Asbach H W
Kreiskrankenhaus, Urologische Klinik, Lübbecke, Germany.
Infection. 1991 Mar-Apr;19(2):85-7. doi: 10.1007/BF01645573.
In a prospective randomized study, the efficacy and safety of 1 and 2 g of cefodizime administered as single intramuscular injections were compared in a total of 50 women having either complicated or uncomplicated lower urinary tract infections (LUTI). Bacteriological culture of urine and safety laboratory tests were performed before and after treatment. 18/25 patients in the 1 g cefodizime group and 22/25 in the 2 g cefodizime group showed satisfactory clinical and bacteriological response to treatment. The inadequately treated patients all had complicating factors on entry to the study (residual urine in six cases, a bladder malignancy in two, neurogenic bladder and diabetes mellitus with glucosuria in one case each). Cefodizime proved efficacious in female patients with uncomplicated LUTI, as well as in those aged over 65 years, patients having mild renal insufficiency, mild glucosuria, unsuccessful oral antibiotic pretreatment or recurrent and postoperative infections. In no case were there any systemic adverse reactions to cefodizime or clinically significant changes in laboratory tests.
在一项前瞻性随机研究中,对50例患有复杂性或非复杂性下尿路感染(LUTI)的女性患者,比较了单次肌内注射1克和2克头孢地嗪的疗效和安全性。在治疗前后进行了尿液细菌学培养和安全性实验室检查。头孢地嗪1克组的18/25例患者和2克组的22/25例患者对治疗显示出满意的临床和细菌学反应。治疗不充分的患者在进入研究时均有复杂因素(6例有残余尿,2例有膀胱恶性肿瘤,1例有神经源性膀胱,1例有糖尿病伴糖尿)。头孢地嗪对患有非复杂性LUTI的女性患者、65岁以上的患者、轻度肾功能不全的患者、轻度糖尿的患者、口服抗生素预处理失败的患者或复发性及术后感染的患者均有效。在任何情况下,均未出现对头孢地嗪的全身性不良反应或实验室检查的临床显著变化。