ArticleBMC pregnancy and childbirth2016
Experiences and preferences of care among Swedish immigrants following a prenatal diagnosis of congenital heart defect in the fetus: a qualitative interview study.
Article in BMC pregnancy and childbirth, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.
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Who cites it
11 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.
- Ethical dilemmas in continuing pregnancy after a prenatal diagnosis of congenital heart defects: a systematic review and narrative synthesis.BMC medical ethics · 2025Pooled it
- Perspectives of Challenges in Counseling for Congenital Heart Defects.Pediatric cardiology · 2025Article
- The role of spirituality in the well-being of families with children with congenital heart disease: scoping review.Translational pediatrics · 2024Article
- Approaches for enhancing patient-reported experience measurement with ethnically diverse communities: a rapid evidence synthesis.International journal for equity in health · 2024Review
- Family Counseling after the Diagnosis of Congenital Heart Disease in the Fetus: Scoping Review.Healthcare (Basel, Switzerland) · 2023Article
- Mapping parents' journey following prenatal diagnosis of CHD: a qualitative study.Cardiology in the young · 2023Article
- What is important in family counseling in cases of fetuses with congenital heart disease?Revista da Associacao Medica Brasileira (1992) · 2023Article
- Breastfeeding experiences of Latina migrants living in Spain: a qualitative descriptive study.International breastfeeding journal · 2021Article
- Implementing Artificial Intelligence and Digital Health in Resource-Limited Settings? Top 10 Lessons We Learned in Congenital Heart Defects and Cardiology.Omics : a journal of integrative biology · 2020Review
- Uncertainty of Prenatally Diagnosed Congenital Heart Disease: A Qualitative Study.JAMA network open · 2020Article
- "It was God's will": Continuing pregnancy after perinatal infection by Zika virus.Revista latino-americana de enfermagem · 2020Article
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Authors and funding
4 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundImmigrants experience significant challenges when in contact with healthcare and report less satisfaction with maternity care compared to native Swedes. Research that gives voice to pregnant immigrant women and their partners following a prenatal diagnosis of a fetal anomaly is scarce. Thus, the aim of this study was to explore experiences and preferences of care following a prenatal diagnosis of congenital heart defect among Swedish immigrants.
methodsPregnant immigrants and their partners were consecutively recruited following a prenatal diagnosis of a congenital heart defect in the fetus. Nine respondents were interviewed in five interviews, four with the aid of a professional interpreter. The material was analyzed using manifest qualitative content analysis.
resultsThe analysis resulted in five categories: 1) "Trustworthy information", 2) "Language barriers", 3) "Psychosocial situation", 4) "Peer support", and 5) "Religious positions".
conclusionThe potential need for interpreter services, visual information, psychosocial support, coordination with welfare officers, and respect for religious positions about termination of pregnancy are all important aspects for health professionals to consider when consulting immigrants faced with a prenatal diagnosis of fetal anomaly in the fetus. Peer support within this context needs to be further explored in future studies.
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