The Effects of High-Energy Enteral Feeds in Newborn Babies/Infants With CHD For Adequate Weight Gain
The Effects of High-Energy Enteral Feeds in Newborn Babies/Infants With CHD For Adequate Weight Gain
The Effects of High-Energy Enteral Feeds in Newborn Babies/Infants With CHD For Adequate Weight Gain
Katie Page
11/17/2023
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Background:
This review article is going to explore the effects of high-energy enteral nutrition feeds
within newborn infants (birth to one year) who have a congenital heart defect/disease. Infants
who are under such critical, clinical stress tend to undergo nutritional deficits, such as poor
growth rates, due to the severity of their disease state. Specifically, this review will discuss
providing high-energy enteral formula to infants with CHD and the effects this on has adequate
growth rates. CHD or “Congenital Heart Defects” is defined as the most common birth defect
and alters the structure of a child’s heart and its functionality. 1 CHD can affect how the blood
flows throughout the body and interfere with oxygenation to the organ systems. 1 One of the most
common congenital heart defects in newborns is PDA or Patent Ductus Arteriosus which is when
the connection of the aorta and the pulmonary artery does not adjoin after birth. 1 The PDA
usually closes shortly after a baby is born, but when it does not, the blood cannot flow in the
proper manner that it should and puts the baby at risk for severe clinical complications and
mortality.1 Other common CHD’s include Atrial Septal Defect, Pulmonary Atresia, Tetralogy of
Fallot, Atrioventricular Septal Defect, etc. 1 The causes of CHD within newborns are not known,
although studies have been conducted that links genetic and chromosomal changes in utero to a
possible etiology of this disease state. 1 Other factors that could contribute to the cause of CHD
include maternal diet during pregnancy, maternal health conditions, or medication use during
pregnancy, but overall, there is no concrete cause for the disease. 1 Studies show that cardiac
defects are present in one percent of around 40,000 births a year, and about 25% of them have
The normal infant’s nutritional needs vary as the infant is growing at a quick and
consistent rate, but generally a preterm infant needs 110-130 kcal/kg/d and term infant needs
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100-110 kcals/kg/d according to the Texas Children’s Hospital Pediatric Nutrition Reference
Guide- 13th Edition.2 The protein needs of a preterm infant is 3.5-4.3 g/kg/d and for a healthy
term infant, the protein requirements are around 1.5 g/kg/d. 2 Fluid needs and total fluid intake are
dependent on the clinical status of the infant and the number of drips and IV lines the patient is
receiving but are usually restricted within cardiology ICU patients. 2 An infant with CHD’s
energy needs is around 40-60 kcal/kg/d, increasing moderately to a goal of 90-120 kcal/kg/d, and
protein requirements are 1.8-2.2 g/kg/d with lipids at around 35% of total calories. 3 Total fluid
intake (TFI) should not exceed 150 mL/kg/d within this population as well. 3 These nutrition
recommendations may differ from the ranges slightly as each patient may have other clinical
diagnoses and/or specific clinical manifestation parameters, but they usually do not stray far
from the CHD recommendations as this disease state is usually at great severity. Overall, infants
with CHD may have stunted or impaired growth and likely will become underdeveloped and
undernourished overtime due to excess energy expenditure and increased needs. 4 It is of much
importance as a dietitian working within this patient population to ensure CHD infant’s
nutritional needs are met to combat these growth and development obstacles. This review article
will investigate the use of high-energy enteral nutrition support to analyze the nutritional
implications it has on adequate growth within this target population. Different Randomized
Control Trials will be utilized to analyze research findings associated with this intervention.
Multiple randomized control trials have been conducted to analyze if high-energy enteral
nutrition support can increase growth rates within the patient population. This review paper will
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begin by interpreting the data collected from the intervention groups receiving high-energy
formulas versus patients receiving normal enteral nutrition formula as the control groups. The
evaluation measures such as weight, length/height, weight gain, growth velocity, tolerance to
feeds, GI complications, etc. will be used to evaluate the effectiveness of the intervention on
adequate growth.
