University of Queensland Centre for Clinical Research (UQCCR), Faculty of Medicine, The University of Queensland, Royal Brisbane & Women's Hospital Campus Herston, Brisbane, QLD, 4029, Australia.
Department of Anaesthesiology, Critical Care and Peri-Operative Medicine, University Hospital of Nancy, Nancy, France.
Crit Care. 2023 Nov 20;27(1):449. doi: 10.1186/s13054-023-04742-w.
Intra-abdominal candidiasis (IAC) is one of the most common of invasive candidiasis observed in critically ill patients. It is associated with high mortality, with up to 50% of deaths attributable to delays in source control and/or the introduction of antifungal therapy. Currently, there is no comprehensive guidance on optimising antifungal dosing in the treatment of IAC among the critically ill. However, this form of abdominal sepsis presents specific pharmacokinetic (PK) alterations and pharmacodynamic (PD) challenges that risk suboptimal antifungal exposure at the site of infection in critically ill patients. This review aims to describe the peculiarities of IAC from both PK and PD perspectives, advocating an individualized approach to antifungal dosing. Additionally, all current PK/PD studies relating to IAC are reviewed in terms of strength and limitations, so that core elements for the basis of future research can be provided.
腹腔内念珠菌病(IAC)是危重病患者中最常见的侵袭性念珠菌病之一。它与高死亡率相关,高达 50%的死亡归因于源控制的延迟和/或抗真菌治疗的引入。目前,在危重病患者中治疗 IAC 时,没有关于优化抗真菌药物剂量的综合指导。然而,这种形式的腹部脓毒症表现出特定的药代动力学(PK)改变和药效学(PD)挑战,这使得在感染部位的抗真菌药物暴露不足,从而导致治疗效果不佳。本综述旨在从 PK 和 PD 的角度描述 IAC 的特殊性,提倡对抗真菌药物剂量进行个体化治疗。此外,还从强度和局限性两个方面回顾了所有与 IAC 相关的 PK/PD 研究,为未来研究提供了核心要素。