Rimola A, Salmerón J M, Clemente G, Rodrigo L, Obrador A, Miranda M L, Guarner C, Planas R, Solá R, Vargas V
Liver Unit, Hospital Clinic i Provincial, Barcelona, Spain.
Hepatology. 1995 Mar;21(3):674-9.
Cefotaxime (CTX) is considered one of the first-choice antibiotics in the therapy of spontaneous bacterial peritonitis (SBP) in cirrhosis. Because CTX is largely metabolized in the liver, this drug may also be effective in SBP by administering lower doses than those habitually used. To investigate this possibility, a prospective, randomized, multicenter study was performed to compare the therapeutic efficacy of two different dosages of CTX in 143 patients with SBP: 71 (group I) were allocated to receive a high dose (2 g every 6 hours, which is one of the most frequently recommended doses in this infection), and 72 (group II) were allocated to receive a low dose (2 g every 12 hours). At inclusion, both groups were similar in relation to clinical and laboratory data, with the exception of a higher incidence of positive ascitic fluid culture in group I than in group II (59% vs. 40%; P = .029). The rate of infection resolution was similar for both groups (77% vs. 79%). Hospital survival was also similar in both groups (69% vs. 79%). No difference was observed between patients with positive or negative ascitic fluid cultures with regard to infection resolution and patient survival. The duration of antibiotic therapy was similar in both groups (9.0 +/- 3.3 days in group I vs. 8.8 +/- 3.1 days in group II). In a subset of 13 patients from group I and 11 patients from group II CTX levels were determined in serum (peak and trough) and ascitic fluid (concomitantly with trough serum). Peak serum levels were similar in patients from both groups.(ABSTRACT TRUNCATED AT 250 WORDS)
头孢噻肟(CTX)被认为是肝硬化自发性细菌性腹膜炎(SBP)治疗中的首选抗生素之一。由于CTX主要在肝脏代谢,通过给予低于常用剂量,该药在SBP治疗中可能也有效。为研究这种可能性,进行了一项前瞻性、随机、多中心研究,比较143例SBP患者使用两种不同剂量CTX的治疗效果:71例(I组)接受高剂量(每6小时2g,这是该感染最常推荐的剂量之一),72例(II组)接受低剂量(每12小时2g)。纳入时,两组在临床和实验室数据方面相似,但I组腹水培养阳性发生率高于II组(59%对40%;P = 0.029)。两组感染缓解率相似(77%对79%)。两组的医院生存率也相似(69%对79%)。腹水培养阳性或阴性患者在感染缓解和患者生存方面未观察到差异。两组抗生素治疗持续时间相似(I组为9.0±3.3天,II组为8.8±3.1天)。在I组的13例患者和II组的11例患者亚组中,测定了血清(峰值和谷值)和腹水(与谷值血清同时)中的CTX水平。两组患者的血清峰值水平相似。(摘要截断于250字)