Evidence map›Paper›PMID 30130800›Full record

ArticleFetal diagnosis and therapy2019

Clinical and Economic Impact of Adopting Noninvasive Prenatal Testing as a Primary Screening Method for Fetal Aneuploidies in the General Pregnancy Population.

Emilia Kostenko, Frederic Chantraine, Katleen Vandeweyer, Maximilian Schmid, Alex Lefevre, Deanna Hertz, Laura Zelle, Jose Luis Bartha, Gian Carlo Di Renzo

Open access · hybridAbstract read
In one paragraph

Article in Fetal diagnosis and therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
5.4field-weighted citation impact, top 4% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Impact of Structural Differences on the Modeled Cost-Effectiveness of Noninvasive Prenatal Testing.Medical decision making : an international journal of the Society for Medical Decision Making · 2024
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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

9 authors at 7 institutions in 5 countries.

Emilia KostenkoRoche Sequencing Solutions, Inc., Prague, Czechia, emilia.kostenko@roche.com.
Frederic ChantraineDepartment of Obstetrics and Gynecology, CHR Citadelle, Liège, Belgium.
Katleen VandeweyerRoche Sequencing Solutions, Inc., Vilvoorde, Belgium.
Maximilian SchmidRoche Sequencing Solutions, Inc., San Jose, California, USA.
Alex LefevreRoche Sequencing Solutions, Inc., Vilvoorde, Belgium.
Deanna HertzGfK, Waltham, Massachusetts, USA.
Laura ZelleGfK, Waltham, Massachusetts, USA.
Jose Luis BarthaLa Paz Hospital, Madrid, Spain.
Gian Carlo Di RenzoCenter for Perinatal and Reproductive Medicine, University of Perugia, Perugia, Italy.
GfK (United States) · USRoche (Belgium) · BECentre hospitalier régional de la Citadelle · BEHospital Universitario La Paz · ESRoche (Czechia) · CZRoche (United States) · USUniversity of Perugia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo evaluate the clinical and economic impact of adopting noninvasive prenatal testing (NIPT) using circulating cell-free DNA as a first-line screening method for trisomy 21, 18, and 13 in the general pregnancy population.

methodsA decision-analytical model was developed to assess the impact of adopting NIPT as a primary screening test compared to conventional screening methods. The model takes the Belgium perspective and includes only the direct medical cost of screening, diagnosis, and procedure-related complications. NIPT costs are EUR 260. Clinical outcomes and the cost per trisomy detected were assessed. Sensitivity analysis measured the impact of NIPT false-positive rate (FPR) on modelled results.

resultsThe cost per trisomy detected was EUR 63,016 for conventional screening versus EUR 66,633 for NIPT, with a difference of EUR 3,617. NIPT reduced unnecessary invasive tests by 94.8%, decreased procedure-related miscarriages by 90.8%, and increased trisomies detected by 29.1%. Increasing the FPR of NIPT (from < 0.01 to 1.0%) increased the average number of invasive procedures required to diagnose a trisomy from 2.2 to 4.5, respectively.

conclusionNIPT first-line screening at a reasonable cost is cost-effective and provides better clinical outcomes. However, modelled results are dependent on the adoption of an NIPT with a low FPR.

Indexed as

AneuploidyGenetic TestingNoninvasive Prenatal TestingCost-Benefit AnalysisDecision Support TechniquesFemaleHumansPregnancyUncertaintyCell-free DNACost effectivenessDown syndromeEconomic evaluationFetal diagnosisGenetic testingMaternal serum screeningNoninvasive prenatal diagnosisPrenatal screeningTrisomy

Identifiers

PMID30130800
PMCPMC6604265
OpenAlexW2888577192

What OpenQuestion holds

Textmetadata
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.