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This study was performed to assess the system accuracy of the blood glucose monitoring system SD GlucoNavii Mentor (SD Biosensor Inc, Korea). The study procedures were based on International Organization for Standardization 15197:2013, in that capillary blood samples from 100 participants’ fingertips were measured with three reagent system lots of the self-monitoring blood glucose system. Samples were collected for comparison measurements on a hexokinase-based glucose analyzer (Cobas Integra400 Plus, Roche Instrument Center, Switzerland). Glucose concentrations were distributed as required by International Organization for Standardization 15197. For each of the 100 evaluable samples, duplicate measurements were taken from three different reagent lots, for a total of 600 measurements. Overall, 98.3% (590/600) of individual measurement results (185/186, 99.5% for glucose values <100 mg/dl and 405/414, 97.8% for glucose values ≥100 mg/dl) were within ±15 mg/dl or ±15% of the corresponding comparison method results. All results (100%) fell into the consensus error grid zones A and B, indicating only clinically acceptable results. In conclusion, the blood glucose monitoring system SD GlucoNavii Mentor device fulfilled the system accuracy criteria of the International Organization for Standardization 15197, indicating measurement accuracy sufficient for diabetes therapy.
Measurement accuracy of blood glucose monitoring systems (BGMSs) is a relevant aspect in diabetes management. The International Organization for Standardization’s (ISO) 15197:2013 [
This study was performed to assess the system accuracy of the BGMS SD GlucoNavii Mentor (SD Biosensor Inc, Korea). According to the manufacturer, this BGMS is substantially equivalent to the BGMS Pic GlucoTest (PIKDARE S.p.A., Italy) and Pic GlucoTest Diary (PIKDARE), which has additional Bluetooth connectivity (data on file).
The study was conducted at the Institut für Diabetes-Technologie, Forschungs- und Entwicklungsgesellschaft mbH an der Universität Ulm, Ulm, Germany. Ethics approval was obtained from the Ethik-Kommission der Landesärztekammer Baden-Württemberg (MP-2012-009). In addition, the study was exempted from approval by the regulatory authority Bundesinstitut für Arzneimittel und Medizinprodukte (95.06 - 5661 - 7848).
Study procedures were based on ISO 15197:2013, in that capillary blood samples from at least 100 participants’ fingertips were measured with three reagent system lots of the self-monitoring blood glucose (SMBG) system. Samples were collected for comparison measurements on a hexokinase-based glucose analyzer (Cobas Integra400 Plus, Roche Instrument Center, Switzerland), which is traceable according to the requirements of ISO 17511 [
For data analysis, system accuracy criteria of ISO 15197 were applied: at least 95% of each individual reagent system lot’s results have to be found within ±15 mg/dl or ±15% of comparison method results (for glucose concentrations <100 mg/dl and ≥100 mg/dl, respectively), and at least 99% of all results have to fall into clinically acceptable consensus error grid zones A and B [
Overall, 98.3% (590/600) of individual measurement results (185/186, 99.5% for glucose values <100 mg/dl and 405/414, 97.8% for glucose values ≥100 mg/dl) were within ±15 mg/dl or ±15% of the corresponding comparison method results (
System accuracy results for the SD GlucoNavii Mentor.
| Glucose concentration range | Results within prespecified ranges of the comparison method results, n (%) | ||
|
|
±5 mg/dl or ±5%a | ±10 mg/dl or ±10%a | ±15 mg/dl or ±15%a |
| <100 mg/dl (n=186) | 109 (58.6) | 164 (88.2) | 185 (99.5) |
| ≥100 mg/dl (n=414) | 231 (55.8) | 363 (87.7) | 405 (97.8) |
| Overall (n=600) | 340 (56.7) | 527 (87.8) | 590 (98.3) |
aDifferences were assessed for comparison method glucose concentrations <100 mg/dl, and relative differences were assessed for comparison method glucose concentrations ≥100 mg/dl.
In conclusion, in this study, the investigated BGMS SD GlucoNavii Mentor device fulfilled the system accuracy criteria of ISO 15197, indicating measurement accuracy sufficient for diabetes therapy.
blood glucose monitoring system
International Organization for Standardization
self-monitoring blood glucose
The study was funded by SD Biosensor, Inc, Korea, and the medical writing was funded by PIKDARE S.p.A., Italy.
HH is an employee of SD Biosensor, Republic of Korea. LL is an employee of PIKDARE S.p.A., Italy. AN received research grants from PIKDARE S.p.A., Italy.