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versão impressa ISSN 0080-6234
Rev. esc. enferm. USP vol.46 no.3 São Paulo jun. 2012
Julyana Gomes de FreitasI; Marli Teresinha Gimeniz GalvãoII; Maria Fátima Maciel AraujoIII; Ênia CostaIV; Ivana Cristina Vieira de LimaV
IRN. Doctoral student in Nursing, by the Nursing Graduate Program,
Federal University of Ceará. FUNCAP fellow. Caucaia, CE, Brazil, E-mail:
IIRN. Ph.D. in Tropical Diseases. Professor of the Nursing Undergraduate and Graduate Programs at Federal University of Ceará. Researcher with CNPq. Fortaleza, CE, Brazil, E-mail: email@example.com
IIIRN. Ph.D. in Nursing. Professor of the Nursing Undergraduate Program, Federal University of Ceará. Fortaleza, CE, Brazil, E-mail: firstname.lastname@example.org
IVRN. Master in Nursing by the Nursing Graduate Program, Federal University of Ceará. CNPq fellow. Fortaleza, CE, Brazil, E-mail: email@example.com
VRN. Master student of the Nursing Graduate Program, Federal University of Ceará. CAPES fellow. Fortaleza, CE, Brazil, E-mail: firstname.lastname@example.org
The objective of this study was to understand the coping mechanisms of men living with HIV/AIDS in terms of their work environment. A qualitative study was carried out at a specialized outpatient clinic in Fortaleza-Ceará between March and June 2010, involving eleven men infected with the virus. Semi-structured and audio-recorded interviews were used. The statements were categorized through content analysis into the following categories: absence from work due to the infection; subterfuges used to hide the disease; disrespect for confidentiality in the work environment; suffering associated with the fear of rejection and prejudice; ways of coping after diagnosis of the disease; and the importance of work for personal accomplishment. In conclusion, men infected with HIV face counterproductive situations in the work environment, mainly evidenced by fear of discovery of the infection and prejudice. Associated with coping, absences for health monitoring purposes interfered with performance at work and increased the risk of losing their job.
Descriptors: Men; HIV; Acquired Immunodeficiency Syndrome; Working environment; Prejudice; Nursing
When a person discovers that she/he is infected with HIV, it marks the course of their and their family's lives because of the acceptance, adaptation and incorporation of new behaviors to keep healthy and, thus, prolong life to the longest.
In view of the increased life expectancy of infected individuals, AIDS is now referred to as a chronic disease, which implies new challenges to patients and healthcare professionals, which include: the social reinsertion in the labor market and in school, the promotion of healthy habits, including eating with quality and exercising, as well as maintaining sexuality, with the right to motherhood and fatherhood(1).
The social inclusion of HIV-positive individuals in the workplace is considered positive for their quality of life. However, the reality that is observed is one of discrimination by employers as well as co-workers. This fact culminated in the exclusion of the most elementary citizenship rights, with includes work(2).
In addition to this problem, workers suffer several forms of discrimination, which are evidenced by: the obligation to take anti-HIV tests during recruitment and, consequently, not being hired in the case of a positive test result; dismissal because of a positive HIV-test result; being excluded from the training program and from promotion opportunities; ostracism by co-workers; exclusion from the company's health plan, among other forms of prejudice(3).
In order to focus on the coping experiences of men with HIV in the labor market there is a need for a renewed view, which, in turn, requires a scientific and intellectual attitude that integrates social inclusion and its relationships with the working world(2).
Workers have to foster the pathways to live in a structure and assign new meanings to life values and healthcare. Here, one's perception of the contradictions regarding their body emerges as a fully concrete fact. They gain a destructuring outline that is far from being organized or controlled, being fascinating and frightening at the same time. The body, initially criticized as a source of pleasure purged by the infection, is now seen as a working tool, which generates a duality between the anxiety towards the disease and the production regulation that apparently has no direct relationship with the training and qualification for the job, gender, age, competence and abilities, time and movement, rational and logical investments of the act of working, technology, workers' rights, and others.
