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Updated: Aug 10, 2026

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Homogeneous Time-resolved Förster Resonance Energy Transfer-based Assay for Detection of Insulin Secretion
Published on: May 10, 2018
[Octreotide therapy for persistent hyperinsulinemic hypoglycemia of infancy]
Dênis Paiva Ferraz1, Marco Aurélio S Almeida, Bernardo Freire de Mello
1Serviço de Endocrinologia, Santa Casa de Misericórdia de Juiz de Fora, MG.
Arquivos Brasileiros De Endocrinologia E Metabologia
|March 18, 2006
Summary
Persistent hyperinsulinemic hypoglycemia of infancy (PHHI) is a serious condition. Octreotide offers a viable treatment option before surgery, crucial for infant neurodevelopment.
Area of Science:
- Pediatric Endocrinology
- Neonatology
- Surgical Gastroenterology
Background:
- Persistent hyperinsulinemic hypoglycemia of infancy (PHHI) is the leading cause of persistent hyperinsulinism in infants.
- PHHI poses significant risks to central nervous system development.
- Limited effective clinical treatment options exist for PHHI.
Observation:
- A case report of a newborn experiencing hypoglycemic episodes within 24 hours of birth.
- Successful initial management of the infant's condition using octreotide.
- The case highlights the challenges in managing PHHI.
Findings:
- Octreotide demonstrated efficacy as a pre-surgical treatment for PHHI.
- Preoperative evaluation is critical for differentiating focal and diffuse pancreatic disease.
- Distinguishing between focal and diffuse PHHI guides surgical approach and improves outcomes.
Implications:
- Octreotide represents a valuable therapeutic option for PHHI prior to surgical intervention.
- Accurate preoperative assessment is essential for optimizing surgical resection and minimizing complications.
- Partial pancreatectomy is the preferred surgical method for focal PHHI, enhancing patient outcomes.
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