TY - JOUR
T1 - One year outcomes in patients with acute lung injury randomised to initial trophic or full enteral feeding
T2 - Prospective follow-up of EDEN randomised trial
AU - Needham, Dale M.
AU - Dinglas, Victor D.
AU - Bienvenu, O. Joseph
AU - Colantuoni, Elizabeth
AU - Wozniak, Amy W.
AU - Rice, Todd W.
AU - Hopkins, Ramona O.
PY - 2013/4/20
Y1 - 2013/4/20
N2 - Objective: To evaluate the effect of initial low energy permissive underfeeding ("trophic feeding") versus full energy enteral feeding ("full feeding") on physical function and secondary outcomes in patients with acute lung injury. Design: Prospective longitudinal follow-up evaluation of the NHLBI ARDS Clinical Trials Network's EDEN trial Setting: 41hospitals in the United States. Participants: 525 patients with acute lung injury. Interventions: Randomised assignment to trophic or full feeding for up to six days; thereafter, all patients still receiving mechanical ventilation received full feeding. Measurements: Blinded assessment of the age and sex adjusted physical function domain of the SF-36 instrument at 12 months after acute lung injury. Secondary outcome measures included survival; physical, psychological, and cognitive functioning; quality of life; and employment status at six and 12 months. Results: After acute lung injury, patients had substantial physical, psychological, and cognitive impairments, reduced quality of life, and impaired return to work. Initial trophic versus full feeding did not affect mean SF-36 physical function at 12 months (55 (SD 33) v 55 (31), P=0.54), survival to 12 months (65% v 63%, P=0.63), or nearly all of the secondary outcomes. Conclusion: In survivors of acute lung injury, there was no difference in physical function, survival, or multiple secondary outcomes at 6 and 12 month follow-up after initial trophic or full enteral feeding. Trial Registration: NCT No 00719446.
AB - Objective: To evaluate the effect of initial low energy permissive underfeeding ("trophic feeding") versus full energy enteral feeding ("full feeding") on physical function and secondary outcomes in patients with acute lung injury. Design: Prospective longitudinal follow-up evaluation of the NHLBI ARDS Clinical Trials Network's EDEN trial Setting: 41hospitals in the United States. Participants: 525 patients with acute lung injury. Interventions: Randomised assignment to trophic or full feeding for up to six days; thereafter, all patients still receiving mechanical ventilation received full feeding. Measurements: Blinded assessment of the age and sex adjusted physical function domain of the SF-36 instrument at 12 months after acute lung injury. Secondary outcome measures included survival; physical, psychological, and cognitive functioning; quality of life; and employment status at six and 12 months. Results: After acute lung injury, patients had substantial physical, psychological, and cognitive impairments, reduced quality of life, and impaired return to work. Initial trophic versus full feeding did not affect mean SF-36 physical function at 12 months (55 (SD 33) v 55 (31), P=0.54), survival to 12 months (65% v 63%, P=0.63), or nearly all of the secondary outcomes. Conclusion: In survivors of acute lung injury, there was no difference in physical function, survival, or multiple secondary outcomes at 6 and 12 month follow-up after initial trophic or full enteral feeding. Trial Registration: NCT No 00719446.
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U2 - 10.1136/bmj.f1532
DO - 10.1136/bmj.f1532
M3 - Article
C2 - 23512759
AN - SCOPUS:84876158749
SN - 0959-8146
VL - 346
JO - BMJ (Online)
JF - BMJ (Online)
IS - 7904
M1 - f1532
ER -