Evidence map›Paper›PMID 32959110›Full record

Trial reportEuropean journal of clinical pharmacology2021

The impact of acetylsalicylic acid dosed at bedtime on circadian rhythms of blood pressure in the high-risk group of cardiovascular patients-a randomized, controlled trial.

Beata Krasińska, Lech Paluszkiewicz, Ewa Miciak-Ławicka, Maciej Krasinski, Piotr Rzymski, Andrzej Tykarski, Zbigniew Krasiński

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in European journal of clinical pharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 2 pooled it
0.9field-weighted citation impact, top 22% 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

7 citing papers in PubMed, 2 syntheses or guidelines pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Circadian rhythms in cardiovascular disease.European heart journal · 2025
    Review
  5. Article
  6. Article
  7. Circadian Rhythms, Disease and Chronotherapy.Journal of biological rhythms · 2021
    Review
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

7 authors at 3 institutions in 3 countries.

Beata KrasińskaDepartment of Hypertension, Angiology and Internal Diseases, Poznan University of Medical Sciences, Długa 1/2, 61-848, Poznań, Poland. beata.bkrasinska@gmail.com.ORCID http://orcid.org/0000-0002-3464-1645
Lech PaluszkiewiczDepartment of Thoracic And Cardiovascular Surgery/Perioperative diagnostics Bad Oeynhausen, Heart and Diabetes Center NRW, Ruhr-University of Bochum, Bochum, Germany.
Ewa Miciak-ŁawickaDepartment of Hypertension, Angiology and Internal Diseases, Poznan University of Medical Sciences, Długa 1/2, 61-848, Poznań, Poland.
Maciej KrasinskiImperial College London School of Medicine, London, UK.
Piotr RzymskiDepartment of Environmental Medicine, Poznan University of Medical Sciences, Poznan, Poland.
Andrzej TykarskiDepartment of Hypertension, Angiology and Internal Diseases, Poznan University of Medical Sciences, Długa 1/2, 61-848, Poznań, Poland.
Zbigniew KrasińskiDepartment of General and Vascular Surgery, Poznan University of Medical Sciences, Poznan, Poland.
Poznan University of Medical Sciences · PLHeart and Diabetes Center North Rhine-Westphalia · DEImperial College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTime of drug administration may significantly influence its effect. The aim of the present study was to investigate the effect of ASA (administrated in the morning or in the evening) on the anti-hypertensive effect and diurnal blood pressure profile in the high-risk group of cardiovascular patients.

methodsAll patients (n = 114) had been diagnosed with coronary heart disease and arterial hypertension prior to the enrolment and had been treated with 75 mg per day of ASA in the morning. The patients were randomly assigned to one of the two study groups receiving 75 mg of ASA per day in a single antiplatelet therapy for 3 months in the morning (n = 58) or in the evening (n = 56). The control group (n = 61) consisted of patients with arterial hypertension but without coronary heart disease, not receiving ASA. In all the patients, during each visit, clinical blood pressure (BP) and ambulatory blood pressure measurements (ABPM) were performed.

resultsThere was a significant reduction in 24-h BP and blood pressure at night in the ASA group evening group compared with the ASA morning group and the control group.

conclusionsThe present study demonstrated that compared with the use of ASA in the morning, its administration in the evening may lead to favourable drop in the ABPM and an improvement of the diurnal profile in the high-risk group of cardiovascular patients who are not naïve to ASA.

Indexed as

AgedAntihypertensive AgentsAspirinBlood PressureCircadian RhythmCoronary DiseaseDrug Administration ScheduleFemaleHumansHypertensionMaleMiddle AgedRiskAntihypertensive AgentsAspirinAcetylsalicylic acidAnti-hypertensive effectBedtime administrationChronotherapyCircadian rhythmRandomized controlled trial

Identifiers

PMID32959110
PMCPMC7782434
OpenAlexW3087523712

What OpenQuestion holds

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Registered trials

None linked

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.