Evidence map›Paper›PMID 32845542›Full record

ArticleAnnals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc2021

Prognostic value of initial QRS analysis in anterior STEMI: Correlation with left ventricular systolic dysfunction, serum biomarkers, and cardiac outcomes.

Marta López-Castillo, Álvaro Aceña, Ana M Pello-Lázaro, Vanessa Viegas, Beatriz Merchán Muñoz, Rocío Carda, Juan Franco-Peláez, Maria Luisa Martín-Mariscal, Sem Briongos-Figuero, Jose Tuñón

Open access · goldAbstract read
In one paragraph

Article in Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 25% 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, 9 citations in OpenAlex.

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  7. Prognostic value of initial QRS analysis in anterior STEMI: Correlation with left ventricular systolic dysfunction, serum biomarkers, and cardiac outcomes.Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc · 2021
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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

10 authors at 5 institutions in 1 country.

Marta López-CastilloDepartment of Cardiology, IIS-Fundación Jiménez Díaz, Madrid, Spain.ORCID 0000-0001-7056-3501
Álvaro AceñaDepartment of Cardiology, IIS-Fundación Jiménez Díaz, Madrid, Spain.
Ana M Pello-LázaroDepartment of Cardiology, IIS-Fundación Jiménez Díaz, Madrid, Spain.
Vanessa ViegasDepartment of Urology, Hospital La Princesa, Madrid, Spain.
Beatriz Merchán MuñozDepartment of Hematology, Hospital de Guadalajara, Guadalajara, Spain.
Rocío CardaDepartment of Cardiology, IIS-Fundación Jiménez Díaz, Madrid, Spain.
Juan Franco-PeláezDepartment of Cardiology, IIS-Fundación Jiménez Díaz, Madrid, Spain.
Maria Luisa Martín-MariscalDepartment of Cardiology, Hospital Rúber Juan Bravo, Madrid, Spain.
Sem Briongos-FigueroDepartment of Cardiology, Hospital Infanta Leonor, Madrid, Spain.
Jose TuñónDepartment of Cardiology, IIS-Fundación Jiménez Díaz, Madrid, Spain.
Hospital Universitario Fundación Jiménez Díaz · ESHospital Ruber Internacional · ESHospital Universitario de Guadalajara · ESHospital Universitario de La Princesa · ESHospital Universitario Infanta Leonor · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe presence of pathologic Q waves on admission electrocardiogram (ECG) in patients with anterior ST-elevated myocardial infarction (STEMI) has been related to adverse cardiac outcomes. Our study evaluates the prognostic value of QRS complex and Q waves in patients with STEMI undergoing percutaneous coronary intervention.

methodsWe prospectively analyzed the specific characteristics of QRS complex and pathologic Q waves on admission and on discharge ECG in 144 patients hospitalized for anterior STEMI. We correlated these findings with the development of left ventricular systolic dysfunction (LVSD), appearance of heart failure (HF) or death during follow-up, and levels of several biomarkers obtained 6 months after the index event.

resultsMultivariate logistic regression analysis showed that QRS width (odds ratios [OR] 1.05, p = .001) on admission ECG and the sum of Q-wave depth (OR 1.06, p = .002) on discharge ECG were independent predictors of LVSD development. Moreover, QRS width on admission ECG was related to an increased risk of HF or death (OR 1.03, p = .026). Regarding biomarkers, QRS width on admission ECG revealed a statistically significant relationship with the levels of NT-pro-BNP at 6 months (0.29, p = .004); the sum of Q-wave depth (0.27, p = .012) and width (0.25, p = .021) on admission ECG was related to the higher levels of hs-cTnI; the sum of the voltages in precordial leads both on admission ECG (-0.26, p = .011) and discharge ECG (0.24, p = .046) was related to the lower levels of parathormone.

conclusionsAssessment of QRS complex width and pathologic Q waves on admission and discharge ECGs aids in predicting long-term prognosis in patients with STEMI.

Indexed as

BiomarkersElectrocardiographyFemaleHeartHumansMaleMiddle AgedNatriuretic Peptide, BrainPeptide FragmentsPrognosisProspective StudiesST Elevation Myocardial InfarctionTroponin IVentricular Dysfunction, LeftBiomarkersNatriuretic Peptide, BrainPeptide Fragmentspro-brain natriuretic peptide (1-76)Troponin Ielectrocardiogrammyocardial infarctionQRS complexQ wavessystolic dysfunction

Identifiers

PMID32845542
PMCPMC7816810
OpenAlexW3080392723

What OpenQuestion holds

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LicenceCC BY
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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.