Reflecting about these aspects, it is worth illustrating that the AIDS epidemics accounted for the death of 28 million workers worldwide until 2005. The problem and its solution still require further explorations and the discovery of meanings that would minimize the restlessness before the social neglect that still persists in society. We live a tendency without setbacks or hesitations. By 2015, the toll of the disease will have been 74 million lives. This situation places AIDS as a significant cause of death in the working world, definitely affecting the social, economic and cultural structure of countries, and, thus, consisting of a serious threat to the working world(4).
The challenge for creating devices to support initiatives to cope with the disease, assumed by government leaders and institutions such as the World Health Organization (WHO) and International Labour Organization (ILO) originated the Consensus Statement on AIDS and the Workplace. As stated, work does not promote any risk of the virus being acquired or transmitted from one worker to another, or from a worker to a client, or from a client to a worker. It is also reinforced that HIV infection is no reason to end the work relationship(5).
In Brazil, since the early 1990's, it has been legally prohibited, in the federal public service, to demand HIV tests in pre-employment and periodical health examinations; it is stated that being HIV-positive does not harm the individual's working capacity, and maintaining a social and professional contact with HIV-positive individuals does not configure a risk of becoming infected(6).
The highlight on establishing risk-free relationships in the workplace encompassed new elements of the working condition; however, the everyday existence of this relationship does not set limits to sharing cultural values and ideas that permeate the whole process of being inserted in the working world, and, for this reason, the referred consensus statement does not address the thought that the worker is exposed to other life fragments that limit their interactions within the workplace.
From the perspective of labor relationships/employment, AIDS brings the following issues into discussion: the management of the working processes, the fundamental rights of the worker and changes in the working world that involve a network of complex relationships mechanisms and activities of HIV-positive workers. It is important to outline that many workers express wishes different from that of the other workers, which directly refer to clear acknowledgement that work is a factor that links health and disease. Factors such as unemployment, informal employment, and, most of all, being excluded from the labor market become associated and lead the individual towards a worsened health condition(7). On one side, there is a contradiction that defends the individual's right, as a citizen, to work, not being discriminated, and the confidentiality of their health condition, while on the other side, there is the community's right to health(8) and also the authority and power of the organization, which is prepared to generate profits and defend the economical interests.
In the workplace, AIDS is not understood as a disease similar to others to which the company and institutions owe certain responsibilities, as segments of civil society. Contrarily, the disease causes problems in the workplace, as the companies are incapable of managing the situation(9).
There is evidence of the need for companies to disseminate the recommendations reported by public organization such as the ILO so that the rights of HIV-positive individuals are respected, which include: not performing an anti-HIV test in the pre-employment examination; maintaining workplace confidentiality of any information regarding the disease as well as avoiding any situation that could cause constraint or prejudice towards the worker and strict rules regarding the confidentiality when accessing the personal data about a worker's HIV.
Within this context, recognizing the contradiction of the working world and the ways of coping used by the HIV-positive men in their everyday practice in view of the scarcity of studies on this issue, justify developing the present study.
To understand the coping situations that HIV-positive men experience in the workplace.
This is an exploratory, descriptive, qualitative study. Literature states that the qualitative approach permits to elaborate answers to intricate and particular questions, because it works with the universe of meanings, values, beliefs, motives, aspirations and attitudes. Thus, its focus transcends the mere operationalization of variables, and encompasses a deeper area of relationships, processes and phenomena(10).
This study was developed during the months of March and June of 2010, at the HIV specialist ambulatory service, at Hospital São José de Doenças Infecciosas (São José Infectious Disease Hospital) in Fortaleza-Ceará. The participants were eleven HIV-positive men. The selection criteria were: 18 years of age or older; male; refer being employed or having been employed some time after becoming aware about their being positive for HIV. The number of subjects was not determined based on a numerical representation criterion, but on the representation regarding the sharing of experiences considered fundamental for the investigated issue. The sample size was not determined, but the group of participants was considered appropriate to portray, by means of interviews, the experiences, meanings, values and behaviors associated to coping with various situations in the workplace in view of the HIV infection.
Data collection was performed using a semi-structured form aimed at gathering information regarding the participants' identification and the situations they have experienced in the workplace that are associated to their being HIV-positive. With the purpose to unveil the study objective, the following guiding question was used: Could you tell me if you have ever experienced any situation of constraint or happiness at the workplace related to your positive diagnosis for HIV?
