Literature DB >> 25068391

Palliative care for severely affected patients with multiple sclerosis: when and why? Results of a Delphi survey of health care professionals.

Julia Strupp1, Vanessa Romotzky, Maren Galushko, Heidrun Golla, Raymond Voltz.   

Abstract

BACKGROUND: Patients severely affected by multiple sclerosis (MS) present with complex symptoms and needs requiring an interdisciplinary care approach.
OBJECTIVE: Analysis of when and why specialized palliative care integration would be beneficial via examining health care professionals' attitudes.
DESIGN: A two-round online Delphi study and expert workshop were undertaken and analyzed descriptively. SETTING/
SUBJECTS: Following an extensive online search, 164 professionals with expertise in treating and caring for severely affected patients with MS were contacted. Professionals included neurologists, urologists, general practitioners, MS nurses, speech therapists, physiotherapists, psychologists, and palliative care physicians. Forty-six consented to participate: 33 of 46 (71.4%) and 15 of 33 (45.5%) experts responded in the first and second round, respectively.
RESULTS: Consensus was reached among all respondents (100%) defining the term "severely affected": 78.8% and 86.7%, respectively, thought that specialized palliative care should begin once the disease has progressed (Expanded Disability Status Scale [EDSS]>6 and nursing care required). When the need exists for communication about disease progression (93.3%), psychological support (93.3%), relatives support (93.3%), and pain medication (86.7%) specialized palliative care should be consulted. Specialized palliative homecare was rated (93.3%) "very important." The workshop documented the paucity of home visits and specialized MS care in nursing homes.
CONCLUSIONS: Our results clearly identified specific areas in which palliative care will likely prove to be a valuable asset in the treatment course of MS. This information should serve clinicians, indicating when to consider palliative care services and help further reduce or eliminate uncertainty about how palliative care can be integrated in the course of MS.

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Year:  2014        PMID: 25068391      PMCID: PMC4195346          DOI: 10.1089/jpm.2013.0667

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


  30 in total

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3.  Self-rating makes the difference: identifying palliative care needs of patients feeling severely affected by multiple sclerosis.

Authors:  Julia Strupp; Heidrun Golla; Maren Galushko; Raphael Buecken; Nicole Ernstmann; Moritz Hahn; Holger Pfaff; Raymond Voltz
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5.  Evaluation of a new model of short-term palliative care for people severely affected with multiple sclerosis: a randomised fast-track trial to test timing of referral and how long the effect is maintained.

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

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Journal:  J Palliat Med       Date:  2014-02-14       Impact factor: 2.947

8.  Applying the Delphi process to palliative care tool development: lessons learned.

Authors:  Patricia D Biondo; Cheryl L Nekolaichuk; Carla Stiles; Robin Fainsinger; Neil A Hagen
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10.  Multiple sclerosis and palliative care - perceptions of severely affected multiple sclerosis patients and their health professionals: a qualitative study.

Authors:  Heidrun Golla; Maren Galushko; Holger Pfaff; Raymond Voltz
Journal:  BMC Palliat Care       Date:  2014-03-19       Impact factor: 3.234

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4.  The effect of nurse practitioner (NP-led) care on health-related quality of life in people with multiple sclerosis - a randomized trial.

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

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6.  Informing patients with progressive neurological disease of their health status, and their adaptation to the disease.

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  6 in total

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