# Enhancing Home Blood Pressure Management: Implementation of the Sacubitril/Valsartan Treatment in Practical Clinical Settings

**Authors:** Tsugiyoshi Yamazaki

PMC · DOI: 10.31662/jmaj.2024-0262 · JMA Journal · 2025-01-31

## TL;DR

Switching from azilsartan to sacubitril/valsartan improves home blood pressure control in patients with hypertension.

## Contribution

Demonstrates the effectiveness of sacubitril/valsartan in improving home BP targets in real-world clinical settings.

## Key findings

- Switching to sacubitril/valsartan increased home systolic BP target attainment by 60% after 48 weeks.
- Significant reductions in systolic and diastolic BP, pulse rate, and serum uric acid were observed within 8 weeks.
- The positive effects of sacubitril/valsartan were sustained for 48 weeks.

## Abstract

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.

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.

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.

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.

## Linked entities

- **Chemicals:** Sacubitril/Valsartan (PubChem CID 24755620), azilsartan (PubChem CID 135415867)

## Full-text entities

- **Diseases:** hypertension (MESH:D006973)
- **Chemicals:** Valsartan (MESH:D000068756), azilsartan (MESH:C521273), Sacubitril (MESH:C000717211), UA (MESH:D014527), potassium (MESH:D011188)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

19 references — full list in the complete paper: https://tomesphere.com/paper/PMC12095859/full.md

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Source: https://tomesphere.com/paper/PMC12095859