With a view to guarantee the quality and trustworthiness of the data, the interviews, which lasted forty-five minutes, were audio-recorded upon the participants' consent and were performed in a private room.
As recommended, the interview contents were fully transcribed and subjected to content analysis. Literature defines this method as a group of communication analysis techniques that aims to achieve, by means of systematic and objective description procedures of the message contents, indicators that would allow for inferring knowledge related to the conditions in which these messages were produced and received. Therefore, it permits to analyze the participants' opinion, in between the lines, i.e., not being exclusively restricted to words that are stated directly, but also those that are implied in the discourse(11).
The analysis originated the following categories: absence from work due to the infection; subterfuges used to hide the disease; disrespect for confidentiality in the workplace; suffering associated with the fear of rejection and prejudice; ways of coping after diagnosis of the disease; and the importance of work for personal accomplishment.
As required, the study complied with the recommendations of resolution 196/96 regarding studies involving human beings and was approved by the Research Ethics Committee at Hospital São José de Doenças Infecciosas, under protocol number 60/2009. All the participants provided written consent. Aiming at preserving the subjects' identity, they were referred to by using the letter "I" (interviewee) follower by numerals according to the order in which the interviews were performed.
As mentioned above, the participants were eleven HIV-positive men, of age between 25 and 50 years. The mean education time of the participants was 8.7 years, while the interval time since they became aware about the infection was from one to nine years. In terms of their employment situation, four men were unemployed, three had a formal job, three had informal jobs, and one was retired due to the serious effects of the disease. The income of most participants was between one and two minimum salaries (at the time the minimum salary was R$ 465.00, or US$ 233.00).
The participants' statements or discourses are presented in Chart 1. This chart shows the categories and main excerpts related to the participants' experiences and their ways of coping with situations at the workplace associated with being HIV-positive.
The analysis of the data in the category Absence from work due to the infection revealed that men stated that in order to look after their health, it was required continuous and periodical medical follow up. These conditions are inherent to the HIV treatment, which require monthly or periodical appointments at the health service, causing work absences or delays because the health service is open only during business hours. Therefore, the workers' constant presentation of medical notes, despite not including any information stating HIV/AIDS, marks the beginning of a process of visibility of their condition and their stigmatization.
It was observed that the individual's health status affected their decision about staying or not in the job. In order to avoid embarrassing situations, in addition to choosing to remain silent, the patient quits the job if any collateral effects of the antiretroviral medication or symptoms that indicate an advanced disease status emerge.
Within this context, it was evidenced that companies have weaknesses in terms of dealing with issues specific to the disease, such as the workers' having to leave work because of medical appointments and the fear of transmission within the workplace. In fact, the logic of the capitalism at the national level contributes with this deficit, most of all because of the legal determination regarding the responsibility that companies and institutions have towards their employees with HIV. This issue is present in between the lines of the recorded statements(9).
As indicated in the category Subterfuges to hide the disease, studies show these situations when they reveal that HIV-positive workers are often dismissed, or not hired, because, in order to follow their health condition with medical care, the employee has to be away quite often, due to appointments, examinations, or, yet, to obtain medications (12).
Also regarding the statements of this category, as can be seen, workers with HIV/AIDS choose not to reveal their diagnosis, fearing embarrassment and losses at work, besides likely being dismissed.
In general, the coping phenomena understood through the subjects' statements reveal a diversity of anguishing feelings, such as fear, shame, stigma, and the social isolation in view of their discovering the diagnosis, issues mentioned in the category and found in literature(13).
Regarding the category Disrespect for confidentiality in the workplace, confidentiality regarding the disease is justified by the subjects as a form of protecting themselves from prejudice, discrimination and shame, set by the social representations of HIV/AIDS.
After becoming aware about the diagnosis of the disease, the HIV-positive patient faces, within their environment of social interaction, the experience of being exposed, discriminated against and isolated. Therefore, the individuals are required to learn how to cope with the situation, which requires obtaining social and personal resources. In view of this situation, these patients prefer not to comment about their health condition with others, and, therefore, try to hide any information that would disclose their condition, by establishing certain criteria to avoid any socialization(14).
