive pulmonary physiology)

6. * Decreased lymphatic drainage or complete
lymphatic vessel blockage, including thoracic duct
obstruction or rupture (eg, malignancy, trauma)
* Movement of fluid from pulmonary edema
across the visceral pleura
* Persistent increase in pleural fluid oncotic
pressure from an existing pleural effusion,
causing further fluid accumulation

7. Pleural effusions are generally classified
as transudates or exudates, based on the
mechanism of fluid formation and pleural
fluid chemistry. Transudates result from an
imbalance of oncotic and hydrostatic
pressures, whereas exudates are the
result of inflammatory processes of the
pleura and/or decreased lymphatic
drainage. In some cases, it is not rare for
pleural fluid to exhibit mixed
characteristics of transudate and exudate.

8. Transudate
Transudates are caused by a small, defined group of etiologies,
including the following:
 Congestive heart failure
 Cirrhosis (hepatic hydrothorax)
 Atelectasis (may be due to occult malignancy or pulmonary
embolism)
 Hypoalbuminemia
 Nephrotic syndrome
 Peritoneal dialysis
 Constrictive pericarditis
 Cerebrospinal fluid (CSF) leaks to the pleura (in the setting of
ventriculopleural shunting or of trauma/surgery to the thoracic
spine)
 Extravascular migration of central venous catheter

9. Exudates
• Produced by a variety of inflammatory conditions
(and often requiring a more extensive evaluation and
treatment strategy than transudates), exudative
effusions develop from inflammation of the pleura or
from decreased lymphatic drainage at pleural edges.
• Mechanisms of exudative formation include pleural
or parenchymal inflammation, impaired lymphatic
drainage of the pleural space, altered permeability of
pleural membranes, and/or increased capillary wall
permeability or vascular disruption. Pleural
membranes are involved in the pathogenesis of the
fluid formation. Of note, the permeability of pleural
capillaries to proteins is increased in disease states
with elevated protein content.

10.  The more common causes of exudates include the following:
 Parapneumonic causes
 Malignancy (most commonly lung or breast cancer, lymphoma, and leukemia; less
commonly ovarian carcinoma, stomach cancer, sarcomas, melanoma) [9]
 Pulmonary embolism
 Collagen-vascular conditions (rheumatoid arthritis, systemic lupus erythematosus
 Tuberculosis (TB)
 Pancreatitis
 Trauma
 Esophageal perforation
 Sarcoidosis
 Pericardial disease
 Uremia
 Chylothorax (acute illness with elevated triglycerides in pleural fluid)
 Fistula (ventriculopleural, biliopleural, gastropleural)

12. Distinguishing Transudates From
Exudates
• The initial diagnostic consideration is distinguishing transudates
from exudates. Although a number of chemical tests have been
proposed to differentiate pleural fluid transudates from
exudates, the tests first proposed by Light et al have become the
criterion standards.
• The fluid is considered an exudate if any of the following are
found:
• Ratio of pleural fluid to serum protein greater than 0.5
• Ratio of pleural fluid to serum LDH greater than 0.6
• Pleural fluid LDH greater than two thirds of the upper limits of
normal serum value

13. Pleural Effusion Clinical Presentation
Some patients with pleural effusion have no
symptoms, with the condition discovered on a chest
x-ray that is performed for another reason. The
patient may have unrelated symptoms due to the
disease or condition that has caused the effusion .
Symptoms of pleural effusion include:
Chest pain
Dry, nonproductive cough
Dyspnea
Orthopnea (the inability to breathe easily unless the
person is sitting up straight or standing erect)

14. Physical Examination
 Physical findings in pleural effusion are variable and
depend on the volume of the effusion. Typically, there are
no clinical findings for effusions less than 300 mL. With
effusions greater than 300 mL, chest wall/pulmonary
findings may include the following:
 Dullness to percussion, and asymmetrical chest expansion, with
diminished or delayed expansion on the side of the effusion: These
are the most reliable physical findings of pleural effusion.
 Mediastinal shift away from the effusion: This finding is observed
with effusions greater than 1000 mL. Displacement of the trachea
and mediastinum toward the side of the effusion is an important
clue to obstruction of a lobar bronchus by an endobronchial lesion,
which can be due to malignancy or, less commonly, to a
nonmalignant cause, such as a foreign body obstruction.
 Diminished or inaudible breath sounds
 Pleural friction rub

15. Other physical and extrapulmonary findings may
suggest the underlying cause of the pleural effusion.
Peripheral edema, distended neck veins, and S3 gallop
suggest congestive heart failure. Edema may also be a
manifestation of nephrotic syndrome or pericardial
disease .
Cutaneous changes and ascites suggest liver disease.
Lymphadenopathy or a palpable mass suggests
malignancy.

