Searchable abstracts of presentations at key conferences in endocrinology
Endocrine Abstracts (2018) 53 P07 | DOI: 10.1530/endoabs.53.P07

OU2018 Poster Presentations (1) (9 abstracts)

The use of ketogenic diet in a patient with post-prandial hyperinsulinemic hypoglycaemia after m Roux-en-Y Gastric Bypass surgery: a case study

Sally Abbott 1, , Naomi Dindol 1, , Rishi Singhal 1, , Ahmed Helmy 1 , Mohamed Ahmed 1 , Sri Bellary 1, & Abd Tahrani 1,


1Heart of England NHS Foundation Trust, Birmingham, UK; 2University of Birmingham, Birmingham, UK; 3Aston University, Birmingham, UK.


Background: Hyperinsulinemic hypoglycaemia (HH) after Roux-en-Y gastric bypass (RYGB) is rare. Patients typically present with post-prandial hypoglycaemia >1 year after surgery and once weight loss has plateaued. Despite multiple treatment options, the management of these patients remains challenging.

Clinical case: A 31-year-old female was referred for bariatric surgery with a BMI of 41.4 kg/m2. In the year preceding the referral to bariatric surgery she attended tier 3 services and managed to lose 29% of her body weight with life style intervention. She was known to have Type 2 diabetes, which was now well controlled with metformin (HbA1c 34 mmol/mol) following this weight loss. Twelve months after undergoing RYGB, her BMI had reduced to 25.5 kg/m2 and she presented with excessive sweating, headaches, palpitations and hunger. At this point she had lost 56% of her total body weight over a 30-month period. Two 16-h fasting tests did not elicit any proven hypoglycaemia. She was admitted as an inpatient for a 72-h fasting test, during which the lowest glucose level was 3.9 mmol/l, which was associated with insulin levels of <10 mU/l and C-peptide of 284 pmol/l. An endoscopic ultrasound showed no evidence of pancreatic tumours. A mixed meal test was then performed which showed hypoglycaemia (glucose 2.6, and 2.8 mmol/l) with inappropriate levels of Insulin (51 mU/l) and C-peptide (1056 pmol/l) 30 min post-prandial. She remained highly symptomatic despite dietary measures (small frequent meals, avoiding simple carbohydrates), and treatment with Acarbose. Hypoglycaemic events remained frequent despite a very low carbohydrate diet (<30 g per day). A restrictive dietary intervention using a ketogenic diet was thus initiated. The patient’s symptoms resolved entirely when carbohydrate intake was reduced gradually to 10–12 g of carbohydrate per day.

Conclusion: Ketogenic dietary intervention might dramatically improve the situation in patients with post-RYGB HH that failed to respond to other measures or wish to avoid pharmacological intervention.

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