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1.
Pharmacotherapy ; 44(7): 488-493, 2024 Jul.
Article de Anglais | MEDLINE | ID: mdl-39005161

RÉSUMÉ

Five long-acting (LA) antiretrovirals (ARVs) are currently available in a limited number of countries worldwide for HIV-1 prevention or treatment - cabotegravir, rilpivirine, lenacapavir, ibalizumab, and dapivirine. Implementing use of LA ARVs in routine clinical practice requires significant changes to the current framework of HIV-1 prevention, treatment, and service provision. Given the novelty, complexity, and interdisciplinary requirements of safe and optimal use of LA ARVs, consensus recommendations on the use of LA ARVs will assist clinicians in optimizing use of these agents. The purpose of these recommendations is to provide guidance for the clinical use of LA ARVs for HIV-1 treatment and prevention. In addition, future areas of research are identified and discussed.


Sujet(s)
Agents antiVIH , Infections à VIH , VIH-1 (Virus de l'Immunodéficience Humaine de type 1) , Humains , Infections à VIH/traitement médicamenteux , Infections à VIH/prévention et contrôle , VIH-1 (Virus de l'Immunodéficience Humaine de type 1)/effets des médicaments et des substances chimiques , Agents antiVIH/usage thérapeutique , Agents antiVIH/administration et posologie , Préparations à action retardée , Consensus , Antirétroviraux/usage thérapeutique , Antirétroviraux/administration et posologie
2.
Pharmacotherapy ; 44(7): 494-538, 2024 Jul.
Article de Anglais | MEDLINE | ID: mdl-39005160

RÉSUMÉ

Five long-acting (LA) antiretrovirals (ARVs) are currently available in a limited number of countries worldwide for HIV-1 prevention or treatment-cabotegravir, rilpivirine, lenacapavir, ibalizumab, and dapivirine. Implementing use of LA ARVs into routine clinical practice requires significant changes to the current framework of HIV-1 prevention, treatment, and service provision. Given the novelty, complexity, and interdisciplinary requirements needed to safely and optimally utilize LA ARVs, consensus recommendations on the use of LA ARVs will assist clinicians in optimizing use of these agents. The purpose of these recommendations is to provide guidance for the clinical use of LA ARVs for HIV-1 treatment and prevention. In addition, future areas of research are also identified and discussed.


Sujet(s)
Agents antiVIH , Infections à VIH , VIH-1 (Virus de l'Immunodéficience Humaine de type 1) , Humains , Infections à VIH/traitement médicamenteux , Infections à VIH/prévention et contrôle , VIH-1 (Virus de l'Immunodéficience Humaine de type 1)/effets des médicaments et des substances chimiques , Agents antiVIH/usage thérapeutique , Agents antiVIH/administration et posologie , Préparations à action retardée , Consensus , Antirétroviraux/usage thérapeutique , Antirétroviraux/administration et posologie
3.
Sci Rep ; 14(1): 14234, 2024 06 20.
Article de Anglais | MEDLINE | ID: mdl-38902326

RÉSUMÉ

Whether, and how, cardioprotective effects of antiretroviral treatment (ART) in adolescents with perinatal HIV infection (APHIV) vary with age at treatment initiation is unknown. We used magnetic resonance imaging to compare cardiac status between APHIV initiated on ART at < 5 years of age (early ART, n = 37) and ≥ 5 years of age (delayed ART, n = 34) versus HIV-uninfected peers (n = 21), reporting z-score mean differences adjusted for confounders. Relative to HIV-uninfected adolescents, APHIV with early ART had higher left ventricular (LV) global circumferential strain (GCS) [adjusted mean (95%CI) z-score: 0.53 (0.13, 0.92)] and maximum indexed left atrium volume (LAVi) [adjusted z-score: 0.55 (0.08, 1.02)]. In contrast, APHIV with delayed ART had greater indexed LV end-diastolic volume (LVEDVi) [adjusted z-score: 0.47 (0.09, 0.86)] and extracellular volume fraction [adjusted z-score: 0.79 (0.20, 1.37)], but lower GCS [adjusted z-score: -0.51 (-0.91, -0.10)] than HIV-uninfected peers. APHIV had distinct albeit subclinical cardiac phenotypes depending on ART initiation age. Changes in early ART suggested comparatively worse diastology with preserved systolic function while delayed ART was associated with comparatively increased diffuse fibrosis and LV dilatation with reduced systolic function. The long-term clinical significance of these changes remains to be determined.


