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Neural network based clinical decision support system for the calculation the initial continuous subcutaneous insulin infusion settings

https://doi.org/10.14341/DM13081

Abstract

BACKGROUND: Despite existing recommendations for the initial calculation of insulin pump settings, the process is largely subjective and depends on the physician’s personal experience.

AIM: Development of a clinical decision support system (CDSS) that determines the initial settings of the insulin pump, which would have satisfactory agreement with the expert opinion of physicians.

MATERIALS AND METHODS: Neural network model developed using data (continuous subcutaneous insulin infusion (CSII) settings, age, weight, total daily dose, and HbA1c) from 2850 children with T1D who were switched to CSII and achieved optimal glycemic control according to glucose levels. CDSS utilizing the model implemented as a computer program in Python.

A prospective assessment of the agreement between the recommendations of the CDSS and the physician conducted on 35 data sets of children with T1D (median age 9.3 years [6.4, 11.5]), and 840 points for decisions were analyzed. 4 degrees of agreement were used: complete consistency, when the physicians agreed with the CDSS recommendations; partial consistency, when the physicians didn’t agree with the CDSS recommendations, but the difference was in the range of ±15%; complete inconsistency — the difference more than ±15%; acceptable consistency is the sum of full and partial consistency (± 15% error is clinically acceptable). The null hypothesis of the study was the absence of difference in consistency/inconsistency between physicians and the CDSS.

RESULTS: The frequency of full consistency between CDSS and physician recommendations for initiating insulin pump therapy is 29.8-43.8%, and inconsistency is 33.7-41.1%. Acceptable consistency is 58.9–66.3%. There were no significant differences in mean insulin pump parameters between CDSS and physicians.

CONCLUSION: The results obtained are consistent with previous studies. Proposed model demonstrates acceptable performance regarding initial CSII settings, without significant deviations between various parameters.

About the Authors

D. N. Laptev
Endocrinology Research Centre
Russian Federation

Dmitry N. Laptev - MD, PhD, Professor; Researcher ID: O-1826-2013; Scopus Author ID: 24341083800.

Moscow


Competing Interests:

Имеется конфликт интересов - клиническое исследование проводилось группой лиц, принимавших участие в разработке СППВР.



D. Y. Sorokin
Endocrinology Research Centre
Russian Federation

Daniil Yu. Sorokin; Researcher ID: HJY-5714-2023.

11 Dm. Ulyanova street, 117036 Moscow


Competing Interests:

Имеется конфликт интересов - клиническое исследование проводилось группой лиц, принимавших участие в разработке СППВР.



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Supplementary files

1. Figure 1. Coefficient of determination (R²) of the model obtained on the validation dataset, depending on the number of predictors added sequentially in descending order of statistical significance.
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2. Figure 2. Loss function value (A) and coefficient of determination (R²) (B) on the training dataset.
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3. Figure 3. Interface of the clinical decision support system.
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4. Figure 4. Levels of agreement in recommendations between the clinical decision support system and physicians (Me, Q1–Q3, min, max).
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Type Исследовательские инструменты
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5. Figure 5. Comparison of median pump parameter values over 24 hours between the clinical decision support system and physicians (Me, Q1–Q3, min, max).
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Review

For citations:


Laptev D.N., Sorokin D.Y. Neural network based clinical decision support system for the calculation the initial continuous subcutaneous insulin infusion settings. Diabetes mellitus. 2024;27(6):555-564. (In Russ.) https://doi.org/10.14341/DM13081

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ISSN 2072-0351 (Print)
ISSN 2072-0378 (Online)