# Two-Drug Combinations Therapy of Different Doses of Valsartan Existing Diverse Significance for Hypertensive Patients

**Authors:** Zerong Wang, Shixiong Wang, Liqiong Zhang, Jiaxuan Wang, Rong Wang, Shude Chen, Qiling Shi, Hongye Wu, Liuyang Wang, Ningyin Li

PMC · DOI: 10.31083/j.rcm2407187 · Reviews in Cardiovascular Medicine · 2023-06-29

## TL;DR

This study evaluates how combining high-dose valsartan with other drugs affects blood pressure and side effects in hypertension patients.

## Contribution

The study identifies optimal drug combinations with high-dose valsartan for effective blood pressure control without significant adverse effects.

## Key findings

- Combining valsartan 320 mg with amlodipine 10 mg showed the best antihypertensive effect with minimal adverse effects.
- High-dose valsartan combined with hydrochlorothiazide 25 mg did not further reduce blood pressure or increase adverse effects.
- Combination therapy with high-dose valsartan effectively controls blood pressure and clinical complications.

## Abstract

The incidence of hypertension and clinical complications 
(e.g., heart, cerebrovascular and kidney injury) is increasing worldwide. It is 
widely known that a relatively large dose of valsartan (320 mg) could alleviate 
clinical complications. The current network meta-analysis assessed which drug 
could be combined with a relatively large dose of valsartan to control blood 
pressure (BP) more effectively. And which combination therapy with different 
dosages of valsartan did not induce excessive BP reduction with increasing 
dosages of valsartan.

The PubMed, Embase, Medline, Cochrane 
Library, CNKI, Wanfang, and CSTJ databases were searched from inception to 
October 2022 for relevant randomized controlled trials (RCTs). The search 
strategies included concepts related to hypertension and two-drug combination 
therapy of different doses of valsartan, and there were no language or data 
restrictions. The outcomes included adverse effects and changes in systolic BP 
and diastolic BP. Permanent discontinuations related to treatment were the most 
accurate and objective measure of adverse effects. The common adverse effects of 
most studies (i.e., dizziness, headache, nasopharyngitis, asthenia and urticaria) 
were also included. A Bayesian network meta-analysis was performed, and mean 
differences with 95% confidence intervals were calculated. ADDIS and STATA were 
used for Bayesian model network meta-calculation.

Thirty-four 
RCTs were included involving 26,752 patients, and the interventions included 
different doses of valsartan combined with various types and doses of drugs. 
Among many combination therapies, the combination of valsartan 320 mg with 
amlodipine 10 mg (p 
< 0.01) had the best antihypertensive effect 
without significant adverse effects. Compared with valsartan 80 mg and 160 mg, 
valsartan 320 mg combined with hydrochlorothiazide 25 mg (p 
> 0.05) 
did not further reduce BP and was not shown to increase the incidence of adverse 
effects.

Combination therapy with a relatively large dose 
of valsartan could control BP and improve clinical complications effectively. 
However, for hypertensive patients with different treatment requirements, 
specific choices should be made regarding whether to control BP, treat clinical 
complications, or both.

## Linked entities

- **Chemicals:** valsartan (PubChem CID 60846), amlodipine (PubChem CID 2162), hydrochlorothiazide (PubChem CID 3639)

## Full-text entities

- **Diseases:** Hypertensive (MESH:D006973), urticaria (MESH:D014581), dizziness (MESH:D004244), asthenia (MESH:D001247), heart, cerebrovascular and kidney injury (MESH:D007674), headache (MESH:D006261), nasopharyngitis (MESH:D009304), BP reduction (MESH:D007022)
- **Chemicals:** hydrochlorothiazide (MESH:D006852), amlodipine (MESH:D017311), Valsartan (MESH:D000068756)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC11266496/full.md

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Source: https://tomesphere.com/paper/PMC11266496