Evidence map›Paper›PMID 38274311›Full record

ArticleFrontiers in cardiovascular medicine2023

Arrhythmias in children undergoing orthotopic heart transplantation.

Eser Doğan, Fırat Ergin, Mehmet B Beyter, Gülçin K Kaşıkçı, Şeyma Ş Ön, Oğuzhan Ay, Reşit E Levent, Çağatay Engin, Zülal Ülger

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cardiovascular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.6field-weighted citation impact, top 38% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

9 authors at 1 institution in 1 country.

Eser DoğanDepartment of Pediatric Cardiology, Faculty of Medicine, Ege University, İzmir, Türkiye.
Fırat ErginDepartment of Pediatric Cardiology, Faculty of Medicine, Ege University, İzmir, Türkiye.
Mehmet B BeyterDepartment of Pediatric Cardiology, Faculty of Medicine, Ege University, İzmir, Türkiye.
Gülçin K KaşıkçıDepartment of Pediatric Cardiology, Faculty of Medicine, Ege University, İzmir, Türkiye.
Şeyma Ş ÖnDepartment of Pediatric Cardiology, Faculty of Medicine, Ege University, İzmir, Türkiye.
Oğuzhan AyDepartment of Pediatric Cardiology, Faculty of Medicine, Ege University, İzmir, Türkiye.
Reşit E LeventDepartment of Pediatric Cardiology, Faculty of Medicine, Ege University, İzmir, Türkiye.
Çağatay EnginDepartment of Cardiovascular Surgery, Faculty of Medicine, Ege University, İzmir, Türkiye.
Zülal ÜlgerDepartment of Pediatric Cardiology, Faculty of Medicine, Ege University, İzmir, Türkiye.
Ege University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Heart transplantation (HT) is the only treatment option in children with heart failure secondary to cardiomyopathies and non-reparable congenital heart diseases. Methods: We performed a retrospective clinical data review of all consecutive pediatric patients (aged 2-18 years) who underwent orthotopic HT for advanced heart failure at our institution between January 2007 and January 2023. Clinical, procedural, and follow-up data were collected and comprehensively analyzed. Results: We identified 27 children (66.7% males) with a median age of 15 years (IQR: 7-16) and a median weight of 45 kg (IQR: 22-66) at the time of the intervention. 24 patients (88.8%) were diagnosed with dilated cardiomyopathy, 2 (7.4%) with restrictive cardiomyopathy, and 1 (3.7%) with hypertrophic cardiomyopathy. On a median follow-up of 35.07 months (IQR: 13.13-111.87), arrhythmias were detected in 9 (33%) patients. Three patients developed symptomatic sinus node dysfunction at 18, 25, and 38 days and received permanent pacemakers. One patient developed a complete AV block during acute rejection at 76 months and received a temporary pacemaker. Two patients developed chronic sinus tachycardia at 4 and 16 months and were treated with Beta-blockers after eliminating all causes of sinus tachycardia. One patient developed a complete right bundle branch block at 12 months. One patient developed ventricular extrasystole at 10 months and was found to have grade 2 rejection. An Atrial extrasystole was detected in one patient at 96 months. We did not identify significant risk factors for arrhythmias post-HT. Discussion: After pediatric HT, early-onset rhythm disturbances, often attributed to surgery-related issues such as sinus node dysfunction, may necessitate invasive treatments like permanent pacemaker therapy. Close monitoring post-transplantation is crucial, and routine follow-up with Holter ECG is necessary to identify potential rhythm disorders even in the absence of symptoms. Rhythm disturbances that develop during follow-up can serve as early indicators of graft rejection and should be carefully evaluated.

Indexed as

arrhythmiaECGHolter ECGpediatrictransplantation (heart)

Identifiers

PMID38274311
PMCPMC10808697
OpenAlexW4390745131

What OpenQuestion holds

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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.