Sujet(s)
Infections à VIH , Humains , Infections à VIH/traitement médicamenteux , Femelle , Adolescent , Mâle , VIH-1 (Virus de l'Immunodéficience Humaine de type 1)/effets des médicaments et des substances chimiques , Imagerie par résonance magnétique , Enfant , Agents antiVIH/usage thérapeutique , Agents antiVIH/administration et posologie , Antirétroviraux/administration et posologie , Antirétroviraux/usage thérapeutique , Transmission verticale de maladie infectieuse/prévention et contrôle , Enfant d'âge préscolaire
4.
J Clin Invest ; 134(14)2024 Jun 04.
Article de Anglais | MEDLINE | ID: mdl-38833307

RÉSUMÉ

Despite effective antiretroviral therapy (ART), persons living with HIV harbor reservoirs of persistently infected CD4+ cells, which constitute a barrier to cure. Initiation of ART during acute infection reduces the size of the HIV reservoir, and we hypothesized that in addition, it would favor integration of proviruses in HIV-specific CD4+ T cells, while initiation of ART during chronic HIV infection would favor relatively more proviruses in herpesvirus-specific cells. We further hypothesized that proviruses in acute ART initiators would be integrated into antiviral genes, whereas integration sites (ISs) in chronic ART initiators would favor genes associated with cell proliferation and exhaustion. We found that the HIV DNA distribution across HIV-specific versus herpesvirus-specific CD4+ T cells was as hypothesized. HIV ISs in acute ART initiators were significantly enriched in gene sets controlling lipid metabolism and HIF-1α-mediated hypoxia, both metabolic pathways active in early HIV infection. Persistence of these infected cells during prolonged ART suggests a survival advantage. ISs in chronic ART initiators were enriched in a gene set controlling EZH2 histone methylation, and methylation has been associated with diminished long terminal repeat transcription. These differences that we found in antigen specificities and IS distributions within HIV-infected cells might be leveraged in designing cure strategies tailored to the timing of ART initiation.


Sujet(s)
Lymphocytes T CD4+ , Infections à VIH , VIH-1 (Virus de l'Immunodéficience Humaine de type 1) , Provirus , Intégration virale , Humains , Infections à VIH/traitement médicamenteux , Infections à VIH/génétique , Infections à VIH/virologie , Infections à VIH/immunologie , Provirus/génétique , Lymphocytes T CD4+/immunologie , Lymphocytes T CD4+/virologie , VIH-1 (Virus de l'Immunodéficience Humaine de type 1)/génétique , Mâle , Femelle , Adulte , Protéine-2 homologue de l'activateur de Zeste/génétique , Protéine-2 homologue de l'activateur de Zeste/métabolisme , ADN viral/génétique , Antirétroviraux/administration et posologie , Antirétroviraux/usage thérapeutique
5.
Br J Nurs ; 33(11): S12-S17, 2024 Jun 06.
Article de Anglais | MEDLINE | ID: mdl-38850143

RÉSUMÉ

Oral antiretroviral therapy (ART) is extremely effective, allowing people living with HIV to have a normal life expectancy. Most treatments consist of oral tablets that must be taken at the same time every day for the rest of an individual's life. For a variety of reasons, some people cannot adhere to a daily regimen, resulting in a deterioration in their health. The introduction in 2021 of long-acting injectable ART has provided an alternative option for those who would prefer not to take oral therapy. This article provides an overview of the practicalities and challenges of setting up nurse clinics to administer these injections. It also highlights how this type of treatment has improved the quality of life for people receiving them. HIV nurse specialists are leading the way in delivering this innovative new treatment, and the article concludes by discussing which patients may benefit from injectables in the future. This guide is aimed at nurses who work within the HIV field or are supporting this treatment in other settings, for example in outpatient parenteral antimicrobial therapy (OPAT) services.


Sujet(s)
Infections à VIH , Humains , Infections à VIH/traitement médicamenteux , Infections à VIH/soins infirmiers , Injections , Agents antiVIH/administration et posologie , Agents antiVIH/usage thérapeutique , Guides de bonnes pratiques cliniques comme sujet , Antirétroviraux/usage thérapeutique , Antirétroviraux/administration et posologie , Qualité de vie
6.
Pan Afr Med J ; 47: 113, 2024.
Article de Anglais | MEDLINE | ID: mdl-38828427

RÉSUMÉ

Introduction: the increasing number of people receiving antiretroviral therapy (ART) in sub-Saharan Africa has stressed already overburdened health systems. A care model utilizing community-based peer-groups (ART Co-ops) facilitated by community health workers (CHW) was implemented (2016-2018) to address these challenges. In 2018, a post-intervention study assessed perceptions of the intervention. Methods: forty participants were engaged in focus group discussions consisting of ART Co-op clients, study staff, and health care providers from Kitale HIV clinic. Data were analyzed thematically for content on the intervention, challenges, and recommendations for improvement. Results: all participants liked the intervention. However, some reported traveling long distances to attend ART Co-op meetings and experiencing stigma with ART Co-ops participation. The ART Co-op inclusion criteria were considered appropriate; however, additional outreach to deliberately include spouses living with HIV, the disabled, the poor, and HIV pregnant women was recommended. Participants liked CHW-directed quarterly group meetings which included ART distribution, adherence review, and illness identification. The inability of the CHW to provide full clinical care, inconvenient meeting venues, poor timekeeping, and non-attendance behaviors were noted as issues. Participants indicated that program continuation, regular CHW training, rotating meetings at group members´ homes, training ART Co-ops leaders to assume CHW tasks, use of pill diaries to check adherence, nutritional support, and economically empowering members through income generation projects would be beneficial. Conclusion: the intervention was viewed positively by both clinic staff and clients. They identified specific challenges and generated actionable key considerations to improve access and acceptability of the community-based model of care.


