Evidence map›Paper›PMID 25960712›Full record

ArticleTransfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie2015

Non-Invasive Prenatal RHD Genotyping Using Cell-Free Fetal DNA from Maternal Plasma: An Italian Experience.

Elena Picchiassi, Gian Carlo Di Renzo, Federica Tarquini, Vittorio Bini, Michela Centra, Luana Pennacchi, Fabiana Galeone, Mara Micanti, Giuliana Coata

Abstract read
In one paragraph

Article in Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Non-invasive prenatal rhesus D genotyping using cell-free foetal DNA.The Indian journal of medical research · 2019
    Article
  3. 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

9 authors.

Elena PicchiassiDepartment of Obstetrics and Gynecology, University Hospital of Perugia, Perugia, Italy.
Gian Carlo Di RenzoDepartment of Obstetrics and Gynecology, University Hospital of Perugia, Perugia, Italy.
Federica TarquiniDepartment of Obstetrics and Gynecology, University Hospital of Perugia, Perugia, Italy.
Vittorio BiniDepartment of Internal Medicine, University Hospital of Perugia, Perugia, Italy.
Michela CentraDepartment of Obstetrics and Gynecology, University Hospital of Perugia, Perugia, Italy.
Luana PennacchiDepartment of Obstetrics and Gynecology, University Hospital of Perugia, Perugia, Italy.
Fabiana GaleoneDepartment of Obstetrics and Gynecology, University Hospital of Perugia, Perugia, Italy.
Mara MicantiDepartment of Obstetrics and Gynecology, University Hospital of Perugia, Perugia, Italy.
Giuliana CoataDepartment of Obstetrics and Gynecology, University Hospital of Perugia, Perugia, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study assessed the diagnostic accuracy of a non-invasive approach to fetal RHD genotyping using cell-free fetal DNA in maternal plasma and a combination of methodological strategies.

methodsReal-time PCR (qPCR) was performed on 216 RhD-negative women between weeks 10+0 and 14+6 of gestation (1st qPCR). qPCR was repeated (2nd qPCR) to increase the amount of each sample for analysis, on 95 plasma aliquots that were available from first trimester blood collection (group 1) and on 13 samples that were collected between weeks 18+0 and 25+6 of gestation (group 2). qPCR was specific for exons 5 and 7 of the RHD gene (RHD5 and RHD7). The results were interpreted according to the number of positive replicates of both exons.

results1st qPCR: diagnostic accuracy was of 93.3%. Diagnostic accuracy increased from 90.5% (1st qPCR) to 93.7% (2nd qPCR) in group 1 and from 84.6% (1st qPCR) to 92.3% (2nd qPCR) in group 2. These increments were not statistically significant.

conclusionOur approach to RHD genotyping in early pregnancy yielded high diagnostic accuracy. Increasing the amount of DNA analyzed in each sample did not improve significantly the diagnostic accuracy of the test.

Indexed as

Fetal DNAHemolytic disease of the fetus and newbornPrenatal RHD genotyping

Identifiers

PMID25960712
PMCPMC4404929

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