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Erschienen in: Journal of Genetic Counseling 4/2018

02.01.2018 | Original Research

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

verfasst von: Allyn McConkie-Rosell, Stephen R. Hooper, Loren D. M. Pena, Kelly Schoch, Rebecca C. Spillmann, Yong-Hui Jiang, Heidi Cope, Christina Palmer, Vandana Shashi, Undiagnosed Diseases Network

Erschienen in: Journal of Genetic Counseling | Ausgabe 4/2018

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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.
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Literatur
Zurück zum Zitat Bally, J., Holtslander, L., Duggleby, W., Wright, K., Thomas, R., Spurr, S., & Mpofu, C. (2014). Understanding parental experiences through their narratives of restitution, chaos, and quest: improving care for families experiencing childhood cancer. Journal of Family Nursing, 20, 287–312.CrossRefPubMed Bally, J., Holtslander, L., Duggleby, W., Wright, K., Thomas, R., Spurr, S., & Mpofu, C. (2014). Understanding parental experiences through their narratives of restitution, chaos, and quest: improving care for families experiencing childhood cancer. Journal of Family Nursing, 20, 287–312.CrossRefPubMed
Zurück zum Zitat Bandura, A. (1997). Self efficacy: the exercise of control. New York: W.H. Freeman. Bandura, A. (1997). Self efficacy: the exercise of control. New York: W.H. Freeman.
Zurück zum Zitat Cohen, J. (1988). Statistical power analysis for the behavioral sciences. Hillsdale, NJ: Lawrence Earlbaum Associates. Cohen, J. (1988). Statistical power analysis for the behavioral sciences. Hillsdale, NJ: Lawrence Earlbaum Associates.
Zurück zum Zitat Cohen, M. (1999). Families coping with childhood chronic illness: a research review. Families, Systems & Health, 149–164. Cohen, M. (1999). Families coping with childhood chronic illness: a research review. Families, Systems & Health, 149–164.
Zurück zum Zitat Dear, B. F., Titov, N., Sunderland, M., McMillan, D., Anderson, T., Lorian, C., & Robinson, E. (2011). Psychometric comparison of the generalized anxiety disorder scale-7 and the Penn State Worry Questionnaire for measuring response during treatment of generalised anxiety disorder. Cognitive Behaviour Therapy, 40(3), 216–227. https://doi.org/10.1080/16506073.2011.582138.CrossRefPubMed Dear, B. F., Titov, N., Sunderland, M., McMillan, D., Anderson, T., Lorian, C., & Robinson, E. (2011). Psychometric comparison of the generalized anxiety disorder scale-7 and the Penn State Worry Questionnaire for measuring response during treatment of generalised anxiety disorder. Cognitive Behaviour Therapy, 40(3), 216–227. https://​doi.​org/​10.​1080/​16506073.​2011.​582138.CrossRefPubMed
Zurück zum Zitat Dellve, L. (2006). Stress and well-being among parents of children with rare diseases: a prospective intervention study. Journal of Advanced Nursing, 53(4), 392–402.CrossRefPubMed Dellve, L. (2006). Stress and well-being among parents of children with rare diseases: a prospective intervention study. Journal of Advanced Nursing, 53(4), 392–402.CrossRefPubMed
Zurück zum Zitat Frank, A. (1995). The wounded storyteller. Chicago: The University of Chicago Press.CrossRef Frank, A. (1995). The wounded storyteller. Chicago: The University of Chicago Press.CrossRef
Zurück zum Zitat Guillamon, N., Nieto, R., Pousada, M., Redolar, D., Munoz, E., Hernandez, E., et al. (2013). Quality of life and mental health among parents of children with cerebral palsy: the influence of self-efficacy and coping strategies. Journal of Clinical Nursing, 22(11–12), 1579–1590. https://doi.org/10.1111/jocn.12124.CrossRefPubMed Guillamon, N., Nieto, R., Pousada, M., Redolar, D., Munoz, E., Hernandez, E., et al. (2013). Quality of life and mental health among parents of children with cerebral palsy: the influence of self-efficacy and coping strategies. Journal of Clinical Nursing, 22(11–12), 1579–1590. https://​doi.​org/​10.​1111/​jocn.​12124.CrossRefPubMed
Zurück zum Zitat Kim, K. R., Lee, E., Namkoong, K., Lee, Y. M., Lee, J. S., & Kim, H. D. (2010). Caregiver’s burden and quality of life in mitochondrial disease. Pediatric Neurology, 42(4), 271–271.CrossRefPubMed Kim, K. R., Lee, E., Namkoong, K., Lee, Y. M., Lee, J. S., & Kim, H. D. (2010). Caregiver’s burden and quality of life in mitochondrial disease. Pediatric Neurology, 42(4), 271–271.CrossRefPubMed
Zurück zum Zitat Kroenke, K., Spitzer, R. L., & Williams, J. B. (2001). The PHQ-9: validity of a brief depression severity measure. Journal of General Internal Medicine, 16(9), 606–613.CrossRefPubMedPubMedCentral Kroenke, K., Spitzer, R. L., & Williams, J. B. (2001). The PHQ-9: validity of a brief depression severity measure. Journal of General Internal Medicine, 16(9), 606–613.CrossRefPubMedPubMedCentral