Sujet(s)
Agents antiVIH , Agents de santé communautaire , Groupes de discussion , Infections à VIH , Humains , Kenya , Infections à VIH/traitement médicamenteux , Femelle , Agents de santé communautaire/organisation et administration , Mâle , Adulte , Agents antiVIH/administration et posologie , Stigmate social , Groupe de pairs , Antirétroviraux/usage thérapeutique , Antirétroviraux/administration et posologie , Adhésion au traitement médicamenteux , Adulte d'âge moyen , Jeune adulte , Services de santé communautaires/organisation et administration , Perception
8.
Expert Rev Clin Pharmacol ; 17(7): 589-614, 2024 Jul.
Article de Anglais | MEDLINE | ID: mdl-38753455

RÉSUMÉ

INTRODUCTION: People with HIV are living longer due to advances in antiretroviral therapy. With improved life expectancy comes an increased lifetime risk of comorbid conditions - such as cardiovascular disease and cancer - and polypharmacy. Older adults, particularly those living with HIV, are more vulnerable to drug interactions and adverse effects, resulting in negative health outcomes. AREA COVERED: Antiretrovirals are involved in many potential drug interactions with medications used to treat common comorbidities and geriatric conditions in an aging population of people with HIV. We review the mechanisms and management of significant drug-drug interactions involving antiretroviral medications and non-antiretroviral medications commonly used among older people living with HIV. The management of these interactions may require dose adjustments, medication switches to alternatives, enhanced monitoring, and considerations of patient- and disease-specific factors. EXPERT OPINION: Clinicians managing comorbid conditions among older people with HIV must be particularly vigilant to side effect profiles, drug-drug interactions, pill burden, and cost when optimizing treatment. To support healthier aging among people living with HIV, there is a growing need for antiretroviral stewardship, multidisciplinary care models, and advances that promote insight into the correlations between an individual, their conditions, and their medications.


Sujet(s)
Agents antiVIH , Interactions médicamenteuses , Infections à VIH , Polypharmacie , Humains , Infections à VIH/traitement médicamenteux , Sujet âgé , Agents antiVIH/administration et posologie , Agents antiVIH/effets indésirables , Agents antiVIH/pharmacologie , Comorbidité , Facteurs âges , Relation dose-effet des médicaments , Espérance de vie , Antirétroviraux/effets indésirables , Antirétroviraux/administration et posologie , Surveillance des médicaments/méthodes
10.
Sci Rep ; 14(1): 11573, 2024 05 21.
Article de Anglais | MEDLINE | ID: mdl-38773172

RÉSUMÉ

GSK2838232 (GSK8232) is a second-generation maturation inhibitor (MI) developed for the treatment of HIV with excellent broad-spectrum virological profiles. The compound has demonstrated promising clinical results as an orally administered agent. Additionally, the compound's physical and pharmacological properties present opportunities for exploitation as long-acting parenteral formulations. Despite unique design constraints including solubility and dose of GSK8232, we report on three effective tunable drug delivery strategies: active pharmaceutical ingredient (API) suspensions, ionic liquids, and subdermal implants. Promising sustained drug release profiles were achieved in rats with each approach. Additionally, we were able to tune drug release rates through a combination of passive and active strategies, broadening applicability of these formulation approaches beyond GSK8232. Taken together, this report is an important first step to advance long-acting formulation development for critical HIV medicines that do not fit the traditional profile of suitable long-acting candidates.


Sujet(s)
Libération de médicament , Animaux , Rats , Interactions hydrophobes et hydrophiles , Préparations à action retardée , Agents antiVIH/administration et posologie , Agents antiVIH/composition chimique , Agents antiVIH/pharmacologie , Agents antiVIH/pharmacocinétique , Systèmes de délivrance de médicaments/méthodes , Liquides ioniques/composition chimique , Rat Sprague-Dawley , Mâle , Solubilité , Infections à VIH/traitement médicamenteux , Antirétroviraux/administration et posologie , Antirétroviraux/composition chimique
11.
Med. infant ; 31(1): 44-50, Marzo 2024. Ilus, Tab
Article de Espagnol | LILACS, UNISALUD, BINACIS | ID: biblio-1553048

