Literature DB >> 20702680

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

Agatha M Gallo1, Diana Wilkie, Marie Suarez, Richard Labotka, Robert Molokie, Alexis Thompson, Patricia Hershberger, Bonnye Johnson.   

Abstract

In the context of an inherited condition such as sickle cell disease (SCD), it is critical to understand how people with SCD or carriers (sickle cell trait [SCT]) face the challenges of making informed reproductive health decisions. The purpose of this analysis was to examine the beliefs, attitudes, and personal feelings of people with sickle cell disease or sickle cell trait related to making informed reproductive health decisions. Three focus groups were conducted with a total of 15 people who had either SCD or SCT. Five themes were identified: health-related issues in sickle cell disease, testing for sickle cell trait, partner choice, sharing sickle cell status with partners, and reproductive options. These findings enhance understanding of the reproductive experiences in people with SCD and SCT and provide the groundwork for developing an educational intervention focused on making informed decisions about becoming a parent.

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Year:  2010        PMID: 20702680      PMCID: PMC3590021          DOI: 10.1177/0193945910371482

Source DB:  PubMed          Journal:  West J Nurs Res        ISSN: 0193-9459            Impact factor:   1.967


  9 in total

1.  Pregnancy Risk Assessment Monitoring System (PRAMS): unintended pregnancy among women having a live birth. PRAMS Working Group.

Authors:  I B Ahluwalia; C Johnson; M Rogers; C Melvin
Journal:  J Womens Health Gend Based Med       Date:  1999-06

2.  US newborn screening system guidelines II: follow-up of children, diagnosis, management, and evaluation. Statement of the Council of Regional Networks for Genetic Services (CORN).

Authors:  K A Pass; P A Lane; P M Fernhoff; C F Hinton; S R Panny; J S Parks; M Z Pelias; W J Rhead; S I Ross; D L Wethers; L J Elsas
Journal:  J Pediatr       Date:  2000-10       Impact factor: 4.406

Review 3.  Sickle cell disease in childhood: Part I. Laboratory diagnosis, pathophysiology and health maintenance.

Authors:  D L Wethers
Journal:  Am Fam Physician       Date:  2000-09-01       Impact factor: 3.292

4.  A pilot study to explore knowledge, attitudes, and beliefs about sickle cell trait and disease.

Authors:  Kruti Acharya; Colleen Walsh Lang; Lainie Friedman Ross
Journal:  J Natl Med Assoc       Date:  2009-11       Impact factor: 1.798

5.  The influence of faith and religion and the role of religious and community leaders in prenatal decisions for sickle cell disorders and thalassaemia major.

Authors:  Shenaz Ahmed; Karl Atkin; Jenny Hewison; Josephine Green
Journal:  Prenat Diagn       Date:  2006-09       Impact factor: 3.050

6.  On the validity of retrospective assessments of pregnancy intention.

Authors:  Ted Joyce; Robert Kaestner; Sanders Korenman
Journal:  Demography       Date:  2002-02

Review 7.  A primary care provider's guide to preventive and acute care management of adults and children with sickle cell disease.

Authors:  Ardie Pack-Mabien; Johnson Haynes
Journal:  J Am Acad Nurse Pract       Date:  2009-05

8.  Understanding sickle cell carrier status identified through newborn screening: a qualitative study.

Authors:  Fiona A Miller; Martha Paynter; Robin Z Hayeems; Julian Little; June C Carroll; Brenda J Wilson; Judith Allanson; Jessica P Bytautas; Pranesh Chakraborty
Journal:  Eur J Hum Genet       Date:  2009-10-07       Impact factor: 4.246

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

Authors:  Shanna L Gustafson; Elizabeth A Gettig; Margaret Watt-Morse; Lakshmanan Krishnamurti
Journal:  Genet Med       Date:  2007-05       Impact factor: 8.822

  9 in total
  20 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.  Reproductive health choices for young adults with sickle cell disease or trait: randomized controlled trial immediate posttest effects.

Authors:  Diana J Wilkie; Agatha M Gallo; Yingwei Yao; Robert E Molokie; Christine Stahl; Patricia E Hershberger; Zhongsheng Zhao; Marie L Suarez; Robert J Labotka; Bonnye Johnson; Rigo Angulo; Veronica Angulo; Jesus Carrasco; David Shuey; Stephanie Pelligra; Edward Wang; Dennie T Rogers; Alexis A Thompson
Journal:  Nurs Res       Date:  2013 Sep-Oct       Impact factor: 2.381

3.  Reproductive Health CHOICES for Young Adults with Sickle Cell Disease or Trait: Randomized Controlled Trial Outcomes over Two Years.

Authors:  Agatha M Gallo; Diana J Wilkie; Yingwei Yao; Robert E Molokie; Christiane Stahl; Patricia E Hershberger; Zhongsheng Zhao; Marie L Suarez; Bonnye Johnson; Rigoberto Angulo; Jesus Carrasco; Veronica Angulo; Alexis A Thompson
Journal:  J Genet Couns       Date:  2015-08-28       Impact factor: 2.537

4.  Community engagement to inform the development of a sickle cell counselor training and certification program in Ghana.

Authors:  Kofi A Anie; Marsha J Treadwell; Althea M Grant; Jemima A Dennis-Antwi; Mabel K Asafo; Mary E Lamptey; Jelili Ojodu; Careema Yusuf; Ayo Otaigbe; Kwaku Ohene-Frempong
Journal:  J Community Genet       Date:  2016-04-18

5.  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

6.  Should Premarital Screening for Blood Disorders be an Obligatory Measure in Oman?

Authors:  Amal A Al-Balushi; Budoor Al-Hinai
Journal:  Sultan Qaboos Univ Med J       Date:  2018-04-04

7.  Perception of young adults with sickle cell disease or sickle cell trait about participation in the CHOICES randomized controlled trial.

Authors:  Patricia E Hershberger; Agatha M Gallo; Robert Molokie; Alexis A Thompson; Marie L Suarez; Yingwei Yao; Diana J Wilkie
Journal:  J Adv Nurs       Date:  2015-06-15       Impact factor: 3.187

8.  The Measure of Sickle Cell Stigma: Initial findings from the Improving Patient Outcomes through Respect and Trust study.

Authors:  Shawn M Bediako; Sophie Lanzkron; Marie Diener-West; Gladys Onojobi; Mary C Beach; Carlton Haywood
Journal:  J Health Psychol       Date:  2014-07-04

9.  Toward understanding family-related characteristics of young adults with sickle-cell disease or sickle-cell trait in the USA.

Authors:  Patricia E Hershberger; Agatha M Gallo; Robert Molokie; Alexis A Thompson; Marie L Suarez; Yingwei Yao; Constance M Dallas; Diana J Wilkie
Journal:  J Clin Nurs       Date:  2016-03-11       Impact factor: 3.036

10.  Effort required to contact primary care providers after newborn screening identifies sickle cell trait.

Authors:  Stephanie A Christopher; Jenelle L Collins; Michael H Farrell
Journal:  J Natl Med Assoc       Date:  2012 Nov-Dec       Impact factor: 1.798

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