TY - JOUR
T1 - A Comparative Study of Ceftizoxime and Cefazolin Prophylaxis in Upper Digestive Tract and Biliary Surgery
T2 - A Prospective Randomised Clinical Trial
AU - The Cooperative Study Group
AU - Hashizume, M.
AU - Sugimachi, K.
N1 - Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 1993/1
Y1 - 1993/1
N2 - In a prospective randomised multicentre study, the effects of cefazolin sodium and ceftizoxime on the prevention of postoperative infection were investigated in 117 patients undergoing abdominal surgery. Each drug was administered intravenously twice daily (cefazolin 4 g/day or ceftizoxime 2 g/day) for 5 days postoperatively. No statistically significant difference was noted in the incidence of infection between the 2 treated groups (cefazolin 11.5% and ceftizoxime 8.9%), and there were no serious adverse events in either group. The fever index was significantly higher in patients with postoperative infections when compared with noninfected individuals in both treatment groups, but showed no correlation with age, time of surgery or blood loss. In terms of cost, prophylactic treatment with cefazolin is recommended for such patients with a low level of anaerobic contamination.
AB - In a prospective randomised multicentre study, the effects of cefazolin sodium and ceftizoxime on the prevention of postoperative infection were investigated in 117 patients undergoing abdominal surgery. Each drug was administered intravenously twice daily (cefazolin 4 g/day or ceftizoxime 2 g/day) for 5 days postoperatively. No statistically significant difference was noted in the incidence of infection between the 2 treated groups (cefazolin 11.5% and ceftizoxime 8.9%), and there were no serious adverse events in either group. The fever index was significantly higher in patients with postoperative infections when compared with noninfected individuals in both treatment groups, but showed no correlation with age, time of surgery or blood loss. In terms of cost, prophylactic treatment with cefazolin is recommended for such patients with a low level of anaerobic contamination.
UR - http://www.scopus.com/inward/record.url?scp=0027510688&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0027510688&partnerID=8YFLogxK
U2 - 10.1007/BF03259229
DO - 10.1007/BF03259229
M3 - Article
AN - SCOPUS:0027510688
SN - 1173-2563
VL - 5
SP - 63
EP - 68
JO - Clinical Drug Investigation
JF - Clinical Drug Investigation
IS - 1
ER -