Evidence map›Paper›PMID 28631226›Full record

ArticleJIMD reports2018

Introduction of a Simple Second Tier Screening Test for C5 Isobars in Dried Blood Spots: Reducing the False Positive Rate for Isovaleric Acidaemia in Expanded Newborn Screening.

R S Carling, D Burden, I Hutton, R Randle, K John, J R Bonham

Abstract read
In one paragraph

Article in JIMD reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.9field-weighted citation impact, top 8% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

R S CarlingSouth East Thames Regional Newborn Screening Laboratory, Biochemical Sciences, Viapath, Guys & St Thomas' NHSFT, 4th Floor, North Wing, Westminster Bridge Road, London, SE1 7EH, UK. rachel.carling@viapath.co.uk.
D BurdenSouth East Thames Regional Newborn Screening Laboratory, Biochemical Sciences, Viapath, Guys & St Thomas' NHSFT, 4th Floor, North Wing, Westminster Bridge Road, London, SE1 7EH, UK.
I HuttonSouth East Thames Regional Newborn Screening Laboratory, Biochemical Sciences, Viapath, Guys & St Thomas' NHSFT, 4th Floor, North Wing, Westminster Bridge Road, London, SE1 7EH, UK.
R RandleSouth East Thames Regional Newborn Screening Laboratory, Biochemical Sciences, Viapath, Guys & St Thomas' NHSFT, 4th Floor, North Wing, Westminster Bridge Road, London, SE1 7EH, UK.
K JohnSouth East Thames Regional Newborn Screening Laboratory, Biochemical Sciences, Viapath, Guys & St Thomas' NHSFT, 4th Floor, North Wing, Westminster Bridge Road, London, SE1 7EH, UK.
J R BonhamDivision of Pharmacy, Diagnostics and Genetics, Sheffield Children's (NHS) FT, Sheffield, UK.
Sheffield Children's NHS Foundation Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In 2015 the English Newborn Screening programme expanded to include Isovaleric Acidaemia (IVA). Screening is performed by flow injection analysis tandem mass spectrometry of isovalerylcarnitine. Isovalerylcarnitine is isobaric with pivaloylcarnitine which can be present in blood due to the use of pivalic ester pro-drugs or pivalic acid derivatives used as emollients in some nipple creams; the potential for false positives (FP) is well documented. A pilot study in England screened 438,164 babies, 18 had presumptive positive results but only 4 were confirmed as true positives (TP). We developed a simple test to separate the isobaric compounds and investigate these samples further.We studied newborn screening blood spots from 122 randomised controls and 34 infants with an initial raised C5 result. Dried blood spots were eluted with 30% acetonitrile (150 μL) and injected into a Waters Acquity UPLC coupled to a Waters Premier XE tandem mass spectrometer operating in positive ion mode. Isocratic separation of isovalerylcarnitine, pivaloylcarnitine, valerylcarnitine and 2-methylbutyrylcarnitine was achieved within 8 min. Assay performance characteristics were acceptable and non-parametric reference ranges (n = 122) were determined for each analyte.If this method had been used as a second tier test for the 34 presumptive positive samples, the number of FP's would have reduced from 24 to 8 and the positive predictive value of the screening test would have increased from 29 to 56%. Introduction of this test into the screening protocol has the potential to significantly reduce FP results for IVA and prevent unnecessary anxiety.

Identifiers

PMID28631226
PMCPMC5874210
OpenAlexW2664379683

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.