Adwaney Anamika, Randall David W, Blunden Mark J, Prowle John R, Kirwan Christopher J
Department of Renal Medicine and Transplantation, Barts Health NHS Trust, Whitechapel, London, UK.
Department of Adult Critical Care, Royal London Hospital, Barts Health NHS Trust, Whitechapel, London, UK.
Clin Kidney J. 2017 Dec;10(6):838-844. doi: 10.1093/ckj/sfx040. Epub 2017 Jun 29.
Kidney transplant recipients often receive large volumes of intravenous fluid replacement in the peri-operative period. Administration of 0.9% saline has previously been associated with acidosis, hyperkalaemia and acute kidney injury. The perioperative use of physiologically balanced replacement fluids may reduce the incidence of post-operative renal replacement therapy and hyperkalaemia.
A retrospective review of consecutive renal transplants before and after a change in perioperative fluid prescription from 0.9% saline to Plasma-Lyte 148.
A total of 97 patients were included in the study, 59 receiving exclusively 0.9% saline and 38 receiving exclusively Plasma-Lyte. Patients in the Plasma-Lyte group were less likely to require emergency postoperative dialysis than those receiving 0.9% saline [odds ratio (OR) 0.15 (95% confidence interval 0.03-0.48), P = 0.004], and these patients had more favourable biochemical parameters with less hyperkalaemia, less acidosis and better diuresis. Patients in the Plasma-Lyte group also had a shorter length of hospital stay (7 days versus 11 days; P < 0.0001) and better graft function at 3 months postoperatively (estimated glomerular filtration rate 51 versus 44 mL/min/1.73 m; P = 0.03); however, there was no difference in graft function at 1 year.
Plasma-Lyte in the perioperative period is safe in renal transplantation and is associated with a favourable biochemical profile, including a reduced incidence of hyperkalaemia, better diuresis and less frequent use of renal replacement therapy early after surgery. In patients receiving Plasma-Lyte, graft function was better at 3 months, but this difference did not persist up to 1 year after transplantation.
肾移植受者在围手术期常接受大量静脉补液。此前,输注0.9%生理盐水与酸中毒、高钾血症及急性肾损伤有关。围手术期使用生理平衡的补液可能会降低术后肾脏替代治疗及高钾血症的发生率。
对围手术期补液处方从0.9%生理盐水改为聚磺基乙酸电解质注射液(Plasma-Lyte 148)前后的连续肾移植病例进行回顾性研究。
该研究共纳入97例患者,其中59例仅接受0.9%生理盐水,38例仅接受聚磺基乙酸电解质注射液。聚磺基乙酸电解质注射液组患者术后需要紧急透析的可能性低于接受0.9%生理盐水的患者[比值比(OR)为0.15(95%置信区间0.03 - 0.48),P = 0.004],且这些患者的生化指标更优,高钾血症较轻、酸中毒较轻且利尿更好。聚磺基乙酸电解质注射液组患者的住院时间也较短(7天对11天;P < 0.0001),术后3个月时移植肾功能更好(估计肾小球滤过率为51对44 mL/min/1.73 m²;P = 0.03);然而,术后1年时移植肾功能无差异。
围手术期使用聚磺基乙酸电解质注射液在肾移植中是安全的,且与良好的生化指标相关,包括降低高钾血症发生率、更好的利尿效果以及术后早期较少使用肾脏替代治疗。接受聚磺基乙酸电解质注射液的患者在术后3个月时移植肾功能更好,但这种差异在移植后1年时并未持续存在。