The Clinical Case for the Integration of a Ketone Sensor as Part of a Closed Loop Insulin Pump System.


Journal

Journal of diabetes science and technology
ISSN: 1932-2968
Titre abrégé: J Diabetes Sci Technol
Pays: United States
ID NLM: 101306166

Informations de publication

Date de publication:
09 2019
Historique:
pubmed: 11 1 2019
medline: 5 9 2020
entrez: 11 1 2019
Statut: ppublish

Résumé

Closed loop (CL) systems deliver insulin with a rapid onset and offset in action. Although favorable overall, the absence of a long-acting insulin increases the risk of diabetic ketoacidosis (DKA) which can occur with insulin delivery failure, acute illness, low carbohydrate diets, sodium glucose-linked transporter inhibitors, and high intensity exercise. A CL system relying entirely on interstitial glucose measurements may not provide an alert for DKA and many people with type 1 diabetes (T1D) do not carry a blood ketone meter and test-strips. Ketone sensing is theoretically feasible. A multianalyte platform incorporating a ketone sensor could provide an additional CL input without an increase in burden for the person with T1D, warning of impending DKA to allow remedial action to be taken. We outline the clinical case for inclusion of continuous ketone sensing as part of future CL systems.

Identifiants

pubmed: 30628470
doi: 10.1177/1932296818822986
pmc: PMC6955455
doi:

Substances chimiques

Ketones 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

967-973

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Auteurs

Melissa H Lee (MH)

1 Department of Medicine, University of Melbourne, St. Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia.
2 Department of Endocrinology and Diabetes, St Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia.

Barbora Paldus (B)

1 Department of Medicine, University of Melbourne, St. Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia.

Balasubramanium Krishnamurthy (B)

1 Department of Medicine, University of Melbourne, St. Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia.
3 St Vincent's Institute, Melbourne, Fitzroy, Victoria, Australia.

Sybil A McAuley (SA)

1 Department of Medicine, University of Melbourne, St. Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia.
2 Department of Endocrinology and Diabetes, St Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia.

Rajiv Shah (R)

4 Percusense, Valencia, CA, USA.

Alicia J Jenkins (AJ)

1 Department of Medicine, University of Melbourne, St. Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia.
5 NHMRC Clinical Trials Centre, University of Sydney, Sydney, NSW, Australia.

David N O'Neal (DN)

1 Department of Medicine, University of Melbourne, St. Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia.
2 Department of Endocrinology and Diabetes, St Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia.

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