Open Access

Rest energy expenditure is decreased during the acute as compared to the recovery phase of sepsis in newborns

  • Rubens Feferbaum1Email author,
  • Cláudio Leone2,
  • Arnaldo AF Siqueira2,
  • Vitor E Valenti3, 4,
  • Paulo R Gallo2,
  • Alberto OA Reis2,
  • Ary C Lopes1,
  • Viviane G Nascimento,
  • Adriana G de Oliveira2,
  • Tatiana Dias de Carvalho3,
  • Rubens Wajnsztejn2, 4,
  • Claudia de Castro Selestrin2 and
  • Luiz Carlos de Abreu2, 4
Nutrition & Metabolism20107:63

https://doi.org/10.1186/1743-7075-7-63

Received: 9 March 2010

Accepted: 23 July 2010

Published: 23 July 2010

Abstract

Background

Little is known with respect to the metabolic response and the requirements of infected newborns. Moreover, the nutritional needs and particularly the energy metabolism of newborns with sepsis are controversial matter. In this investigation we aimed to evaluate the rest energy expenditure (REE) of newborns with bacterial sepsis during the acute and the recovery phases.

Methods

We studied nineteen neonates (27.3 ± 17.2 days old) with bacterial sepsis during the acute phase and recovery of their illness. REE was determined by indirect calorimetry and VO2 and VCO2 measured by gas chromatography.

Results

REE significantly increased from 49.4 ± 13.1 kcal/kg/day during the acute to 68.3 ± 10.9 kcal/kg/day during recovery phase of sepsis (P < 0.01). Similarly, VO2 (7.4 ± 1.9 vs 10 ± 1.5 ml/kg/min) and VCO2 (5.1 ± 1.7 vs 7.4 ± 1.5 ml/kg/min) were also increased during the course of the disease (P < 0.01).

Conclusion

REE was increased during recovery compared to the sepsis phase. REE of septic newborns should be calculated on individualized basis, bearing in mind their metabolic capabilities.

Introduction

As compared with birth the body weight doubles at five months of age and is three-fold greater at the end of the first year of life. Their length increases approximately 25-30 cm in the first year of life, which represents 75 to 85% of the length at birth. As a result of such a rapid growth the requirements of nutrients and energy are higher during the neonatal period (especially preterm) as compared to later in life [1]. The most frequent infections during the neonatal period not only contribute to enhance morbidity and mortality rates [2], but may also impact on the energy and nutrient requirements.

In the presence of severe infection, the metabolic response is characteristically elevated, and in adults energy metabolism is higher following septicemia. Significant changes in protein metabolism and severe proteolysis occurs in muscle and visceral protein. As a consequence of these changes protein re-synthesis of immune factors, such as antibodies and acute phase reactants which the C-reactive protein (CRP) are generated [3, 4].

Resting energy expenditure (REE) is the amount of energy expended while at rest in a neutrally temperate environment in the post-absorptive state. The release of energy in this state is sufficient only for vital organs. REE decreases with age and is directly proportional to lean body mass [58].

Albeit previous studies assessed the metabolism of adults with sepsis, little is known regarding the metabolic response in septic infants. In addition, conflicting data are available about the nutritional requirements and the energy metabolism of infants [9, 10]. Therefore, we aimed to evaluate REE in newborns with bacterial sepsis during the acute and the recovery phases of illness. We hypothesized that the newborn's metabolic demands are increased during recovery, when compared to the acute phase.

Materials and methods

Study Population

This study protocol was approved by the University of Sao Paulo Research Ethics Board and subjects were only enrolled following parental consent.

We studied 19 children admitted in the University of Sao Paulo Neonatal Intensive Care Unit with the diagnosis of a bacterial sepsis. The subjects' were 20 ± 17 days old, birth weight of 2966 ± 502 grams and a male:female ratio of 10:9. Except for one (gestational age 35 weeks), all infants were full term.

