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Treatment of mild-to-moderate hypoglycemia in patients with type 1 diabetes treated with insulin pump therapy: are current recommendations effective?

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Abstract

Aims

Mild-to-moderate hypoglycemia (blood glucose < 4.0 mmol/L) is recommended to be treated with 15 g of carbohydrates and to repeat the treatment if hypoglycemia persists after 15 min. This recommendation was established before intensive insulin therapy and based on studies using insulin with different pharmacokinetic profiles from actual insulin analogs showing that 15 g of glucose increases blood glucose by ~ 1.5 mmol/L in 15 min. We aimed to explore the effect of current recommended treatment of mild-to-moderate hypoglycemia in type 1 diabetes (T1D) participants and factors associated with treatment effectiveness.

Methods

This is a secondary analysis from three observational inpatient studies with a standardized and supervised treatment (16 g carbohydrates) of hypoglycemia (< 3.3 mmol/L with symptoms or < 3.0 mmol/L without symptom) in participants (47 adults–10 adolescents) with T1D using continuous subcutaneous insulin infusion (“insulin pumps”; CSII)).

Results

Twenty-seven participants presented a total of 48 hypoglycemia episodes treated by a single intake of 16 g of carbohydrates. Time required for normoglycemia recovery was 19.5 ± 12.0 min. The rise in plasma glucose following treatment was 0.85 ± 0.66 mmol/L in 15 min. Eighteen episodes (38%) were resolved (> 4.0 mmol/L) 15-min post-treatment. Glycemia at the time of treatment (< 3.2 mmol/L; p < 0.001) and a higher proportion of total daily insulin from basal doses (p = 0.03) were associated with a slower post-treatment plasma glucose rise.

Conclusions

These results raise the possibility that sixteen grams of carbohydrates could be insufficient to treat a large proportion of hypoglycemia episodes in T1D patients treated with CSII. Factors affecting treatment effectiveness need to be investigated.

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Acknowledgements

We are grateful to all participants from the studies that were included in this secondary analysis. The J-A DeSève Foundation to RRL supported this analysis, while data collection was supported by studies funded by Diabetes Canada, Diabète Québec and the Canadian Institute for Health Research operating grants to RRL. VG is a research scholar of FRQS (Fonds de Recherche du Québec en Santé). MRS was supported by a postdoctoral fellowship from the Fonds de Recherche du Québec Nature et Technologies (FRQNT).

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Correspondence to Rémi Rabasa-Lhoret.

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Conflict of interest

RRL has received consultant/speaker honorariums and/or his institution received grants from Astra-Zeneca, Becton–Dickinson, Bohringer, Eli Lilly, Janssen, Insulet, Lifescan, Medtronic, Merck, Novartis, Neomed, Novo Nordisk, Roche, Sanofi-Aventis, Takeda and Valeant. AH has received consultant fees and grants from Medtronic, Eli Lilly and AgaMatrix. LL has received consultant/speaker honorariums and/or his institution received grants from Eli Lilly, Medtronic, Novo Nordisk, Merck and Sanofi. No other competing financial interests were reported.

Human and animal rights

All procedures performed in the initial studies involving human participants were in accordance with the ethical standards of the institutional research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.

Informed consent

The IRCM ethics committee approved the studies and all participants gave their informed consent prior to their inclusion in the studies.

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Gingras, V., Desjardins, K., Smaoui, M.R. et al. Treatment of mild-to-moderate hypoglycemia in patients with type 1 diabetes treated with insulin pump therapy: are current recommendations effective?. Acta Diabetol 55, 227–231 (2018). https://doi.org/10.1007/s00592-017-1085-8

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  • DOI: https://doi.org/10.1007/s00592-017-1085-8

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