Literature DB >> 26306645

Mothers' psychological adaptation to Duchenne/Becker muscular dystrophy.

Holly L Peay1,2, Bettina Meiser3, Kathleen Kinnett1, Pat Furlong1, Kathryn Porter1, Aad Tibben2.   

Abstract

Duchenne and Becker muscular dystrophy (DBMD) cause significant emotional and care-related burden on caregivers, but no studies have evaluated predictors of positive caregiver outcomes, including disorder-specific psychological adaptation. Using a community-engaged approach focused on supporting mothers in positive aspects of caregiving, this prospective study aims to assess (i) the association between child's baseline functional status and mothers' illness perceptions, resilience, and coping self-efficacy; and (ii) predictors of mothers' psychological adaptation to caring for a child with DBMD. Biological mothers with at least one living child with DBMD completed a baseline survey (n=205) with 1-year (n=147) and 2-year (n=144) follow-up surveys. Worse child's baseline function was associated not only with increased caregiver burden and reduced maternal resilience, but also with perception of positive disease impact on the family. At two follow-ups, increased psychological adaptation to DBMD was predicted by resilience (β=0.264, P=0.001) and perceived positive impact (β=0.310, P<0.001), controlling for mother's age (β=-0.305, P<0.001) and income (β=-0.088, P=0.245). Child's functional status and caregiver burden of DBMD did not predict DBMD-specific adaptation. Though clinicians caring for families with DBMD should anticipate increased caregiver burden as the disorder progresses, interventions focused on caregiver burden are not expected to influence mothers' psychosocial adaptation. Efforts to improve mothers' well-being should focus on fostering mothers' resilience and enhancing perceptions of positive disease impact (benefit finding). Results suggest that psychosocial interventions can highlight strengths and well-being rather than burden and deficit.

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Year:  2015        PMID: 26306645      PMCID: PMC4930093          DOI: 10.1038/ejhg.2015.189

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  31 in total

1.  Subjective caregiver burden of parents of adults with Duchenne muscular dystrophy.

Authors:  Robert F Pangalila; Geertrudis A M van den Bos; Henk J Stam; N Job A van Exel; Werner B F Brouwer; Marij E Roebroeck
Journal:  Disabil Rehabil       Date:  2011-12-09       Impact factor: 3.033

Review 2.  Youth Resilience Framework for reducing health-risk behaviors in adolescents.

Authors:  Lynn Rew; Sharon D Horner
Journal:  J Pediatr Nurs       Date:  2003-12       Impact factor: 2.145

3.  Benefit-finding among patients with rheumatoid arthritis: positive effects on interpersonal relationships.

Authors:  Sharon Danoff-Burg; Tracey A Revenson
Journal:  J Behav Med       Date:  2005-02

4.  Resilience in relation to personality and intelligence.

Authors:  Oddgeir Friborg; Dag Barlaug; Monica Martinussen; Jan H Rosenvinge; Odin Hjemdal
Journal:  Int J Methods Psychiatr Res       Date:  2005       Impact factor: 4.035

5.  Uncertainty and perceived personal control among parents of children with rare chromosome conditions: the role of genetic counseling.

Authors:  Shawn E Lipinski; Michael J Lipinski; Leslie G Biesecker; Barbara B Biesecker
Journal:  Am J Med Genet C Semin Med Genet       Date:  2006-11-15       Impact factor: 3.908

6.  The effect of caregiving on women in families with Duchenne/Becker muscular dystrophy.

Authors:  Aileen Kenneson; Janet Kay Bobo
Journal:  Health Soc Care Community       Date:  2010-06-16

Review 7.  Adaptation to living with a genetic condition or risk: a mini-review.

Authors:  B B Biesecker; L Erby
Journal:  Clin Genet       Date:  2008-09-24       Impact factor: 4.438

Review 8.  Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management.

Authors:  Katharine Bushby; Richard Finkel; David J Birnkrant; Laura E Case; Paula R Clemens; Linda Cripe; Ajay Kaul; Kathi Kinnett; Craig McDonald; Shree Pandya; James Poysky; Frederic Shapiro; Jean Tomezsko; Carolyn Constantin
Journal:  Lancet Neurol       Date:  2009-11-27       Impact factor: 44.182

Review 9.  Duchenne and Becker muscular dystrophies.

