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Low Dose Parenteral Fat for Prevention of Parenteral Nutrition Associated Cholestasis in Preterm Neonates

Low Dose Parenteral Fat for Prevention of Parenteral Nutrition Associated Cholestasis in Preterm Neonates

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01050660
Enrollment
136
Registered
2010-01-15
Start date
2009-06-30
Completion date
2013-01-31
Last updated
2014-10-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parenteral Nutrition-Associated Liver Disease

Keywords

Parenteral nutrition associated liver disease, Direct bilirubin, Intravenous fat emulsion, Very low birth weight infants, PNAC

Brief summary

The goal of the study is to determine if parenteral nutrition-associated cholestasis (PNAC) is related to the amount of parenteral (intravenous) fat administered to premature babies until full enteral nutrition is achieved.

Detailed description

In the neonatal intensive care unit, parenteral nutrition is widely used to provide protein, energy, vitamins and minerals to infants who cannot accept enteral feeds. Intravenous fat emulsion is an important component of parenteral nutrition because of the important caloric supply that it brings, but also for the essential fatty acids (linoleic and linolenic acid) that it provides. Because intravenous fat emulsion is the only supply of essential fatty acids, at least until the enteral feeds are established, there is a minimum of fat that has to be administered with at least 0.25g/kg /day for preterm babies and 0.1g/kg/day for term infants (Lee EJ, 1993). The maximal dose of intravenous fat safe to administer is difficult to determine. Although in larger preterm infants intravenous fat is tolerated well based on measurement of serum triglycerides, there are still question regarding tolerance in extremely low birth weight infants. Parenteral nutrition has been associated with the development of liver disease-parenteral nutrition associated liver disease (PNALD). PNALD can range from cholestasis and a transient elevation of liver enzymes to more severe forms including fibrosis, liver cirrhosis and hepatic failure. Cholestasis, defined as hyperbilirubinemia with a direct bilirubin above 2 mg/dL or more than 15% of total bilirubin, is a hepatocellular injury of the liver that manifests after the administration of parenteral nutrition for at least two weeks. The mechanism by which the liver injury occurs is unknown and probably multifactorial. Risk factors associated with the development of PNAC include: prematurity, low birth weight, absence of enteral feeds, bacterial sepsis, necrotizing enterocolitis, prolonged use of parenteral nutrition, and multiple surgical procedures on the gastro-intestinal tract. In addition, many of the nutrients contained in parenteral nutrition, have been linked with the development of cholestasis. Specific factors associated with intravenous fat emulsions that have been related to PNAC include : phytosterols, the rate of administration of the intravenous emulsion, the total amount of fat administered and toxic metabolites of intravenous fat emulsions. The total amount of lipids was found to be a risk factor for cholestasis in children on long-term parenteral nutrition and decreased amount of fat was recommended for the prevention of this hepatic complication (Colomb V, 2000). In the adult population parenteral lipid intake of less than 1gr/kg of body weight decreased the risk of cholestasis in parenteral nutrition treated patients (Cavicchi, 2000). Current Nutritional Management for VLBW infants in the NBSCU: The administration of parenteral nutrition to all the preterm babies with a gestational age less than or equal to 29 weeks' is standard practice in the NBSCU for infants not receiving full enteral nutrition. Fat, as an integral part of the intravenous alimentation, is started in the first day of life at a dose of 0.5 grams/kg/day of an 20% fat emulsion(eg, Lyposyn II, Abbott Laboratories Chicago, IL). The amount of fat is then gradually increased by 0.5-1 grams/kg/day to total amount of 3 grams/kg/day as tolerated. The tolerance is checked by measuring serum triglyceride level the morning after 3 grams/kg/day has been reached for the first time serum triglyceride level ≤200 mg/dl are accepted for infants ≤52 weeks postmenstrual age. If the serum triglyceride level is \>200 mg/dL, the intravenous fat emulsion is reduced for 24 hours, then the triglyceride level is checked again to ensure that it has dropped below 200 mg/dL. The fat emulsion is then restarted at 1-1.5 grams/kg/day and the serum triglyceride level is monitored as it is slowly increased. Enteral nutrition is started initially as minimal enteral feedings, also called non-nutritive feedings, usually by 48±12 hours of age with about 12 ml/kg/day. The feedings are then advanced as tolerated with the goal to reach full enteral nutrition (\>120 ml/kg/day) between 14-21days of life. As the enteral volumes reach 1/3, 1/2, and 2/3 of the total daily fluid volume, the rate of administration of the lipid emulsion is decreased in steps (ie, from 2 grams/kg/day to 1.5 to 1.0) , until the intravenous fat emulsion is stopped. As part of standard NBSCU management guidelines screening of liver function consists of measuring serum direct bilirubin level after the baby has been on TPN for 10 days to two weeks and then biweekly, if PN continues. In addition, if the direct bilirubin level is greater than 2.5mg/dL, then liver enzymes will be checked . Study Procedure: All preterm babies with a gestational age less than or equal to 29 weeks' born at YNHH who will receive intravenous fat emulsion as part of their nutrition management are eligible to participate in the study. The parents of these babies will be approached during the first 24 hours of life, regarding the possible participation in the study. After informed consent will be obtained, the subjects will be randomized by YNHH Investigator pharmacy to one of the two groups: intervention (restricted intravenous fat intake) and control (standard intravenous fat intake). Therefore, the purpose of this study will be to determine if PNAC is related to the amount of parenteral fat administered to premature babies until full enteral nutrition is reached.

