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Description of the life style of patients and families during the course of long term HPN.
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Gastrointestinal diseases may cause intestinal failure (IF) requiring long term parenteral nutrition (PN) which is, most of the time, performed at home (HPN).
However such conditions represent a great burden for the parents and the family.
The birth of a child with such disease changes the life of the entire family including life style, leisures, social relationships and professional activities.
These condition obligate to change the personal and familial organization according to the course of the disease. The PN treatment which was seen as life saving when first started might become a burden altogether physically and psychologically for the child and his/her family.
The Necker-Enfants Malades hospital developed home PN in the early eighties as an alternative to very long hospitalizations.
Nowadays, there are 7 expert centers for HPN in France. The Necker HPN program is the oldest and the largest looking after i a third of the 400 children on HPN in France.
Our organization is based on a specializednursing team together with medical doctors specialized in pediatric clinical nutrition.
The nursing team is also a teaching team for training the parents for daily PN care. The HPN team works in collaboration with professional partners: pharmacists, dieticians, psychologists, occupational therapistsand speech specialists as well as with social workers.
Results of our clinical activities have been published in international peer review journals. However those publications reported only clinical data in terms of diagnosis, prognosis, mortality, morbidity and growth.There was any data on family quality of life (QOL) and on life style changes (LSC). In other words, by reporting only on medical aspects, there was any analyze on familial, psychosocial and professional impact of long term HPN.
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Isabelle Eicher, MSC; Yasmine Ainouz
Data sourced from clinicaltrials.gov
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