16. Approach Considerations
Thoracentesis should be performed for new and
unexplained pleural effusions when sufficient fluid is
present to allow a safe procedure. Observation of
pleural effusion is reasonable when benign etiologies
are likely, as in the setting of overt congestive heart
failure, viral pleurisy, or recent thoracic or abdominal
surgery.
Laboratory testing helps to distinguish pleural fluid
transudates from exudates. However, certain types of
exudative pleural effusions might be suspected simply
by observing the gross characteristics of the fluid
obtained during thoracentesis. Note the following:

17. Frankly purulent fluid indicates an empyema
A putrid odor suggests an anaerobic empyema
A milky, opalescent fluid suggests a chylothorax,
resulting most often from lymphatic obstruction by
malignancy or thoracic duct injury by trauma or
surgical procedure
Grossly bloody fluid may result from trauma,
malignancy or asbestos-related effusion and indicates
the need for a spun hematocrit test of the sample. A
pleural fluid hematocrit level of more than 50% of the
peripheral hematocrit level defines a hemothorax,
which often requires tube thoracostomy

18. Normal pleural fluid
 Normal pleural fluid has the following characteristics:
 Clear ultrafiltrate of plasma that originates from the parietal
pleura
 A pH of 7.60-7.64
 Protein content of less than 2% (1-2 g/dL)
 Fewer than 1000 white blood cells (WBCs) per cubic
millimeter
 Glucose content similar to that of plasma
 Lactate dehydrogenase (LDH) less than 50% of plasma

19. Pleural Fluid LDH, Glucose, and pH
Pleural fluid LDH
• Pleural fluid LDH levels greater than 1000 IU/L
suggest empyema, malignant effusion,
rheumatoid effusion. Pleural fluid LDH levels are
also increased in effusions from Pneumocystis
jiroveci (formerly, P carinii) pneumonia. The
diagnosis is suggested by a pleural fluid/serum
LDH ratio of greater than 1, with a pleural
fluid/serum protein ratio of less than 0.5.

20. Pleural fluid glucose and pH
• In addition to the previously discussed tests,
glucose and pleural fluid pH should be measured
during the initial thoracentesis in most situations.
• A low pleural glucose concentration (30-50 mg/dL)
suggests malignant effusion, tuberculous pleuritis,
esophageal rupture, or lupus pleuritis. A very low
pleural glucose concentration (ie, < 30 mg/dL)
further restricts diagnostic possibilities, to
rheumatoid pleurisy or empyema.

21. • Pleural fluid pH is highly correlated with pleural fluid glucose
levels. A pleural fluid pH of less than 7.30 with a normal
arterial blood pH level is caused by the same diagnoses as
listed above for low pleural fluid glucose. However, for
parapneumonic effusions, a low pleural fluid pH level is
more predictive of complicated effusions (that require
drainage) than is a low pleural fluid glucose level. In such
cases, a pleural fluid pH of less than 7.1-7.2 indicates the
need for urgent drainage of the effusion, while a pleural
fluid pH of more than 7.3 suggests that the effusion may be
managed with systemic antibiotics alone.
• In malignant effusions, a pleural fluid pH of less than 7.3 has
been associated in some reports with more extensive
pleural involvement, higher yield on cytology, decreased
success of pleurodesis, and shorter survival times

22. Pleural Fluid Cell Count Differential
• If an exudate is suspected clinically or is confirmed
by chemistry test results, send the pleural fluid for
total and differential cell counts, Gram stain,
culture, and cytology.
• Pleural fluid lymphocytosis, with lymphocyte values
greater than 85% of the total nucleated cells,
suggests TB, lymphoma, sarcoidosis, chronic
rheumatoid pleurisy, and chylothorax. Pleural
lymphocyte values of 50-70% of the nucleated cells
suggest malignancy.

23. • Pleural fluid eosinophilia (PFE), with eosinophil
values greater than 10% of nucleated cells, is seen
in approximately 10% of pleural effusions and is
not correlated with peripheral blood eosinophilia.
PFE is most often caused by air or blood in the
pleural space. Blood in the pleural space causing
PFE may be the result of pulmonary embolism with
infarction or benign asbestos pleural effusion. PFE
may be associated with other nonmalignant
diseases, including parasitic disease , fungal
infection and a variety of medications.

