Literature DB >> 19877061

Psychosocial aspects of patients with Niemann-Pick disease, type B.

Shelly L Henderson1, Wendy Packman, Seymour Packman.   

Abstract

Health-care providers have only begun to understand the medical aspects of Niemann-Pick disease type B (NPDB), a relatively rare disease. Even less information is known about the psychological effects of living with NPDB. Patients with NPDB and their families face numerous psychological stressors including extensive medical testing, uncertainty of diagnosis, living and coping with a chronic illness, and grief and bereavement surrounding this progressively debilitating, and, ultimately, fatal disease. We used a qualitative case study approach to explore the human experiences of NPDB patients and families. To assess psychosocial adjustment, all participants were administered a semi-structured, qualitative interview, as well as quantitative measures. Five major findings emerged: (1) limited physical activity, social isolation, and peer rejection were identified as significant stressors; (2) stressors had a specific impact during the age span of 10-16 years; (3) parents and adult patients expressed frustration regarding the lack of available information and treatment; (4) patients described close family relationships as a way of coping with illness; and (5) adult patients identified early medical experiences as having a considerable psychological impact. The results of this investigation highlight and expand awareness of the psychological and social needs of NPDB patients and families. This study calls for a collaborative, multidisciplinary effort in the treatment of these patients and their families. Copyright 2009 Wiley-Liss, Inc.

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Mesh:

Year:  2009        PMID: 19877061     DOI: 10.1002/ajmg.a.33077

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  10 in total

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Journal:  J Inherit Metab Dis       Date:  2015-07-25       Impact factor: 4.982

3.  Experiences of caregivers of children with inherited metabolic diseases: a qualitative study.

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Review 4.  Disease manifestations and burden of illness in patients with acid sphingomyelinase deficiency (ASMD).

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Review 5.  Psychosocial Considerations for the Child with Rare Disease: A Review with Recommendations and Calls to Action.

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Journal:  Children (Basel)       Date:  2022-06-21

Review 6.  A systematic review and integrative sequential explanatory narrative synthesis: The psychosocial impact of parenting a child with a lysosomal storage disorder.

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7.  Australian families living with rare disease: experiences of diagnosis, health services use and needs for psychosocial support.

Authors:  Matilda Anderson; Elizabeth J Elliott; Yvonne A Zurynski
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9.  Choosing between medical management and liver transplant in urea cycle disorders: A conceptual framework for parental treatment decision-making in rare disease.

Authors:  Maya T Gerstein; Anne R Markus; Kan Z Gianattasio; Cynthia Le Mons; Janice Bartos; David M Stevens; Nicholas Ah Mew
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10.  Impact and burden of acid sphingomyelinase deficiency from a patient and caregiver perspective.

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  10 in total

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