Evidence map›Paper›PMID 35748048›Full record

ArticleEuropean journal of heart failure2022

Clinical implications of left atrial changes after optimization of medical therapy in patients with heart failure.

Riccardo M Inciardi, Matteo Pagnesi, Carlo M Lombardi, Stefan D Anker, John G Cleland, Kenneth Dickstein, Gerasimos S Filippatos, Chim C Lang, Leong L Ng, Pierpaolo Pellicori and 7 more

Open access · hybridAbstract read
In one paragraph

Article in European journal of heart failure, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 13 institutions in 9 countries.

Riccardo M Inciardi *Institute of Cardiology, ASST Spedali Civili, Department of Medical and Surgical Specialties, Radiological Sciences and Public Health, University of Brescia, Brescia, Italy.
Matteo Pagnesi *Institute of Cardiology, ASST Spedali Civili, Department of Medical and Surgical Specialties, Radiological Sciences and Public Health, University of Brescia, Brescia, Italy.
Carlo M LombardiInstitute of Cardiology, ASST Spedali Civili, Department of Medical and Surgical Specialties, Radiological Sciences and Public Health, University of Brescia, Brescia, Italy.
Stefan D AnkerDivision of Cardiology and Metabolism, Department of Cardiology (CVK) and Berlin-Brandenburg Center for Regenerative Therapies (BCRT), German Centre for Cardiovascular Research (DZHK) Partner Site Berlin, Charité Universitätsmedizin Berlin, Berlin, Germany.
John G ClelandNational Heart and Lung Institute, Royal Brompton and Harefield Hospitals, Imperial College, London, UK.
Kenneth DicksteinUniversity of Bergen, Bergen, Norway.
Gerasimos S FilippatosDepartment of Cardiology, Attikon University Hospital, National and Kapodistrian University of Athens, Athens, Greece.
Chim C LangSchool of Medicine Centre for Cardiovascular and Lung Biology, Division of Molecular and Clinical Medicine, University of Dundee, Ninewells Hospital & Medical School, Dundee, UK.
Leong L NgDepartment of Cardiovascular Sciences, University of Leicester, Glenfield Hospital, Leicester, UK.
Pierpaolo PellicoriRobertson Centre for Biostatistics and Clinical Trials, University of Glasgow, Glasgow, UK.
Piotr PonikowskiDepartment of Heart Diseases, Wroclaw Medical University, Wrocław, Poland.
Nilesh J SamaniDepartment of Cardiovascular Sciences, University of Leicester, Glenfield Hospital, Leicester, UK.
Faiez ZannadUniversite de Lorraine, Inserm Centre d'Investigations Cliniques 1433 and F-CRIN INI-CRCT, Nancy, France.
Dirk J van VeldhuisenDepartment of Cardiology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Scott D SolomonCardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Adriaan A VoorsDepartment of Cardiology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Marco MetraInstitute of Cardiology, ASST Spedali Civili, Department of Medical and Surgical Specialties, Radiological Sciences and Public Health, University of Brescia, Brescia, Italy.
University of Brescia · ITUniversity of Groningen · NLBrigham and Women's Hospital · USCharité - Universitätsmedizin Berlin · DEGlasgow Royal Infirmary · GBGlenfield Hospital · GBImperial College London · GBNational and Kapodistrian University of Athens · GRStavanger University Hospital · NOUniversité de Lorraine · FRUniversity of Dundee · GBUniversity of Leicester · GBWroclaw Medical University · PL

Funding

European Commission EudraCT 2010-020808-29European Commission FP7-242209-BIOSTAT-CHFFP7 Ideas: European Research Council Grant Agreement n;242209
6 · The paper itself

Abstract

aimsLimited data exist regarding the prognostic relevance of changes in left atrial (LA) dimensions in patients with heart failure (HF). We assessed changes in LA dimension and their relation with outcomes after optimization of guideline-directed medical therapy (GDMT) in patients with new-onset or worsening HF. METHODS AND

resultsLeft atrial diameter was assessed at baseline and 9 months after GDMT optimization in 632 patients (mean age 65.8 ± 12.1 years, 22.3% female) enrolled in BIOSTAT-CHF. LA adverse remodelling (LAAR) was defined as an increase in LA diameter on transthoracic echocardiography between baseline and 9 months. After the 9-month visit, patients were followed for a median of 13 further months. LAAR was observed in 247 patients (39%). Larger baseline LA diameter (odds ratio [OR] 0.90; 95% confidence interval [CI] 0.87-0.93; p < 0.001) and up-titration to higher doses of angiotensin-converting enzyme inhibitors or angiotensin receptor blockers (ACEi/ARBs) (OR 0.56; 95% CI 0.34-0.92; p = 0.022) were independently associated with lower likelihood of LAAR. LAAR was associated with an increased risk of the composite of all-cause mortality or HF hospitalization (log-rank p = 0.007 and adjusted hazard ratio 1.73, 95% CI 1.22-2.45, p = 0.002). The association was more pronounced in patients without a history of atrial fibrillation (p for interaction = 0.009).

conclusionAmong patients enrolled in BIOSTAT-CHF, LAAR was associated with an unfavourable outcome and was prevented by ACEi/ARB up-titration. Changes in LA dimension may be a useful marker of response to treatment and improve risk stratification in patients with HF.

Indexed as

Atrial FibrillationHeart FailureAgedAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor AntagonistsFemaleHumansMaleMiddle AgedAngiotensin-Converting Enzyme InhibitorsAngiotensin Receptor AntagonistsGuideline-directed medical therapyHeart failureLeft atrium

Identifiers

PMID35748048
PMCPMC10084101
OpenAlexW4283459153

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.