Pleural Effusion Aspiration

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PatientPlus articles are written by UK doctors and are based on research evidence, UK and European Guidelines. They are designed for health professionals to use, so you may find the language more technical than the condition leaflets.

See also: Pleural Effusion written for patients

Synonym: thoracentesis, pleural tap

See also the separate Pleural Effusion article.

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Percutaneous pleural effusion aspiration is carried out:

To investigate the cause of pleural effusion
The British Thoracic Society (BTS) guidelines suggest that pleural aspiration should be reserved for the investigation of unilateral exudative pleural effusions. It should not be carried out if a unilateral or bilateral transudative effusion is suspected, unless there are atypical features or there is failure of response to therapy.[1] 

As symptom relief for breathlessness

  • Urgent decompression of the pleural space may be required to alleviate respiratory distress.[2] 
  • Repeated 'tapping' of fluid may be useful in palliative care. However, there is a high recurrence rate if pleurodesis (intrapleural instillation of a sclerosant) is not carried out simultaneously.[3] 
  • Very small volume of fluid.
  • Bleeding diathesis.
  • Anticoagulant therapy.
  • Mechanical ventilation (increased likelihood of tension pneumothorax or bronchopleural fistula if the lung is punctured).
  • Cutaneous disease over the proposed skin puncture site.
Lungs and airways with pleural effusion

This can be performed in the clinic or by the bedside.[1] 

Radiological guidance (particularly using ultrasound) is increasingly used and reduces the risk of complications.[4] 

  • Sit the patient as upright as possible. A pillow can be used to support arms and head on an adjustable table or couch. If the patient leans forward too much it increases the risk of liver/spleen injury.
  • Use an aseptic technique throughout the procedure.
  • Use percussion to determine the upper level of fluid.
  • The conventional site for aspiration is posteriorly, approximately 10 cm lateral to the spine (mid-scapular line) and 1-2 intercostal spaces below the upper level of the fluid.
  • Mark the spot and clean the area using antiseptic.
  • Use local anaesthetic (5-10 ml of 1% lidocaine) to infiltrate the skin and underlying tissues. A 25G needle can be used for this.
  • Avoid the intercostal nerves and vessels that run immediately beneath the rib by inserting the needle just above the upper border of the rib, below your mark.
  • You can confirm the correct location for pleural aspiration by aspirating a small amount of fluid through this smaller needle.
  • Attach a 21G needle to a 50 ml syringe.
  • Again, avoid the intercostal nerves and vessels by inserting the needle just above the upper border of the rib below your mark. Aspirate while you are advancing the needle.
  • 50-100 ml of fluid is usually adequate for diagnostic purposes.
  • Look at the fluid obtained and note any odour: purulent fluid suggests empyema; milky, opalescent fluid suggests chylothorax; grossly bloody fluid suggests haemothorax; anaerobic infection has a pungent odour.
  • Separate the pleural fluid into different sterile pots to be sent for biochemistry, microbiology, cytology ± immunology. Some fluid should also be added to blood culture bottles.
  • A post-procedure CXR to look for pneumothorax is not generally needed provided the patient is asymptomatic and the procedure was uncomplicated.

If the procedure is being carried out to relieve breathlessness, a greater volume of fluid usually needs to be drained:

  • Use a 14G intravenous cannula instead of the 21G needle.
  • Administer oxygen and use pulse oximetry throughout the procedure.
  • Follow the same steps as above.
  • When the cannula is inserted, remove the stylet and connect a closed pleural aspiration kit.
  • The fluid should still be sent for analysis.
  • It is best to remove fluid slowly.
  • Monitor for chest pressure or pain during fluid removal. This can be a sign of lung entrapment due to extensive pleural involvement or endobronchial obstruction which will prevent re-expansion of the lung when the fluid is removed. If this occurs, stop the procedure.
  • Rarely, if more than 1.5 litres of fluid are drained off, fluid shifts can cause haemodynamic instability or pulmonary oedema. The recommended fluid drainage limit is 1.5 litres.[4] 

A chest drain can also be inserted for pleural fluid drainage.[5][6]

The BTS suggests the following initial investigations:[1]

Microbiology

  • It is generally recommended that pleural fluid samples from pleural effusions of unknown cause be cultured for bacteria, mycobacteria and fungi. However, the positive yield of smears and cultures on pleural fluid specimens is low.[7] 
  • Send one pot for Gram stain, acid-alcohol fast bacilli (AAFB) stain, microscopy, culture and sensitivity.
  • Send some fluid in blood culture bottles (increases yield, especially for anaerobic organisms).

