Involving Fathers in Ante-Natal Screening for Sickle Cell Disorders: Improving Informed Decision-Making
dc.contributor.author | Berghs, Maria | en |
dc.contributor.author | Atkin, Karl | en |
dc.contributor.author | Dyson, Simon | en |
dc.date.accessioned | 2015-02-09T14:23:09Z | |
dc.date.available | 2015-02-09T14:23:09Z | |
dc.date.issued | 2014 | |
dc.description.abstract | There are many reasons why fathers find it difficult to be involved in ante-natal screening for sickle cell disorders. Some are the consequence of disadvantage and inequalities, others are associated with how services are organised. Men’s perceptions about the relevance of screening are equally important, along with their relationship with their partners and families. Examples of good practice also exist and we can learn from these. Our report includes findings and recommendations for policy and practice. | en |
dc.explorer.multimedia | No | en |
dc.funder | National Institute for Health Research, Research for Patient Benefit | en |
dc.identifier.citation | Berghs, M., Atkin, K. and Dyson, S.M. (2014) Involving Fathers in Ante-Natal Screening for Sickle Cell Disorders: Improving Informed Decision-Making Research for Patient Benefit Report PB-PG-0610-22196. York: University of York | en |
dc.identifier.uri | http://hdl.handle.net/2086/10632 | |
dc.language.iso | en | en |
dc.peerreviewed | No | en |
dc.projectid | Research for Patient Benefit PB-PG-0610-22196 | en |
dc.publisher | University of York | en |
dc.researchgroup | Unit for the Social Study of Thalassaemia and Sickle Cell | en |
dc.researchinstitute | Institute for Allied Health Sciences Research | en |
dc.researchinstitute | Institute of Health, Health Policy and Social Care | en |
dc.subject | sickle cell | en |
dc.subject | ante-natal screening | en |
dc.subject | fathers | en |
dc.subject | reproductive technology | en |
dc.title | Involving Fathers in Ante-Natal Screening for Sickle Cell Disorders: Improving Informed Decision-Making | en |
dc.type | Other | en |
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