Evidence map›Paper›PMID 38398730›Full record

ArticleLife (Basel, Switzerland)2024

Familiar Disposition of May-Thurner Syndrome-A Case Series.

Stefanie Nowak, André Jakob, Robert Dalla Pozza, Sebastian Michel, Nikolaus A Haas, Joseph Pattathu

Open access · goldAbstract readCase Reports
In one paragraph

Article in Life (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.6field-weighted citation impact, top 20% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

6 authors at 1 institution in 1 country.

Stefanie NowakDepartment of Paediatric Cardiology and Paediatric Intensive Care, University Hospital, Ludwig-Maximilians-University, 81377 Munich, Germany.
André JakobDepartment of Paediatric Cardiology and Paediatric Intensive Care, University Hospital, Ludwig-Maximilians-University, 81377 Munich, Germany.ORCID 0000-0003-3580-2268
Robert Dalla PozzaDepartment of Paediatric Cardiology and Paediatric Intensive Care, University Hospital, Ludwig-Maximilians-University, 81377 Munich, Germany.
Sebastian MichelDepartment of Paediatric Cardiology and Paediatric Intensive Care, University Hospital, Ludwig-Maximilians-University, 81377 Munich, Germany.
Nikolaus A HaasDepartment of Paediatric Cardiology and Paediatric Intensive Care, University Hospital, Ludwig-Maximilians-University, 81377 Munich, Germany.
Joseph PattathuDepartment of Paediatric Cardiology and Paediatric Intensive Care, University Hospital, Ludwig-Maximilians-University, 81377 Munich, Germany.
Ludwig-Maximilians-Universität München · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

May-Thurner syndrome is a venous compression syndrome of the pelvic vessels that represents a relevant risk factor for thrombus formation. The standard procedure to secure a diagnosis is venography, followed by endovascular therapy as the preferred treatment choice if the patient is symptomatic. In our case series, there are three related patients with May-Thurner syndrome. A 16-year-old female was admitted with pulmonary embolism, dyspnoea and hip pain. The compression syndrome was diagnosed with interventional venography, and the patient received venous stent implantation. Due to her family history, we also suspected her mother to be affected by the syndrome and elucidated the diagnosis shortly afterwards by invasive venography. Subsequently, we examined the patient's 19-year-old brother, and magnetic resonance imaging confirmed May-Thurner syndrome. A similar case series has not been published before. In this case, the family relation indicates a possible hereditary aspect of May-Thurner syndrome. This hypothesis should be the subject of further research. In conclusion, it is essential to assess family history thoroughly when treating patients with May-Thurner syndrome.

Indexed as

case serieschildhoodhereditaryiliac compression syndromeMay–Thurner syndromepulmonary embolism

Identifiers

PMID38398730
PMCPMC10890414
OpenAlexW4391540214

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.