Evidence map›Paper›PMID 33450092›Full record

ArticlePrenatal diagnosis2021

Evaluating the efficacy of three carrier screening workflows designed to identify at-risk carrier couples.

Aishwarya Arjunan, Raul Torres, Anna Gardiner, Kristjan Eerik Kaseniit, Jeff Wootton, Rotem Ben-Shachar, Katherine Johansen Taber

Open access · hybridAbstract read
In one paragraph

Article in Prenatal diagnosis, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 14% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. 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

7 authors at 2 institutions in 2 countries.

Aishwarya ArjunanMyriad Women's Health, South San Francisco, California, USA.ORCID https://orcid.org/0000-0002-7863-2388
Raul TorresMyriad Genetics, Inc., Salt Lake City, Utah, USA.
Anna GardinerMyriad Genetics, Inc., Salt Lake City, Utah, USA.
Kristjan Eerik KaseniitMyriad Genetics, Inc., Salt Lake City, Utah, USA.
Jeff WoottonMyriad Women's Health, South San Francisco, California, USA.
Rotem Ben-ShacharMyriad Genetics, Inc., Salt Lake City, Utah, USA.
Katherine Johansen TaberMyriad Women's Health, South San Francisco, California, USA.
Myriad Genetics · USMyriad (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo evaluate the efficacy of three different carrier screening workflows designed to identify couples at risk for having offspring with autosomal recessive conditions.

methodsPartner testing compliance, unnecessary testing, turnaround time, and ability to identify at-risk couples (ARCs) were measured across all three screening strategies (sequential, tandem, or tandem reflex).

resultsA total of 314,100 individuals who underwent carrier screening were analyzed. Sequential, tandem, and tandem reflex screening yielded compliance frequencies of 25.8%, 100%, and 95.9%, respectively. Among 14,595 couples tested in tandem, 42.2% of females were screen-negative, resulting in unnecessary testing of the male partner. In contrast, less than 1% of tandem reflex couples included unnecessary male testing. The median turnaround times were 29.2 days (sequential), 8 days (tandem), and 13.3 days (tandem reflex). The proportion of ARCs detected per total number of individual screens were 0.5% for sequential testing and 1.3% for both tandem and tandem reflex testing.

conclusionThe tandem reflex strategy simplifies a potentially complex clinical scenario by providing a mechanism by which providers can maximize partner compliance and the detection of at-risk couples while minimizing workflow burden and unnecessary testing and is more efficacious than both sequential and tandem screening strategies.

Indexed as

HeterozygoteFemaleGenetic Carrier ScreeningGenetic TestingHumansParentsPreconception CarePregnancyRetrospective StudiesWorkflow

Identifiers

PMID33450092
PMCPMC8248057
OpenAlexW3125765495

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.