TY - JOUR
T1 - A comparison of albumin and saline for fluid resuscitation in the intensive care unit
AU - SAFE Study Investigators
AU - Finfer, S.
AU - Bellomo, R.
AU - Boyce, N.
AU - French, J.
AU - Myburgh, J.
AU - Norton, R.
AU - Doig, G.
AU - Hayek, M.
AU - O'Donnell, S.
AU - Bell, A.
AU - Blythe, D.
AU - Cade, J.
AU - Chapman, M.
AU - Cole, L.
AU - Cooper, J.
AU - Davies, A.
AU - French, C.
AU - Joyce, C.
AU - McArthur, C.
AU - MacMahon, S.
AU - Neal, B.
AU - Presneill, J.
AU - Saul, P.
AU - Seppelt, I.
AU - Stephens, D.
AU - Turner, A.
AU - Williams, A.
AU - Woolfe, C.
AU - Peto, R.
AU - Sandercock, P.
AU - Sprung, C.
AU - Young, D.
AU - Correction Lo, S. K.
AU - Sivarajasingham, S.
AU - Francis, L.
AU - Woodward, M.
AU - Charlton, J.
AU - Cooper, J.
AU - Davies, A.
AU - Harry, C.
AU - Higgins, L.
AU - Moulden, K.
AU - Vallance, S.
AU - Chadderton, J.
AU - Newby, L.
AU - McArthur, C.
AU - Bates, S.
AU - Goldsmith, D.
AU - Voss, A.
AU - Blythe, D.
AU - Palermo, A.
AU - Francis, L.
AU - French, J.
AU - Hayek, M.
AU - Jayne, K.
AU - MacMahon, S.
AU - Merai, M.
AU - Neal, B.
AU - Norton, R.
AU - Pandey, S.
AU - O'Donnell, S.
AU - Schmidt, M.
AU - Sivarajasingham, S.
AU - Woodward, M.
AU - Carroll, R.
AU - McFadyen, B.
AU - Saul, P.
AU - Clarke, J.
AU - Powell, J.
AU - Williams, A.
AU - Tai, J.
AU - Cole, L.
AU - Hynesova, I.
AU - Seppelt, I.
AU - Weisbrodt, L.
AU - Bradley, L.
AU - Joyce, C.
AU - Kelly, T.
AU - Limpus, A.
AU - Moore, R.
AU - Chapman, M.
AU - Creed, S.
AU - Kaplan, S.
AU - Rivett, J.
AU - Stephens, D.
AU - Thomas, J.
AU - Bell, A.
AU - Marsden, K.
AU - Turner, A.
AU - Boyce, C.
AU - Cade, J.
AU - Howe, B.
AU - Presneill, J.
AU - Robertson, M.
AU - Doig, G.
AU - Finfer, S.
AU - O'Connor, A.
AU - Potter, J.
AU - Ramakrishnan, N.
AU - Powell, C.
AU - Rajbhandari, D.
AU - Woolfe, C.
AU - Girling, K.
AU - Hodgetts, M.
AU - Jovanovska, A.
AU - Myburgh, J.
AU - French, C.
AU - Little, L.
PY - 2004/5/27
Y1 - 2004/5/27
N2 - BACKGROUND: It remains uncertain whether the choice of resuscitation fluid for patients in intensive care units (ICUs) affects survival. We conducted a multicenter, randomized, double-blind trial to compare the effect of fluid resuscitation with albumin or saline on mortality in a heterogeneous population of patients in the ICU. METHODS: We randomly assigned patients who had been admitted to the ICU to receive either 4 percent albumin or normal saline for intravascular-fluid resuscitation during the next 28 days. The primary outcome measure was death from any cause during the 28-day period after randomization. RESULTS: Of the 6997 patients who underwent randomization, 3497 were assigned to receive albumin and 3500 to receive saline; the two groups had similar baseline characteristics. There were 726 deaths in the albumin group, as compared with 729 deaths in the saline group (relative risk of death, 0.99; 95 percent confidence interval, 0.91 to 1.09; P=0.87). The proportion of patients with new single-organ and multiple-organ failure was similar in the two groups (P=0.85). There were no significant differences between the groups in the mean (±SD) numbers of days spent in the ICU (6.5±6.6 in the albumin group and 6.2±6.2 in the saline group, P=0.44), days spent in the hospital (15.3±9.6 and 15.6±9.6, respectively; P=0.30), days of mechanical ventilation (4.5±6.1 and 4.3±5.7, respectively; P=0.74), or days of renal-replacement therapy (0.5±2.3 and 0.4±2.0, respectively; P=0.41). CONCLUSIONS: In patients in the ICU, use of either 4 percent albumin or normal saline for fluid resuscitation results in similar outcomes at 28 days.
AB - BACKGROUND: It remains uncertain whether the choice of resuscitation fluid for patients in intensive care units (ICUs) affects survival. We conducted a multicenter, randomized, double-blind trial to compare the effect of fluid resuscitation with albumin or saline on mortality in a heterogeneous population of patients in the ICU. METHODS: We randomly assigned patients who had been admitted to the ICU to receive either 4 percent albumin or normal saline for intravascular-fluid resuscitation during the next 28 days. The primary outcome measure was death from any cause during the 28-day period after randomization. RESULTS: Of the 6997 patients who underwent randomization, 3497 were assigned to receive albumin and 3500 to receive saline; the two groups had similar baseline characteristics. There were 726 deaths in the albumin group, as compared with 729 deaths in the saline group (relative risk of death, 0.99; 95 percent confidence interval, 0.91 to 1.09; P=0.87). The proportion of patients with new single-organ and multiple-organ failure was similar in the two groups (P=0.85). There were no significant differences between the groups in the mean (±SD) numbers of days spent in the ICU (6.5±6.6 in the albumin group and 6.2±6.2 in the saline group, P=0.44), days spent in the hospital (15.3±9.6 and 15.6±9.6, respectively; P=0.30), days of mechanical ventilation (4.5±6.1 and 4.3±5.7, respectively; P=0.74), or days of renal-replacement therapy (0.5±2.3 and 0.4±2.0, respectively; P=0.41). CONCLUSIONS: In patients in the ICU, use of either 4 percent albumin or normal saline for fluid resuscitation results in similar outcomes at 28 days.
UR - http://www.scopus.com/inward/record.url?scp=84926232888&partnerID=8YFLogxK
U2 - 10.1056/NEJMoa040232
DO - 10.1056/NEJMoa040232
M3 - Article
C2 - 15163774
AN - SCOPUS:84926232888
SN - 0028-4793
VL - 350
SP - 2247
EP - 2256
JO - New England Journal of Medicine
JF - New England Journal of Medicine
IS - 22
ER -