Knowledge and perceptions of haemoglobinopathy carrier screening among general practitioners in Cardiff.
Open Access
- 1 February 1989
- journal article
- research article
- Published by BMJ in Journal of Medical Genetics
- Vol. 26 (2) , 109-112
- https://doi.org/10.1136/jmg.26.2.109
Abstract
A questionnaire was sent to 164 principal general practitioners working in Cardiff. A response rate of 81% was achieved. A total of 70% of respondents had had professional contact with a carrier for thalassaemia and a similar number for sickle cell disease, while 57% had recommended that a patient should be screened for haemoglobinopathy status. GPs tended to underestimate greatly the prevalence of haemoglobinopathies in South Glamorgan, and were uncertain of the ethnic minorities that were at particular risk. A carrier screening programme was considered justified by the majority of GPs in Cardiff and reasons for this opinion were examined. However, before a screening programme is started, information on whom to screen and their relative risk needs to be made more widely available.This publication has 4 references indexed in Scilit:
- King's Fund forum consensus statement: screening for fetal and genetic abnormality.BMJ, 1987
- Haemoglobinopathy Screening in a ‘Low-Risk’ Area of the United Kingdom: South Glamorgan, WalesActa Haematologica, 1987
- Effect of introducing antenatal diagnosis on reproductive behaviour of families at risk for thalassaemia major.BMJ, 1980
- Advocacy and Compliance in Genetic ScreeningNew England Journal of Medicine, 1974