Literature DB >> 12525733

Fatigue and depression are associated with poor quality of life in ALS.

Jau-Shin Lou1, Alexa Reeves, Theodore Benice, Gary Sexton.   

Abstract

Twenty-five ALS subjects filled out five questionnaires: the ALS Functional Rating Scale, Multidimensional Fatigue Inventory, multidimensional McGill Quality of Life, Center of Epidemiologic Study--Depression Scale, and the Epworth Sleepiness Scale. Fatigue, depression, and excessive somnolence are more pronounced in ALS subjects than in normal controls. Both fatigue and depression are associated with poorer quality of life in subjects with ALS, and should be treated aggressively.

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Year:  2003        PMID: 12525733     DOI: 10.1212/01.wnl.0000042781.22278.0a

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  39 in total

1.  A cross sectional study on determinants of quality of life in ALS.

Authors:  A Chiò; A Gauthier; A Montuschi; A Calvo; N Di Vito; P Ghiglione; R Mutani
Journal:  J Neurol Neurosurg Psychiatry       Date:  2004-11       Impact factor: 10.154

2.  Depression in amyotrophic lateral sclerosis.

Authors:  Nazem Atassi; Amanda Cook; Cristiana M E Pineda; Padmaja Yerramilli-Rao; Darlene Pulley; Merit Cudkowicz
Journal:  Amyotroph Lateral Scler       Date:  2010-11-24

3.  Apathy and its impact on patient outcome in amyotrophic lateral sclerosis.

Authors:  J Caga; S Hsieh; E Highton-Williamson; M C Zoing; E Ramsey; E Devenney; R M Ahmed; M C Kiernan
Journal:  J Neurol       Date:  2017-11-30       Impact factor: 4.849

4.  Depression in amyotrophic lateral sclerosis.

Authors:  Elin Roos; Daniela Mariosa; Caroline Ingre; Cecilia Lundholm; Karin Wirdefeldt; Per M Roos; Fang Fang
Journal:  Neurology       Date:  2016-04-22       Impact factor: 9.910

Review 5.  Amyotrophic Lateral Sclerosis: An update for 2013 Clinical Features, Pathophysiology, Management and Therapeutic Trials.

Authors:  Paul H Gordon
Journal:  Aging Dis       Date:  2013-10-01       Impact factor: 6.745

6.  Quality of life of ALS and LIS patients with and without invasive mechanical ventilation.

Authors:  Marie-Christine Rousseau; Stéphane Pietra; José Blaya; Anne Catala
Journal:  J Neurol       Date:  2011-04-02       Impact factor: 4.849

Review 7.  Symptom Management and End-of-Life Care in Amyotrophic Lateral Sclerosis.

Authors:  Carlayne E Jackson; April L McVey; Stacy Rudnicki; Mazen M Dimachkie; Richard J Barohn
Journal:  Neurol Clin       Date:  2015-11       Impact factor: 3.806

8.  Depression and wish to die in a multicenter cohort of ALS patients.

Authors:  Judith G Rabkin; Raymond Goetz; Pam Factor-Litvak; Jonathan Hupf; Martin McElhiney; Jessica Singleton; Hiroshi Mitsumoto
Journal:  Amyotroph Lateral Scler Frontotemporal Degener       Date:  2014-12-08       Impact factor: 4.092

Review 9.  Evaluation of quality of life in individuals with severe chronic motor disability: A major challenge.

Authors:  Marie-Christine Rousseau; Karine Baumstarck; Thierry Billette de Villemeur; Pascal Auquier
Journal:  Intractable Rare Dis Res       Date:  2016-05

10.  Depression and quality of life in patients with amyotrophic lateral sclerosis.

Authors:  Dorothée Lulé; Sonja Häcker; Albert Ludolph; Niels Birbaumer; Andrea Kübler
Journal:  Dtsch Arztebl Int       Date:  2008-06-06       Impact factor: 5.594

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