Evidence map›Paper›PMID 31073477›Full record

ArticleJournal of pediatric intensive care2018

Innovative Strategies for the Management of a Massive Neonatal Rhabdomyoma.

N Prabhu, N Osifodunrin, D Murphy, S Butler, L E Hunter

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in Journal of pediatric intensive care, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–field-weighted citation impact, top 85% 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, 1 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Pooled it
  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

5 authors at 1 institution in 1 country.

N PrabhuDepartment of Paediatric Cardiology, Royal Hospital for Children, Glasgow, United Kingdom.
N OsifodunrinDepartment of Paediatric Oncology, Royal Hospital for Children, Glasgow, United Kingdom.
D MurphyDepartment of Paediatric Oncology, Royal Hospital for Children, Glasgow, United Kingdom.
S ButlerDepartment of Paediatric Radiology, Royal Hospital for Children, Glasgow, United Kingdom.
L E HunterDepartment of Paediatric Cardiology, Royal Hospital for Children, Glasgow, United Kingdom.
Royal Hospital for Children · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rhabdomyomas are histologically benign tumors known to be associated with tuberous sclerosis. The natural history predicts the majority of tumors to be asymptomatic and regress within the first year of life. We describe a neonate presenting on day 1 of life with cardiovascular collapse secondary to a massive rhabdomyoma. Surgical resection was excluded due to the extensive nature of the lesion and oral sirolimus, a mammalian target of rapamycin inhibitor, was commenced to promote tumor regression. The patient developed intractable arrhythmias requiring extracorporeal life support during therapy.

Indexed as

extracorporeal life supportmTOR inhibitorsrhabdomyoma

Identifiers

PMID31073477
PMCPMC6260344
OpenAlexW2755215844

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.