Inclusion Criteria

The following inclusion was utilized: 1) age up to 90 days old; 2) birth weight higher than 1500 g; 3) clinical evidence of bacterial sepsis defined according to positive blood culture and/or modified clinical laboratory criteria of Bone [11]. We considered the measurement of C-reactive protein (CRP) higher than 5 mg/liter as suggestive of infection [12]. Other laboratory tests such as cerebrospinal fluid changes suggesting bacterial meningitis [13], chest X-rays with the image of bronchopneumonia were also considered auxiliary criteria for the diagnosis of bacterial sepsis.

Exclusion Criteria

Infants were excluded if presenting with liver or respiratory failure. The latter was defined or mechanical ventilation.

Variables analysis

The infant's medical management was determined by their attending physicians. The infants were evaluated time-in two periods: sepsis and recovery phases. The sepsis phase was characterized by a positive blood culture. The recovery phase was characterized by the normalization of blood count, CRP and a negative blood culture. Laboratory exams were performed according to the following techniques:

Blood culture: collected in media for aerobic and anaerobic bacteria and plated on agar-blood;

Blood cell count: automated method for the laser hematology counter CELL-DYN 3000® that performs global and differential counts of platelets and formed elements with the confirmation of results for optical microscopy;

CRP: measured by nephelometric technique using reagents "High sensitive CRP" and "Reagent additional Oumu-15" brand in Behring® device Behring® Nephelometer 100;

Cerebrospinal fluid: according to the technique proposed by Spina-França, 1971.

Weight was measured daily throughout the hospitalization in an electronic scale accurate to 5 grams, with a capacity of 10 kg, calibrated before each measurement. We calculated Z scores based on weight and chronological age. In order to calculate it we used the ANTHRO 1.01 program of the Nutrition Division of the Center for Disease Control (CDC-USA) and Nutrition Unit/World Health Organization, December, 1990.

Newborns received only parenteral nutrition, which was based on glucose as an energy source, especially in preterm infants, a fact also noted previously [14]. Test measurements were evaluated at least 12 hours after feeding.

The gestational age was calculated by the last menstrual period reported by the mother (Naegele's rule) and when possible we used the somatic Capurro method [15]. The classification of newborns with respect to birth weight and gestational age was based on the Brazilian Ramos curve [16].

Determination of indirect calorimetry was performed in two stages of the child evolution, always by the same investigator:

On the acute phase of bacterial sepsis after hemodynamic stabilization which corresponds to the flow restoration level;

On recovery phase of bacterial sepsis, when the newborn was considered clinically and biochemically free of infection by the attending physician, with the registry of the weight gain and at least 10 days after the first testing.

Assessment of indirect calorimetry is part of the routine tests performed in our center for newborns with metabolic and/or severe nutritional disorders requiring nutritional support. Details of our method to measure REE in newborns have been previously published by Cardoso et al [17]. They used the same technique of indirect calorimetry measurement in our study and demonstrated that the REE in malnourished infants was approximately 58.3+/-10.9 kcal/kg on hospitalization. Validation studies have shown the technique to give results equivalent to direct measurements [16, 18]. The calorimeter used was developed by Hamamoto [19] and built from the incubator model C-86 of Fanem. Routine calibration was performed prior to each study using a 0.5 L syringe and primary standard calibration gases. Physical activity was assessed by the scale of Scopes and Ahmed [20], considering the scores 0 (sleep, eyes closed) and 1 (eyes open, physically still).

The volume of air in the system was measured geometrically (140 liters), and the air flow around the fan was 75 liters per minute. On the anterior portion of the calorimeter there was a system of three-way taps to collect gas which is made with glass syringe fitted with locks and sealed with silicone. The test measurement involved placing the newborn in the incubator after feeding, keeping the ventilation ports opened, while temperature and humidity of the system and the newborn's home stabilize.

