Evidence map›Paper›PMID 35535120›Full record

ArticleAmerican journal of nuclear medicine and molecular imaging2022

PET/CT in congenital hyperinsulinism: transforming patient's lives by molecular hybrid imaging.

Milena Pizzoferro, Gabriele Masselli, Arianna Maiorana, Emanuele Casciani, Saadi Sollaku, Carlo Dionisi-Vici, Marco Spada, Claudio Altini, Maria Felicia Villani, Vittoria Rufini and 2 more

Open access · greenAbstract read
In one paragraph

Article in American journal of nuclear medicine and molecular imaging, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. KFrontiers in endocrinology · 2023
    Review
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

12 authors at 4 institutions in 2 countries.

Milena PizzoferroNuclear Medicine Unit/Imaging Department, IRCCS Bambino Gesù Children's Hospital Rome, Italy.
Gabriele MasselliNuclear Medicine Section, Pio XI Private Hospital Rome, Italy.
Arianna MaioranaDivision of Metabolic Diseases, Department of Pediatric Specialties, IRCCS Bambino Gesù Children's Hospital Rome, Italy.
Emanuele CascianiNuclear Medicine Section, Pio XI Private Hospital Rome, Italy.
Saadi SollakuNuclear Medicine Section, Pio XI Private Hospital Rome, Italy.
Carlo Dionisi-ViciDivision of Metabolic Diseases, Department of Pediatric Specialties, IRCCS Bambino Gesù Children's Hospital Rome, Italy.
Marco SpadaDivision of Abdominal Transplantation and Hepatobiliopancreatic Surgery, IRCCS Bambino Gesù Children's Hospital Rome, Italy.
Claudio AltiniNuclear Medicine Unit/Imaging Department, IRCCS Bambino Gesù Children's Hospital Rome, Italy.
Maria Felicia VillaniNuclear Medicine Unit/Imaging Department, IRCCS Bambino Gesù Children's Hospital Rome, Italy.
Vittoria RufiniInstitute of Nuclear Medicine, Policlinico Gemelli Foundation, Catholic University of The Sacred Heart Rome, Italy.
Gianfranco GualdiNuclear Medicine Section, Pio XI Private Hospital Rome, Italy.
Maria Carmen GarganeseNuclear Medicine Unit/Imaging Department, IRCCS Bambino Gesù Children's Hospital Rome, Italy.
Bambino Gesù Children's Hospital · ITSt. Eugenio Hospital · ITPoliclinico Umberto I · ITUniversity of the Sacred Heart · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital hyperinsulinism (HI) is a life-threatening condition characterized by severe and recurrent episodes of hypoglycaemia due to defects in key genes involved in regulating insulin secretion. The delay in diagnosis and inappropriate management of HI lead to high risk of permanent hypoglycemic brain injury. The management of HI is challenging as each form of HI (focal, diffuse, and atypical) requires its own therapeutic strategy. In HI diagnostic work-up, integrated PET/CT scan is currently the first-line imaging technique allowing to differentiate between diffuse and focal form and, in the latter case, to localize the focus within the pancreas with high precision. Only in focal HI partial pancreatectomy is the treatment of choice and a curative surgical treatment means a real chance of transforming patient's lives and HI patient's future. The aim of this review is to discuss the role of PET/CT imaging in HI scenario, its technical advantages and limitations and how successful surgery is strongly dependent on accurate preoperative assessment (genetic analysis and PET/CT scan). A multidisciplinary approach in HI diagnosis and treatment inside a single team (involving different expertise) allows to manage children safely and properly, supporting their families in an organized care network.

Indexed as

Congenital hyperinsulinismDOPAmolecular hybrid imagingpediatricPET/CT

Identifiers

PMID35535120
PMCPMC9077170
OpenAlexW4285744413

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.