Enteral Nutrition, Oral Aversion, Parenteral Nutrition, Tube Feeding
Conditions
Brief summary
The goal of this Retrospective Cohort Study is to compare the patients from before and after the implementation of the pre-convention for infants with feeding difficulties needing tube feeding or having received tube feeding in the past, but able to develop normal feeding behavior. The main objectives it aims to compare are: * To characterize the patients taking part in a multi-disciplinary follow-up for feeding difficulties over time and to evaluate their progress before and after the institution of a multidisciplinary team in the context of the pre-convention for feeding difficulties from the RIZIV/INAMI. * To evaluate if the multi-disciplinary approach is more efficient for treatment and follow-up in infants with eating difficulties before and after the start of the pre-convention. * To calculate the probability of reaching full oral intake after having feeding difficulties within two years.
Interventions
Since 2010, a structured multidisciplinary team was formed to evaluate the child medically, support its nutrition, teach, treat and educate the children and parents and guide them through the process to obtain a normal and independent feeding behavior. The multidisciplinary team must have special expertise regarding digestive and nutritional as well as sensory and oral motor problems in children requiring artificial nutrition. The team must at least consist of a pediatrician, a dietician with experience in artificial nutrition in children, a speech therapist and/or physical therapist and a psychologist or orthopedagogue. The team should also be able to rely on a nurse with experience in artificial nutrition, a social assistant and a secretary.
Sponsors
Study design
Eligibility
Inclusion criteria
* Children consulting a pediatric gastroenterologist for feeding problems in UZB between the 1st of January 2000 and the 31st of December 2021 and receiving the label feeding difficulties. The infants have a pediatric feeding disorder that prevent them from feeding normally by oral means. * The infants need or have needed (enteral or parenteral) artificial nutrition. * The infants are aged between 0 and 12 years at their first presentation. * The infants are capable of developing normal feeding behavior.
Exclusion criteria
* Have no 6-months follow-up available. * Parents refusal to enter a multi-disciplinary approach for the feeding problems of their children.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Growth (weight-for-height Z-scores) | at 3, 6, 12, 18 months and 2 years |
Secondary
| Measure | Time frame |
|---|---|
| Comparing the mean of the 2 groups of total number of days tube fed | At 3, 6, 12, 18 months and 2 years |
| Comparing the mean of the 2 groups of the percentage of intake through tube feeding | At 3, 6, 12, 18 months and 2 years |
Other
| Measure | Time frame |
|---|---|
| Compare how many infants completed full oral intake after two years before and after the implementation of the pre-convention for feeding difficulties. | 2 years |
| Compare the percentage of tube feeding that remains in the group that was unable to achieve full oral intake after one year, before and after the implementation of the pre-convention for feeding difficulties. | 1 year |
Countries
Belgium