A Pilot Study of the Continuous Glucose Monitoring System
A Pilot Study of the Continuous Glucose Monitoring System Clinical decisions and glycemic control after its use in pediatric type 1 diabetic subjects Francine R. Kaufman , MD , Leena C. Gibson , MA , Mary Halvorson , RN, MSN, CDE , Sue Carpenter , BA, RN, CDE , Lynda K. Fisher , MD and Pisit Pitukch...
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| Published in | Diabetes care Vol. 24; no. 12; pp. 2030 - 2034 |
|---|---|
| Main Authors | , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
American Diabetes Association
01.12.2001
|
| Online Access | Get full text |
| ISSN | 0149-5992 1935-5548 1935-5548 |
| DOI | 10.2337/diacare.24.12.2030 |
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| Abstract | A Pilot Study of the Continuous Glucose Monitoring System
Clinical decisions and glycemic control after its use in pediatric type 1 diabetic subjects
Francine R. Kaufman , MD ,
Leena C. Gibson , MA ,
Mary Halvorson , RN, MSN, CDE ,
Sue Carpenter , BA, RN, CDE ,
Lynda K. Fisher , MD and
Pisit Pitukcheewanont , MD
Division of Endocrinology and Metabolism, Childrens Hospital Los Angeles and the Department of Pediatrics, University of Southern
California School of Medicine, Los Angeles, California
Abstract
OBJECTIVE —To determine whether the continuous glucose monitoring system (CGMS) (MiniMed, Sylmar, CA) could be used to make clinical
decisions and whether it has an impact on glycemia in pediatric type 1 diabetic subjects.
RESEARCH DESIGN AND METHODS —Pediatric subjects were recruited if they had HbA 1c >8.0% with management problems ( n = 35) or episodes of severe or nocturnal hypoglycemia or hypoglycemia unawareness associated with HbA 1c ≤8.0% ( n = 12). A total of 47 patients with a mean HbA 1c value of 8.6 ± 1.6% (mean age 11.8 ± 4.6 years, youngest 2.7 years, and diabetes duration 5.5 ± 3.5 years) on three to four
insulin injections/day ( n = 24) or insulin pump therapy ( n = 23) were followed with the CGMS for a mean of 69.5 ± 28 h. Comparisons were made between the number of high (>150 mg/dl)
and low (<70 mg/dl) glucose patterns discerned with the sensor or the logbook, and HbA 1c levels were evaluated.
RESULTS —In patients on injection therapy, 30 high or low glucose patterns were discerned with the logbook records and 120 patterns
with the CGMS. Specific alterations of the diabetes regimen were made. An overall significant change in HbA 1c , from 3 months before wearing the sensor to 6 months after (analysis of variance 0.04), was found in the subjects. Post hoc
analysis showed a significant change in HbA 1c from 8.6 ± 1.5% at baseline to 8.4 ± 1.3% at 3 months (paired Student’s t test 0.03).
CONCLUSIONS —The CGMS can be used by pediatric patients to detect abnormal patterns of glycemia. The information that was obtained could
be used to alter the diabetes regimen and impact glycemic outcome.
ANOVA, analysis of variance
CGMS, continuous glucose monitoring system
CSII, continuous subcutaneous insulin infusion
Footnotes
Address correspondence and reprint requests to Francine R. Kaufman, 4650 Sunset Blvd, MS #61, Los Angeles, CA 90027. E-mail:
fkaufman{at}chla.usc.edu .
Received for publication 27 December 2000 and accepted in revised form 17 August 2001.
F.R.C. has received consultantships from and served on advisory panels for Minimed, Integ, Novo Nordisk, Genentech, Medisense
Ketone, Inverness, Johnson & Johnson, Takeda Pharmaceuticals, Cygnus, Ortho McNeil, and Amylin; is a stockholder in MiniMed
and Clincal Products; has received grant/research support from Bristol Myers Squibb, Genentech, Pharmacia & Upjohn, Eli Lilly,
Novo Nordisk, Pfizer, MiniMed, and Takeda Pharmaceuticals; and is on the the speaker’s bureau for Eli Lilly, Novo Nordisk,
and MiniMed. M.H. is a stock shareholder in MiniMed and Inhale; has received honoraria for speaking engagements from MiniMed,
Novo Nordisk, Lilly, and Medisense; and has received grant/research support from MiniMed, Lilly, Starbright, and NovoNordisk.
S.C. is a stockholder in MiniMed.
