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Rapid exome sequencing as a first-tier test in neonates with suspected genetic disorder: results of a prospective multicenter clinical utility study in the Netherlands.
Olde Keizer, Richelle A C M; Marouane, Abderrahim; Kerstjens-Frederikse, Wilhelmina S; Deden, A Chantal; Lichtenbelt, Klaske D; Jonckers, Tinneke; Vervoorn, Marieke; Vreeburg, Maaike; Henneman, Lidewij; de Vries, Linda S; Sinke, Richard J; Pfundt, Rolph; Stevens, Servi J C; Andriessen, Peter; van Lingen, Richard A; Nelen, Marcel; Scheffer, Hans; Stemkens, Daphne; Oosterwijk, Cor; van Amstel, Hans Kristian Ploos; de Boode, Willem P; van Zelst-Stams, Wendy A G; Frederix, Geert W J; Vissers, Lisenka E L M.
Afiliación
  • Olde Keizer RACM; Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
  • Marouane A; Department of Human Genetics, Radboud University Medical Center, Radboud Institute for Health Sciences, Nijmegen, Netherlands.
  • Kerstjens-Frederikse WS; Department of Genetics, University Medical Center, University of Groningen, Groningen, Netherlands.
  • Deden AC; Department of Human Genetics, Radboud University Medical Center, Radboud Institute for Health Sciences, Nijmegen, Netherlands.
  • Lichtenbelt KD; Department of Genetics, Utrecht University Medical Center, Utrecht, Netherlands.
  • Jonckers T; Department of Pediatrics and Neonatology, Máxima Medical Center, Veldhoven, Netherlands.
  • Vervoorn M; Department of Pediatrics and Neonatology, Máxima Medical Center, Veldhoven, Netherlands.
  • Vreeburg M; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, Netherlands.
  • Henneman L; Department of Human Genetics and Amsterdam Reproduction and Development Research Institute, Amsterdam UMC, Vrije Universiteit, Amsterdam, Netherlands.
  • de Vries LS; Department of Neonatology, University Medical Center Utrecht, Utrecht, Netherlands.
  • Sinke RJ; Department of Genetics, University Medical Center, University of Groningen, Groningen, Netherlands.
  • Pfundt R; Department of Human Genetics, Radboud University Medical Center, Radboud Institute for Health Sciences, Nijmegen, Netherlands.
  • Stevens SJC; Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, Netherlands.
  • Andriessen P; Department of Pediatrics, Máxima Medical Center, Veldhoven, Netherlands.
  • van Lingen RA; Department of Applied Physics, Eindhoven University of Technology, Eindhoven, Netherlands.
  • Nelen M; Department of Neonatology, Isala, Zwolle, Netherlands.
  • Scheffer H; Department of Human Genetics, Radboud University Medical Center, Radboud Institute for Health Sciences, Nijmegen, Netherlands.
  • Stemkens D; Department of Human Genetics, Radboud University Medical Center, Radboud Institute for Health Sciences, Nijmegen, Netherlands.
  • Oosterwijk C; VSOP - National Patient Alliance for Rare and Genetic Diseases, Soest, Netherlands.
  • van Amstel HKP; VSOP - National Patient Alliance for Rare and Genetic Diseases, Soest, Netherlands.
  • de Boode WP; Department of Genetics, Utrecht University Medical Center, Utrecht, Netherlands.
  • van Zelst-Stams WAG; Department of Neonatology, Radboud University Medical Center, Radboud Institute for Health Sciences, Amalia Children's Hospital, Nijmegen, Netherlands.
  • Frederix GWJ; Department of Human Genetics, Radboud University Medical Center, Radboud Institute for Health Sciences, Nijmegen, Netherlands. wendy.vanzelst-stams@radboudumc.nl.
  • Vissers LELM; Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
Eur J Pediatr ; 182(6): 2683-2692, 2023 Jun.
Article en En | MEDLINE | ID: mdl-36997769
The introduction of rapid exome sequencing (rES) for critically ill neonates admitted to the neonatal intensive care unit has made it possible to impact clinical decision-making. Unbiased prospective studies to quantify the impact of rES over routine genetic testing are, however, scarce. We performed a clinical utility study to compare rES to conventional genetic diagnostic workup for critically ill neonates with suspected genetic disorders. In a multicenter prospective parallel cohort study involving five Dutch NICUs, we performed rES in parallel to routine genetic testing for 60 neonates with a suspected genetic disorder and monitored diagnostic yield and the time to diagnosis. To assess the economic impact of rES, healthcare resource use was collected for all neonates. rES detected more conclusive genetic diagnoses than routine genetic testing (20% vs. 10%, respectively), in a significantly shorter time to diagnosis (15 days (95% CI 10-20) vs. 59 days (95% CI 23-98, p < 0.001)). Moreover, rES reduced genetic diagnostic costs by 1.5% (€85 per neonate). CONCLUSION:  Our findings demonstrate the clinical utility of rES for critically ill neonates based on increased diagnostic yield, shorter time to diagnosis, and net healthcare savings. Our observations warrant the widespread implementation of rES as first-tier genetic test in critically ill neonates with disorders of suspected genetic origin. WHAT IS KNOWN: • Rapid exome sequencing (rES) enables diagnosing rare genetic disorders in a fast and reliable manner, but retrospective studies with neonates admitted to the neonatal intensive care unit (NICU) indicated that genetic disorders are likely underdiagnosed as rES is not routinely used. • Scenario modeling for implementation of rES for neonates with presumed genetic disorders indicated an expected increase in costs associated with genetic testing. WHAT IS NEW: • This unique prospective national clinical utility study of rES in a NICU setting shows that rES obtained more and faster diagnoses than conventional genetic tests. • Implementation of rES as replacement for all other genetic tests does not increase healthcare costs but in fact leads to a reduction in healthcare costs.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pruebas Genéticas / Enfermedad Crítica Tipo de estudio: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans / Newborn País/Región como asunto: Europa Idioma: En Revista: Eur J Pediatr Año: 2023 Tipo del documento: Article País de afiliación: Países Bajos Pais de publicación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pruebas Genéticas / Enfermedad Crítica Tipo de estudio: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans / Newborn País/Región como asunto: Europa Idioma: En Revista: Eur J Pediatr Año: 2023 Tipo del documento: Article País de afiliación: Países Bajos Pais de publicación: Alemania