Evidence map›Paper›PMID 39780945›Full record

ArticlePorto biomedical journal

Platelet distribution width-a prognosis marker in patients with chronic heart failure.

Ana Neves, Rita Gouveia, Sérgio Madureira, Catarina Elias, Pedro Ribeirinho-Soares, Marta Soares-Carreira, Joana Pereira, Jorge Almeida, Patrícia Lourenço

Abstract read
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Article in Porto biomedical journal. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Ana NevesInternal Medicine Department, Unidade Local de Saúde São João, Porto, Portugal.
Rita GouveiaInternal Medicine Department, Unidade Local de Saúde São João, Porto, Portugal.
Sérgio MadureiraInternal Medicine Department, Unidade Local de Saúde São João, Porto, Portugal.
Catarina EliasInternal Medicine Department, Unidade Local de Saúde São João, Porto, Portugal.
Pedro Ribeirinho-SoaresInternal Medicine Department, Unidade Local de Saúde São João, Porto, Portugal.
Marta Soares-CarreiraInternal Medicine Department, Unidade Local de Saúde São João, Porto, Portugal.
Joana PereiraInternal Medicine Department, Unidade Local de Saúde São João, Porto, Portugal.
Jorge AlmeidaInternal Medicine Department, Unidade Local de Saúde São João, Porto, Portugal.
Patrícia LourençoInternal Medicine Department, Unidade Local de Saúde São João, Porto, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Increased levels of platelet distribution width (PDW) can predict cardiac death and infarction recurrence in acute myocardial infarction. PDW appears to be a prognosis marker in acute heart failure (HF); however, its impact on chronic HF is still unknown. We investigated the impact of PDW on chronic HF. Methods: We retrospectively analyzed outpatients with chronic HF with left ventricular systolic dysfunction (LVSD) from January 2012 to May 2018. Patients with no data on PDW levels or with preserved or recovered ejection fraction were excluded. The primary end point was all-cause mortality. Multivariable Cox regression analysis was used to evaluate the association between PDW and mortality. A multivariate model was built adjusting for age, sex, comorbidities, brain-type natriuretic peptide, New York Heart Association (NYHA) class, evidence-based therapy, and severity of LVSD. Results: In our cohort of 766 patients, 65.7% were male, the mean age was 70 years, and 35.4% were in NYHA class I; 38.3% had diabetes mellitus, 51.4% had severe LVSD, and 3.9% had an inflammatory or autoimmune disease. The median (interquartile range) PDW was 13.5 (12.1-14.9) fL. During a median follow-up of 49 (30-79) months, 372 patients (48.6%) died. Patients with PDW ≥ 14.3 fL presented a multivariate-adjusted higher risk of all-cause death than those with lower values (hazard ratio: 1.32, 95% confidence interval [CI]: 1.05-1.64, Conclusions: Patients with PDW ≥14.3 fL (upper tercile for PDW) presented a multivariate-adjusted 32% (95% CI: 5-64%) higher risk of all-cause death than those with lower values. PDW can help clinicians stratify patients with chronic HF; it is a practical, inexpensive, and widely available parameter.

Indexed as

chronic heart failureplatelet distribution widthprognosis

Identifiers

PMID39780945
PMCPMC11706588

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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.