Examination of a Pleural Effusion

Pleural effusion is a pathological (abnormal) increase in fluid content between the pleura parietalis (pleura) and the pleura visceralis (pleura of the lung), which can be caused by a wide variety of diseases. As part of the diagnosis and treatment of the various forms of pleural effusion, the fluid obtained by puncture is subjected to laboratory analysis. The following forms of pleural effusion can be distinguished:

  • Hemorrhagic (bloody) secretion.
  • Purid (purulent) secretion
  • Lymph
  • Exudate (see below) – more or less turbid fluid of inflammatory origin.
  • Transsudate (see below) – mostly serous fluid of non-purulent origin, which is low in cells and protein.

The procedure

Material needed

  • Pleural punctate

Preparation of the patient

  • Not necessary

Disruptive factors

  • Not known

Indications

  • Unclear pleural effusion

Interpretation

Inspection (color and consistency of the punctate).

Color and consistency Assessment
Light amber and clear normal
clear and viscous
  • Parapneumonic pleural effusion (see below: pleural effusion/classification).
  • Pulmonary pleural effusions
  • Tuberculous pleural effusions
  • Cardiac pleural effusions
  • Hypoproteinemic pleural effusions
pus-cloudy Pus: pleural empyema (with foul fetid odor; massive leukocyte-rich secretion in pleural space) or abdominal abscesses
Milky-cloudy A milky effusion contains fats: chylothorax:

  • Triglycerides > 110 mg/dl) or.
  • Pseudochylothorax (cholesterol > 200 mg/dl
bloody Hematothorax:

  • Pleural hematocrit > 50% of blood hematocrit or
  • Hemorrhagic effusion:
    • Malignant disease of the lung, pleura or mamma.
    • Pulmonary embolism
    • Tuberculosis
    • Thoracic trauma

Differentiation between exudate and transudate.

Transudate Exudate
Total white in g/l < 30 > 30
Specific weight < 1.016 > 1.016
Pleural TP: serum TP (total protein quotient; total protein, TP). < 0,5 > 0,5
LDH in U/l < 200 > 200
Pleural LDL: serum LDL (LDL quotient). < 0,6 > 0,6

Diseases that may be associated with transudate:

  • Heart failure (cardiac insufficiency): decompensated left heart failure.
  • Hypalbuminemia (decreased concentration of the plasma protein albumin in blood plasma):
    • Exudative enteropathy (protein-losing intestinal disease; enteral protein loss syndrome).
    • Liver cirrhosis – connective tissue remodeling of the liver leading to functional impairment.
    • Nephrotic syndrome – collective term for symptoms that occur in various diseases of the glomerulus (renal corpuscles); symptoms are proteinuria (excretion of protein with urine) with a protein lossof more than 1 g/m²/body surface per day; hypoproteinemia, peripheral edema due to hypalbuminemia of < 2.5 g/dl in serum, hyperlipoproteinemia (lipid metabolism disorder).
    • Malnutrition
  • Renal insufficiency (kidney weakness)

Diseases that may be associated with exudate:

Other laboratory parameters in unclear pleural effusion:

  • Differential blood count
  • Hematocrit
  • PH value
  • Amylase
  • Glucose (blood glucose determination)
  • Triglycerides
  • Microbiological examination
  • Cytology
Biochemical studies
  • Pleural pH:
    • PH 7.1-7.3: complicated effusion.
    • PH < 7.1: pleural empyema (accumulation of pus (empyema) within the pleura) with indication for surgical therapy
    • 7.2-7.0: Parapneumonic effusion.
    • PH > 7.3: uncomplicated pleural effusion (antibiosis if necessary).
  • Pleural glucose < 60 mg/dl: infections, collagenoses.
  • Pleural amylase: acute pancreatitis.
  • Further: see above under “Differentiation between exudate and transudate”.
Microbiology
  • Usual bacteriology as well as examination for mycobacteria. For reliable bacterial detection native material is required, which arrives at the laboratory without delay!
Cytology
  • Neutrophil proliferation: acute inflammation (e.g., pneumonia/pneumonia).
  • Eosinophils (rare): eosinophilic granulomatosis with polyangiitis (EGPA; formerly Churg-Strauss syndrome (CSS)), Dressler syndrome, pleural asbestosis, pneumothorax (entry of air into pleural space), caused by drugs
  • Lymphocytosis: tuberculosis, tumors.
  • Monocyte proliferation: chronic inflammation.
  • Tumor cells?