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 25 April 2018

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News

Diagnostic approach and current management of chylous ascites

A study published in the latest issue of the Alimentary Pharmacology & Therapeutics reviewed the current diagnostic approach and management of chylous ascites.

News image

Chylous ascites is rare, accounting for less than 1% of cases.

An appropriate and stepwise approach to its diagnosis and management is of key importance.

Dr Cardenas and colleagues from Spain reviewed the current diagnostic approach and management of chylous ascites.

The team conducted a literature search using PubMed with the key words ‘chylous’, ‘ascites’, ‘cirrhosis’, ‘pathophysiology’, ‘nutritional therapy’, ‘paracentesis”, “transjugular intrahepatic portosystemic shunt” and “TIPSS’.

Only articles in English were included.

Chylous ascites is caused by the traumatic or obstructive disruption of the lymphatic system that leads to extravasation of thoracic or intestinal lymph into the abdominal space, and the accumulation of a milky fluid rich in triglycerides.

An ascitic triglyceride concentration above 200 mg/dL is consistent with chylous ascites
Alimentary Pharmacology & Therapeutics

The team found that the most common causes are malignancy, cirrhosis and trauma after abdominal surgery.

The researchers report that this condition can lead to chyle depletion, which results in nutritional, immunologic and metabolic deficiencies.

An ascitic triglyceride concentration above 200 mg/dL is consistent with chylous ascites.

Treatment is based on management of the underlying cause and nutritional support.

Dr Cardenas' team comments, "Chylous ascites is mostly due to malignancy and cirrhosis in adults, and congenital lymphatic disorders in children."

"Treatment with nutritional optimization and management of the underlying etiology are the cornerstones of therapy."

"When conservative measures fail, other interventions such as octreotide/somatostatin analogues, surgical ligation, embolization and transjugular intrahepatic portosystemic shunt in patients with cirrhosis can be considered."

Aliment Pharmacol Ther 2017: 46(9): 816–824
19 October 2017

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