Literature DB >> 16115832

GPs' opinions of their role in prenatal genetic services: a cross-sectional survey.

Nadeem Qureshi1, Sarah Armstrong, Bernadette Modell.   

Abstract

BACKGROUND: In the UK about 4.5% of the population carry cystic fibrosis, whilst in the inner city areas an even higher proportion carry one of the haemoglobin disorders such as thalassaemia. Couples who both carry the same recessive disorder have a 1 in 4 risk of an affected child in every pregnancy.
OBJECTIVES: To assess GPs' confidence in their ability to provide initial prenatal advice for couples carrying common autosomal recessive disorders (either the cystic fibrosis or thalassaemia gene), and their opinions of different approaches for referral to prenatal diagnostic services for such at-risk couples.
METHODS: A cross-sectional postal survey of all 644 GPs in 388 general practices in Nottinghamshire. Practices were randomly allocated to receive either the cystic fibrosis or the thalassaemia scenario survey. The survey questions predominantly used six-point Likert scales to assess confidence and opinions of prenatal services.
RESULTS: The questionnaire was returned by 62% (397) of GPs. Only 23% (91) were confident in providing prenatal advice to the at-risk carrier couples. GPs were more confident about advising cystic fibrosis carriers than thalassaemia carriers (P = 0.01). The least popular approach to prenatal service provision was direct referral to prenatal services after counselling with 52% (194) scoring this as useful, whilst 60.5% (233) of GPs scored referral to the obstetric services with the prenatal diagnosis organised by the obstetrician as useful.
CONCLUSIONS: GPs perceive that they lack the confidence to provide basic prenatal genetic advice to women at risk of the commonest recessive disorders, with particularly low confidence where the couple both carry thalassaemia. A significant knowledge gap was demonstrated by the poor awareness of the importance of rapid referral to prenatal diagnostic services.

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Mesh:

Year:  2005        PMID: 16115832     DOI: 10.1093/fampra/cmi088

Source DB:  PubMed          Journal:  Fam Pract        ISSN: 0263-2136            Impact factor:   2.267


  13 in total

1.  Carrier screening in preconception consultation in primary care.

Authors:  Sylvia A Metcalfe
Journal:  J Community Genet       Date:  2011-12-20

2.  Interactive genetic counseling role-play: a novel educational strategy for family physicians.

Authors:  Sean M Blaine; June C Carroll; Andrea L Rideout; Gord Glendon; Wendy Meschino; Cheryl Shuman; Deanna Telner; Natasha Van Iderstine; Joanne Permaul
Journal:  J Genet Couns       Date:  2008-01-30       Impact factor: 2.537

3.  Attitudes of health care professionals toward carrier screening for cystic fibrosis. A review of the literature.

Authors:  S Janssens; A De Paepe; P Borry
Journal:  J Community Genet       Date:  2012-12-29

4.  Attitudes and opinions of pregnant women who are not offered cystic fibrosis carrier screening.

Authors:  Liane Ioannou; John Massie; Sharon Lewis; Veronica Collins; Belinda McClaren; Martin B Delatycki
Journal:  Eur J Hum Genet       Date:  2013-11-20       Impact factor: 4.246

5.  Prenatal genetic counseling in cross-cultural medicine: A framework for family physicians.

Authors:  Ashvinder K Bhogal; Fern Brunger
Journal:  Can Fam Physician       Date:  2010-10       Impact factor: 3.275

6.  Genetic education for primary care providers: improving attitudes, knowledge, and confidence.

Authors:  June C Carroll; Andrea L Rideout; Brenda J Wilson; Judith Md Allanson; Sean M Blaine; Mary Jane Esplen; Sandra A Farrell; Gail E Graham; Jennifer MacKenzie; Wendy Meschino; Fiona Miller; Preeti Prakash; Cheryl Shuman; Anne Summers; Sherry Taylor
Journal:  Can Fam Physician       Date:  2009-12       Impact factor: 3.275

7.  Prenatal diagnostic services in three regional centers in Vietnam.

Authors:  Bui Thi Thu Ha; Nguyen Thi Thu Huong; Doan Thi Thuy Duong
Journal:  Int J Public Health       Date:  2016-09-15       Impact factor: 3.380

Review 8.  A systematic review of factors that act as barriers to patient referral to genetic services.

Authors:  Türem Delikurt; Graham R Williamson; Violetta Anastasiadou; Heather Skirton
Journal:  Eur J Hum Genet       Date:  2014-09-10       Impact factor: 4.246

9.  Parents' experiences of universal screening for haemoglobin disorders: implications for practice in a new genetics era.

Authors:  Louise Locock; Joe Kai
Journal:  Br J Gen Pract       Date:  2008-03       Impact factor: 5.386

10.  Health practitioners' perceptions of the barriers and enablers to the implementation of reproductive genetic carrier screening: A systematic review.

Authors:  Stephanie Best; Janet Long; Tahlia Theodorou; Sarah Hatem; Rebecca Lake; Alison Archibald; Lucinda Freeman; Jeffrey Braithwaite
Journal:  Prenat Diagn       Date:  2021-03-05       Impact factor: 3.050

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