Evidence map›Paper›PMID 39589769›Full record

ArticleFuture cardiology2024

Primary congenital abdominal aortic aneurysm associated with renovascular hypertension in pediatric patient.

Emad M Al-Osail, Caroline Rousset-Rouviere, Philippe Piquet, Marine Gaudry

Abstract readCase Reports
In one paragraph

Article in Future cardiology, 2024. 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

4 authors.

Emad M Al-OsailDepartment of Vascular Surgery, Aortic Centre, Hôpital de la Timone, Marseille, France.
Caroline Rousset-RouviereDepartment of Nephrology, Hôpital de la Timone, Marseille, France.
Philippe PiquetDepartment of Vascular Surgery, Aortic Centre, Hôpital de la Timone, Marseille, France.
Marine GaudryDepartment of Vascular Surgery, Aortic Centre, Hôpital de la Timone, Marseille, France.ORCID 0000-0001-9717-475X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Idiopathic congenital abdominal aortic aneurysm (AAA) is rare, with only a few cases reported in the literature. We present a case of a 3-year-old girl with a fusiform AAA measuring 19 mm in segments 4 and 5, associated with renal artery stenosis and severe hypertension. She was treated with three antihypertensive medications. Initially, left nephrectomy was performed due to the persistence of hypertension. Subsequently, we conducted a hepatorenal bypass and open surgical repair of the AAA via left thoracolumbar approach. At the 4-year follow-up, there were no complications. Pediatric CAAA is very rare. Case-by-case discussion and management are essential; the open approach with synthetic grafts is the gold standard and has resulted in good outcomes.

Indexed as

Aortic Aneurysm, AbdominalHypertension, RenovascularChild, PreschoolComputed Tomography AngiographyFemaleHumansTomography, X-Ray Computedaneurysmcongenitalhypertensionpediatricrenovascular

Identifiers

PMID39589769
PMCPMC11622790

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.