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The cost implications of continuous glucose monitoring in pregnant women with type 1 diabetes in 3 Canadian provinces: a posthoc cost analysis of the CONCEPTT trial

BACKGROUND: The Continuous Glucose Monitoring in Women with Type 1 Diabetes in Pregnancy Trial (CONCEPTT) found improved health outcomes for mothers and their infants among those randomized to self-monitoring of blood glucose (SMBG) with continuous glucose monitoring (CGM) compared with SMBG alone....

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Autores principales: Ahmed, Rashid J., Gafni, Amiram, Hutton, Eileen K., Hu, Zheng Jing, Sanchez, J. Johanna, Murphy, Helen R., Feig, Denice S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: CMA Joule Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8191590/
https://www.ncbi.nlm.nih.gov/pubmed/34088734
http://dx.doi.org/10.9778/cmajo.20200128
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author Ahmed, Rashid J.
Gafni, Amiram
Hutton, Eileen K.
Hu, Zheng Jing
Sanchez, J. Johanna
Murphy, Helen R.
Feig, Denice S.
author_facet Ahmed, Rashid J.
Gafni, Amiram
Hutton, Eileen K.
Hu, Zheng Jing
Sanchez, J. Johanna
Murphy, Helen R.
Feig, Denice S.
author_sort Ahmed, Rashid J.
collection PubMed
description BACKGROUND: The Continuous Glucose Monitoring in Women with Type 1 Diabetes in Pregnancy Trial (CONCEPTT) found improved health outcomes for mothers and their infants among those randomized to self-monitoring of blood glucose (SMBG) with continuous glucose monitoring (CGM) compared with SMBG alone. In this study, we evaluated whether CGM or standard SMBG was more or less costly from the perspective of a third-party payer. METHODS: We conducted a posthoc analysis of data from the CONCEPTT trial (Mar. 25, 2013, to Mar. 22, 2016). Health care resource data from 215 pregnant women, randomized to CGM or SMBG, were collected from 31 hospitals in 7 countries. We determined resource costs posthoc based on prices from hospitals in 3 Canadian provinces (Ontario, British Columbia, Alberta). The primary outcome was the difference between groups in the mean total cost of care for mother and infant dyads, paid by each government (i.e., the third-party payer) from randomization to hospital discharge (time horizon). The secondary outcome included CGM and SMBG costs not paid by governments (e.g., glucose monitoring devices and supplies). RESULTS: The mean total cost of care was lower in the CGM group compared with the SMBG group in each province (Ontario: $13 270.25 v. $18 465.21, difference in mean total cost [DMT] −$5194.96, 95% confidence interval [CI] −$9841 to −$1395; BC: $13 480.57 v. $18 762.17, DMT −$5281.60, 95% CI −$9964 to −$1382; Alberta: $13 294.39 v. $18 674.45, DMT −$5380.06, 95% CI −$10 216 to −$1490). There was no difference in the secondary outcome. INTERPRETATION: Government health care costs are lower when CGM is paid by the patient, driven by lower costs from reduced use of the neonatal intensive care unit in the CGM group; however, when governments pay for CGM equipment, there is no overall cost difference between CGM and SMBG. Governments should consider paying for CGM, as it results in improved maternal and neonatal outcomes with no added overall cost. TRIAL REGISTRATION: ClinicalTrials.gov, no. NCT01788527
