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dc.contributor.authorHidalgo Tenorio, Carmen
dc.contributor.authorPasquau, Juan
dc.contributor.authorVinuesa, David
dc.contributor.authorFerra, Sergio
dc.contributor.authorTerrón, Alberto
dc.contributor.authorPayeras, Albertp
dc.contributor.authorSanJoaquin, Isabel
dc.contributor.authorMartinez, Onofre Juan
dc.contributor.authorLópez Ruz, Miguel Ángel 
dc.contributor.authorOmar, Mohamed
dc.contributor.authorDe la Torre Lima, Javier
dc.contributor.authorLópez Lirola, Ana
dc.contributor.authorPalomares, Jesús
dc.contributor.authorBlanco, José Ramón
dc.contributor.authorMontero, Marta
dc.contributor.authorGarcía Vallecillos, Coral
dc.date.accessioned2024-04-19T06:41:19Z
dc.date.available2024-04-19T06:41:19Z
dc.date.issued2022-03
dc.identifier.citationViruses . 2022 Mar 4;14(3):524es_ES
dc.identifier.urihttps://hdl.handle.net/10481/90899
dc.description.abstractBrief: Real-world data in naïve HIV-1 patients demonstrate that dolutegravir plus lamivudine in a multiple tablet regimen is effective, safe, and satisfactory; it causes moderately increasing weight and abdominal circumference and is administrable on a test-and-treat strategy. Background: Our objectives were to determine the real-life effectiveness and safety of DT with dolutegravir (50 mg/QD) plus lamivudine (300 mg/QD) in a multiple-tablet regimen (MTR) in naïve PLHIV followed up for 48 weeks and to evaluate the compliance and satisfaction of patients. Material and methods: An open, single-arm, multicenter, non-randomized clinical trial from May 2019 through September 2020 with a 48-week follow-up. Results: The study included 88 PLHIV patients (87.5% male) with a mean age of 35.9 years; 76.1% were MSM patients. The mean baseline CD4 was 516.4 cells/uL, with a viral load (VL) of 4.49 log10, and 11.4% were in the AIDS stage. DT started within 7 days of first specialist consultation in all patients and the same day in 84.1%; 3.4% had baseline resistance mutations (K103N, V106I + E138A, and V108I); 12.5% were lost to follow-up. At week 48, 86.3% had VL < 50 cop/uL by intention-to-treat analysis and 98.7% by per-protocol (PP) analysis. Virological failure (VF) was recorded in 1.1%, with no resistance mutation. One blip was detected in 5.2% without VF. Three reported anxiety, dizziness, and cephalgia, respectively, at week 4 and one reported insomnia at week 24; none reported adverse events at week 48. The mean weight was 4 kg higher at 48 weeks (p = 0.0001) and abdominal circumference 3 cm larger at 24 weeks (p = 0.022). No forgetfulness occurred in 98.7% of patients. Patient satisfaction was 90/100 at 4, 24, and 48 weeks. Conclusion: Real-world data demonstrate that dolutegravir plus lamivudine in MTR is effective, safe, and satisfactory, moderately increasing weight and abdominal circumference and administrable on a test-and-treat strategy.es_ES
dc.language.isoenges_ES
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs 3.0 Licensees_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es_ES
dc.titleDOLAVI Real-Life Study of Dolutegravir Plus Lamivudine in Naive HIV-1 Patients (48 Weeks)es_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.doi10.3390/v14030524


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