The gas collected (20 mL) were sent to the laboratory and analyzed by GC-35 chromatograph calibrated, the reading of the concentrations of oxygen and carbon dioxide were made in integrating CG processor 300 coupled to the gas chromatograph. One gas sample was needed to get a stable result. VO2 and VCO2 were corrected to standard conditions of pressure and temperature and we calculated REE using the modified Weir equation [21]:

VO2 = Oxygen uptake (ml/Kg/min)

VCO2 = Carbon dioxide production (ml/Kg/min)

REE = Resting Energy Expenditure (Kcal/Kg/day)

Statistical Analysis

Data distribution was evaluated by D'Agostino Pearson normality test. Considering that all variables presented parametric distribution we used paired Student t-test to compare the acute and recovery phase values. The significance level were adopted for 1% (p < 0.01). The statistical analysis was conducted with Sigma Stat software.

Results

Four infants died during the study period due to worsening of their clinical condition. Table 1 lists the complete blood count, CRP and cultures results for the acute phase, while Table 2 shows similar data relative to the recovery phase.
Table 1

Complete blood count, CRP and cultures on acute phase of sepsis.

Subject

Hb (g/dl)

Hct (%)

NI

Leukocyte/mm3

Platelet/mm3

CRP (mg/l)

Identified bacteria

1

8.8

24

0.23

23500

32000

-

HMC: Staphylococcus coagulase

2

10.6

30

0.02

12000

31400

9.82

HMC: Klebsiella pneumoniae

3

14.4

41

0.20

8000

480000

-

HMC: Escherichia coli

4

9.6

27

0.11

18700

72000

36.40

HMC: Streptococcus pyogenes

5

13.6

39

0.02

16400

16000

9.30

HMC: Enterobacter cloacae

6

13.6

38

0.20

21000

193000

-

HMC: Streptococcus pyogenes

7

14.7

42

0.01

14900

560000

-

HMC: Staphylococcus aureus

8

18.3

52

0.10

6500

111000

14.20

HMC: Enterobacter aglomerans

9

7.8

21.1

0.22

4900

72000

203.00

HMC: Staphylococcus aureus

10

12.0

34

0.21

10100

206000

3.30

HMC: Enterobacter aglomerans

11

8.5

24

0.02

10300

610000

-

HMC: Enterobacter cloacae

12

9.2

26

0.20

11000

72000

132.20

HMC: Staphylococcus aureus

13

10.6

32

0.21

20600

144000

57.50

Pus articulation Staphylococcus aureus

14

7.9

24

0.04

3700

200000

37.30

LCR: Neisseria meningitidis

15

12.5

36

0.20

11800

272000

21.00

HMC: Corynebacterium sp

16

10.0

28

0.30

4800

80000

-

HMC: Enterococcus faecalis

17

11.5

31

0.30

3900

186000

-

Ascitic liquid: Pseudomonas aeruginosa

18

11.1

32

0.20

21700

350000

-

HMC: Staphylococcus aureus

19

9.4

27

0.20

24900

429000

-

HMC: Enterococcus faecalis

CRP: C-reactive protein; Hb: Hemoglobin; Hct: Hematocrit; NI: Neutrophil Index.

Table 2

Complete blood count, CRP and cultures on recovery phase of sepsis.

Case

Hb (g/dl)

Hct (%)

Leukocyte/mm3

NI

Platelet/mm3

CRP (mg/l)

Cultures

1

14.6

42

7900

0.06

200000

2.98

Negative

2

11.2

32

10700

0.04

75000

2.00

Negative

3

12.0

35

10000

0.05

130000

-

-

4

9.3

28

11700

0.06

400000

3.30

Negative

5

13.3

36

11400

0.09

120000

-

Negative

6

12.0

34

12000

0.08

146000

-

-

7

13.1

40

9600

0.05

210000

-

Negative

8

11.5

35

11800

0.01

210000

7.00

Negative

9

11.7

35

12800

0.05

390000

9.00

Negative

10

9.9

28

8500

0.10

250000

3.40

Negative

11

12.5

36

9700

0.07

395000

6.00

Negative

12

10.4

30

8100

0.05

570000

3.40

Negative

13

9.1

27

7400

0.04

319000

8.00

Negative

14

10.6

31

13600

0.10

190000

-

Negative

15

12.2

36

12100

0.10

177000

-

Negative

16

14.6

42

7900

0.06

200000

2.98

Negative

17

11.2

32

10700

0.04

75000

2.00

Negative

18

12.0

35

10000

0.05

130000

-

-

19

9.3

28

11700

0.06

400000

3.30

Negative

CRP: C-reactive protein; Hb: Hemoglobin; Hct: Hematocrit; NI: Neutrophil Index.

