Empyema is diagnosed after a thorough review of the individual’s medical history and
conduction of a physical examination. The healthcare provider may
auscultate the chest with a stethoscope in order to identify signs of
pneumonia and
fluid accumulation. Further diagnostic testing is frequently needed as many conditions may present similarly. Initially,
chest X-rays are typically ordered to evaluate the presence of any
pleural effusion. This characteristically appears on X-ray as blunting of the costodiaphragmatic angles, which means that the angle created by the
diaphragm and
rib disappears or has vague borders due to the accumulation of fluid.
If the X-ray is not indicative, an ultrasound can be performed at any time. Empyema may be suspected when the parietal and visceral pleura is thickened and separated by fluid, which appears on ultrasound as a homogenous anechoic accumulation.
Chest CT scans are also necessary for individuals with empyema, preferably with an intravenous (IV) injection of contrast. Both ultrasound and CT scans are useful diagnostic tools with great sensitivity at revealing the empyema. Similarly, on CT, the pleura may be thickened, separated, and enhanced by the contrast. Additionally, the CT also offers better imaging of the lung parenchyma to evaluate for other pathologies.
After all the necessary preliminary imaging, a
thoracentesis (i.e., minimally invasive procedure during which a needle is inserted between the
pleural space to drain the pus) is usually performed in order to drain the fluid and send it for analysis and culture. Notably, all
pleural fluids should be cultivated and sent for further analysis. However, negative cultures do not exclude the diagnosis as some bacteria are more difficult to cultivate.