Please use this identifier to cite or link to this item: http://repo.knmu.edu.ua/handle/123456789/15447
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dc.contributor.authorLlibre, Josep M.-
dc.contributor.authorCozzi-Lepri, Alessandro-
dc.contributor.authorPedersen, Court-
dc.contributor.authorRistola, Matti-
dc.contributor.authorMocrof, Amanda-
dc.contributor.authorMitsura, Viktar-
dc.contributor.authorMaltez, Fernando-
dc.contributor.authorFalconer, Karolin-
dc.contributor.authorBeniowsk, Marek-
dc.contributor.authorVullo, Vincenzo-
dc.contributor.authorGamal, Hassoun-
dc.contributor.authorKuzovatova, Elena-
dc.contributor.authorSzlavik, János-
dc.contributor.authorKuznetsova, Anastasiia-
dc.contributor.authorHans-Jürgen, Stellbrink-
dc.contributor.authorClaudine, Duvivier-
dc.contributor.authorSimon, Edwards-
dc.contributor.authorKamilla, Laut-
dc.contributor.authorRoger, Paredes-
dc.date.accessioned2016-12-16T10:38:28Z-
dc.date.available2016-12-16T10:38:28Z-
dc.date.issued2016-
dc.identifier.citationLong-term effectiveness of unboosted atazanavir plus abacavir/lamivudine in subjects with virological suppression: A prospective cohort study / J. M. Llibre, A. Cozzi-Lepri, C. Pedersen, M. Ristola, M. Losso, A. Mocroft, V. Mitsura, K. Falconer, F. Maltez, M. Beniowski, V. Vullo, G. Hassoun, E. Kuzovatova, J. Szlavik, A. Kuznetsova [et all.] // Medicine. – 2016. – № 95 (40). – DOI:10.1097/MD.0000000000005020.ru_RU
dc.identifier.urihttps://repo.knmu.edu.ua/handle/123456789/15447-
dc.description.abstractEffectiveness data of an unboosted atazanavir (ATV) with abacavir/lamivudine (ABC/3TC) switch strategy in clinical routine are scant. We evaluated treatment outcomes of ATV + ABC/3TC in pretreated subjects in the EuroSIDA cohort when started with undetectable plasma HIV-1 viral load (pVL), performing a time to loss of virological response (TLOVR <50 copies/mL) and a snapshot analysis at 48, 96, and 144 weeks. Virological failure (VF) was defined as confirmed pVL >50 copies/mL. We included 285 subjects, 67% male, with median baseline CD4 530 cells, and 44 months with pVL 50 copies/mL. The third drug in the previous regimen was ritonavir-boosted atazanavir (ATV/r) in 79 (28%), and another ritonavir-boosted protease inhibitor (PI/r) in 29 (10%). Ninety (32%) had previously failed with a PI. Proportions of people with virological success at 48/96/144 weeks were 90%/87%/88% (TLOVR) and 74%/67%/59% (snapshot analysis), respectively. The rates of VF were 8%/8%/6%. Rates of adverse events leading to study discontinuation were 0.4%/1%/2%. The multivariable adjusted analysis showed an associationru_RU
dc.language.isoenru_RU
dc.subjectabacavir/lamivudineru_RU
dc.subjectvirological suppressionru_RU
dc.titleLong-term effectiveness of unboosted atazanavir plus abacavir/lamivudine in subjects with virological suppressionru_RU
dc.typeArticleru_RU
Appears in Collections:Наукові праці. Кафедра інфекційних хвороб

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