Burkhalter Felix, Clemenger Michelle, Haddoub San San, McGrory Jacqueline, Hisole Nora, Brown Edwina
Clinic for Transplant Immunology and Nephrology , University Hospital Basel , Basel , Switzerland.
Imperial College Renal and Transplant Centre , Hammersmith Hospital , London , UK.
Clin Kidney J. 2015 Dec;8(6):781-4. doi: 10.1093/ckj/sfv089. Epub 2015 Sep 12.
Although, Pseudomonas exit-site infection (ESI) is recognized as a major complication of peritoneal dialysis (PD) with high risk of catheter loss due to refractory/recurrent infection or peritonitis, there is remarkably little literature about treatment outcomes. International Society for Peritoneal Dialysis guidelines advise the use of one to two antibiotics; in addition, we change standard exit-site care by stopping prophylactic mupirocin and starting regular use of gentamicin 1% cream.
Retrospective review of outcomes of Pseudomonas ESI from January 2012 to March 2015.
During the study period, a total of 135 patients were on PD with an overall incidence of any ESI of 0.36/patient-year. There were 14 patients with ESI episodes with Pseudomonas with a rate of 0.12/patient-year. In total, 13 of 14 patients with ESI episodes were treated with oral ciprofloxacin and/or intraperitoneal (IP) gentamicin or ceftazidime, plus topical gentamicin, with a success rate of 38% (5/13). One patient had gentamicin-resistant Pseudomonas species and was treated successfully with topical polymyxin/bacitracin cream. Median follow-up time in cured patients was 385 days (range 74-1107). Six patients had associated with Pseudomonas peritonitis, four during follow-up and two at initial presentation. Three patients had recurrent ESI with Pseudomonas, with one successfully re-treated with topical and IP gentamicin. In total, in only 50% of the patients was Pseudomonas ESI successfully treated. Five of the patients (36%) changed modality to permanent haemodialysis following catheter removal.
Eradication of Pseudomonas ESI remains difficult even with the addition of topical gentamicin to the exit site. There should be a low threshold for catheter replacement.
尽管假单胞菌出口处感染(ESI)被认为是腹膜透析(PD)的主要并发症,因难治性/复发性感染或腹膜炎导致导管丢失的风险很高,但关于治疗结果的文献却非常少。国际腹膜透析学会指南建议使用一至两种抗生素;此外,我们通过停止预防性使用莫匹罗星并开始定期使用1%庆大霉素乳膏来改变标准的出口处护理。
回顾性分析2012年1月至2015年3月假单胞菌ESI的治疗结果。
在研究期间,共有135例患者接受腹膜透析,任何ESI的总体发生率为0.36/患者年。有14例患者发生假单胞菌ESI发作,发生率为0.12/患者年。总共有14例ESI发作患者中的13例接受了口服环丙沙星和/或腹腔内(IP)庆大霉素或头孢他啶治疗,外加局部使用庆大霉素,成功率为38%(5/13)。1例患者感染了对庆大霉素耐药的假单胞菌,经局部使用多粘菌素/杆菌肽乳膏成功治疗。治愈患者的中位随访时间为385天(范围74 - 1107天)。6例患者合并假单胞菌腹膜炎,4例在随访期间发生,2例在初次就诊时发生。3例患者发生假单胞菌ESI复发,其中1例经局部和腹腔内使用庆大霉素成功再次治疗。总共只有50%的患者假单胞菌ESI得到成功治疗。5例患者(36%)在拔除导管后改为永久性血液透析。
即使在出口处添加局部庆大霉素,根除假单胞菌ESI仍然困难。更换导管的阈值应该较低。