Abrams Paul, Hashim Hashim, Tomson Charles, Macgowan Alasdair, Skews Rachel, Warren Katherine
Bristol Urological Institute, Southmead Hospital, Bristol, United Kingdom.
Freeman Hospital, Newcastle upon Tyne, United Kingdom.
Neurourol Urodyn. 2017 Nov;36(8):2109-2116. doi: 10.1002/nau.23250. Epub 2017 May 15.
To assess the use of intravesical gentamicin to treat intractable recurrent urinary tract infections in lower urinary tract dysfunction.
A two-center retrospective cohort study of 27 patients treated with intravesical gentamicin was performed over a 2-year period. A treatment protocol was developed, reviewed, and accepted by the clinical effectiveness committee of both hospitals. Patients were taught to instill the gentamicin into the bladder on a nightly basis. Inclusion criteria included failure to respond to standard therapy, having six or more cultured confirmed UTIs over a 12-month period, or at least one hospital admission with sepsis. Serum gentamicin levels were taken after 7 days and the treatment was discontinued if the level was >1 mg/L. Patients were counseled about the limited evidence base for this treatment.
Twenty-seven patients have been treated with intravesical gentamicin for an average of 26 months. Seventeen were performing ISC, five had suprapubic catheters, three were voiding, and two had ileal conduits at the time of instituting treatment. All patients started on daily 80 mg gentamicin. Twenty two patients had less frequently occurring infections after starting intravesical gentamicin treatment. Six stopped the treatment and none had side effects as a result of the instillations.
This study has shown that in a small group of adult patients who have multiple symptomatic UTIs refractory to conventional treatment, intravesical gentamicin is effective in reducing the frequency of infections. The treatment is well tolerated with no evidence of systemic absorption.
评估膀胱内注射庆大霉素治疗下尿路功能障碍所致顽固性复发性尿路感染的疗效。
进行一项为期2年的两中心回顾性队列研究,纳入27例接受膀胱内注射庆大霉素治疗的患者。制定了治疗方案,并经两家医院的临床疗效委员会审核通过。指导患者每晚将庆大霉素注入膀胱。纳入标准包括对标准治疗无反应、在12个月内有6次或更多次经培养确诊的尿路感染,或至少有1次因败血症住院治疗。7天后检测血清庆大霉素水平,若水平>1mg/L则停止治疗。向患者告知了该治疗方法证据有限的情况。
27例患者接受了膀胱内注射庆大霉素治疗,平均治疗时间为26个月。开始治疗时,17例患者进行间歇性导尿,5例患者留置耻骨上膀胱造瘘管,3例患者可自主排尿,2例患者有回肠膀胱术。所有患者开始时每日使用80mg庆大霉素。22例患者在开始膀胱内注射庆大霉素治疗后感染发作频率降低。6例患者停止治疗,且均未因注射出现副作用。
本研究表明,对于一小部分对传统治疗有多种症状性尿路感染且难治的成年患者,膀胱内注射庆大霉素可有效降低感染频率。该治疗耐受性良好,无全身吸收的证据。