ABSTRACT
Previous studies showed that Erotic industry sShows (ES) were appropriate events for sexual health promotion and testing interventions. A cross-sectional survey exploring screening practices, sexual behaviors, substance use, and sexual motives for substance use was conducted in ES in December 2017 and completed by 781 respondents. Overall, . Eighteen18% percent reported substance use in the last 3 months (51% alcohol), 26%. Twenty-six percent reported a sexual purpose for substance use. Main sexual partners were spouse (68%), regular (21%), unknown (18%) and several (17%) partners. Main sexual practices were libertinism (22%), partner swapping (15%) and threesome (15%). Twenty-seven percent of respondents reported cContactless sex was reported by 27% of the respondents. 18% reported no previous HIV test. Univariate analysis showed that having or not previous HIV test was linked to male sex (76.8% vs. 54.5%, p < 10-3), alcohol consumption in the last three months (58.7% vs. 49.4%, p = .043), number of drugs in a lifetime (1.3% vs. 1.6%, p = .022), sexual partnership with spouse/long-term partner (57.3% vs. 70.5%; p = .002), at least one multiple-partner sexual practice (23.1% vs. 31.8%, p = .040) and type of sexual attraction (p = <10-3). Results contribute to establishing the usefulness of HIV-testing and awareness campaigns in ES eventsand informing potential combined risk behaviors and related interventions.
Subject(s)
HIV Infections , Substance-Related Disorders , Male , Humans , Cross-Sectional Studies , HIV Infections/diagnosis , HIV Infections/epidemiology , HIV Infections/prevention & control , Sexual Behavior , Sexual Partners , Substance-Related Disorders/diagnosis , Substance-Related Disorders/epidemiology , Risk-TakingABSTRACT
BACKGROUND: At the request of the Hospitalization Regional Agency (ARH)--in the context of the 2007-2011 plan aimed at improving the quality of life for patients affected by chronic diseases--the purpose of this work was to draw up a clear assessment of the 2008 Therapeutic Education programmes in the Provence-Alpes-Côte d'Azur (PACA) region. The study was carried out before the publication of the therapeutic education statutory orders and ARS (regional health agency) authorizations. METHODS: Cross-sectional study, carried out in the three sectors of medical management in the region--namely health-care institutions, ambulatory structures and health networks--made it possible to identify, first, which structures had actually launched therapeutic education programmes and then, how the procedures had been designed and set up. RESULTS: Among all the medical structures investigated, the study has listed 491 programmes, heterogeneously located throughout the PACA region. These programmes primarily target diabetes, respiratory and cardiovascular diseases. Their main objectives are the patients' quality of life, adherence to treatment and protective health behaviour (health improvement). The hospitalization sector programmes preferentially target the 30 to 60 years old, whereas the ambulatory and health networks programmes are more inclined to target the over 60 years old part of the population. More than 50% of the professionals involved in the programmes have never benefited from a specific training concerning the patients' therapeutic education. CONCLUSION: This study has pointed out a great number of important aspects which need drastic improvement in terms of therapeutic education organization - the involvement and training of health professionals, for instance.
Subject(s)
Chronic Disease/rehabilitation , Medication Adherence , Patient Education as Topic , Quality of Life , Adolescent , Adult , Aged , Ambulatory Care , Cardiac Rehabilitation , Chronic Disease/therapy , Cross-Sectional Studies , Diabetes Mellitus/rehabilitation , Female , France , Health Personnel/education , Hospitals , Humans , Male , Middle Aged , Patient Education as Topic/methods , Quality of Health Care , Respiratory Tract Diseases/rehabilitation , Surveys and QuestionnairesABSTRACT
OBJECTIVE: Post-exposure prophylaxis (PEP) is recommended for the management of sexual HIV-risk exposure. However, a high percentage of exposed patients discontinue both their 28-day prophylaxis course before 15 days and HIV testing follow-up before M3. The objective of this study is to assess the efficacy of a counseling intervention in enhancing both adherence to PEP and HIV testing follow-up. METHODS: Between 1 June 2004 and 31 December 2005, 54 patients exposed to sexual HIV-risk exposure were included in a multicenter, prospective, controlled, randomized trial, comparing a group receiving a counseling intervention in addition to traditional medical management (intervention group (IG), n=28) vs. a control group (CG, n=26). Patients in the IG received interactive counseling interventions focused on adherence to PEP and to HIV testing follow-up, led by specially trained nurses. The main outcome measures were proportion of patients achieving 100% adherence to PEP as evaluated on D15 by a self-completed patient questionnaire and on HIV testing on D45 and M3. RESULTS: Groups were well balanced at baseline for age, sex, and circumstances of exposure. The proportion of 100% adherent patients to PEP was significantly higher in the IG compared to the CG (54% vs. 23%, p=0.036). Patients in the IG were more likely to complete the HIV testing follow-up at D45 (86% vs. 54%, p=0.023) and M3 (68% vs. 38%, p=0.056). CONCLUSIONS: This study suggests the effectiveness of a counseling program to enhance adherence to both PEP and HIV testing follow-up after sexual exposure.