Interventions

OTHERIntravenous fat emulsion

An infusion of intravenous fat will start at 0.5 grams/kg on the first day of life, with increments of 0.5 -1.0 grams/kg every day, until a total dose of 3 grams/kg is reached.

OTHERRestriction of intravenous fat emulsion to 1 gm/kg/d

Intravenous fat will be started at 0.5 grams/kg on the first day of life and then increase to a dose of 1gram/kg/day the next day. There will be no further increase in the amount of intravenous fat.

Sponsors

University of California, Los Angeles
CollaboratorOTHER
Northwestern University Feinberg School of Medicine
CollaboratorOTHER
Yale University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
12 Hours to 48 Hours
Healthy volunteers
No

Inclusion criteria

* Preterm infants less than or equal to 29 weeks' gestation * Age less than 48 hours

Exclusion criteria

* Congenital intrauterine infection, known to be associated with liver involvement and cholestasis * Known structural liver abnormalities that are associated with cholestasis * Known genetic disorders: trisomy 21, trisomy 13 and trisomy 18 * Inborn errors of metabolism * Infants meeting the criteria for terminal illness (eg, pH \< 6.8 \> 2 hours) * Inability to obtain informed consent

Design outcomes

Primary

MeasureTime frame
The Presence of Cholestasis at Age of 28 Days or When Full Enteral Nutrition is Achieved, Whichever is Longer.28 days of age or when full enteral nutrition is acheived, whichever is longer

Secondary

MeasureTime frameDescription
Incidence of Bronchopulmonary Dysplasia (BPD)36 weeks PMA or discharge home,whichever comes first
Incidence of Necrotizing Enterocolitis (NEC)At discharge from Newborn ICU
Incidence of Retinopathy of Prematurity (ROP)At discharge from Newborn ICU
Late Onset SepsisAt the discharge from Newborn ICUBloodstream infection, defined as a positive blood culture obtained after 72 hours of life.
Mortality Rate- Death Rate Before Discharge From the HospitalDischarge from the Newborn ICU
Anthropometric Measurements(Body Weight)At age of 28 days and at dischargeChange in body weight measurement reported in g/week
Anthropometric Measurements(Length)At age of 28 days and at dischargeChange in body length measurement reported in cm/week
Anthropometric Measurements(Head Circumference)At age of 28 days and at dischargeChange in head circumference measurement reported in cm/week
Length of StayAt discharge from Newborn ICU/deathDefines time to discharge or death.

Countries

United States

Participant flow

Recruitment details

Bewtween May 2009 -November 2012- infants born and admitted to NICU were enrolled.

Participants by arm

ArmCount
3 gm/kg/Day Intravenous Lipid Emulsion
Intravenous fat emulsion : An infusion of intravenous fat will start at 0.5 grams/kg on the first day of life, with increments of 0.5 -1.0 grams/kg every day, until a total dose of 3 grams/kg is reached.
67
Intravenous Fat Emulsion-restricted
Restriction of intravenous fat emulsion to 1 gm/kg/d : Intravenous fat will be started at 0.5 grams/kg on the first day of life and then increase to a dose of 1gram/kg/day the next day. There will be no further increase in the amount of intravenous fat.
69
Total136

Baseline characteristics

Characteristic3 gm/kg/Day Intravenous Lipid EmulsionIntravenous Fat Emulsion-restrictedTotal
Age, Categorical
<=18 years
67 Participants69 Participants136 Participants
Age, Categorical
>=65 years
0 Participants0 Participants0 Participants
Age, Categorical
Between 18 and 65 years
0 Participants0 Participants0 Participants
Gestational age at enrollement26.4 weeks
STANDARD_DEVIATION 1.8
26.6 weeks
STANDARD_DEVIATION 1.8
26.5 weeks
STANDARD_DEVIATION 1.8
Region of Enrollment
United States
67 participants69 participants136 participants
Sex: Female, Male
Female
26 Participants23 Participants49 Participants
Sex: Female, Male
Male
41 Participants46 Participants87 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
0 / 670 / 69
serious
Total, serious adverse events
5 / 676 / 69

Outcome results

Primary

The Presence of Cholestasis at Age of 28 Days or When Full Enteral Nutrition is Achieved, Whichever is Longer.

