Evidence map›Paper›PMID 41248336›Full record

ArticleBMJ open2025

Prognostic impact of heart failure, chronic kidney disease and atherosclerotic disease alone or combined in an elderly population: a retrospective cohort study based on electronic health record data.

João Pedro Ferreira, Tiago Taveira-Gomes, Rita Lopes, Daniel Seabra-Carvalho, Filipa Bernardo, Cristina Gavina

Abstract read
In one paragraph

Article in BMJ open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

6 authors.

João Pedro FerreiraCentre d'Investigation Clinique Plurithématique de Nancy, Vandœuvre-lès-Nancy, Grand Est, France jpferreira@med.up.pt.ORCID http://orcid.org/0000-0002-2304-6138
Tiago Taveira-GomesUniversity of Porto Faculty of Medicine, Porto, Portugal.
Rita LopesDepartment of Community Medicine, Health Information and Decision, University of Porto, Porto, Portugal.
Daniel Seabra-CarvalhoUnidade Local de Saúde de Matosinhos, Matosinhos, Portugal.
Filipa BernardoMedical Department, AstraZeneca, Lisbon, Portugal.
Cristina GavinaDepartment of Medicine, Faculdade de Medicina da Universidade do Porto, Porto, Portugal.ORCID http://orcid.org/0000-0003-2553-8264

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesHeart failure (HF), chronic kidney disease (CKD) and atherosclerotic cardiovascular disease (ASCVD) are highly prevalent conditions that often coexist. Using electronic health records (EHRs), we evaluated the 1-year risk of all-cause death, major cardiovascular and kidney events in patients with HF, CKD, ASCVD and with combinations of these conditions, compared with an unselected control population aged ≥75 years.

designRetrospective cohort study based on EHR data.

settingIntegrated primary and secondary health unit located in the North of Portugal. Eligible adult patients were identified using EHRs from 2008 to June 2022.

participantsEight cohorts were defined: (1) control: patients with ≥75 years; (2) ASCVD alone; (3) HF alone; (4) CKD alone; (5) cardiorenal syndrome (CRS): combined HF+CKD; (6) atherosclerotic HF: combined ASCVD+HF without CKD; (7) atherosclerotic CKD: combined ASCVD+CKD without HF and (8) combined ASCVD+CRS. The risk of these conditions was compared with controls using propensity score age-sex matching. We identified 19 129 patients with ASCVD alone, 13 640 patients with HF alone, 40 545 with CKD alone and 10 499 with CRS. The control group comprised 36 532 patients aged 75 years or older. PRIMARY AND SECONDARY OUTCOME MEASURES: The primary outcome was all-cause mortality. The main secondary outcomes were cardiovascular death, HF hospitalisations and end-stage renal disease.

resultsThe 1-year mortality rate was 0.65% in the control cohort, 5.6% for patients with ASCVD alone, 6.05% for patients with HF alone and 3.53% for patients with CKD alone. Adjusted risk of all-cause death was significantly increased in the ASCVD-alone (HR: 8.42, 95% CI 7.12 to 9.95), HF-alone (HR: 9.19, 95% CI 7.75 to 10.9) and CKD-alone (HR: 5.35, 95% CI 4.62 to 6.19) cohorts, compared with control population; however, patients with the combination of all three conditions (ie, ASCVD+CRS) had the highest mortality risk (HR: 14.18, 95% CI 11.62 to 17.3). A similar association pattern was observed for cardiovascular death, HF events and end-stage renal disease.

conclusionsOur results support the concept of an atherosclerotic cardiorenal phenotype, with a very high risk of mortality, cardiovascular and renal adverse events. Implementation strategies are required to target these conditions simultaneously.

Indexed as

AtherosclerosisElectronic Health RecordsHeart FailureRenal Insufficiency, ChronicAgedAged, 80 and overFemaleHumansMalePortugalPrognosisRetrospective StudiesRisk FactorsCoronary heart diseaseDIABETES & ENDOCRINOLOGYHeart failureKidney & urinary tract disorders

Identifiers

PMID41248336
PMCPMC12625902

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LicenceCC BY-NC
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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.