Literature DB >> 12663586

Accuracy of an electrochemical sensor for measuring capillary blood ketones by fingerstick samples during metabolic deterioration after continuous subcutaneous insulin infusion interruption in type 1 diabetic patients.

Bruno Guerci1, Muriel Benichou, Michèle Floriot, Philip Bohme, Sebastien Fougnot, Patricia Franck, Pierre Drouin.   

Abstract

OBJECTIVE: This study was designed to test the accuracy of capillary ketonemia for diagnosis of ketosis after interruption of insulin infusion. RESEARCH DESIGN AND METHODS: A total of 18 patients with type 1 diabetes treated by external pump were studied during pump stop for 5 h. Plasma and capillary ketonemia and ketonuria were determined every hour from 7:00 A.M. (time 0 min = T0) to 12:00 P.M. (time 300 min = T300). Plasma beta-hydroxybutyrate (beta-OHB) levels were measured by an enzymatic end point spectrophotometric method, and capillary beta-OHB levels were measured by an electrochemical method (MediSense Optium meter). Ketonuria was measured by a semiquantitative test (Ketodiastix). Positive ketosis was defined by a value of >/=0.5 mmol/l for ketonemia and >/=4 mmol/l (moderate) for ketonuria.
RESULTS: After stopping the pump, concentrations of beta-OHB in both plasma and capillary blood increased significantly at time 60 min (T60) compared with T0 (P < 0.001), reaching maximum levels at T300 (1.30 +/- 0.49 and 1.23 +/- 0.78 mmol/l, respectively). Plasma and capillary beta-OHB values were highly correlated (r = 0.94, P < 0.0001). For diagnosis of ketosis, capillary ketonemia has a higher sensitivity and negative predictive value (80.4 and 82.5%, respectively) than ketonuria (63 and 71.8%, respectively). For plasma glucose levels >/=250 mg/dl, plasma and capillary ketonemia were found to be more frequently positive (85 and 78%, respectively) than ketonuria (59%) (P = 0.017). The time delay to diagnosis of ketosis was significantly higher for ketonuria than for plasma ketonemia (212 +/- 67 vs. 140 +/- 54 min, P = 0.0023), whereas no difference was noted between plasma and capillary ketonemia.
CONCLUSIONS: The frequency of screening for ketosis and the efficiency of detection of ketosis definitely may be improved by the use of capillary blood ketone determination in clinical practice.

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Year:  2003        PMID: 12663586     DOI: 10.2337/diacare.26.4.1137

Source DB:  PubMed          Journal:  Diabetes Care        ISSN: 0149-5992            Impact factor:   19.112


  21 in total

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2.  Ketone production in children with type 1 diabetes, ages 4-14 years, with and without nocturnal insulin pump suspension.

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3.  Outpatient safety assessment of an in-home predictive low-glucose suspend system with type 1 diabetes subjects at elevated risk of nocturnal hypoglycemia.

Authors:  Bruce A Buckingham; Fraser Cameron; Peter Calhoun; David M Maahs; Darrell M Wilson; H Peter Chase; B Wayne Bequette; John Lum; Judy Sibayan; Roy W Beck; Craig Kollman
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4.  The Population Pharmacokinetics of D-β-hydroxybutyrate Following Administration of (R)-3-Hydroxybutyl (R)-3-Hydroxybutyrate.

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6.  Blood versus urine ketone monitoring in a pediatric cohort of patients with type 1 diabetes: a crossover study.

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Review 9.  Endocrine emergencies.

Authors:  M W Savage; P M Mah; A P Weetman; J Newell-Price
Journal:  Postgrad Med J       Date:  2004-09       Impact factor: 2.401

10.  Current concepts and controversies in prevention and treatment of diabetic ketoacidosis in children.

Authors:  Arleta Rewers
Journal:  Curr Diab Rep       Date:  2012-10       Impact factor: 4.810

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