Literature DB >> 24527993

Unmet needs of patients feeling severely affected by multiple sclerosis in Germany: a qualitative study.

Maren Galushko1, Heidrun Golla, Julia Strupp, Ute Karbach, Claudia Kaiser, Nicole Ernstmann, Holger Pfaff, Christoph Ostgathe, Raymond Voltz.   

Abstract

BACKGROUND: The needs of patients feeling severely affected by multiple sclerosis (MS) have rarely been investigated. However this is essential information to know before care can be improved, including adding palliative care (PC) services where helpful. Since it remains unclear at what point specialized palliative care should begin for this patient group, this study focuses on needs in general.
OBJECTIVE: The objective was to explore the subjectively unmet needs of patients feeling severely affected by MS.
METHODS: The study used a qualitative cross-sectional approach for needs assessment. Fifteen patients self-reporting feeling severely affected by MS were recruited and interviewed using a combination of purposive and convenience sampling (five were accompanied by a caregiver relative). Interviews were recorded and transcribed verbatim, followed by qualitative content analysis.
RESULTS: Unmet needs were identified in the main categories "support of family and friends," "health care services," "managing everyday life," and "maintaining biographical continuity." Patients expressed the desire for more support from their families and to be viewed as distinct individuals. They see a substantial deficit in the physician-patient relationship and in the coordination of services. A decrease in expressed unmet needs was found for patients more severely affected and less socially integrated.
CONCLUSIONS: To address the unmet needs of severely affected MS patients, health care services need to be improved and linked with existing PC services. Special attention is required to form supporting professional-patient relationships. Multiprofessional services should be accessible for patients, while integrating relatives. All services should have an individual approach to provide needs-tailored support.

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Year:  2014        PMID: 24527993      PMCID: PMC3952521          DOI: 10.1089/jpm.2013.0497

Source DB:  PubMed          Journal:  J Palliat Med        ISSN: 1557-7740            Impact factor:   2.947


  39 in total

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Review 4.  Renovating the Pyramid of Needs: Contemporary Extensions Built Upon Ancient Foundations.

Authors:  Douglas T Kenrick; Vladas Griskevicius; Steven L Neuberg; Mark Schaller
Journal:  Perspect Psychol Sci       Date:  2010-05

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Review 7.  Historical and clinical perspectives of the expanded disability status scale.

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Authors:  Judy Ann Wollin; Patsy M Yates; Linda J Kristjanson
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Authors:  Thomas Klauer; Wolfgang Schneider; Uwe K Zettl
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Authors:  P Edmonds; B Vivat; R Burman; E Silber; I J Higginson
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  21 in total

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3.  Identifying Barriers to and Facilitators of Health Service Access Encountered by Individuals with Multiple Sclerosis.

Authors:  Chantel D Mayo; Negar Farzam-Kia; Setareh Ghahari
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4.  Home-based palliative approach for people with severe multiple sclerosis and their carers: study protocol for a randomized controlled trial.

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5.  Managing the transition (ManTra): a resource for persons with secondary progressive multiple sclerosis and their health professionals: protocol for a mixed-methods study in Italy.

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Review 6.  Palliative Care Intervention Trials for Adults Living With Progressive Central Nervous System Diseases and Their Caregivers: A Systematic Review.

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7.  A Swiss Health Care Professionals' Perspective on the Meaning of Interprofessional Collaboration in Health Care of People with MS-A Focus Group Study.

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8.  Multiple sclerosis and palliative care - perceptions of severely affected multiple sclerosis patients and their health professionals: a qualitative study.

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9.  Unmet needs of people with severe multiple sclerosis and their carers: qualitative findings for a home-based intervention.

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Journal:  PLoS One       Date:  2014-10-06       Impact factor: 3.240

10.  Progressive Dwindling in Multiple Sclerosis: An Opportunity to Improve Care.

Authors:  Jessica E Martin; Joel Raffel; Richard Nicholas
Journal:  PLoS One       Date:  2016-07-21       Impact factor: 3.240

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