Stevenson Sarah, Tang Wen, Cho Yeoungjee, Mudge David W, Hawley Carmel M, Badve Sunil V, Johnson David W
Department of Nephrology, University of Queensland at Princess Alexandra Hospital, Brisbane, Australia.
Department of Nephrology, University of Queensland at Princess Alexandra Hospital, Brisbane, Australia Division of Nephrology, Peking University Third Hospital, Beijing, China.
Perit Dial Int. 2015 Mar-Apr;35(2):222-8. doi: 10.3747/pdi.2013.00156. Epub 2014 Mar 1.
There is limited available evidence regarding the role of monitoring serum vancomycin concentrations during treatment of peritoneal dialysis (PD)-associated peritonitis.
A total of 150 PD patients experiencing 256 episodes of either gram-positive or culture-negative peritonitis were included to investigate the relationship between measured serum vancomycin within the first week and clinical outcomes of cure, relapse, repeat or recurrence of peritonitis, catheter removal, temporary or permanent transfer to hemodialysis, hospitalization and death.
Vancomycin was used as an initial empiric antibiotic in 54 gram-positive or culture-negative peritonitis episodes among 34 patients. The median number of serum vancomycin level measurements in the first week was 3 (interquartile range; IQR 1 - 4). The mean day-2 vancomycin level, measured in 34 (63%) episodes, was 17.5 ± 5.2 mg/L. Hospitalized patients were more likely to have serum vancomycin levels measured on day 2 and ≥ 3 measurements in the first week. The peritonitis cure rates were similar between patients with < 3 and ≥ 3 measurements in the first week (77% vs 57%, p = 0.12) and if day-2 vancomycin levels were measured or not (68% vs 65%, p = 0.84). The average day-2 (18.0 ± 5.9 vs 16.6 ± 3.2, p = 0.5), first-week average (18.6 ± 5.1 vs 18.6 ± 4.3, p = 0.9) and nadir (14.5 ± 4.1 vs 13.6 ± 4.2, p = 0.5) vancomycin levels were comparable in patients who did or did not achieve peritonitis cure. Similar results were observed for all other clinical outcomes.
The clinical outcomes of gram-positive and culture-negative peritonitis episodes are not associated with either the frequency or levels of serum vancomycin measurements in the first week of treatment when vancomycin is dosed according to International Society for Peritoneal Dialysis (ISPD) Guidelines.
关于在腹膜透析(PD)相关性腹膜炎治疗期间监测血清万古霉素浓度的作用,现有证据有限。
共纳入150例经历256次革兰氏阳性或培养阴性腹膜炎发作的PD患者,以研究治疗第一周内测得的血清万古霉素与腹膜炎治愈、复发、重复发作或再发、导管拔除、临时或永久转为血液透析、住院及死亡等临床结局之间的关系。
在34例患者的54次革兰氏阳性或培养阴性腹膜炎发作中,万古霉素被用作初始经验性抗生素。第一周血清万古霉素水平测量的中位数为3次(四分位间距;IQR 1 - 4)。在34次(63%)发作中测得的第2天万古霉素平均水平为17.5±5.2mg/L。住院患者在第2天更有可能进行血清万古霉素水平测量,且在第一周测量次数≥3次。第一周测量次数<3次和≥3次的患者之间腹膜炎治愈率相似(77%对57%,p = 0.12),无论是否测量第2天万古霉素水平(68%对65%,p = 0.84)。腹膜炎治愈和未治愈的患者之间,第2天平均水平(18.0±5.9对16.6±3.2,p = 0.5)、第一周平均水平(18.6±5.1对18.6±4.3,p = 0.9)和最低点水平(14.5±4.1对13.6±4.2,p = 0.5)相当。所有其他临床结局也观察到类似结果。
当按照国际腹膜透析学会(ISPD)指南给药万古霉素时,革兰氏阳性和培养阴性腹膜炎发作的临床结局与治疗第一周血清万古霉素测量的频率或水平均无关。