Literature DB >> 22325346

The impact of vasculitis on patients' social participation and friendships.

Delesha M Carpenter1, Amy E Meador, Emily A Elstad, Susan L Hogan, Robert F DeVellis.   

Abstract

OBJECTIVES: Our objective is to explore how vasculitis affects patients' friendships and social participation.
METHODS: Vasculitis patients (n=221) completed an online questionnaire that asked if, and how, relationships with friends have changed since receiving a vasculitis diagnosis. Participants' written responses were imported into Atlas.ti, and two independent researchers used both structured and unstructured coding to identify themes. After reaching 100% consensus on the themes present in each participant's responses, the coders determined how themes were interrelated across participants.
RESULTS: Over half of patients (52%) expressed that vasculitis negatively impacted their friendships and 25% noted a negative impact on their social participation. At times, this negative impact was related to structural changes in patients' social networks due to loss of friendships. Reduced social participation was also associated with friends' inability to understand vasculitis and its effects, vasculitis-related fatigue, and lifestyle changes such as not being able to drink alcohol and avoiding infection-prone events. Additionally, patients withdrew from social engagements due to fatigue or because of physical symptoms and side effects.
CONCLUSIONS: The unique circumstances associated with a rare chronic illness like vasculitis can create significant barriers to friendships, including loss of these relationships. Interventions designed to help patients cope with the social impact of vasculitis are implicated, especially if they increase patients' ability to engage in dialogue about their illness with their friends.

Entities:  

Mesh:

Year:  2012        PMID: 22325346      PMCID: PMC3760766     

Source DB:  PubMed          Journal:  Clin Exp Rheumatol        ISSN: 0392-856X            Impact factor:   4.473


  21 in total

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7.  Health-related quality of life for patients with vasculitis and their spouses.

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8.  Investigation of quality of life, mood, pain, disability, and disease status in primary systemic vasculitis.

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2.  The relationship between peer support, medication adherence, and quality of life among patients with vasculitis.

Authors:  D S Alexander; S L Hogan; J M Jordan; R F DeVellis; D M Carpenter
Journal:  Clin Exp Rheumatol       Date:  2015-05-26       Impact factor: 4.473

3.  Predictors of medication non-adherence for vasculitis patients.

Authors:  Delesha M Carpenter; Susan L Hogan; Robert F Devellis
Journal:  Clin Rheumatol       Date:  2013-01-12       Impact factor: 2.980

4.  Patient and physician perspectives on the impact of health-related quality of life in Mexican patients with ANCA-associated vasculitis.

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Journal:  Rheumatol Int       Date:  2017-12-15       Impact factor: 2.631

5.  Public health awareness of autoimmune diseases after the death of a celebrity.

Authors:  Nicola Luigi Bragazzi; Abdulla Watad; Francesco Brigo; Mohammad Adawi; Howard Amital; Yehuda Shoenfeld
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6.  Examining whether the information-motivation-behavioral skills model predicts medication adherence for patients with a rare disease.

Authors:  Dayna S Alexander; Susan L Hogan; Joanne M Jordan; Robert F DeVellis; Delesha M Carpenter
Journal:  Patient Prefer Adherence       Date:  2017-01-12       Impact factor: 2.711

7.  How do patients with systemic autoimmune rheumatic disease perceive the use of their medications: a systematic review and thematic synthesis of qualitative research.

Authors:  Hans Haag; Tim Liang; J Antonio Avina-Zubieta; Mary A De Vera
Journal:  BMC Rheumatol       Date:  2018-04-02

8.  Addressing the transition to a chronic condition: exploring independent adoption of self-management by patients with ANCA-associated vasculitis.

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9.  Patients with rare diseases using pharmacists for medication information.

Authors:  Delesha M Carpenter; Susan J Blalock; Robert F DeVellis
Journal:  J Am Pharm Assoc (2003)       Date:  2012

10.  Treatment of fatigue with physical activity and behavioural change support in vasculitis: study protocol for an open-label randomised controlled feasibility study.

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Journal:  BMJ Open       Date:  2018-10-30       Impact factor: 2.692

  10 in total

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