Publication:
Choice of the initial antiretroviral treatment for HIV-positive individuals in the era of integrase inhibitors

dc.contributor.authorAlejos, Belén
dc.contributor.authorSuárez-García, Inés
dc.contributor.authorBisbal, Otilia
dc.contributor.authorIribarren, José Antonio
dc.contributor.authorAsensi, Víctor
dc.contributor.authorGórgolas, Miguel
dc.contributor.authorMuga, Roberto
dc.contributor.authorMoreno, Santiago
dc.contributor.authorJarrin Vera, Inmaculada
dc.contributor.authorCoRIS Cohort
dc.contributor.funderRed de Investigación Cooperativa en Investigación en Sida (España)
dc.contributor.funderInstituto de Salud Carlos III
dc.contributor.funderUnión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF)
dc.date.accessioned2019-11-21T10:19:51Z
dc.date.available2019-11-21T10:19:51Z
dc.date.issued2019
dc.description.abstractBackground: We aimed to describe the most frequently prescribed initial antiretroviral therapy (ART) regimens in recent years in HIV-positive persons in the Cohort of the Spanish HIV/AIDS Research Network (CoRIS) and to investigate factors associated with the choice of each regimen. Methods: We analyzed initial ART regimens prescribed in adults participating in CoRIS from 2014 to 2017. Only regimens prescribed in >5% of patients were considered. We used multivariable multinomial regression to estimate Relative Risk Ratios (RRRs) for the association between sociodemographic and clinical characteristics and the choice of the initial regimen. Results Among 2874 participants, abacavir(ABC)/lamivudine(3TC)/dolutegavir(DTG) was the most frequently prescribed regimen (32.1%), followed by tenofovir disoproxil fumarate (TDF)/emtricitabine (FTC)/elvitegravir(EVG)/cobicistat(COBI) (14.9%), TDF/FTC/rilpivirine (RPV) (14.0%), tenofovir alafenamide (TAF)/FTC/EVG/COBI (13.7%), TDF/FTC+DTG (10.0%), TDF/FTC+darunavir/ritonavir or darunavir/cobicistat (bDRV) (9.8%) and TDF/FTC+raltegravir (RAL) (5.6%). Compared with ABC/3TC/DTG, starting TDF/FTC/RPV was less likely in patients with CD4<200 cells/mu L and HIV-RNA> 100.000 copies/mL. TDF/FTC+DTG was more frequent in those with CD4< 200 cells/mu L and HIV-RNA>100.000 copies/mL. TDF/FTC+FTC+bDRV were also more frequent among patients with CD4< 200 cells//mu L and with transmission categories other than men who have sex with men. Compared with ABC/3TC/DTG, the prescription of other initial ART regimens decreased from 2014-2015 to 2016-2017 with the exception of TDF/FTC+DTG. Differences in the choice of the initial ART regimen were observed by hospitals' location. Conclusions: The choice of initial ART regimens is consistent with Spanish guidelines' recommendations, but is also clearly influenced by physician's perception based on patient's clinical and sociodemographic variables and by the prescribing hospital location.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipThe RIS cohort (CoRIS) is supported by the Instituto de Salud Carlos III through the Red Temática de Investigación Cooperativa en Sida (RD06/006, RD12/0017/0018 and RD16/0002/0006) as part of the Plan Nacional I+D+i and cofinanced by ISCIII-Subdirección General de Evaluación and the Fondo Europeo de Desarrollo Regional (FEDER). This study was funded by ViiV Healthcare. ViiV Healthcare was given the opportunity to review a preliminary version of this manuscript for factual accuracy. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The authors are solely responsible for final content and interpretation of the results.es_ES
dc.format.number8es_ES
dc.format.pagee0221598es_ES
dc.format.volume14es_ES
dc.identifier.citationPLoS One. 2019 Aug 26;14(8):e0221598.es_ES
dc.identifier.doi10.1371/journal.pone.0221598es_ES
dc.identifier.e-issn1932-6203es_ES
dc.identifier.issn1932-6203es_ES
dc.identifier.journalPloS onees_ES
dc.identifier.otherhttp://hdl.handle.net/20.500.13003/15375
dc.identifier.pubmedID31449566es_ES
dc.identifier.puiL2002705342
dc.identifier.scopus2-s2.0-85071299637
dc.identifier.urihttp://hdl.handle.net/20.500.12105/8623
dc.identifier.wos485044000026
dc.language.isoenges_ES
dc.publisherPublic Library of Science (PLOS)
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/RD06/006es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/RD12/0017/0018es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/RD16/0002/0006es_ES
dc.relation.publisherversionhttps://doi.org/10.1371/journal.pone.0221598es_ES
dc.repisalud.centroISCIII::Centro Nacional de Epidemiologíaes_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.decsHumanos
dc.subject.decsInhibidores de Integrasa
dc.subject.decsPersona de Mediana Edad
dc.subject.decsOportunidad Relativa
dc.subject.decsSeropositividad para VIH
dc.subject.decsAntirretrovirales
dc.subject.decsFemenino
dc.subject.decsAnálisis Multivariante
dc.subject.decsAdulto
dc.subject.decsTerapia Antirretroviral Altamente Activa
dc.subject.decsMasculino
dc.subject.meshMale
dc.subject.meshMultivariate Analysis
dc.subject.meshAdult
dc.subject.meshFemale
dc.subject.meshAnti-Retroviral Agents
dc.subject.meshHIV Seropositivity
dc.subject.meshHumans
dc.subject.meshOdds Ratio
dc.subject.meshAntiretroviral Therapy, Highly Active
dc.subject.meshIntegrase Inhibitors
dc.subject.meshMiddle Aged
dc.titleChoice of the initial antiretroviral treatment for HIV-positive individuals in the era of integrase inhibitorses_ES
dc.typeresearch articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
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