Human Milk Fortification in Extremely Preterm Infants
- Conditions
- Necrotizing EnterocolitisMortalitySepsis
- Interventions
- Dietary Supplement: H2MFDietary Supplement: Bovine milk-based fortifier
- Registration Number
- NCT03797157
- Lead Sponsor
- Thomas Abrahamsson, MD, PhD
- Brief Summary
This is a randomised controlled multi-centre trial comparing the effect of diet supplementation of a human breast milk-based nutrient fortifier (H2MF®) with standard bovine protein-based nutrient fortifier in 222 extremely preterm infants (born before gestational week 28+0) exclusively fed with human breast milk (own mother´s milk and/or donor milk). The infants will be randomised to receive either the human breast-milk based H2MF® or the standard bovine protein-based nutrient fortifier when oral feeds have reached \<100 ml/kg/day.
The randomised intervention, stratified by centre, will continue until the target gestational week 34+0. The infant must not be fed with formula during the intervention period. The allocation will be concealed before inclusion, but after randomisation the study is not blinded.
Primary endpoint of the intervention is the composite variable necrotizing enterocolitis (NEC), sepsis and mortality.
The enrolled infants are characterised with clinical data including growth, feeding intolerance, use of enteral and parenteral nutrition, treatment, antibiotics and complications collected daily in a study specific case report form from birth until discharge from the hospital (not longer than gestational week 44+0). A follow up focusing on neurological development, growth and feeding problems will be performed at 2 years of age (corrected) and 5.5 years of age.
- Detailed Description
This is a randomised controlled multi-centre trial comparing the effect of diet supplementation of a human breast milk-based nutrient fortifier (H2MF®) with standard bovine protein-based nutrient fortifier in 222 extremely preterm infants (born before gestational week 28+0) exclusively fed with human breast milk (own mother´s milk and/or donor milk). The infants will be randomised to receive either the human breast-milk based H2MF® or the standard bovine protein-based nutrient fortifier when oral feeds have reached \<100 ml/kg/day. If fortification with extra enteral lipids is needed during the intervention period, the infants receiving H2MF® will be supplemented with the human milk-based Prolact CR®, while the infants receiving standard bovine protein-based fortification will be supplemented with the standard lipid products used at the unit. The study subject will be enrolled at level III neonatal intensive care unit (NICU)s. Only infants with a home clinic with the logistics to maintain the intervention until gestational week 34+0 will be included.
The randomised intervention, stratified by centre, will continue until the target gestational week 34+0. The infant must not be fed with formula during the intervention period. The allocation will be concealed before inclusion, but after randomisation the study is not blinded. It would not be possible to prescribe the fortifier and prepare of the breast milk in a blinded fashion, since the fortifiers are not exactly equal in nutrient content and also look different. Instead the assessment of several of the outcomes will be made blinded, such as the assessment of X-ray images in NEC cases.
The enrolled infants are characterised with clinical data including growth, feeding intolerance, use of enteral and parenteral nutrition, treatment, antibiotics and complications collected daily in a study specific case report form from birth until discharge from the hospital (not longer than gestational week 44+0). A follow up focusing on neurological development, growth and feeding problems will be performed at 2 years of age (corrected) and 5.5 years.
Since it is often difficult to distinguish between the diagnoses of NEC and sepsis, and their clinical consequences, the investigator's primary endpoint of the intervention is the composite variable NEC, sepsis and mortality. Secondary endpoints are feeding intolerance and other severe complication such as Bronchopulmonary dysplasia (BPD), Retinopathy of prematurity (ROP) and neurological impairment. Stool, urine and blood samples are also collected for microbiology, metabolomic and immunology analysis in order to study underlying mechanisms. Health economic analyses will be made to evaluate the costs and benefits of an introduction of human milk-based fortifier in NICUs in the Nordic countries.
Analyses will be conducted using an intention to treat approach. An evaluation will be performed when 20 infants have been included to evaluate feasibility and make it possible to adjust the protocol for the remaining part of the study. Safety analyses will be performed by an independent data and safety monitoring board (DSMB) when 50, 100 and 150 infants have been included. A sample size re-estimation will be made by an independent statistician when 150 infants have been included. Thus, the definitive sample size might be increased (never decreased) based on this interim analysis. The study can be terminated before 322 infants have been enrolled based on a decision of the sponsor and the DSMB, if the primary outcome is significantly lower (with a significance level \<0.001) in the H2MF® than in the standard fortification group in the interim analysis made after 150 infants have completed the neonatal period. The study subject will be enrolled at level III NICUs in the Nordic Countries. All study subjects will be followed during the neonatal period until discharge (not longer than gestational week 44+0) and also be included in a follow up at 2 and 5.5 years of age based on the national follow up program for extremely preterm infants.
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 229
- Gestational age at birth 22+0-27+6: based on prenatal ultrasonography.
- Enteral feeds < 100 mL/kg/day at the day of randomisation.
