Skip to main content

01.12.2018 | Research | Ausgabe 1/2018 Open Access

Critical Care 1/2018

Validation of carbon dioxide production (VCO2) as a tool to calculate resting energy expenditure (REE) in mechanically ventilated critically ill patients: a retrospective observational study

Critical Care > Ausgabe 1/2018
I. Kagan, O. Zusman, I. Bendavid, M. Theilla, J. Cohen, P. Singer


The use of indirect calorimetry (IC) to assess resting energy expenditure (REE) based on the measurement of oxygen consumption (VO 2) and carbon dioxide production (VCO 2) has been demonstrated in several studies and meta-analyses to be more accurate when compared with predictive equations [ 14]. Since its use remains limited (mainly for financial and technical reasons), the use of VCO 2 alone has recently been suggested as an alternative method to calculate REE in children as well as in adults in various settings [ 57]. This method is based on the Weir equation, where VO 2 is not measured but is derived as being equal to VCO 2/RQ, where RQ is the respiratory quotient which in turn is derived from VCO 2/VO 2 [ 8]. This is defined as the REE-VCO 2. However, the level of accuracy of REE-VCO 2 is uncertain, and a comparison between REE derived from the VCO 2 calculated from the calorimeter and REE derived from VO 2 and VCO 2 from the mechanical ventilator has shown significant differences [ 8]. The RQ value may vary according to substrate utilization and therefore the REE calculation may differ accordingly. The present study was conducted to compare the REE-VCO 2 compared with the REE derived from IC (REE-IC).


This retrospective observational study was performed at a 16-bed mixed medical-surgical intensive care department of a university-affiliated tertiary hospital. Data were derived from the database of a computerized information system (MetaVision ICU ®, iMDs oft, Tel Aviv, Israel). All patients from 2003 to 2015 who underwent IC measurements (Deltatrac II, Datex-Ohmeda, part of GE Healthcare, Madison, WI, USA) were included in this study. The calorimeter was calibrated with ethanol on a monthly basis and for test gases (ambient air and O 2 95% and CO 2 5%) before all measurements. Prior to testing, patients were required to be in stable condition for at least 30 min, ventilated with fraction of inspired oxygen (FiO 2) of less than 60%, and positive end-expiratory pressure (PEEP) of less than 10 cm H 2O without any discernable air leaks. Only stable measurements for at least 20 min were considered acceptable. Oxygen consumption and CO 2 production were measured, and the RQ and REE were calculated by using the Weir equation. The timing and number of IC measurement per patient were determined by the treating physician. All patients hospitalized between 2014 and 2017 who had an IC measurement and a simultaneous VCO 2 measurement obtained from the ventilator (Evita 4, Dräger, Lübeck, Germany) were included in the study. Demographic data noted included age, sex, weight, height, body mass index, and Sequential Organ Failure Assessment (SOFA) score. VO 2, VCO 2, REE, and RQ were obtained from the IC measurements [ 9]. In addition, VCO 2 was obtained from the ventilator over 6-h blocks and was used to calculate REE-VCO 2. RQ values were chosen arbitrarily as 0.8, 0.85, and 0.89 because these values are the most commonly used values to derive REE from VO 2 [ 10].
The study was approved by the institution’s review board, and informed consent was waived since the data were recorded retrospectively.
REE-IC and REE-VCO 2 were compared by using mean difference, standard deviation, percentage of error, percentage of difference, correlation, concordance, agreement with the equation 5.5 × VCO 2 × 1.44 (within 85% and 115% of measured REE), and tight agreement within 95% and 105% of measured REE). In addition, we used ridge regression, a form of penalized linear regression, to estimate REE from VCO 2 measurements derived from the ventilator. A Bland–Altman graph and a scatter plot were performed to study the precision of the method.


