Measuring and reporting glycemic control in clinical trials: building a path to consensus

Clinical trials over time have used a variety of approaches for both measuring tight glycemic control and reporting results. The review by Finfer and colleagues in this issue of Critical Care is a step toward consensus within the research community to standardize the way blood glucose is measured and reported in clinical trials. The authors propose using specific measures of central tendency and dispersion for reporting glucose, advocate the use of blood gas analyzers and elimination of point-of-care glucose monitors in the intensive care unit, and comment on performance of continuous glucose monitors. As we await the release of updated rules from the International Standards Organization and process the new rules from the Clinical Laboratory and Standards Institute to regulate glucose monitoring, these recommendations should trigger many more conversations within the field as we strive for uniformity. However, we need to be cautious in prematurely proposing and adopting standards of care that fail to account for newer technology and data in this rapidly growing area of research.

the fi eld, present a compelling case for uniformity in assessment and reporting of future trials.
Th e group discussed and made recommendations in fi ve areas: (a) measurement of intermittent blood glucose (BG) and characterization of those measurements, (b) performance standards for BG measurement devices, (c) use of continuous glucose monitoring (CGM), (d) assessment of CGM, and (e) performance of CGM. Although they cited much of the relevant published literature over the last several years, their task was daunting, particularly with new and improved BG measurement technology just recently brought to the inpatient setting [2]. Th e authors ultimately produced consensus recommen dations, which are excellent fi rst steps toward the laudable goal of uniform assessment and reporting.
In considering adoption of new standards, one has to take into account the quality and quantity of evidence that supports them as well as the structure of the formal analysis of the data. Finfer and colleagues put forth many resolutions to open questions. If adopted by clinical researchers, these standards would allow the signal to be noticed above the noise. However, some of the 'noise' that exists in the TGC literature represents reasonable variability in experimental approaches to performing and measuring TGC as well as in real-world implementation. For example, the authors acknowledge that protocols that increase BG sampling frequency as BG drops below a certain range will have a lower BG mean. However, the meeting consensus stipulates that the central tendency be reported as a median of patients' individual means, which does not mitigate the acknowledged bias.
When stipulating methods of measuring BG at the bedside in the ICU, the authors review performance of hospital meters from the prior generation of technology and rightly conclude that the meters are inadequate for ICU monitoring. But with a new generation of hospital BG meters on the market, new ICU evaluations are surely warranted [2]. Similarly, the cited International Standards Organization (ISO) and Clinical Laboratory and Standards Institute (CLSI) rules for BG meters are inappropriately generous for ICU use [3,4]; however, new rules have been developed by both organizations and are

Abstract
Clinical trials over time have used a variety of approaches for both measuring tight glycemic control and reporting results. The review by Finfer and colleagues in this issue of Critical Care is a step toward consensus within the research community to standardize the way blood glucose is measured and reported in clinical trials. The authors propose using specifi c measures of central tendency and dispersion for reporting glucose, advocate the use of blood gas analyzers and elimination of point-ofcare glucose monitors in the intensive care unit, and comment on performance of continuous glucose monitors. As we await the release of updated rules from the International Standards Organization and process the new rules from the Clinical Laboratory and Standards Institute to regulate glucose monitoring, these recommendations should trigger many more conversations within the fi eld as we strive for uniformity. However, we need to be cautious in prematurely proposing and adopting standards of care that fail to account for newer technology and data in this rapidly growing area of research.
currently being rolled out [5,6]. Although blood gas analyzers are widely accepted to have outstanding precision and accuracy, they are not present in every ICU. Stipulation in a consensus document that glucose meters are unacceptable on the basis of prior generations of devices might discourage investigators from conducting clinical trials. In fact, the largest adult and pediatric trials published to date used this prior generation of devices with relatively low rates of severe hypoglycemia (7% and 3%), although the pediatric trial also used a computerized algorithm augmented with CGM [7,8]. Th e authors make similarly strong statements about the use of CGM in TGC, concluding that there are insuffi cient data about perfor mance in the ICU.
Finfer and colleagues provide a fi rst attempt at addressing the major issues in the fi eld of conducting TGC in a clinical trial. Th e authors take a defi nitive position on a host of challenges facing TGC investigators, allowing the fi eld to move forward. Th e phrase 'the devil is in the details' was not coined to describe clinical research, but those of us engaged in its conception and design know that it may as well have been. In trying to pin down many of those details, the authors are to be congratulated. However, it behooves all of us in the fi eld to continue to advance and refi ne the conversation and to update our conclusions with the most recently available devices and data so that, ultimately, in both adult and pediatric critical care, we can discern which populations derive what benefi t when a well-defi ned therapy is applied to their care.

Competing interests
MA is a consultant to Roche Diagnostics (Basel, Switzerland) on their hospitalbased glucose meter and to Medtronic Diabetes (Northridge, CA, USA) on their hospital-based continuous glucose monitor. CS-R declares that she has no competing interests.