In an attempt to hide the disease, many patients omit their true health conditions when asked about the treatment that force them to attend the health service so frequently. However, according to the statements of the present study subjects, not always is it possible to maintain confidentiality, and, when their health condition regarding HIV is disclosed, employers and co-workers demonstrate prejudice, exposing the patient to a situation of constraint or even their voluntary or arbitrary dismissal(14).
The infection by HIV does not justify dismissing the individual from work. People with HIV and any associated disease are capable of working in a location considered appropriate and clinically adequate for performing the professional activities.
What has been defended for long is guaranteeing the job of individuals with HIV: their job contract cannot be terminated by theme simple fact that they carry the virus in their body. Thus, the guarantee of employment would be the workers' right to remain in their job, protected under the Constitution of 1988(15).
In the category Suffering associated with the fear of rejection and prejudice, the individuals with HIV feared that if their co-workers found out about their health condition, there would be prejudice. In some cases, the fear of transmission also generates a certain discomfort at work, while in others, discrimination becomes a strong factor for their not returning to work(16).
When referring to AIDS, fear was often emphasized and the existence of the disease appears as a threat. The possibility of being infected raises concern, because AIDS is represented with great dread. Furthermore, the fact that there is no cure for the disease and the risk of infection suggest a catastrophe that, often, should not even be mentioned (17).
When diagnosed, AIDS overwhelms the patient with doubts and uncertainties; such as whether the disease will develop or not and how painful and inevitable its progress will be, forcing the patient to live permanently with the certainty of an early death(18). In addition, the patients' concern about their infection being revealed is often self-imposed by the fear of being subjected to prejudice and stigmatization(12).
As observed, some patients who were employed, quit their jobs because of the fear of being known to have HIV; others were fired because of prejudice; and others gave up on looking for a job due to their fear of pre-employment examinations.
However, it is illegal to force candidates to taking an anti-HIV test, in addition to being highly discriminatory, as determined in several legal ordinances, such as Law number 9029/95. Similarly, the ministerial decree 869, of 11 August 1992 prohibits: in the federal public service, to demand a test to detect the human immunodefi-ciency virus in either pre-employment or periodical health examinations(6).
According to the statements, today, many of the subjects are either unemployed or keep an informal job. They fight to get their retirement or right to sickness allowance to minimize their financial burdens. Jobless, they become anxious and depressed. They were once contributors and now they see themselves as a burden to society.
In the study, some reports referred to episodes of discrimination at the workplace due to the lack of confidentiality by others who became aware of the worker's HIV infection.
Hence, it is understood that the issue regarding the disclosure, at the workplace, of the worker's condition of being HIV-positive is complex and represents a threat to their continuing in the job. When their HIV-positive status is revealed to their superiors or co-workers, they face difficult situations at the workplace. It is, therefore, necessary to deal with the prejudice of withdraw from peers. Within this context, the results confirm that their silence represents a search for self-protection and a way of coping with HIV/AIDS.
Thus, one of the problems revealed in the workplace is the fear of their co-workers finding out about their infection, and the resulting prejudice. In some cases, the fear of transmission also causes a certain discomfort at work(16).
Many of the perverse
consequences of the stigmatization of people and/or specific groups involve
discrimination in public spaces and private institutions, which generate
hostility, segregation, exclusion and/or self-exclusion of individuals whose
HIV-positive status is revealed. The AIDS stigma overlaps the
preexisting stigma associated with different social groups, such as
homosexuals, sex workers and drug users, thus evoking multiple meanings. These
pre-conceived concepts and images are part of a cultural and social matrix that
establishes differences, creates hierarchies, and sanctions structures of
The few subjects that revealed their HIV-positive condition to some people reported experiencing prejudice from their friends or at the workplace.
By observing the statements in the category Ways of coping after diagnosis of the disease, it is evidenced that the subjects seek different forms of minimizing the suffering in face of their unemployment.
Facing or coping with these situations triggers deep stress in these individuals. According to literature, this type of coping has been defined as the cognitive and behavioral efforts towards managing the intrinsic and extrinsic demands of the individuals, which are evaluated as an overburden to their personal resources (20).
