Representations and practices of patients with vasculogenic ulcers on quality of life

ABSTRACT Objective: To identify the social representations and practices of patients with vasculogenic ulcer about their quality of life. Method: Qualitative research that applied the Social Representations theory. Participants were 30 patients with vasculogenic ulcers registered at a health unit in...

Full description

Saved in:
Bibliographic Details
Main Authors: Nathália Nunes Gomes (Author), Lara Mariana Monteiro de Santa Rosa (Author), Márcia de Assunção Ferreira (Author), Rafael Celestino da Silva (Author)
Format: Book
Published: Universidade Federal do Rio Grande do Sul, 2021-12-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000 am a22000003u 4500
001 doaj_3a11a2f7c259479380d2f9a8875f8b5d
042 |a dc 
100 1 0 |a Nathália Nunes Gomes  |e author 
700 1 0 |a Lara Mariana Monteiro de Santa Rosa  |e author 
700 1 0 |a Márcia de Assunção Ferreira  |e author 
700 1 0 |a Rafael Celestino da Silva  |e author 
245 0 0 |a Representations and practices of patients with vasculogenic ulcers on quality of life 
260 |b Universidade Federal do Rio Grande do Sul,   |c 2021-12-01T00:00:00Z. 
500 |a 1983-1447 
500 |a 10.1590/1983-1447.2021.20200098 
520 |a ABSTRACT Objective: To identify the social representations and practices of patients with vasculogenic ulcer about their quality of life. Method: Qualitative research that applied the Social Representations theory. Participants were 30 patients with vasculogenic ulcers registered at a health unit in Rio de Janeiro. Data was collected through semi-structured interviews, and lexical analysis was applied. Results: The social representations about the quality of life of the patients were built from the affections arising from the changes in their lives. Thus, losses arising from the reconfiguration of daily life led to a negative symbolic construction about themselves and their lives, which resulted, on the one hand, in proactive self-care behaviors and, on the other, in less self-care. Conclusion: Care for health promotion and social support is required to re-signification of life with ulcer and the adoption of new coping practices. 
546 |a EN 
546 |a ES 
546 |a PT 
690 |a Quality of life 
690 |a Leg ulcer 
690 |a Psychology social 
690 |a Nursing 
690 |a Primary health care 
690 |a Nursing 
690 |a RT1-120 
655 7 |a article  |2 local 
786 0 |n Revista Gaúcha de Enfermagem, Vol 42 (2021) 
787 0 |n http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1983-14472021000100459&tlng=en 
787 0 |n http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1983-14472021000100459&tlng=pt 
787 0 |n https://doaj.org/toc/1983-1447 
856 4 1 |u https://doaj.org/article/3a11a2f7c259479380d2f9a8875f8b5d  |z Connect to this object online.