Padilla S L, Spence M R, Beauchamp P J
Obstet Gynecol. 1983 Apr;61(4):463-6.
A single 2-g dose of ampicillin or a placebo identical in appearance was administered intravenously in a randomized, prospective, double-blind manner to 71 patients undergoing cesarean section. The solutions were given either on call to the operating room or during the intraoperative period. Postoperative morbidity from infection occurred in 59.4% of patients receiving placebo and in 14.7% of those receiving ampicillin (P less than .0001). In those individuals undergoing primary cesarean section the incidence of infection with placebo was 65% and with ampicillin 6.3% (P less than .0004). In patients undergoing repeat cesarean section the incidence was 53% in the placebo group and 22% in the treatment group (P greater than .05). There were no differences in the effectiveness of the drug whether given preoperatively or intraoperatively. Serious infections and wound infections were not encountered in patients receiving ampicillin.
对71例行剖宫产手术的患者,以随机、前瞻性、双盲的方式静脉注射一剂2克的氨苄青霉素或外观相同的安慰剂。溶液在接到手术室通知时或手术期间给予。接受安慰剂的患者中59.4%发生术后感染,接受氨苄青霉素的患者中14.7%发生术后感染(P<0.0001)。在初次剖宫产的患者中,安慰剂组感染发生率为65%,氨苄青霉素组为6.3%(P<0.0004)。在再次剖宫产的患者中,安慰剂组发生率为53%,治疗组为22%(P>0.05)。术前或术中给药,药物疗效无差异。接受氨苄青霉素的患者未出现严重感染和伤口感染。