Stiver H G, Forward K R, Livingstone R A, Fugère P, Lemay M, Verschelden G, Hunter J D, Carson G D, Beresford P, Tyrrell D L
Am J Obstet Gynecol. 1983 Jan 15;145(2):158-63. doi: 10.1016/0002-9378(83)90483-0.
A randomized double-blind placebo-controlled comparison of prophylactic cefoxitin, an antibiotic with good activity against anaerobic bacteria, with cefazolin, an agent effective predominantly against aerobes, was undertaken in 354 women who underwent nonelective cesarean section (124 receiving cefoxitin, 119 cefazolin, and 111 placebo). Among the placebo group, 24.3% developed genital tract-related infection, in comparison to 5.6% of the cefoxitin patients and 6.7% of the cefazolin patients (P less than 0.001). Standard febrile morbidity, fever index, and duration of postoperative hospital stay were also significantly less in the antibiotic prophylactic groups. For patients with febrile morbidity, the mean fever index was less in the cefoxitin group (24.8 degree-hours) than that in the cefazolin group (42.7 degree-hours), and this difference approached statistical significance (P less than 0.1, greater than 0.05). Postoperative hospital stay longer than 1 week for infectious morbidity occurred in 26% of cefoxitin patients, a significantly lower incidence compared to the 66% rate for patients who received cefazolin, and the 57% incidence for patients in the placebo group (P less than 0.05).
对354例行非选择性剖宫产的女性进行了一项随机双盲安慰剂对照试验,比较了对厌氧菌有良好活性的抗生素头孢西丁与主要对需氧菌有效的头孢唑林。其中124例接受头孢西丁,119例接受头孢唑林,111例接受安慰剂。安慰剂组中,24.3%发生了与生殖道相关的感染,而头孢西丁组为5.6%,头孢唑林组为6.7%(P<0.001)。抗生素预防组的标准发热发病率、发热指数和术后住院时间也显著更低。对于有发热发病率的患者,头孢西丁组的平均发热指数(24.8度时)低于头孢唑林组(42.7度时),且这种差异接近统计学意义(P<0.1,>0.05)。因感染性疾病术后住院时间超过1周的情况在26%的头孢西丁患者中出现,与接受头孢唑林的患者66%的发生率以及安慰剂组患者57%的发生率相比,发生率显著更低(P<0.05)。