Tolerance, adherence, and acceptability of a ketogenic 2.5:1 ratio, nutritionally complete, medium chain triglyceride-containing liquid feed in children and adults with drug-resistant epilepsy following a ketogenic diet.

enteral feed gastrointestinal tolerance ketogenic diet medium chain triglycerides seizures

Journal

Epilepsia open
ISSN: 2470-9239
Titre abrégé: Epilepsia Open
Pays: United States
ID NLM: 101692036

Informations de publication

Date de publication:
27 Feb 2024
Historique:
revised: 22 01 2024
received: 17 11 2023
accepted: 23 01 2024
medline: 27 2 2024
pubmed: 27 2 2024
entrez: 27 2 2024
Statut: aheadofprint

Résumé

To investigate incorporating a ready-to-use 2.5:1 ratio liquid feed into a ketogenic diet (KD) in children and adults with drug-resistant epilepsy. Following a three-day baseline, patients (n = 19; age: 19 years [SD 13], range: 8-46 years) followed a KD for 28 days (control period), then incorporated ≥200 mL/day of a ready-to-use liquid feed, made with a ratio of 2.5 g of fat to 1 g of protein plus carbohydrate and including medium chain triglycerides ([MCTs]; 25.6% of total fat/100 mL) for 28 days as part of their KD (intervention period). Outcome measures (control vs intervention period) included gastrointestinal (GI) tolerance, adherence to KD and intervention feed, dietary intake, blood ß-hydroxybutyrate (BHB) concentration, seizure outcomes, health-related quality of life (HRQoL), acceptability and safety. Compared to the control period, during the intervention period, the percentage of patients reporting no GI symptoms increased (+5% [SD 5], p = 0.02); adherence to the KD prescription was similar (p = 0.92) but higher in patients (n = 5) with poor adherence (<50%) to KD during the control period (+33% [SD 26], p = 0.049); total MCT intake increased (+12.1 g/day [SD 14.0], p = 0.002), driven by increases in octanoic (C8; +8.3 g/day [SD 6.4], p < 0.001) and decanoic acid (C10; +5.4 g/day [SD 5.4], p < 0.001); KD ratio decreased (p = 0.047), driven by a nonsignificant increase in protein intake (+11 g/day [SD 44], p = 0.29); seizure outcomes were similar (p ≥ 0.63) but improved in patients (n = 6) with the worst seizure outcomes during the control period (p = 0.04); and HRQoL outcomes were similar. The intervention feed was well adhered to (96% [SD 8]) and accepted (≥88% of patients confirmed). These findings provide an evidence-base to support the effective management of children and adults with drug-resistant epilepsy following a KD with the use of a ready-to-use, nutritionally complete, 2.5:1 ratio feed including MCTs. This study examined the use of a ready-to-use, nutritionally complete, 2.5:1 ratio (2.5 g of fat to 1 g of protein plus carbohydrate) liquid feed, including medium chain triglycerides (MCTs), into a ketogenic diet (KD) in children and adults with drug-resistant epilepsy. The results show that the 2.5:1 ratio feed was well tolerated, adhered to, and accepted in these patients. Increases in MCT intake (particularly C8 and C10) and improvements in seizure outcomes (reduced seizure burden and intensity) and KD adherence also occurred with the 2.5:1 ratio feed in patients with the worst seizures and adherence, respectively.

Identifiants

pubmed: 38411329
doi: 10.1002/epi4.12910
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Nutricia Ltd.

Informations de copyright

© 2024 Nutricia Ltd. Epilepsia Open published by Wiley Periodicals LLC on behalf of International League Against Epilepsy.

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Auteurs

Corbin Griffen (C)

Clinical Research, Nutricia Ltd., Trowbridge, UK.

Natasha E Schoeler (NE)

UCL Great Ormond Street Institute of Child Health, London, UK.
Great Ormond Street Hospital for Children, London, UK.

Robert Browne (R)

Clinical Research, Nutricia Ltd., Trowbridge, UK.

Tracy Cameron (T)

Tayside Children's Hospital, Dundee, UK.
Royal Aberdeen Children's Hospital, Aberdeen, UK.

Martin Kirkpatrick (M)

Tayside Children's Hospital, Dundee, UK.

Seema Thowfeek (S)

The Barberry, Birmingham and Solihull Mental Health NHS Foundation Trust, Birmingham, UK.

Judith Munn (J)

The Barberry, Birmingham and Solihull Mental Health NHS Foundation Trust, Birmingham, UK.

Helena Champion (H)

Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.

Nicole Mills (N)

Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.

Siân Phillips (S)

Southampton Children's Hospital, Southampton General Hospital, Southampton, UK.

Linda Air (L)

Great North Children's Hospital, Newcastle Upon Tyne, UK.

Anita Devlin (A)

Great North Children's Hospital, Newcastle Upon Tyne, UK.

Claire Nicol (C)

Great North Children's Hospital, Newcastle Upon Tyne, UK.

Susan Macfarlane (S)

Tayside Children's Hospital, Dundee, UK.

Victoria Bittle (V)

Bristol Royal Hospital for Children, Bristol, UK.

Phillipa Thomas (P)

Bristol Royal Hospital for Children, Bristol, UK.

Lisa Cooke (L)

Bristol Royal Hospital for Children, Bristol, UK.

Julia Ackril (J)

Birmingham Women's and Children's NHS Trust, Birmingham, UK.

Astrid Allford (A)

Birmingham Women's and Children's NHS Trust, Birmingham, UK.

Vanessa Appleyard (V)

Birmingham Women's and Children's NHS Trust, Birmingham, UK.

Clare Szwec (C)

Clinical Research, Nutricia Ltd., Trowbridge, UK.

Kiranjit Atwal (K)

Independent Researcher, Phoenix, Arizona, USA.

Gary P Hubbard (GP)

Clinical Research, Nutricia Ltd., Trowbridge, UK.

Rebecca J Stratton (RJ)

Clinical Research, Nutricia Ltd., Trowbridge, UK.
University of Southampton, Southampton, UK.

Classifications MeSH