TY - JOUR
T1 - Hextend®, a physiologically balanced plasma expander for large volume use in major surgery
T2 - A randomized phase III clinical trial
AU - Gan, T. J.
AU - Bennett-Guerrero, E.
AU - Phillips-Bute, B.
AU - Wakeling, H.
AU - Moskowitz, D. M.
AU - Olufolabi, Y.
AU - Konstadt, S. N.
AU - Bradford, C.
AU - Glass, P. S.A.
AU - Machin, S. J.
AU - Mythen, M. G.
AU - Booth, J. V.
AU - Bronheim, D. S.
AU - Robertson, C.
AU - Feierman, D. E.
AU - Kucmeroski, D.
AU - Gabrielson, G. V.
AU - Dufore, S.
AU - Sampson, I. H.
AU - Robertson, K. M.
AU - Scarola, S. B.
AU - Hilton, A. B.
AU - Winfree, W. J.
AU - Woolf, R. L.
AU - Mackie, I. J.
PY - 1999
Y1 - 1999
N2 - Hextend® (BioTime, Inc., Berkeley, CA) is a new plasma volume expander containing 6% hetastarch, balanced electrolytes, a lactate buffer, and physiological levels of glucose. In preclinical studies, its use in shock models was associated with an improvement in outcome compared with alternatives, such as albumin or 6% hetastarch in saline. In a prospective, randomized, two-center study (n = 120), we compared the efficacy and safety of Hextend® versus 6% hetastarch in saline (HES) for the treatment of hypovolemia during major surgery. Patients at one center had a blood sample drawn at the beginning and the end of surgery for thromboelastographic (TEG) analysis. Hextend® was as effective as HES for the treatment of hypovolemia. Patients received an average of 1596 mL of Hextend®: 42% received >20 mL/kg up to a total of 5000 mL. No patient received albumin. Hextend®-treated patients required less intraoperative calcium (4 vs 220 mg; P < 0.05). In a subset analysis of patients receiving red blood cell transfusions (n = 56; 47%), Hextend®-treated patients had a lower mean estimated blood loss (956 mL less; P = 0.02) and were less likely to receive calcium supplementation (P = 0.04). Patients receiving HES demonstrated significant prolongation of time to onset of clot formation (based on TEG) not seen in the Hextend® patients (P < 0.05). No Hextend® patient experienced a related serious adverse event, and there was no difference in the total number of adverse events between the two groups. The results of this study demonstrate that Hextend®, with its novel buffered, balanced electrolyte formulation, is as effective as 6% hetastarch in saline for the treatment of hypovolemia and may be a safe alternative even when used in volumes up to 5 L. Implications: Hextend® (BioTime, Inc., Berkeley, CA) is a new plasma volume expander containing 6% hetastarch, balanced electrolytes, a lactate buffer, and a physiological level of glucose. It is as effective as 6% hetastarch in saline for the treatment of hypovolemia but has a more favorable side effects profile in volumes of up to 5 L compared with 6% hetastarch in saline.
AB - Hextend® (BioTime, Inc., Berkeley, CA) is a new plasma volume expander containing 6% hetastarch, balanced electrolytes, a lactate buffer, and physiological levels of glucose. In preclinical studies, its use in shock models was associated with an improvement in outcome compared with alternatives, such as albumin or 6% hetastarch in saline. In a prospective, randomized, two-center study (n = 120), we compared the efficacy and safety of Hextend® versus 6% hetastarch in saline (HES) for the treatment of hypovolemia during major surgery. Patients at one center had a blood sample drawn at the beginning and the end of surgery for thromboelastographic (TEG) analysis. Hextend® was as effective as HES for the treatment of hypovolemia. Patients received an average of 1596 mL of Hextend®: 42% received >20 mL/kg up to a total of 5000 mL. No patient received albumin. Hextend®-treated patients required less intraoperative calcium (4 vs 220 mg; P < 0.05). In a subset analysis of patients receiving red blood cell transfusions (n = 56; 47%), Hextend®-treated patients had a lower mean estimated blood loss (956 mL less; P = 0.02) and were less likely to receive calcium supplementation (P = 0.04). Patients receiving HES demonstrated significant prolongation of time to onset of clot formation (based on TEG) not seen in the Hextend® patients (P < 0.05). No Hextend® patient experienced a related serious adverse event, and there was no difference in the total number of adverse events between the two groups. The results of this study demonstrate that Hextend®, with its novel buffered, balanced electrolyte formulation, is as effective as 6% hetastarch in saline for the treatment of hypovolemia and may be a safe alternative even when used in volumes up to 5 L. Implications: Hextend® (BioTime, Inc., Berkeley, CA) is a new plasma volume expander containing 6% hetastarch, balanced electrolytes, a lactate buffer, and a physiological level of glucose. It is as effective as 6% hetastarch in saline for the treatment of hypovolemia but has a more favorable side effects profile in volumes of up to 5 L compared with 6% hetastarch in saline.
UR - http://www.scopus.com/inward/record.url?scp=0033124320&partnerID=8YFLogxK
U2 - 10.1097/00000539-199905000-00005
DO - 10.1097/00000539-199905000-00005
M3 - Article
C2 - 10320157
AN - SCOPUS:0033124320
SN - 0003-2999
VL - 88
SP - 992
EP - 998
JO - Anesthesia and Analgesia
JF - Anesthesia and Analgesia
IS - 5
ER -