Continuous Glucose Monitoring in Patients Undergoing Extracorporeal Ventricular Assist Therapy

PLoS One. 2016 Mar 10;11(3):e0148778. doi: 10.1371/journal.pone.0148778. eCollection 2016.

Abstract

Background: Dysregulations of blood glucose (BG) are associated with adverse outcome in critical illness; controlling BG to target appears to improve outcome. Since BG-control is challenging in daily intensive care practice BG-control remains poor especially in patients with rapidly fluctuating BG. To improve BG-control and to avoid deleterious hypoglycemia, automated online-measurement tools are advocated. We thus evaluated the point-accuracy of the subcutaneous Sentrino® Continuous Glucose Monitoring System (CGM, Medtronic Diabetes, Northridge, California) in patients undergoing extracorporeal cardiac life support (ECLS) for cardiogenic shock.

Methods: Management of BG was performed according to institute's standard aiming at BG-levels between 100-145 mg/dl. CGM-values were recorded without taking measures into therapeutic account. Point-accuracy in comparison to intermittent BG-measurement by the ABL-blood-gas analyzer was determined.

Results: CGM (n = 25 patients) correlated significantly with ABL-values (r = 0.733, p<0.001). Mean error from standard was 15.0 mg/dl (11.9%). 44.2% of the readings were outside a 15% range around ABL-values. In one of 635 paired data-points, ABL revealed hypoglycemia (BG 32 mg/dl) whereas CGM did not show hypoglycemic values (132mg/dl).

Conclusions: CGM reveals minimally invasive BG-values in critically ill adults with dynamically impaired tissue perfusion. Because of potential deviations from standard, CGM-readings must be interpreted with caution in specific ICU-populations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Blood Glucose Self-Monitoring*
  • Demography
  • Female
  • Heart-Assist Devices*
  • Humans
  • Male
  • Middle Aged
  • Regression Analysis

Grants and funding

This work was supported from institutional and departmental sources and from Medtronic GmbH, Earl-Bakken-Platz 1, 40670 Meerbusch, Germany. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.