Time frame: 28 days of age or when full enteral nutrition is acheived, whichever is longer

Population: Incidence of PNALD at Yale and UCLA NICU prior to the start of the study was around 40%.~Our goal was to decrease incidence by 50%/ Alpha of 5%/ Power of 80% We calculated a sample size of 65 infants in each group

ArmMeasureValue (NUMBER)
3 gm/kg/Day Intravenous Lipid EmulsionThe Presence of Cholestasis at Age of 28 Days or When Full Enteral Nutrition is Achieved, Whichever is Longer.39 participants who developed Cholestasis
Intravenous Fat Emulsion-restrictedThe Presence of Cholestasis at Age of 28 Days or When Full Enteral Nutrition is Achieved, Whichever is Longer.45 participants who developed Cholestasis
Secondary

Anthropometric Measurements(Body Weight)

Change in body weight measurement reported in g/week

Time frame: At age of 28 days and at discharge

ArmMeasureValue (MEAN)Dispersion
3 gm/kg/Day Intravenous Lipid EmulsionAnthropometric Measurements(Body Weight)66.6 g/weekStandard Deviation 34
Intravenous Fat Emulsion-restrictedAnthropometric Measurements(Body Weight)62.9 g/weekStandard Deviation 39
Secondary

Anthropometric Measurements(Head Circumference)

Change in head circumference measurement reported in cm/week

Time frame: At age of 28 days and at discharge

ArmMeasureValue (MEAN)Dispersion
3 gm/kg/Day Intravenous Lipid EmulsionAnthropometric Measurements(Head Circumference)0.5 cm/weekStandard Deviation 0.3
Intravenous Fat Emulsion-restrictedAnthropometric Measurements(Head Circumference)0.6 cm/weekStandard Deviation 0.3
Secondary

Anthropometric Measurements(Length)

Change in body length measurement reported in cm/week

Time frame: At age of 28 days and at discharge

ArmMeasureValue (MEAN)Dispersion
3 gm/kg/Day Intravenous Lipid EmulsionAnthropometric Measurements(Length)0.8 cm/weekStandard Deviation 0.5
Intravenous Fat Emulsion-restrictedAnthropometric Measurements(Length)0.9 cm/weekStandard Deviation 0.5
Secondary

Incidence of Bronchopulmonary Dysplasia (BPD)

Time frame: 36 weeks PMA or discharge home,whichever comes first

ArmMeasureValue (NUMBER)
3 gm/kg/Day Intravenous Lipid EmulsionIncidence of Bronchopulmonary Dysplasia (BPD)27 participants who developed BPD
Intravenous Fat Emulsion-restrictedIncidence of Bronchopulmonary Dysplasia (BPD)26 participants who developed BPD
Secondary

Incidence of Necrotizing Enterocolitis (NEC)

Time frame: At discharge from Newborn ICU

ArmMeasureValue (NUMBER)
3 gm/kg/Day Intravenous Lipid EmulsionIncidence of Necrotizing Enterocolitis (NEC)8 participants who developed NEC
Intravenous Fat Emulsion-restrictedIncidence of Necrotizing Enterocolitis (NEC)11 participants who developed NEC
Secondary

Incidence of Retinopathy of Prematurity (ROP)

Time frame: At discharge from Newborn ICU

ArmMeasureValue (NUMBER)
3 gm/kg/Day Intravenous Lipid EmulsionIncidence of Retinopathy of Prematurity (ROP)7 participants who developed ROP
Intravenous Fat Emulsion-restrictedIncidence of Retinopathy of Prematurity (ROP)9 participants who developed ROP
Secondary

Late Onset Sepsis

Bloodstream infection, defined as a positive blood culture obtained after 72 hours of life.

Time frame: At the discharge from Newborn ICU

ArmMeasureValue (NUMBER)
3 gm/kg/Day Intravenous Lipid EmulsionLate Onset Sepsis3 participants who developed LOS
Intravenous Fat Emulsion-restrictedLate Onset Sepsis5 participants who developed LOS
Secondary

Length of Stay

Defines time to discharge or death.

Time frame: At discharge from Newborn ICU/death

ArmMeasureValue (MEAN)
3 gm/kg/Day Intravenous Lipid EmulsionLength of Stay81.5 Days
Intravenous Fat Emulsion-restrictedLength of Stay87 Days
Secondary

Mortality Rate- Death Rate Before Discharge From the Hospital

Time frame: Discharge from the Newborn ICU

ArmMeasureValue (NUMBER)
3 gm/kg/Day Intravenous Lipid EmulsionMortality Rate- Death Rate Before Discharge From the Hospital5 participants
Intravenous Fat Emulsion-restrictedMortality Rate- Death Rate Before Discharge From the Hospital6 participants

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026