Evidence map›Paper›PMID 38718428›Full record

ArticleArchivos de cardiologia de Mexico2024

[Diagnosis and treatment in a series of patients with cardiac corrected transposition of the great arteries (double discordance)].

Jesús De Rubens-Figueroa, Paulina Villamar-García, Diana G Ruiz-Meléndez, Carlos González-Rebeles, Alexis Palacios-Macedo

Abstract readEnglish Abstract
In one paragraph

Article in Archivos de cardiologia de Mexico, 2024. 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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0citing papers 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

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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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

5 authors.

Jesús De Rubens-FigueroaServicio de Cardiología, Laboratorio de Ecocardiografía, Instituto Nacional de Pediatría, Ciudad de México, México.
Paulina Villamar-GarcíaServicio de Pediatría, Instituto Nacional de Pediatría, Ciudad de México, México.
Diana G Ruiz-MeléndezServicio de Cardiología, Instituto Nacional de Pediatría, Ciudad de México, México.
Carlos González-RebelesServicio de Cardiología, Laboratorio de Electrofisiología, Instituto Nacional de Pediatría, Ciudad de México, México.
Alexis Palacios-MacedoServicio de Cirugía Cardiaca, Instituto Nacional de Pediatría, Ciudad de México, México.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: The atrio-ventricular and ventricle-arterial double discordance (DD) or corrected transposition of the great arteries is a rare heart disease, it occurs in 0.02-0.07 of every 1,000 live newborns. The objective of the study is to describe the diagnosis, treatment and evolution of a series of patients with DD. Method: A retrospective and descriptive study was carried out, reviewing the records of patients diagnosed with DD in the last 22 years. Descriptive statistics were performed. Numerical variables were obtained using means and standard deviation and categorical variables using frequencies and percentages. Results: Thirty patients were studied in 22 years with a ratio of 1.5:1 for men, with a mean age of 20 months. The situs was solitus in 24/29 patients (82.7%). Ventricular septal defect was the most frequent lesion in 25/29 (86.2%) Tricuspid insufficiency in 70%. Four patients diagnosed with pulmonary atrial hypertension. With atrio-ventricular block 20%. One with Wolff-Parkinson-White syndrome. Surgical treatment was carried out in 70% of patients. Eight with Glenn procedure (26.6%) and 4 with Fontan surgery (13.3%). Follow-up ranged from 1 month to 17 years. Five died (16.6%). Of the 25 patients in follow-up, 18 patients (72%) had normal ventricular function, 5 with Grade II Ross classification (20%) and 2 in Grade III (8%). Conclusions: The quality of life of these patients is improving and there is still controversy in the literature about the ideal time to perform the most appropriate surgical procedure.

Indexed as

Congenital heart diseaseCongenitally corrected transposition of the great arteriesDoublediscordanceVentricular inversion

Identifiers

PMID38718428
PMCPMC12148540

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