Evidence map›Paper›PMID 38817264›Full record

ArticleAnnals of pediatric cardiology

Anomalous right coronary artery from the pulmonary artery in an infant with tetralogy of Fallot.

Swati Garekar, Ronak Sheth, Sachin Patil, Bharat Soni, Dhananjay P Malankar

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Annals of pediatric cardiology. 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. Article
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.

Swati GarekarDepartment of Paediatric Cardiology, Fortis Pediatric and Congenital Heart Centre, Mumbai, Maharashtra, India.
Ronak ShethDepartment of Paediatric Cardiology, Fortis Pediatric and Congenital Heart Centre, Mumbai, Maharashtra, India.
Sachin PatilDepartment of Pediatric Cardiac Anaesthesia and Critical Care, Fortis Paediatric and Congenital Heart Centre, Mumbai, Maharashtra, India.
Bharat SoniDepartment of Paediatric Cardiac Surgery, Fortis Pediatric and Congenital Heart Centre, Mumbai, Maharashtra, India.
Dhananjay P MalankarDepartment of Paediatric Cardiac Surgery, Fortis Pediatric and Congenital Heart Centre, Mumbai, Maharashtra, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An anomalous right coronary artery from the pulmonary artery (ARCAPA) is a rare congenital anomaly that does not have the typical presentation of the more common anomalous left coronary artery. We present an infant with tetralogy of Fallot with atypical findings on the preoperative echocardiogram. A cardiac computerized tomographic (CT) scan showed ARCAPA. This was confirmed intraoperatively and repaired successfully. Close attention to coronaries on echocardiography and a low threshold for additional imaging can successfully diagnose ARCAPA in the presence of additional congenital heart defects.

Indexed as

Anomalous right coronary artery from the pulmonary arterycongenital heart defectcoronary artery anomalytetralogy of Fallot

Identifiers

PMID38817264
PMCPMC11135895

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.