Subject(s)
Anti-HIV Agents/therapeutic use , Counseling/methods , HIV Infections/drug therapy , Patient Compliance , Post-Exposure Prophylaxis/methods , Sexual Behavior/psychology , Adult , Female , France , HIV Infections/prevention & control , HIV Infections/psychology , Humans , Male , Prospective Studies , Risk Factors , Treatment OutcomeABSTRACT
OBJECTIVE: This study had for aim to evaluate the immuno-virological and therapeutic profile of a cohort of 7416 HIV-1 infected patients followed in six French hospital with the Nadis software. METHOD: This cross sectional and retrospective study was performed between June 1, 2004 and June 1, 2005. We analyzed the demographic (sex, age, HIV infection route), immunovirological, and therapeutic characteristics (last treatment prescribed) of the 7416 cohort patients. RESULTS: The mean age was 43 years, 29% were women and 29% HCV/HBV co infected. The viral load was 1.9 log(10)copies/ml (IQR: 1.5-3.3) and the CD4 cells count was 452/mm(3) [IQR: 306-630]. Among the 5,913 antiretroviral treated patients, VL was less than 200 copies/ml for 74.7% of patients and 50% of them had a CD4 cell count superior to 500/mm(3); the drug regimen was 2 or 3 nucleosides reverse transcriptase inhibitors (NRTI) combined with one protease inhibitor (88% Ritonavir boosted) in 42% of the patients, 26% of them were treated with 2 NRTI and 1 non-NRTI, and 14% with 3NRTI. Patients with undetectable VL were followed 5.1/year versus 7.2 for non- VL controlled patients (P<10(-3)). The heterosexual route predominated among the new 531 HIV-diagnosed patients among whom 25% had a median CD4 cell count of 242/ m(3). CONCLUSION: Close to 75% of antiretroviral treated patients had a VL<200 copies/ml but 15% kept a low CD4 cell count. The characteristics of recently diagnosed HIV positive patients stresses the need for more information on prevention and an early diagnosis.
Subject(s)
Anti-HIV Agents/therapeutic use , HIV Infections/drug therapy , Adult , Antiviral Agents/therapeutic use , Cohort Studies , Female , France/epidemiology , HIV Infections/complications , HIV Infections/epidemiology , HIV Infections/transmission , Hepatitis B/complications , Hepatitis B/epidemiology , Heterosexuality/statistics & numerical data , Homosexuality/statistics & numerical data , Humans , Incidence , Male , Risk Factors , SoftwareABSTRACT
OBJECTIVE: The Nadis electronic medical patient record allows real time constitution of a database including the clinical, therapeutic, biological, and epidemiological features of HIV-positive patients. METHODS: Data concerning HIV-infected patients followed-up in 6 French University Hospitals was collected. Data quality was assessed on a regular basis in each center. RESULTS: The 6 first University hospitals using Nadis agreed to group their data on March 15, 2004, concerning 6236 patients having consulted at least once in the previous year. Among these, 29% were female patients, 80% were under treatment on March 15, 2004, 9% were off treatment, 29% were co-infected by hepatitis B or C virus, 57% had an undetectable viral load, 15% of the treated patients were in a worrying immunovirological situation, 358 were diagnosed HIV-positive in 2003. 35% of these "new patients" were women, the mode of infection was sexual in 80%, 45% were under treatment on March 15, 04. This recent data allowed us to have an accurate assessment of this population's management in 2004.
