dc.date.accessioned2019-04-24T18:23:56Z
dc.date.available2019-04-24T18:23:56Z
dc.date.created2019-04-24T18:23:56Z
dc.date.issued2016
dc.identifierhttps://hdl.handle.net/20.500.12866/6489
dc.identifierhttps://doi.org/10.1371/journal.pone.0153921
dc.description.abstractBackground: Since 2009, earlier initiation of highly active antiretroviral therapy (HAART) after an opportunistic infection (OI) has been recommended based on lower risks of death and AIDS-related progression found in clinical trials. Delay in HAART initiation after OIs may be an important barrier for successful outcomes in patients with advanced disease. Timing of HAART initiation after an OI in "real life" settings in Latin America has not been evaluated. Methods: Patients in the Caribbean, Central and South America network for HIV Epidemiology (CCA-SAnet) ≥18 years of age at enrolment, from 2001-2012 who had an OI before HAART initiation were included. Patients were divided in an early HAART (EH) group (those initiating within 4 weeks of an OI) and a delayed HAART (DH) group (those initiating more than 4 weeks after an OI). All patients with an AIDS-defining OI were included. In patients with more than one OI the first event reported was considered. Calendar trends in the proportion of patients in the EH group (before and after 2009) were estimated by site and for the whole cohort. Factors associated with EH were estimated using multivariable logistic regression models. Results: A total of 1457 patients had an OI before HAART initiation and were included in the analysis: 213 from Argentina, 686 from Brazil, 283 from Chile, 119 from Honduras and 156 from Mexico. Most prevalent OI were Tuberculosis (31%), followed by Pneumocystis pneumonia (24%), Invasive Candidiasis (16%) and Toxoplasmosis (9%). Median time from OI to HAART initiation decreased significantly from 5.7 (interquartile range [IQR] 2.8-12.1) weeks before 2009 to 4.3 (IQR 2.0-7.1) after 2009 (p<0.01). Factors associated with starting HAART within 4 weeks of OI diagnosis were lower CD4 count at enrolment (p-<0.001), having a non-tuberculosis OI (p<0.001), study site (p<0.001), and more recent years of OI diagnosis (p<0.001). Discussion: The time from diagnosis of an OI to HAART initiation has decreased in Latin America coinciding with the publication of evidence of its benefit. We found important heterogeneity between sites which may reflect differences in clinical practices, local guidelines, and access to HAART. The impact of the timing of HAART initiation after OI on patient survival in this "real life" context needs further evaluation.
dc.languageeng
dc.publisherPublic Library of Science
dc.relationPLoS ONE
dc.relation1932-6203
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectCD4 antigen
dc.subjectnonnucleoside reverse transcriptase inhibitor
dc.subjectproteinase inhibitor
dc.subjectacquired immune deficiency syndrome
dc.subjectadult
dc.subjectArgentina
dc.subjectArticle
dc.subjectatypical mycobacteriosis
dc.subjectbrain disease
dc.subjectBrazil
dc.subjectCaribbean
dc.subjectCD4 lymphocyte count
dc.subjectCentral America
dc.subjectChile
dc.subjectcoccidioidomycosis
dc.subjectcohort analysis
dc.subjectcontrolled study
dc.subjectcryptococcal meningitis
dc.subjectcryptosporidiosis
dc.subjectcytomegalovirus infection
dc.subjectCytomegalovirus retinitis
dc.subjectfemale
dc.subjectfollow up
dc.subjectherpes simplex
dc.subjecthighly active antiretroviral therapy
dc.subjecthistoplasmosis
dc.subjectHonduras
dc.subjecthuman
dc.subjectHuman immunodeficiency virus infection
dc.subjectinvasive candidiasis
dc.subjectisosporiasis
dc.subjectmajor clinical study
dc.subjectmale
dc.subjectMexico
dc.subjectopportunistic infection
dc.subjectPneumocystis pneumonia
dc.subjectprevalence
dc.subjectprogressive multifocal leukoencephalopathy
dc.subjectsalmonellosis
dc.subjectSouth America
dc.subjectSouth and Central America
dc.subjecttherapy delay
dc.subjecttoxoplasmosis
dc.subjecttuberculosis
dc.subjectAIDS-Related Opportunistic Infections
dc.subjectclinical trial
dc.subjectdisease free survival
dc.subjecthighly active antiretroviral therapy
dc.subjectHuman immunodeficiency virus 1
dc.subjectmortality
dc.subjectmulticenter study
dc.subjectsurvival rate
dc.subjecttime factor
dc.subjectAdult
dc.subjectAIDS-Related Opportunistic Infections
dc.subjectAntiretroviral Therapy, Highly Active
dc.subjectDisease-Free Survival
dc.subjectFemale
dc.subjectHIV-1
dc.subjectHumans
dc.subjectLatin America
dc.subjectMale
dc.subjectPrevalence
dc.subjectSurvival Rate
dc.subjectTime Factors
dc.titleTime to HAART initiation after diagnosis and treatment of opportunistic infections in patients with AIDS in Latin America
dc.typeinfo:eu-repo/semantics/article


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