24. Pleural Fluid Culture and Cytology
• Cultures of infected pleural fluids yield positive results
in approximately 60% of cases. This occurs even less
often for anaerobic organisms. Diagnostic yields,
particularly for anaerobic pathogens, may be
increased by directly culturing pleural fluid into blood
culture bottles.
• Malignancy is suspected in patients with known
cancer or with lymphocytic, exudative effusions,
especially when bloody. Direct tumor involvement of
the pleura is diagnosed most easily by performing
pleural fluid cytology

25. Chest Radiography
• Effusions of more than 175 mL are usually
apparent as blunting of the costophrenic angle on
upright posteroanterior chest radiographs. On
supine chest radiographs, which are commonly
used in the intensive care setting, moderate to
large pleural effusions may appear as a
homogenous increase in density spread over the
lower lung fields. Apparent elevation of the
hemidiaphragm, lateral displacement of the dome
of the diaphragm, or increased distance between
the apparent left hemidiaphragm and the gastric
air bubble suggests subpulmonic effusions.

30. Diagnostic Thoracentesis
• A diagnostic thoracentesis should be performed if
the etiology of the effusion is unclear or if the
presumed cause of the effusion does not respond
to therapy as expected. Pleural effusions do not
require thoracentesis if they are too small to safely
aspirate or, in clinically stable patients, if their
presence can be explained by underlying
congestive heart failure (especially bilateral
effusions) or by recent thoracic or abdominal
surgery.

31. Contraindications
• Relative contraindications to diagnostic thoracentesis
include a small volume of fluid (< 1 cm thickness on a
lateral decubitus film), bleeding diathesis or systemic
anticoagulation, mechanical ventilation, and
cutaneous disease over the proposed puncture site.
Reversal of coagulopathy or thrombocytopenia may
not be necessary as long as the procedure is
performed under ultrasound guidance by an
experienced operator. Mechanical ventilation with
positive end-expiratory pressure does not increase
the risk of pneumothorax after thoracentesis, but it
increases the likelihood of severe complications
(tension pneumothorax or persistent bronchopleural
fistula) if the lung is punctured. An uncooperative
patient is an absolute contraindication for this
procedure

32. Complications
• Complications of diagnostic thoracentesis include
pain at the puncture site, cutaneous or internal
bleeding from laceration of an intercostal artery or
spleen/liver puncture, pneumothorax, empyema,
reexpansion pulmonary edema, malignant seeding
of the thoracentesis tract, and adverse reactions
to anesthetics used in the procedure.
Pneumothorax complicates approximately 6% of
thoracenteses but requires treatment with a chest
tube drainage of the pleural space in less than 2%
of cases

33. Biopsy
• Pleural biopsy should be considered, only if
TB or malignancy is suggested. Medical
thoracoscopy with the patient under
conscious sedation and local anesthesia has
emerged as a diagnostic tool to directly
visualize and take a biopsy specimen from
the parietal pleura in cases of undiagnosed
exudative effusions.

34. How is pleural effusion treated?
• Treatment of pleural effusion is based on the
underlying condition and whether the effusion is
causing severe respiratory symptoms, such as
shortness of breath or difficulty breathing.
• Diuretics and other heart failure medications are used
to treat pleural effusion caused by congestive heart
failure or other medical causes. A malignant effusion
may also require treatment with chemotherapy,
radiation therapy or a medication infusion within the
chest.
• A pleural effusion that is causing respiratory symptoms
may be drained using therapeutic thoracentesis or
through a chest tube (called tube thoracostomy).

35. • For patients with pleural effusions that are
uncontrollable or recur due to a malignancy
despite drainage, a sclerosing agent (a type of drug
that deliberately induces scarring) occasionally may
be instilled into the pleural cavity through a tube
thoracostomy to create a fibrosis (excessive fibrous
tissue) of the pleura (pleural sclerosis).
• Pleural sclerosis performed with sclerosing agents
(such as talc, doxycycline, and tetracycline) is 50
percent successful in preventing the recurrence of
pleural effusions.

36. Surgery
• Pleural effusions that cannot be managed through
drainage or pleural sclerosis may require surgical
treatment.
• The two types of surgery include:
Video-assisted thoracoscopic surgery (VATS)
Thoracotomy (Also referred to as traditional,
“open” thoracic surgery)