International Consensus on Use of Continuous Glucose Monitoring
Measurement of glycated hemoglobin (HbA ) has been the traditional method for assessing glycemic control. However, it does not reflect intra- and interday glycemic excursions that may lead to acute events (such as hypoglycemia) or postprandial hyperglycemia, which have been linked to both microvascu...
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| Vydané v: | Diabetes care Ročník 40; číslo 12; s. 1631 |
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| Hlavní autori: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
| Médium: | Journal Article |
| Jazyk: | English |
| Vydavateľské údaje: |
United States
01.12.2017
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| Predmet: | |
| ISSN: | 1935-5548, 1935-5548 |
| On-line prístup: | Zistit podrobnosti o prístupe |
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| Abstract | Measurement of glycated hemoglobin (HbA
) has been the traditional method for assessing glycemic control. However, it does not reflect intra- and interday glycemic excursions that may lead to acute events (such as hypoglycemia) or postprandial hyperglycemia, which have been linked to both microvascular and macrovascular complications. Continuous glucose monitoring (CGM), either from real-time use (rtCGM) or intermittently viewed (iCGM), addresses many of the limitations inherent in HbA
testing and self-monitoring of blood glucose. Although both provide the means to move beyond the HbA
measurement as the sole marker of glycemic control, standardized metrics for analyzing CGM data are lacking. Moreover, clear criteria for matching people with diabetes to the most appropriate glucose monitoring methodologies, as well as standardized advice about how best to use the new information they provide, have yet to be established. In February 2017, the Advanced Technologies & Treatments for Diabetes (ATTD) Congress convened an international panel of physicians, researchers, and individuals with diabetes who are expert in CGM technologies to address these issues. This article summarizes the ATTD consensus recommendations and represents the current understanding of how CGM results can affect outcomes. |
|---|---|
| AbstractList | Measurement of glycated hemoglobin (HbA1c) has been the traditional method for assessing glycemic control. However, it does not reflect intra- and interday glycemic excursions that may lead to acute events (such as hypoglycemia) or postprandial hyperglycemia, which have been linked to both microvascular and macrovascular complications. Continuous glucose monitoring (CGM), either from real-time use (rtCGM) or intermittently viewed (iCGM), addresses many of the limitations inherent in HbA1c testing and self-monitoring of blood glucose. Although both provide the means to move beyond the HbA1c measurement as the sole marker of glycemic control, standardized metrics for analyzing CGM data are lacking. Moreover, clear criteria for matching people with diabetes to the most appropriate glucose monitoring methodologies, as well as standardized advice about how best to use the new information they provide, have yet to be established. In February 2017, the Advanced Technologies & Treatments for Diabetes (ATTD) Congress convened an international panel of physicians, researchers, and individuals with diabetes who are expert in CGM technologies to address these issues. This article summarizes the ATTD consensus recommendations and represents the current understanding of how CGM results can affect outcomes.Measurement of glycated hemoglobin (HbA1c) has been the traditional method for assessing glycemic control. However, it does not reflect intra- and interday glycemic excursions that may lead to acute events (such as hypoglycemia) or postprandial hyperglycemia, which have been linked to both microvascular and macrovascular complications. Continuous glucose monitoring (CGM), either from real-time use (rtCGM) or intermittently viewed (iCGM), addresses many of the limitations inherent in HbA1c testing and self-monitoring of blood glucose. Although both provide the means to move beyond the HbA1c measurement as the sole marker of glycemic control, standardized metrics for analyzing CGM data are lacking. Moreover, clear criteria for matching people with diabetes to the most appropriate glucose monitoring methodologies, as well as standardized advice about how best to use the new information they provide, have yet to be established. In February 2017, the Advanced Technologies & Treatments for Diabetes (ATTD) Congress convened an international panel of physicians, researchers, and individuals with