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Serum potassium and clinical outcomes in heart failure patients: results of risk calculations in 21?334 patients in the UK

机译:心力衰竭患者的血钾和临床结局:英国21 334位患者的风险计算结果

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Aims At present, the clinical burden of hypokalaemia and hyperkalaemia among European heart failure patients, and relationships between serum potassium and adverse clinical outcomes in this population, is not well characterized. The aim of this study was to investigate associations between mortality, major adverse cardiac events, and renin–angiotensin–aldosterone system inhibitor (RAASi) discontinuation across serum potassium levels, in a UK cohort of incident heart failure patients. Methods and results This was a retrospective observational cohort study of newly diagnosed heart failure patients listed in the Clinical Practice Research Datalink, with a first record of heart failure (index date) between 2006 and 2015. Hypokalaemia and hyperkalaemia episodes were defined as the number of serum potassium measurements exceeding each threshold (3.5, ≥5.0, ≥5.5, and ≥6.0?mmol/L), without such a measurement in the preceding 7?days. Risk equations developed using Poisson generalized estimating equations were utilized to estimate adjusted incident rate ratios (IRRs) relating serum potassium and clinical outcomes (death, major adverse cardiac event, and RAASi discontinuation). Among 21,334 eligible heart failure patients, 1969 (9.2%), 7648 (35.9%), 2725 (12.8%), and 763 (3.6%) experienced episodes of serum potassium 3.5, ≥5.0, ≥5.5, and ≥6.0?mmol/L, respectively. The adjusted IRRs for mortality exhibited a U‐shaped association pattern with serum potassium. Relative to the reference category (4.5 to 5.0?mmol/L), adjusted IRRs for mortality were estimated as 1.98 (95% confidence interval: 1.69–2.33), 1.23 (1.12–1.36), 1.35 (1.14–1.60), and 3.02 (2.28–4.02), for patients with serum potassium 3.5, ≥5.0 to 5.5, ≥5.5 to 6.0, and ≥6.0?mmol/L, respectively. The adjusted IRRs for major adverse cardiac events demonstrated a non‐statistically significant relationship with serum potassium. Discontinuation of RAASi therapy exhibited a J‐shaped trend in association with serum potassium. Compared with the reference category (4.5 to 5.0?mmol/L), adjusted IRRs were estimated as 1.07 (0.89–1.28) in patients with serum potassium 3.5?mmol/L, increasing to 1.32 (1.14–1.53) and 2.19 (1.63–2.95) among those with serum potassium ≥5.5 to 6.0 and ≥6.0?mmol/L, respectively. Conclusions In UK patients with new onset heart failure, both hypokalaemia and hyperkalaemia were associated with increased mortality risk, and hyperkalaemia was associated with increased likelihood of RAASi discontinuation. Our results demonstrate the potential importance of serum potassium monitoring for heart failure outcomes and management.
机译:目的目前,欧洲心力衰竭患者低钾血症和高钾血症的临床负担以及该人群中血钾与不良临床结局之间的关系尚不十分清楚。这项研究的目的是调查英国突发性心力衰竭患者队列中死亡率,主要心脏不良事件和肾素-血管紧张素-醛固酮系统抑制剂(RAASi)中断血清钾水平之间的相关性。方法和结果这是一项对临床实践研究数据链中列出的新诊断出的心力衰竭患者的回顾性观察性队列研究,首次记录了2006年至2015年之间的心力衰竭(索引日期)。低钾血症和高钾血症发作的定义为血清钾测量值超过每个阈值(<3.5,≥5.0,≥5.5和≥6.0?mmol / L),而在之前的7天中未进行此测量。使用泊松广义估计方程开发的风险方程用于估计与血清钾和临床结果(死亡,严重的不良心脏事件和RAASi停药)相关的调整后的发生率比率(IRR)。在21334名合格的心力衰竭患者中,1969年(9.2%),7648(35.9%),2725(12.8%)和763(3.6%)经历了血清钾<3.5,≥5.0,≥5.5和≥6.0?mmol发作/ L。调整后的死亡率IRR与血清钾呈U型关联模式。相对于参考类别(4.5至<5.0?mmol / L),调整后的死亡率IRR估计为1.98(95%置信区间:1.69–2.33),1.23(1.12-1.36),1.35(1.14-1.60)和血钾<3.5,≥5.0至<5.5,≥5.5至<6.0和≥6.0?mmol / L的患者的血氧饱和度分别为3.02(2.28–4.02)。调整后的严重不良心脏事件的IRR与血清钾无统计学意义。 RAASi治疗的中止表现出与血清钾相关的J型趋势。与参考类别(4.5至<5.0?mmol / L)相比,血清钾<3.5?mmol / L患者的调整后IRRs估计为1.07(0.89–1.28),分别增至1.32(1.14–1.53)和2.19(血钾≥5.5至<6.0和≥6.0?mmol / L的人群分别为1.63–2.95)。结论在英国新发性心力衰竭患者中,低钾血症和高钾血症均与死亡风险增加相关,而高钾血症则与RAASi停药可能性增加相关。我们的结果证明了血清钾监测对心力衰竭结果和治疗的潜在重要性。

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