RESUMEN
OBJECTIVE: To describe HIV-infected people's experience of the HIV test procedure in Europe. METHODS: Between August 1996 and September 1997, anonymous self-administered questionnaires were distributed to HIV-infected people in 11 European countries. RESULTS: A total of 1366 people completed the questionnaire (50% response rate). Of these, 194 (16%) had more than five negative HIV tests before being diagnosed as HIV positive, 179 (14%) were tested without consent and 192 (15%) were informed about the HIV positive test result by mail or by telephone. Of the 963 people who received a positive test result during a consultation, 247 (26%) reported that this visit lasted less than 10 min, 336 (35%) between 10 and 20 min, and 289 (30%) more than 20 min. Over half the total respondents (591, 54%) felt they did not receive adequate support when they were informed about being HIV positive, with 249 (19%) experiencing feelings of rejection. People who were diagnosed as HIV positive after 1994 reported more frequently receiving adequate support, information and understanding when the positive test result was revealed compared with those diagnosed before 1990. CONCLUSION: A large number of our study participants did not endorse the way HIV tests were conducted and positive test results revealed. Although there was an improvement over time in the way HIV tests were conducted, they often did not conform to international guidelines.
Asunto(s)
Serodiagnóstico del SIDA/métodos , Serodiagnóstico del SIDA/psicología , Actitud Frente a la Salud , Infecciones por VIH/diagnóstico , Infecciones por VIH/psicología , Revelación de la Verdad , Serodiagnóstico del SIDA/normas , Adaptación Psicológica , Adolescente , Adulto , Anciano , Escolaridad , Europa (Continente) , Femenino , Infecciones por VIH/transmisión , Humanos , Consentimiento Informado , Masculino , Persona de Mediana Edad , Motivación , Guías de Práctica Clínica como Asunto , Derivación y Consulta , Rechazo en Psicología , Apoyo Social , Encuestas y Cuestionarios , Factores de TiempoRESUMEN
BACKGROUND: A high proportion of individuals receiving highly active antiretroviral treatment (HAART) complain of sexual dysfunction (SD), encompassing a lack of desire or erectile dysfunction. OBJECTIVE: To determine whether SD was associated with particular components of the HAART regimens and to identify risk factors for the development of SD in patients on HAART. METHODS: A survey among patients with HIV infection using an anonymous questionnaire was conducted in 10 European countries between December 1998 and December 1999. A total of 904 individuals currently receiving antiretroviral agents were included in the analyses. RESULTS: A decrease in sexual interest was significantly more frequently reported by subjects (men and women) using HAART containing protease inhibitors (PI) (308/766, 40%), compared with PI-naive patients (22/138, 16%; OR 3.55; 95% CI 2.15--5.89). In addition, a significantly larger number of PI-experienced men reported a decrease in sexual potency (216/628, 34%) compared with PI-naive men (12/99, 12%; OR 2.56; 95% CI 1.33--5.03). In multivariate analyses the following factors were associated with a decrease in sexual interest: a current PI-containing regimen, a history of a PI regimen, symptomatic HIV infection, age and homosexual contact as HIV transmission mode. Factors associated with a decrease in sexual potency were: current use of a PI-containing regimen, symptomatic HIV disease, age and the use of tranquillisers. CONCLUSION: SD appears to be a common side-effect of HAART regimens containing a PI. The potential association between SD and other side-effects of HAART, such as lipodystrophy syndrome and neuropathy, should be investigated further.
