AutoICD API

81637-1

Laboratory

Glucose meter to reference method correlation [Ratio] in Serum, Plasma or Blood by calculation

Definition

The glucose correlation is a charted value used to monitor the accuracy of glucose meter results as compared to reference method results for quality assurance purposes. According to draft guidance from the Food and Drug Administration in 2014, for point-of-care blood glucose meter devices used by healthcare providers, 99% of all values should be within 10% of the reference method for glucose concentrations > 70 mg/dL and within 7 mg/dL for glucose concentrations < 70 mg/dL.[http://www.fda.gov/downloads/medicaldevices/deviceregulationandguidance/guidancedocuments/ucm380325.pdf] For self-monitoring blood glucose meters used by patients, 95% of all results should be within 15% of the reference method result and 99% of all results should be within 20% of the reference method result across the entire claimed measuring range of the instrument. [http://www.fda.gov/downloads/medicaldevices/deviceregulationandguidance/guidancedocuments/ucm380327.pdf]

LOINC 6-Axis Classification

Component

Glucose meter to reference method correlation

Property

Ratio

Time Aspect

Pt

System

Ser/Plas/Bld

Scale Type

Qn

Method Type

Calculated

Details

Class

CHEM

Order/Observation

Both

Short Name

Glucose correlation SerPlBld Calc-Rto

Display Name

Glucose meter to reference method correlation Calc (S/P/Bld) [Ratio]

Related Names

BloodCalcCalculationChemistryGluGlucGlucose correlationGlucoseurMethMethod ofPlPlasBldPlasmaPlsmPoint in timeQNTQuanQuantQuantitativeRandomRatiosRtoSerPSerPlSerPlasSerPlBldSerumSerum or plasmaSerum, plasma or whole bloodSRWBWhole blood

Frequently Asked Questions

What is LOINC code 81637-1?

LOINC code 81637-1 identifies "Glucose meter to reference method correlation [Ratio] in Serum, Plasma or Blood by calculation". The glucose correlation is a charted value used to monitor the accuracy of glucose meter results as compared to reference method results for quality assurance purposes. According to draft guidance from the Food and Drug Administration in 2014, for point-of-care blood glucose meter devices used by healthcare providers, 99% of all values should be within 10% of the reference method for glucose concentrations > 70 mg/dL and within 7 mg/dL for glucose concentrations < 70 mg/dL.[http://www.fda.gov/downloads/medicaldevices/deviceregulationandguidance/guidancedocuments/ucm380325.pdf] For self-monitoring blood glucose meters used by patients, 95% of all results should be within 15% of the reference method result and 99% of all results should be within 20% of the reference method result across the entire claimed measuring range of the instrument. [http://www.fda.gov/downloads/medicaldevices/deviceregulationandguidance/guidancedocuments/ucm380327.pdf]

What does 81637-1 measure?

This code measures Glucose meter to reference method correlation in Ser/Plas/Bld. It belongs to the CHEM class in the LOINC classification.

What is LOINC?

LOINC (Logical Observation Identifiers Names and Codes) is a universal standard for identifying laboratory and clinical observations. It is maintained by the Regenstrief Institute and used worldwide for health data exchange.