Evidence map›Paper›PMID 23404215›Full record

ReviewJournal of endocrinological investigation2013

The Italian screening program for primary congenital hypothyroidism: actions to improve screening, diagnosis, follow-up, and surveillance.

A Cassio, C Corbetta, I Antonozzi, F Calaciura, U Caruso, G Cesaretti, R Gastaldi, E Medda, F Mosca, E Pasquini and 14 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Journal of endocrinological investigation, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 3 pooled it
–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

24 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Guideline
  3. The molecular causes of thyroid dysgenesis: a systematic review.Journal of endocrinological investigation · 2013
    Pooled it
  4. Review
  5. Observational
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. An Overview on Different L-Thyroxine (l-TFrontiers in endocrinology · 2022
    Review
  16. Article
  17. Article
  18. Transoral thyroidectomy: advantages and limitations.Journal of endocrinological investigation · 2017
    Article
  19. Article
  20. Screening of HHEX Mutations in Chinese Children with Thyroid Dysgenesis.Journal of clinical research in pediatric endocrinology · 2016
    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

24 authors.

A CassioDepartment of Pediatrics, University of Bologna, Bologna, Italy.
C Corbetta
I Antonozzi
F Calaciura
U Caruso
G Cesaretti
R Gastaldi
E Medda
F Mosca
E Pasquini
M C Salerno
V Stoppioni
M Tonacchera
G Weber
A Olivieri
Italian Society for Pediatric Endocrinology and Diabetology
Italian Society for the Study of Metabolic Diseases and Neonatal Screening
Italian National Institute of Health
Italian National Coordinating Group for Congenital Hypothyroidism
Italian Thyroid Association
Italian Society of Pediatrics
Italian Society of Neonatology
Italian Society of Endocrinology
Associazione Medici Endocrinologi

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Italian screening program for primary congenital hypothyroidism (CH) is an integrated system including neonatal screening, diagnosis, treatment, follow-up, and nationwide surveillance of the disease. The aim of the Italian screening program for CH is to identify not only babies with severe permanent CH (core target), but also babies with mild persistent and transient forms of CH who could have a benefit from an early replacement therapy (secondary target). In the last years, despite the important results obtained in terms of standardization of screening and follow-up procedures, it has become clear the need of optimizing the program in order to harmonize the screening strategy and the screening procedures among Regions, and to improve the diagnostic and therapeutic approach in all affected infants. On the basis of available guidelines, the experience of the Italian screening and clinical reference centers, and the knowledge derived from the nation-wide surveillance activity performed by the Italian National Registry of Infants with CH, the Italian Society for Pediatric Endocrinology and Diabetology together with the Italian Society for the Study of Metabolic Diseases and Neonatal Screening and the Italian National Institute of Health promoted actions aimed at improving diagnosis, treatment, follow-up and surveillance of CH in our country. In this paper the most important actions to improve the Italian screening program for CH are described.

Indexed as

Population SurveillanceCongenital HypothyroidismFollow-Up StudiesHumansInfant, NewbornItalyNeonatal ScreeningQuality ImprovementReference ValuesThyrotropinThyrotropin

Identifiers

PMID23404215

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.