Table 3 presents the clinical profile of all subjects.
Table 3

Clinical profile of each newborn during acute phase of sepsis.

Case

Infection

Hypothermy

(T<36°C)

Hyperthermy

(T>37,5°C)

Tachycardia

(>120 bpm)

Tachypnea (>40/min)

Antibiotics

1

YES

YES

NO

YES

YES

Vancomycin and Cefotaxime

2

YES

NO

NO

YES

YES

Ceftazidime and Imipenem

3

YES

NO

YES

YES

NO

Ceftriaxone

4

YES

YES

NO

YES

YES

Penicillin and Amicacine

5

YES

NO

YES

YES

YES

Vancomycin and Cefotaxime

6

YES

YES

NO

YES

YES

Ampicillin and Amicacine

7

YES

NO

YES

YES

YES

Oxacillin

8

YES

YES

NO

NO

YES

Vancomycin and Cefotaxime

9

YES

NO

YES

YES

YES

Vancomycin and Ceftriaxone

10

YES

NO

NO

YES

YES

Penicilyin and Amicacine

11

YES

NO

NO

YES

YES

Vancomycin and Cefotaxime

12

YES

NO

YES

YES

YES

Vancomycin and Ceftriaxona

13

YES

NO

NO

YES

YES

Vancomycin and Ceftriaxona

14

YES

NO

YES

YES

YES

Penicillin and Amicacine

15

YES

NO

YES

YES

YES

Vancomycin and Cefotaxime

16

YES

YES

NO

YES

YES

Oxacillin and Amicacine

17

YES

YES

NO

YES

YES

Vancomycin and Imipenem

18

YES

YES

NO

YES

YES

Vancomycin and Cefoxitin

19

YES

NO

YES

YES

YES

Meropenen

We noted no changes in newborns oxygen saturation and axillary temperature. The respiratory quotient (RQ) data showed an average of 0.7 during sepsis, which is indicative of the predominant combustion of fat and ketone bodies, resulting in lower CO2 production.

During the acute phase of sepsis the REE was 49.4 ± 13.1 kcal/kg/day and on recovery it significantly increased to 68.3 ± 10.9 kcal/kg/day (p < 0.01) (Figure 1). Moreover, VO2 (7.4 ± 1.9 vs 10 ± 1.5 ml/kg/min) (Figure 2) and VCO2 (5.1 ± 1.7 vs 7.4 ± 1.5 ml/kg/min) (Figure 3) also increased during the recovery phase (p < 0.01). Those findings support the hypothesis that the whole body metabolic rate is enhanced after sepsis recovery.
Figure 1

Comparison of REE (kcal/kg/day) between sepsis and recovery phase.

Figure 2

Comparison of VO 2 (ml/kg/min) between sepsis and recovery phase.

Figure 3

Comparison of VCO 2 (ml/kg/min) between sepsis and recovery phase.

Table 4 shows data relative to age and weight changes during sepsis and recovery phase.
Table 4

Age (days) and weight (g) at sepsis and recovery phase of sepsis.

Case

Age (days)

Weight (g)

 

