Literature DB >> 18990100

A grounded theory study of information preference and coping styles following antenatal diagnosis of foetal abnormality.

Joan G Lalor1, Cecily M Begley, Eoin Galavan.   

Abstract

AIM: This paper is a report of a study to explore the information-seeking behaviour of women following an antenatal diagnosis of foetal abnormality.
BACKGROUND: The identification of a foetal abnormality on routine ultrasound in pregnancy is both shocking and distressing for women, and seeking information in this stressful situation is a common response. There is evidence that women's information needs are not always adequately met, and in some cases they recall little from the initial consultation.
METHOD: A longitudinal study involving 42 women was conducted using a classical grounded theory design. Data were collected in 2004-2006 through in-depth interviews at three time intervals: within 4-6 weeks of diagnosis, 4-6 weeks before the birth and 6-12 weeks postnatally.
FINDINGS: Women described their main concern from diagnosis until the time to give birth in terms of regulating the information received in order to cope with the situation. Two main categories were identified: 'Getting my head around it' and 'I'll cross that bridge when I come to it'. These two differing information-seeking preferences are described as monitoring and blunting.
CONCLUSION: Matching of information preferences with coping styles may support individuals to cope with this stressful event. Women with high information needs (monitors) respond well to detail. However, those with information avoidance behaviours (blunters) should be facilitated to 'opt-in' to information when they are ready, in order to reduce the stress caused by perceived information overload.

Entities:  

Mesh:

Year:  2008        PMID: 18990100     DOI: 10.1111/j.1365-2648.2008.04778.x

Source DB:  PubMed          Journal:  J Adv Nurs        ISSN: 0309-2402            Impact factor:   3.187


  10 in total

Review 1.  Health-care provider communication with expectant parents during a prenatal diagnosis: an integrative review.

Authors:  A L Kratovil; W A Julion
Journal:  J Perinatol       Date:  2016-08-11       Impact factor: 2.521

2.  Reciprocal Relationships: the Genetic Counselor-Patient Relationship Following a Life-Limiting Prenatal Diagnosis.

Authors:  S R Williams; K L Berrier; K Redlinger-Grosse; J G Edwards
Journal:  J Genet Couns       Date:  2016-10-22       Impact factor: 2.537

3.  Parents of children with congenital heart disease prefer more information than cardiologists provide.

Authors:  Bhawna Arya; Julie S Glickstein; Stéphanie M Levasseur; Ismeé A Williams
Journal:  Congenit Heart Dis       Date:  2012-08-14       Impact factor: 2.007

4.  "Have no regrets:" Parents' experiences and developmental tasks in pregnancy with a lethal fetal diagnosis.

Authors:  Denise Côté-Arsenault; Erin Denney-Koelsch
Journal:  Soc Sci Med       Date:  2016-02-26       Impact factor: 4.634

5.  Facets of parenting a child with hypoplastic left heart syndrome.

Authors:  Gwen R Rempel; Laura G Rogers; Vinitha Ravindran; Joyce Magill-Evans
Journal:  Nurs Res Pract       Date:  2012-04-02

6.  Women's Experiences With Palliative Care During Pregnancy.

Authors:  Andrea Crawford; Amelia Hopkin; Mary Rindler; Erin Johnson; Lauren Clark; Erin Rothwell
Journal:  J Obstet Gynecol Neonatal Nurs       Date:  2021-03-26

7.  When fetal hydronephrosis is suspected antenatally--a qualitative study.

Authors:  Marie Oscarsson; Tomas Gottvall; Katarina Swahnberg
Journal:  BMC Pregnancy Childbirth       Date:  2015-12-22       Impact factor: 3.007

8.  Coping with worry while waiting for diagnostic results: a qualitative study of the experiences of pregnant couples following a high-risk prenatal screening result.

Authors:  Stina Lou; Camilla P Nielsen; Lone Hvidman; Olav B Petersen; Mette B Risør
Journal:  BMC Pregnancy Childbirth       Date:  2016-10-21       Impact factor: 3.007

9.  Insights from parents about caring for a child with birth defects.

Authors:  Jodi Lemacks; Kristin Fowles; Amanda Mateus; Kayte Thomas
Journal:  Int J Environ Res Public Health       Date:  2013-08-07       Impact factor: 3.390

10.  Experiences of informational needs and received information following a prenatal diagnosis of congenital heart defect.

Authors:  Tommy Carlsson; Gunnar Bergman; Barbro Wadensten; Elisabet Mattsson
Journal:  Prenat Diagn       Date:  2016-04-24       Impact factor: 3.050

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.