透析患者高血压:当前临床方法综述

Colm Rowan, Stephen Mahony, L. Redahan
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引用次数: 0

摘要

心血管疾病是终末期肾病(ESRD)发病和死亡的主要原因。高血压起主要作用,导致进行性左心室肥厚,增加心源性猝死的风险。其患病率和病理生理机制与非透析依赖人群有根本的不同。钠限制可以像抗高血压药物一样有效地减轻由钠处理受损引起的血流动力学影响。调整透析液钠可以增强扩散并促进钠的更大消除,而单独的饮食措施是无效的。与广泛人群中的高血压不同,容量超载在ESRD中起着主要的病理生理作用。在血液透析患者中,检测干重可以显著降低临床血压(BP),并转化为未来心血管发病率和死亡率指标的改善。药物治疗仍然是控制透析患者高血压的一个重要方面。虽然没有大规模的研究确定最佳的药物治疗方法,但大量的荟萃分析和随机对照试验(RCT)已经证明了血管紧张素转换酶(ACE)抑制剂和血管紧张素II受体阻滞剂(ARB)、钙通道阻滞剂、β阻滞剂和肼嗪/硝酸异山梨酯治疗ESRD高血压的疗效。矿物皮质激素受体拮抗剂的有益血流动力学特性是否大于高钾血症的风险是正在进行的随机对照试验的主题。许多荟萃分析表明,充分的药理学控制血压转化为改善心血管发病率和死亡率。透析期间/透析期间容量状态的波动使ESRD患者高血压的诊断复杂化。与未接受透析的患者一样,24小时血压监测在诊断高血压和预测高血压预后方面似乎具有最大的敏感性。在资源有限的情况下,家庭血压监测似乎具有最大的价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hypertension in Patients Receiving Dialysis: A Review of the Current Clinical Approach
Cardiovascular disease is a leading cause of morbidity and mortality in end-stage renal disease (ESRD). Hypertension plays a major contributory role, resulting in progressive left ventricular hypertrophy, and increasing the risk of sudden cardiac death. The prevalence and pathophysiological mechanisms differ fundamentally from the non-dialysis-dependent population. Sodium restriction can be as effective as antihypertensive medication in mitigating the haemodynamic effects resulting from impaired sodium handling. Tailoring dialysate sodium may enhance diffusion and facilitate greater sodium elimination where dietary measures alone prove ineffective. Unlike hypertension in the wider population, volume overload plays a major pathophysiological role in ESRD. Probing dry weight in patients on dialysis who are seemingly euvolaemic enables clinically significant blood pressure (BP) reduction, and translates to improvements in markers of future cardiovascular morbidity and mortality. Pharmacotherapy remains an important aspect in controlling hypertension in dialysis. Although no large-scale studies have identified the optimal medical therapy, numerous meta-analyses and randomised control trials (RCT) have demonstrated the efficacy of angiotensin-converting enzyme (ACE) inhibitors and angiotensin II receptor blockers (ARB), calcium channel blockers, β-blockers, and hydralazine/isosorbide dinitrate in the treatment of hypertension in ESRD. Whether the beneficial haemodynamic properties of mineralocorticoid receptor antagonists outweigh the risk of hyperkalaemia is the subject of ongoing RCTs. Numerous meta-analyses have demonstrated that adequate pharmacological control of BP translates to improved cardiovascular morbidity and mortality. The fluctuation of volume status in the inter/intra-dialytic period complicates the diagnosis of hypertension in ESRD. As with patients not receiving dialysis, 24-hour blood pressure monitoring appears to have the greatest sensitivity in diagnosing hypertension and predicting outcomes from hypertension. Where resources are limited, home BP monitoring appears to have the greatest value.
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