Subject(s)
HIV Infections/epidemiology , Medical Records Systems, Computerized , Adult , Anti-HIV Agents/therapeutic use , Cohort Studies , Comorbidity , Databases, Factual , Disease Transmission, Infectious , Female , Follow-Up Studies , France/epidemiology , HIV Infections/drug therapy , HIV Infections/transmission , Hepatitis B/epidemiology , Hepatitis C/epidemiology , Hospitals, University/statistics & numerical data , Humans , Male , Middle Aged , Quality Control , Sexual Behavior , Substance Abuse, Intravenous/epidemiology , Transfusion Reaction , Viral LoadABSTRACT
OBJECTIVES: To identify factors related to delayed testing, and delayed or interrupted care-seeking or treatment uptake, among HIV-infected patients. DESIGN: HIV-infected patients hospitalized for an opportunistic infection (OI) cases were included in a prospective study and compared with controls matched by age and sex who had regular follow-up and treatment. Patients were asked to complete a questionnaire about their therapeutic itinerary and their socioeconomic, psychological and medical characteristics. RESULTS: Seventy patients were matched with 140 controls. According to their therapeutic itinerary prior to admission, cases were subdivided into four groups among which three will be more particularly studied: nontested patients (NT) (24%; n=17), known HIV-infected patients with no medical follow-up (NF) (30%; n=21); and noncompliant patients (NC) (36%, n=25). Characteristics of NT and NF patients included a predominantly sexual mode of contamination (P=0.01), continuing occupational activity (P=0.01) despite a low mean Karnofsky index (P=0.001) and unfavourable virological and immunological parameters. NT patients displayed a low degree of anxiety, and lacked awareness concerning risk of contamination and HIV-related symptoms. HIV-status announcement (P=0.04) and the benefits of medical follow-up (P=0.05) were less favourably perceived by NF patients than by controls, and were associated with a high degree of anxiety in NF patients. NC patients had a weaker commitment to follow-up and treatment, and more frequent treatment discontinuation associated with a higher rate of interruption of follow-up in a context of social difficulties. CONCLUSIONS: Patients ignorant of their HIV status, patients NF and NC have very specific characteristics. More appropriate approaches are needed regarding screening and access to care in order to reduce the incidence of delayed care-seeking.
Subject(s)
AIDS-Related Opportunistic Infections/drug therapy , AIDS-Related Opportunistic Infections/diagnosis , AIDS-Related Opportunistic Infections/psychology , Adult , Antiretroviral Therapy, Highly Active/methods , Anxiety/psychology , Attitude to Health , Awareness , Communication , Female , Hospitalization , Humans , Male , Middle Aged , Patient Acceptance of Health Care/psychology , Patient Compliance , Prospective Studies , Socioeconomic FactorsSubject(s)
Anti-HIV Agents/blood , Anti-HIV Agents/cerebrospinal fluid , Didanosine/blood , Didanosine/cerebrospinal fluid , HIV Infections/blood , HIV Infections/cerebrospinal fluid , Adult , Anti-HIV Agents/therapeutic use , CD4 Lymphocyte Count/methods , Didanosine/therapeutic use , Female , HIV Infections/drug therapy , Humans , Magnetic Resonance Spectroscopy , Male , Middle Aged , Retrospective Studies , Viral Load/methodsABSTRACT
OBJECTIVE: to develop an electronic medical record for patients living with HIV, HBV or HCV in order to improve their management, facilitate communication between all the caregivers, and to create a useful medical database for research and assessments. This project (NADIS 2000) involved 6 centres of Infectious Diseases in France in partnership with Fédialis Médica (subsidiary of the GSK group in France). METHODS: A specifications sheets was drawn-up by a piloting Committee regrouping the various correspondents in each centre and a computer expert representing Fédialis Médica. A Scientific and Development committee regrouped the heads of departments of each centre and the representatives from Fédialis Médica and GSK and was charged with defining the general concept of the project and guaranteeing the scientific and clinical aspects. RESULTS: NADIS 2000 version 1.0 was activated in the departments of infectious diseases in Nice and Toulouse in November 2000 and in others Units at the end of 2001. NADIS 2000 permitted real-time use by the physicians in the Outpatients and Day-care Units and was easily handled by all the practitioners. Its use was eased by the principles clearly defined before its application (department project, progressive but exhaustive use), an intuitive interface simulating a consultation, and functions proposing direct benefits for the physicians (graphical visualization of the biological variables, printing of prescriptions and letters). CONCLUSION: The activation and input methods of NADIS 2000 are user friendly and the physicians find it rapidly easy to use. New functional aspects are being developed as well as its use in other hospital departments.
