Clinical Chemistry AACC Online Job Center
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Clinical Chemistry 39: 2329-2332, 1993;
This Article
Right arrow Full Text (PDF)
Right arrow Submit an electronic Letter to
the Editor about this paper
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Vadasdi, E.
Right arrow Articles by Jacobs, E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Vadasdi, E.
Right arrow Articles by Jacobs, E.

Clinical Chemistry, Vol 39, 2329-2332, Copyright © 1993 by American Association for Clinical Chemistry

HemoCue beta-glucose photometer evaluated for use in a neonatal intensive care unit

E Vadasdi and E Jacobs
Center for Clinical Laboratories, Mount Sinai Hospital, New York, NY.

We evaluated the HemoCue beta-Glucose Photometer system for use in our neonatal intensive care unit by assaying 178 heparinized whole-blood samples obtained by heel stick. The required sample size is 5 microL. Plasma glucose was analysed by a glucose oxidase/oxygen electrode methodology. Across the glucose range of 1.28-21.87 mmol/L, the regression slope was 0.976 (r = 0.976, Sy/x = 0.475). For samples with hematocrit < or = 0.30, the regression slope was 0.981 (r = 0.950, Sy/x = 0.415); for hematocrit of 0.31-0.49, the regression slope was 0.984 (r = 0.972, Sy/x = 0.508); and for hematocrit > or = 0.50, the regression slope was 0.959 (r = 0.988, Sy/x = 0.394). Human whole blood, bovine whole blood, and bovine serum-based quality-control materials were studied. Except for assays of the low-concentration human control material, the total CV was < 3.5%. The accuracy and precision of the HemoCue system were comparable with those of conventional laboratory instrumentation.


The following articles in journals at HighWire Press have cited this article:


Home page
Eur J EndocrinolHome page
A. D M Stork, H. Kemperman, D W. Erkelens, and T. F Veneman
Comparison of the accuracy of the hemocue glucose analyzer with the Yellow Springs Instrument glucose oxidase analyzer, particularly in hypoglycemia
Eur. J. Endocrinol., August 1, 2005; 153(2): 275 - 281.
[Abstract] [Full Text] [PDF]


Home page
Clin. Chem.Home page
P. L. M. Lynch and M. J. O'Kane
Methemoglobin Interferes with the HemoCue B-Glucose Analyzer
Clin. Chem., March 1, 2002; 48(3): 581 - 583.
[Full Text] [PDF]


Home page
Clin. Chem.Home page
J. M. Lorenz
Assessing fluid and electrolyte status in the newborn
Clin. Chem., January 1, 1997; 43(1): 205 - 210.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1993 by the American Association for Clinical Chemistry.