Content and Quality of Information Websites About Congenital Heart Defects Following a Prenatal Diagnosis
BackgroundPregnant women and their partners use the Internet to search for information following a prenatal diagnosis of congenital heart defect. ObjectiveOur aim was to explore central subjects of content and to assess the accessibility, reliability, usability, a...
Main Authors: | Carlsson, Tommy, Bergman, Gunnar, Karlsson, Anna-Malin, Mattsson, Elisabet |
---|---|
Format: | Article |
Language: | English |
Published: |
JMIR Publications
2015-01-01
|
Series: | Interactive Journal of Medical Research |
Online Access: | http://www.i-jmr.org/2015/1/e4/ |
Similar Items
-
Information following a diagnosis of congenital heart defect: experiences among parents to prenatally diagnosed children.
by: Tommy Carlsson, et al.
Published: (2015-01-01) -
Emotional and cognitive experiences during the time of diagnosis and decision-making following a prenatal diagnosis: a qualitative study of males presented with congenital heart defect in the fetus carried by their pregnant partner
by: Tommy Carlsson, et al.
Published: (2018-01-01) -
To Grasp the Unexpected : Information Following a Prenatal Diagnosis of Congenital Heart Defect in the Fetus
by: Carlsson, Tommy
Published: (2017) -
Being involved in research as a collaborator with experience of a prenatal diagnosis of congenital heart defect in the fetus: a qualitative study
by: Tommy Carlsson, et al.
Published: (2020-03-01) -
Written narratives from immigrants following a prenatal diagnosis: qualitative exploratory study
by: Tommy Carlsson, et al.
Published: (2019-05-01)