Results of the first Russian multicenter non-interventional study of Contour® TS glucometer

Aim. To evaluate fitness of Contour® TS glucometer (Contour® TS, Bayer/Ascensia*) – a system for blood glycemia level control, and its characteristics in everyday use for Russian patients with insulin dependent diabetes mellitus (DM) types 1 and 2 and endocrinologists. Study design. According to th...

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Main Authors: Marina V. Shestakova, Liubov L. Bolotskaya, Mariia V. Verbovaia
Format: Article
Language:Russian
Published: ZAO "Consilium Medicum" 2019-04-01
Series:Consilium Medicum
Subjects:
Online Access:http://consilium.orscience.ru/en/archive/2019/vol-21-4-2019/results-of-the-first-russian-multicenter-non-interventional-study-of-contour-ts-glucometer_5458/?element
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spelling doaj-598f5e3583224a3bb4168442acac3fe72021-08-02T18:46:39ZrusZAO "Consilium Medicum"Consilium Medicum2075-17532542-21702019-04-01214263410.26442/20751753.2019.4.190308Results of the first Russian multicenter non-interventional study of Contour® TS glucometerMarina V. Shestakova0Liubov L. Bolotskaya1Mariia V. Verbovaia2National Medical Research Center for Endocrinology, Moscow, RussiaNational Medical Research Center for Endocrinology, Moscow, RussiaCenter "Diabetes", Samara, RussiaAim. To evaluate fitness of Contour® TS glucometer (Contour® TS, Bayer/Ascensia*) – a system for blood glycemia level control, and its characteristics in everyday use for Russian patients with insulin dependent diabetes mellitus (DM) types 1 and 2 and endocrinologists. Study design. According to the inclusion criteria, 3759 patients were registered in the program, of which 3599 patients have completed the study as per 3 visits. The non-interventional study was conducted in 84 medical centers in RF during the period from October 2013 to June 2015. Age of insulin-dependent patients and patients on hypoglycaemic therapy was 18 years and older. Results. Observational program included – 1126 (31.29%) patients with type 1 diabetes mellitus and 2473 (68.71%) patients with type 2 diabetes mellitus. Following switch to Contour® TS, while insulin therapy regimens were maintained, it was noted that the rate of blood glucose measurement increased compared with Visit 1 (p<0.0001). Upon assessment of satisfaction with the device, virtually all questions were answered as “good” and “perfect” by more than 90% patients and 95% study doctors. Upon assessment of the quality of life by EQ-5D, increase of this parameter was noted in 6 months, at Visit 3 (p<0.0001). No glucometer-associated malfunction were registered during the study. Additional data from general clinical experience of each patient that allowed to establish significant reduction of the levels of glycosilated haemoglobin and pre-prandial blood glucose just in 3 months at Visit 2, significant reduction of reported hypoglycaemia episodes as calculated per one patient have been obtained during the study. Additional data on the prevalence of macro- and microvascular complications were obtained during the study, and the highest per cent was for non-proliferative retinopathy and nephropathy at the stage of albuminuria. The most common among concomitant diseases were arterial hypertension, dyslipidemia and coronary artery disease. Conclusion. Use of Contour® TS glucometer by the patients, while insulin therapy regimens were maintained, led to increase in the rate of blood glucose measurements by up to 4–6 times during the day and statistically significant improvement in blood glucose control.http://consilium.orscience.ru/en/archive/2019/vol-21-4-2019/results-of-the-first-russian-multicenter-non-interventional-study-of-contour-ts-glucometer_5458/?elementnon-interventional studydiabetes mellitusinsulin therapyglucometerglycaemic control
collection DOAJ
language Russian
format Article
sources DOAJ
author Marina V. Shestakova
Liubov L. Bolotskaya
Mariia V. Verbovaia
spellingShingle Marina V. Shestakova
Liubov L. Bolotskaya
Mariia V. Verbovaia
Results of the first Russian multicenter non-interventional study of Contour® TS glucometer
Consilium Medicum
non-interventional study
diabetes mellitus
insulin therapy
glucometer
glycaemic control
author_facet Marina V. Shestakova
Liubov L. Bolotskaya
Mariia V. Verbovaia
author_sort Marina V. Shestakova
title Results of the first Russian multicenter non-interventional study of Contour® TS glucometer
title_short Results of the first Russian multicenter non-interventional study of Contour® TS glucometer
title_full Results of the first Russian multicenter non-interventional study of Contour® TS glucometer
title_fullStr Results of the first Russian multicenter non-interventional study of Contour® TS glucometer
title_full_unstemmed Results of the first Russian multicenter non-interventional study of Contour® TS glucometer
title_sort results of the first russian multicenter non-interventional study of contour® ts glucometer
publisher ZAO "Consilium Medicum"
series Consilium Medicum
issn 2075-1753
2542-2170
publishDate 2019-04-01
description Aim. To evaluate fitness of Contour® TS glucometer (Contour® TS, Bayer/Ascensia*) – a system for blood glycemia level control, and its characteristics in everyday use for Russian patients with insulin dependent diabetes mellitus (DM) types 1 and 2 and endocrinologists. Study design. According to the inclusion criteria, 3759 patients were registered in the program, of which 3599 patients have completed the study as per 3 visits. The non-interventional study was conducted in 84 medical centers in RF during the period from October 2013 to June 2015. Age of insulin-dependent patients and patients on hypoglycaemic therapy was 18 years and older. Results. Observational program included – 1126 (31.29%) patients with type 1 diabetes mellitus and 2473 (68.71%) patients with type 2 diabetes mellitus. Following switch to Contour® TS, while insulin therapy regimens were maintained, it was noted that the rate of blood glucose measurement increased compared with Visit 1 (p<0.0001). Upon assessment of satisfaction with the device, virtually all questions were answered as “good” and “perfect” by more than 90% patients and 95% study doctors. Upon assessment of the quality of life by EQ-5D, increase of this parameter was noted in 6 months, at Visit 3 (p<0.0001). No glucometer-associated malfunction were registered during the study. Additional data from general clinical experience of each patient that allowed to establish significant reduction of the levels of glycosilated haemoglobin and pre-prandial blood glucose just in 3 months at Visit 2, significant reduction of reported hypoglycaemia episodes as calculated per one patient have been obtained during the study. Additional data on the prevalence of macro- and microvascular complications were obtained during the study, and the highest per cent was for non-proliferative retinopathy and nephropathy at the stage of albuminuria. The most common among concomitant diseases were arterial hypertension, dyslipidemia and coronary artery disease. Conclusion. Use of Contour® TS glucometer by the patients, while insulin therapy regimens were maintained, led to increase in the rate of blood glucose measurements by up to 4–6 times during the day and statistically significant improvement in blood glucose control.
topic non-interventional study
diabetes mellitus
insulin therapy
glucometer
glycaemic control
url http://consilium.orscience.ru/en/archive/2019/vol-21-4-2019/results-of-the-first-russian-multicenter-non-interventional-study-of-contour-ts-glucometer_5458/?element
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AT mariiavverbovaia resultsofthefirstrussianmulticenternoninterventionalstudyofcontourtsglucometer
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