HIV/AIDS Information in Public Libraries

Abstract

Despite well-publicized advances in the development of antiretroviral therapies, HIV infection remains an incurable condition. Worldwide, the disease threatens to gravely impact a wide range of developing nations, especially in Sub-Saharan Africa, South and Southeast Asia and South America. In the United States, the poor and particularly women of color are at great, and increasing, risk for infection. Public libraries, as trusted public institutions for the dissemination of information, can continue to play an important role in promoting public health information surrounding HIV/AIDS prevention and education. Public libraries are not immune, however, to the political and value-driven public discourse surrounding HIV infection. Through carefully identifying the issues, taking a nonjudgmental service approach, and building collaborations with community based organizations, public libraries can become common ground for providing proactive prevention-focused information services. This article examines the current state of epidemic HIV/AIDS infection, reviews the literature on public library responses, and identifies highly select consumer health and biomedical monographic, serial, audio-visual and Web-based HIV/AIDS information tools.     

Knowledge and Attitude of Women to HIV/AIDS in a Farming Community in Southwestern Nigeria: Challenges for Public Libraries

The HIV/AIDS epidemic is one of the major setbacks to the achievement of the 2015 millennium development targets in Africa, generally, and Nigeria, in particular, where it is the leading cause of death. In terms of age and gender distribution, the most severely affected are sexually active females in their most economically reproductive years. A greater percentage of the Nigerian population lives in rural areas where there is low access to health information. This study assesses the knowledge level and attitudes of women in a farming community to HIV/AIDS, and suggests intervention strategies by the public libraries to bridge the knowledge gap on HIV/AIDS. This article suggests that public libraries as custodians of knowledge should play a significant role in transmitting information about how to prevent and control HIV/AIDS.     

Museums of Malawi Case Study: Tackling HIV/AIDS by Creating Awareness of Rights and Cultural Practices

The HIV/AIDS epidemic has greatly impacted the lives of many Malawians. In 2007, one million people in a population of 13 million were infected with the HIV virus. There are 91,000 cases of children living with HIV and over 550,000 orphans who lost their parents to this disease (UNAIDS 2008 Report on Global AIDS Epidemic). At the Museums of Malawi, many staff have died of HIV/AIDS‐related illnesses. The gravity of this matter prompted the Museums of Malawi to join hands with other stakeholders in a concerted effort to address the HIV/AIDS pandemic. The Museums of Malawi has found that the most significant reasons for HIV transmission are specific cultural beliefs and practices that abuse people’s rights, and that are as dangerous as the disease itself. The museum created activities that look at these beliefs in order to achieve behavioral change among youth and adults during the program.     

The Ethics of Keeping HIV/AIDS Newsworthy in Tanzania

This study focuses on the negotiation of ethical challenges when reporting HIV/AIDS in Tanzania by investigating how two newspapers, the Daily News and the Guardian, operate in an environment with marked limitations on resources. Interviews with journalists reveal how economic concerns and reluctance to invest money in reporting a disease, now perceived as “old news,” has opened up space for official news sources to gain privileged access to disseminate their messages, shaping the discourse on HIV/AIDS. Organizational news sources use many strategies, including providing a “transport allowance” and offering all-expenses paid trips to the field in order to gain media attention, raising ethical dilemmas for journalists and concerns about the quality of the news that gets published.     

Stigma in the line of face: Self‐disclosure of patients' HIV status to health care providers

Patients who are HIV+ are often faced with the choice of whether or not they should tell their health care providers that they are HIV+. Although appropriate health care and safety require the communication of such information, the stigmatization associated with HIV puts at risk the patients’ pride, dignity, and ultimately the quality of their health. Using Goffman's (1963, 1967) notions of face and stigma, the present study described the major influential factors prompting the act of disclosure of HIV, the act itself, and the effect that act appears to have had on the patient/provider relationship. Phase I of the study gathered pilot data through in‐depth interviews, leading to a quantitative questionnaire used in Phase II. A sample was obtained through AIDS organizations around the U.S. and via electronic mail addresses for AIDS/HIV electronic discussion groups. The interviews and surveys asked respondents to recall a time when they had to make the decision to disclose or not disclose their HIV+ status to a care provider. The results indicated that patients typically did disclose their HIV+ status despite their strong feelings of stigmatization. Three key factors were related to their decisions: 1) perceived necessity of disclosure; 2) subjective feelings of comfort about the disclosure; and 3) perceptions of stigmatization. Patient satisfaction levels were also related to these factors. Implications for face maintenance and health care management as well as the determinants of subjective comfort are discussed.     

