TY - JOUR
T1 - Plasma aluminum levels during sucralfate prophylaxis for stress ulceration in critically ill patients on continuous venovenous hemofiltration
T2 - A randomized, controlled trial
AU - Mulla, Hussain
AU - Peek, Giles
AU - Upton, David
AU - Lin, Edward
AU - Loubani, Mahmoud
PY - 2001
Y1 - 2001
N2 - Objective: To investigate plasma aluminum levels in critically ill patients requiring continuous venovenous hemofiltration (CVVH), while receiving sucralfate for stress ulcer prophylaxis. Design: Randomized, controlled study. Setting: Cardiothoracic intensive care unit. Patients: Twenty postoperative cardiac surgical patients Interventions: Twenty patients requiring CVVH support for acute renal failure were randomized into two groups for concurrent stress ulcer prophylaxis. Group 1 (n = 10) received nasogastric sucralfate, and group 2 patients received intravenous ranitidine. Plasma aluminum samples were analyzed at baseline and on days 1, 4, 8, and 14. Measurements and Main Results: In both the sucralfate and ranitidine groups, clinical characteristics, number of days the patients were on CVVH support (median, 5.5 [range, 2-32] days, and median, 3 [range, 2-18] days, respectively) and duration of prophylaxis (median, 12 [range, 4-42] days, and median, 16 [range, 3-62] days, respectively) were similar. There were no significant differences in the baseline aluminum concentrations (median, 0.37 [range, 0.15-1.63] μmol/L, vs. median, 0.32 [range, 0.11-1.0] μmol/L; p = .79). On initiation of therapy, aluminum levels in the sucralfate group increased dramatically on day 1 (median, 0.87 [range, 0.26-4.4] μmol/L) and peaked on day 4 (median, 2.84 [range, 1.52-4.44] μmol/L) with seven of the ten patients exhibiting levels of >2 μmol/L. In the ranitidine group, there were no significant elevations in aluminum levels above baseline. Analysis of the two groups at the four time points revealed that aluminum levels in the sucralfate group were up to 14 times higher, with the confidence intervals suggesting that the true value may be 2-27 times higher (p < .0001). On cessation of CVVH, a rapid decline in aluminum levels was observed. No clinical manifestations of these potentially toxic levels were observed. Conclusions: The use of sucralfate for stress ulcer prophylaxis in patients requiring CVVH results in toxic elevations in plasma aluminum levels. Alternative agents should be considered for prophylaxis in these patients.
AB - Objective: To investigate plasma aluminum levels in critically ill patients requiring continuous venovenous hemofiltration (CVVH), while receiving sucralfate for stress ulcer prophylaxis. Design: Randomized, controlled study. Setting: Cardiothoracic intensive care unit. Patients: Twenty postoperative cardiac surgical patients Interventions: Twenty patients requiring CVVH support for acute renal failure were randomized into two groups for concurrent stress ulcer prophylaxis. Group 1 (n = 10) received nasogastric sucralfate, and group 2 patients received intravenous ranitidine. Plasma aluminum samples were analyzed at baseline and on days 1, 4, 8, and 14. Measurements and Main Results: In both the sucralfate and ranitidine groups, clinical characteristics, number of days the patients were on CVVH support (median, 5.5 [range, 2-32] days, and median, 3 [range, 2-18] days, respectively) and duration of prophylaxis (median, 12 [range, 4-42] days, and median, 16 [range, 3-62] days, respectively) were similar. There were no significant differences in the baseline aluminum concentrations (median, 0.37 [range, 0.15-1.63] μmol/L, vs. median, 0.32 [range, 0.11-1.0] μmol/L; p = .79). On initiation of therapy, aluminum levels in the sucralfate group increased dramatically on day 1 (median, 0.87 [range, 0.26-4.4] μmol/L) and peaked on day 4 (median, 2.84 [range, 1.52-4.44] μmol/L) with seven of the ten patients exhibiting levels of >2 μmol/L. In the ranitidine group, there were no significant elevations in aluminum levels above baseline. Analysis of the two groups at the four time points revealed that aluminum levels in the sucralfate group were up to 14 times higher, with the confidence intervals suggesting that the true value may be 2-27 times higher (p < .0001). On cessation of CVVH, a rapid decline in aluminum levels was observed. No clinical manifestations of these potentially toxic levels were observed. Conclusions: The use of sucralfate for stress ulcer prophylaxis in patients requiring CVVH results in toxic elevations in plasma aluminum levels. Alternative agents should be considered for prophylaxis in these patients.
KW - Acute
KW - Aluminum
KW - Critical illness
KW - Drug toxicity
KW - Hemofiltration
KW - Histamine H
KW - Kidney failure
KW - Mechanical ventilation
KW - Plasma
KW - Receptor antagonists
KW - Renal replacement therapy
KW - Stress ulcer prophylaxis
KW - Sucralfate
UR - http://www.scopus.com/inward/record.url?scp=0035113409&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0035113409&partnerID=8YFLogxK
U2 - 10.1097/00003246-200102000-00008
DO - 10.1097/00003246-200102000-00008
M3 - Article
C2 - 11246304
AN - SCOPUS:0035113409
SN - 0090-3493
VL - 29
SP - 267
EP - 271
JO - Critical care medicine
JF - Critical care medicine
IS - 2
ER -