Impact of SPN on Infection Rate, Duration of Mechanical Ventilation & Rehabilitation in ICU Patients
Critically Ill
About this trial
This is an interventional supportive care trial for Critically Ill focused on measuring Critically ill, nutrition, randomised controlled clinical trial, human, adult, Supplemental parenteral nutrition
Eligibility Criteria
Inclusion Criteria:
- Expected ICU stay > 5 days
- Expected survival > 7 days
- No contraindication to EN
- Obtained informed consent
Exclusion Criteria:
- Refusal of consent
- Age < 18 years
- Short bowel syndrome
- Significant persistent gastrointestinal dysfunction with ileus
- High output proximal fistula (> 1.5 liter/d)
- Patients receiving PN
Sites / Locations
- Service of Intensive Care, Geneva University Hospital,
- Service de Médecine Intensive Adulte et Centre des Brûlés
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
SPN group
Control gr
experimental arm: Supplemental Parenteral Nutrition (SPN) is added to enteral nutrition (EN) to reach 100% of their predicted energy needs from ICU day 4. In the treated group, SPN is started if at day 4 energy input by EN is < 60% of energy target in order to reach 100% of energy target by peripheral or central line. Nutritional products as currently used in our institution. SPN is composed of EN and PN, both techniques being currently used in our institution.
EN : start EN at 20-30 ml/h per day up to maximal 150 ml/h per day; or day1: 500 ml, day2: 1000 ml, day3: 1500 ml of EN dependant on gastrointestinal tolerance (gastric residue volume more than 500ml). Nutritional products as currently used in our institution.