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Evaluation of repeat testing of a non-sequencing based NIPT test on a Finnish general-risk population.
Karlsson, Filip; Ahola, Tarja; Dahlberg, Jenny; Prensky, Lawrence; Moilanen, Helena; Spalding, Heli.
Afiliação
  • Karlsson F; PerkinElmer Inc., Vanadis Diagnostics, Stockholm, Sweden.
  • Ahola T; PerkinElmer Inc., Vanadis Diagnostics, Stockholm, Sweden.
  • Dahlberg J; PerkinElmer Inc., Vanadis Diagnostics, Stockholm, Sweden.
  • Prensky L; PerkinElmer Inc., Waltham, MA, USA.
  • Moilanen H; Nordlab, Oulu, Finland.
  • Spalding H; Obstetrics and Gynecology, Terveystalo Healthcare Services, Helsinki, Finland.
Acta Obstet Gynecol Scand ; 100(8): 1497-1500, 2021 08.
Article em En | MEDLINE | ID: mdl-33576010
ABSTRACT

INTRODUCTION:

To evaluate the effect of repeating test failures using an automated, non-sequencing based non-invasive prenatal testing test on a general-risk population in Finland. MATERIAL AND

METHODS:

A total of 545 samples from women who represent the average-risk population in Oulu, Finland were analyzed with Vanadis® non-invasive prenatal testing. Repeat testing of test failures was performed using a second sample. Results before and after repeat testing were compared with the reference outcome, as determined by clinical examination of neonates.

RESULTS:

There were eight test failures after first-pass analysis, representing 1.5% of samples (95% CI 0.6%-2.9%). Seven out of eight failures could be resolved by analysis of a second sample, thereby reducing the test failure rate from 1.5% to 0.2% (95% CI 0.0%-1.0%).

CONCLUSIONS:

Repeating test failures with a second plasma sample could significantly reduce the effective failure rate, thereby providing a way to effectively minimize test failures and further improving clinical utility and test performance.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diagnóstico Pré-Natal / Testes Genéticos / Erros de Diagnóstico / Síndrome da Trissomia do Cromossomo 13 / Síndrome da Trissomía do Cromossomo 18 Tipo de estudo: Diagnostic_studies / Etiology_studies / Evaluation_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Pregnancy País/Região como assunto: Europa Idioma: En Revista: Acta Obstet Gynecol Scand Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Suécia

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Diagnóstico Pré-Natal / Testes Genéticos / Erros de Diagnóstico / Síndrome da Trissomia do Cromossomo 13 / Síndrome da Trissomía do Cromossomo 18 Tipo de estudo: Diagnostic_studies / Etiology_studies / Evaluation_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Pregnancy País/Região como assunto: Europa Idioma: En Revista: Acta Obstet Gynecol Scand Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Suécia