Skip to main content

Table 4 Primary end points in included studies and results for EPN, LPN and EN groups

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

  1. RCT, randomized control trial; ICU, intensive care unit; x, not investigated as a primary end point; LPN, late parenteral nutrition; EPN, early parenteral nutrition; HR, hazard ratio; 95% CI, 95% confidence interval; p, p-value; vs, versus; RD, risk difference; EN, enteral nutrition. NB: studies used different definitions for EPN, LPN and EN. In the study by Cahill et al. [12], no primary end point was described.