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Comparing the psychological outcomes of donor and non-donor conceived people: A systematic review.
Talbot, Charlotte; Hodson, Nathan; Rose, Joanne; Bewley, Susan.
Afiliação
  • Talbot C; University of Birmingham, Birmingham, UK.
  • Hodson N; Division of Mental Health and Wellbeing, Warwick Medical School, Coventry, UK.
  • Rose J; Centre for Paediatrics and Child Health & Department of Infectious Disease, Imperial College London, London, UK.
  • Bewley S; Department of Women and Children's Health, King's College London, London, UK.
BJOG ; 2024 Jun 27.
Article em En | MEDLINE | ID: mdl-38936405
ABSTRACT

BACKGROUND:

Over 70 000 donor-conceived (DC) people have been born in the UK since 1991. Little is known about their long-term psychological outcomes and no systematic review has assessed these.

OBJECTIVES:

To conduct a systematic review of the psychological experiences of DC people through childhood and adulthood (Prospero CRD42021257863). SEARCH STRATEGY Searches of Cumulative Index to Nursing and Allied Health Literature (CINHAL), the Excerpta Medica database (Embase), MEDLINE® and PsycINFO, conducted on 4 January 2024. SELECTION CRITERIA Quantitative and qualitative studies were included if there were five or more participants; they were peer reviewed; and any DC psychological outcomes were assessed. No limits on date, language or country were applied. DATA COLLECTION AND

ANALYSIS:

Double screening, selection, data extraction and quality assessment were performed, using Joanna Briggs Institute (JBI) scoring. MAIN

RESULTS:

Fifty studies (with 4666 DC participants), mostly from high-income anglophone countries, with heterogeneity of design, populations and outcome measures, were included. Of 19 comparative studies, 14 found no difference in outcomes between DC and non-DC people, ten found better outcomes (in health, well-being, self-esteem and emotional warmth) and six found worse outcomes (increased autism spectrum disorder and attention deficit hyperactivity disorder, addiction issues, mental illness, disruptive behaviour and identity problems). Qualitative data revealed common themes relating to identity formation, mistrust and concerns regarding genetic heritage. The evidence regarding adulthood outcomes was very limited.

CONCLUSIONS:

The research on DC individuals presents a nuanced picture, with most studies suggesting comparable or improved outcomes in terms of well-being and relationships, but with a notable minority indicating higher rates of mental health and identity struggles. Qualitative findings underscore common negative experiences, whereas the early disclosure of DC status appears beneficial for psychological well-being.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article