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1.
Eur J Hum Genet ; 4(2): 108-12, 1996.
Artigo em Inglês | MEDLINE | ID: mdl-8744029

RESUMO

Women's opinion on the maternal serum screening programme offered at one maternity unit in East Northumberland (1991-1992) was evaluated. The responses from 1,774/2,633 women showed a general acceptance of the test but 722/1,774 (40%) wanted more information and a third, more explanation. Recommendations, which included a 'gold standard' protocol, a video to complement revised patient information literature and a coordinator to facilitate interdisciplinary communication and training with support for midwives, were introduced. The audit cycle was completed by a repeat questionnaire survey of 2,489 women from the postnatal ward (1992-1994) with a 67.3% response. An overall improvement in levels of satisfaction with reduction in, but not eradication of, the need for more information and explanation had occurred. These findings have relevance to the current controversy surrounding the counselling implications of maternal serum screening and have led to the formation of a network of professionals to develop the programme in our region.


Assuntos
Síndrome de Down/diagnóstico , Aconselhamento Genético , Testes Genéticos , Diagnóstico Pré-Natal , Feminino , Conhecimentos, Atitudes e Prática em Saúde , Humanos , Entrevistas como Assunto , Gravidez , Opinião Pública , Risco , Inquéritos e Questionários
4.
Public Health ; 111(6): 383-5, 1997 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-9392969

RESUMO

The lack of consensus regarding the implementation of maternal serum screening, has led to a widespread variation in practice. The importance of the role of midwives within the service has been recognised. All maternity units in the Northern region now have a designated 'co-ordinator' in an attempt to improve service delivery, professional liaison and training. This study was designed to obtain midwives' views about maternal serum screening in principle and to assess whether any changes had occurred since the introduction of co-ordinators. Semi-structured, postal questionnaires were sent to all midwives in one health authority for them to complete and return. Within this authority, one maternity unit offered universal screening whereas the other maintained a selective policy. Responses were obtained from 90 out of 133 (67.7%). There was almost unanimous support for the principle of screening 86 out of 90 (95.5%) and most midwives considered the offer of screening should be an NHS service, independent of age 78 out of 90 (86.7%). Half of the respondents 46 out of 90 (51.2%) reported that the introduction of a co-ordinator had been successful in improving staff education but requests for further training and updating were made by 69 out of 90 (76.6%) despite having had this organized training input: although those midwives who were regularly involved with screening made significantly fewer requests 27 out of 45 (60%). These findings confirmed our previous recommendation that ongoing responsibility for such provision would be required. The results of the study provided a useful contribution towards the review of screening policy undertaken by the health authority, as well as evidence upon which to base further development of the role of the co-ordinators in their support of midwives.


Assuntos
Atitude do Pessoal de Saúde , Síndrome de Down/diagnóstico , Tocologia , Diagnóstico Pré-Natal , Aconselhamento , Síndrome de Down/sangue , Feminino , Humanos , Inquéritos e Questionários
5.
J R Coll Physicians Lond ; 26(1): 69-70, 1992 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-1573590

RESUMO

We report a questionnaire survey of 216 adults (aged 16-68) attending the dental hospital in Newcastle. This was undertaken to provide a representative assessment of the level of knowledge in the community of cystic fibrosis and attitudes towards testing for carrier status. Knowledge of inheritance and symptomatology of the condition was scored and found to be less than previously reported in selected population groups. In the majority the source of information reported was the mass media; only 27 respondents had any contact with an affected individual. The questionnaire provided information about the inheritance and effects of cystic fibrosis. Three-quarters of the respondents accepted the idea of carrier testing for themselves, which included most of those of reproductive age, and all considered that testing should be available to those planning a family. General practice surgeries were the most favoured venue for testing. The implications of these findings for those involved in the planning of population screening programmes are considered.


Assuntos
Atitude Frente a Saúde , Fibrose Cística/genética , Escolaridade , Triagem de Portadores Genéticos , Adolescente , Adulto , Idoso , Fibrose Cística/epidemiologia , Fibrose Cística/prevenção & controle , Feminino , Humanos , Incidência , Masculino , Meios de Comunicação de Massa , Pessoa de Meia-Idade , Inquéritos e Questionários
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