diabetes who are expert in CGM technologies to address these issues. This article summarizes the ATTD consensus recommendations and represents the current understanding of how CGM results can affect outcomes. Measurement of glycated hemoglobin (HbA ) has been the traditional method for assessing glycemic control. However, it does not reflect intra- and interday glycemic excursions that may lead to acute events (such as hypoglycemia) or postprandial hyperglycemia, which have been linked to both microvascular and macrovascular complications. Continuous glucose monitoring (CGM), either from real-time use (rtCGM) or intermittently viewed (iCGM), addresses many of the limitations inherent in HbA testing and self-monitoring of blood glucose. Although both provide the means to move beyond the HbA measurement as the sole marker of glycemic control, standardized metrics for analyzing CGM data are lacking. Moreover, clear criteria for matching people with diabetes to the most appropriate glucose monitoring methodologies, as well as standardized advice about how best to use the new information they provide, have yet to be established. In February 2017, the Advanced Technologies & Treatments for Diabetes (ATTD) Congress convened an international panel of physicians, researchers, and individuals with diabetes who are expert in CGM technologies to address these issues. This article summarizes the ATTD consensus recommendations and represents the current understanding of how CGM results can affect outcomes. |
| Author | Nimri, Revital Doyle, 3rd, Francis J Hovorka, Roman Kowalski, Aaron Buckingham, Bruce Heller, Simon Cobelli, Claudio Beck, Roy Garg, Satish Kordonouri, Olga Kovatchev, Boris Phillip, Moshe Battelino, Tadej Maahs, David Renard, Eric Jia, Weiping Amiel, Stephanie A Hirsch, Irl Bergenstal, Richard M Tamborlane, William V Laffel, Lori Saboo, Banshi Murphy, Helen R Danne, Thomas Dassau, Eyal Parkin, Christopher G Close, Kelly L DeVries, J Hans Heinemann, Lutz Scharf, Mauro Jones, Tim Bosi, Emanuele Nørgaard, Kirsten Weinzimer, Stuart A |
| Author_xml | – sequence: 1 givenname: Thomas orcidid: 0000-0003-0773-6961 surname: Danne fullname: Danne, Thomas email: danne@hka.de organization: Diabetes Centre for Children and Adolescents, Children's and Youth Hospital "Auf Der Bult," Hannover, Germany danne@hka.de – sequence: 2 givenname: Revital surname: Nimri fullname: Nimri, Revital organization: The Myrtle and Henry Hirsch National Center for Childhood Diabetes, The Jesse and Sara Lea Shafer Institute of Endocrinology and Diabetes, Schneider Children's Medical Center of Israel, Petah Tikva, Israel – sequence: 3 givenname: Tadej orcidid: 0000-0002-0273-4732 surname: Battelino fullname: Battelino, Tadej organization: Department of Pediatric Endocrinology, Diabetes and Metabolic Diseases, University Children's Hospital, Ljubljana University Medical Centre, and Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia – sequence: 4 givenname: Richard M surname: Bergenstal fullname: Bergenstal, Richard M organization: International Diabetes Center at Park Nicollet, Minneapolis, MN – sequence: 5 givenname: Kelly L surname: Close fullname: Close, Kelly L organization: Close Concerns, San Francisco, CA – sequence: 6 givenname: J Hans orcidid: 0000-0001-9196-9906 surname: DeVries fullname: DeVries, J Hans organization: Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands – sequence: 7 givenname: Satish surname: Garg fullname: Garg, Satish organization: University of Colorado Denver and Barbara Davis Center for Diabetes, Aurora, CO – sequence: 8 givenname: Lutz surname: Heinemann fullname: Heinemann, Lutz organization: Science & Co, Düsseldorf, Germany – sequence: 9 givenname: Irl surname: Hirsch fullname: Hirsch, Irl organization: Division of Metabolism, Endocrinology, and Nutrition, Department of Medicine, University of Washington School of Medicine, Seattle, WA – sequence: 10 givenname: Stephanie A surname: Amiel fullname: Amiel, Stephanie A organization: Diabetes Research Group, King's College London, London, U.K – sequence: 11 givenname: Roy orcidid: 0000-0002-5194-8446 surname: Beck fullname: Beck, Roy organization: Jaeb Center for Health Research, Tampa, FL – sequence: 12 givenname: Emanuele surname: Bosi fullname: Bosi, Emanuele organization: Diabetes Research Institute, University "Vita-Salute" San Raffaele, Milan, Italy – sequence: 13 givenname: Bruce surname: Buckingham fullname: Buckingham, Bruce organization: Division of Endocrinology and Diabetes, Department of Pediatrics, Stanford University Medical Center, Stanford, CA – sequence: 14 givenname: Claudio orcidid: 0000-0002-0169-6682 surname: Cobelli fullname: Cobelli, Claudio organization: Department of Information Engineering, University of Padova, Padova, Italy – sequence: 15 givenname: Eyal orcidid: 0000-0001-5333-6892 surname: Dassau fullname: Dassau, Eyal organization: John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA – sequence: 16 givenname: Francis J orcidid: 0000-0002-3293-9114 surname: Doyle, 3rd fullname: Doyle, 3rd, Francis J organization: John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, MA – sequence: 17 givenname: Simon orcidid: 0000-0002-2425-9565 surname: Heller fullname: Heller, Simon organization: Academic Unit of Diabetes, Endocrinology & Metabolism, The University of Sheffield, Sheffield, U.K – sequence: 18 givenname: Roman surname: Hovorka fullname: Hovorka, Roman organization: Wellcome Trust-MRC Institute of Metabolic Science and Department of Paediatrics, University of Cambridge, Cambridge, U.K – sequence: 19 givenname: Weiping surname: Jia fullname: Jia, Weiping organization: Department of Endocrinology and Metabolism, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai Diabetes Institute, Shanghai Key Laboratory of Diabetes Mellitus, Shanghai Clinical Center of Diabetes, Shanghai, China – sequence: 20 givenname: Tim orcidid: 0000-0002-7989-1998 surname: Jones fullname: Jones, Tim organization: Telethon Kids Institute and School of Paediatrics and Child Health, The University of Western Australia, and Department of Endocrinology and Diabetes, Princess Margaret Hospital for Children, Perth, Australia – sequence: 21 givenname: Olga surname: Kordonouri fullname: Kordonouri, Olga organization: Diabetes Centre for Children and Adolescents, Children's and Youth Hospital "Auf Der Bult," Hannover, Germany – sequence: 22 givenname: Boris surname: Kovatchev fullname: Kovatchev, Boris organization: Center for Diabetes Technology, University of Virginia School of Medicine, Charlottesville, VA – sequence: 23 givenname: Aaron orcidid: 0000-0002-0979-5343 surname: Kowalski fullname: Kowalski, Aaron organization: JDRF, New York, NY – sequence: 24 givenname: Lori orcidid: 0000-0002-9675-3001 surname: Laffel fullname: Laffel, Lori organization: Pediatric, Adolescent and Young Adult Section and Section on Clinical, Behavioral and Outcomes Research, Joslin Diabetes Center, Harvard Medical School, Boston, MA – sequence: 25 givenname: David surname: Maahs fullname: Maahs, David organization: Division of Endocrinology and Diabetes, Department of Pediatrics, Stanford University Medical Center, Stanford, CA – sequence: 26 givenname: Helen R surname: Murphy fullname: Murphy, Helen R organization: Norwich Medical School, University of East Anglia, Norwich, U.K – sequence: 27 givenname: Kirsten surname: Nørgaard fullname: Nørgaard, Kirsten organization: Department of Endocrinology, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark – sequence: 28 givenname: Christopher G orcidid: 0000-0001-6838-5355 surname: Parkin fullname: Parkin, Christopher G organization: CGParkin Communications, Boulder City, NV – sequence: 29 givenname: Eric surname: Renard fullname: Renard, Eric organization: Department of Endocrinology, Diabetes, and Nutrition, Montpellier University Hospital, and Institute of Functional Genomics, University of Montpellier, and INSERM Clinical Investigation Centre, Montpellier, France – sequence: 30 givenname: Banshi surname: Saboo fullname: Saboo, Banshi organization: DiaCare, Ahmedabad, Gujarat, India – sequence: 31 givenname: Mauro surname: Scharf fullname: Scharf, Mauro organization: Centro de Diabetes Curitiba and Division of Pediatric Endocrinology, Hospital Nossa Senhora das Graças, Curitiba, Brazil – sequence: 32 givenname: William V surname: Tamborlane fullname: Tamborlane, William V organization: Department of Pediatrics, Yale School of Medicine, New Haven, CT – sequence: 33 givenname: Stuart A surname: Weinzimer fullname: Weinzimer, Stuart A organization: Department of Pediatrics, Yale School of Medicine, New Haven, CT – sequence: 34 givenname: Moshe surname: Phillip fullname: Phillip, Moshe organization: The Myrtle and Henry Hirsch National Center for Childhood Diabetes, The Jesse and Sara Lea Shafer Institute of Endocrinology and Diabetes, Schneider Children's Medical Center of Israel, Petah Tikva, Israel |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29162583$$D View this record in MEDLINE/PubMed |
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| Snippet | Measurement of glycated hemoglobin (HbA
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| Title | International Consensus on Use of Continuous Glucose Monitoring |
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