Therefore, living with a disease that implies discrimination, such as AIDS, requires the individuals to deal with different situations. In this setting, the search for religious support has been one way of achieving adaptive results in the process of coping with AIDS.
In the present study, taking initiative and having the courage to face the disease start with believing in a God; next, the patient's decision to seek alternative therapies is used as an attempt to dodge the different coping situations.
As observed in the category The importance of work for personal accomplishment, having a job surpasses the individuals' economical needs, it is, most of all, a source of well-being, self-respect, dignity, self-esteem, and citizenship. These feelings can improve their quality of life, and promote social reinsertion, considering that working means they are contributing with the society, hence they feel useful(21). This is further evidence when gender issues are considered, because for men work is a source of social identity(16).
The process of disseminating the news about the HIV infection proliferates an epidemics of meaning, implying that the individual must constantly cope, either in silence or explicitly, with stigma and discrimination(16). To men, living intensively and with quality of life requires relating with the world, and, most of all, counting on the support from family, friends and from those from the workplace(22).
In general, it appears that living with HIV in the work environment is not a harmonious situation. The diagnosis of the disease triggered a series of experiences with different effects on the HIV-positive individual, most of which are counterproductive. Furthermore, the need to feel useful and productive contrasts with the obligation of being absent from work due to the manifestations of the disease and attending clinical follow up.
In view of the fear of having their diagnosis revealed and, thus, produce feelings of prejudices and rejection from employers and co-workers, the HIV-positive men choose to be silent about their disease and consciously decide to quit their jobs as a coping strategy. There were also reports of the embodiment of prejudice, evidenced by the disrespect of the confidentiality, dismissal after knowing about their diagnosis and several other situations that caused constraint at the workplace.
This study reinforces the thesis that understanding the issues related to HIV infection among productive men is a complex task, as they carry the stereotype of a disease associated with connotations of devaluation, which have an impacting effect on their right to work. From this perspective, the present study findings may help companies and employers reflect about how to support and include HIV-positive workers in the work environment. On the other hand, workers should also seek asserting their legal rights, through and active by notifying situations involving prejudice and exclusion at the workplace.
This study does not aim to exhaust the investigation about experiences and the ways that HIV-positive men cope with the disease in the labor market. Rather, the purpose is to raise awareness about the theme, as a first step to implement specific methodological approaches, as well as the utilization of a larger study sample. Further studies should investigate the social representations of employers towards HIV. Moreover, interventional studies should be performed, in addition to investigations of public policy studies that encourage including HIV-positive individuals in the context of labor should be prioritized.
In view of this reality, it is highlighted that nurses, particularly those who specialize in occupational nursing, are promoters of the support and inclusion of HIV-positive individuals in the workplace. Therefore, we hope to encourage equal and humanized treatment, free from prejudice, that would promote, above all, the quality of life of this clientele in terms of work, which is considered one of the main forms of affirmation of men.
The authors thank FUNCAP - Fundação Cearense de Apoio ao Desenvolvimento Científico e Tecnológico, CNPq National Council for Scientific and Technological Development and CAPES - Coordenação de Aperfeiçoamento de Pessoal de Nível Superior for the fellowships granted to the students during their Master studies.