Authors:  Kevin M Flanigan
Journal:  Neurol Clin       Date:  2014-08       Impact factor: 3.806

10.  Parental stress in mothers of boys with duchenne muscular dystrophy.

Authors:  Nancy E Nereo; Robert J Fee; Veronica J Hinton
Journal:  J Pediatr Psychol       Date:  2003 Oct-Nov
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  12 in total

1.  Factors Associated with Parental Adaptation to Children with an Undiagnosed Medical Condition.

Authors:  Tatiane Yanes; Linda Humphreys; Aideen McInerney-Leo; Barbara Biesecker
Journal:  J Genet Couns       Date:  2016-12-30       Impact factor: 2.537

2.  Psychosocial Needs and Facilitators of Mothers Caring for Children with Duchenne/Becker Muscular Dystrophy.

Authors:  Holly L Peay; Bettina Meiser; Kathleen Kinnett; Aad Tibben
Journal:  J Genet Couns       Date:  2017-08-12       Impact factor: 2.537

3.  The genome empowerment scale: An assessment of parental empowerment in families with undiagnosed disease.

Authors:  Allyn McConkie-Rosell; Kelly Schoch; Jennifer Sullivan; Heidi Cope; Rebecca Spillmann; Christina G S Palmer; Loren Pena; Yong-Hui Jiang; Nicole Daniels; Nicole Walley; Khoon G Tan; Stephen R Hooper; Vandana Shashi
Journal:  Clin Genet       Date:  2019-10-08       Impact factor: 4.438

4.  Psychosocial Profiles of Parents of Children with Undiagnosed Diseases: Managing Well or Just Managing?

Authors:  Allyn McConkie-Rosell; Stephen R Hooper; Loren D M Pena; Kelly Schoch; Rebecca C Spillmann; Yong-Hui Jiang; Heidi Cope; Christina Palmer; Vandana Shashi
Journal:  J Genet Couns       Date:  2018-01-02       Impact factor: 2.537

5.  Cases from the Undiagnosed Diseases Network: The continued value of counseling skills in a new genomic era.

Authors:  Ellen F Macnamara; Kelly Schoch; Emily G Kelley; Elizabeth Fieg; Elly Brokamp; Rebecca Signer; Kimberly LeBlanc; Allyn McConkie-Rosell; Christina G S Palmer
Journal:  J Genet Couns       Date:  2019-01-24       Impact factor: 2.537

Review 6.  Ethical issues in using the internet to engage participants in family and child research: A scoping review.

Authors:  Stacey Hokke; Naomi J Hackworth; Nina Quin; Shannon K Bennetts; Hnin Yee Win; Jan M Nicholson; Lawrie Zion; Jayne Lucke; Patrick Keyzer; Sharinne B Crawford
Journal:  PLoS One       Date:  2018-09-27       Impact factor: 3.240

7.  Gene therapy as a potential therapeutic option for Duchenne muscular dystrophy: A qualitative preference study of patients and parents.

Authors:  Holly Landrum Peay; Ryan Fischer; Janice P Tzeng; Sharon E Hesterlee; Carl Morris; Amy Strong Martin; Colin Rensch; Edward Smith; Valeria Ricotti; Katherine Beaverson; Hannah Wand; Carol Mansfield
Journal:  PLoS One       Date:  2019-05-01       Impact factor: 3.240

8.  Priorities when deciding on participation in early-phase gene therapy trials for Duchenne muscular dystrophy: a best-worst scaling experiment in caregivers and adult patients.

Authors:  Ryan S Paquin; Ryan Fischer; Carol Mansfield; Brennan Mange; Katherine Beaverson; Annie Ganot; Amy Strong Martin; Carl Morris; Colin Rensch; Valeria Ricotti; Leo J Russo; Alesia Sadosky; Edward C Smith; Holly L Peay
Journal:  Orphanet J Rare Dis       Date:  2019-05-09       Impact factor: 4.123

9.  Needs management in families affected by childhood-onset dystrophinopathies.

Authors:  Kristin M Conway; Katy Eichinger; Christina Trout; Paul A Romitti; Katherine D Mathews; Shree K Pandya
Journal:  SAGE Open Med       Date:  2019-03-02

Review 10.  An Integrative Review Exploring Psycho-Social Impacts and Therapeutic Interventions for Parent Caregivers of Young People Living with Duchenne's Muscular Dystrophy.

Authors:  Debra Porteous; Barbara Davies; Christine English; Joanne Atkinson
Journal:  Children (Basel)       Date:  2021-03-11
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