Human Milk for Congenital Gastrointestinal Disorders (HM for CGD)
Congenital Gastrointestinal Disorders
About this trial
This is an interventional other trial for Congenital Gastrointestinal Disorders focused on measuring Digestive Disease and Disorders, Neonatal, Pediatric Disorders
Eligibility Criteria
Inclusion Criteria:
- Admission to participating NICU at less than 7 days of age
- Birthweight >1250g and/or gestational age at birth >32 weeks
- Less than 7 days of enteral feedings
- Diagnosis of eligible primary "Congenital Gastointestinal Disorders" defined as: gastroschisis, omphalocele and intestinal atresias
- Consent to the use of donor human milk products
- Consent to participate in this study
Exclusion Criteria:
- Admission to participating NICU at >7 days of age
- Birthweight <1250g and/or gestational age <32 weeks
- Diagnosis of non-eligible gastrointestinal disorders: congenital diaphragmatic hernia, midgut volvulus, Hirschsprung's disease, esophageal atresia, imperforate anus
- Evidence of significant liver dysfunction at time of enrollment (direct bilirubin >4 and transaminases elevated more than 2 SD above upper limit of normal for age)
- Liver malformations such as biliary atresia and choledochal cyst
- Refusal of consent
Sites / Locations
- Children's Healthcare of Atlanta-Egleston
Arms of the Study
Arm 1
Arm 2
No Intervention
Experimental
Retrospective Control Group
Exclusive Human Milk Diet Group
Approximately 150 patients with congenital gastrointestinal disorders who were treated in the neonatal intensive care unit (NICU) at Children's Healthcare of Atlanta-Egleston and other participating institutions from 2012 to 2015, who had non-human milk (HM) diets will be identified as retrospective controls using the electronic medical records system.
A minimum of 150 patients with CGD admitted to participating NICUs who meet inclusion criteria and provide informed consent will be enrolled in the prospective arm of the study. These patients will be fed an EHMD comprised of mother's own milk (MOM) or pasteurized donor human milk (DM). Fortification will be provided with human milk derived human milk fortifier, either a human milk-based fortifier (Prolact+ H2MF®) for infants born at less than 37 weeks GA or <2,200g birth weight or the term-equivalent version (PBCLN-002) formulated for infants >37 weeks and/or >2,200g at birth. Infants will receive this EHMD until they have achieved full enteral feedings for 7 days with bowel in continuity