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首页> 外文期刊>Chemotherapy: International Journal of Experimental and Clinical Chemotherapy >Comparative randomized pilot study of azithromycin and doxycycline efficacy and tolerability in the treatment of prostate infection caused by Ureaplasma urealyticum.
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Comparative randomized pilot study of azithromycin and doxycycline efficacy and tolerability in the treatment of prostate infection caused by Ureaplasma urealyticum.

机译:比较阿奇霉素和多西环素在治疗解脲支原体引起的前列腺感染中的功效和耐受性的随机对照研究。

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A total of 1,442 patients with symptoms of chronic prostatitis were examined over a 4-year period at the Outpatient Department for Urogenital Infections, University Hospital for Infectious Diseases Dr. Fran Mihaljevic, Zagreb, Croatia. The inclusion criteria for chronic prostatitis caused by Ureaplasma urealyticum were the presence of clinical symptoms, presence of U. urealyticum in expressed prostatic secretion (EPS) or voided urine collected immediately after prostatic massage (VB(3)), absence of U. urealyticum in urethral swabs and absence of other possible pathogens of chronic prostatitis in EPS or VB(3). A total of 63 patients with prostate infection caused by U. urealyticum were available for this pilot study. The patients were randomized according to a computer randomization list to receive a total dose of 4.5 g of azithromycin given as a 3-day therapy of 1 x 500 mg weekly for 3 weeks or doxycyline 100 mg b.i.d. for 21 days. Patients' sexual partners were treated at the same time. Clinical efficacy and tolerability of the administered drug as well as possible adverse events were evaluated during, at the end and 4-6 weeks after completion of therapy. Bacteriological efficacy was evaluated 4-6 weeks after completion of therapy. Treatment groups did not differ regarding age, distribution of urethral, prostatic, sexual and other symptoms, or digitorectal prostatic examination. Five patients treated with doxycycline had nausea. In the group of patients with prostate infection caused by U. urealyticum, the eradication rate was not significantly different with regard to the administered azithromycin (25/32) or doxycycline (23/31). Clinical cure did not significantly differ with regard to the administered azithromycin (22/32) or doxycycline (21/31).
机译:在4年期间,在克罗地亚萨格勒布大学传染病医院门诊部泌尿生殖系统感染科共检查了1,442例患有慢性前列腺炎的患者。由解脲脲原体引起的慢性前列腺炎的纳入标准是临床症状的存在,在表达前列腺分泌物(EPS)中存在解脲脲原体或在前列腺按摩后立即收集排尿(VB(3)),在体内不存在解脲脲原体。 EPS或VB中没有尿道拭子且没有其他可能的慢性前列腺炎病原​​体(3)。共有63名由解脲脲原体引起的前列腺感染患者可用于该初步研究。根据计算机随机表对患者进行随机分组,以接受总剂量为4.5 g的阿奇霉素,以3天每周3次每周1 x 500 mg的疗法或100 mg b.i.d的多西环素进行治疗。持续21天。患者的性伴侣同时接受治疗。在治疗完成后,治疗结束时和治疗结束后的4-6周,评估所用药物的临床疗效和耐受性以及可能的不良事件。治疗结束后4-6周评估细菌学功效。治疗组在年龄,尿道分布,前列腺,性和其他症状或直肠直肠检查方面无差异。用强力霉素治疗的五名患者恶心。在由解脲支原体引起的前列腺感染的患者中,根除率相对于阿奇霉素(25/32)或强力霉素(23/31)而言没有显着差异。就所用阿奇霉素(22/32)或强力霉素(21/31)而言,临床治愈率无显着差异。

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