A review of standards and statistics used to describe blood glucose monitor performance.

J Diabetes Sci Technol

Krouwer Consulting, Sherborn, Massachusetts 01770, USA.

Published: January 2010

AI Article Synopsis

  • The review discusses glucose performance by considering total error, which encompasses various sources of error beyond just analytical errors.
  • Many standards allow for up to 5% of glucose test results to be medically unacceptable, raising concerns about patient safety and the adequacy of current regulatory standards.
  • The article suggests that existing evaluation methods for glucose meters may underestimate errors, highlighting the need for improved clinical standards and more effective protocols to ensure accurate glucose monitoring.

Article Abstract

Glucose performance is reviewed in the context of total error, which includes error from all sources, not just analytical. Many standards require less than 100% of results to be within specific tolerance limits. Analytical error represents the difference between tested glucose and reference method glucose. Medical errors include analytical errors whose magnitude is great enough to likely result in patient harm. The 95% requirements of International Organization for Standardization 15197 and others make little sense, as up to 5% of results can be medically unacceptable. The current American Diabetes Association standard lacks a specification for user error. Error grids can meaningfully specify allowable glucose error. Infrequently, glucose meters do not provide a glucose result; such an occurrence can be devastating when associated with a life-threatening event. Nonreporting failures are ignored by standards. Estimates of analytical error can be classified into the four following categories: imprecision, random patient interferences, protocol-independent bias, and protocol-dependent bias. Methods to estimate total error are parametric, nonparametric, modeling, or direct. The Westgard method underestimates total error by failing to account for random patient interferences. Lawton's method is a more complete model. Bland-Altman, mountain plots, and error grids are direct methods and are easier to use as they do not require modeling. Three types of protocols can be used to estimate glucose errors: method comparison, special studies and risk management, and monitoring performance of meters in the field. Current standards for glucose meter performance are inadequate. The level of performance required in regulatory standards should be based on clinical needs but can only deal with currently achievable performance. Clinical standards state what is needed, whether it can be achieved or not. Rational regulatory decisions about glucose monitors should be based on robust statistical analyses of performance.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2825627PMC
http://dx.doi.org/10.1177/193229681000400110DOI Listing

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