Evidence map›Paper›PMID 34591219›Full record

ReviewClinical and experimental medicine2022

Special situations in pheochromocytomas and paragangliomas: pregnancy, metastatic disease, and cyanotic congenital heart diseases.

Marta Araujo-Castro, Lía Nattero Chavez, Alberto Martínez Lorca, Javier Molina-Cerrillo, Teresa Alonso-Gordoa, Eider Pascual-Corrales

Abstract readReview
PubMed Publisher
In one paragraph

Review in Clinical and experimental medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 23% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. 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 2 institutions in 1 country.

Marta Araujo-CastroDepartment of Endocrinology and Nutrition, Instituto de Investigación Sanitaria Ramón y Cajal (IRYCIS), Hospital Universitario Ramón y Cajal, Colmenar Viejo Street km. 9,100, 28034, Madrid, Spain. marta.araujo@salud.madrid.org.ORCID http://orcid.org/0000-0002-0519-0072
Lía Nattero ChavezDepartment of Endocrinology and Nutrition, Instituto de Investigación Sanitaria Ramón y Cajal (IRYCIS), Hospital Universitario Ramón y Cajal, Colmenar Viejo Street km. 9,100, 28034, Madrid, Spain.ORCID http://orcid.org/0000-0002-9758-9397
Alberto Martínez LorcaDepartment of Nuclear Medicine, Hospital Universitario Ramón y Cajal, Madrid, Spain.ORCID http://orcid.org/0000-0003-3218-2550
Javier Molina-CerrilloDepartment of Medical Oncology, Hospital Universitario Ramón y Cajal, IRYCIS, Madrid, Spain.ORCID http://orcid.org/0000-0003-4616-0598
Teresa Alonso-GordoaDepartment of Medical Oncology, Hospital Universitario Ramón y Cajal, IRYCIS, Madrid, Spain.ORCID http://orcid.org/0000-0002-8966-7236
Eider Pascual-CorralesDepartment of Endocrinology and Nutrition, Instituto de Investigación Sanitaria Ramón y Cajal (IRYCIS), Hospital Universitario Ramón y Cajal, Colmenar Viejo Street km. 9,100, 28034, Madrid, Spain.
Instituto Ramón y Cajal de Investigación Sanitaria · ESHospital Universitario Ramón y Cajal · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of our study was to describe the epidemiology, diagnosis, and treatment of the most complex pheochromocytoma and paraganglioma (PGL) cases, including pheochromocytoma/PGL during pregnancy, in cyanotic congenital heart diseases (CCHDs), and metastatic pheochromocytoma. The English and Spanish literature was thoroughly evaluated searching for articles reporting clinical studies, case reports, or reviews of pheochromocytoma/PGL in pregnancy and in CCHD and metastatic pheochromocytoma/PGL. Particular settings in the diagnosis and management of pheochromocytoma and PGLs remain challenging. Those special situations include the diagnosis during pregnancy or in the context of CCHD since the typical clinical features of pheochromocytoma may be confounded with preeclampsia during pregnancy and with the complications commonly observed in CCHD. In addition, although some clinical and genetic features have been associated with higher risk of metastatic pheochromocytoma, the detection and prediction of the development of metastatic disease involve another complex situation that may require special hormonal determinations as plasmatic 3-methoxytyramine and nuclear medicine studies including

Indexed as

Adrenal Gland NeoplasmsHeart Defects, CongenitalNeoplasms, Second PrimaryParagangliomaPheochromocytomaFemaleHumansPositron Emission Tomography Computed TomographyPregnancyCyanotic congenital heart diseasesMetastatic pheochromocytomaPheochromocytomaPregnancy

Identifiers

PMID34591219
OpenAlexW3202912997

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.