RCT 1:
The research trial being analyzed is a prospective, open-label, single-arm growth, safety,
and tolerance RCT with CHD infants aged one to eight months who are experiencing poor
growth. The intervention group received energy and protein enriched formula (EPFE) and the
control group received normal enteral nutrition formula. This study lasted 35 days and used stool
weight-for-age (WAZ) to analyze the effectiveness of the intervention.5 The study showed high-
energy and protein enriched formula to be tolerated well, improving the CHD infants’ weight
gain.5 The mean improvement in WAZ was 0.79 (+0.76) within baseline and the end of
participation of the study, with P=0.0001.5 Eighty-three percent of the participating infants
achieved a growth velocity greater or equal to the median during the study.5 Also, the P value for
important to note that feeding tolerances increased as the study went on as well.5 Overall, this
study seemed to show a correlation with weight gain and adequate growth within CHD infants
who uses high-energy and protein formula, but the study did have a few limitations. These
included having a difficult time recruiting participants and increased breastfeeding rates, leading
to a multitude of infants being excluded from the research criteria.5 It was also noted within the
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study that using a high-energy and protein dense formula accommodates with fluid restrictions
that this population might have due to their cardiological clinical status.5
RCT 2:
The second research trial investigating this topic is a parallel randomized control trial
using 68 infants with CHD who underwent cardiovascular corrective surgery.6 The study uses an
intervention of high-density formula (90 kcal/100 mL) with the control group receiving standard
density formula (67 kcal/100 mL).6 It is also important to add that the participants were allowed
breastmilk and/or complimentary foods in addition to their formula.6 The measures used to
determine the effectiveness of the study were weight, length measurements, head circumference,
MUAC, and WAZ.6 The results of the study demonstrated a mean standard deviation for weight
z-scores of -2.38 ± 10.04 to -1.38 + 0.97 in the standard formula group, and -2.69 ± 1.19 to -0.89
± 0.90 in the high-density formula group at baseline to 8 weeks of the study.6 The P value
between the groups for weight z-scores was P=0.0001.6 The standard formula infants
demonstrated a drop in length z-scores, whereas the high-density formula infants had no decrease
within length.6 An additional point to note is serum albumin levels were increased within the
high-density group, but four parents of infants in this group reported constipation even though
tolerance was not factored into the research collection methods.6 The limitations on this study
were a small window to follow-up on participants, lack of a frequent food intake collection
within the duration of the study and no measurements taken for subcutaneous fat loss
evaluations.6 The research conducted concluded that infants receiving the higher-density formula
displayed better results within weight gain and a greater increase in WAZ scores.6
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RCT 3:
The third research trial being evaluated was a randomized control trial in Brazil using 59
CHD infants who just underwent heart surgery. The intervention group received energy-enriched
formula at 1 kcal/mL, while the control group received “normocaloric” formula. 7 The study
lasted for thirty days post heart surgery and measured weight-for-age, weight-for-height, weight
gain, GI side effects, RACHS score, and readmission rates to determine the effectiveness of the
intervention on adequate growth.7 Along the duration of the study or during the follow-up
evaluation period, eight patients in the intervention group and four patients within the control
group passed away due to different etiologies (sepsis, multiorgan failure or heart failure) with
P=0.20.7 The mean discharge rate was 14 days within the intervention infants and 20 days in the
control infants, which was of decent significance at P=0.057.7 The research also discusses that
the use of antibiotics was lower in the intervention group (16 infants) versus the control group
(24 infants) with P=0.047.7 For the purpose of this review, the most important factor to analyze
within this study is weight gain variation. The weight gain rate within the intervention group was
higher than the control group and had a P value of 0.03.7 The control group had a mean growth
velocity of 10 g/d, while the intervention group was higher with a mean growth velocity of 16
g/d.7 Factors that limited the research design within this study include reduced sample size,
deaths during the research period and complementary intake and tolerance levels being reported
by parents which could lead to bias or inaccuracy.7 As a whole, this study concluded to
hospitalization stays being shorter within the intervention group, and a statistical significance in
increase of weight gain in the intervention group compared to the control group.7
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RCT 4:
The next research trial being analyzed is a parallel randomized control trial including a
sample size of 59 infants who were diagnosed with CHD and undergoing open heart surgery.4
The intervention group within this study received high-energy formula of 100 kcal/100 mL as
opposed to the control group receiving standard formula of 67 kcal/mL.4 The factors used to
measure outcomes of the trial were weight gain trends, emesis frequency, abdominal distention,
GRV, and diarrhea amount.4 Along the duration of the study, five infants were excluded due to
death or admission to another outside hospital.4 It is also important to note that each participant
did not vary significantly in weight before the trial had begun.4 The study resulted with infants
that received high-energy formula having increased weight gain in comparison to the control
group with P=0.001.4 Although the intervention group had a higher weight gain rate and
improved nutritional status, they also experienced more feeding intolerance and GI
complications while using the high-energy formula.4 There was not a significant difference of
time on ventilation between the two groups with a P value of 0.749.4 The intervention limitations
within the study included bias of reports from medical staff, a limited follow-up time depending
on CICU admission period, and cariology limitations like fluid restriction or edema altering
weight trends.4 The research concluded that there can be improvement to weight status using the
RCT 5:
The last research trial that will be analyzed within this review is another parallel
randomized control trial including a larger sample size of 244 CHD infants who experienced
cardiac surgery between 2016 and 2018.8 The duration of this study is slightly longer than the
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others at around two years using a 100 kcal/mL high-energy formula for the intervention group
and a standard formula for the control group.8 Evaluation measurements include age, weight, and
height at the time of surgery, time on ventilation, length of stay in the ICU, infection rate, and
nutrition recovery.8 At the conclusion of the study, patients in the intervention group had a higher
significantly lower ventilation support time (P=0.004), infection rate (P=0.001) and ICU stay (P=
0.045).8 It was also demonstrated that the intervention group was found to have a higher recovery
rate from malnutrition 3 months post-op in comparison to the control group at P=0.002.8 The
study limitations consisted of only short-term assessments and implementations being confined
to inpatient only with limited research and follow-up conducted outside hospitalization. 8
Conclusively, this study determined that high-energy formula within CHD infants increases
growth rates, reduces ICU admission time, decreases infection rate and ventilation support time,
Comparison of Findings:
Overall, each clinical research trial concluded to increased weight and adequate growth
with using a higher-energy formula versus a standard formula within CHD infants. Other
findings such as improved length of stay, infection rate and tolerance levels were included and
varied slightly. Differences in the number of participants and the duration of each study need to
be accounted for when analyzing the data as a whole. It is also important to note that some of the
trials included complementary food and supplement intake as others did not, which can alter
weight gain and growth trends. Another factor to consider is scale-variation between different
facilities and edema within patients as both factors can cause weight inaccuracy or fluctuations.
