Evidence map›Paper›PMID 33073033›Full record

ArticleInternational journal of neonatal screening2020

Expanded Screening of One Million Swedish Babies with R4S and CLIR for Post-Analytical Evaluation of Data.

Lene Sörensen, Ulrika von Döbeln, Henrik Åhlman, Annika Ohlsson, Martin Engvall, Karin Naess, Carolina Backman-Johansson, Yvonne Nordqvist, Anna Wedell, Rolf H Zetterström

Open access · goldAbstract read
In one paragraph

Article in International journal of neonatal screening, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

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  11. Towards Achieving Equity and Innovation in Newborn Screening across Europe.International journal of neonatal screening · 2022
    Review
  12. Article
  13. Use of Molecular Genetic Analyses in Danish Routine Newborn Screening.International journal of neonatal screening · 2021
    Article
  14. Article
  15. Article
  16. 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

10 authors at 1 institution in 1 country.

Lene SörensenCentre for Inherited Metabolic Diseases, Karolinska University Hospital Solna, SE-171 76 Stockholm, Sweden; ulrika.vondobeln@sll.se (U.v.D.); henrik.ahlman@sll.se (H.Å.); annika.ohlsson@eskilstuna.se (A.O.); martin.engvall@sll.se (M.E.); karin.naess@ki.se (K.N.); carolina.backman-johansson@sll.se (C.B.-J.); yvonne.m.nordqvist@sll.se (Y.N.); anna.wedell@ki.se (A.W.); rolf.zetterstrom@sll.se (R.H.Z.).ORCID 0000-0002-0309-4247
Ulrika von DöbelnCentre for Inherited Metabolic Diseases, Karolinska University Hospital Solna, SE-171 76 Stockholm, Sweden; ulrika.vondobeln@sll.se (U.v.D.); henrik.ahlman@sll.se (H.Å.); annika.ohlsson@eskilstuna.se (A.O.); martin.engvall@sll.se (M.E.); karin.naess@ki.se (K.N.); carolina.backman-johansson@sll.se (C.B.-J.); yvonne.m.nordqvist@sll.se (Y.N.); anna.wedell@ki.se (A.W.); rolf.zetterstrom@sll.se (R.H.Z.).ORCID 0000-0003-4137-970X
Henrik ÅhlmanCentre for Inherited Metabolic Diseases, Karolinska University Hospital Solna, SE-171 76 Stockholm, Sweden; ulrika.vondobeln@sll.se (U.v.D.); henrik.ahlman@sll.se (H.Å.); annika.ohlsson@eskilstuna.se (A.O.); martin.engvall@sll.se (M.E.); karin.naess@ki.se (K.N.); carolina.backman-johansson@sll.se (C.B.-J.); yvonne.m.nordqvist@sll.se (Y.N.); anna.wedell@ki.se (A.W.); rolf.zetterstrom@sll.se (R.H.Z.).
Annika OhlssonCentre for Inherited Metabolic Diseases, Karolinska University Hospital Solna, SE-171 76 Stockholm, Sweden; ulrika.vondobeln@sll.se (U.v.D.); henrik.ahlman@sll.se (H.Å.); annika.ohlsson@eskilstuna.se (A.O.); martin.engvall@sll.se (M.E.); karin.naess@ki.se (K.N.); carolina.backman-johansson@sll.se (C.B.-J.); yvonne.m.nordqvist@sll.se (Y.N.); anna.wedell@ki.se (A.W.); rolf.zetterstrom@sll.se (R.H.Z.).ORCID 0000-0002-4115-1775
Martin EngvallCentre for Inherited Metabolic Diseases, Karolinska University Hospital Solna, SE-171 76 Stockholm, Sweden; ulrika.vondobeln@sll.se (U.v.D.); henrik.ahlman@sll.se (H.Å.); annika.ohlsson@eskilstuna.se (A.O.); martin.engvall@sll.se (M.E.); karin.naess@ki.se (K.N.); carolina.backman-johansson@sll.se (C.B.-J.); yvonne.m.nordqvist@sll.se (Y.N.); anna.wedell@ki.se (A.W.); rolf.zetterstrom@sll.se (R.H.Z.).
