Kidney Center, Turku University Hospital and University of Turku, Turku, Finland.
Department of Anaesthesiology and Intensive Care, Turku University Hospital and University of Turku, Turku, Finland.
Acta Anaesthesiol Scand. 2021 Jul;65(6):778-784. doi: 10.1111/aas.13798. Epub 2021 Mar 2.
The safety of continuous veno-venous hemodialysis (CVVHD) with citrate-calcium anticoagulation for acute kidney injury (AKI) with coincident hyponatremia remains unclear. We aimed to explore the feasibility of CVVHD with standard dialysate and citrate-calcium anticoagulation in hyponatremic critically ill AKI patients.
Thirty-seven of the 493 critically ill AKI patients requiring CVVHD and admitted to our intensive care unit during a 10-year period had hyponatremia (<130 mmol/L) and were included in this retrospective study. All patients received CVVHD with citrate-calcium anticoagulation and standard commercial dialysate and plasma sodium concentrations were frequently controlled until death or CVVHD discontinuation. Clinical data, mortalities and cases of central pontine myelinolysis within one-year follow-up were recorded.
Median plasma sodium concentration was 127 (IQR 124-129) mmol/L at CVVHD initiation. CVVHD duration was median 3 (IQR 1.5-5.5) days and the mean daily sodium load of the trisodium citrate solution during the first 3 days of CVVHD was 1754 (SD 730) mmol. The plasma sodium concentration increased a median 8 (IQR 5-10) mmol/L during the first 24 hours of CVVHD and excessively high plasma sodium correction (>8 mmol/L/24 h) was observed in 18 (48.6%) patients. However, increased mortality in association to rapid plasma sodium correction was not observed in this study.
CVVHD using standard citrate-calcium anticoagulation effectively increased plasma sodium concentration in this study. However, excessively high plasma sodium correction was observed in half of the patients and the sodium load provided by the standard citrate anticoagulation solutions was substantial.
在并发低钠血症的急性肾损伤(AKI)患者中,使用柠檬酸钠-钙抗凝的连续静脉-静脉血液透析(CVVHD)的安全性尚不清楚。我们旨在探索在伴有低钠血症的危重症 AKI 患者中,使用标准透析液和柠檬酸钠-钙抗凝进行 CVVHD 的可行性。
在 10 年期间,我们重症监护病房共收治了 493 例需要 CVVHD 的危重症 AKI 患者,其中 37 例患者伴有低钠血症(<130mmol/L),并纳入本回顾性研究。所有患者均接受柠檬酸钠-钙抗凝和标准商业透析液的 CVVHD,并频繁控制血浆钠浓度,直至死亡或 CVVHD 停止。记录临床数据、死亡率和一年内随访时的桥脑中央髓鞘溶解症病例。
CVVHD 开始时的中位血浆钠浓度为 127(IQR 124-129)mmol/L。CVVHD 持续时间中位数为 3(IQR 1.5-5.5)天,CVVHD 前 3 天的柠檬酸钠三钠溶液的日平均钠负荷为 1754(SD 730)mmol。CVVHD 开始后 24 小时内,中位血浆钠浓度升高 8(IQR 5-10)mmol/L,18 例(48.6%)患者出现过高的血浆钠纠正(>8mmol/L/24h)。然而,在本研究中,并未观察到与快速血浆钠纠正相关的增加死亡率。
在本研究中,使用标准柠檬酸钠-钙抗凝的 CVVHD 有效地增加了血浆钠浓度。然而,一半的患者出现了过高的血浆钠纠正,且标准柠檬酸钠抗凝溶液提供的钠负荷量较大。