Evidence map›Paper›PMID 37754773›Full record

ArticleInternational journal of neonatal screening2023

Neonatal Screening for Cystic Fibrosis in Hungary-First-Year Experiences.

Andrea Xue, István Lénárt, Judit Kincs, Hajnalka Szabó, Andrea Párniczky, István Balogh, Anna Deák, Péter Béla Monostori, Krisztina Hegedűs, Attila J Szabó and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of neonatal screening, 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
0.5field-weighted citation impact, top 29% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

11 authors at 4 institutions in 1 country.

Andrea XuePaediatric Centre, MTA Centre of Excellence, Semmelweis University, 1083 Budapest, Hungary.ORCID 0000-0002-6224-9886
István LénártDepartment of Paediatrics, Albert Szent-Györgyi Medical School, University of Szeged, 6725 Szeged, Hungary.
Judit KincsPaediatric Centre, MTA Centre of Excellence, Semmelweis University, 1083 Budapest, Hungary.
Hajnalka SzabóDepartment of Paediatrics, Albert Szent-Györgyi Medical School, University of Szeged, 6725 Szeged, Hungary.
Andrea PárniczkyHeim Pál National Paediatric Institute, 1089 Budapest, Hungary.
István BaloghDivision of Clinical Genetics, Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.ORCID 0000-0003-3397-2829
Anna DeákDivision of Clinical Genetics, Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary.
Péter Béla MonostoriDepartment of Paediatrics, Albert Szent-Györgyi Medical School, University of Szeged, 6725 Szeged, Hungary.ORCID 0000-0003-3591-6054
Krisztina HegedűsPaediatric Centre, MTA Centre of Excellence, Semmelweis University, 1083 Budapest, Hungary.
Attila J SzabóPaediatric Centre, MTA Centre of Excellence, Semmelweis University, 1083 Budapest, Hungary.
Ildikó SzatmáriPaediatric Centre, MTA Centre of Excellence, Semmelweis University, 1083 Budapest, Hungary.ORCID 0000-0003-1040-145X
Semmelweis University · HUUniversity of Szeged · HUUniversity of Debrecen · HUHeim Pál Országos Gyermekgyógyászati Intézet · HU

Funding

Ministry of Human Capacities 10541-4/2019/EGST
6 · The paper itself

Abstract

The aim of this study is to evaluate the strategy of the cystic fibrosis newborn screening (CFNBS) programme in Hungary based on the results of the first year of screening. A combined immunoreactive trypsinogen (IRT) and pancreatitis-associated protein (PAP) CFNBS protocol (IRT/IRT×PAP/IRT) was applied with an IRT-dependent safety net (SN). Out of 88,400 newborns, 256 were tested screen-positive. Fourteen cystic fibrosis (CF) and two cystic fibrosis-positive inconclusive diagnosis (CFSPID) cases were confirmed from the screen-positive cases, and two false-negative cases were diagnosed later. Based on the obtained results, a sensitivity of 88% and a positive predictive value (PPV) of 5.9% were calculated. Following the recognition of false-negative cases, the calculation method of the age-dependent cut-off was changed. In purely biochemical CFNBS protocols, a small protocol change, even after a short period, can have a significant positive impact on the performance. CFNBS should be monitored continuously in order to fine-tune the screening strategy and define the best local practices.

Indexed as

cystic fibrosis (CF)immunoreactive trypsinogen (IRT)newborn screening (NBS)pancreatitis-associated protein (PAP)

Identifiers

PMID37754773
PMCPMC10531581
OpenAlexW4386099869

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.