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终末期肾病中的抗高血压药物

Antihypertensive Medications in End-Stage Renal Disease.

作者信息

Denker Matthew G, Cohen Debbie L

机构信息

Renal, Electrolyte and Hypertension Division, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.

出版信息

Semin Dial. 2015 Jul-Aug;28(4):330-6. doi: 10.1111/sdi.12369. Epub 2015 Apr 15.

Abstract

Hypertension is almost universal in end-stage renal disease (ESRD) and contributes to the substantial cardiovascular (CV) morbidity and mortality observed in these patients. The management of blood pressure (BP) in ESRD is complicated by a number of factors, including missed dialysis treatments, intradialytic changes in BP, medication removal with dialysis, and poor correlation of BPs obtained in the dialysis unit with those at home and with CV outcomes. Control of extracellular volume with ultrafiltration and dietary sodium restriction represents the principal strategy to manage hypertension in ESRD, and antihypertensive medications are subsequently added if this strategy is inadequate. While reduction in BP with medication improves CV outcomes, few head-to-head clinical trials have been performed to firmly establish the superiority of one antihypertensive medication class over another. Therefore, individualization of therapy is necessary, and patient comorbidities must be considered. Angiotensin-converting enzyme (ACE) inhibitors, angiotensin receptor blockers (ARBs), and beta-blockers are reasonable first-line agents for most patients. ACE inhibitors and ARBs exert cardioprotective effects that are independent of BP reduction. Medications that are removed with dialysis may be preferred in patients who are prone to develop intradialytic hypotension. Intradialytic hypertension can be managed with challenging the patient's dry weight and using nondialyzable medications. Within a class of antihypertensive medications, there may be large variability in drug removal with dialysis, which must be considered upon medication selection. Studies demonstrate that even thrice-weekly dosing of medication after dialysis has robust BP-lowering effects, which may be a useful regimen in nonadherent patients.

摘要

高血压在终末期肾病(ESRD)中几乎普遍存在,并导致这些患者出现大量心血管(CV)发病和死亡情况。ESRD患者的血压(BP)管理因多种因素而变得复杂,包括透析治疗不充分、透析过程中血压的变化、透析导致的药物清除,以及在透析单元测得的血压与在家中测得的血压及CV结局之间的相关性较差。通过超滤和饮食限钠来控制细胞外液量是ESRD患者高血压管理的主要策略,如果该策略不足,则随后添加抗高血压药物。虽然药物降压可改善CV结局,但很少有直接比较的临床试验来明确确立一种抗高血压药物类别优于另一种。因此,治疗个体化是必要的,必须考虑患者的合并症。对于大多数患者而言,血管紧张素转换酶(ACE)抑制剂、血管紧张素受体阻滞剂(ARB)和β受体阻滞剂是合理的一线药物。ACE抑制剂和ARB具有独立于降压作用的心脏保护作用。对于容易发生透析中低血压的患者,可优先选用可被透析清除的药物。透析中高血压可通过调整患者的干体重和使用不可透析的药物来进行管理。在一类抗高血压药物中,透析导致的药物清除可能存在很大差异,在选择药物时必须予以考虑。研究表明,即使在透析后每周给药三次也具有强大的降压作用,这对于依从性差的患者可能是一种有用的给药方案。

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