Biochemistry
Send one pot for protein, lactate dehydrogenase (LDH) and pH.

Cytology

  • Send a 20 ml sample in a sterile pot for cytological examination. Some cytologists prefer samples to be sent in a citrate bottle to prevent clots (discuss with your laboratory).
  • The sample needs to be fresh.
  • Malignant effusions can be diagnosed by pleural fluid cytology alone in 60% of cases.[8] A second sample can increase diagnostic yield.

Additional investigations should be requested under specific circumstances:

  • If empyema is suspected send some fluid for centrifuge to differentiate from chylothorax.
  • If chylothorax is suspected send some fluid for centrifuge, cholesterol and triglyceride levels and investigation for the presence of cholesterol crystals and chylomicrons.
  • If haemothorax is suspected, or the pleural fluid is grossly bloody, send some fluid for haematocrit level.
  • If rheumatoid disease is suspected send some fluid for glucose and complement levels.
  • If pancreatitis is suspected send some fluid for amylase level.

See the separate Pleural Effusion article.

  • Pain during and after the procedure at the puncture site.
  • Pneumothorax complicates 12-30% of pleural aspirations but chest drain treatment is required in <5% of these.
  • Persistent air leak.
  • Bleeding (may be cutaneous or intrapleural).
  • Empyema.
  • Inadvertent liver/spleen puncture.
  • Re-expansion pulmonary oedema.
  • Malignant metastatic seeding (rare).

Further reading & references

  1. Pleural Disease Guidelines; British Thoracic Society (September 2010)
  2. Maslove DM, Chen BT, Wang H, et al; The diagnosis and management of pleural effusions in the ICU. J Intensive Care Med. 2013 Jan-Feb;28(1):24-36. doi: 10.1177/0885066611403264. Epub 2011 Nov 11.
  3. Antunes G, Neville E, Duffy J, et al; BTS guidelines for the management of malignant pleural effusions. Thorax. 2003 May;58 Suppl 2:ii29-38.
  4. Corcoran JP, Psallidas I, Wrightson JM, et al; Pleural procedural complications: prevention and management. J Thorac Dis. 2015 Jun;7(6):1058-67. doi: 10.3978/j.issn.2072-1439.2015.04.42.
  5. Zisis C, Tsirgogianni K, Lazaridis G, et al; Chest drainage systems in use. Ann Transl Med. 2015 Mar;3(3):43. doi: 10.3978/j.issn.2305-5839.2015.02.09.
  6. George RS, Papagiannopoulos K; Advances in chest drain management in thoracic disease. J Thorac Dis. 2016 Feb;8(Suppl 1):S55-64. doi: 10.3978/j.issn.2072-1439.2015.11.19.
  7. Barnes TW, Olson EJ, Morgenthaler TI, et al; Low yield of microbiologic studies on pleural fluid specimens. Chest. 2005 Mar;127(3):916-21.
  8. Porcel JM, Light RW; Diagnostic approach to pleural effusion in adults. Am Fam Physician. 2006 Apr 1;73(7):1211-20.
  9. Daniels CE, Ryu JH; Improving the safety of thoracentesis. Curr Opin Pulm Med. 2011 Jul;17(4):232-6. doi: 10.1097/MCP.0b013e328345160b.
  10. Duncan DR, Morgenthaler TI, Ryu JH, et al; Reducing iatrogenic risk in thoracentesis: establishing best practice via experiential training in a zero-risk environment. Chest. 2009 May;135(5):1315-20. doi: 10.1378/chest.08-1227. Epub 2008 Nov 18.

Disclaimer: This article is for information only and should not be used for the diagnosis or treatment of medical conditions. EMIS has used all reasonable care in compiling the information but make no warranty as to its accuracy. Consult a doctor or other health care professional for diagnosis and treatment of medical conditions. For details see our conditions.

Original Author:
Dr Michelle Wright
Current Version:
Peer Reviewer:
Prof Cathy Jackson
Document ID:
2979 (v24)
Last Checked:
05/05/2016
Next Review:
04/05/2021

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