Continuous renal replacement therapy: individualization of the prescription

被引:10
作者
Haines, Ryan W. [1 ,2 ]
Kirwan, Christopher J. [1 ,2 ,3 ]
Prowle, John R. [1 ,2 ,3 ]
机构
[1] Barts Hlth NHS Trust, Royal London Hosp, Adult Crit Care Unit, London E1 1BB, England
[2] Queen Mary Univ London, William Harvey Res Inst, London, England
[3] Barts Hlth NHS Trust, Royal London Hosp, Dept Renal Med & Transplantat, London, England
关键词
acute kidney injury; continuous renal replacement therapy; critical care; CRITICALLY-ILL PATIENTS; ACUTE KIDNEY INJURY; REGIONAL CITRATE; SEPTIC SHOCK; MANAGEMENT; INITIATION; INTENSITY; CARE; HEMODIAFILTRATION; HEMOFILTRATION;
D O I
10.1097/MCC.0000000000000546
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Purpose of review 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. Recent findings 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.
引用
收藏
页码:443 / 449
页数:7
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