Adult Critical Care Unit, The Royal London Hospital, Barts Health NHS Trust.
William Harvey Research Institute, Queen Mary University of London.
Curr Opin Crit Care. 2018 Dec;24(6):443-449. doi: 10.1097/MCC.0000000000000546.
Continuous renal replacement therapy (CRRT) is now the mainstay of renal organ support in the critically ill. As our understanding of CRRT delivery and its impact on patient outcomes improves there is a focus on researching the potential benefits of tailored, patient-specific treatments to meet dynamic needs.
The most up-to-date studies investigating aspects of CRRT prescription that can be individualized: CRRT dose, timing, fluid management, membrane selection, anticoagulation and vascular access are reviewed. The use of different doses of CRRT lack conventional high-quality evidence and importantly studies reveal variation in assessment of dose delivery. Research reveals conflicting evidence for clinicians in distinguishing which patients will benefit from 'watchful waiting' vs. early initiation of CRRT. Both dynamic CRRT dosing and precision fluid management using CRRT are difficult to investigate and currently only observational data supports individualization of prescriptions. Similarly, individualization of membrane choice is largely experimental.
Clinicians have limited evidence to individualize the prescription of CRRT. To develop this, we need to understand the requirements for renal support for individual patients, such as electrolyte imbalance, fluid overload or clearance of systemic inflammatory mediators to allow us to target these abnormalities in appropriately designed randomized trials.
连续肾脏替代治疗(CRRT)现已成为危重症患者肾脏器官支持的主要方法。随着我们对 CRRT 实施及其对患者预后影响的理解的提高,我们专注于研究量身定制、针对患者个体的治疗方法的潜在益处,以满足动态需求。
对可个体化的 CRRT 处方的各个方面的最新研究进行了综述:CRRT 剂量、时机、液体管理、膜选择、抗凝和血管通路。不同剂量的 CRRT 使用缺乏常规的高质量证据,重要的是研究揭示了剂量输送评估的差异。研究为临床医生提供了相互矛盾的证据,表明哪些患者将受益于“静观其变”与早期开始 CRRT。动态 CRRT 剂量和使用 CRRT 进行精确液体管理都难以进行研究,目前仅观察性数据支持处方的个体化。同样,膜选择的个体化在很大程度上是实验性的。
临床医生对 CRRT 处方的个体化证据有限。为了实现这一点,我们需要了解个体患者对肾脏支持的需求,例如电解质失衡、液体超负荷或全身炎症介质的清除,以便我们能够在适当设计的随机试验中针对这些异常进行靶向治疗。