Evidence map›Paper›PMID 39229379›Full record

ReviewFrontiers in endocrinology2024

Prevention and management of hypertensive crises in children with pheochromocytoma and paraganglioma.

Chiara Bima, Chiara Lopez, Gerdi Tuli, Jessica Munarin, Stefano Arata, Matteo Procopio, Martina Bollati, Mauro Maccario, Luisa De Sanctis, Mirko Parasiliti-Caprino

Abstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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. Article
  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

10 authors.

Chiara BimaEndocrinology, Diabetes and Metabolism; Department of Medical Sciences; University of Turin, Turin, Italy.
Chiara LopezEndocrinology, Diabetes and Metabolism; Department of Medical Sciences; University of Turin, Turin, Italy.
Gerdi TuliDepartment of Sciences of Public Health and Pediatrics, University of Turin, Turin, Italy.
Jessica MunarinDepartment of Sciences of Public Health and Pediatrics, University of Turin, Turin, Italy.
Stefano ArataEndocrinology, Diabetes and Metabolism; Department of Medical Sciences; University of Turin, Turin, Italy.
Matteo ProcopioEndocrinology, Diabetes and Metabolism; Department of Medical Sciences; University of Turin, Turin, Italy.
Martina BollatiEndocrinology, Diabetes and Metabolism; Department of Medical Sciences; University of Turin, Turin, Italy.
Mauro MaccarioEndocrinology, Diabetes and Metabolism; Department of Medical Sciences; University of Turin, Turin, Italy.
Luisa De SanctisDepartment of Sciences of Public Health and Pediatrics, University of Turin, Turin, Italy.
Mirko Parasiliti-CaprinoEndocrinology, Diabetes and Metabolism; Department of Medical Sciences; University of Turin, Turin, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypertensive crises in pediatric patients are rare conditions. However, determining their precise prevalence is more challenging than in adults due to the heterogeneity in the definition itself. These crises frequently occur without a prior diagnosis of hypertension and may indicate an underlying cause of secondary hypertension, including pheochromocytoma/paraganglioma (PPGL). The mechanisms of hypertensive crises in the pediatric population with PPGL are directly related to different types of catecholamine excess. Noradrenergic tumors typically present with sustained hypertension due to their predominant action on α1-adrenoceptors in the vasculature. Conversely, adrenergic tumors, through epinephrine binding to β2-adrenoceptors in addition to stimulation of α1- and α2-adrenoceptors, more frequently cause paroxysmal hypertension. Furthermore, the biochemical phenotype also reflects the tumor localization and the presence of a genetic mutation. Recent evidence suggests that more than 80% of PPGL in pediatric cases have a hereditary background. PPGL susceptibility mutations are categorized into three clusters; mutations in cluster 1 are more frequently associated with a noradrenergic phenotype, whereas those in cluster 2 are associated with an adrenergic phenotype. Consequently, the treatment of hypertensive crises in pediatric patients with PPGL, reflecting the underlying pathophysiology, requires first-line therapy with alpha-blockers, potentially in combination with beta-blockers only in the case of tachyarrhythmia after adequate alpha-blockade. The route of administration for treatment depends on the context, such as intraoperative or pre-surgical settings, and whether it presents as a hypertensive emergency (elevated blood pressure with acute target organ damage), where intravenous administration of antihypertensive drugs is mandatory. Conversely, in cases of hypertensive urgency, if children can tolerate oral therapy, intravenous administration may initially be avoided. However, managing these cases is complex and requires careful consideration of the selection and timing of therapy administration, particularly in pediatric patients. Therefore, facing these conditions in tertiary care centers through interdisciplinary collaboration is advisable to optimize therapeutic outcomes.

Indexed as

Adrenal Gland NeoplasmsHypertensionParagangliomaPheochromocytomaChildDisease ManagementHumansHypertensive Crisiscatecholamineschildrenhypertensive crisisjuvenile hypertensionparagangliomapheochromocytomasecondary hypertension

Identifiers

PMID39229379
PMCPMC11368778

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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.