Eighty patients were included in the study, and 497 REE-IC measurements with a corresponding mean of the 6-h block VCO 2 were performed. The median number of measurements per patients was 3 (interquartile range of 2–7). Patients’ characteristics are presented in Table 1.
Table 1
Patient characteristics
N = 80
Standard deviation
53% male, 47% female
Age, years
SOFA score
Weight, kg
Height, m
Body mass index, kg/m 2
Enteral energy delivered, kcal/d
Parenteral energy delivered, kcal/d
Abbreviations: APACHE Acute Physiology and Chronic Health Evaluation; SOFA Sequential Organ Failure Assessment
The mean caloric intake from enteral sources was 1278 ± 654 kcal, whereas the mean caloric intake from parenteral sources was 333 ± 439 kcal. Mean protein intake was 68 g/day and comprised 18% of calories, and 38% of energy was derived from lipids and 44% from carbohydrates.
The mean REE-IC was 2059.5 ± 491.7 kcal/d, and the mean RQ was 0.75 ± 0.07. The mean 6-h block VCO 2 was 244.5 ± 85.9 mL/min. The mean REE-RQs corresponding to RQs of 0.80, 0.85, and 0.89 were 1936.8 ± 680.0, 2017.8 ± 708.8, and 2122.1 ± 745.4 kcal/d, respectively.
The VCO 2 performance is presented in Table  2. The mean RQ of all patients in the intensive care unit who had REE-IC measurements ( n = 3326) was 0.79 ± 0.11 (personal data). A Bland–Altman figure (Fig.  1) shows a wide variability but without a consistent bias suggesting that the measurement could widely under- or overestimate REE. A scatter plot (Fig.  2) confirms these findings.
Table 2
The VCO 2 performance
Mean difference
Standard deviation
% Error
% Difference
Agreement a
Tight agreement b
VCO 2 with 0.89 RQ c
− 122.78
0.51 (0.44–0.57)
0.37 (0.27–0.47)
VCO 2 with 0.85 RQ
0.51 (0.44–0.57)
0.37 (0.27–0.47)
VCO 2 with 0.80 RQ
0.51 (0.44–0.57)
0.37 (0.26–0.47)
VCO 2 with 0.75 RQ
aWithin 85% and 115% of measured REE
bWithin 95% and 105% of measured REE
cEquivalent to REE calculation of 5.5*VCO 2*1.44
Abbreviations: REE resting energy expenditure, RQ respiratory quotient, VCO 2 carbon dioxide production
REE-VCO 2 derived from an RQ of 0.85 had the lowest mean difference from REE-IC and the same percentage error, difference, correlation, and concordance with REE-VCO 2-RQ derived from RQs of 0.80 and 0.89. The agreement (between 85% and 115%) was slightly lower than for REE-RQ derived from 0.89 but better than REE-RQ derived from 0.80 with the same results as the tight agreement.
When we estimated REE using only VCO 2 measurements made by the calorimeter using penalized regression as described, VCO 2 was found to be significantly associated with REE-IC ( P <0.001, R 2 = 0.84). A simplified formula (i.e. REE = 135 +8*VCO 2) was then derived. Using this formula resulted in a difference of 52 kcal, standard deviation of 220 kcal, 9% percent error, 6% percent difference, 92% correlation, 72% concordance, 82% agreement, and 33% tight agreement. However, application of this formula to the 80 ventilated patients resulted in similar performance to predefined RQ (agreement of 0.43).


