Literature DB >> 25052100

Participation in life situations by persons with systemic sclerosis.

Janet L Poole1, Annandhi Chandrasekaran, Kristal Hildebrand, Betty Skipper.   

Abstract

PURPOSE: To measure the frequency of participation in life situations.
METHODS: A sample of 83 persons with systemic sclerosis (SSc) completed questionnaires regarding the presence and severity of disease symptoms, disability [the Health Assessment Questionnaire (HAQ)], depression [the Center for Epidemiologic Studies Depression Scale (CES-D)], and participation [the Adelaide Activities Profile (AAP)]. On the AAP, individuals rate the frequency of participation in four domains: domestic chores, household maintenance, service to others and social activities.
RESULTS: Participants were predominantly female, married, educated, white, and had diffuse SSc. Mean age was 53.7 years and mean disease duration was 9.9 years. On the AAP, participation was significantly more frequent for domestic chores than for household maintenance, service to others, and social activities. More fatigue (p < 0.05), disability (p < 0.001), and fatigue (p < 0.05) resulted in lower total AAP scores. More fatigue, pain, severe gastrointestinal symptoms, and depression related to lower household maintenance scores, while the presence of ulcers and more disability and depression were associated with lower domestic chores scores.
CONCLUSIONS: Participation in life situations in persons with SSc is related to higher disability, depression, and severity of disease symptoms. Interventions to address the disability, depression and symptoms may increase participation.

Entities:  

Keywords:  Adelaide activities profile; participation; scleroderma; systemic sclerosis

Mesh:

Year:  2014        PMID: 25052100     DOI: 10.3109/09638288.2014.944624

Source DB:  PubMed          Journal:  Disabil Rehabil        ISSN: 0963-8288            Impact factor:   3.033


  7 in total

Review 1.  Productivity Losses and Costs in the Less-Common Systemic Autoimmune Rheumatic Diseases.

Authors:  Natalie McCormick; Carlo A Marra; J Antonio Aviña-Zubieta
Journal:  Curr Rheumatol Rep       Date:  2017-10-30       Impact factor: 4.592

2.  Diverging illness perceptions between physicians about patients with systemic lupus erythematosus and systemic sclerosis: a vignette-based study.

Authors:  Seher Arat; Philip Moons; Joris Vandenberghe; Jan L Lenaerts; Kurt de Vlam; René Westhovens
Journal:  Rheumatol Int       Date:  2017-02-28       Impact factor: 2.631

3.  Fatigue and Its Association With Social Participation, Functioning, and Quality of Life in Systemic Sclerosis.

Authors:  Susan L Murphy; Anna L Kratz; Daniel Whibley; Janet L Poole; Dinesh Khanna
Journal:  Arthritis Care Res (Hoboken)       Date:  2021-02-05       Impact factor: 4.794

4.  Rehabilitation Interventions in Systemic Sclerosis: A Systematic Review and Future Directions.

Authors:  Susan L Murphy; Janet L Poole; Yen T Chen; Alain Lescoat; Dinesh Khanna
Journal:  Arthritis Care Res (Hoboken)       Date:  2021-12-22       Impact factor: 5.178

5.  Illness representations of systemic lupus erythematosus and systemic sclerosis: a comparison of patients, their rheumatologists and their general practitioners.

Authors:  Seher Arat; Jan L Lenaerts; Ellen De Langhe; Patrick Verschueren; Philip Moons; Joris Vandenberghe; Veerle Taelman; Rene Westhovens
Journal:  Lupus Sci Med       Date:  2017-11-14

6.  Prospective associations between illness perceptions and health outcomes in patients with systemic sclerosis and systemic lupus erythematosus: a cross-lagged analysis.

Authors:  Seher Arat; Jessica Rassart; Philip Moons; Koen Luyckx; Joris Vandenberghe; René Westhovens
Journal:  Rheumatol Adv Pract       Date:  2018-03-06

7.  Fatigue Predicts Future Reduced Social Participation, not Reduced Physical Function or Quality of Life in People with Systemic Sclerosis.

Authors:  Susan L Murphy; Daniel Whibley; Anna L Kratz; Janet L Poole; Dinesh Khanna
Journal:  J Scleroderma Relat Disord       Date:  2020-09-20
  7 in total

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