在接受万科米治疗的患者中,早期急性损伤的潜在风险因素
Aiju Endo1, Kazumi Hanawa2, Daiki Asakawa1
1Department of Pharmacy, Yamanashi Prefectural Central Hospital, Kofu, 400-8506, Yamanashi, Japan.
概括
范科米辛诱导的急性损伤 (AKI) 可以发生在早期. 监测万科米辛的血度,并以AUC0-48低于910.2μg/mL·h为目标,可能有助于预防早期的AKI.
科学领域:
- 药理学 药理学是指药理学的学科.
- 腎臟病學 (nephrology) 是一種醫學專業.
- 临床药房 临床药房
背景情况:
- 范科米辛 (VCM) 是治疗严重的格拉姆阳性细菌感染的关键抗生素.
- 急性损伤 (AKI) 是众所周知的万科米辛的副作用,通常与其血液度有关.
- 与万科米辛相关的早期AKI需要了解度依赖性毒性和识别预测标记.
研究的目的:
- 调查接受万科米的患者早期AKI的发生率.
- 确定新的指标来预测和潜在地避免早期的万科米辛诱导的AKI.
- 确定与早期AKI相关的血度-时间曲线 (AUC) 下面区域的值.
主要方法:
- 参与了接受万科米辛超过4天的成年患者.
- 监测了血清肌素和万科米辛的最低水平.
- 分析了各种AUC间隔与早期AKI (7天内) 之间的关联,并确定了AUC截止值.
主要成果:
- 在164名患者中,21人患有早期AKI,最常见的是4日.
- 所有评估的AUC间隔 (AUC0-24,AUC24-48,AUC48-72,AUC0-48,AUC24-72,AUC0-72) 都与早期的AKI显著相关.
- 确定了早期AKI的特定AUC截止值,包括AUC0-48的910.2μg/mL·h.
结论:
- 范科米辛的累积毒性是AKI的潜在原因.
- 早期监测万科米辛血度至关重要.
- 保持AUC0-48低于910.2μg/mL·h可能会降低早期AKI的风险.
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