Literature DB >> 22183783

Carrier screening in preconception consultation in primary care.

Sylvia A Metcalfe1.   

Abstract

Discussing carrier screening during preconception consultation in primary care has a number of advantages in terms of promoting autonomy and enabling the greatest range of reproductive choices. For those with a family history of an inherited condition, this ought to be a routine discussion; however, this can be expanded to include the wider population, especially for those conditions for which carrier frequencies are considered relatively common. There is published literature from around the world regarding experiences with carrier screening in primary care for cystic fibrosis, haemoglobinopathies, fragile X syndrome, Tay-Sachs disease and spinal muscular atrophy, although many of these have tended to focus on consultations during rather than before pregnancy. Overall, these studies reveal that population carrier screening is well received by the participants with apparent minimal psychosocial harms; however, challenges exist in terms of approaches to ensure couples receive adequate information to make personally relevant decisions and for ongoing health professional engagement.

Entities:  

Year:  2011        PMID: 22183783      PMCID: PMC3419291          DOI: 10.1007/s12687-011-0071-z

Source DB:  PubMed          Journal:  J Community Genet        ISSN: 1868-310X


  121 in total

Review 1.  Screening for fragile X syndrome: a literature review and modelling study.

Authors:  F J Song; P Barton; V Sleightholme; G L Yao; A Fry-Smith
Journal:  Health Technol Assess       Date:  2003       Impact factor: 4.014

2.  Cystic fibrosis: community knowledge and attitudes towards carrier screening and prenatal diagnosis.

Authors:  M Decruyenaere; G Evers-Kiebooms; L Denayer; H Van den Berghe
Journal:  Clin Genet       Date:  1992-04       Impact factor: 4.438

3.  Attitudes towards reproductive issues and carrier testing among adult patients and parents of children with cystic fibrosis (CF).

Authors:  L Henneman; I Bramsen; T A Van Os; I E Reuling; H G Heyerman; J van der Laag; H M van der Ploeg; L P ten Kate
Journal:  Prenat Diagn       Date:  2001-01       Impact factor: 3.050

4.  Antenatal thalassaemia carrier testing: women's perceptions of "information" and "consent".

Authors:  Shenaz Ahmed; Josephine Green; Jenny Hewison
Journal:  J Med Screen       Date:  2005       Impact factor: 2.136

5.  Twenty-year outcome analysis of genetic screening programs for Tay-Sachs and beta-thalassemia disease carriers in high schools.

Authors:  J J Mitchell; A Capua; C Clow; C R Scriver
Journal:  Am J Hum Genet       Date:  1996-10       Impact factor: 11.025

6.  Screening for carriers of cystic fibrosis--a general practitioner's perspective.

Authors:  M Modell
Journal:  BMJ       Date:  1993-10-02

7.  Fragile X carrier screening and FMR1 allele distribution in the Japanese population.

Authors:  Susumu Otsuka; Yumiko Sakamoto; Haruhiko Siomi; Mituo Itakura; Kenji Yamamoto; Hideo Matumoto; Tsukasa Sasaki; Nobumasa Kato; Eiji Nanba
Journal:  Brain Dev       Date:  2009-02-10       Impact factor: 1.961

8.  Offering cystic fibrosis carrier screening to an HMO population: factors associated with utilization.

Authors:  E S Tambor; B A Bernhardt; G A Chase; R R Faden; G Geller; K J Hofman; N A Holtzman
Journal:  Am J Hum Genet       Date:  1994-10       Impact factor: 11.025

9.  Identification of the cystic fibrosis gene: chromosome walking and jumping.

Authors:  J M Rommens; M C Iannuzzi; B Kerem; M L Drumm; G Melmer; M Dean; R Rozmahel; J L Cole; D Kennedy; N Hidaka
Journal:  Science       Date:  1989-09-08       Impact factor: 47.728

10.  Needs assessment study of genetics education for general practitioners in Australia.

Authors:  Sylvia Metcalfe; Rosalind Hurworth; Jennifer Newstead; Rosemary Robins
Journal:  Genet Med       Date:  2002 Mar-Apr       Impact factor: 8.822

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  18 in total

1.  "It gives them more options": preferences for preconception genetic carrier screening for fragile X syndrome in primary healthcare.

Authors:  Alison D Archibald; Chriselle L Hickerton; Samantha A Wake; Alice M Jaques; Jonathan Cohen; Sylvia A Metcalfe
Journal:  J Community Genet       Date:  2016-02-03

2.  Editorial: genetic aspects of preconception consultation in primary care.

Authors:  Jon D Emery; Anne L Dunlop; Leo P Ten Kate
Journal:  J Community Genet       Date:  2012-06-29

3.  Evaluation of two-year Jewish genetic disease screening program in Atlanta: insight into community genetic screening approaches.

Authors:  Yunru Shao; Shuling Liu; Karen Grinzaid
Journal:  J Community Genet       Date:  2015-01-07

4.  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

5.  The changing landscape of carrier screening: expanding technology and options?.

Authors:  Michelle L McGowan; Deborah Cho; Richard R Sharp
Journal:  Health Matrix Clevel       Date:  2013

Review 6.  The measurement of patient attitudes regarding prenatal and preconception genetic carrier screening and translational behavioral medicine: an integrative review.

Authors:  Jennifer J Shiroff; Mathew J Gregoski
Journal:  Transl Behav Med       Date:  2017-06       Impact factor: 3.046

7.  Preconception carrier screening for multiple disorders: evaluation of a screening offer in a Dutch founder population.

Authors:  Inge B Mathijssen; Kim C A Holtkamp; Cecile P E Ottenheim; Janneke M C van Eeten-Nijman; Phillis Lakeman; Hanne Meijers-Heijboer; Merel C van Maarle; Lidewij Henneman
Journal:  Eur J Hum Genet       Date:  2018-01-10       Impact factor: 4.246

8.  Family Communication and Cascade Testing for Fragile X Syndrome.

Authors:  Melissa Raspa; Anne Edwards; Anne C Wheeler; Ellen Bishop; Donald B Bailey
Journal:  J Genet Couns       Date:  2016-03-09       Impact factor: 2.537

9.  How people in Benin assess a couple's risk of having a baby with sickle cell disease.

Authors:  Ornheilia Zounon; Paul Clay Sorum; Etienne Mullet
Journal:  J Community Genet       Date:  2014-11-25

10.  What can be offered to couples at (possibly) increased genetic risk?

Authors:  Andrew P Read; Dian Donnai
Journal:  J Community Genet       Date:  2012-07-04
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