Brewster S F, MacGowan A P, Gingell J C
Bristol Urological Institute, UK.
Br J Urol. 1995 Sep;76(3):351-4. doi: 10.1111/j.1464-410x.1995.tb07713.x.
To compare the clinical and microbiological outcome of a single-dose administration of cefuroxime or combined piperacillin/tazobactam (PT) after transrectal prostatic core-biopsy (TPB) in a prospective, randomized, open-label study.
Of 111 eligible men consecutively undergoing ultrasonographically guided TPB, 56 received 1.5 g cefuroxime and 55 received 4.5 g PT intravenously 20 min before the procedure. The anterior rectal wall was cleaned with an antiseptic swab and four biopsies were taken. Urine and blood cultures were evaluated before the procedure and again after 48 h, and oral temperature and symptoms recorded for 72 h after TPB.
A clinically successful outcome (no symptoms to indicate urinary or systemic sepsis or pyrexia > or = 37.5 degrees C after TPB) was achieved in 100 of 108 men (92.6%), of whom 51 received cefuroxime and 49 PT. Microbiological success (no bacteriuria > 10(5) organisms/mL, or bacteraemia, after TPB) was observed in 98 of 103 men (95%), of whom 48 received PT and 50 cefuroxime. Bacteriuria was present 48 h after TPB in 5% of the men. One man randomized to receive cefuroxime became bacteraemic (with Escherichia coli) and required hospital admission. Four of the five microbiological failures were caused by organisms sensitive to the administered antimicrobial agent. No anaerobic organisms were cultured. The most common adverse event recorded was transient diarrhoea, reported by 16 men receiving PT and two receiving cefuroxime.
With this prophylactic regimen, there was no significant difference in outcome between the groups. Most of the organisms isolated were sensitive to the administered antimicrobial agent. Thus, further reductions in sepsis after TPB may be achieved by the administration of additional oral antimicrobial prophylaxis.
在一项前瞻性、随机、开放标签研究中,比较经直肠前列腺穿刺活检(TPB)后单剂量应用头孢呋辛或联合应用哌拉西林/他唑巴坦(PT)的临床和微生物学结果。
111例连续接受超声引导下TPB的符合条件男性中,56例在操作前20分钟静脉注射1.5克头孢呋辛,55例静脉注射4.5克PT。用消毒拭子清洁直肠前壁并取4块活检组织。操作前及48小时后评估尿培养和血培养,并记录TPB后72小时的口腔温度和症状。
108例男性中有100例(92.6%)取得临床成功结果(TPB后无提示泌尿系统或全身败血症或发热≥37.5℃的症状),其中51例接受头孢呋辛,49例接受PT。103例男性中有98例(95%)取得微生物学成功结果(TPB后无细菌尿>10⁵菌落形成单位/毫升或菌血症),其中48例接受PT,50例接受头孢呋辛。5%的男性在TPB后48小时出现细菌尿。1例随机接受头孢呋辛的男性发生菌血症(大肠杆菌)并需要住院治疗。5例微生物学失败中有4例是由对所用抗菌药物敏感的微生物引起。未培养出厌氧菌。记录到的最常见不良事件是短暂腹泻,16例接受PT的男性和2例接受头孢呋辛的男性报告有此症状。
采用这种预防方案,两组结果无显著差异。分离出的大多数微生物对所用抗菌药物敏感。因此,通过额外口服抗菌预防可能进一步降低TPB后的败血症发生率。