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Impact of protein-losing enteropathy in children who underwent the Fontan operation
Baneen Alkofair1, Abdulmajeed Alruwaili1, Jiaxiang Gai2
1Department of Pediatrics, George Washington University School of Medicine, Washington, DC, USA.
Insights
Post-Fontan protein-losing enteropathy significantly reduces transplant-free survival and increases healthcare costs. This condition necessitates higher resource utilization and medication use compared to patients without the complication.
Area of Science:
- Pediatric Cardiology
- Gastroenterology
- Health Economics
Background:
- Protein-losing enteropathy (PLE) is a known complication following Fontan surgery.
- Limited data exists on the economic impact and resource utilization of post-Fontan PLE in the current healthcare landscape.
- Understanding these factors is crucial for optimizing patient care and resource allocation.
Purpose of the Study:
- To evaluate the impact of post-Fontan PLE on transplant-free survival.
- To describe resource utilization and treatment variations in patients with post-Fontan PLE.
- To analyze healthcare charges and medication use associated with post-Fontan PLE.
Main Methods:
- Retrospective, single-center study of patients who underwent Fontan surgery between 2009 and 2017.
- Patients were divided into two groups: those with and without post-Fontan PLE.
- Data collected included demographics, hospital admissions, resource utilization, medications, and charges.
Main Results:
- 19% of eligible patients (28 out of 147) developed post-Fontan PLE.
- The PLE group showed significantly higher encounters, hospital length of stay, and total charges.
- Ten-year transplant-free survival was markedly lower in patients with PLE (65.7%) compared to those without (97.3%).
Conclusions:
- Post-Fontan PLE is associated with reduced transplant-free survival and increased healthcare resource utilization and costs.
- Significant practice variation exists in the management of post-Fontan PLE.
- Further research is needed to establish standardized treatment protocols to improve outcomes for these patients.
Abstract:
Previous reports have identified risk factors associated with development of post-Fontan protein-losing enteropathy. Less is known about the economic impact and resource utilisation required for post-Fontan protein-losing enteropathy in the current era. We conducted a single-centre retrospective study to assess the impact of post-Fontan protein-losing enteropathy on transplant-free survival. We also described resource utilisation and treatment variations among post-Fontan protein-losing enteropathy patients. Children who received care at our centre between 2009 and 2017 after the Fontan surgery were eligible. Initial admissions for the Fontan operative procedure were excluded. Demographics, hospital admissions, resource utilisation, medications and charges were reviewed. Patients were divided into two groups based on the presence of post-Fontan protein-losing enteropathy. Of the 343 patients screened, 147 met the eligibility criteria. Of these, 28 (19%) developed protein-losing enteropathy. After adjusting for follow-up duration, the protein-losing enteropathy group had higher number of encounters (2.15 ± 2.16 versus 1.47 ± 2.56, p 0.002), hospital length of stay (days) (25 ± 51.3 versus 11.4 ± 41.7, p < 0.0001) and total charges (2018US$) (388,489 ± 759,859 versus 202,725 ± 1,076,625, p < 0.0001). Encounters for patients with protein-losing enteropathy utilised more therapies. Among those with protein-losing enteropathy, use of digoxin was associated with slightly decreased odds for mortality and/or transplant (0.95, confidence interval 0.90-0.99, p 0.021). The 10-year transplant-free survival for patients with/without protein-losing enteropathy was 65.7/97.3% (p 0.002), respectively. Post-Fontan protein-losing enteropathy is associated with reduced 10-year transplant-free survival, higher resource utilisation, charges and medication use compared with the non-protein-losing enteropathy group. Practice variation among post-Fontan protein-losing-enteropathy patients is common. Further larger studies are needed to assess the impact of standardisation on the well-being of children with post-Fontan protein-losing enteropathy.
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