Cargando…
Prenatal screening for congenital anomalies: exploring midwives’ perceptions of counseling clients with religious backgrounds
BACKGROUND: In the Netherlands, prenatal screening follows an opting in system and comprises two non-invasive tests: the combined test to screen for trisomy 21 at 12 weeks of gestation and the fetal anomaly scan to detect structural anomalies at 20 weeks. Midwives counsel about prenatal screening te...
Autores principales: | Gitsels–van der Wal, Janneke T, Manniën, Judith, Gitsels, Lisanne A, Reinders, Hans S, Verhoeven, Pieternel S, Ghaly, Mohammed M, Klomp, Trudy, Hutton, Eileen K |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4223558/ https://www.ncbi.nlm.nih.gov/pubmed/25037919 http://dx.doi.org/10.1186/1471-2393-14-237 |
Ejemplares similares
-
Factors affecting the uptake of prenatal screening tests for congenital anomalies; a multicentre prospective cohort study
por: Gitsels - van der Wal, Janneke T, et al.
Publicado: (2014) -
Counselling for prenatal anomaly screening to migrant women in the Netherlands: An interview study of primary care midwives’ perceived barriers with client–midwife communication
por: Koopmanschap, Isabel, et al.
Publicado: (2022) -
Maternal characteristics associated with referral to obstetrician-led care in low-risk pregnant women in the Netherlands: A retrospective cohort study
por: Niessink-Beckers, Susan, et al.
Publicado: (2023) -
The DELIVER study; the impact of research capacity building on research, education, and practice in Dutch midwifery
por: Spelten, Evelien, et al.
Publicado: (2023) -
Perinatal outcomes of frequent attendance in midwifery care in the Netherlands: a retrospective cohort study
por: Gitsels-van der Wal, Janneke T., et al.
Publicado: (2020)