- Written informed consent from the legal guardians of the infant.
- The home clinic of the infant has the logistics of maintaining the intervention until gestational week 34+0
- Lethal or complicated malformation known at the time of inclusion
- Chromosomal anomalies known at the time of inclusion
- No realistic hope for survival at the time of inclusion
- Gastrointestinal malformation known at the time of inclusion
- Abdominal surgery before the time of inclusion
- Participation in another intervention trial aiming at having an effect on growth, nutrition, feeding intolerance or severe complications such as NEC and sepsis
- Infants having nutrient fortifier or formula prior to randomisation
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description H2MF H2MF Human milk-based breast milk fortifier Standard fortifier Bovine milk-based fortifier Standard care: bovine milk-based breast milk fortifier
- Primary Outcome Measures
Name Time Method The incidence of the composite of necrotizing enterocolitis, culture-proven sepsis and mortality From birth until discharge from hospital (but not longer than gestational week 44+0) An infant should have had any of these diagnoses to fulfil the criterion
- Secondary Outcome Measures
Name Time Method The incidence culture-proven sepsis From birth until discharge from hospital (but not loner than gestational week 44+0) Number of feeding interruptions From birth until discharge from hospital (but not longer than gestational week 44+0) Number of days feedings held for ≥12 hours or feeds reduced by \>50% (ml/kg/d) not due to a clinical procedure or transitioning to the breast
Stool frequency From birth until discharge from hospital (but not longer than gestational week 44+0) Numbers of days with parenteral nutrition From birth until discharge from hospital (but not longer than gestational week 44+0) Number of days of parental amino acid and/or lipid infusion. Only days when the enteral feed \<150mL/kg/day should be included
Change in head circumference in centimeters At 7, 14, 21 and 28 days, the end of intervention (gestational week 34+0), gestational week 36+0, at discharge from neonatal ward (or at gestational week 44+0, whatever comes first) and at 2 years of age (corrected) and 5.5 years of age (uncorrected). The mortality incidence From birth until discharge from hospital (but not loner than gestational week 44+0) Change in length in centimeters At 7, 14, 21 and 28 days, the end of intervention (gestational week 34+0), gestational week 36+0, at discharge from neonatal ward (or at gestational week 44+0, whatever comes first) and at 2 years of age (corrected) and 5.5 years of age (uncorrected). The incidence spontaneous intestinal perforation From birth until discharge from hospital (but not loner than gestational week 44+0) The number of infants needing extra oxygen and/or ventilatory support after discharge from the hospital at the neonatal period From gestational week 44 until 2 years of age The incidence of severe infections after discharge from the neonatal unit From gestational week 44 until 2 years of age The prevalence of neurocognitive development at 5.5 years At 5.5 years of age Wechsler Preschool and Primary Scale of Intelligence IV (WPPSI-IV TM) and Movement ABC-2: the total scale points as well as the points of sub scales (motor, cognitive, language) will be presented. The prevalence of infants with a realist below 2 standard deviations will be defined to have mental retardation.
The prevalence of wheeze and/or asthma at 5.5 years of age At 5.5 years of age Levels of subclasses of T and B cells and granulocytes in blood samples At 1, 2 and 4 weeks of age and gestational week 36+0 T helper subsets (TH1, Th2, TH17, Treg), T cells subsets associated with the intestinal mucosa (gamma/delta-T cells, MAIT cells) and neutrophils will be assessed using masscytometry
Levels of growth factors in plasma samples At 1, 2 and 4 weeks of age and gestational week 36+0 The levels of growth factors such as IGF-1 and the associated IGFBP-3 will be analysed.
Levels of neurotransmitters in plasma samples At 1, 2 and 4 weeks of age and gestational week 36+0 Neurotransmitters such as GABA and serotonin in plasma
Time to reach full enteral feeds From birth until discharge from hospital (but not longer than gestational week 44+0) The day of life the infant has received at least 150 mL/kg enteral feeds
Time to regain birth weight From birth until discharge from hospital (but not longer than gestational week 44+0) The incidence of suspected sepsis, not culture-proven From birth until discharge from hospital (but not loner than gestational week 44+0) The incidence of periventricular leukomalacia From birth until discharge from hospital (but not loner than gestational week 44+0) Criteria according to de Vries
Number of days with intensive care From birth until discharge from hospital (but not loner than gestational week 44+0) Need of respirator or CPAP until discharge (not later than gestational week 44+0).
Prevalence of squint and/or impaired vision at 2 years At 2 years of age The number of infants needing extra nutritional support after discharge from the hospital at the neonatal period From gestational week 44 until 2 years of age The incidence of the composite of necrotizing enterocolitis and culture-proven sepsis From birth until discharge from hospital (but not longer than gestational week 44+0) An infant should have had any of these diagnoses to fulfil the criterion
The incidence of the composite of necrotizing enterocolitis culture-proven sepsis, bronchopulmonary dysplasia, retinopathy of prematurity and mortality (Mortality and morbidity index) From birth until discharge from hospital (but not longer than gestational week 44+0) An infant should have had any of these diagnoses to fulfil the criterion
Number of large gastric aspirates per day From birth until discharge from hospital (but not longer than gestational week 44+0) ≥100% pre-feed volume (2 hours feeding volume if continuous feeding). Lower limit=2 ml/kg.
