Evidence map›Paper›PMID 34223227›Full record

ArticleF&S reports2020

Consistency in rates of diagnosis of embryonic mosaicism, segmental abnormalities, and "no call" results among experienced embryologists performing preimplantation genetic testing for aneuploidy.

Emily K Osman, Shelby A Neal, Ashley W Tiegs, Brent M Hanson, Julia G Kim, Jason M Franasiak, Richard T Scott

Open access · goldAbstract read
In one paragraph

Article in F&S reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-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

6 citing papers in PubMed, 9 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

7 authors at 2 institutions in 1 country.

Emily K OsmanIVI/RMA New Jersey, Basking Ridge, New Jersey.
Shelby A NealIVI/RMA New Jersey, Basking Ridge, New Jersey.
Ashley W TiegsIVI/RMA New Jersey, Basking Ridge, New Jersey.
Brent M HansonIVI/RMA New Jersey, Basking Ridge, New Jersey.
Julia G KimIVI/RMA New Jersey, Basking Ridge, New Jersey.
Jason M FranasiakIVI/RMA New Jersey, Basking Ridge, New Jersey.
Richard T ScottIVI/RMA New Jersey, Basking Ridge, New Jersey.
Reproductive Medicine Associates of New Jersey · USThomas Jefferson University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo determine whether differences exist in rates of subchromosomal abnormalities, mosaicism, and "no call" results among embryologists performing and loading trophectoderm biopsies for preimplantation genetic testing for aneuploidy (PGT-A).

designRetrospective cohort.

settingLarge infertility center. PATIENTS: All patients undergoing in vitro fertilization with PGT-A.

interventionsThe NexCCS next generation sequencing platform was used for PGT-A. The χ

main outcome measuresInteroperator variability in rates of mosaic, segmental, and no call results.

resultsFour embryologists performed 30,899 biopsies and 6 embryologists loaded specimens into designated tubes. Among individuals performing trophectoderm sampling, rates of mosaicism were 4.3% to 6.1%, segmental errors were 9.0% to 10.7%, and inconclusive results were 1.1% to 2.9%. For those loading, the incidence of mosaicism was 4.2% to 5.9%, subchromosomal abnormalities was 9.7% to 10.4%, and no call results was 1.2% to 2.2%. The intraclass correlation coefficient was 0.978 for embryologists performing biopsies and 0.981 for those loading. Differences in mean MAPD scores were within 0.6% and 0.2% of each other for doing biopsies and loading embryologists, respectively.

conclusionsRates of mosaicism, segmental, and no call PGT-A results are consistent among experienced embryologists. Due to the large sample size included, differences within 1% of the mean were deemed clinically irrelevant despite statistical significance.

Indexed as

IVF laboratoryMosaicismnonconcurrent and unamplified resultspreimplantation genetic testing for aneuploidy (PGT-A)segmental abnormalities

Identifiers

PMID34223227
PMCPMC8244265
OpenAlexW3090656960

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.