RÉSUMÉ

El uso de antirretrovirales (ARV) en el embarazo, el parto y el recién nacido y la aplicación de tratamientos combinados en los niños se han asociado con una disminución del sida en pediatría y el aumento de la sobrevida. La introducción de los inhibidores de integrasa en una dosis diaria ha eliminado barreras para la adherencia, pero los medicamentos orales diarios continúan planteando problemas de privacidad y estigma. Las nuevas tecnologías de administración de los medicamentos y las nuevas drogas junto con la combinación de ARV y los anticuerpos ampliamente neutralizantes (bNAb), ofrecen un potencial de opciones futuras para el tratamiento pediátrico del HIV. Los bNAb son anticuerpos que pueden reconocer diferentes tipos de HIV, bloquear su entrada en las células sanas y ayudar a destruir las células ya infectadas, pueden administrarse por vía parenteral y constituyen un enfoque novedoso y seguro con potencial para el tratamiento y la prevención del HIV, incluida la transmisión vertical. En los lactantes que contraen HIV, los bNAb podrían ofrecer ventajas terapéuticas al reducir el reservorio del virus, mejorar la inmunidad adquirida y, en el futuro, proporcionar un camino hacia la cura funcional. Dentro de los ARV inyectables de acción prolongada, cabotegravir/ rilpivirina se ha incorporado en las guías internacionales de adultos y adolescentes tanto para el tratamiento como para la prevención. A medida que el tratamiento del HIV en adultos va evolucionando, es fundamental asegurar que los neonatos, lactantes, niños y adolescentes tengan acceso a las mejores opciones de tratamiento y prevención a lo largo de su vida (AU)


The use of antiretrovirals (ARVs) during pregnancy, delivery, and in the newborn and the use of combination therapy in children have been associated with a decrease in pediatric AIDS and increased survival. The introduction of once-daily integrase inhibitors has removed barriers to adherence, but daily oral medications continue to pose privacy and stigma issues. New drug delivery technologies and new drugs along with the combination of ARVs and broadly neutralizing antibodies (bNAbs) offer potential future options for pediatric HIV treatment. bNAbs are antibodies that can recognize different types of HIV, block their entry into healthy cells and help destroy already infected cells, can be delivered parenterally, and represent a novel and safe approach with potential for the treatment and prevention of HIV, including mother-to-child transmission. In infants who contract HIV, bNBAs could offer therapeutic advantages by reducing the viral reservoir, enhancing acquired immunity and, in the future, providing a pathway to a functional cure. Within the long-acting injectable ARVs, cabotegravir/rilpivirine has been incorporated into international guidelines for adults and adolescents for both treatment and prevention. As adult HIV treatment evolves, it is critical to ensure that newborns, infants, children and adolescents have access to the best treatment and prevention options throughout their lives (AU)


Sujet(s)
Infections à VIH/prévention et contrôle , Infections à VIH/traitement médicamenteux , Antirétroviraux/administration et posologie , Antirétroviraux/usage thérapeutique , Transmission verticale de maladie infectieuse/prévention et contrôle , Préparation de médicament
13.
CPT Pharmacometrics Syst Pharmacol ; 13(5): 781-794, 2024 05.
Article de Anglais | MEDLINE | ID: mdl-38429889

RÉSUMÉ

There is growing interest in the use of long-acting (LA) injectable drugs to improve treatment adherence. However, their long elimination half-life complicates the conduct of clinical trials. Physiologically-based pharmacokinetic (PBPK) modeling is a mathematical tool that allows to simulate unknown clinical scenarios for LA formulations. Thus, this work aimed to develop and verify a mechanistic intramuscular PBPK model. The framework describing the release of a LA drug from the depot was developed by including both the physiology of the injection site and the physicochemical properties of the drug. The framework was coded in Matlab® 2020a and implemented in our existing PBPK model for the verification step using clinical data for LA cabotegravir, rilpivirine, and paliperidone. The model was considered verified when the simulations were within twofold of observed data. Furthermore, a local sensitivity analysis was conducted to assess the impact of various factors relevant for the drug release from the depot on pharmacokinetics. The PBPK model was successfully verified since all predictions were within twofold of observed clinical data. Peak concentration, area under the concentration-time curve, and trough concentration were sensitive to media viscosity, drug solubility, drug density, and diffusion layer thickness. Additionally, inflammation was shown to impact the drug release from the depot. The developed framework correctly described the release and the drug disposition of LA formulations upon intramuscular administration. It can be implemented in PBPK models to address pharmacological questions related to the use of LA formulations.


Sujet(s)
Simulation numérique , Modèles biologiques , Rilpivirine , Humains , Injections musculaires , Rilpivirine/pharmacocinétique , Rilpivirine/administration et posologie , Palmitate de palipéridone/pharmacocinétique , Palmitate de palipéridone/administration et posologie , Préparations à action retardée/pharmacocinétique , Mâle , Adulte , Antirétroviraux/pharmacocinétique , Antirétroviraux/administration et posologie , Libération de médicament , Adulte d'âge moyen , Agents antiVIH/pharmacocinétique , Agents antiVIH/administration et posologie , Femelle , Pyridones , Pipérazinediones
14.
Pharm. pract. (Granada, Internet) ; 22(1): 1-14, Ene-Mar, 2024. tab, graf
Article de Anglais | IBECS | ID: ibc-231365