Subject(s)
HIV Infections/therapy , Hepatitis B/therapy , Hepatitis C/therapy , Medical Records Systems, Computerized/organization & administration , Computer Communication Networks/organization & administration , Computer Graphics , Databases, Factual , France , HIV Infections/diagnosis , Hepatitis B/diagnosis , Hepatitis C/diagnosis , Humans , Patient Care Team , Remote Consultation , Software , User-Computer InterfaceABSTRACT
The prognosis of melanoma is closely related to tumor thickness at the time of surgical excision. Thickness depends on the duration of disease before diagnosis. This underlines the importance of information campaigns to promote early diagnosis of melanoma. The purpose of this study was to estimate the cost and effectiveness of a media campaign for the early screening of malignant melanoma (MM) at national level. This trial, the first of its kind in France, was conducted in the spring of 1989 in the Provence-Alpes-Côte d'Azur-Corse region. The campaign combined an effort to inform and heighten awareness in the medical community and the broadcast of an information movie for the general population on a regional TV channel. Following the campaign, the number of MM diagnosed in a representative selection of pathology laboratories increased significantly compared with the same period of the previous year: + 108 p. 100 over the 10 first weeks, + 47.6 p. 100 over 6 months. This increase was mostly for MM of low thickness (less than 1 mm) which have a good prognosis: + 74 p. 100 over 6 months. However MM distribution by thickness was not significantly different from one year to the next. Although the number of added cost generated by this campaign could not be precisely determined, these positive initial results argue for a national prevention campaign based on the lessons of this experience.
Subject(s)
Health Education , Melanoma/prevention & control , Skin Neoplasms/prevention & control , Costs and Cost Analysis , France , Health Education/methods , Humans , Melanoma/diagnosis , Melanoma/epidemiology , Primary Prevention/education , Skin Neoplasms/diagnosis , Skin Neoplasms/epidemiology , Sunburn/complications , TelevisionSubject(s)
Acquired Immunodeficiency Syndrome , Blood Donors , Blood Transfusion , HIV Seropositivity , International Cooperation , Internationality , Patients , Public Policy , Tissue Donors , AIDS Serodiagnosis , Blood Banks , Confidentiality , Contact Tracing , Databases, Factual , Directed Tissue Donation , Fees and Charges , Health Facilities , Humans , Informed Consent , Jurisprudence , Liability, Legal , Malpractice , Preventive Medicine , Records , Tissue and Organ Procurement , United StatesSubject(s)
Acquired Immunodeficiency Syndrome , Confidentiality , HIV Seropositivity , Public Policy , Codes of Ethics , Communicable Diseases , Contact Tracing , Duty to Warn , Ethics, Medical , Ethics, Professional , History , Humans , International Cooperation , Internationality , Jurisprudence , Moral Obligations , Patients , Physician-Patient Relations , Physicians , Privacy , Public Health , Social ResponsibilitySubject(s)
Acquired Immunodeficiency Syndrome , Coercion , HIV Seropositivity , Human Rights , Mandatory Programs , Patients , Public Policy , Voluntary Programs , AIDS Serodiagnosis , Blood Donors , Civil Rights , Confidentiality , Contact Tracing , Freedom , Health Education , Homosexuality , Humans , Informed Consent , Mass Screening , Prejudice , Privacy , Public Health , Quarantine , Research , Social Justice , Social Welfare , Therapeutic Human ExperimentationSubject(s)
Acquired Immunodeficiency Syndrome , Health Personnel , Occupational Exposure , Patient Care , Refusal to Treat , AIDS Serodiagnosis , Confidentiality , Contact Tracing , Duty to Warn , Humans , Iatrogenic Disease , Mass Screening , Moral Obligations , Nurses , Organizational Policy , Patients , Physicians , Social Responsibility , Societies , StereotypingSubject(s)
Acquired Immunodeficiency Syndrome , Patient Advocacy , Patient Rights , AIDS Serodiagnosis , Codes of Ethics , Coercion , Confidentiality , Contact Tracing , Duty to Warn , Ethics, Medical , Ethics, Professional , HIV Seropositivity , Health Personnel , Humans , Informed Consent , International Cooperation , Internationality , Jurisprudence , Mandatory Programs , Mass Screening , Occupational Exposure , Prejudice , Privacy , Public Health , Public Policy , Refusal to Treat , Research , Stereotyping , Therapeutic Human Experimentation , Truth Disclosure , Voluntary ProgramsABSTRACT
At present, we can observe an evolution in ideas about the detection of HIV seropositivity through a qualitative analysis of specialised literature on the ethical aspects of AIDS. In the case of this disease, systematic screening of the population does not correspond to epidemiological criteria: it is wasteful, troublesome and costly. Whether it is voluntary, and therefore biased, or compulsory, and therefore controversial, systematic screening seems an unlikely option. This situation has prompted many versions of target-group screening, which correspond to two options: systematic screening of known risk-groups, discriminatory, confidential and anonymous; target-group screening linked to particular circumstances: recognised as necessary by blood-donors and well-accepted by pregnant mothers. This method can be institutionalised and applied in the armed forces and in prisons,.... Lastly, we consider measures taken by different countries and organisations.
