Cargando…

What's out there for parents? A systematic review of online information about prenatal microarray and exome sequencing

OBJECTIVE: To identify what online patient information (presented in English) is available to parents about prenatal microarray (CMA) and exome sequencing (ES), and evaluate its content, quality, and readability. METHOD: Systematic searches (Google and Bing) were conducted, and websites were categor...

Descripción completa

Detalles Bibliográficos
Autores principales:	Peter, Michelle, McInnes‐Dean, Hannah, Fisher, Jane, Tapon, Dagmar, Chitty, Lyn S., Hill, Melissa
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2021
Materias:	Original Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9298227/ https://www.ncbi.nlm.nih.gov/pubmed/34747021 http://dx.doi.org/10.1002/pd.6066

Ejemplares similares

Implementing a rapid fetal exome sequencing service: What do parents and health professionals think?
por: Mellis, Rhiannon, et al.
Publicado: (2022)

Optimising Exome Prenatal Sequencing Services (EXPRESS): a study protocol to evaluate rapid prenatal exome sequencing in the NHS Genomic Medicine Service
por: Hill, Melissa, et al.
Publicado: (2022)

Couples experiences of receiving uncertain results following prenatal microarray or exome sequencing: A mixed‐methods systematic review
por: Harding, Eleanor, et al.
Publicado: (2020)

Diagnostic yield of exome sequencing for prenatal diagnosis of fetal structural anomalies: A systematic review and meta‐analysis
por: Mellis, Rhiannon, et al.
Publicado: (2022)

Lessons learnt from prenatal exome sequencing
por: Chandler, Natalie J., et al.
Publicado: (2022)

A qualitative study looking at informed choice in the context of non‐invasive prenatal testing for aneuploidy
por: Lewis, Celine, et al.
Publicado: (2016)

Development and evaluation of training resources to prepare health professionals for counselling pregnant women about non-invasive prenatal testing for Down syndrome: a mixed methods study
por: Oxenford, Kerry, et al.
Publicado: (2017)

Has noninvasive prenatal testing impacted termination of pregnancy and live birth rates of infants with Down syndrome?
por: Hill, Melissa, et al.
Publicado: (2017)

Offering non‐invasive prenatal testing as part of routine clinical service. Can high levels of informed choice be maintained?
por: Lewis, Celine, et al.
Publicado: (2017)

Women’s Experiences and Preferences for Service Delivery of Non-Invasive Prenatal Testing for Aneuploidy in a Public Health Setting: A Mixed Methods Study
por: Lewis, Celine, et al.
Publicado: (2016)

Development and validation of a measure of informed choice for women undergoing non-invasive prenatal testing for aneuploidy
por: Lewis, Celine, et al.
Publicado: (2016)

Development and mixed-methods evaluation of an online animation for young people about genome sequencing
por: Lewis, Celine, et al.
Publicado: (2020)

The clinical utility of microarray technologies applied to prenatal cytogenetics in the presence of a normal conventional karyotype: a review of the literature
por: Callaway, Jonathan L A, et al.
Publicado: (2013)

Model-Based Analysis of Costs and Outcomes of Non-Invasive Prenatal Testing for Down’s Syndrome Using Cell Free Fetal DNA in the UK National Health Service
por: Morris, Stephen, et al.
Publicado: (2014)

Preferences for Prenatal Tests for Cystic Fibrosis: A Discrete Choice Experiment to Compare the Views of Adult Patients, Carriers of Cystic Fibrosis and Health Professionals
por: Hill, Melissa, et al.
Publicado: (2014)

Prenatal genetic diagnosis of omphalocele by karyotyping, chromosomal microarray analysis and exome sequencing
por: Shi, Xiaomei, et al.
Publicado: (2021)

“The communication and support from the health professional is incredibly important”: A qualitative study exploring the processes and practices that support parental decision‐making about postmortem examination
por: Lewis, Celine, et al.
Publicado: (2019)

Preferences for prenatal diagnosis of sickle‐cell disorder: A discrete choice experiment comparing potential service users and health‐care providers
por: Hill, Melissa, et al.
Publicado: (2017)