The incidence of abdominal surgery From birth until discharge from hospital (but not loner than gestational week 44+0) The incidence of pneumonia From birth until discharge from hospital (but not loner than gestational week 44+0) Pathological X-ray confirmed by an independent radiologist, need of increased respiratory support/oxygen and laboratory inflammatory response
The incidence of bronchopulmonary dysplasia At gestational week 36+0 Need of extra oxygen, continuous positive air pressure (CPAP) or ventilator at gestational week 36+0
The incidence of intraventricular haemorrhage From birth until discharge from hospital (but not loner than gestational week 44+0) Classified into grade I-IV according to Papile
Length of stay at the hospital From birth until discharge from hospital (but not loner than gestational week 44+0) Gestational week and day at discharge (not later than gestational week 44+0).
Prevalence of cerebral palsy at 2 years At 2 years of age Prevalence of impaired hearing at 2 years At 2 years of age Change in weight in gram At 7, 14, 21 and 28 days, the end of intervention (gestational week 34+0), gestational week 36+0, at discharge from neonatal ward (or at gestational week 44+0, whatever comes first) and at 2 years of age (corrected) and 5.5 years of age (uncorrected). The incidence of retinopathy of the prematurity From birth until gestational week 42+0 Classified into stage I-V. The diagnosis is set after gestational week 42+0
Prevalence of epilepsy at 2 years At 2 years of age Levels of immune markers in plasma At 1, 2 and 4 weeks of age and gestational week 36+0 Pre planned analyses are anti-inflammatory (e.g. IL-10) and proinflammatory (e.g. TNF) cytokines and chemokines (e.g. CXCL11, CCL18).
Levels of lipids in plasma samples At 1, 2 and 4 weeks of age and gestational week 36+0 Fatty acids in plasma
Levels of metabolic peptides in urine samples At 1, 2, 3 and 4 weeks of age and gestational week 36+0 Metabolic peptide will be measured with proton nuclear magnetic resonance spectroscopy (NMR), liquid chromatography (LC) and mass spectroscopy couple to gas chromatography (GC-MC).
Levels of proteins in breast milk samples At 1, 2, 3 and 4 weeks of age and gestational week 36+0 Protein composition will be measured with multiplex methods
Levels of human milk oligosaccharides in breast milk samples At 1, 2, 3 and 4 weeks of age and gestational week 36+0 The levels of human milk oligosaccharides will be measured with high-performance anion-exchange chromatography with pulsed amperometric detection.
The incidence of necrotising enterocolitis: Bell´s stage II-III From birth until discharge from hospital (but not loner than gestational week 44+0) Length of need of feeding tube From birth until discharge from hospital (but not loner than gestational week 44+0) Gestational week and day when the infant does not need it anymore (not later than gestational week 44+0)
Neurocognitive development at 2 years At 2 years of age Bayleys III, PARCA-R (Parental Report of Children´s Abilities-Revised) and ASQ-3 (Ages and stages questionnaire)
The incidence of wheeze and/or asthma From birth until 2 years of life The number of infants needing feeding tube after discharge from the hospital at the neonatal period From gestational week 44 until 2 years of age The prevalence of cerebral palsy at 5.5 years At 5.5 years of age The prevalence of epilepsy at 5.5 years of age At 5.5 years of age The prevalence of squint and/or impaired vision at 5.5 years of age At 5.5 years of age The prevalence of children with impaired hearing at 5.5 years of age At 5.5 years of age Microbiome composition in stool samples At 1, 2, 3 and 4 weeks of age and gestational week 36+0 The relative abundance and diversity of microbial taxa will be analyses with next generation sequencing and be related till the study intervention
Levels of markers of central nervous system (CNS) damage in plasma samples At 1, 2 and 4 weeks of age and gestational week 36+0 Markers of CNS damage such as neurofilament light protein will be measured in plasma
Health care costs From birth until discharge from hospital (but not loner than gestational week 44+0) The number of days at each level of care will be recorded until discharge from the hospital (not longer than gestational week 44+0). The cost will be calculated by multiplying the number of days at each level of care by the average cost
Trial Locations
- Locations (5)
Queen Silvia Children´s Hospital
🇸🇪Göteborg, Sweden
Karolinska Hospital
🇸🇪Stockholm, Sweden
Akademiska Barnsjukhuset
🇸🇪Uppsala, Sweden
Crown Princess Victoria Children´s Hospital
🇸🇪Linköping, Sweden
Norrlands Universitetssjukhus
🇸🇪Umeå, Sweden