1. Brasil. Ministério da Saúde; Secretaria de Vigilância em Saúde. Programa Nacional de DST e Aids. Diretrizes para o fortalecimento das ações de adesão ao tratamento para pessoas que vivem com HIV e aids. Brasília; 2007. [ Links ]
2. Ferreira RCM, Figueiredo MAC. Reinserção no mercado de trabalho: barreiras e silêncio no enfrentamento da exclusão por pessoas com HIV/aids. Medicina (Ribeirão Preto). 2006;39(4):591-600. [ Links ]
3. International Labour Organization (ILO). Manual sobre HIV/Aids para os inspetores do trabalho [Internet]. 2006 [citado 2010 out. 31]. Disponível em: http://www.ilo.org/wcmsp5/groups/public/---ed_protect/---protrav/---ilo_aids/documents/publication/wcms_114277.pdf [ Links ]
4. Organização Internacional do Trabalho (OIT); Escritório no Brasil. Recomendações sobre o HIV e a AIDS no mundo do trabalho [Internet]. 2010 [citado 2011 jan. 19]. Disponível em: http://www.oit.org.br/content/recomenda%C3%A7%C3%A3o-sobre-o-hiv-e-aids-e-o-mundo-do-trabalho [ Links ]
5. Valentim JH. Teletrabalho e relações de trabalho. Rev Minist Público Trab. 2003;19(1):96-104. [ Links ]
6. Brasil. Ministério da Saúde; Ministério do Trabalho e Administração. Portaria Interministerial n. 869, de 11 de agosto de 1992. Proíbe, no âmbito do Serviço Público Federal, a exigência de teste para detecção do vírus de imunodeficiência adquirida, tanto nos exames pré-admissionais quanto nos exames periódicos de saúde. Brasília; 1992. [ Links ]
7. Giatti L, Barreto SM. Situação do indivíduo no mercado de trabalho e iniqüidade em saúde no Brasil. Rev Saúde Pública. 2006;40(1):99-106. [ Links ]
8. Barros AM. Aids no local de trabalho um enfoque de direito internacional e comparado. Rev Trib Reg Trab. 2000;32(62):67-86. [ Links ]
9. Bastos FI, Swarcwald CL. Aids e pauperização: principais conceitos e evidências empíricas. Cad Saúde Pública. 2000;16(1):65-76. [ Links ]
10. Minayo MCS. O desafio do conhecimento: pesquisa qualitativa em saúde. São Paulo: Hucitec; 2004. [ Links ]
11. Bardin L. Análise de conteúdo. Lisboa: Edições 70; 2009. [ Links ]
12. Galvão MTG, Cerqueira ATAR, Marcondes-Machado J. Avaliação da qualidade de vida de mulheres com HIV/AIDS através do HAT-QoL. Cad Saúde Pública. 2004;20(2):430-7. [ Links ]
13. Teixeira MG, Silva GA. Representation of the HIV carriers about antiretroviral treatment. Rev Esc Enferm USP [cited 2011 May 10]. 2008;42(4):729-36. Available from: http://www.scielo.br/pdf/reeusp/v42n4/en_v42n4a15.pdf [ Links ]
14. Gaspar J, Reis RK, Pereira FMV, Neves L, Castrighini C, Gir E. Quality of life in women with HIV/aids in a municipality in the State of São Paulo. Rev Esc Enferm USP [Internet]. 2011 [cited 2011 May 10];45(1):230-6.Available from: http://www.scielo.br/pdf/reeusp/v45n1/en_32.pdf [ Links ]
15. Maciel JAC. Garantia no emprego já em vigor. São Paulo: LTr; 1994. [ Links ]
16. Cardoso GP, Arruda A. As representações sociais da soropositividade e sua relação com a observância terapêutica. Ciênc Saúde Coletiva. 2004;10(1):151-62. [ Links ]
17. Andrade LS, Nóbrega-Therrien SM. A sexualidade masculina e a vulnerabilidade ao HIV/aids. J Bras Doenças Sex Transm. 2005;17(2):121-6. [ Links ]
18. Carvalho CML, Galvão MTG. Enfrentamento da AIDS entre mulheres infectadas em Fortaleza - CE. Rev Esc Enferm USP. 2008;42(1):90-7. [ Links ]
19. Garcia S, Koyama MAH. Estigma, discriminação e HIV/aids no contexto brasileiro, 1998 e 2005. Rev Saúde Pública. 2008;42(1 Supl):72-83. [ Links ]
20. Faria JB, Seidl EMF. Religiosidade, enfrentamento e bem-estar subjetivo em pessoas vivendo com HIV/aids. Psicol Estud. 2006;11(1):155-64. [ Links ]
21. Reis RK, Haas VJ, Santos CB, Teles AS, Galvão MTG, Gir E. Symptoms of depression and quality of life of people living with HIV/AIDS. Rev Latino Am Enferm. 2011;19(4):874-81. [ Links ]
22. Castanha AR, Coutinho MPL, Saldanha AAW, Ribeiro CG. Avaliação da qualidade de vida em soropositivos para o HIV. Estud Psicol. 2007;24(1):21-31. [ Links ]