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Protein-losing enteropathy after the Fontan operation: associations and predictors of clinical outcome

Suchaya Silvilairat1, Allison K Cabalka, Frank Cetta

  • 1Division of Pediatric Cardiology, Mayo Clinic, Rochester, MN 55905, USA.

Congenital Heart Disease
|August 22, 2008
PubMed

Insights

Protein-losing enteropathy (PLE) in Fontan patients is linked to poorer outcomes. Short deceleration time, NYHA class III/IV, and low serum albumin predict mortality in these patients.

Area of Science:

  • Pediatric Cardiology
  • Congenital Heart Disease
  • Cardiac Surgery Outcomes

Background:

  • Protein-losing enteropathy (PLE) is a severe complication following Fontan surgery.
  • While pre- and perioperative factors for PLE are known, postoperative predictors of outcome remain unclear.

Purpose of the Study:

  • To identify clinical parameters associated with the long-term outcomes of Fontan patients who develop protein-losing enteropathy (PLE).

Main Methods:

  • A matched-pair analysis compared 44 Fontan patients with PLE to controls without PLE.
  • Survival analyses were conducted using Kaplan-Meier and Cox proportional hazard models.

Main Results:

  • Fontan patients with PLE showed reduced short-axis and apical fractional area change (Delta FA) compared to controls.
  • Five- and 10-year survival rates for the PLE group were 49% and 30%, respectively.
  • Independent predictors of mortality in PLE patients included deceleration time <120 ms, NYHA class III/IV, and low serum albumin.

Conclusions:

  • Mild reduction in Delta FA was the sole late echocardiographic finding linked to PLE development.
  • Short deceleration time, advanced NYHA class, and low serum albumin identify high-risk Fontan patients with PLE.
  • These high-risk indicators warrant aggressive management and potential early consideration for heart transplantation.
Abstract

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