The Multi-disciplinary Approach of Children With Feeding Difficulties and Tube Feeding in UZB Between 2000 and 2021

NCT06161350 | Unknown

• 1 other identifier: ORALAV
• Study Type: observational
• Target: 330
• Locations: 1 country
• Sites: 1

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.

Conditions

Oral Aversion; Enteral Nutrition; Parenteral Nutrition; Tube Feeding

Outcome Measures

Primary Outcomes (1)

• Growth (weight-for-height Z-scores)

  at 3, 6, 12, 18 months and 2 years

Secondary Outcomes (2)

• 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 Outcomes (2)

• 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

Study Arms (2)

Group 1

Infants who consulted between January 1st 2000 and December 31st 2009 (this is before the implementation of the pre-convention). Inclusion criteria: * Children consulting a pediatric gastroenterologist for feeding problems in UZB between the 1st of January 2000 and the 31st of December 2009 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. Infants will be excluded from this study if they: * Have no 6-months follow-up available. * Parents refusal to enter a multi-disciplinary approach for the feeding problems of their children.

Group 2

Infants who consulted after the implementation of the pre-convention, who consulted between January 1st 2010 and December 31st 2021. Inclusion criteria: * Children consulting a pediatric gastroenterologist for feeding problems in UZB between the 1st of January 2010 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. Infants will be excluded from this study if they: * Have no 6-months follow-up available. * Parents refusal to enter a multi-disciplinary approach for the feeding problems of their children.

Combination Product: Structured multi-disciplinary approach

Interventions

Structured multi-disciplinary approach COMBINATION_PRODUCT

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.

Group 2

Eligibility Criteria

• Age: Up to 12 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17)
• Sampling Method: Non-Probability Sample

Study Population

Infants with feeding difficulties needing tube feeding or having received tube feeding in the past, capable of developing normal feeding behavior.

You may qualify if:

• 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.

You may not qualify if:

• Have no 6-months follow-up available.
• Parents refusal to enter a multi-disciplinary approach for the feeding problems of their children.

Sponsors & Collaborators

• Universitair Ziekenhuis Brussel: lead

Study Sites (1)

Universitair Ziekenhuis Brussel

Jette, Brussels Capital, 1090, Belgium

Location

MeSH Terms

Conditions

Hyperphagia

Condition Hierarchy (Ancestors)

Signs and Symptoms, Digestive; Signs and Symptoms; Pathological Conditions, Signs and Symptoms

Study Officials

• Elisabeth De Greef, MD, PhD

  Universitair Ziekenhuis Brussel

  PRINCIPAL INVESTIGATOR

• Koen Huysentruyt, MD, PhD

  Universitair Ziekenhuis Brussel

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: RETROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Prof. Dr. De Greef

Study Record Dates

• First Submitted: November 29, 2023
• First Posted: December 7, 2023
• Study Start: November 8, 2023
• Primary Completion: September 30, 2024
• Study Completion: September 30, 2024
• Last Updated: December 7, 2023

Record last verified: 2023-11

Locations

BE (1)