Department of Medicine, Monash University School of Clinical Sciences at Monash Health, Clayton, Victoria, Australia
General Medicine, Monash Health, Clayton, Victoria, Australia.
BMJ Open. 2021 Oct 22;11(10):e051201. doi: 10.1136/bmjopen-2021-051201.
To determine if liver cirrhosis is associated with reduced efficacy of insulin-glucose treatment in moderate to severe hyperkalaemia.
Retrospective, cohort study.
Two secondary and one tertiary care hospital at a large metropolitan healthcare network in Melbourne, Australia.
This study included 463 adults with a mean age of 68.7±15.8 years, comprising 79 patients with cirrhosis and 384 without cirrhosis as controls, who received standard insulin-glucose treatment for a serum potassium ≥6.0 mmol/L from October 2016 to March 2020. Patients were excluded if they received an insulin infusion, or if there was inadequate follow-up data for at least 6 hours after IDT due to death, lost to follow-up or inadequate biochemistry monitoring. The mean Model for End-stage Liver Disease score in patients with cirrhosis was 22.2±7.5, and the distribution of the Child-Pugh score for cirrhosis was: class A (24%), class B (46%), class C (30%).
The primary outcome was the degree of potassium lowering and the secondary outcome was the proportion of patients who achieved normokalaemia, within 6 hours of treatment.
The mean pretreatment potassium for the cohort was 6.57±0.52 mmol/L. After insulin-glucose treatment, mean potassium lowering was 0.84±0.58 mmol/L in patients with cirrhosis compared with 1.33±0.75 mmol/L for controls (p<0.001). The proportion of patients achieving normokalaemia was 33% for patients with cirrhosis, compared with 53% for controls (p=0.001). By multivariable regression, on average, liver cirrhosis was associated with a reduced potassium lowering effect of 0.42 mmol/L (95% CI 0.22 to 0.63 mmol/L, p<0.001) from insulin-glucose treatment, after adjusting for age, serum creatinine, cancer, pretreatment potassium level, β-blocker use and cotreatments (sodium polystyrene sulfonate, salbutamol, sodium bicarbonate).
Our observational data suggest reduced efficacy of insulin-glucose treatment for hyperkalaemia in patients with cirrhosis.
确定肝硬化是否与中重度高钾血症胰岛素-葡萄糖治疗的疗效降低有关。
回顾性队列研究。
澳大利亚墨尔本大型都市医疗保健网络的两家二级和一家三级医院。
本研究纳入了 463 名平均年龄为 68.7±15.8 岁的成年人,其中 79 名患者患有肝硬化,384 名作为对照的患者无肝硬化,他们在 2016 年 10 月至 2020 年 3 月期间因血清钾≥6.0mmol/L 接受标准胰岛素-葡萄糖治疗。如果患者接受胰岛素输注,或由于死亡、失访或生化监测不足而在 IDT 后至少 6 小时内没有足够的随访数据,则将患者排除在外。肝硬化患者的平均终末期肝病模型评分(MELD)为 22.2±7.5,肝硬化患者的 Child-Pugh 评分分布为:A级(24%)、B 级(46%)、C 级(30%)。
主要结局为治疗后 6 小时内血钾降低程度,次要结局为达到正常血钾的患者比例。
该队列的平均预处理血钾为 6.57±0.52mmol/L。在胰岛素-葡萄糖治疗后,肝硬化患者的平均血钾降低 0.84±0.58mmol/L,而对照组为 1.33±0.75mmol/L(p<0.001)。肝硬化患者达到正常血钾的比例为 33%,而对照组为 53%(p=0.001)。通过多变量回归,平均而言,肝硬化与胰岛素-葡萄糖治疗的血钾降低效果降低 0.42mmol/L(95%CI 0.22 至 0.63mmol/L,p<0.001)相关,调整年龄、血清肌酐、癌症、预处理血钾水平、β受体阻滞剂使用和联合治疗(聚苯乙烯磺酸钠、沙丁胺醇、碳酸氢钠)后。
我们的观察性数据表明,肝硬化患者的高钾血症胰岛素-葡萄糖治疗效果降低。