Community Radio Stations as Community Technology Centers: An Evaluation of the Development Impact of Technological Hybridization on Stakeholder Communities in South Africa

This study investigated the impact of using community radio stations to extend information and communication technology (ICT) benefits to poor communities in South Africa. Six community radio stations in six rural South African communities were studied, using face-to-face interviews, community conversations, and observation method. The study found these radio stations have ICT presence, but because of a lack of resources they are only able to allow their stakeholder communities' indirect access to these technologies. It concludes that for these stations to realize their full development potential of extending ICTs to poor rural communities in South Africa, collaborative innovative strategies will have to be instituted.     

Sex differences in communication and the construction of HIV/AIDS

This paper reports analyses of sex differences in knowledge, attitudes, and behavior related to HIV/AIDS and communication about HIV I'AIDS in the heterosexual college population. Men and women differed in their assessments of risk to HIV infection for various behaviors; in each case women perceived greater risk. Women were more favorable than men regarding talking about AIDS and attitudes about condom use. Men reported a greater number of sexual partners for the previous five years than did women. Men, more often than women, appear to have changed their behavior in a direction of greater risk. Only two sex differences were found for prevention‐related behaviors. First, men more often reported having purchased a condom. However, no sex differences were found for actual condom use. Second, as reported in previous studies, women were more likely to engage in AIDS‐related talk with a sexual partner. Because of their many differences, men and women need to be targeted as separate audiences for HIV/AIDS prevention. Further, because women have emerged as the most rapidly growing group at risk for HIV infection and because women appear to be more willing than men to implement HIV/AIDS prevention in their relationships, they should be considered a primary audience for HIV/AIDS‐prevention programs designed for influencing the behavior of heterosexual couples.     

Meeting health information needs of people with HIV/AIDS: sources and means of collaboration

Background: Internet‐based applications, in particular those that allow communication, have great potential to meet information needs. Limited research has indicated that people with human immunodeficiency virus/acquired immune deficiency syndrome (HIV/AIDS; PHAs) use these technologies, but it has not yet been examined how resources are used collaboratively and in conjunction with offline sources. Objectives: The purpose of this study was to determine in what ways PHAs collaborate to meet treatment information needs and what role Internet‐based computer‐mediated communication (CMC) played in meeting this goal. Methods: This exploratory study was implemented using surveys and focus groups with 23 participants in Toronto, Canada. The purposive sample included men and women. Results: A variety of both off‐ and online resources were used to learn about HIV/AIDS treatment information, including web‐based and print. All participants were communicating with others, primarily in person, and most desired anecdotal treatment information. However, few reported using CMC to accomplish this goal. Harris and Dewdney's Principles of Information Seeking was used to frame the findings. Conclusions: Despite technical proficiency with CMC, few participants in this study reported use of this communication tool. Information professionals need to ensure access to HIV health information including those in remote areas who have fewer resources.     

“From food silos to community kitchens”—Retooling African libraries

This article explores reasons why the Western library system does not adequately address Africa's vision for a library and why it does not meet the local needs for information. With a focus on the AIDS pandemic, the role and mission of libraries are revisited as a customized tool that is culturally localized to effectively participate as a proactive disseminator of information, specifically to support the three key public health objectives regarding HIV/AIDS, namely, to have people tested for the virus, to inform those infected about their best options to sustain life, and to support efforts to prevent the spread of HIV. A progressive Africanized vision of the role of libraries is proposed—to retool libraries from their current passive roles as the guardians of books, to active, live, and customized disseminators of socially relevant and culturally appropriate information.     

Information and communication: a library’s local response to HIV/AIDS in Zambia

Objective: To document and describe the University of Zambia Medical library’s responses to the fight against HIV/AIDS in Zambia. Methods: The methodology adopted was a case study approach combined with an analysis of the literature such as annual reports and official documents. This was augmented by personal reflections of the author having worked at the Medical Library. Results: The University of Zambia Medical library has over the years instituted and implemented HIV/AIDS information provision programmes that include the provision of information in various formats ‐‐ print or electronic and, in addition, capacity building in HIV/AIDS information literacy skills. Conclusion: A library’s social responsibility calls for it to be part of national responses to crises that arise in society. As HIV/AIDS has affected every aspect of Zambian society prevention, treatment, care and support there is an understanding that the library’s role should be using the cri tical and strategic resource at its disposal – information ‐‐ as part of their contribution to the fight against HIV/AIDS. In this context, libraries should source, collect, organize and disseminate information on HIV/AIDS in a way that is easily accessible to researchers, HIV/AIDS programme implementation agencies and the ordinary public.     

HIV/AIDS and Subaltern Autonomous Rationality: A Call to Recenter Health Communication in Marginalized Sex Worker Spaces

Sex workers in India constitute a marginalized population. They are considered at high risk of HIV/AIDS and are stigmatized for “selling sex” in a culture that generally censures sex outside marriage. HIV/AIDS initiatives targeted at this population have mostly adhered to promoting condom use, increasing awareness, and encouraging blood tests to screen for HIV/AIDS. Missing from this discourse are voices of sex workers and their autonomous consciousness. Based on an analysis of interview data from an eight-week field project, this paper seeks to centralize sex worker subaltern rationality in a call to reframe expert-led HIV/AIDS communication efforts that cater to sex worker communities.     

