Hirano Ryuichi, Sakamoto Yuichi, Kitazawa Junichi, Yamamoto Shoji, Tachibana Naoki
Department of Pharmacy.
Laboratory Medicine and Blood Transfusion, Aomori Prefectural Central Hospital, Aomori-shi, Japan.
Infect Drug Resist. 2016 Oct 14;9:243-252. doi: 10.2147/IDR.S109485. eCollection 2016.
Vancomycin (VCM) requires dose adjustment based on therapeutic drug monitoring. At Aomori Prefectural Central Hospital, physicians carried out VCM therapeutic drug monitoring based on their experience, because pharmacists did not participate in the dose adjustment. We evaluated the impact of an Antimicrobial Stewardship Program (ASP) on attaining target VCM trough concentrations and pharmacokinetics (PK)/pharmacodynamics (PD) parameters in patients with methicillin-resistant (MRSA) infections.
The ASP was introduced in April 2012. We implemented a prospective audit of prescribed VCM dosages and provided feedback based on measured VCM trough concentrations. In a retrospective pre- and postcomparison study from April 2007 to December 2011 (preimplementation) and from April 2012 to December 2014 (postimplementation), 79 patients were treated for MRSA infection with VCM, and trough concentrations were monitored (pre, n=28; post, n=51). In 65 patients (pre, n=15; post, n=50), 24-hour area under the concentration-time curve (AUC 0-24 h)/minimum inhibitory concentration (MIC) ratios were calculated.
Pharmacist feedback, which included recommendations for changing dose or using alternative anti-MRSA antibiotics, was highly accepted during postimplementation (88%, 29/33). The number of patients with serum VCM concentrations within the therapeutic range (10-20 μg/mL) was significantly higher during postimplementation (84%, 43/51) than during preimplementation (39%, 11/28) (<0.01). The percentage of patients who attained target PK/PD parameters (AUC 0-24 h/MIC >400) was significantly higher during postimplementation (84%, 42/50) than during preimplementation (53%, 8/15; =0.013). There were no significant differences in nephrotoxicity or mortality rate.
Our ASP increased the percentage of patients that attained optimal VCM trough concentrations and PK/PD parameters, which contributed to the appropriate use of VCM in patients with MRSA infections.
万古霉素(VCM)需要根据治疗药物监测进行剂量调整。在青森县中央医院,由于药剂师未参与剂量调整,医生根据经验进行VCM治疗药物监测。我们评估了抗菌药物管理计划(ASP)对耐甲氧西林金黄色葡萄球菌(MRSA)感染患者达到目标VCM谷浓度及药代动力学(PK)/药效学(PD)参数的影响。
2012年4月引入ASP。我们对开具的VCM剂量进行前瞻性审核,并根据测得的VCM谷浓度提供反馈。在一项2007年4月至2011年12月(实施前)和2012年4月至2014年12月(实施后)的回顾性前后比较研究中,79例患者接受VCM治疗MRSA感染,并监测谷浓度(实施前,n = 28;实施后,n = 51)。在65例患者中(实施前,n = 15;实施后,n = 50),计算了24小时浓度-时间曲线下面积(AUC0-24 h)/最低抑菌浓度(MIC)比值。
在实施后,药剂师的反馈,包括更改剂量或使用替代抗MRSA抗生素的建议,得到了高度认可(88%,29/33)。血清VCM浓度在治疗范围内(10 - 20μg/mL)的患者数量在实施后(84%,43/51)显著高于实施前(39%,11/28)(<0.01)。达到目标PK/PD参数(AUC0-24 h/MIC >400)的患者百分比在实施后(84%,42/50)显著高于实施前(53%,8/15;P = 0.013)。肾毒性或死亡率无显著差异。
我们的ASP提高了达到最佳VCM谷浓度和PK/PD参数的患者百分比,这有助于MRSA感染患者合理使用VCM。