Evidence map›Paper›PMID 37401055›Full record

ArticleAnnals of pediatric endocrinology & metabolism2023

Cushing disease in pediatrics: an update.

Marcio José Concepción-Zavaleta, Cristian David Armas, Juan Eduardo Quiroz-Aldave, Eilhart Jorge García-Villasante, Ana Cecilia Gariza-Solano, María Del Carmen Durand-Vásquez, Luis Alberto Concepción-Urteaga, Francisca Elena Zavaleta-Gutiérrez

Open access · diamondAbstract read
In one paragraph

Article in Annals of pediatric endocrinology & metabolism, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. 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

8 authors at 4 institutions in 1 country.

Marcio José Concepción-ZavaletaUniversidad Cientifica del Sur, Lima, Perú.
Cristian David ArmasSchool of Medicine, National University of Trujillo, Trujillo, Perú.
Juan Eduardo Quiroz-AldaveDivision of Medicine, Hospital de Apoyo Chepén, Chepén, Perú.
Eilhart Jorge García-VillasanteDivision of Endocrinology, Clínica Javier Prado, Lima, Perú.
Ana Cecilia Gariza-SolanoDivision of Pediatric Endocrinology, Hospital Nacional Hipólito Unanue, Lima, Perú.
María Del Carmen Durand-VásquezDivision of Family Medicine, Hospital de Apoyo Chepén, Chepén, Perú.
Luis Alberto Concepción-UrteagaSchool of Medicine, National University of Trujillo, Trujillo, Perú.
Francisca Elena Zavaleta-GutiérrezDivision of Pediatrics, Hospital Belén de Trujillo, Trujillo, Perú.
National University of Trujillo · PEHospital Nacional Cayetano Heredia · PEPrivate University of Trujillo · PEUniversidad Científica del Sur · PE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cushing disease (CD) is the main cause of endogenous Cushing syndrome (CS) and is produced by an adrenocorticotropic hormone (ACTH)-producing pituitary adenoma. Its relevance in pediatrics is due to the retardation of both growth and developmental processes because of hypercortisolism. In childhood, the main features of CS are facial changes, rapid or exaggerated weight gain, hirsutism, virilization, and acne. Endogenous hypercortisolism should be established after exogenous CS has been ruled out based on 24-hour urinary free cortisol, midnight serum or salivary cortisol, and dexamethasone suppression test; after that, ACTH dependence should be established. The diagnosis should be confirmed by pathology. The goal of treatment is to normalize cortisol level and reverse the signs and symptoms. Treatment options include surgery, medication, radiotherapy, or combined therapy. CD represents a challenge for physicians owing to its multiple associated conditions involving growth and pubertal development; thus, it is important to achieve an early diagnosis and treatment in order to control hypercortisolism and improve the prognosis. Its rarity in pediatric patients has led physicians to have limited experience in its management. The objective of this narrative review is to summarize the current knowledge about the pathophysiology, diagnosis, and treatment of CD in the pediatric population.

Indexed as

Cushing diseaseCushing syndromeDiagnosisNeuroendocrinologyTreatment

Identifiers

PMID37401055
PMCPMC10329946
OpenAlexW4382195887

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.