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dc.contributor.authorBuscher, April
dc.contributor.authorMugavero, Michael
dc.contributor.authorWestfall, Andrew O
dc.contributor.authorKeruly, Jeanne
dc.contributor.authorMoore, Richard
dc.contributor.authorDrainoni, Mari-Lynn
dc.contributor.authorSullivan, Meg
dc.contributor.authorWilson, Tracey E
dc.contributor.authorRodriguez, Allan
dc.contributor.authorMetsch, Lisa
dc.contributor.authorGardner, Lytt
dc.contributor.authorMarks, Gary
dc.contributor.authorMalitz, Faye
dc.contributor.authorGiordano, Thomas P
dc.date.accessioned2023-10-13T16:44:05Z
dc.date.available2023-10-13T16:44:05Z
dc.date.issued2013-07-26
dc.identifier.citationBuscher A, Mugavero M, Westfall AO, Keruly J, Moore R, Drainoni ML, Sullivan M, Wilson TE, Rodriguez A, Metsch L, Gardner L, Marks G, Malitz F, Giordano TP. The association of clinical follow-up intervals in HIV-infected persons with viral suppression on subsequent viral suppression. AIDS Patient Care STDS. 2013 Aug;27(8):459-66. doi: 10.1089/apc.2013.0105. Epub 2013 Jul 26. PMID: 23886048; PMCID: PMC3739946.en_US
dc.identifier.eissn1557-7449
dc.identifier.doi10.1089/apc.2013.0105
dc.identifier.pmid23886048
dc.identifier.urihttp://hdl.handle.net/20.500.12648/13044
dc.description.abstractThe recommendation for the frequency for routine clinical monitoring of persons with well-controlled HIV infection is based on evidence that relies on observed rather than intended follow-up intervals. We sought to determine if the scheduled follow-up interval is associated with subsequent virologic failure. Participants in this 6-clinic retrospective cohort study had an index clinic visit in 2008 and HIV viral load (VL) ≤400 c/mL. Univariate and multivariate tests evaluated if scheduling the next follow-up appointment at 3, 4, or 6 months predicted VL >400 c/mL at 12 months (VF). Among 2171 participants, 66%, 26%, and 8% were scheduled next follow-up visits at 3, 4, and 6 months, respectively. With missing 12-month VL considered VF, 25%, 25%, and 24% of persons scheduled at 3, 4, and 6 months had VF, respectively (p=0.95). Excluding persons with missing 12-month VL, 7.1%, 5.7%, and 4.5% had VF, respectively (p=0.35). Multivariable models yielded nonsignificant odds of VF by scheduled follow-up interval both when missing 12-month VL were considered VF and when persons with missing 12-month VL were excluded. We conclude that clinicians are able to make safe decisions extending follow-up intervals in persons with viral suppression, at least in the short-term.
dc.language.isoenen_US
dc.relation.urlhttps://www.liebertpub.com/doi/epub/10.1089/apc.2013.0105en_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleThe association of clinical follow-up intervals in HIV-infected persons with viral suppression on subsequent viral suppression.en_US
dc.typeArticle/Reviewen_US
dc.source.journaltitleAIDS patient care and STDsen_US
dc.source.volume27
dc.source.issue8
dc.source.beginpage459
dc.source.endpage66
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.description.versionVoRen_US
refterms.dateFOA2023-10-13T16:44:07Z
html.description.abstractThe recommendation for the frequency for routine clinical monitoring of persons with well-controlled HIV infection is based on evidence that relies on observed rather than intended follow-up intervals. We sought to determine if the scheduled follow-up interval is associated with subsequent virologic failure. Participants in this 6-clinic retrospective cohort study had an index clinic visit in 2008 and HIV viral load (VL) ≤400 c/mL. Univariate and multivariate tests evaluated if scheduling the next follow-up appointment at 3, 4, or 6 months predicted VL >400 c/mL at 12 months (VF). Among 2171 participants, 66%, 26%, and 8% were scheduled next follow-up visits at 3, 4, and 6 months, respectively. With missing 12-month VL considered VF, 25%, 25%, and 24% of persons scheduled at 3, 4, and 6 months had VF, respectively (p=0.95). Excluding persons with missing 12-month VL, 7.1%, 5.7%, and 4.5% had VF, respectively (p=0.35). Multivariable models yielded nonsignificant odds of VF by scheduled follow-up interval both when missing 12-month VL were considered VF and when persons with missing 12-month VL were excluded. We conclude that clinicians are able to make safe decisions extending follow-up intervals in persons with viral suppression, at least in the short-term.
dc.description.institutionSUNY Downstateen_US
dc.description.departmentCommunity Health Sciencesen_US
dc.description.degreelevelN/Aen_US
dc.identifier.journalAIDS patient care and STDs


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