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1.
Enferm Infecc Microbiol Clin ; 30(8): 472-8, 2012 Oct.
Artículo en Español | MEDLINE | ID: mdl-22939565

RESUMEN

The immigrant population in Spain, whether legal or not, has been entitled to healthcare under the same conditions as the Spanish population since the year 2000. The entry into vigour of the Royal Decree-Law 12/2012 of 20 April has significantly restricted this right, so that unauthorized or non-resident foreigners may now only receive emergency care, if they are under 18 or pregnant women. Out of an estimated 459,909 illegal immigrants in our country, 2,700 to 4,600 are probably infected with HIV; 1,800 to 3,220 know that they are infected, and 80% of the latter could receive antiretroviral treatment. The Royal Decree-Law is likely to cause many undesirable consequences in this population infected with HIV: increasing mortality, promoting the emergence of opportunistic diseases, increasing hospital admissions, increasing infections in the population (by HIV and other pathogens), or contributing to mother to child transmission of HIV. The expected increase in morbidity and mortality will be a greater cost in patient care, a cost which will be significantly higher in the more immunosuppressed patients. Therefore, the enforcement of the Royal Decree-Law will be much less cost-effective in the short term than was expected, and will negatively affect our country's public health, especially for those patients infected with HIV who will not be covered, thus increasing healthcare medium to long term costs, and moving away from the international health goals that were established.


Asunto(s)
Infecciones por VIH/epidemiología , Accesibilidad a los Servicios de Salud/legislación & jurisprudencia , Programas Nacionales de Salud/legislación & jurisprudencia , Migrantes/legislación & jurisprudencia , Infecciones Oportunistas Relacionadas con el SIDA/economía , Infecciones Oportunistas Relacionadas con el SIDA/etnología , Fármacos Anti-VIH/economía , Fármacos Anti-VIH/uso terapéutico , Análisis Costo-Beneficio , Femenino , Predicción , Objetivos , Infecciones por VIH/tratamiento farmacológico , Infecciones por VIH/economía , Infecciones por VIH/etnología , Infecciones por VIH/transmisión , Costos de la Atención en Salud , Política de Salud/economía , Política de Salud/legislación & jurisprudencia , Política de Salud/tendencias , Recursos en Salud/economía , Recursos en Salud/estadística & datos numéricos , Accesibilidad a los Servicios de Salud/economía , Humanos , Masculino , Morbilidad/tendencias , Mortalidad/tendencias , Programas Nacionales de Salud/economía , Embarazo , Complicaciones Infecciosas del Embarazo/etnología , Política Pública/economía , Política Pública/legislación & jurisprudencia , Política Pública/tendencias , España/epidemiología , Migrantes/estadística & datos numéricos , Cobertura Universal del Seguro de Salud/legislación & jurisprudencia
3.
Enferm Infecc Microbiol Clin ; 26 Suppl 16: 12-20, 2008 Dec.
Artículo en Español | MEDLINE | ID: mdl-19572439

RESUMEN

Simplification of triple antiretroviral therapy to lopinavir/ritonavir (LPV/r) monotherapy in patients with well-controlled viremia for prolonged periods (more than 6 months) without prior failure with a protease inhibitor has been proposed as a strategy that could reduce the toxicity and costs of antiretroviral therapy in the long term while also preserving other therapeutic options. The results of several studies are currently available, some of which had a large number of patients and follow-up of up to 4 years. These studies indicate that this strategy is safe and efficacious, thus allowing its clinical use when indicated. This strategy may be especially useful in reducing the costs of treatment in countries with scarce economic resources. The role of LPV/r monotherapy in the prevention and management of lipodystrophy and in improving the selection of patients with an optimal risk-benefit ratio remains to be defined.


Asunto(s)
Infecciones por VIH/tratamiento farmacológico , Inhibidores de la Proteasa del VIH/uso terapéutico , VIH-1/efectos de los fármacos , Pirimidinonas/uso terapéutico , Ritonavir/uso terapéutico , Fármacos Anti-VIH/efectos adversos , Ensayos Clínicos como Asunto/estadística & datos numéricos , Control de Costos , Países en Desarrollo , Combinación de Medicamentos , Estudios de Seguimiento , Infecciones por VIH/economía , Inhibidores de la Proteasa del VIH/administración & dosificación , Inhibidores de la Proteasa del VIH/efectos adversos , Inhibidores de la Proteasa del VIH/economía , VIH-1/enzimología , VIH-1/fisiología , Síndrome de Lipodistrofia Asociada a VIH/prevención & control , Humanos , Lopinavir , Estudios Multicéntricos como Asunto , Proyectos Piloto , Estudios Prospectivos , Pirimidinonas/administración & dosificación , Pirimidinonas/efectos adversos , Pirimidinonas/economía , Ensayos Clínicos Controlados Aleatorios como Asunto/estadística & datos numéricos , Ritonavir/administración & dosificación , Ritonavir/efectos adversos , Ritonavir/economía , Resultado del Tratamiento , Carga Viral , Viremia/tratamiento farmacológico , Replicación Viral/efectos de los fármacos
4.
Med Clin (Barc) ; 119(19): 721-4, 2002 Nov 30.
Artículo en Español | MEDLINE | ID: mdl-12487966

RESUMEN

BACKGROUND AND OBJECTIVE: To know the durability of consecutive regimens of antiretroviral treatment is important to design a long-term therapy, but there is not much information about this subject. PATIENTS AND METHOD: Retrospective epidemiological study of a sample of 401 patients who began antiretroviral treatment between January 1997 and April 2000 at ten Spanish hospitals. The duration of each consecutive antiretroviral regimen was calculated and the reasons for modification and discontinuation were described. RESULTS: In the 3 years and 3 months covered by the study, 48.6% of the patients received more than one regimen of therapy. Seventy five of the initial prescribed combinations included protease inhibitors. Median duration of consecutive lines of therapy was decreasing: 560, 360, 330 and 202 days for the first, second, third and fourth regimens, respectively. The main reason to modification was intolerance or toxicity (46.2, 49.1 and 47.1% for the first, second and third modification). A fifth of changes was originated by difficulties to follow the therapy. Virological failure was the reason for modification in 21.8, 24.5 and 26.5% of first, second and third changes. CONCLUSIONS: Duration of consecutive antiretroviral regimens progressively decreases. Intolerance or drug toxicity were the main reasons conditioning the change of treatment.


Asunto(s)
Fármacos Anti-VIH/uso terapéutico , Infecciones por VIH/tratamiento farmacológico , Infecciones por VIH/epidemiología , Adulto , Femenino , Humanos , Masculino , Estudios Retrospectivos , España , Factores de Tiempo
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