Literature DB >> 15702359

[Quality of life in multiple sclerosis. Measures, relevance, problems, and perspectives].

W Pöllmann1, C Busch, R Voltz.   

Abstract

Measuring quality of life (QOL) has made essential contributions for the management of patients with multiple sclerosis (MS). QOL measures may be used for helping to assess the complex changes which patients with MS have to go through during the disease trajectory, and they may be used for pharmacoeconomic research. The large number of tests available includes generic ones such as Short Form SF-36 and Sickness Impact Profile, health-related ones such as MSQOL-54, FAMS, or HAQUAMS, and patient generated measures such as the Patient Generated Index and SEIQOL-DW. Depression, cognitive impairment, and fatigue are important factors influencing QOL. Since the different tests measure quite different facets of QOL, this review intends to help the reader select a tool suited to the aim and specific question. It is hoped that QOL measures may help to better understand patients, to become a more helpful medical partner, to assist patients to develop perspectives for their future, and to decide about therapies or even palliative interventions.

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Year:  2005        PMID: 15702359     DOI: 10.1007/s00115-004-1790-8

Source DB:  PubMed          Journal:  Nervenarzt        ISSN: 0028-2804            Impact factor:   1.214


  100 in total

1.  Type I interferons and the quality of life of multiple sclerosis patients. Results from a clinical trial on interferon alfa-2a.

Authors:  M W Nortvedt; T Riise; K M Myhr; H I Nyland; B R Hanestad
Journal:  Mult Scler       Date:  1999-10       Impact factor: 6.312

2.  Autobiographical memory, depression and quality of life in multiple sclerosis.

Authors:  P M Kenealy; G J Beaumont; T Lintern; R Murrell
Journal:  J Clin Exp Neuropsychol       Date:  2000-02       Impact factor: 2.475

3.  Reduced quality of life among multiple sclerosis patients with sexual disturbance and bladder dysfunction.

Authors:  M W Nortvedt; T Riise; K M Myhr; A M Landtblom; A Bakke; H I Nyland
Journal:  Mult Scler       Date:  2001-08       Impact factor: 6.312

4.  Disease specific quality of life instruments in multiple sclerosis: validation of the Hamburg Quality of Life Questionnaire in Multiple Sclerosis (HAQUAMS).

Authors:  S M Gold; C Heesen; H Schulz; U Guder; A Mönch; J Gbadamosi; C Buhmann; K H Schulz
Journal:  Mult Scler       Date:  2001-04       Impact factor: 6.312

5.  Quality of life in multiple sclerosis: the disability and impact profile (DIP).

Authors:  G J Lankhorst; F Jelles; R C Smits; C H Polman; D J Kuik; L E Pfennings; L Cohen; H M van der Ploeg; P Ketelaer; L Vleugels
Journal:  J Neurol       Date:  1996-06       Impact factor: 4.849

6.  An examination of suicidal intent in patients with multiple sclerosis.

Authors:  Anthony Feinstein
Journal:  Neurology       Date:  2002-09-10       Impact factor: 9.910

7.  Validity and reliability of the MSQLI in cognitively impaired patients with multiple sclerosis.

Authors:  Ruth Ann Marrie; Deborah M Miller; Gordon J Chelune; Jeffrey A Cohen
Journal:  Mult Scler       Date:  2003-12       Impact factor: 6.312

8.  "Sticking jewels in your life": exploring women's strategies for negotiating an acceptable quality of life with multiple sclerosis.

Authors:  Frances Reynolds; Sarah Prior
Journal:  Qual Health Res       Date:  2003-11

9.  Does adding MS-specific items to a generic measure (the SF-36) improve measurement?

Authors:  J A Freeman; J C Hobart; A J Thompson
Journal:  Neurology       Date:  2001-07-10       Impact factor: 9.910

Review 10.  The needs and experiences of caregivers of individuals with multiple sclerosis: a systematic review.

Authors:  L P McKeown; A P Porter-Armstrong; G D Baxter
Journal:  Clin Rehabil       Date:  2003-05       Impact factor: 3.477

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  5 in total

Review 1.  Twelve years' experience with the Patient Generated Index (PGI) of quality of life: a graded structured review.

Authors:  Faith Martin; Laura Camfield; Karen Rodham; Petra Kliempt; Danny Ruta
Journal:  Qual Life Res       Date:  2007-02-01       Impact factor: 4.147

2.  Individualized quality of life of severely affected multiple sclerosis patients: practicability and value in comparison with standard inventories.

Authors:  A M Giovannetti; E Pietrolongo; A Giordano; V Cimino; A Campanella; G Morone; A Fusco; A Lugaresi; P Confalonieri; F Patti; M G Grasso; M Ponzio; S Veronese; A Solari
Journal:  Qual Life Res       Date:  2016-04-28       Impact factor: 4.147

3.  Home-based palliative approach for people with severe multiple sclerosis and their carers: study protocol for a randomized controlled trial.

Authors:  Alessandra Solari; Andrea Giordano; Maria Grazia Grasso; Paolo Confalonieri; Francesco Patti; Alessandra Lugaresi; Lucia Palmisano; Roberta Amadeo; Giovanni Martino; Michela Ponzio; Giuseppe Casale; Claudia Borreani; Renzo Causarano; Simone Veronese; Paola Zaratin; Mario Alberto Battaglia
Journal:  Trials       Date:  2015-04-23       Impact factor: 2.279

Review 4.  Anxiety, depression and impaired health-related quality of life are therapeutic challenges in patients with multiple sclerosis.

Authors:  Dominik Michalski; Stefanie Liebig; Eva Thomae; Susanne Singer; Andreas Hinz; Florian Then Bergh
Journal:  Ment Illn       Date:  2010-05-14

5.  Integrated Imaginative Distention Therapy to Cope with Fatigue. DIMMI SI Study: The First Randomized Controlled Trial in Multiple Sclerosis.

Authors:  Annalisa Sgoifo; Angelo Bignamini; Loredana La Mantia; Maria G Celani; Piero Parietti; Maria A Ceriani; Maria R Marazzi; Paola Proserpio; Lino Nobili; Alessandra Protti; Elio C Agostoni
Journal:  Neurol Ther       Date:  2017-08-09
  5 in total

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