Literature DB >> 17505208

Health beliefs among African American women regarding genetic testing and counseling for sickle cell disease.

Shanna L Gustafson1, Elizabeth A Gettig, Margaret Watt-Morse, Lakshmanan Krishnamurti.   

Abstract

PURPOSE: The Health Belief Model can help in understanding low acceptance of disease prevention and screening. We studied health beliefs of African American women to determine causes of low acceptance of genetic testing and counseling despite high prevalence of sickle cell disease and heterozygotes in this population.
METHODS: An anonymous questionnaire using a 12-question measure with a 5-point Likert scale response was administered to 101 African American women attending an obstetrics and gynecology clinic to determine knowledge of sickle cell disease, perception of risk, severity, likelihood of benefit and barriers to counseling.
RESULTS: The cumulative mean perceived scores on the 5-point Likert scale were 4.22 +/- 0.88 for severity of sickle cell disease, 4.10 +/- 1.03 for benefit of genetic testing, 2.28 +/- 1.00 for barriers to testing, and 2.62 +/- 1.06 for risk of having a child with sickle cell disease. High average level knowledge was associated with high perception of severity and benefit to screening (P < 0.05).
CONCLUSION: African American women have a relatively high belief of the severity of sickle cell disease and benefits of genetic counseling but frequently do not appear to believe that they are at risk of having a child with the disease. This should be taken into account in the design of educational and counseling strategies.

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Year:  2007        PMID: 17505208     DOI: 10.1097/gim.0b013e3180534282

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  12 in total

1.  Sickle cell carriers' unmet information needs: Beyond knowing trait status.

Authors:  Tilicia L Mayo-Gamble; David Schlundt; Jennifer Cunningham-Erves; Velma McBride Murry; Kemberlee Bonnet; Delores Quasie-Woode; Charles P Mouton
Journal:  J Genet Couns       Date:  2019-04-10       Impact factor: 2.537

2.  Knowledge and Health Beliefs Regarding Sickle Cell Disease Among Omanis in a Primary Healthcare Setting: Cross-sectional study.

Authors:  Mohammed H Al-Azri; Rajaa Al-Belushi; Muna Al-Mamari; Robin Davidson; Anil C Mathew
Journal:  Sultan Qaboos Univ Med J       Date:  2016-11-30

3.  Identifying Factors Underlying the Decision for Sickle Cell Carrier Screening Among African Americans Within Middle Reproductive Age.

Authors:  Tilicia L Mayo-Gamble; Susan E Middlestadt; Hsien-Chang Lin; Jennifer Cunningham-Erves; Priscilla Barnes; Pamela Braboy Jackson
Journal:  J Genet Couns       Date:  2018-03-24       Impact factor: 2.537

4.  Attitudes and beliefs of African-Americans toward genetics, genetic testing, and sickle cell disease education and awareness.

Authors:  Katie A Long; Stephen B Thomas; Robin E Grubs; Elizabeth A Gettig; Lakshmanan Krishnamurti
Journal:  J Genet Couns       Date:  2011-07-12       Impact factor: 2.537

5.  Feasibility of a Community-Based Sickle Cell Trait Testing and Counseling Program.

Authors:  Ashley J Housten; Regina A Abel; Terianne Lindsey; Allison A King
Journal:  J Health Dispar Res Pract       Date:  2016

6.  Reproductive decisions in people with sickle cell disease or sickle cell trait.

Authors:  Agatha M Gallo; Diana Wilkie; Marie Suarez; Richard Labotka; Robert Molokie; Alexis Thompson; Patricia Hershberger; Bonnye Johnson
Journal:  West J Nurs Res       Date:  2010-08-11       Impact factor: 1.967

7.  Developing community-based health education strategies with family history: Assessing the association between community resident family history and interest in health education.

Authors:  Elizabeth C Prom-Wormley; James S Clifford; Jessica L Bourdon; Peter Barr; Courtney Blondino; Kevin M Ball; Joshua Montgomery; Jonathan K Davis; Joseph E Real; Alexis C Edwards; Dawn L Thiselton; Gwen Corley Creighton; De'Nisha Wilson; Cynthia Newbille
Journal:  Soc Sci Med       Date:  2019-02-19       Impact factor: 4.634

8.  Impact of education on APOL1 testing attitudes among prospective living kidney donors.

Authors:  Jordan G Nestor; Amber J Li; Kristen L King; S Ali Husain; Tristan J McIntosh; Deirdre Sawinski; Ana S Iltis; Melody S Goodman; Heidi A Walsh; James M DuBois; Sumit Mohan
Journal:  Clin Transplant       Date:  2021-10-28       Impact factor: 3.456

9.  Maternal knowledge and attitudes about newborn screening for sickle cell disease and cystic fibrosis.

Authors:  Colleen Walsh Lang; Alex P Stark; Kruti Acharya; Lainie Friedman Ross
Journal:  Am J Med Genet A       Date:  2009-11       Impact factor: 2.802

10.  Some ethical issues in the prenatal diagnosis of sickle cell anaemia.

Authors:  Joseph O Fadare
Journal:  Ann Ib Postgrad Med       Date:  2009-12
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