Our study shows a small mean difference in the REE derived from the REE-VCO 2 using the derived equation but with low agreement when compared with the gold-standard REE obtained by IC. In addition, we demonstrated the ability of VCO 2 to predict REE based on measurements by the calorimeter and specific regression with very high accuracy (agreement). This represents the “ceiling” of possibility of using VCO 2, but it remains unclear whether this applies to VCO 2 measurements made by the ventilator. Using VCO 2 to estimate energy expenditure is challenged by a medical hazard: the quite unpredicted error as compared with the gold standard. If mean (median) values presented may perhaps be acceptable, the larger scatter is not. Individual subjects may not have an inaccurate evaluation, as clearly shown in Figs.  1 and  2).
Stapel et al. [ 5] found that 10% and less than 15% accuracy rates of REE-VCO 2 were 61% and 79%, respectively. Less than 25% and less than 30% inaccuracy rates of REE-VCO 2 were 2% and 0%, respectively. There results were superior to those derived from predictive equations. The differences between their results and those we have shown may be explained by methodological details. First, the VCO 2 measurements in the study by Stapel et al. were obtained as a mean of 24 h and not from a block of 6 h as in our study. In our study, VCO 2 measurements were obtained as a mean of 6 h and compared with a measurement of 20 min using the Deltatrac II instrument. Second, we used a different ventilator (Dräger) from that used in the study by Stapel et al. (Maquet, Rastatt, Germany), and since our study was retrospective, there was no calibration before each measurement. Finally, we did not use an RQ according to nutritional intake but rather three values representing common clinical states, including the RQ of 0.86 used in the study by Stapel et al., which is the most frequent RQ resulting from nutrition. The use of RQ according to nutrition intake has been applied by others in children [ 6]. Mehta et al. used an RQ defined by macronutrient administration defined as VCO 2RQmacro (kcal/day) = [3.941(VCO 2/RQmacro) + 1.106(VCO 2)] × 1440. VCO 2-REE was obtained using an RQ of 0.9 using the equation: REE = [3.941 (VCO 2/0.89) + 1.106(VCO 2)] × 1440 = [4.428(VCO 2) + 1.106(VCO 2)] × 1440 = 5.534(VCO 2) × 1440. The authors described a mean bias (limits) for agreement between measured REE and REE-VCO 2 or VCO 2-RQmacro of −0.6 (−14.4 to 13.1) and −2.0 (−42.9 to 38.8), respectively, using REE-VCO 2 in comparison with REE-IC. When patients were classified as hypometabolic or hypermetabolic according to REE-IC divided by the Schoeffield equation, the accuracy, sensitivity, and specificity were 0.86, 1.00, and 0.83 and 0.82, 0.62, and 1.00, respectively. The conclusions of the authors were in favor of using an RQ of 0.89 (the mean of the measurements in their study) and evaluating REE from VCO 2 alone as being an acceptable method. Others [ 7] compared REE-IC obtained by a GE module giving continuous VO 2, VCO 2, and REE to an REE-VCO 2 obtained by VCO 2 and a fixed RQ of 0.85. In most patients (89%), accuracy (± 10%) was obtained. However, the authors noted the problems linked to variations in minute volume limiting the validity of the measurements. These variations have been described previously [ 11], and a stable ventilation setting has been a condition to validate REE measurements. Finally, Oshima et al. [ 8] used another methodology to compare REE-IC with REE-VCO 2. All measurements (VO 2, VCO 2, and REE) were obtained from IC measurements and not from the ventilator. They compared REE-IC with REE-VCO 2 obtained using an RQ of 0.85 or RQ related to nutritional intake. Mean biases (lower, upper 95% confidence intervals) for REE-VCO 2_0.85 and REE-VCO 2_FQ (derived from Food Quotient) were −21 kcal/d (−41, 1) and −48 kcal/d (−67, −28), respectively. The limits of agreement in Bland–Altman plots were (+314, −356) and (+272, −367), respectively. The 5% accuracy rates compared with REE-IC were 46.0% and 46.4%, and 10% accuracy rates were 77.7% and 77.3%, respectively. The authors confirmed the finding from McClave et al. [ 12] that RQ is neither a reliable indicator of the feeding status nor strongly associated with non-nutritional factors such as mode of ventilation and acid-base disturbances. RQ based on VCO 2 cannot be as accurate for REE evaluation when compared with VO 2-based equations. The authors concluded that REE-VCO 2 was not accurate enough to be considered an alternative to IC. Using the same methodology, Mouzaki et al. [ 12] also evaluated REE-VCO 2 compared with REE-IC in a cardiac pediatric population and reached results similar to those of Oshima et al. Wide limits of agreement and a high percentage error suggested that the REE derived from VCO 2 was inaccurate only when compared with the gold standard. These findings were explained by a large RQ distribution.
Our study has several limitations. It is retrospective and did not take into account sedation, ventilator types, and settings but used a VCO 2 measurement over the 6 h preceding the assessment. The RQ examined used predefined common values and was not obtained according to nutritional intake. Although the sample size was comparable to that of other studies, it was small and single-centered. Finally, there is a limitation in the reliability of some calorimeters when compared with Deltatrac II. Sundström et al. [ 13] found higher limits of agreement when comparing Deltatrac II with the Quark device than Stapel et al. found between Datex and the VCO 2 respirator-derived approach. Graf et al. [ 14] confirmed these increased limits of agreement when comparing Quark and the CCM device with Deltatrac II. The reliability of the reference calorimetry therefore should be ensured.


In this retrospective study, we did not find tight agreement between REE-IC and REE-VCO 2 using various RQ values. Thus, for defining the appropriate calorie target in critically ill patients, IC remains the best tool. In recent years, great efforts have been made to develop easier-to-use and more accurate IC devices at lower costs, reflecting the clinicians’ needs. Some of them stand alone and some are integrated in monitors or ventilators. All of these new devices require careful evaluation and validation but will allow a more accurate evaluation of the energy expenditure of critically ill patients. Where IC is not possible, REE derived from VCO 2 obtained from the ventilator may be the best alternative. However, it must be stressed that using VCO 2 from the ventilator and an arbitrary RQ to derive REE remains less accurate than IC.

Ethics approval and consent to participate


Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://​creativecommons.​org/​licenses/​by/​4.​0/​), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://​creativecommons.​org/​publicdomain/​zero/​1.​0/​) applies to the data made available in this article, unless otherwise stated.
Über diesen Artikel

Weitere Artikel der Ausgabe 1/2018

Critical Care 1/2018 Zur Ausgabe

Neu im Fachgebiet AINS

Mail Icon II Newsletter

Bestellen Sie unseren kostenlosen Newsletter Update AINS und bleiben Sie gut informiert – ganz bequem per eMail.