Microarray Technology for the Diagnosis of Fetal Chromosomal Aberrations: Which Platform Should We Use?
por: Karampetsou, Evangelia, et al.
Publicado: (2014)

Non‐invasive prenatal diagnosis (NIPD) for single gene disorders: cost analysis of NIPD and invasive testing pathways
por: Verhoef, Talitha I., et al.
Publicado: (2016)

Delivering genome sequencing for rapid genetic diagnosis in critically ill children: parent and professional views, experiences and challenges
por: Hill, Melissa, et al.
Publicado: (2020)

Dealing with uncertain results from chromosomal microarray and exome sequencing in the prenatal setting: An international cross‐sectional study with healthcare professionals
por: Lewis, Celine, et al.
Publicado: (2021)

Parents’ motivations, concerns and understanding of genome sequencing: a qualitative interview study
por: Lewis, Celine, et al.
Publicado: (2020)

Chromosome Microarray Analysis and Exome Sequencing: Implementation in Prenatal Diagnosis of Fetuses with Digestive System Malformations
por: Wang, You, et al.
Publicado: (2023)

Non-invasive prenatal diagnosis (NIPD): how analysis of cell-free DNA in maternal plasma has changed prenatal diagnosis for monogenic disorders
por: Hanson, Britt, et al.
Publicado: (2022)

RAPIDR: an analysis package for non-invasive prenatal testing of aneuploidy
por: Lo, Kitty K., et al.
Publicado: (2014)

Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study
por: Lord, Jenny, et al.
Publicado: (2019)

Availability of less invasive prenatal, perinatal and paediatric autopsy will improve uptake rates: a mixed‐methods study with bereaved parents
por: Lewis, C, et al.
Publicado: (2019)

Diagnosis of lethal or prenatal‐onset autosomal recessive disorders by parental exome sequencing
por: Stals, Karen L., et al.
Publicado: (2017)

Evaluation of non-invasive prenatal testing (NIPT) for aneuploidy in an NHS setting: a reliable accurate prenatal non-invasive diagnosis (RAPID) protocol
por: Hill, Melissa, et al.
Publicado: (2014)

Non-invasive prenatal diagnosis for cystic fibrosis: detection of paternal mutations, exploration of patient preferences and cost analysis
por: Hill, Melissa, et al.
Publicado: (2015)

The Performance of Clinics for Out-Patient Control of Anticoagulation
por: McInnes, Gordon T., et al.
Publicado: (1987)

Stakeholder views and attitudes towards prenatal and postnatal transplantation of fetal mesenchymal stem cells to treat Osteogenesis Imperfecta
por: Hill, Melissa, et al.
Publicado: (2019)

Routine testing of fetal Rhesus D status in Rhesus D negative women using cell-free fetal DNA: an investigation into the preferences and information needs of women
por: Oxenford, Kerry, et al.
Publicado: (2013)

Confined placental mosaicism: implications for fetal chromosomal analysis using microarray comparative genomic hybridization
por: Karampetsou, Evangelia, et al.
Publicado: (2014)

Diabetic foot disease in the United Kingdom: about time to put feet first
por: McInnes, Alistair D
Publicado: (2012)

Implementing Prenatal Diagnosis Based on Cell-Free Fetal DNA: Accurate Identification of Factors Affecting Fetal DNA Yield
por: Barrett, Angela N., et al.
Publicado: (2011)

Safe, accurate, prenatal diagnosis of thanatophoric dysplasia using ultrasound and free fetal DNA
por: Chitty, Lyn S, et al.
Publicado: (2013)

Cytogenetic microarray in prenatal and postnatal diagnosis
por: Phadke, Shubha
Publicado: (2014)

Uptake, outcomes, and costs of implementing non-invasive prenatal testing for Down’s syndrome into NHS maternity care: prospective cohort study in eight diverse maternity units
por: Chitty, Lyn S, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_j9pmk2p0r5opl2hvb86a688du0