Ventilator‐free days up to day 28 · critically ill adults admitted to the ICU for trauma, emergency, or post‐surgical care; population excludes participants with acute…
1 finding from 1 review
Adverse events: aspiration (as reported by study authors at end of study · critically ill adults admitted to the ICU for trauma, emergency, or post‐surgical care; population excludes participants with acute…
It is very uncertain whether enteral changes adverse events: aspiration (as reported by study authors at end of… compared with parenteral nutrition (very low certainty).
1 finding from 1 review
Adverse events: sepsis (as reported by study authors at end of study · critically ill adults admitted to the ICU for trauma, emergency, or post‐surgical care; population excludes participants with acute…
Enteral may leads to lower adverse events: sepsis (as reported by study authors at end of study compared with parenteral nutrition (low certainty).
1 finding from 1 review
Adverse events ‐ pneumonia · critically ill adults admitted to the ICU for trauma, emergency, or post‐surgical care; population excludes participants with acute…
Enteral showed no clear difference in adverse events: pneumonia (as reported by study authors at end of… compared with parenteral nutrition (low certainty).
1 finding from 1 review
Adverse events: Vomiting · critically ill adults admitted to the ICU for trauma, emergency, or post‐surgical care; population excludes participants with acute…
It is very uncertain whether enteral changes adverse events: vomiting (as reported by study authors at end of study compared with parenteral nutrition (very low certainty).
1 finding from 1 review
All‐cause mortality · critically ill adults admitted to the ICU for trauma, emergency, or post‐surgical care; population excludes participants with acute…
Enteral showed no clear difference in mortality compared with enteral and parenteral nutrition (low certainty).
1 finding from 1 review
Number of ICU‐free days up to day 28 · critically ill adults admitted to the ICU for trauma, emergency, or post‐surgical care; population excludes participants with acute…
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Intervention not reported
Quantity and quality of sleep as measured through reports of participants or of family members or by personnel assessments Data collected at end of · adult patients in the ICU
1 finding from 1 review
Intervention not reported
Quantity and quality of sleep as measured by PSG, actigraphy, BIS, or EEG Data collected at end of · adult patients in the ICU
1 finding from 1 review
Intervention not reported
Anxiety or depression, or both Data collected at end of · adult patients in the ICU
1 finding from 1 review
Intervention not reported
Mortality Study authors did not report final timepoint for data collection. · adult patients in the ICU
1 finding from 1 review
Intervention not reported
Length of stay in the ICU · adult patients in the ICU
1 finding from 1 review
Intervention not reported
Adverse events (such as nausea, dizziness and headache) Data collected at end of · adult patients in the ICU
1 finding from 1 review
Intervention not reported
Functional exercise capacity Multiple different outcome measures used SF‐36 PF and AT (at 9 and 26 weeks) (Batterham 2014) SF‐36 PF and 6MWT (at 8 and 26 weeks) (Elliott 2011) ABC, Katz, TUAG (at 3 months) (Jackson 2012) SF‐36 PCS ( · adult survivors of critical illness
1 finding from 1 review
Intervention not reported
Health‐related quality of life Multiple different outcome measures used EQ‐5D and EQ‐5D VAS (9 and 26 weeks) (Batterham 2014) SF‐36 PCS and MCS (8 and 26 weeks) (Elliott 2011) · adult survivors of critical illness
1 finding from 1 review
Intervention not reported
Withdrawals Participant withdrawal following randomization before or during receipt of the intervention because of consent or medical reason · adult survivors of critical illness
1 finding from 1 review
Intervention not reported
Adherence Participant completion of the intervention as described in the trial method · adult survivors of critical illness
1 finding from 1 review
Intervention not reported
Mortality Death at any point during the trial duration · adult survivors of critical illness
1 finding from 1 review
Intervention not reported
Loss to · adult survivors of critical illness
1 finding from 1 review
Intervention not reported
Other adverse events Non‐mortality · adult survivors of critical illness
1 finding from 1 review