Role of Indian public libraries to increase the awareness of the community on HIV/AIDS

Abstract

Today Indian society is at high risk. AIDS, the most devastating disease humankind has ever faced, has become a conflagration on the Indian subcontinent and nearly 5.134 million people in the country are estimated to be HIV-positive. There is a perceived need for public libraries to provide necessary information to make the community aware of the threat of HIV/AIDS. Today's challenge is to reinvent the public libraries to respond to community needs. This paper explores the avenues created by ICT-enabled networking processes in providing HIV/AIDS information to the unprivileged population in India. It concludes with a number of recommendations that are intended to address the core problems and thereby improve the overall situation.     

Complementary and alternative medicine as represented in the HIV/AIDS body of knowledge: a bibliometric analysis

Although the HIV/AIDS epidemic began more than twenty years ago, there still is no cure for the disease and no vaccine to prevent infection. As with the general population, individuals with HIV/AIDS have sought care using a variety of traditional and nontraditional approaches. The popularity of complementary and alternative interventions among the HIV/AIDS community continues. To understand better the distribution of the HIV/AIDS body of knowledge concerning complementary and alternative medicine (CAM), this study sought to (1) examine the literature specific to the use of complementary and alternative medicine where HIV/AIDS is concerned to determine publication patterns; (2) determine the degree of overlap among bibliographic citation databases that index the literature concerning the use of CAM practices in treating HIV/AIDS; and (3) facilitate access to this body of literature.     

Malevolence,stigma, and social distance: Maximizing intergroup differences in HIV/AIDS discourse

This study examined the intergroup language used by young heterosexual Australians in conversations about HIV/AIDS and safe sex. Sixty male and 72 female heterosexuals participated in four‐person facilitated conversations (same‐sex or mixed‐sex) about HIV/AIDS and safe sex, which were recorded and transcribed. We focused on extracts concerning strangers or malevolent individuals who appear to be group members, along with extracts involving foreign national groups. Discourse analysis showed that groups at lower levels of social distance were constructed mainly in terms of individual responsibility. At moderate social distance, stereotypes were more negative, but sub‐typing was common, whereas at the highest levels, people were constructed entirely in intergroup terms. The findings of this study suggest that HTV prevention programs should make reference to all salient outgroups, so as to neutralize communicative strategies that strengthen intergroup boundaries as a means of reducing perceived personal threat of HIV infection.     

韩国图书情报学教育简史

[目的/意义] 考察韩国图书情报学教育历史,有利于把握其发展特点和建设规律。[方法/过程] 通过阅读国内外与韩国图书情报教育相关的文献,凝练出韩国图书情报教育的发展规律,进而得出韩国图书情报教育的未来发展趋势。[结果/结论] 韩国早期的图书馆学教育主要由教育培训机构施行,基本延续了美国图书馆学教育的模式。20世纪80年代中期以后,图书情报教育进入高学历繁荣阶段,课程设置与研究领域向外扩展,社会需求量大于人才培养量,毕业生更愿意到图书馆就业,图书情报学教育走上繁荣与稳定发展之路。     

Compliance with freedom of information legislation by public bodies in South Africa

In South Africa, freedom of information (FOI) is entrenched in section 32 of the Constitution, which guarantees every citizen the right of access to any information held by the state or by any other person that is to be used for the protection or exercise of any right. The Promotion of Access to Information Act (PAIA) is the law that gives effect to section 32 of the Constitution. Regardless of a remarkable trend towards the adoption of FOI laws, international trends have shown this does not automatically translate into fulfilment of people's right to information. This study utilised mixed method research through the explanatory sequential design to assess compliance with FOI legislation by public bodies in South Africa, with a view to develop a model for implementation of FOI. The study first conducted a quantitative study by analysing the reports of the South African Human Rights Commission from the reporting years 2006/07 to 2016/07 to assess compliance with sections 14, 15, 16, 17 and 32 of the PAIA. Thereafter, a qualitative study through interviews with purposively chosen participants was conducted to substantiate the findings of a quantitative study. Key results suggest that over the years, there were problems in the implementation of the FOI legislation in South Africa and its use was limited. Where implementation has taken place, it has been partial and inconsistent. The responsibility for the implementation of FOI legislation in most public bodies is assigned to legal departments that do not have knowledge of what records are created, and where and how they are kept. With regard to compliance, in terms of the degree of comparison, the situation was better in national departments, worse in provincial departments and worst in municipalities. The study recommends the establishment of an information governance unit to implement FOI in public bodies. Failure to assign responsibility to a relevant unit would perpetuate the non-compliance with FOI legislation by public bodies in South Africa. A model for the implementation of PAIA within a public body is suggested.