RÉSUMÉ

Objective: This study assessed antiretroviral adherence and treatment outcomes among outpatients with human immunodeficiency virus (HIV). Methods: A cross-sectional study was performed on patients with HIV over 18 years old receiving antiretroviral therapy for at least six months at an Indonesian clinic, from January to March 2021. The previously validated self-reported adherence questionnaire was used to recall antiretroviral use. Viral load and CD4 were indicators of treatment outcomes. Binary logistic regression was used to explore factors associated with nonadherence and poor treatment outcomes. Results: Ninety-five patients were included in the study (male 70.5%, median [interquartile range, IQR] age 35 [29–42] years, and median [IQR] treatment duration 29 [15–49] months). Adherence greater than 95% was observed in 89.5%, 88.4%, 95.8% of the patients in the past week, month, and three months, respectively. Patients with secondary education or lower were associated with low adherence (adjusted odds ratio, aOR: 7.73, 95%CI: 1.12– 53.19). Viral suppression and improved CD4 were observed in 83.2% and 68.4% of the patients, respectively. Taking non-nucleoside reverse transcriptase inhibitors (NNRTIs)-based regimen was associated with viral suppression (aOR: 0.01, 95%CI: 0.00–0.14) as well as high CD4 count (aOR: 0.16, 95%CI: 0.03– 0.83). Being diagnosed with stage 4 of HIV (aOR: 72.38, 95%CI: 3.11–1687.28) and having adherence of 95% or lower (aOR: 68.84, 95%CI: 4.86–974.89) were associated with non-suppressed viral load, and having HIV stage 3 (aOR: 7.81, 95%CI: 1.26–48.40) or 4 (aOR: 26.15, 95%CI: 3.42–200.10) at diagnosis was associated with low CD4. Conclusion: Rates of self-reported adherence and treatment outcomes were high. Secondary education or lower was a predictor of low adherence. Using NNRTIs-based therapy was associated with good treatment outcomes; meanwhile, stage 3 or 4 of HIV at diagnosis and low adherence were predictors of poor outcomes. Therefore, strategies to improve adherence and treatment outcomes are warranted.(AU)


Sujet(s)
Humains , Mâle , Femelle , Résultat thérapeutique , Adhésion et observance thérapeutiques , Antirétroviraux/administration et posologie , VIH (Virus de l'Immunodéficience Humaine) , Charge virale , Numération des lymphocytes CD4 , Indonésie , Études transversales , Enquêtes et questionnaires
16.
Farm Hosp ; 48(3): 101-107, 2024.
Article de Anglais, Espagnol | MEDLINE | ID: mdl-38336553

RÉSUMÉ

INTRODUCTION: In the context of the advancement of antiretroviral therapy and as the characteristics of people living with HIV progress toward an ageing population, understanding the causes of treatment interruption becomes crucial. The aim of the study was to determine the change in reasons for antiretroviral treatment discontinuation for 12 years. Secondarily, compare annual antiretroviral regimen discontinuation rate and factors associated. METHODS: We conducted an analysis using data from people living with HIV who were receiving antiretroviral therapy and discontinued it for any reason. The study included people with HIV infection who visited an outpatient hospital pharmacy clinic from January 2010 to December 2021. Two periods were differentiated for the analysis: 2010-2015 and 2016-2021. The reasons for antiretroviral treatment discontinuation followed classification described by Swiss cohort. In the context of this study, it is pertinent to note that the term "discontinuation" is employed synonymously with "interruption". The term "discontinuation" will be consistently used in this article to refer to the act of switching or stopping antiretroviral treatment. To examine factors associated with antiretroviral therapy discontinuation, we utilised Kaplan-Meier methods and Cox proportional models. RESULTS: We included 789 people living with HIV, predominantly male (81.5%). The main reason for discontinuation was clinical decision (50.2%) followed by adverse effects (37.9%). Focusing on clinical decision, we observed a trend change that went from antiretroviral treatment simplification regimen (56.1%) in the first part of the period analysed to the therapeutic optimisation (53.6%) in the second half. Furthermore, factors that were statistically significantly associated with antiretroviral treatment discontinuation were people with HIV≥50 years (HR 1.60; 95%CI 1.25-2.04), post-discontinuation single-tablet regimen (HR 1.49; 95%CI 1.06-2.11) and antiretroviral drug classes. CONCLUSION: Over the 12 years, there has been a change in the main cause of antiretroviral treatment discontinuation, currently therapeutic optimisation being the main reason. Integrase inhibitors-based regimens and single-tablet regimen strategies were less likely to be discontinued than others antiretroviral drug classes, allowing for better clinical management due to the efficacy profile, especially in people living with HIV≥50 years with comorbidities.


