Literature DB >> 29297108

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

Allyn McConkie-Rosell1, Stephen R Hooper2, Loren D M Pena3, Kelly Schoch3, Rebecca C Spillmann3, Yong-Hui Jiang3, Heidi Cope3, Christina Palmer4, Vandana Shashi3.   

Abstract

Little is known about the psychosocial profiles of parents who have a child with an undiagnosed chronic illness. The National Institutes of Health Undiagnosed Diseases Network (UDN) evaluates individuals with intractable medical findings, with the objective of discovering the underlying diagnosis. We report on the psychosocial profiles of 50 parents whose children were accepted to one of the network's clinical sites. Parents completed questionnaires assessing anxiety, depression, coping self-efficacy, and health care empowerment at the beginning of their child's UDN clinical evaluation. Parents of undiagnosed children had high rates of anxiety and depression (~ 40%), which were significantly inversely correlated with coping self-efficacy, but not with health care empowerment. Coping self-efficacy, depressive, and anxiety symptoms were better in parents with older children and with longer duration of illness. Gender differences were identified, with mothers reporting greater health care engagement than fathers. Overall, our findings suggest that parents of children with undiagnosed diseases maintain positive coping self-efficacy and remain actively engaged in health care and to a lesser degree tolerance for uncertainty, but these come with a high emotional cost to the parents. As the parents' psychological needs may not be obvious, these should be ascertained and the requisite support provided.

Entities:  

Keywords:  Anxiety; Coping self-efficacy; Depression; Diagnostic odyssey; Health care empowerment; Parent; Tolerance of uncertainty; Undiagnosed disease; Whole exome sequencing

Mesh:

Year:  2018        PMID: 29297108      PMCID: PMC6028305          DOI: 10.1007/s10897-017-0193-5

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  43 in total

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Review 2.  The supportive care needs of parents caring for a child with a rare disease: A scoping review.

Authors:  Lemuel J Pelentsov; Thomas A Laws; Adrian J Esterman
Journal:  Disabil Health J       Date:  2015-04-07       Impact factor: 2.554

3.  The PHQ-9: validity of a brief depression severity measure.

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4.  Using Path Analysis to Evaluate the Healthcare Empowerment Model Among Persons Living with HIV for Antiretroviral Therapy Adherence.

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Journal:  AIDS Patient Care STDS       Date:  2016-11       Impact factor: 5.078

5.  Differences on psychosocial outcomes between male and female caregivers of children with life-limiting illnesses.

Authors:  Monica Schneider; Rose Steele; Susan Cadell; David Hemsworth
Journal:  J Pediatr Nurs       Date:  2010-02-25       Impact factor: 2.145

6.  Not the End of the Odyssey: Parental Perceptions of Whole Exome Sequencing (WES) in Pediatric Undiagnosed Disorders.

Authors:  Allyn McConkie Rosell; Loren D M Pena; Kelly Schoch; Rebecca Spillmann; Jennifer Sullivan; Stephen R Hooper; Yong-Hui Jiang; Nicolas Mathey-Andrews; David B Goldstein; Vandana Shashi
Journal:  J Genet Couns       Date:  2016-02-12       Impact factor: 2.537

7.  Quest, chaos and restitution: living with chronic fatigue syndrome/myalgic encephalomyelitis.

Authors:  Lisa Claire Whitehead
Journal:  Soc Sci Med       Date:  2005-10-19       Impact factor: 4.634

8.  Understanding Parental Experiences Through Their Narratives of Restitution, Chaos, and Quest: Improving Care for Families Experiencing Childhood Cancer.

