The hypoglycemia-prevention effect of sensor-augmented pump therapy with predictive low glucose management in Japanese patients with type 1 diabetes mellitus: a short-term study.

Hypoglycemia Predictive low glucose management (PLGM) Sensor-augmented pump therapy (SAP) Type 1 diabetes mellitus (T1DM)

Journal

Diabetology international
ISSN: 2190-1678
Titre abrégé: Diabetol Int
Pays: Japan
ID NLM: 101553224

Informations de publication

Date de publication:
Apr 2020
Historique:
received: 25 06 2019
accepted: 10 09 2019
entrez: 25 3 2020
pubmed: 25 3 2020
medline: 25 3 2020
Statut: epublish

Résumé

The predictive low glucose management (PLGM) system was introduced in March 2018 in Japan. Although there are some reports demonstrating the benefit of PLGM in preventing hypoglycemia, no data are currently available in Japanese patients with type 1 diabetes mellitus (T1DM). The aim of the present study is to evaluate the effect of PLGM with sensor-augmented pump therapy in the prevention of hypoglycemia in Japanese patients. We included 16 patients with T1DM who used the MiniMed The area under the curve (AUC) of hypoglycemia of < 70 mg/dL was lowered from 0.42 ± 0.43 mg/dL day to 0.18 ± 0.18 mg/dL day ( The hypoglycemia avoidance rate was comparable to those in previous reports. In addition, we demonstrated that PLGM can markedly suppress severe hypoglycemia without deteriorating glycemic control in Japanese T1DM patients. It is necessary to further investigate the effective use of the PLGM feature such as establishing a lower limit and the timing of resumption.

Identifiants

pubmed: 32206479
doi: 10.1007/s13340-019-00408-7
pii: 408
pmc: PMC7082487
doi:

Types de publication

Journal Article

Langues

eng

Pagination

97-104

Informations de copyright

© The Japan Diabetes Society 2019.

Déclaration de conflit d'intérêts

Conflict of interestAuthor Atsuhito T. received lecture fees from Medtronic Japan, Sanofi and Eli Lilly. Author Jun W. received lecture fees from Astellas, Astra Zeneca, Boeringer Ingelheim Japan, Daiichi Sankyo, MSD, Novartis, Tanabe Mitsubishi and Taisho Toyama, and received research funding from Bayer, Baxter, Chugai, Dainippon Sumitomo, Kyowa Hakko Kirin, MSD, Novartis, Novo Nordisk, Ono, Takeda, Tanabe Mitsubishi and Teijin. Other authors declare that they have no conflict of interest associated with this research.

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Auteurs

Akihiro Katayama (A)

1Diabetes Center, Okayama University Hospital, 2-5-1 Shikata-cho, Kita-ku, Okayama, 700-8558 Japan.

Atsuhito Tone (A)

2Diabetes Center, Okayama Saiseikai General Hospital, Kita-ku, Okayama, 700-8511 Japan.

Mayu Watanabe (M)

3Department of Primary Care and Medical Education, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Kita-ku, Okayama, 700-8558 Japan.

Sanae Teshigawara (S)

2Diabetes Center, Okayama Saiseikai General Hospital, Kita-ku, Okayama, 700-8511 Japan.

Satoshi Miyamoto (S)

4Center for Innovative Clinical Medicine, Okayama University Hospital, Kita-ku, Okayama, 700-8558 Japan.

Jun Eguchi (J)

5Department of Nephrology, Rheumatology, Endocrinology and Metabolism, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Kita-ku, Okayama, 700-8558 Japan.

Atsuko Nakatsuka (A)

5Department of Nephrology, Rheumatology, Endocrinology and Metabolism, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Kita-ku, Okayama, 700-8558 Japan.

Kenichi Shikata (K)

4Center for Innovative Clinical Medicine, Okayama University Hospital, Kita-ku, Okayama, 700-8558 Japan.

Jun Wada (J)

5Department of Nephrology, Rheumatology, Endocrinology and Metabolism, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Kita-ku, Okayama, 700-8558 Japan.

Classifications MeSH