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Critical Care

Open Access

Preliminary ICU experience of a novel intravascular blood glucose sensor

  • KP Mulavisala1,
  • PB Gopal2,
  • B Crane3 and
  • A Mackenzie3
Critical Care201216(Suppl 1):P175

Published: 20 March 2012


Glycaemic ControlBlood Glucose MonitoringHypoglycaemic EpisodeGlucose VariabilityTight Glycaemic Control


A need for continuous blood glucose monitoring has always been expressed by critical care practitioners. The results from several iterations of a novel optical fluorescence-based intravascular blood glucose sensor were examined for correlation with an accepted laboratory assay. Ever since Van Den Berghe's group demonstrated reductions in hospital mortality and morbidity from the application of tight glycaemic control [1], many groups have attempted to replicate those results with limited success. Practitioners have speculated upon the reasons behind this observation, and have cited manpower implications and incidence of hypoglycaemic episodes as contributing factors [2]. Investigators have speculated that a continuous blood glucose sensor might contribute towards safe effective glycaemic control [3].


A series of postoperative and direct admission ICU patients had an optical fluorescence-based intravascular glucose sensor (GlySure Ltd, Abingdon, UK) placed into the left internal jugular vein on admission to the ICU. The sensor remained in situ throughout the ICU stay. Periodic blood samples and simultaneous real-time values of blood glucose measured by the sensor were recorded. The results were correlated with the results of blood sample analysed by a Yellow Springs Instrument glucose analyser. The sensor, which has a heparin coating on its surface, required no further heparinisation; a 'keep vein open' rate of normal saline infusion was maintained throughout the period of operation.


Sixteen patients received the current configuration blood glucose sensor; during their combined length of stay, 296 paired values were obtained for correlation purposes. A total 99.6% of these values fall within the A+B areas of the Clarke error grid. All sensors continued to function throughout the length of stay, maximum 92 hours, and were withdrawn immediately prior to discharge from the ICU.


The pre-production intravascular blood glucose sensors successfully track blood glucose values, with improved insight into blood glucose variability in ICU patients.

Authors’ Affiliations

Axon Anaesthesia Associates Care Hospital Nampally, India
Apollo Hospitals, India
Glysure, UK


  1. Van den Berghe G, et al.: Intensive insulin therapy in critically ill patients. N Engl J Med 2001, 345: 1359-1367. 10.1056/NEJMoa011300View ArticlePubMedGoogle Scholar
  2. Aragon D, et al.: Evaluation of nurse work effort and perception about blood glucose testing in TGC. Am J Crit Care 2006, 15: 370-377.PubMedGoogle Scholar
  3. Krinsley J, Preiser JC: Moving beyond TGC to safe effective glycemic control (SEGC). Crit Care 2008, 12: 149. 10.1186/cc6889PubMed CentralView ArticlePubMedGoogle Scholar


© Mulavisala et al.; licensee BioMed Central Ltd. 2012

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.