Subject(s)
Acquired Immunodeficiency Syndrome/psychology , Ethics, Medical , HIV Seropositivity/diagnosis , Acquired Immunodeficiency Syndrome/diagnosis , Confidentiality , HIV Seropositivity/psychology , Humans , Internationality , Mandatory Programs , Mass Screening , Prejudice , Risk Assessment , Risk Factors , Voluntary ProgramsABSTRACT
At present questions are being asked world-wide about the risk of the AIDS epidemic. The discovery of an anti-HIV vaccine has become an urgent priority, but it also raises a number of sensitive questions. Ethical problems in this field are particularly delicate, since the perspectives of individual health and public health do not seem to coincide. Our research team conducted a review of more than 400 articles on the ethical problems raised by AIDS. We concentrated particularly on the ethical and legal issues raised by research on anti-HIV vaccine. These problems fall into three main categories: therapeutic assays, which must be controlled by a strict agreement defined by international norms; manufacture of the future vaccine, raising legal difficulties which must be faced and solved now; distribution of the vaccine to the population, which should be conducted on a general basis, i.e. it should be offered to all individuals and not only to risk groups.
Subject(s)
Ethics, Medical , HIV Infections/prevention & control , Vaccination/psychology , Animal Experimentation , Government Regulation , HIV Infections/psychology , Humans , Internationality , Mandatory Programs , Mass Media , Nontherapeutic Human Experimentation , Patient Selection , Research Subjects , Therapeutic Human Experimentation , Vaccination/economics , Vaccination/legislation & jurisprudence , Voluntary ProgramsABSTRACT
This bibliographical study involved first the exploitation of four data-banks: Medline, CNRS, Bioethics and AIDS, with the following key words (in conjunction with AIDS): ethics, human rights, confidentiality, legislation, jurisprudence. A total of 412 references were listed between 1983 and the end of 1987. Examination of the quantitative increase of articles over these years shows that, while references to AIDS and/or HIV infection--referred to as 'AIDS' for brevity--increased by about one third per year, the number of papers treating ethical problems linked to AIDS doubled each year. This increase makes it clear that these problems are important and pressing, that they are evolving rapidly and can be given no easy solution. After reading and analysis of accessible articles in readily comprehensible languages, the different themes can be classified in two categories: 1: Measures intended to protect society (starting with the most coercive); quarantine and isolation; discriminatory measures concerning specific groups; non-respect of the confidential nature of medical information; application of the penal code; screening; obligatory declaration and registration; testing of blood given by donors; vaccination and medical innovations, therapeutic assays; information, education. 2. Measures intended to protect the individual: fundamental rights of the patient: his/her right to confidentiality, to information and to treatment; civil rights: civil liberty, right to education, right to work, etc...; rights of the healthy individual: right of those in contact with the patients, safety of hospital staff, of those receiving blood-transfusions, etc... The legislation adopted in the various countries and the main opinions to be found in these articles are listed and analysed, and for each particular theme it is possible to refer to a list of the 232 most important articles. While the debate seems to concentrate on the conflict between the right of society to protect itself against the spread of infection and the 'civil' rights of the infected minorities, our conclusion tends to reduce this antagonism, showing that, particularly as far as the confidential nature of medical information is concerned, measures intended to protect the individual also protect society.