Sujet(s)
Infections à VIH , Humains , Infections à VIH/traitement médicamenteux , Mâle , Femelle , Adulte d'âge moyen , Adulte , Agents antiVIH/usage thérapeutique , Agents antiVIH/administration et posologie , Antirétroviraux/usage thérapeutique , Antirétroviraux/administration et posologie , Sujet âgé , Adhésion au traitement médicamenteux/statistiques et données numériques , Études rétrospectives
17.
Rev. esp. quimioter ; 36(6): 604-611, dec. 2023. tab, graf
Article de Espagnol | IBECS | ID: ibc-228247

RÉSUMÉ

Objetivos. Analizar las modificaciones de la terapia antirre troviral (TAR) y su impacto económico en la práctica clínica diaria. Material y métodos. Estudio observacional, retrospectivo de los pacientes que iniciaron TAR entre 01/2017-12/2021 (se guimiento hasta 12/2022). Variables recogidas: TAR, duración, motivo del cambio y costes del tratamiento. Resultados. 280 pacientes iniciaron TAR. La mediana de durabilidad de la 1ª línea fue: 19,9 meses en 2017 (IC95% 13,9-25,9), 12,2 meses en 2018 (IC95% 4,7-19,7), 27,4 meses en 2019 (IC95% 6,8-48,1) y no se alcanzó la mediana para los años 2020 y 2021 (p p<0,001). De un total de 541 líneas prescri tas, la triple terapia con inhibidores de la proteasa se modificó en el 63,8% (81/127), seguido de los inhibidores de la integrasa 52,1% (159/305), mientras que, la terapia dual (DTG/3TC) solo en el 8,3% (7/84). De un total de 261 modificaciones, la simpli ficación/optimización 47,5% (124/261) fue el principal motivo, seguido de efectos adversos 21,8% (57/261), siendo el 2017 el único año donde ambos motivos se encontraban al mismo nivel. El impacto económico de los cambios supusieron una re ducción del coste medio de 34,0€ [-391,4 a +431,4] al mes/ paciente. El año 2019 es el único año donde estos cambios se asociaron con un incremento del coste adicional medio (23,4€ [-358,3 a +431,4]). Conclusiones. Dejando atrás el fracaso virológico, la sim plificación a regímenes de un solo comprimido y de mayor tolerancia han marcado la nueva la era TAR. Con un impacto económico que, a pesar del punto de inflexión del 2019, refleja una reducción progresiva de costes mantenida en el tiempo (AU)


Objectives. To analyze the modifications of antiretrovi ral therapy (ART) and their economic impact on daily clinical practice. Material and methods. Observational, retrospective study of patients who started ART between 01/2017-12/2021 (follow-up until 12/2022). Variables collected: prescribed ART, duration, the reason for the change, and treatment costs. Results. A total of 280 patients initiated ART therapy. The median durability of 1st line was: 19.9 months in 2017 (95%CI 13.9-25.9), 12.2 months in 2018 (95%CI 4.7-19.7), 27.4 months in 2019 (95%CI 6.8-48.1) and the median was not reached for the years 2020 and 2021 (p<0.001). Triple therapy with protease inhibitors was changed in 63.8% (81/127) of cases, followed by integrase inhibitors 52.1% (159/305), while dual therapy (DTG/3TC) only in 8.3% (7/84). The main cause of dis continuation was simplification/optimization 47.5% (124/261), followed by adverse effects 21.8% (57/261), with 2017 being the only year where simplification/optimization was at the same level as adverse effects. The economic impact of ART changes resulted in an average cost reduction of 34.0€ [-391.4 to +431.4] per month per patient. The year 2019 stands out as the only year where these changes were associated with an increase in mean additional cost (23.4€ [-358.3 to +431.4]). Conclusions. Optimization/simplification accounts for almost half of the reasons for TAR change, with an econom ic impact that, despite the inflection point of 2019, each year manages to exceed the previous one, achieving a progressive cost reduction maintained over time (AU)


Sujet(s)
Humains , Mâle , Femelle , Adulte , Adulte d'âge moyen , Infections à VIH/traitement médicamenteux , Infections à VIH/économie , Agents antiVIH/administration et posologie , Agents antiVIH/économie , Antirétroviraux/administration et posologie , Antirétroviraux/économie , Études rétrospectives
18.
Maputo; s.n; Sn; set 15, 2023. 54 p. tab, graf.
Thèse de Portugais | RSDM | ID: biblio-1527420