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spelling pubmed-81915902021-06-11 The cost implications of continuous glucose monitoring in pregnant women with type 1 diabetes in 3 Canadian provinces: a posthoc cost analysis of the CONCEPTT trial Ahmed, Rashid J. Gafni, Amiram Hutton, Eileen K. Hu, Zheng Jing Sanchez, J. Johanna Murphy, Helen R. Feig, Denice S. CMAJ Open Research BACKGROUND: The Continuous Glucose Monitoring in Women with Type 1 Diabetes in Pregnancy Trial (CONCEPTT) found improved health outcomes for mothers and their infants among those randomized to self-monitoring of blood glucose (SMBG) with continuous glucose monitoring (CGM) compared with SMBG alone. In this study, we evaluated whether CGM or standard SMBG was more or less costly from the perspective of a third-party payer. METHODS: We conducted a posthoc analysis of data from the CONCEPTT trial (Mar. 25, 2013, to Mar. 22, 2016). Health care resource data from 215 pregnant women, randomized to CGM or SMBG, were collected from 31 hospitals in 7 countries. We determined resource costs posthoc based on prices from hospitals in 3 Canadian provinces (Ontario, British Columbia, Alberta). The primary outcome was the difference between groups in the mean total cost of care for mother and infant dyads, paid by each government (i.e., the third-party payer) from randomization to hospital discharge (time horizon). The secondary outcome included CGM and SMBG costs not paid by governments (e.g., glucose monitoring devices and supplies). RESULTS: The mean total cost of care was lower in the CGM group compared with the SMBG group in each province (Ontario: $13 270.25 v. $18 465.21, difference in mean total cost [DMT] −$5194.96, 95% confidence interval [CI] −$9841 to −$1395; BC: $13 480.57 v. $18 762.17, DMT −$5281.60, 95% CI −$9964 to −$1382; Alberta: $13 294.39 v. $18 674.45, DMT −$5380.06, 95% CI −$10 216 to −$1490). There was no difference in the secondary outcome. INTERPRETATION: Government health care costs are lower when CGM is paid by the patient, driven by lower costs from reduced use of the neonatal intensive care unit in the CGM group; however, when governments pay for CGM equipment, there is no overall cost difference between CGM and SMBG. Governments should consider paying for CGM, as it results in improved maternal and neonatal outcomes with no added overall cost. TRIAL REGISTRATION: ClinicalTrials.gov, no. NCT01788527 CMA Joule Inc. 2021-06-04 /pmc/articles/PMC8191590/ /pubmed/34088734 http://dx.doi.org/10.9778/cmajo.20200128 Text en © 2021 CMA Joule Inc. or its licensors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY-NC-ND 4.0) licence, which permits use, distribution and reproduction in any medium, provided that the original publication is properly cited, the use is noncommercial (i.e., research or educational use), and no modifications or adaptations are made. See: https://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Research
Ahmed, Rashid J.
Gafni, Amiram
Hutton, Eileen K.
Hu, Zheng Jing
Sanchez, J. Johanna
Murphy, Helen R.
Feig, Denice S.
The cost implications of continuous glucose monitoring in pregnant women with type 1 diabetes in 3 Canadian provinces: a posthoc cost analysis of the CONCEPTT trial
title The cost implications of continuous glucose monitoring in pregnant women with type 1 diabetes in 3 Canadian provinces: a posthoc cost analysis of the CONCEPTT trial
title_full The cost implications of continuous glucose monitoring in pregnant women with type 1 diabetes in 3 Canadian provinces: a posthoc cost analysis of the CONCEPTT trial
title_fullStr The cost implications of continuous glucose monitoring in pregnant women with type 1 diabetes in 3 Canadian provinces: a posthoc cost analysis of the CONCEPTT trial
title_full_unstemmed The cost implications of continuous glucose monitoring in pregnant women with type 1 diabetes in 3 Canadian provinces: a posthoc cost analysis of the CONCEPTT trial
title_short The cost implications of continuous glucose monitoring in pregnant women with type 1 diabetes in 3 Canadian provinces: a posthoc cost analysis of the CONCEPTT trial
title_sort cost implications of continuous glucose monitoring in pregnant women with type 1 diabetes in 3 canadian provinces: a posthoc cost analysis of the conceptt trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8191590/
https://www.ncbi.nlm.nih.gov/pubmed/34088734
http://dx.doi.org/10.9778/cmajo.20200128
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