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Early Impact of Fontan Operation on Enteric Protein Loss
Jyoti K Patel1, Kathleen M Loomes1, David J Goldberg1
1Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Insights
The Fontan operation rarely causes immediate protein-losing enteropathy (PLE). However, children may experience increased enteric protein loss, especially with hemodynamic issues, before or after surgery.
Area of Science:
- Pediatric Cardiology
- Gastroenterology
- Vascular Physiology
Background:
- Protein-losing enteropathy (PLE) is a significant complication following Fontan operations.
- Subclinical enteric protein loss can precede overt PLE development.
- The study investigates acute effects of Fontan circulation on protein loss and mesenteric vascular resistance.
Purpose of the Study:
- To evaluate acute changes in enteric protein loss after Fontan operations.
- To assess mesenteric vascular resistance in the context of Fontan circulation.
- To identify potential predictors or associated factors of enteric protein loss.
Main Methods:
- Prospective cohort study of children undergoing Fontan operations.
- Measurement of stool alpha-1 antitrypsin (A1AT) preoperatively, early postoperatively, and 3-9 months postoperatively.
- Assessment of superior mesenteric artery (SMA) resistance indices and serum albumin/protein levels.
Main Results:
- No clinical PLE observed in 33 participants.
- Elevated stool A1AT found in 6 of 93 samples, with 2 cases associated with hemodynamic disturbances.
- No significant change in SMA resistance; serum albumin decreased postoperatively but did not correlate with A1AT or SMA resistance.
Conclusions:
- The Fontan operation does not typically lead to acute increases in enteric protein loss.
- Increased enteric protein loss can occur in children around the time of Fontan surgery, particularly with hemodynamic instability.
Background:
Protein-losing enteropathy (PLE) is a challenging complication after a Fontan operation. Subclinical enteric protein loss may precede development of overt PLE. We evaluated the acute effects of Fontan circulation on enteric protein loss and mesenteric vascular resistance.
Methods:
A prospective cohort study was performed evaluating enteric protein loss in children undergoing Fontan operations. Stool alpha-1 antitrypsin (A1AT) concentration was measured in the preoperative, early postoperative, and intermediate postoperative (3-9 months) periods. The intestinal circulation was characterized by Doppler-derived resistance indices of the superior mesenteric artery (SMA), and serum albumin and protein levels were obtained.
Results:
We enrolled 33 participants at a median age at operation of 3.0 years (interquartile range [IQR], 2.5-3.3 years). No clinical PLE was observed. Six of the 93 stool samples obtained had elevated A1AT levels (>54 mg/dL), with 2 abnormal samples at each of the 3 time points. Two of the 5 participants with elevated stool A1AT values had significant hemodynamic disturbances requiring intervention (junctional bradycardia or tricuspid stenosis). There was no difference in SMA resistance in the preoperative versus early postoperative periods (p = 0.9). Serum albumin levels were lower in the early postoperative period compared with the preoperative period (3.2 mg/dL [{IQR}, 2.9-3.5] versus 4.1 mg/dL; IQR, 3.4-4.5; p = 0.01) but did not correlate with abnormal stool A1AT concentration or SMA resistance indices.
Conclusions:
The Fontan operation does not commonly result in acute development of increased enteric protein loss. However, increased enteric protein loss may occur in children before or after a Fontan operation, particularly when hemodynamic disturbances are present.
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