RÉSUMÉ

: Introdução: O HIV e SIDA é um problema de saúde pública global, responsável por cerca de 32.7 milhões de mortes de doenças relacionadas à SIDA desde o início da epidemia até o final de 2019, comprometendo a saúde, a força de produção e produtividade. Esse cenário tende a ser mais grave, quando se trata de forças militares, cuja a responsabilidade da defesa e manutenção da paz, recai sobre eles. O objectivo foi avaliar o perfil clinico-epidemiológico e factores associados a não supressão viral em pacientes vivendo com HIV/SIDA assistidas no Centro Integrado de Tratamento no Hospital Militar de Maputo (CITRA/HMM). Métodos: Tratou-se de um estudo transversal analítico com uma abordagem quantitativa, utilizando dados secundários de pacientes em seguimento entre os anos de 2019-2020 no CITRA/HMM. A amostra foi composta por 9.015 indivíduos com idade igual ou superiora 15 anos de idade. A analise de dados foi feita com pacote estatístico STATA versão 16, onde recorreu-se os testes Qui-quadrado de Pearson e a razão de chances/OR com Intervalos de Confiança/IC de 95% e p<0,05, para verificar as diferenças entre às proporções e a associação entre as variáveis em análise, considerando como desfecho o estado de supressão viral: suprimido (<1000 cópias de RNA do HIV/ml) e não suprimido (≥1000 cópias de RNA do HIV/ml). Para o modelo de regressão logística múltipla, apenas foram seleccionadas as variáveis que se mostraram estatisticamente significativas na análise bivariada. Resultados: Dos 9.105 indivíduos inclusos na análise, 4.808 (52,8%) eram do sexo feminino e 1.235 (13,6%) eram militares. A média de idade foi de 47,9 anos (DP±12,1), sendo o grupo etário mais prevalente composto por indivíduos com idades entre 25 e 59 anos, totalizando 7.297 (80,2%) participantes. Entre os analisados, 5.395 (53,3%) tinham resultados de última carga viral, e destes, 4.148 (76,9%) tinham a carga viral suprimida. Embora a maior proporção de supressão viral tenha sido verificada em civis, quando ajustada, essa diferença não demonstrou significância estatística…


Introduction: HIV and AIDS is a global public health problem, responsible for about 32.7 million deaths from AIDS-related diseases from the beginning of the epidemic to the end of 2019, compromising health, workforce and productivity. This scenario tends to be more serious when it comes to military forces, whose responsibility for the defense and maintenance of peace falls on them. The objective was to evaluate the clinical and epidemiological profile and factors associated with viral load non-suppression in patients living with HIV/AIDS at the Military Hospital (CITRA/HMM). Methods: This is a analytic cross-sectional study with a quantitative approach, using secondary data from patients being followed up between the years 2019-2020 at CITRA/HMM. The sample consisted of 9,015 individuals aged 15 years and over. Data analysis was performed with the statistical package STATA, Version 16. Pearson's chi-square test and odds ratio/OR with a confidence interval of 95%CI and p<0,05 were used to verify the differences between the proportions and association between the variables under analysis, considering the state of viral suppression as an outcome: suppressed (<1000 HIV RNA copies/ml) and non-suppressed (≥1000 HIV RNA copies/ml). For the multiple logistic regression model, only the variables that proved to be statistically significant in the bivariate analysis were selected. Results: Of the 9,105 individuals included in the analysis, 4,808 (52.8%) were female and 1,235 (13.6%) were military personnel. The average age was 47.9 years (SD±12.1), with the most prevalent age group being individuals aged between 25 and 59, totalling 7,297 (80.2%) participants. Among those analysed, 5,395 (53.3%) had their last viral load results, and of these, 4,148 (76.9%) had a suppressed viral load. Although the highest proportion of viral suppression was seen in civilians, when adjusted, this difference was not statistically significant…


Sujet(s)
Humains , Mâle , Femelle , Adolescent , Adulte , Adulte d'âge moyen , Charge virale/immunologie , Antirétroviraux/administration et posologie , Syndrome d'immunodéficience acquise/prévention et contrôle , VIH (Virus de l'Immunodéficience Humaine)/classification , Réponse virologique soutenue , Mozambique
19.
JAMA ; 330(8): 736-745, 2023 08 22.
Article de Anglais | MEDLINE | ID: mdl-37606666

RÉSUMÉ

Importance: An estimated 1.2 million persons in the US currently have HIV, and more than 760 000 persons have died of complications related to HIV since the first cases were reported in 1981. Although treatable, HIV is not curable and has significant health consequences. Therefore, effective strategies to prevent HIV are an important public health and clinical priority. Objective: The US Preventive Services Task Force (USPSTF) commissioned a systematic review to evaluate the benefits and harms of preexposure prophylaxis with antiretroviral therapy for the prevention of HIV acquisition, and the diagnostic accuracy of risk assessment tools to identify persons at increased risk of HIV acquisition. Population: Adolescents and adults who do not have HIV and are at increased risk of HIV. Evidence Assessment: The USPSTF concludes with high certainty that there is a substantial net benefit from the use of effective antiretroviral therapy to reduce the risk of acquisition of HIV in persons at increased risk of acquiring HIV. Recommendation: The USPSTF recommends that clinicians prescribe preexposure prophylaxis using effective antiretroviral therapy to persons at increased risk of HIV acquisition to decrease the risk of acquiring HIV. (A recommendation).


