Non‐recovery of vancomycin‐associated nephrotoxicity is related to worsening survival outcomes: Combined retrospective analyses of two real‐world databases

医学 危险系数 回顾性队列研究 比例危险模型 优势比 内科学 置信区间 数据库 万古霉素 急性肾损伤 肾毒性 队列 病历 重症监护医学 生物 计算机科学 细菌 遗传学 金黄色葡萄球菌
作者
Masayuki Chuma,Hirofumi Hamano,Takashi Bando,Masateru Kondo,Naoto Okada,Yuki Izumi,Shunichi Ishida,Toshihiko Yoshioka,Mizuho Asada,Takahiro Niimura,Yoshito Zamami,Kenshi Takechi,Mitsuhiro Goda,Kôji Miyata,Kenta Yagi,Sachiko Kasamo,Yuki Izawa‐Ishizawa,Momoyo Azuma,Hiroaki Yanagawa,Yoshikazu Tasaki,Keisuke Ishizawa
出处
期刊:Basic & Clinical Pharmacology & Toxicology [Wiley]
卷期号:131 (6): 525-535
标识
DOI:10.1111/bcpt.13799
摘要

There has been growing concern in worsening survival and renal outcomes following vancomycin-associated nephrotoxicity (VAN) onset, but the factors associated with these phenomena remain unclear. To examine these factors, we performed a retrospective study combining the analysis of two real-world databases. Initially, the FDA Adverse Event Reporting System (FAERS) was used to evaluate the relationship between VAN and mortality using odds ratios (ORs) and 95% confidence intervals (CIs). Next, electronic medical records (EMRs) were examined in a more robust cohort for evaluation of the association between renal outcomes and worsening survival using Cox proportional hazards regression models. FAERS analysis revealed a significant correlation between VAN occurrence and increased mortality (OR: 1.30; 95% CI: 1.17-1.46). EMR analysis showed that non-recovery of VAN was associated with increased hospital mortality (hazard ratio [HR]: 4.05; 95% CI: 2.42-6.77) and 1-year mortality (HR: 3.03, 95% CI: 1.98-4.64). The HR for VAN recovery was lower for patients with acute kidney injury (AKI) stage ≥2 (HR: 0.09; 95% CI: 0.02-0.40). Thus, worsening survival outcomes were associated with non-recovery of VAN, whereby AKI stage ≥2 was a significant risk factor. Progression to severe VAN should be prevented for better survival outcomes.
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