A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances. |
|---|---|
| AbstractList | OBJECTIVE—To determine whether the continuous glucose monitoring system (CGMS) (MiniMed, Sylmar, CA) could be used to make clinical decisions and whether it has an impact on glycemia in pediatric type 1 diabetic subjects.
RESEARCH DESIGN AND METHODS—Pediatric subjects were recruited if they had HbA1c >8.0% with management problems (n = 35) or episodes of severe or nocturnal hypoglycemia or hypoglycemia unawareness associated with HbA1c ≤8.0% (n = 12). A total of 47 patients with a mean HbA1c value of 8.6 ± 1.6% (mean age 11.8 ± 4.6 years, youngest 2.7 years, and diabetes duration 5.5 ± 3.5 years) on three to four insulin injections/day (n = 24) or insulin pump therapy (n = 23) were followed with the CGMS for a mean of 69.5 ± 28 h. Comparisons were made between the number of high (>150 mg/dl) and low (<70 mg/dl) glucose patterns discerned with the sensor or the logbook, and HbA1c levels were evaluated.
RESULTS—In patients on injection therapy, 30 high or low glucose patterns were discerned with the logbook records and 120 patterns with the CGMS. Specific alterations of the diabetes regimen were made. An overall significant change in HbA1c, from 3 months before wearing the sensor to 6 months after (analysis of variance 0.04), was found in the subjects. Post hoc analysis showed a significant change in HbA1c from 8.6 ± 1.5% at baseline to 8.4 ± 1.3% at 3 months (paired Student’s t test 0.03).
CONCLUSIONS—The CGMS can be used by pediatric patients to detect abnormal patterns of glycemia. The information that was obtained could be used to alter the diabetes regimen and impact glycemic outcome. A Pilot Study of the Continuous Glucose Monitoring System Clinical decisions and glycemic control after its use in pediatric type 1 diabetic subjects Francine R. Kaufman , MD , Leena C. Gibson , MA , Mary Halvorson , RN, MSN, CDE , Sue Carpenter , BA, RN, CDE , Lynda K. Fisher , MD and Pisit Pitukcheewanont , MD Division of Endocrinology and Metabolism, Childrens Hospital Los Angeles and the Department of Pediatrics, University of Southern California School of Medicine, Los Angeles, California Abstract OBJECTIVE —To determine whether the continuous glucose monitoring system (CGMS) (MiniMed, Sylmar, CA) could be used to make clinical decisions and whether it has an impact on glycemia in pediatric type 1 diabetic subjects. RESEARCH DESIGN AND METHODS —Pediatric subjects were recruited if they had HbA 1c >8.0% with management problems ( n = 35) or episodes of severe or nocturnal hypoglycemia or hypoglycemia unawareness associated with HbA 1c ≤8.0% ( n = 12). A total of 47 patients with a mean HbA 1c value of 8.6 ± 1.6% (mean age 11.8 ± 4.6 years, youngest 2.7 years, and diabetes duration 5.5 ± 3.5 years) on three to four insulin injections/day ( n = 24) or insulin pump therapy ( n = 23) were followed with the CGMS for a mean of 69.5 ± 28 h. Comparisons were made between the number of high (>150 mg/dl) and low (<70 mg/dl) glucose patterns discerned with the sensor or the logbook, and HbA 1c levels were evaluated. RESULTS —In patients on injection therapy, 30 high or low glucose patterns were discerned with the logbook records and 120 patterns with the CGMS. Specific alterations of the diabetes regimen were made. An overall significant change in HbA 1c , from 3 months before wearing the sensor to 6 months after (analysis of variance 0.04), was found in the subjects. Post hoc analysis showed a significant change in HbA 1c from 8.6 ± 1.5% at baseline to 8.4 ± 1.3% at 3 months (paired Student’s t test 0.03). CONCLUSIONS —The CGMS can be used by pediatric patients to detect abnormal patterns of glycemia. The information that was obtained could be used to alter the diabetes regimen and impact glycemic outcome. ANOVA, analysis of variance CGMS, continuous glucose monitoring system CSII, continuous subcutaneous insulin infusion Footnotes Address correspondence and reprint requests to Francine R. Kaufman, 4650 Sunset Blvd, MS #61, Los Angeles, CA 90027. E-mail: fkaufman{at}chla.usc.edu . Received for publication 27 December 2000 and accepted in revised form 17 August 2001. F.R.C. has received consultantships