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            "title": "4 Changes in depression in a cohort of Danish HIV-positive individuals: time for routine screening",
            "creators": [
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                    "creatorType": "author",
                    "firstName": "L.",
                    "lastName": "Rodkjaer"
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                {
                    "creatorType": "author",
                    "firstName": "T.",
                    "lastName": "Laursen"
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                {
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                    "firstName": "N.B.",
                    "lastName": "Christensen"
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                    "firstName": "L.",
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                    "firstName": "M.",
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            "abstractNote": "Background: The aim of this study was to follow a cohort of HIV-positive individuals for 3 years in order to assess changes in depression, adherence, unsafe sex and emotional strains from living with HIV. Methods: Participants were assessed for depression, adherence, emotional strain and unsafe sex via a questionnaire. The Beck Depression Inventory II (BDI) was used to assess the prevalence and severity of depressive symptoms. Patients with a BDI score of 20 or above (moderate to major depression) were offered a clinical evaluation by a consultant psychiatrist. Results: In 2005, 205 HIV-positive individuals participated in the study. Symptoms of depression (BDI >14) were observed in 77 (38%) and major depression (BDI ≥20) in 53 (26%) individuals. In 2008, 148 participants were retested (72% of original sample). Depression (BDI >14) was observed in 38 (26%) and symptoms of major depression (BDI ≥20) in 24 (16%) individuals. Patients at risk of moderate to major depression were more likely to be non-adherent to medications, to practice unsafe sex and to suffer from emotional strains compared with patients not at risk of depression, both at baseline (2005) and follow-up (2008). Conclusion: This study demonstrated a decline in depression scores over time and an association between the risk of depression and low medication adherence, stress and unsafe sex. We recommend routine screening for depression to be conducted regularly to provide full evaluations and relevant psychiatric treatment.",
            "publicationTitle": "Sexual Health",
            "publisher": "",
            "place": "",
            "date": "2011",
            "volume": "8",
            "issue": "2",
            "section": "",
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            "partTitle": "",
            "pages": "214-221",
            "series": "",
            "seriesTitle": "",
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            "journalAbbreviation": "Sex. Health",
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            "url": "http://dx.doi.org/10.1071/SH10067",
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                    "type": 1
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            "title": "HIV in East London: ethnicity, gender and risk. Design and methods",
            "creators": [
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                    "firstName": "Jonathan",
                    "lastName": "Elford"
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                {
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                    "firstName": "Jane",
                    "lastName": "Anderson"
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                    "creatorType": "author",
                    "firstName": "Cecilia",
                    "lastName": "Bukutu"
                },
                {
                    "creatorType": "author",
                    "firstName": "Fowzia",
                    "lastName": "Ibrahim"
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            ],
            "abstractNote": "Background\nWhile men who have sex with men remain the group at greatest risk of acquiring HIV infection in the UK, the number of new diagnoses among heterosexuals has risen steadily over the last five years. In the UK, three-quarters of heterosexual men and women diagnosed with HIV in 2004 probably acquired their infection in Africa. This changing epidemiological pattern is particularly pronounced in East London because of its ethnically diverse population.\n\nDesign and methods\nThe objective of the study was to examine the social, economic and behavioural characteristics of patients with HIV infection currently receiving treatment and care in hospitals in East London. The research focused on ethnicity, gender, sexuality, education, employment, housing, HIV treatment, stigma, discrimination, religion, migration and sexual risk behaviour. People diagnosed with HIV infection attending outpatient treatment clinics at St Bartholomew's, the Royal London, Whipp's Cross, Homerton, Newham and Barking hospitals (all in East London) over a 4–6 month period were invited to participate in the study in 2004–2005. Those who agreed to participate completed a confidential, self-administered pen-and-paper questionnaire. During the study period, 2680 patients with HIV attended the outpatient clinics in the six participating hospitals, of whom 2299 were eligible for the study and 1687 completed a questionnaire. The response rate was 73% of eligible patients and 63% of all patients attending the clinics during the survey period.\n\nDiscussion\nA clinic-based study has allowed us to survey nearly 1700 patients with HIV from diverse backgrounds receiving treatment and care in East London. The data collected in this study will provide valuable information for the planning and delivery of appropriate clinical care, social support and health promotion for people living with HIV not only in East London but in other parts of the capital as well as elsewhere in the UK.",
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            "title": "HIV-infected individuals with high coping self-efficacy are less likely to report depressive symptoms: a cross-sectional study from Denmark",
            "creators": [
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                    "creatorType": "author",
                    "firstName": "L.",
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                {
                    "creatorType": "author",
                    "firstName": "M. A.",
                    "lastName": "Chesney"
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            "abstractNote": "Aim To explore the experience of young adults growing up and living with HIV in urban Sweden. Background HIV has become a widespread pandemic. Effective antiretroviral treatment has dramatically increased the survival rate of infected individuals, such that HIV infection is currently considered a chronic disease where treatment is available. Data concerning the experience of living with HIV since early childhood is scarce and more empirical knowledge is needed to direct the development of adequate care and interventions for this growing demographic. Design Exploratory qualitative study. Method Semi-structured interviews were conducted with ten HIV-infected young adults over the period from January–August 2008. Transcripts of the interviews were analysed using qualitative content analysis. Findings The analysis revealed five categories illustrating the experiences of growing up and living with HIV in Sweden: (1) to protect oneself from the risk of being stigmatized; (2) to be in control; (3) losses in life, but HIV is not a big deal; (4) health care/healthcare providers; and (5) belief in the future. Conclusion It is essential to offer a safe, trustworthy, and professional healthcare environment during the upbringing of HIV-infected children. Evidence-based interventions are needed to improve care and support, particularly about the handling of stigma and discrimination.",
            "publicationTitle": "Journal of Advanced Nursing",
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            "place": "",
            "date": "2013",
            "volume": "69",
            "issue": "6",
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            "partTitle": "",
            "pages": "1357–1365",
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            "DOI": "10.1111/j.1365-2648.2012.06127.x",
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            "shortTitle": "",
            "language": "en",
            "libraryCatalog": "Wiley Online Library",
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            "rights": "© 2012 Blackwell Publishing Ltd",
            "extra": "",
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                    "tag": "nursing",
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                },
                {
                    "tag": "quality of life",
                    "type": 1
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                    "tag": "stigma",
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            "title": "3 Gender and Ethnicity Differences in HIV-related Stigma Experienced by People Living with HIV in Ontario, Canada",
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                    "creatorType": "author",
                    "firstName": "Mona R.",
                    "lastName": "Loutfy"
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                {
                    "creatorType": "author",
                    "firstName": "Carmen H.",
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