Authors:  Jill M G Bally; Lorraine Holtslander; Wendy Duggleby; Karen Wright; Roanne Thomas; Shelley Spurr; Christopher Mpofu
Journal:  J Fam Nurs       Date:  2014-04-28       Impact factor: 3.818

9.  How do mothers and fathers who have a child with a disability describe their adaptation/ transformation process?

Authors:  Diane Pelchat; Marie-Josée Levert; Valérie Bourgeois-Guérin
Journal:  J Child Health Care       Date:  2009-09       Impact factor: 1.979

10.  A window into living with an undiagnosed disease: illness narratives from the Undiagnosed Diseases Network.

Authors:  Rebecca C Spillmann; Allyn McConkie-Rosell; Loren Pena; Yong-Hui Jiang; Kelly Schoch; Nicole Walley; Camilla Sanders; Jennifer Sullivan; Stephen R Hooper; Vandana Shashi
Journal:  Orphanet J Rare Dis       Date:  2017-04-17       Impact factor: 4.123

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  13 in total

1.  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

Review 2.  Genomic medicine for undiagnosed diseases.

Authors:  Anastasia L Wise; Teri A Manolio; George A Mensah; Josh F Peterson; Dan M Roden; Cecelia Tamburro; Marc S Williams; Eric D Green
Journal:  Lancet       Date:  2019-08-05       Impact factor: 79.321

3.  ModelMatcher: A scientist-centric online platform to facilitate collaborations between stakeholders of rare and undiagnosed disease research.

Authors:  J Michael Harnish; Lucian Li; Sanja Rogic; Guillaume Poirier-Morency; Seon-Young Kim; Kym M Boycott; Michael F Wangler; Hugo J Bellen; Philip Hieter; Paul Pavlidis; Zhandong Liu; Shinya Yamamoto
Journal:  Hum Mutat       Date:  2022-03-24       Impact factor: 4.700

4.  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

5.  Understanding Adult Participant and Parent Empowerment Prior to Evaluation in the Undiagnosed Diseases Network.

Authors:  Christina G S Palmer; Allyn McConkie-Rosell; Ingrid A Holm; Kimberly LeBlanc; Janet S Sinsheimer; Lauren C Briere; Naghmeh Dorrani; Matthew R Herzog; Sharyn Lincoln; Kelly Schoch; Rebecca C Spillmann; Elly Brokamp
Journal:  J Genet Couns       Date:  2018-03-01       Impact factor: 2.537

Review 6.  Recent developments in genetic/genomic medicine.

Authors:  Rachel H Horton; Anneke M Lucassen
Journal:  Clin Sci (Lond)       Date:  2019-03-05       Impact factor: 6.124

7.  Clinical application of a scale to assess genomic healthcare empowerment (GEmS): Process and illustrative case examples.

Authors:  Allyn McConkie-Rosell; Kelly Schoch; Jennifer Sullivan; Rebecca C Spillmann; Heidi Cope; Queenie K-G Tan; Christina G S Palmer; Stephen R Hooper; Vandana Shashi
Journal:  J Genet Couns       Date:  2021-06-11       Impact factor: 2.537

8.  Family genetic result communication in rare and undiagnosed disease communities: Understanding the practice.

Authors:  Courtney M Studwell; Emily G Kelley; Janet S Sinsheimer; Christina G S Palmer; Kimberly LeBlanc
Journal:  J Genet Couns       Date:  2020-10-27       Impact factor: 2.537

9.  "Doctors can read about it, they can know about it, but they've never lived with it": How parents use social media throughout the diagnostic odyssey.

Authors:  Natalie T Deuitch; Erika Beckman; Meghan C Halley; Jennifer L Young; Chloe M Reuter; Jennefer Kohler; Jonathan A Bernstein; Matthew T Wheeler; Kelly E Ormond; Holly K Tabor
Journal:  J Genet Couns       Date:  2021-06-06       Impact factor: 2.537

10.  Improving diagnosis for rare diseases: the experience of the Italian undiagnosed Rare diseases network.

Authors:  Marco Salvatore; Agata Polizzi; Maria Chiara De Stefano; Giovanna Floridia; Simone Baldovino; Dario Roccatello; Savino Sciascia; Elisa Menegatti; Giuseppe Remuzzi; Erica Daina; Paraskevas Iatropoulos; Bruno Bembi; Rosalia Maria Da Riol; Alessandra Ferlini; Marcella Neri; Giuseppe Novelli; Federica Sangiuolo; Francesco Brancati; Domenica Taruscio
Journal:  Ital J Pediatr       Date:  2020-09-14       Impact factor: 2.638

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