Karin NaessCentre for Inherited Metabolic Diseases, Karolinska University Hospital Solna, SE-171 76 Stockholm, Sweden; ulrika.vondobeln@sll.se (U.v.D.); henrik.ahlman@sll.se (H.Å.); annika.ohlsson@eskilstuna.se (A.O.); martin.engvall@sll.se (M.E.); karin.naess@ki.se (K.N.); carolina.backman-johansson@sll.se (C.B.-J.); yvonne.m.nordqvist@sll.se (Y.N.); anna.wedell@ki.se (A.W.); rolf.zetterstrom@sll.se (R.H.Z.).ORCID 0000-0003-4310-7927
Carolina Backman-JohanssonCentre for Inherited Metabolic Diseases, Karolinska University Hospital Solna, SE-171 76 Stockholm, Sweden; ulrika.vondobeln@sll.se (U.v.D.); henrik.ahlman@sll.se (H.Å.); annika.ohlsson@eskilstuna.se (A.O.); martin.engvall@sll.se (M.E.); karin.naess@ki.se (K.N.); carolina.backman-johansson@sll.se (C.B.-J.); yvonne.m.nordqvist@sll.se (Y.N.); anna.wedell@ki.se (A.W.); rolf.zetterstrom@sll.se (R.H.Z.).
Yvonne NordqvistCentre for Inherited Metabolic Diseases, Karolinska University Hospital Solna, SE-171 76 Stockholm, Sweden; ulrika.vondobeln@sll.se (U.v.D.); henrik.ahlman@sll.se (H.Å.); annika.ohlsson@eskilstuna.se (A.O.); martin.engvall@sll.se (M.E.); karin.naess@ki.se (K.N.); carolina.backman-johansson@sll.se (C.B.-J.); yvonne.m.nordqvist@sll.se (Y.N.); anna.wedell@ki.se (A.W.); rolf.zetterstrom@sll.se (R.H.Z.).
Anna WedellCentre for Inherited Metabolic Diseases, Karolinska University Hospital Solna, SE-171 76 Stockholm, Sweden; ulrika.vondobeln@sll.se (U.v.D.); henrik.ahlman@sll.se (H.Å.); annika.ohlsson@eskilstuna.se (A.O.); martin.engvall@sll.se (M.E.); karin.naess@ki.se (K.N.); carolina.backman-johansson@sll.se (C.B.-J.); yvonne.m.nordqvist@sll.se (Y.N.); anna.wedell@ki.se (A.W.); rolf.zetterstrom@sll.se (R.H.Z.).ORCID 0000-0002-2612-6301
Rolf H ZetterströmCentre for Inherited Metabolic Diseases, Karolinska University Hospital Solna, SE-171 76 Stockholm, Sweden; ulrika.vondobeln@sll.se (U.v.D.); henrik.ahlman@sll.se (H.Å.); annika.ohlsson@eskilstuna.se (A.O.); martin.engvall@sll.se (M.E.); karin.naess@ki.se (K.N.); carolina.backman-johansson@sll.se (C.B.-J.); yvonne.m.nordqvist@sll.se (Y.N.); anna.wedell@ki.se (A.W.); rolf.zetterstrom@sll.se (R.H.Z.).ORCID 0000-0002-3016-0019
Karolinska University Hospital · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sweden has one neonatal screening laboratory, receiving 115 to 120 thousand samples per year. Among the one million babies screened by tandem mass spectrometry from November 2010 until July 2019, a total of 665 babies were recalled and 311 verified as having one of the diseases screened for with this methodology, giving a positive predictive value (PPV) of 47% and an incidence of 1:3200. The PPV was high (41%) already in the first year after start of screening, thanks to the availability of the collaborative project Region 4 Stork database. The PPV is presently 58%. This improvement was achieved by the implementation of second-tier analyses in the screening for methylmalonic aciduria, propionic aciduria, isovaleric aciduria, and homocystinuria, and the employment of various post analytical tools of the Region 4 Stork, and its successor the collaborative laboratory integrated reports.

Indexed as

Collaborative Laboratory Integrated Reports (CLIR)dried blood spots (DBS)expanded screeningnewborn screeningpositive predictive value (PPV)post-analytical evaluationtandem mass spectrometry

Identifiers

PMID33073033
PMCPMC7423009
OpenAlexW3031878838

What OpenQuestion holds

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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.