van der Wall E, Verkooyen R P, Mintjes-de Groot J, Oostinga J, van Dijk A, Hustinx W N, Verbrugh H A
Department of Medical Microbiology, Diakonessen Hospital, Utrecht, Netherlands.
Lancet. 1992 Apr 18;339(8799):946-51. doi: 10.1016/0140-6736(92)91529-h.
Patients receiving antibiotics during bladder drainage have a lower incidence of urinary-tract infections compared with similar patients not on antibiotics. However, antibiotic prophylaxis in patients with a urinary catheter is opposed because of the fear of inducing resistant bacterial strains. We have done a double-blind, placebo-controlled trial of prophylactic ciprofloxacin in selected groups of surgical patients who had postoperative bladder drainage scheduled to last for 3 to 14 days. Patients were randomly assigned to receive placebo (n = 61), 250 mg ciprofloxacin per day (n = 59), or 500 mg ciprofloxacin twice daily (n = 64) from postoperative day 2 until catheter removal. 75% of placebo patients were bacteriuric at catheter removal compared with 16% of ciprofloxacin-treated patients (relative risk [RR] [95% CI] 4.7 [3.0-7.4]). The prevalence of pyuria among placebo patients increased from 11% to 42% while the catheter was in place; by contrast, the rate of pyuria was 11% or less in patients receiving ciprofloxacin (RR 4.0 [2.1-7.3]). 20% of placebo patients had symptomatic urinary-tract infections, including 3 with septicaemia, compared with 5% of the ciprofloxacin groups (RR 4.0 [1.6-10.2]). Bacteria isolated from urines of placebo patients at catheter removal were mostly species of enterobacteriaceae (37%), staphylococci (26%), and Enterococcus faecalis (20%), whereas species isolated from urines of ciprofloxacin patients were virtually all gram-positive. Ciprofloxacin-resistant mutants of normally sensitive gram-negative bacteria were not observed. Ciprofloxacin prophylaxis is effective and safe in the prevention of catheter-associated urinary tract infection and related morbidity in selected groups of patients requiring 3 to 14 days of bladder drainage.
与未使用抗生素的类似患者相比,在膀胱引流期间接受抗生素治疗的患者尿路感染发生率较低。然而,由于担心诱导耐药菌株,反对对留置导尿管的患者进行抗生素预防。我们对选定的术后膀胱引流计划持续3至14天的手术患者组进行了预防性环丙沙星的双盲、安慰剂对照试验。患者从术后第2天开始随机分配接受安慰剂(n = 61)、每天250 mg环丙沙星(n = 59)或每天两次500 mg环丙沙星(n = 64),直至拔除导尿管。拔除导尿管时,75%的安慰剂组患者有菌尿,而环丙沙星治疗组患者为16%(相对风险[RR][95%置信区间]4.7[3.0 - 7.4])。在留置导尿管期间,安慰剂组患者脓尿患病率从11%增加到42%;相比之下,接受环丙沙星治疗的患者脓尿率为11%或更低(RR 4.0[2.1 - 7.3])。20%的安慰剂组患者有症状性尿路感染,包括3例败血症,而环丙沙星组为5%(RR 4.0[1.6 - 10.2])。拔除导尿管时从安慰剂组患者尿液中分离出的细菌大多是肠杆菌科(37%)、葡萄球菌(26%)和粪肠球菌(20%),而从环丙沙星组患者尿液中分离出的细菌几乎都是革兰氏阳性菌。未观察到对通常敏感的革兰氏阴性菌的环丙沙星耐药突变体。环丙沙星预防在预防需要3至14天膀胱引流的选定患者组中与导尿管相关的尿路感染及相关发病率方面是有效且安全的。