Sujet(s)
Antirétroviraux , Infections à VIH , Prophylaxie pré-exposition , Adolescent , Adulte , Humains , Comités consultatifs , Antirétroviraux/administration et posologie , Antirétroviraux/effets indésirables , Antirétroviraux/usage thérapeutique , Infections à VIH/diagnostic , Infections à VIH/épidémiologie , Infections à VIH/étiologie , Infections à VIH/prévention et contrôle , Prophylaxie pré-exposition/méthodes , Prophylaxie pré-exposition/normes , Services de médecine préventive , Santé publique , Appréciation des risques/méthodes , Appréciation des risques/normes , États-Unis/épidémiologie
20.
Rev. chil. infectol ; 40(3): 236-244, jun. 2023. ilus, tab
Article de Espagnol | LILACS | ID: biblio-1515129

RÉSUMÉ

INTRODUCCIÓN: Existe controversia con respecto a los factores que determinan un mayor riesgo de gravedad y complicaciones por COVID-19 en personas que viven con VIH (PVVIH). Asimismo, hay datos limitados sobre el impacto de la vacunación contra SARS-CoV-2 en la hospitalización en esta población. OBJETIVOS: Describir las características clínicas y evolutivas de COVID-19 en PVVIH; Evaluar factores de riesgo para hospitalización; Evaluar el impacto de la vacunación en la hospitalización. Pacientes y MÉTODOS: Estudio observacional, prospectivo, multicéntrico (septiembre de 2020 a junio de 2022). Se registraron variables clínicas, inmunovirológicas, tratamiento antirretroviral (TARV), vacunación contra SARS-CoV-2 y hospitalización en PVVIH con COVID-19. Se realizaron análisis uni y multivariados examinando factores asociados a hospitalización utilizando dos modelos: primer modelo (sin vacunación) y segundo modelo (vacunación, mínimo una dosis). RESULTADOS: Se incluyeron 1.201 PVVIH. La mediana de edad fue 45 años. El 65,3% fueron hombres; el 38,7% presentó comorbilidades. Recibía TARV el 92,8% y presentó carga viral (CV) indetectable el 83,1%. La mediana de linfocitos T CD4+ fue de 600 céls/mm3. El 95,7% presentó síntomas. Las tasas de hospitalización, ingreso a UCI, requerimiento de oxígeno y muerte fueron 17,8%, 2,8%, 10,7% y 1,39%, respectivamente. De acuerdo con el análisis multivariado para el primer modelo, la edad > 60 años y las comorbilidades se asociaron a mayor riesgo de hospitalización, mientras que el sexo femenino y un recuento de linfocitos T CD4+ > 500 céls/mm3 tuvieron un efecto protector. En el segundo modelo sólo las comorbilidades se relacionaron con un mayor riesgo de hospitalización mientras que la vacunación y células CD4+ > 500 céls/mm3 la redujeron. CONCLUSIONES: En PVVIH las comorbilidades se asociaron con mayor tasa de hospitalización, mientras que tener linfocitos T CD4+ elevados y estar vacunado tuvieron un efecto protector. El TARV y la CV no tuvieron impacto en modelo alguno mientras que la edad y el sexo solo influyeron cuando no se consideró la vacunación.


BACKGROUND: There is controversy regarding the factors that determine a greater risk of severity and complications from COVID-19 in people living with HIV (PLHIV). Likewise, there are limited data on the impact of SARS-CoV-2 vaccination on hospitalization in this population. AIMS: To describe clinical characteristics and outcome of COVID-19 in PLHIV; To assess risk factors for hospitalization; To evaluate the impact of vaccination on hospitalization. METHODS: Multicenter, prospective, observational study (September 2020 to June 2022). Clinical and immunovirological variables, antiretroviral treatment (ART), SARS-CoV-2 vaccination, and hospitalization in PLHIV with COVID-19 were recorded. Univariate and multivariate analyzes were performed examining factors associated with hospitalization using two models: first model (without vaccination) and second model (vaccination, minimum one dose). RESULTS: 1,201 PLHIV were included. The median age was 45 years. 65.3% were men; 38.7% presented comorbidities. 92.8% received ART and 83.1% presented undetectable viral load (VL). The median CD4+ T-cell count was 600/mm3. 95.7% presented symptoms. The rates of hospitalization, ICU admission, oxygen requirement, and death were 17.8 %, 2.8%, 10.7% and 1.39%, respectively. According to the multivariate analysis for the first model, age > 60 years and comorbidities were associated with a higher risk of hospitalization, while female sex and CD4+ > 500/mm3 had a protective effect. In the second model, only the comorbidities were associated with a higher risk of hospitalization, while vaccination and CD4+ > 500/mm3 reduced it. CONCLUSIONS: in PLHIV, comorbidities were associated with a higher hospitalization rate, while having elevated CD4+ T-cell counts and being vaccinated had a protective effect. ART and VL had no impact in any model, while age and sex only had an influence when vaccination was not considered.


Sujet(s)
Humains , Mâle , Femelle , Adulte , Adulte d'âge moyen , Infections à VIH/épidémiologie , COVID-19/épidémiologie , Hospitalisation/statistiques et données numériques , Argentine/épidémiologie , Comorbidité , Infections à VIH/complications , Infections à VIH/traitement médicamenteux , Analyse multifactorielle , Études prospectives , Facteurs de risque , Étude multicentrique , Antirétroviraux/administration et posologie , Vaccins contre la COVID-19/administration et posologie , SARS-CoV-2 , COVID-19/complications , COVID-19/diagnostic , COVID-19/prévention et contrôle
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