Faculdade de Medicina da Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Hospital das Clínicas da Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
PLoS One. 2019 Sep 5;14(9):e0222095. doi: 10.1371/journal.pone.0222095. eCollection 2019.
Vancomycin is widely used to treat infections caused by Gram positive bacteria, mostly methicillin-resistant strains. Despite its therapeutic effectiveness, vancomycin is a nephrotoxic drug that has been associated with the occurrence of acute kidney injury (AKI). In this study, we sought to evaluate the variability of serum trough concentrations of vancomycin and to determine the incidence and risk factors of vancomycin-associated nephrotoxicity (VAN) in non-critically ill patients.
This was a prospective cohort including Brazilian public hospital inpatients from April 2017 to June 2018. The participants received intravenous vancomycin therapy for at least 48 hours for any suspected or confirmed infection by Gram positive bacteria. Demographic, clinical and laboratory data were collected. Information on vancomycin therapy and concomitant use of other nephrotoxic drugs were also recorded. Patients were followed up until discontinuation of vancomycin treatment or death, whatever occurred first. The primary outcome was the occurrence of AKI. We performed a Poisson regression to determine risk factors for AKI.
Overall, 98 participants were included in the study. Median age was 55.9 (interquartile range [IQR] 40.6-66.8) years and 58 (59.2%) were men. Most of them showed subtherapeutic (<10mg/L) or supratherapeutic (>20mg/L) trough levels of vancomycin; 42.9% and 15.3%, respectively. A total of 19 (19.4%) patients developed AKI. Poisson regression showed that male sex (odds ratio [OR] 2.90; confidence interval [CI] 95% 1.28-6.53; p = 0.011), concomitant use of piperacillin-tazobactam (OR 4.66; CI 95% 2.26-9.58; p <0.001) and vancomycin trough levels above 20mg/mL (OR 4.21; CI 95% 1.57-11.278; p = 0.004) were independently associated with AKI.
Our study showed that usual doses of vancomycin did not reach recommended therapeutic serum trough levels of vancomycin in non-critically ill patients. Besides that, nephrotoxicity was common in this population, being associated with male sex, concomitant use of piperacillin-tazobactam and supra-therapeutic trough serum levels of vancomycin.
万古霉素被广泛用于治疗由革兰氏阳性菌引起的感染,主要是耐甲氧西林菌株。尽管其治疗效果良好,但万古霉素是一种肾毒性药物,已与急性肾损伤(AKI)的发生有关。在这项研究中,我们试图评估万古霉素的血清谷浓度的可变性,并确定非危重症患者万古霉素相关性肾毒性(VAN)的发生率和危险因素。
这是一项前瞻性队列研究,纳入了 2017 年 4 月至 2018 年 6 月巴西公立医院的住院患者。这些患者因疑似或确诊的革兰氏阳性菌感染而接受至少 48 小时的静脉万古霉素治疗。收集了人口统计学、临床和实验室数据。还记录了万古霉素治疗和同时使用其他肾毒性药物的信息。患者随访至万古霉素治疗停止或死亡,以先发生者为准。主要结局是发生 AKI。我们进行了泊松回归以确定 AKI 的危险因素。
共有 98 名患者纳入研究。中位年龄为 55.9 岁(四分位距 [IQR] 40.6-66.8),58 名(59.2%)为男性。他们中的大多数人显示出治疗性(<10mg/L)或超治疗性(>20mg/L)的万古霉素谷浓度;分别为 42.9%和 15.3%。共有 19 名(19.4%)患者发生 AKI。泊松回归显示,男性(比值比 [OR] 2.90;95%置信区间 [CI] 1.28-6.53;p = 0.011)、同时使用哌拉西林-他唑巴坦(OR 4.66;95%CI 2.26-9.58;p <0.001)和万古霉素谷浓度超过 20mg/mL(OR 4.21;95%CI 1.57-11.278;p = 0.004)与 AKI 独立相关。
我们的研究表明,非危重症患者通常使用的万古霉素剂量并未达到推荐的万古霉素血清谷浓度。此外,该人群中肾毒性很常见,与男性、同时使用哌拉西林-他唑巴坦和超治疗性万古霉素血清谷浓度有关。