Department of Pharmacy, Sultan Qaboos University Hospital, Muscat, Oman.
Oman Medical Specialty Board, Muscat, Oman.
J Infect Public Health. 2022 May;15(5):589-593. doi: 10.1016/j.jiph.2022.04.007. Epub 2022 Apr 20.
Therapeutic drug monitoring (TDM) has proven effectiveness in maintaining efficacy and reducing toxicities associated with vancomycin. A trough level of (15-20 mg/L) for MRSA serious infections is recommended. Therapeutic failure is of concern due to suboptimal routine vancomycin utilization in clinical practice. This study aims to identify factors of vancomycin TDM practice potentially associated with vancomycin-induced nephrotoxicity and therapeutic failure measured by the need to restart vancomycin therapy within 28-days and all-cause mortality in a tertiary hospital in Oman.
A single-center retrospective cohort was conducted in a tertiary care hospital that included all adult patients aged ≥ 18 years treated with IV vancomycin for> 72 h.
Vancomycin therapeutic level was not achieved in 16.8% of the patients, and 47.5% had high levels (>20 mg/L). Vancomycin-induced nephrotoxicity occurred in 31.7% of the patients, it was restarted within 28-days in 18.8% of the patient, and 25.2% of the patients died during the same hospitalization. Univariate analysis showed old age (p < 0.01), higher baseline creatinine reading (p = 0.03), high vancomycin level (p = 0.03), and vancomycin-induced nephrotoxicity (p < 0.01) were associated with increased all-cause mortality. Multivariate analysis identified overweight and vancomycin-induced nephrotoxicity were independent factors associated with increased all-cause mortality (OR:1.04; p = 0.043; 95% CI 1.00-1.08) and (OR:1.96; p = 0.049; 95% CI 1.00-21.61) respectively.
Failure to achieve the recommended therapeutic vancomycin level (15-20 mg/L) is common in clinical practice and associated with poor health outcomes; hence, appropriate TDM practice is an essential exercise to improve efficacy, prevent failure and reduce serious toxicities associated with vancomycin therapy.
治疗药物监测(TDM)已被证明可有效维持疗效并降低万古霉素相关的毒性。对于耐甲氧西林金黄色葡萄球菌(MRSA)严重感染,建议谷浓度(15-20mg/L)。由于万古霉素在临床实践中的常规应用不理想,治疗失败引起了关注。本研究旨在确定与万古霉素 TDM 实践相关的因素,这些因素可能与万古霉素诱导的肾毒性和治疗失败有关,治疗失败的衡量标准是在 28 天内需要重新开始万古霉素治疗以及在阿曼的一家三级医院的全因死亡率。
在一家三级保健医院进行了一项单中心回顾性队列研究,该研究纳入了所有年龄≥18 岁且接受静脉万古霉素治疗>72 小时的成年患者。
16.8%的患者未达到万古霉素治疗水平,47.5%的患者血药浓度较高(>20mg/L)。31.7%的患者发生了万古霉素诱导的肾毒性,其中 18.8%的患者在 28 天内重新开始治疗,25.2%的患者在同一住院期间死亡。单因素分析显示,年龄较大(p<0.01)、较高的基线肌酐读数(p=0.03)、较高的万古霉素水平(p=0.03)和万古霉素诱导的肾毒性(p<0.01)与全因死亡率增加相关。多因素分析确定超重和万古霉素诱导的肾毒性是与全因死亡率增加相关的独立因素(OR:1.04;p=0.043;95%CI 1.00-1.08)和(OR:1.96;p=0.049;95%CI 1.00-21.61)。
在临床实践中,未能达到推荐的治疗性万古霉素水平(15-20mg/L)很常见,并且与不良健康结果相关;因此,适当的 TDM 实践是提高疗效、预防治疗失败和降低与万古霉素治疗相关的严重毒性的重要措施。