加强家庭血压管理:苏比利/缬沙坦治疗在实际临床环境中的实施。

IF 1.5 Q2 MEDICINE, GENERAL & INTERNAL
JMA journal Pub Date : 2025-04-28 Epub Date: 2025-01-31 DOI:10.31662/jmaj.2024-0262
Tsugiyoshi Yamazaki
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引用次数: 0

摘要

导言:虽然家庭血压管理的重要性已被广泛报道,但在日本,家庭血压目标的完成率仍然很低。Sacubitril/缬沙坦是一种新型降压药,具有较强的降压作用。尽管理论上有优势,但在优化家庭血压管理方面,苏比里尔/缬沙坦的实际临床应用仍未得到充分探索。本研究的目的是评估从阿齐沙坦治疗转向苏比里尔/缬沙坦治疗对实现家庭血压目标的影响,并在实际临床环境中完善高血压管理策略。方法:一组55例患者,平均早晨家庭收缩压为135 mmHg或更高,入组阿齐沙坦和钙通道阻滞剂治疗8周。在从20mg阿兹沙坦切换到200mg苏比里尔/缬沙坦后,分别在基线、8周、24周和48周评估早晨血压、脉搏率(PR)、肾小球滤过率、b型利钠肽、血清钾、血清尿酸(UA)和血红蛋白A1c水平。结果:在改用苏比利/缬沙坦48周后,达到家庭收缩压目标的比率增加了60%。Sacubitril/缬沙坦在前8周内显著降低平均收缩压(从143.6±7.0 mmHg降至131.4±8.7 mmHg)、舒张压(从86.9±12.3 mmHg降至80.2±10.7 mmHg)、PR(从74.8±11.0 bpm降至72.1±10.1 bpm)和血清UA(从5.9±1.1 mg/dL降至5.5±0.9 mg/dL)(均p < 0.01)。这些效果维持了48周。结论:从阿齐沙坦到苏比里尔/缬沙坦治疗的转换导致家庭血压目标的实现显著改善,这与我们在实际临床环境中改进高血压管理策略的目标一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhancing Home Blood Pressure Management: Implementation of the Sacubitril/Valsartan Treatment in Practical Clinical Settings.

Introduction: Although the importance of home blood pressure (BP) management has been widely reported, the achievement rate of home BP targets remains low in Japan. Sacubitril/valsartan is a novel antihypertensive agent with potent antihypertensive effects. Despite its theoretical advantages, the real-world clinical application of sacubitril/valsartan in optimizing home BP management remains underexplored. The aim of this study was to evaluate the effect of switching from azilsartan treatment to sacubitril/valsartan treatment on the achievement of home BP targets and to refine hypertension management strategies in practical clinical settings.

Methods: A cohort of 55 patients, with a mean morning home systolic BP of 135 mmHg or more was enrolled for an 8-week treatment phase with azilsartan and calcium-channel blockers. Morning BP, pulse rate (PR), estimated glomerular filtration rate, and B-type natriuretic peptide, serum potassium, serum uric acid (UA), and hemoglobin A1c levels were assessed at baseline and then at 8, 24, and 48 weeks after switching from 20 mg azilsartan to 200 mg sacubitril/valsartan.

Results: At 48 weeks after switching to sacubitril/valsartan, there was a 60% increase in the rate of attainment of home systolic BP targets. Sacubitril/valsartan significantly reduced the mean systolic BP (from 143.6 ± 7.0 mmHg to 131.4 ± 8.7 mmHg), diastolic BP (from 86.9 ± 12.3 mmHg to 80.2 ± 10.7 mmHg), PR (from 74.8 ± 11.0 bpm to 72.1 ± 10.1 bpm), and serum UA (from 5.9 ± 1.1 mg/dL to 5.5 ± 0.9 mg/dL) within the first 8 weeks (all p < 0.01). These effects were maintained for 48 weeks.

Conclusions: The switch from azilsartan to sacubitril/valsartan treatment resulted in a significant improvement in the achievement of home BP targets, which is consistent with our goal of refining hypertension management strategies in practical clinical settings.

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