Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/44223
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dc.contributor.authorMiró Meda, José M.-
dc.contributor.authorManzardo, Christian-
dc.contributor.authorMussini, Cristina-
dc.contributor.authorJohnson, Margaret M.-
dc.contributor.authorD'Arminio Monforte, Antonella-
dc.contributor.authorAntinori, Antonella-
dc.contributor.authorGill, M. John-
dc.contributor.authorSighinolfi, Laura-
dc.contributor.authorUberti-Foppa, Caterina-
dc.contributor.authorBorghi, Vanni-
dc.contributor.authorSabin, Caroline-
dc.contributor.authorLate Presenters Investigators-
dc.date.accessioned2013-06-13T10:51:27Z-
dc.date.available2013-06-13T10:51:27Z-
dc.date.issued2011-10-17-
dc.identifier.issn1932-6203-
dc.identifier.urihttp://hdl.handle.net/2445/44223-
dc.description.abstractObjectives: We analyzed clinical progression among persons diagnosed with HIV at the time of an AIDS-defining event, and assessed the impact on outcome of timing of combined antiretroviral treatment (cART). Methods: Retrospective, European and Canadian multicohort study.. Patients were diagnosed with HIV from 1997-2004 and had clinical AIDS from 30 days before to 14 days after diagnosis. Clinical progression (new AIDS event, death) was described using Kaplan-Meier analysis stratifying by type of AIDS event. Factors associated with progression were identified with multivariable Cox regression. Progression rates were compared between those starting early (< 30 days after AIDS event) or deferred (30-270 days after AIDS event) cART. Results: The median (interquartile range) CD4 count and viral load (VL) at diagnosis of the 584 patients were 42 (16, 119) cells/ mL and 5.2 (4.5, 5.7) log 10 copies/mL. Clinical progression was observed in 165 (28.3%) patients. Older age, a higher VL at diagnosis, and a diagnosis of non-Hodgkin lymphoma (NHL) (vs. other AIDS events) were independently associated with disease progression. Of 366 patients with an opportunistic infection, 178 (48.6%) received early cART. There was no significant difference in clinical progression between those initiating cART early and those deferring treatment (adjusted hazard ratio 1.32 [95% confidence interval 0.87, 2.00], p=0.20). Conclusions: Older patients and patients with high VL or NHL at diagnosis had a worse outcome. Our data suggest that earlier initiation of cART may be beneficial among HIV-infected patients diagnosed with clinical AIDS in our setting.-
dc.format.extent8 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherPublic Library of Science (PLoS)-
dc.relation.isformatofReproducció del document publicat a: http://dx.doi.org/10.1371/journal.pone.0026009-
dc.relation.ispartofPLoS One, 2011, vol. 6, num. 10, p. e26009-
dc.relation.urihttp://dx.doi.org/10.1371/journal.pone.0026009-
dc.rightscc-by (c) Miro, J.M. et al., 2011-
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es-
dc.sourceArticles publicats en revistes (Medicina)-
dc.subject.classificationVIH (Virus)-
dc.subject.classificationSida-
dc.subject.classificationAntiretrovirals-
dc.subject.classificationTerapèutica-
dc.subject.classificationPersones seropositives-
dc.subject.otherHIV (Viruses)-
dc.subject.otherAIDS (Disease)-
dc.subject.otherAntiretroviral agents-
dc.subject.otherTherapeutics-
dc.subject.otherHIV-positive persons-
dc.titleSurvival outcomes and effect of early vs. deferred cART among HIV-infected patients diagnosed at the time of an AIDS-defining event: a cohort analysis.-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec610259-
dc.date.updated2013-06-13T10:51:28Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid22043301-
Appears in Collections:Articles publicats en revistes (Medicina)

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