Hospitalization

Sepsis

Recovery

Birth

Hospitalization

Sepsis

Recovery

1

24

31

41

3030

3295

3570

3620

2

6

28

39

3070

2820

2535

2750

3

13

14

25

3230

3580

3480

3630

4

18

30

50

2630

2730

2685

3520

5

1

10

24

1800

1680

1695

2000

6

1

2

13

2750

2760

2580

2600

7

22

25

35

2730

3640

3565

3750

8

9

11

26

3500

3000

3080

3040

9

16

20

42

3000

3130

2780

2890

10

31

33

44

3640

3580

3570

3980

11

51

57

69

3300

4500

4710

4965

12

15

21

44

3440

3660

4130

3180

13

27

33

54

2580

2760

2490

2990

14

63

69

81

1960

4015

3880

4365

15

4

7

28

3530

3300

3700

3570

16

30

34

-

3200

3900

3885

-

17

6

11

-

2930

2725

3070

-

18

1

45

-

3470

3470

2690

-

19

35

38

-

3150

2430

2510

-

Mean

19.6

27.3

41

2996.8

3209.2

3189.7

3390

Median

16

28

41

3070

3295

3080

3520

SD

17.1

17.2

17.8

502.3

647.9

730.9

737.3

Maximum

63

69

81

3640

4500

4710

4965

Minimum

1

2

13

1800

1680

1695

2000

Discussion

We endeavored to evaluate the REE in newborn with bacterial sepsis at acute and recovery phases. We reported that at the recovery phase REE was increased compared to the acute sepsis phase, probably due to the resumption of growth. Albeit we investigated a small number of newborns, statistical analysis showed significant differences between acute and recovery phases of sepsis.

In adults with bacterial sepsis it has been shown that caloric and protein needs increased by as much as 150% of normal basal metabolism rate [22]. In this age group equations for calculating caloric requirements are often used; one of the best known is the Harris-Benedict. However, this equation tends to overestimate the caloric needs [23].

We reported that VO2 and VCO2 were increased at the recovery phase of sepsis. There are few studies where the energy requirements in children and especially in newborns with bacterial sepsis were evaluated and the clinically utilized data in neonates was extrapolated from adult values [24]. The application of various predictive equations of REE for children under mechanical ventilation as the Harris-Benedict and Talbot equations formulas overestimate the caloric requirement [25, 26].

Nevertheless, other studies have reported decreased basal metabolic rate in sick children. Powis et al [27] evaluated children undergoing major surgery and did not report an increase in basal metabolic rate during the postoperative period of six newborns with necrotizing enterocolitis. Chwals [28] evaluated the overfeeding (over nutrition) associated to the metabolic effects which occur when nutritionally supporting extremely ill children. The author concluded that the caloric requirement of these children are unpredictable and modified by disease, age, previous nutritional status and type of nutrients (especially parenteral use) with varied specific dynamic action. Therefore, the caloric requirements of critically ill children should be assessed individually and measured by appropriate techniques.

In our study we measured REE through indirect calorimetry. Several techniques are used to evaluate the basal metabolism rate or REE. The most used is the indirect calorimetry, due to its accuracy, portability, comfort and safety for the patient, even in seriously ill subjects [29]. The equipment and technique utilized in the present study were developed by Hamamoto [19] and are especially appropriate for newborns and young children. The method validation was performed by measuring REE in newborns and comparing the results with data from studies that used the same technique. During our study there were no changes in the oxygen saturation and axillary temperature of the newborns. The technique is utilized in our center as part of the patient assessment and it is used frequently for children with metabolic disorders and/or to determine adequacy of nutritional support [19].

We found that REE averaged 49.4 ± 13.1. These values are very close to those of a previous study (51.7 ± 6.21 kcal/kg/day), which used the same apparatus and technique. In the present study, the highest REE during sepsis was 70.7 kcal/kg/day. Considering that in normal children the average REE is 58 kcal/kg/day [25], only six study subjects showed REE values above the normal range. Even in one case the REE was 70.7 kcal/kg/day, which represents only 20% above the highest reference value.

We reported that some of the newborns died during our study. The analysis of REE data in these subjects showed that two neonates exhibited REE values (51.7 ± 6.21 kcal/kg/day) within the adopted reference range. However, we observed that newborns showing significantly lower REE values were more likely to have a poor outcome. In fact, the infant who presented one of the lowest REE (27.8 kcal/kg/day) quickly evolved to demise. Briassoulis et al [25] proposed that the measurement of basal metabolism rate may be a prognostic factor for mortality: the lower the value, the greater the odds of a poor prognosis.