Asunto(s)
Infecciones por VIH/tratamiento farmacológico , Inhibidores de la Proteasa del VIH/efectos adversos , Disfunciones Sexuales Psicológicas/inducido químicamente , Adulto , Terapia Antirretroviral Altamente Activa/efectos adversos , Disfunción Eréctil/inducido químicamente , Femenino , Infecciones por VIH/transmisión , Inhibidores de la Proteasa del VIH/uso terapéutico , Humanos , Indinavir/efectos adversos , Indinavir/uso terapéutico , Masculino , Análisis Multivariante , Nelfinavir/efectos adversos , Nelfinavir/uso terapéutico , Prevalencia , Factores de Riesgo , Ritonavir/efectos adversos , Ritonavir/uso terapéutico , Disfunciones Sexuales Psicológicas/epidemiología , Encuestas y CuestionariosRESUMEN
International guidelines for the treatment of human immunodeficiency virus (HIV) infection change rapidly. They are mainly based on results from large-scale randomized clinical trials, but also on hypotheses. The objective of the study was to look at the use of antiretrovirals (ARVs) in different HIV treatment centres in Europe. Between August 1996 and September 1997 self-administered anonymous questionnaires were distributed to persons with HIV infection at inpatient and outpatient departments in 11 European countries; 1,366 people completed the questionnaire. Important differences in use of ARVs were noted between different centres. Zidovudine was the drug that was used predominantly in all countries and by 77% of all patients; the use of didanosine, zalcitabine and stavudine differed widely. Use of ARVs was found to be lower for people who reported intravenous drug use (compared to homosexual transmission), people with a low education level, and those with a monthly income lower than 992 Euro. The use of a protease inhibitor containing ARV treatment regimen was significantly lower in the centres in the south of Europe. Between 1996 and 1997, many persons with HIV infection in Europe received a suboptimal ARV treatment regimen. Use of ARVs should be improved for intravenous drug users, persons with lower educational level and lower income.
Asunto(s)
Fármacos Anti-VIH/uso terapéutico , Infecciones por VIH/tratamiento farmacológico , Adolescente , Adulto , Anciano , Terapia Antirretroviral Altamente Activa/estadística & datos numéricos , Actitud Frente a la Salud , Protocolos Clínicos/clasificación , Protocolos Clínicos/normas , Combinación de Medicamentos , Europa (Continente)/epidemiología , Femenino , Infecciones por VIH/epidemiología , Inhibidores de la Proteasa del VIH/uso terapéutico , Humanos , Masculino , Persona de Mediana Edad , Encuestas y CuestionariosAsunto(s)
Infecciones Oportunistas Relacionadas con el SIDA/tratamiento farmacológico , Antivirales/uso terapéutico , VIH-1/genética , Hepatitis C Crónica/tratamiento farmacológico , Ribavirina/uso terapéutico , Carga Viral , Infecciones Oportunistas Relacionadas con el SIDA/virología , Adulto , Terapia Antirretroviral Altamente Activa , Femenino , Seropositividad para VIH/tratamiento farmacológico , Seropositividad para VIH/virología , Humanos , Interferón alfa-2 , Interferón-alfa/uso terapéutico , Masculino , Persona de Mediana Edad , ARN Viral/sangre , Proteínas RecombinantesAsunto(s)
Infecciones por VIH/tratamiento farmacológico , Infecciones por VIH/inmunología , Anticuerpos Antihepatitis/análisis , Antígenos de Superficie de la Hepatitis B/análisis , Interleucina-2/uso terapéutico , Anticuerpos Antihepatitis/inmunología , Antígenos de Superficie de la Hepatitis B/inmunología , Humanos , Proteínas Recombinantes/uso terapéuticoAsunto(s)
Infecciones Oportunistas Relacionadas con el SIDA/diagnóstico , Síndrome de Inmunodeficiencia Adquirida/complicaciones , Criptococosis/diagnóstico , Adulto , Anfotericina B/uso terapéutico , Antifúngicos/uso terapéutico , Cryptococcus neoformans/aislamiento & purificación , Quimioterapia Combinada , Flucitosina/uso terapéutico , Humanos , Masculino , Peritonitis/microbiologíaRESUMEN
Forty-six heroin abusers were hospitalized and treated with meperidine either alone or in association with clonidine. Meperidine was given orally in rapidly decreasing doses according to three different schedules. The majority of patients (87%) successfully completed the detoxification program. The best meperidine starting posology was 200 mg four times daily, which allowed stoppage of the opioid treatment after gradual reduction of the daily dose in a mean time of 9.5 days. Association with clonidine was not proven to be useful. This study shows that meperidine can be effectively used in rapidly decreasing doses in the pharmacological detoxification treatment of hospitalized heroin addicts.