scholarly journals Social representations of the quality of life of the young people living with HIV

2021 ◽  
Vol 74 (2) ◽  
Author(s):  
Danielle Pinheiro Elias Silva ◽  
Denize Cristina de Oliveira ◽  
Sergio Corrêa Marques ◽  
Rodrigo Leite Hipólito ◽  
Tadeu Lessa da Costa ◽  
...  

ABSTRACT Objectives: to analyze the social representations of the quality of life of the young people living with HIV. Methods: qualitative survey, based on the Social Representations Theory, with 24 young people living with HIV, monitored in specialized services in Rio de Janeiro, through semi-structured interviews, and the analysis supported by the software IRAMUTEQ. Results: multidimensionality of the quality of life was observed unfolding the implications of living with HIV/aids concerning the familiar and social support network, time of diagnosis, healthcare services, antiretroviral therapy, and prejudice expressions. Final Considerations: a conceptual synthesis of quality of life is observed when it is associated with healthy lifestyle habits, interpersonal relationships, and health services and professional practices.

2001 ◽  
Vol 24 (2) ◽  
pp. 227-237 ◽  
Author(s):  
Mary Jane Rotheram-Borus ◽  
Debra A. Murphy ◽  
Richard G. Wight ◽  
Martha B. Lee ◽  
Marguerita Lightfoot ◽  
...  

2016 ◽  
Vol 15 ◽  
pp. 575 ◽  
Author(s):  
Rodrigo Leite Hipolito ◽  
Denize Cristina De Oliveira

Aim:  to  analyze  the  quality  of  life  (QoL)  and  its  representations  in different  diagnostic  times.  Method:  This  is  a  descriptive,  cross-sectional  study  with  a stratified sample by the time of diagnosis, consisting of 100 people living with HIV of a specialized  service  in  the  coastal  lowlands  of  the  municipality  of  Rio  de  Janeiro.  The sociodemographic and health forms were used, followed by the WHOQOL-HIV BREF and semi-structured  interviews.  Descriptive  and  inferential  statistical  analysis  was  used. Lexical analysis was operationalized by the Alceste software. Results: The perception of QoL was intermediate in all areas, as well as the contents of QoL representation pointed to the hypothesis of non-autonomous representation regarding the social representation of AIDS. Conclusion: We observed a representational profile of the quality of life aimed for positive aspects and reinterpretation, based on the new symbology attributed to the object  AIDS.  It  is  necessary  to  consider  satisfaction  with  health and  longer  time  for diagnosis in the physical domain as relevant aspects to nursing care.


2021 ◽  
Vol 42 ◽  
Author(s):  
Nathália Nunes Gomes ◽  
Lara Mariana Monteiro de Santa Rosa ◽  
Márcia de Assunção Ferreira ◽  
Rafael Celestino da Silva

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.


2021 ◽  
Vol 7 (3) ◽  
pp. 227-234
Author(s):  
Mahathir Mahathir ◽  
Wiwin Wiarsih ◽  
Henny Permatasari

Background: The progress of the fight against HIV is highlighted by significant change. HIV of the past is different from HIV of the present. Healthcare services have played an essential role in achieving the optimal goals needed to end the HIV epidemic. However, people living with HIV and those at risk of catching it (PLWH) often misunderstand the rapid growth of HIV healthcare service options.Objective: This study aimed to explore the experiences of PLWH in the healthcare services featured in this study.Methods: A qualitative phenomenological approach was used. Semi-structured interviews were conducted in 2017 with 12 PLWH who engaged with healthcare services in Jakarta, Indonesia, by using a purposive sampling technique. Semi-structured questions were asked which related to their experiences of using the services. Stevick Colaizzi Keen method was used to extract the thematic analysis of the study.Results: The study developed four essential themes of PLWH healthcare use. They were accessibility, availability at all healthcare levels, comprehensiveness of service, and affordability.Conclusion: Providing accessible healthcare services is considered essential by PLWH. It is also pivotal to helping people feel positive about the community-related healthcare services on offer. Nurse-led HIV services must maintain this progress by continuously evaluating the quality-of-service outcomes and promoting the accessibility of the services to the broader population.


2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Moses K. Nyongesa ◽  
Paul Mwangi ◽  
Michael Kinuthia ◽  
Amin S. Hassan ◽  
Hans M. Koot ◽  
...  

Abstract Background In sub-Saharan Africa, common mental disorders (CMDs) like depression and anxiety are under-investigated amongst young people living with HIV (YLWH). To address the gap, in Kenya we: a) determined the prevalence of CMDs among YLWH compared to their uninfected peers; b) investigated HIV status as an independent predictor of CMDs in young people; c) investigated CMDs risk and protective indicators with more focus on YLWH. Methods Between November 2018 and September 2019, 819 young people aged 18–24 years (407 HIV-infected) were recruited from two Counties on the Kenyan coast. Locally adapted pre-existing mental health measures, Patient Health Questionnaire (9-item) and Generalized Anxiety Disorder scale (7-item), were administered among other questionnaires via audio computer-assisted self-interview. Logistic regression was used to determine the correlates of CMDs. Results Prevalence of CMDs was significantly elevated among YLWH compared to their uninfected peers i.e. 29% vs. 12%; p < 0.001 for depressive symptoms, 19% vs. 8%; p < 0.001 for anxiety symptoms, and 16% vs. 5%; p < 0.001 for comorbid depressive and anxiety symptoms. HIV status independently predicted depressive symptoms and its co-occurrence with anxiety symptoms. Among YLWH, negative life events, higher perceived HIV-related stigma and low adherence to antiretroviral therapy were the risk indicators for elevated CMDs. Among HIV-uninfected youths, death of both parents was a risk indicator for elevated depressive symptoms. Protective indicators against CMDs among youths with and without HIV included higher social support and health-related quality of life. Conclusion At the Kenyan coast, YLWH have significantly higher burden of CMDs compared to their uninfected peers. Being HIV-positive as a youth in this setting is predictive of more depressive symptoms and its comorbidity with anxiety symptoms. YLWH at high risk of CMDs in coastal Kenya can benefit from early detection, referral and treatment if routine screening for CMDs is integrated in their care package. The mental wellbeing of bereaving HIV-unaffected youths could be improved through continued support to help them come to terms with their loss. At the community level, programmes strengthening the social capital or improving the overall quality of life of youths with or without HIV may be beneficial to their mental health.


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