Evidence map›Paper›PMID 31496864›Full record

ArticlePediatric health, medicine and therapeutics2019

Prune belly syndrome: current perspectives.

Angela M Arlen, Cayce Nawaf, Andrew J Kirsch

Open access · goldAbstract read
In one paragraph

Article in Pediatric health, medicine and therapeutics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
7.3field-weighted citation impact, top 3% 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

12 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. A case of prune belly syndrome: Experience from a regional hospital in Togo.International journal of surgery case reports · 2023
    Article
  7. Dental treatment of patients with prune belly syndrome.Special care in dentistry : official publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry · 2023
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Two cases of Prune Belly Syndrome from Kagera Region Tanzania.The East African health research journal · 2020
    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

3 authors at 2 institutions in 1 country.

Angela M ArlenYale University School of Medicine, Department of Urology, New Haven, CT 06520, USA.
Cayce NawafYale University School of Medicine, Department of Urology, New Haven, CT 06520, USA.
Andrew J KirschEmory University, Children's Healthcare of Atlanta, Atlanta, GA 30328, USA.
Yale University · USEmory University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prune belly syndrome (PBS) is a rare but morbid congenital disease, classically defined by a triad of cardinal features that includes cryptorchidism, urinary tract dilation and laxity of the abdominal wall musculature. Children often require numerous surgical interventions including bilateral orchidopexy as well as individually tailored urinary tract and abdominal wall reconstruction. Along with the classic features, patients with PBS often experience gastrointestinal, orthopedic, and cardiopulmonary comorbidities.

Indexed as

abdominal wall laxityabdominoplastycryptorchidismprune-belly syndromeurinary tract dilation

Identifiers

PMID31496864
PMCPMC6689549
OpenAlexW2964805862

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.