Based on our results, we found no hypermetabolism, differently from what is established in adults with bacterial sepsis where REE is estimated at 100-150% higher than the values of basal metabolism. The same can be said about the VO2 and VCO2. The average VO2 of our study was 7.4 ± 1.9 ml/kg/min, similar to the value of 7.41 ± 0.88 ml/kg/min verified by Hamamoto [19]. The VCO2 during acute phase of sepsis averaged 5.1 ± 1.7 ml/kg/min, which was below the average of 6.36 ± 1.04 reported by the authors. The lower values likely relate to changes in energy metabolism and burning fat and preferential ketone bodies, which frequently occurs in malnourished children and low-calorie-protein intake. This assumption is also supported by the analysis of the RQ. The RQ = 0.7 we found during sepsis is indicative of the predominant combustion of fat and ketone bodies, resulting in lower CO2 production.

The proposed explanation for our results regarding REE, i.e. the absence of hypermetabolism energy has not been adequately discussed in the literature. Nonetheless, some studies related to bacterial sepsis in children are relevant to our analysis. Uzel and Neyzi [30] studied thyroid function in severely infected children and they reported that the values of thyroxine (T4) and thyroid-stimulating hormone (TSH) were comparable to normal controls, whereas triiodothyronine (T3) were much lower and triiodothyronine (reverse rT3) were higher. Mendoza-Morfin et al [31] investigated infants with bacterial sepsis and observed reduction of T4 and T3 associated to increase of rT3 and TSH. After the recovery of sepsis these values returned to normal in children who survived. The authors suggested that through these hormonal changes positively contributed to prevent sepsis-induced catabolism. Furthermore, Hatherill et al [32] evaluated adrenal function in infants with septic shock and demonstrated adrenal insufficiency in 52% of cases. The consequence of this fact was reflected in higher mortality, severe hypotension and more frequent use of vasoactive drugs to maintain blood pressure. Togari et al [33], on the same line of research, demonstrated a decrease of plasma cortisol in children with endotoxic shock. The analysis of these studies showed a reduction of T3, cortisol and catecholamines mainly caused by adrenal insufficiency, an important fact because the triiodothyronine and catecholamines are hormones that promote the body thermogenesis. Probably the interpretation of our results with respect to the absence of hypermetabolism energy in children during the acute phase of sepsis is explained by hormonal changes described above.

The present study has the following caveats. Firstly, we decided not to use a control group since energy expenditure in healthy newborns is well described in the literature [34] and in this investigation we opted to comparatively evaluate the changes in the same infant over time (acute sepsis phase and recovery phase). Secondly, parenteral [28], enteral and oral feeding influence REE [35] and we evaluated newborns which received parenteral feeding. Thirdly, we did not perform any multivariate analysis in order to assess the study variables although this could have provided more detailed information regarding REE. We suggest further studies to evaluate this issue. Fourthly, newborns did not require higher FIO2 and were not mechanically ventilated. These results are not supported by Kreymann et al [36], who found a normal or only slightly elevated REE in adult patients with severe sepsis or septic shock but a hypermetabolic response in patients with uncomplicated sepsis. It is possible that this apparent conflict can be explained by standardization approach described in our method section.

In summary, during the acute phase of bacterial sepsis REE was significantly reduced, as compared with the subsequent recovery phase of sepsis. We recommend that REE during the acute phase of sepsis be individualized for each child, taking into account the severity of the disease, the degree of malnutrition and the type of energy substrate used with respect to the metabolic capacity of the child.

Declarations

Acknowledgements

We thank Dr. Jaques Belik for critical review English Grammar and neonatal concepts. We thank the Medical School of University of São Paulo for financial support.

Authors’ Affiliations

(1)
Departamento de Pediatria, Universidade de São Paulo (USP)
(2)
Departamento de Saúde Materno-infantil, Universidade de São Paulo (USP)
(3)
Departamento de Medicina, Disciplina de Cardiologia, Universidade Federal de São Paulo (UNIFESP)
(4)
Departamento de Morfologia e Fisiologia, Faculdade de Medicina do ABC

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