Regional Citrate Anticoagulation for PrismaFlex Continuous Renal Replacement Therapy

医学 肾脏替代疗法 代谢性碱中毒 透析 急性肾损伤 钙代谢 重症监护室 堆积红细胞 麻醉 外科 输血 重症监护医学 内科学
作者
Lisa Burry,David Tung,David Hallett,Toni Bailie,Virginia Carvalhana,David D. Lee,Steve Ramganesh,Robert Richardson,Sangeeta Mehta,Stephen E. Lapinsky
出处
期刊:Annals of Pharmacotherapy [SAGE]
卷期号:43 (9): 1419-1425 被引量:17
标识
DOI:10.1345/aph.1m182
摘要

Background: Since Mehta et al. reported the first successful use of regional citrate anticoagulation (RCA) for continuous renal replacement therapy (CRRT) in 1990, RCA is increasingly used for CRRT because it provides filter patency with minimal risk of bleeding. However, RCA has been associated with significant metabolic complications including hypocalcemia, hypernatremia, metabolic alkalosis, and citrate toxicity. Objective: To describe our experience with a newly implemented RCA protocol with acid citrate dextrose formula A (ACD-A) and intravenous calcium gluconate, for use with PrismaFlex CRRT in critically ill patients with acute kidney injury. Methods: A retrospective chart review was conducted from May 1, 2006, until May 1, 2007, in a 16-bed medical-surgical university-affiliated intensive care unit. Data collected included dialysis filter life, patient and circuit metabolic parameters, and units of packed red blood cells transfused. Results: Forty-eight patients received dialysis with citrate (n = 178 fitters). Circuit clotting occurred in 24% of all filters. Mean ± SD filter life was 38.4 ± 25.9 hours, and filter survival at 48 hours was 38.2%. Persistent metabolic alkalosis while on CRRT was identified in 6 of 45 (13.3%) patients. Mild hypocalcemia (ionized calcium <3.6 mg/dL) occurred in 11 (23%) patients, but no patient had an ionized calcium level less than 2.8 mg/dL. Six patients, 3 with acute leukemia, required transfusion of 2 or more units of packed red blood cells in 24 hours. Conclusions: We found that anticoagulation of PrismaFlex CRRT with ACD-A and intravenous calcium gluconate provided reasonable filter patency, but with minor metabolic complications. Close monitoring of electrolyte and acid–base balance is required to minimize metabolic derangements.
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