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For example, the only two trials that included edema within the study limitations was RCT 1 and
4, but a common factor within cardiac clinical outcomes is fluid retention and monitoring.
Clinical needs for a hydrolyzed- formula could also be a factor within participants in each study
Clinical Implications:
It can be determined from the findings above that administering a higher-energy dense
formula versus a standard formula to CHD infants can improve weight gain, adequate growth,
and clinical outcomes of the disease state. From the results of each trial, there were slight
variations depending on the specifics of each participant, but overall, each study resulted in
similar outcomes. As a practitioner, one should take into consideration these findings, and assess
each patient as to whether they could potentially benefit from a high-energy formula. Registered
Dietitians specifically have the responsibility to provide the most accurate and adequate nutrition
recommendations and support to every patient seen. With the research conducted already, energy
enriched formulas should be used at the discretion of the RD. More research needs to be
conducted by dietitians and other practitioners to further explore the nutrition implications high-
energy formula has on CHD infants. Refer to Table 1 for specific recommendations regarding
Most of the research trials mentioned using 1 kcal/mL formulas for the intervention
group. High-energy formulas were discussed as the intervention, but it was not specified within
any trial particular brands to use. Infatrini (Nutricia), Similac High Energy, and SMA High
Energy are a few examples of high-energy infant formulas that could be used to increase weight
gain and adequate growth.9 As clinicians, it is also important to ensure accessibility of formula
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within patients that are seen. Formulas used inpatient will need to be on the hospital’s formulary,
and formulas prescribed for outpatient will need to be affordable and accessible to the patient.
WIC is a commonly used way for many families to access formula at home. WIC is state specific
as to what can be provided, and it is important to know the state’s specific WIC formulary.
Conclusion:
Overall, the research shown concludes that the use of high-energy formula within CHD
infants may increase weight gain, adequate growth, reduce malnutrition and improve clinical
outcomes. It can be recommended to provide energy enriched formula to this patient population
while closely monitoring weight trends and tolerance levels. More research will need to be
conducted to create concrete recommendations for specific formula brands and types, but the
findings within the trials used in this review suggest overall positive outcomes from the use of
Table 1:
Recommendations: Justification:
4. Encourage PO intake along with Teaches infant to use oral motor skills
nutrition support when possible: and allows the infant to practice when
able.
Reduces swallowing difficulty and
aspiration when patient reaches the
ability to take all feeds PO.
Provide all nutrition via nutrition
support that is not taken PO.
Work with SLP if patient is having PO
difficulties.
References:
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1. What are congenital heart defects? Centers for Disease Control and Prevention. February 2,
2023. Accessed November 20, 2023. https://www.cdc.gov/ncbddd/heartdefects/facts.html.
2. Food and nutrition. Texas Children’s Hospital. Accessed November 17, 2023.
https://www.texaschildrens.org/departments/food-and-nutrition.
3. Luca A-C, Miron IC, Mîndru DE, et al. Optimal nutrition parameters for neonates and infants
with congenital heart disease. Nutrients. April 17, 2022. Accessed November 20, 2023.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9029500/.
4. Zhang H;Gu Y;Mi Y;Jin Y;Fu W;Latour JM; High-energy nutrition in paediatric cardiac
critical care patients: A randomized controlled trial. Nursing in critical care. Accessed October 6,
2023. https://pubmed.ncbi.nlm.nih.gov/30548121/.
8. Chen X;Zhang M;Song Y;Luo Y;Wang L;Xu Z;Bao N; Early high-energy feeding in infants
following cardiac surgery: A randomized controlled trial. Translational pediatrics.
Accessed October 6, 2023. https://pubmed.ncbi.nlm.nih.gov/34765467/.
10. Helping children with congenital heart disease stay healthy, active & fit.
HealthyChildren.org. Accessed November 20, 2023.
https://www.healthychildren.org/English/health-issues/conditions/heart/Pages/Helping-
Children-With-Congenital-Heart-Disease-Stay-Healthy,-Active-&-
Fit.aspx#:~:text=Needing%20more%20calories%20in%20early,high%2Dcalorie
%20formula%20or%20supplements.
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