From: Timing of (supplemental) parenteral nutrition in critically ill patients: a systematic review
Primary end points | Studies | |||||
---|---|---|---|---|---|---|
RCT | Prospective observational study | |||||
Bauer 2000[[11]] | Casaer 2011[[13]] | Doig 2013[[14]] | Heidegger 2013[[15]] | Cahill 2011 [[12]] | Kutsogiannis 2011[[16]] | |
ICU length of stay (median days) | x | 3 days (LPN) vs 4 days (EPN); HR 1.06; 95% CI 1.00 to 1.13; p = 0.04 | x | x | x | x |
Mortality; day 60 | x | x | 22.8% (standard care) vs 21.5% (EPN), RD −1.26%; 95% CI −6.6 to 4.1; p = 0.60 | x | x | x |
Nosocomial infection between days 9 to 28 | x | x | x | 27% (EN + LPN) vs 38% (EN); HR 0.65, 95% CI 0.43 to 0.97; p = 0.0338 | x | x |
Alive discharge from hospital | x | x | x | x | x | EN + EPN vs EN: HR 0.75; 95% CI 0.59 to 0.96; EN + LPN vs EN: HR 0.64, 95% CI 0.51 to 0.81 |
Retinol-binding protein (RBP) | Significant increase in EN + EPN vs EN + placebo from day 0 to day 7; p = 0.0496 | x | x | x | x | x |
Prealbumin | Significant increase in EPN vs placebo (day 0 to day 7); p = 0.0369 | x | x | x | x | x |