NeoHemoHapt: Improving Gastrointestinal Function In High-Risk Newborns By Stimulation Of The Enteric Nervous System
Study Details
Study Description
Brief Summary
The goal of this therapeutical intervention trial is to investigate whether tactile-kinesthaetic and oral sensorimotor stimulation can improve gastrointestional function in preterm infants born before gestational age of 30 weeks and newborns with congenital diaphragmatic hernia. The main question it aims to answer is:
• To determine whether HAPTOS- intervention (Handling Adapted to Postnatal age with Tactile-kinaesthetic and Oral sensorimotor Stimulation) in the particpants results in earlier attainment (postnatal days) of full enteral feeding and/or full oral feeding (post menstrual age) compared to standard care. Researchers will compare an intervention group receiving standard of care plus HAPTOS intervention to a group of patients receiving only current standard of care.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
Infants born preterm or with congenital diaphragmatic hernia (CDH) are at risk for several long-term unfavourable outcomes that can be related to feeding difficulties from birth onwards. Adverse nutritional outcomes in both patient groups mainly originate from mechanical dysfunction, based on dysmotility. Mechanical function includes suck-swallow coordination, gastrointestinal sphincter tone, gastric emptying and intestinal motility and is regulated by the complex interplay of the autonomic (ANS) and enteric (ENS) nervous system with modulation by the central nervous system (CNS). The intra-uterine environment provides the fetus with developmentally timed sensory exposures through 'touch' that are necessary for development of sensory control and autonomous coordination of bodily functions. Preterm infants miss out this normal maturation, while newborns with CDH may exhibit a delayed maturation probably as a result of the deviant anatomical situation and the severe illness during the direct postnatal period. In the postnatal situation both patient groups may be confronted with either 'negative' sensory stimulation through exposures such as procedural touch/handling, pain or otherwise a reduction in sensory exposures through avoidance of positive touch in relation to supposed clinical instability. All together this may affect normal development and may lead to sensory deprivation and delayed maturation of the nervous regulation and cerebral maturation. Tactile-kinaesthetic and oral sensorimotor stimulation using positive gentle touch have been shown to positively affect cardiorespiratory stability, weight gain, gastro-intestinal performance, and length of stay in hospital for preterm infants. However, these strategies have not been evaluated in high-risk infants. The current study aims at evaluating an intervention programme that provides positive stimuli through touch adapted to the stage of development of the infant with regard to timing, duration and intensity that supports the maturational development of gastrointestinal functionality. (Handling Adapted to Postnatal age with Tactile-kinaesthetic and Oral sensorimotor Stimulation; HAPTOS intervention). We hypothesize that the HAPTOS intervention will improve the postnatal maturation of the autonomous and enteral nervous system and cause improvements in gastrointestinal motility, enteral and oral feeding and cardiorespiratory stability.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| No Intervention: Standard care Will receive standard of care according to the institutional protocol and principles of developmental care which currently belongs to (inter-) national guidelines and is regarded as safe. |
|
| Experimental: Standard care supplemented with HAPTOS intervention Will receive standard of care according to the principles of developmental care which currently belongs to (inter-) national guidelines plus HAPTOS intervention which includes: tactile/ kinaesthetic massage of the trunk and extremities twice daily and stimulation of oral function by providing perioral stimulation up to 4 times a day. Interventions will be continued until clinical improvement. |
Procedure: HAPTOS (Handling Adapted to Postnatal age with Tactile-kinaesthetic and Oral sensorimotor Stimulation
Tactile-kinaesthetic and Oral sensorimotor Stimulation
|
Outcome Measures
Primary Outcome Measures
- Number of days to achieve full enteral feeding [60 days]
measuring the time from birth until enteral intake reaches 150ml/kg/d
- Postmenstrual age at achievement of full oral feeding [52 weeks]
Number of postmenstrual weeks until gastrointestinal tube is taken out
Secondary Outcome Measures
- First meconium passage [14 days]
Postnatal day at first meconium
- Duration of meconium passage [14 days]
Number of days until normal defecation
- Use of laxatives [60 days]
Number of laxatives given
- Gastrointestinal Motility [100 days]
Volume of gastric residuals per week
- Vomiting [duration of hospitalization up to 15 months]
Number of incidences of vomiting in combination with aspiration
- Periodic breathing [duration of hospitalization up to 15 months]
Number of desaturations < 80% and/or bradycardia < 80/min that require intervention per week
- Feeding difficulties [24 months]
Number of infants with impaired oral motor skills
- Maturation of heart rate variability [duration of intensive care stay up to 60 days]
Number of infants with delayed regulation of the para- and sympathicus tonus measured continuously through monitordata collection
- Growth at postmenstrual age [at 40 weeks, 3, 6, 12, 18 and 24 weeks]
Gain in weight, length, and head circumference including percentiles
- Morbidity [100 days]
Number of infants with necrotizing enterocolitis, spsis, chronic lung disease, retinopathy of prematurity, intra-ventricular hemorrhage
- Duration hospital stay [100 days]
Postnatal age at time of discharge home
- Neurocognitive development [at 24 months]
Measuring cognitive and motor development using Bayley Scores of Infant Development (BSID III)
- Parent participation in care [duration of hospitalization up to 100 days]
Measuring number of parents who participate and frequency of activity
Eligibility Criteria
Criteria
Inclusion Criteria:
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Preterm birth at gestational age < 30 weeks or
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Diagnosis of Congenital Diaphragmatic Hernia
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Born at Amalia Children's Hospital or admitted 1rst day of life
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Written informed consent of both parents or representatives
Exclusion Criteria:
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Preterm infant born at gestational age ≥ 30 weeks
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Perinatal Asphyxia; (Apgar score at 5' < 5 and first pH ≤ 7,0)
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Major congenital anomalies or birth defects other than congenital diaphragmatic hernia;
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Metabolic disease that necessitates a special diet other than human milk or formula feeding and or has a prognosis of impaired neurological development
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Parental refusal of participation
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- Radboud University Medical Center
- Nutricia Research
Investigators
- Principal Investigator: Viola Christmann, MD, PhD, Radboud University Medical Center
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 114536