Protein-energy Enriched Milk for Infants With Bronchiolitis
- Conditions
- Bronchiolitis
- Interventions
- Dietary Supplement: Infatrini® or Infatrini Peptisorb®
- Registration Number
- NCT02316015
- Lead Sponsor
- Universitair Ziekenhuis Brussel
- Brief Summary
The aim of this study is to investigate if a standardized nutritional intervention with a protein and energy enriched milk could help overcome the catabolic state in children hospitalized with a bronchiolitis and thus creating a better nutritional state during hospitalization and at outpatient follow-up.
The investigators also want to assess the clinical repercussion on the number of hospitalization days, the duration of oxygen support and the quality of life at ouptatient follow-up.
- Detailed Description
In this study, the investigators aim to assess the effect protein-energy enriched milk to reverse the catabolic state (weight loss, change in mid-upper arm circumference and tricpes skin fold) on the short term and failure to thrive (degree of weight recovery, change in arm circumference) one week after discharge in infants with moderate to severe bronchiolitis. The secondary short term aims are to investigate the effect on the length of hospital stay, days of oxygen support and the rate of antibiotic use. Secondary long term outcomes are the re-admission rate, the persistence of wheezing and the number of work days missed by the parents.
The investigators hypothesize that in those children who received a protein-energy enriched milk during hospitalization the catabolic state will be reversed more quickly by the intervention and will need less hospitalisation days, less oxygen support, less antibiotic use, less re-admission rate, less persistent wheezing and less work days missed by the parents. The investigators also hypothesize that the effects of the nutritional intervention on the proposed outcome parameters will be greater in children screened at high nutritional risk.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 44
- All children hospitalized at the paediatric wards of UZ Brussel with the diagnosis of moderate to severe bronchiolitis
- Not meeting their normal oral intake are eligible for inclusion between the beginning of December and the end of February 2014
- Bronchiolitis will be defined as a constellation of clinical symptoms and signs that typically begin with rhinitis and cough, and may progress to tachypnea, wheezing, rales, use of accessory muscles and/or nasal flaring
- Children admitted to the paediatric intensive care unit
- Children in whom it is unsafe to place a nasogastric tube (e.g. severe mucositis, platelet count <50.000/µl)
- Children unwilling or unable to participate
- Children that are breast fed
- Children over the age of 12 months
- Children with an underlying malabsorption disease
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Intervention group Infatrini® or Infatrini Peptisorb® Children in the intervention group will receive a protein-energy enriched milk (Infatrini®, or in the case of children on a partial or fully hydrolized milk Infatrini Peptisorb®). The volume of milk offered will be the same quantity as they usually drink at home (within the limits of 120-170 ml/kg/day). The intervention will be carried out during the first 7 days of hospitalisation, or until the day of discharge (if hospitalized for less than 7 days).
- Primary Outcome Measures
Name Time Method Evolution of nutritional status during hospitalization Hospital stay (mean 5 days) The change in followong parameters will be assessed:
* Change in weight for age z-score
* Change in mid upper arm circumference z-score
* Change in triceps skin fold (mm)
- Secondary Outcome Measures
Name Time Method Evolution of nutritional status at outpatient follow-up 1 week after discharge - Change in WFA z-score, weight for height z-score, MUAC z-score and TSF (mm)
Trial Locations
- Locations (1)
UZ Brussel
🇧🇪Jette, Belgium