静脉注射头孢曲松和氟喹诺酮预防抗生素可减少经直肠超声引导前列腺活检后的感染并发症。

Korean Journal of Urology Pub Date : 2015-06-01 Epub Date: 2015-06-02 DOI:10.4111/kju.2015.56.6.466
Chunwoo Lee, Dalsan You, In Gab Jeong, Jun Hyuk Hong, Myung-Soo Choo, Hanjong Ahn, Tai Young Ahn, Choung-Soo Kim
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引用次数: 8

摘要

目的:评价前列腺穿刺活检预防性抗生素方案改变前后感染并发症的发生率。材料与方法:回顾性分析2005年8月~ 2012年7月峨山医院行前列腺穿刺活检的5577例患者的资料。组1 (n= 1743)包括2005年至2009年期间使用氟喹诺酮治疗3天的患者,组2 (n= 2723)包括2009年至2012年期间在活检前使用头孢曲松1次,活检前使用氟喹诺酮并继续治疗3天的患者,组3 (n= 1111)在活检后使用相同治疗7天以上的患者。单变量和多变量logistic回归模型分析了前列腺穿刺活检后感染并发症的相关危险因素。结果:前列腺穿刺活检后出现感染性并发症18例(1组),7例(2组),2例(3组)(p=0.001)。1组7例感染并发症患者血培养阳性,含氟喹诺酮类耐药大肠杆菌,4例头孢曲松敏感,3例广谱β -内酰胺酶阳性大肠杆菌。1组2例患者因感染性休克需要重症监护。在多变量分析中,氟喹诺酮与头孢曲松合用患者感染并发症发生率明显低于氟喹诺酮单用患者(p=0.003)。结论:前列腺穿刺活检前使用头孢曲松和氟喹诺酮预防抗生素可降低潜在严重感染并发症的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Antibiotic prophylaxis with intravenous ceftriaxone and fluoroquinolone reduces infectious complications after transrectal ultrasound-guided prostatic biopsy.

Purpose: To assess the rates of infectious complications before and after the change of prophylactic antibiotic regimens in prostate needle biopsy.

Materials and methods: The records of 5,577 patients who underwent prostate needle biopsy at Asan Medical Center between August 2005 and July 2012 were retrospectively reviewed. Group 1 (n=1,743) included patients treated between 2005 and 2009 with fluoroquinolone for 3 days, group 2 (n=2,723) included those treated between 2009 and 2012 with ceftriaxone once before the biopsy and fluoroquinolone before biopsy and continue therapy for 3 days, and group 3 (n=1,111) received the same treatment for more than 7 days after the biopsy. Univariable and multivariable logistic regression models addressed risk factors associated with infectious complication after prostate needle biopsy.

Results: Infectious complication after prostate needle biopsy developed in 18 (group 1), seven (group 2), and two patients (group 3) (p=0.001). In group 1, seven patients with infectious complication had positive blood cultures and harbored fluoroquinolone-resistant Escherichia coli, four had ceftriaxone susceptible isolates, and three had extended spectrum beta-lactamase-positive E. coli. Two patients in group 1 required intensive care because of septic shock. In multivariable analysis, the patients with combination of fluoroquinolone and ceftriaxone had significantly lower infectious complication rate than the fluoroquinolon alone (p=0.003).

Conclusions: Antibiotic prophylaxis with ceftriaxone and fluoroquinolone before prostate needle biopsy decreased the risk of potentially serious infectious complications.

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