Evidence map›Paper›PMID 37252695›Full record

ArticleArchives of endocrinology and metabolism2023

Epidemiological profile of congenital hypothyroidism at a southern Brazilian state.

Márcia Inês Boff, Cristiane Kopacek, Vandrea Carla de Souza, Sabliny Carreiro Ribeiro, Edmundo Kreisner, Paula Regla Vargas, Livia Silveira Mastella, José Mauro Madi, Simone Martins de Castro, Rosa Maria Rahmi

Abstract read
In one paragraph

Article in Archives of endocrinology and metabolism, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Márcia Inês BoffUniversidade de Caxias do Sul, Caxias do Sul, RS, Brasil, mibrizzotto@ucs.br.
Cristiane KopacekServiço de Referência em Triagem Neonatal do Estado do Rio Grande do Sul, Hospital Materno-Infantil Presidente Vargas, Porto Alegre, RS, Brasil.
Vandrea Carla de SouzaDepartamento de Pediatria, Universidade de Caxias do Sul, Caxias do Sul, RS, Brasil.
Sabliny Carreiro RibeiroServiço de Referência em Triagem Neonatal do Estado do Rio Grande do Sul, Hospital Materno-Infantil Presidente Vargas, Porto Alegre, RS, Brasil.
Edmundo KreisnerServiço de Referência em Triagem Neonatal do Estado do Rio Grande do Sul, Hospital Materno-Infantil Presidente Vargas, Porto Alegre, RS, Brasil.
Paula Regla VargasServiço de Referência em Triagem Neonatal do Estado do Rio Grande do Sul, Hospital Materno-Infantil Presidente Vargas, Porto Alegre, RS, Brasil.
Livia Silveira MastellaSecretaria Municipal de Saúde de Porto Alegre, Porto Alegre, RS, Brasil.
José Mauro MadiDepartamento de Obstetrícia e Ginecologia, Hospital Geral de Caxias do Sul, Universidade de Caxias do Sul, Caxias do Sul, RS, Brasil.
Simone Martins de CastroServiço de Referência em Triagem Neonatal do Estado do Rio Grande do Sul, Hospital Materno-Infantil Presidente Vargas, Porto Alegre, RS, Brasil.
Rosa Maria RahmiDepartamento de Endocrinologia, Universidade de Caxias do Sul, Caxias do Sul, RS, Brasil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To determine the incidence of congenital hypothyroidism (CH) over a 10-year period at the Reference Service in Neonatal Screening of the state of Rio Grande do Sul (RSNS-RS). Subjects and methods: Historical cohort study including all newborns screened for CH by the RSNS-RS from January 2008 until December 2017. Data of all newborns with neonatal TSH (neoTSH; heel prick test) values ≥ 9 mIU/L were collected. According to neoTSH values, the newborns were allocated into two groups: Group 1 (G1), comprising newborns with neoTSH ≥ 9 mIU/L and serum TSH (sTSH) < 10 mIU/L, and Group 2 (G2), comprising those with neoTSH ≥ 9 mIU/L and sTSH ≥ 10 mIU/L. Results: Of 1,043,565 newborns screened, 829 (0.08%) had neoTSH values ≥ 9 mIU/L. Of these, 284 (39.3%) had sTSH values < 10 mIU/L and were allocated to the G1 group, while 439 (60.7%) had sTSH ≥ 10 mIU/L and were allocated to the G2 group, and 106 (12.7%) were considered missing data. The overall incidence of CH was 42.1 per 100,000 newborns screened (95% confidence interval [CI] 38.5-45.7/100,000) or 1:2377 screened newborns. The sensibility and specificity of neoTSH ≥ 9 mIU/L were 97% and 11%; of neoTSH 12.6 mUI/L, 73% and 85% respectively. Conclusion: In this population, the incidence of permanent and transitory CH was 1:2377 screened newborns. The neoTSH cutoff value adopted during the study period showed excellent sensibility, which matters for a screening test.

Indexed as

Congenital HypothyroidismBrazilCohort StudiesHumansInfant, NewbornNeonatal ScreeningThyrotropinThyrotropinCongenital hypothyroidismincidenceneonatal screeningpublic health

Identifiers

PMID37252695
PMCPMC10665071

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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.