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Results of glycated hemoglobin during treatment with insulin analogues dispensed in the public health system of Federal District in Brazil

BACKGROUND: Diabetes treatment requires specialized multi-professional teams, supplies for blood glucose monitoring and training for self-injections of human insulin or insulin analogues. The State Health Secretariat of the Federal District (SHS-FD) has dispensed insulin analogues by means of clinic...

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Autores principales: Leite, Eliziane Brandão, Pedrosa, Hermelinda Cordeiro, Casulari, Luiz Augusto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4539715/
https://www.ncbi.nlm.nih.gov/pubmed/26288660
http://dx.doi.org/10.1186/s13098-015-0061-0
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author Leite, Eliziane Brandão
Pedrosa, Hermelinda Cordeiro
Casulari, Luiz Augusto
author_facet Leite, Eliziane Brandão
Pedrosa, Hermelinda Cordeiro
Casulari, Luiz Augusto
author_sort Leite, Eliziane Brandão
collection PubMed
description BACKGROUND: Diabetes treatment requires specialized multi-professional teams, supplies for blood glucose monitoring and training for self-injections of human insulin or insulin analogues. The State Health Secretariat of the Federal District (SHS-FD) has dispensed insulin analogues by means of clinical validated protocols since 2004. However, data on outcomes of follow-up are still unknown. OBJECTIVE: To evaluate the results of glycated hemoglobin (HbA1c) among diabetic patients treated with insulin analogues. METHODS: It is a retrospective cohort study involving data of type 1(DM1) and type 2 diabetes (DM2) patients 18 years old and above who were registered to participate at the insulin analogues dispense program of the SHS-FD. Evaluation of criteria of insulin treatment continuity was based on HbA1c values achieved in the follow-up period: in the target, <7 %, patients between 18 and 65 years old; <8 % for those above 65 years old; out of target, when values were superior these cut off points for both age groups; and minimum 0.5 % reduction of two HbA1c values during follow-up. RESULTS: Two hundred and fifteen formularies were analyzed: Type 2 patients (63.7 %) and female sex were the most prevalent (63.7 %), (p < 0.05). Mean age and SD were 41.5 ± 23.5 years among DM1 and 60.5 ± 28.5 in those with DM2. HbA1c in the target was found in 26 %, 48 % were out of target and 26 % achieved 0.5 % minimum reduction in HbA1c value (p < 0.05). The main clinical characteristics associated with HbA1c found to be in the target were older age (>65 years), more than three medical appointments in the follow-up and lower mean HbA1c in the patient selection for inclusion criteria in the dispense program (p < 0.05). CONCLUSION: The low number of patients using insulin analogues in the target group, considered to be in good control, implies the need to reevaluate both level of patients self-care knowledge and glucose monitoring prior their inclusion in the insulin analogue dispense program. Reinforcement and training of health professional teams in enrollment procedures should be on mandatory basis to avoid protocol failure or deviations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13098-015-0061-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-45397152015-08-19 Results of glycated hemoglobin during treatment with insulin analogues dispensed in the public health system of Federal District in Brazil Leite, Eliziane Brandão Pedrosa, Hermelinda Cordeiro Casulari, Luiz Augusto Diabetol Metab Syndr Research BACKGROUND: Diabetes treatment requires specialized multi-professional teams, supplies for blood glucose monitoring and training for self-injections of human insulin or insulin analogues. The State Health Secretariat of the Federal District (SHS-FD) has dispensed insulin analogues by means of clinical validated protocols since 2004. However, data on outcomes of follow-up are still unknown. OBJECTIVE: To evaluate the results of glycated hemoglobin (HbA1c) among diabetic patients treated with insulin analogues. METHODS: It is a retrospective cohort study involving data of type 1(DM1) and type 2 diabetes (DM2) patients 18 years old and above who were registered to participate at the insulin analogues dispense program of the SHS-FD. Evaluation of criteria of insulin treatment continuity was based on HbA1c values achieved in the follow-up period: in the target, <7 %, patients between 18 and 65 years old; <8 % for those above 65 years old; out of target, when values were superior these cut off points for both age groups; and minimum 0.5 % reduction of two HbA1c values during follow-up. RESULTS: Two hundred and fifteen formularies were analyzed: Type 2 patients (63.7 %) and female sex were the most prevalent (63.7 %), (p < 0.05). Mean age and SD were 41.5 ± 23.5 years among DM1 and 60.5 ± 28.5 in those with DM2. HbA1c in the target was found in 26 %, 48 % were out of target and 26 % achieved 0.5 % minimum reduction in HbA1c value (p < 0.05). The main clinical characteristics associated with HbA1c found to be in the target were older age (>65 years), more than three medical appointments in the follow-up and lower mean HbA1c in the patient selection for inclusion criteria in the dispense program (p < 0.05). CONCLUSION: The low number of patients using insulin analogues in the target group, considered to be in good control, implies the need to reevaluate both level of patients self-care knowledge and glucose monitoring prior their inclusion in the insulin analogue dispense program. Reinforcement and training of health professional teams in enrollment procedures should be on mandatory basis to avoid protocol failure or deviations. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13098-015-0061-0) contains supplementary material, which is available to authorized users. BioMed Central 2015-08-18 /pmc/articles/PMC4539715/ /pubmed/26288660 http://dx.doi.org/10.1186/s13098-015-0061-0 Text en © Leite et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Leite, Eliziane Brandão
Pedrosa, Hermelinda Cordeiro
Casulari, Luiz Augusto
Results of glycated hemoglobin during treatment with insulin analogues dispensed in the public health system of Federal District in Brazil
title Results of glycated hemoglobin during treatment with insulin analogues dispensed in the public health system of Federal District in Brazil
title_full Results of glycated hemoglobin during treatment with insulin analogues dispensed in the public health system of Federal District in Brazil
title_fullStr Results of glycated hemoglobin during treatment with insulin analogues dispensed in the public health system of Federal District in Brazil
title_full_unstemmed Results of glycated hemoglobin during treatment with insulin analogues dispensed in the public health system of Federal District in Brazil
title_short Results of glycated hemoglobin during treatment with insulin analogues dispensed in the public health system of Federal District in Brazil
title_sort results of glycated hemoglobin during treatment with insulin analogues dispensed in the public health system of federal district in brazil
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4539715/
https://www.ncbi.nlm.nih.gov/pubmed/26288660
http://dx.doi.org/10.1186/s13098-015-0061-0
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