Evidence map›Paper›PMID 30349279›Full record

Trial reportVascular health and risk management2018

Influence of fixed-dose combination perindopril/amlodipine on target organ damage in patients with arterial hypertension with and without ischemic heart disease (results of EPHES trial).

Ganna D Radchenko, Liliya O Mushtenko, Yuriy M Sirenko

Open access · goldAbstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in Vascular health and risk management, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 26% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 9 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Ganna D RadchenkoState Institute "National Scientific Center "Institute of Cardiology named after acad.M.Strazhesko" of Ukrainian National Academy of Medical Science, Kyiv, Ukraine, rganna@bigmir.net.
Liliya O MushtenkoState Institute "National Scientific Center "Institute of Cardiology named after acad.M.Strazhesko" of Ukrainian National Academy of Medical Science, Kyiv, Ukraine, rganna@bigmir.net.
Yuriy M SirenkoState Institute "National Scientific Center "Institute of Cardiology named after acad.M.Strazhesko" of Ukrainian National Academy of Medical Science, Kyiv, Ukraine, rganna@bigmir.net.
National Scientific Center "M.D. Strazhesko Institute of Cardiology" · UA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe EPHES trial (Evaluation of influence of fixed dose combination Perindo-pril/amlodipine on target organ damage in patients with arterial HypErtension with or without iSchemic heart disease) compared the dynamics of target organ damage (TOD) in hypertensive patients with and without ischemic heart disease (IHD) treated with the fixed-dose combination (FDC) perindopril + amlodipine.

methodsThe analysis included 60 hypertensive patients (aged >30 years): 30 without IHD and 30 with IHD. At randomization, FDC was administered at a daily baseline dose of 5/5 mg with uptitration to 10/10 mg every two weeks. If target blood pressure (BP<140/90 mmHg) was not achieved after six weeks, indapamide 1.5 mg was added to the regimen. All patients underwent body mass index measurements, office and ambulatory BP measurements, pulse wave velocity (PWVe) and central systolic BP evaluation, augmentation index adjusted to heart rate 75 (Aix@75) evaluation, biochemical analysis, ECG, echocardiography with Doppler, ankle-brachial index measurement, and intima-media thickness measurement. The follow-up period was 12 months.

resultsTherapy based on FDC perindopril/amlodipine was effective in lowering BP (office, ambulatory, central) in both groups. We noted significant decrease in Aix@75 with the therapy in both groups, but ΔAix@75 was lesser in the group with IHD than the group without IHD. FDC provided significant improvement in PWVe and left ventricular diastolic function, and decrease in albuminuria, left ventricular hypertrophy (LVH), and left atrium size. ΔPWVe was significantly (

conclusionThus, treatment based on FDC was effective in decreasing BP and TOD regression in both patients with and without IHD. However, the dynamics of changes in TOD were different between the two groups, which should be taken into consideration during management of patients with and without IHD.

Indexed as

AdultAmlodipineAngiotensin-Converting Enzyme InhibitorsAntihypertensive AgentsArterial PressureCalcium Channel BlockersDrug CombinationsFemaleHumansHypertensionMaleMiddle AgedMyocardial IschemiaPerindoprilTime FactorsTreatment OutcomeAmlodipineamlodipine, perindopril drug combinationAngiotensin-Converting Enzyme InhibitorsAntihypertensive AgentsCalcium Channel BlockersDrug CombinationsPerindoprilamlodipinearterial hypertensionfixed-dose combinationischemic heart diseaseperindoprilprospective observationtarget organ damage regression

Identifiers

PMID30349279
PMCPMC6188174
OpenAlexW2897833364

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.