from and served on advisory panels for Minimed, Integ, Novo Nordisk, Genentech, Medisense Ketone, Inverness, Johnson & Johnson, Takeda Pharmaceuticals, Cygnus, Ortho McNeil, and Amylin; is a stockholder in MiniMed and Clincal Products; has received grant/research support from Bristol Myers Squibb, Genentech, Pharmacia & Upjohn, Eli Lilly, Novo Nordisk, Pfizer, MiniMed, and Takeda Pharmaceuticals; and is on the the speaker’s bureau for Eli Lilly, Novo Nordisk, and MiniMed. M.H. is a stock shareholder in MiniMed and Inhale; has received honoraria for speaking engagements from MiniMed, Novo Nordisk, Lilly, and Medisense; and has received grant/research support from MiniMed, Lilly, Starbright, and NovoNordisk. S.C. is a stockholder in MiniMed. A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances. |
| Author | Sue Carpenter Lynda K. Fisher Mary Halvorson Leena C. Gibson Francine R. Kaufman Pisit Pitukcheewanont |
| Author_xml | – sequence: 1 givenname: Francine R. surname: Kaufman fullname: Kaufman, Francine R. organization: Division of Endocrinology and Metabolism, Childrens Hospital Los Angeles and the Department of Pediatrics, University of Southern California School of Medicine, Los Angeles, California – sequence: 2 givenname: Leena C. surname: Gibson fullname: Gibson, Leena C. organization: Division of Endocrinology and Metabolism, Childrens Hospital Los Angeles and the Department of Pediatrics, University of Southern California School of Medicine, Los Angeles, California – sequence: 3 givenname: Mary surname: Halvorson fullname: Halvorson, Mary organization: Division of Endocrinology and Metabolism, Childrens Hospital Los Angeles and the Department of Pediatrics, University of Southern California School of Medicine, Los Angeles, California – sequence: 4 givenname: Sue surname: Carpenter fullname: Carpenter, Sue organization: Division of Endocrinology and Metabolism, Childrens Hospital Los Angeles and the Department of Pediatrics, University of Southern California School of Medicine, Los Angeles, California – sequence: 5 givenname: Lynda K. surname: Fisher fullname: Fisher, Lynda K. organization: Division of Endocrinology and Metabolism, Childrens Hospital Los Angeles and the Department of Pediatrics, University of Southern California School of Medicine, Los Angeles, California – sequence: 6 givenname: Pisit surname: Pitukcheewanont fullname: Pitukcheewanont, Pisit organization: Division of Endocrinology and Metabolism, Childrens Hospital Los Angeles and the Department of Pediatrics, University of Southern California School of Medicine, Los Angeles, California |
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| References_xml | – ident: 2022031213233729200_R13 doi: 10.2337/diacare.23.9.1236 – ident: 2022031213233729200_R9 doi: 10.1016/S0168-8227(99)00113-8 – ident: 2022031213233729200_R6 doi: 10.1089/152091500316737 – ident: 2022031213233729200_R2 doi: 10.1002/(SICI)1520-7560(199909/10)15:5<338::AID-DMRR57>3.0.CO;2-Y – ident: 2022031213233729200_R14 – ident: 2022031213233729200_R4 – ident: 2022031213233729200_R5 doi: 10.1152/ajpendo.1999.277.3.E561 – ident: 2022031213233729200_R15 doi: 10.1016/S0022-3476(97)70197-5 – ident: 2022031213233729200_R8 – ident: 2022031213233729200_R7 – ident: 2022031213233729200_R10 doi: 10.1542/peds.107.2.222 – ident: 2022031213233729200_R16 doi: 10.1016/S0022-3476(97)70121-5 – ident: 2022031213233729200_R11 – ident: 2022031213233729200_R1 doi: 10.1542/pir.18.11.383 – ident: 2022031213233729200_R17 doi: 10.2337/diacare.16.3.40 – ident: 2022031213233729200_R12 doi: 10.2337/diacare.21.7.1146 – ident: 2022031213233729200_R3 doi: 10.2337/diacare.22.8.1252 |
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| Snippet | A Pilot Study of the Continuous Glucose Monitoring System
Clinical decisions and glycemic control after its use in pediatric type 1 diabetic subjects
Francine... OBJECTIVE—To determine whether the continuous glucose monitoring system (CGMS) (MiniMed, Sylmar, CA) could be used to make clinical decisions and whether it... |
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| StartPage | 2030 |
| Title | A Pilot Study of the Continuous Glucose Monitoring System |
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