Zurück zum Zitat Lingen, M., Albers, L., Borchers, M., Haass, S., Gärtner, J., Schröder, S., et al. (2016). Obtaining a genetic diagnosis in a child with disability: impact on parental quality of life. Social and Behavioural Research in Clinical Genetics, 89(2258–266). https://doi.org/10.1111/cge.12629. Lingen, M., Albers, L., Borchers, M., Haass, S., Gärtner, J., Schröder, S., et al. (2016). Obtaining a genetic diagnosis in a child with disability: impact on parental quality of life. Social and Behavioural Research in Clinical Genetics, 89(2258–266). https://​doi.​org/​10.​1111/​cge.​12629.
Zurück zum Zitat McConkie-Rosell, A., Pena, L. D., Schoch, K., Spillmann, R., Sullivan, J., Hooper, S. R., et al. (2016). Not the end of the odyssey: parental perceptions of whole exome sequencing (WES) in pediatric undiagnosed disorders. Journal of Genetic Counseling, 25(5), 1019–1031. https://doi.org/10.1007/s10897-016-9933-1.CrossRef McConkie-Rosell, A., Pena, L. D., Schoch, K., Spillmann, R., Sullivan, J., Hooper, S. R., et al. (2016). Not the end of the odyssey: parental perceptions of whole exome sequencing (WES) in pediatric undiagnosed disorders. Journal of Genetic Counseling, 25(5), 1019–1031. https://​doi.​org/​10.​1007/​s10897-016-9933-1.CrossRef
Zurück zum Zitat Muscara, F., McCarthy, M., Woolf, C., Hearps, S., Burke, K., & Anderson, V. (2015b). Early psychological reactions in parents of children with a life threatening illness within a pediatric hospital setting. European Psychiatry, 30(5). Muscara, F., McCarthy, M., Woolf, C., Hearps, S., Burke, K., & Anderson, V. (2015b). Early psychological reactions in parents of children with a life threatening illness within a pediatric hospital setting. European Psychiatry, 30(5).
Zurück zum Zitat Pelentsov, L. J., Laws, T. A., & Esterman, A. J. (2015). The supportive care needs of parents caring for a child with a rare disease: a scoping review. Disability and Health Journal, 8(4), 475–491.CrossRefPubMed Pelentsov, L. J., Laws, T. A., & Esterman, A. J. (2015). The supportive care needs of parents caring for a child with a rare disease: a scoping review. Disability and Health Journal, 8(4), 475–491.CrossRefPubMed
Zurück zum Zitat Perry, A., Sarlo-McGarvey, N., & Factor, D. C. (1992). Stress and family functioning in parents of girls with Rett syndrome. Journal of Autism and Developmental Disorders, 22(2), 235–248.CrossRefPubMed Perry, A., Sarlo-McGarvey, N., & Factor, D. C. (1992). Stress and family functioning in parents of girls with Rett syndrome. Journal of Autism and Developmental Disorders, 22(2), 235–248.CrossRefPubMed
Zurück zum Zitat Rosenthal, E. T., Biesecker, L. G., & Biesecker, B. B. (2001). Parental attitudes toward a diagnosis in children with unidentified multiple congenital anomaly syndromes. American Journal of Medical Genetics, 103(2), 106–114.CrossRefPubMed Rosenthal, E. T., Biesecker, L. G., & Biesecker, B. B. (2001). Parental attitudes toward a diagnosis in children with unidentified multiple congenital anomaly syndromes. American Journal of Medical Genetics, 103(2), 106–114.CrossRefPubMed
Zurück zum Zitat Salas, B. L., Rodríguez, V. Y., Urbieta, C. T., & Cuadrado, E. (2017). The role of coping strategies and self-efficacy as predictors of life satisfaction in a sample of parents of children with autism spectrum disorder. Psicothema, 29(1), 55–60. Salas, B. L., Rodríguez, V. Y., Urbieta, C. T., & Cuadrado, E. (2017). The role of coping strategies and self-efficacy as predictors of life satisfaction in a sample of parents of children with autism spectrum disorder. Psicothema, 29(1), 55–60.
Zurück zum Zitat Spiers, G., & Beresford, B. (2017). “It goes against the grain”: a qualitative study of the experiences of parents’ administering distressing health-care procedures for their child at home. Health Expectations: an International Journal of Public Participation in Health Care and Health Policy. Spiers, G., & Beresford, B. (2017). “It goes against the grain”: a qualitative study of the experiences of parents’ administering distressing health-care procedures for their child at home. Health Expectations: an International Journal of Public Participation in Health Care and Health Policy.
Zurück zum Zitat Truitt, M., Biesecker, B., Capone, G., Bailey, T., & Erby, L. (2012). The role of hope in adaptation to uncertainty: the experience of caregivers of children with Down syndrome. Patient Education and Counseling, 87(2), 233–238.CrossRefPubMed Truitt, M., Biesecker, B., Capone, G., Bailey, T., & Erby, L. (2012). The role of hope in adaptation to uncertainty: the experience of caregivers of children with Down syndrome. Patient Education and Counseling, 87(2), 233–238.CrossRefPubMed
Metadaten
Titel
Psychosocial Profiles of Parents of Children with Undiagnosed Diseases: Managing Well or Just Managing?
verfasst von
Allyn McConkie-Rosell
Stephen R. Hooper
Loren D. M. Pena
Kelly Schoch
Rebecca C. Spillmann
Yong-Hui Jiang
Heidi Cope
Christina Palmer
Vandana Shashi
Undiagnosed Diseases Network
Publikationsdatum
02.01.2018
Verlag
Springer US
Erschienen in
Journal of Genetic Counseling / Ausgabe 4/2018
Print ISSN: 1059-7700
Elektronische ISSN: 1573-3599
DOI
https://doi.org/10.1007/s10897-017-0193-5

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