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September 9, 2012 6:37 am
In my practice, I am asked to give input on patients with Fontan procedure infrequently. A few recent articles though are a good resource:
Both articles review the physiology and therapies available. In essence, the Fontan operation establishes a passive connection between the systemic venous return and the pulmonary circulation. When there are elevated inferior vena cava pressure, this can lead to hepatic dysfunction and protein-losing enteropathy. The latter is related to engorged intestinal lymphatics, similar to that in congenital intestinal lymphangiectasia. When lymphatic proteins leak, PLE only develops when the intestinal leak exceeds the patient’s ability to resynthesize lost proteins.
PLE presenting features: edema, diarrhea, bloating, pain, and pleural or pericardial effusions. PLE places patient at risk for growth failure and associated problems. In more severe cases, hypocalcemia and infections due to lymphopenia can be present.
Potential treatments:
The second reference notes that many centers are delaying the Fontan procedure and accepting some degree of hypoxemia. The problems with this approach include symptoms like headaches and decreased energy levels and the likelihood of developing pulmonary arteriovenous malformations. Ultimately, the authors hypothesize that biomedical engineers may develop better solutions with miniaturized mechanical support devices to improve pulmonary blood flow.
Additional references:
Posted by gutsandgrowth
Categories: Pediatrics
Tags: budesonide, Fontan, PLE, sildenafil, single ventricle
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By Congenital heart disease and the Liver | gutsandgrowth on November 11, 2012 at 6:11 am