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American Journal of Critical Care. 2009;18: 232-239 doi:10.4037/ajcc2009262
Copyright © 2009 by the American Association of Critical-Care Nurses.
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Precision-to-Tolerance Capability: An Important Consideration in Tight Glucose Control

By Catherine Prinzing, APRN, Sarah Rosenlund, RN, MHS, CCRN, Vicki Sukeena, MT(ASCP), CLS, (NCA), Cynthia Malinowski, RN, MSN, CCRN and Lowell C. Wise, RN, DNSc. Catherine Prinzing is a clinical nurse specialist for diabetes, Sarah Rosenlund is manager of the cardiovascular intensive care unit, Vicki Sukeena is the point-of-care testing coordinator, Cynthia Malinowski is a nurse educator in the cardiovascular intensive care unit, and Lowell C. Wise is a Six Sigma black belt at Trinity Health-Saint Alphonsus Regional Medical Center in Boise, Idaho.

Corresponding author: Lowell C. Wise, RN, DNSc, Six Sigma Department, Trinity Health-Saint Alphonsus Regional Medical Center, 1055 N Curtis Rd, Boise, Idaho 83706 (e-mail: lowewise{at}sarmc.org).

Objective To assess clinical implications of bias and variance of point-of-care glucometric measurements in cardiac surgery patients with wide variations in postoperative hematocrit.

Methods Point-of-care glucose measurements were compared with values from laboratory analysis of the same sample of whole blood obtained from cardiac patients early on postoperative days 1 and 2. Twenty nurses collected 89 arterial blood samples from 58 patients during a 4-month period. Bias was measured by using difference scores between paired measurements. Patients were grouped within 5% increments according to hematocrit, and analysis of variance was used to test for differences. Variation was analyzed by precision-to-tolerance analysis within 3 euglycemic tolerance ranges.

Results Laboratory glucose values were 62 to 224 mg/dL; point-of-care measures were 83 to 253 mg/dL. Bias was 10.85 mg/dL across all hematocrit groups. Pairs of laboratory and point-of-care glucose values differed significantly (t174 = 10.03; P < .001). Bias increased from –2.83 mg/dL for patients with hematocrits exceeding 39% to +16.71 mg/dL for patients with hematocrits between 20% and 24%. The standard deviation of difference scores was 11.59 mg/dL overall. The difference between 5% hematocrit groups was significant (F4 = 4.11; P = .004). Precision-to-tolerance capability ratios for specification limits of 70 to 300, 90 to 140, and 80 to 110 mg/dL were 0.30, 1.39, and 2.32, respectively.

Conclusions The direction of bias change between hematocrit groupings was the direction predicted in the manufacturer’s information. Precision-to-tolerance measures indicated that the point-of-care equipment was not suitable for testing glucose within the planned "tighter" glycemic standards.







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Copyright © 2009 by the American Association of Critical-Care Nurses.