OBJECTIVES: The relationship between lopinavir trough plasma concentration at baseline and virological efficacy 3 months after the beginning of the therapy was investigated in an unselected cohort of HIV-1-infected patients METHODS: According to initial trough lopinavir plasma level, patients were classified into three groups: the subtherapeutic group (<3 mg/L, n=18), the therapeutic group (between 3 and 8 mg/L, n=50) and the toxic group (>8 mg/L, n=16). The virological response after 3 months of lopinavir treatment, defined as a viral load <200 HIV-1 RNA copies/mL, was compared amongst these groups. RESULTS: The virological response was significantly different (P<0.05) between the subtherapeutic group (22.% of patients with viral load<200 copies/mL) and the other groups (56.0% of patients with a viral load<200 copies/mL in the therapeutic group and 56.2% in the toxic group). CONCLUSIONS: A lower virological efficacy should be expected for experienced or naive patients with plasma trough lopinavir concentrations<3 mg/L at the beginning of treatment.
OBJECTIVES: The relationship between lopinavir trough plasma concentration at baseline and virological efficacy 3 months after the beginning of the therapy was investigated in an unselected cohort of HIV-1-infectedpatients METHODS: According to initial trough lopinavir plasma level, patients were classified into three groups: the subtherapeutic group (<3 mg/L, n=18), the therapeutic group (between 3 and 8 mg/L, n=50) and the toxic group (>8 mg/L, n=16). The virological response after 3 months of lopinavir treatment, defined as a viral load <200 HIV-1 RNA copies/mL, was compared amongst these groups. RESULTS: The virological response was significantly different (P<0.05) between the subtherapeutic group (22.% of patients with viral load<200 copies/mL) and the other groups (56.0% of patients with a viral load<200 copies/mL in the therapeutic group and 56.2% in the toxic group). CONCLUSIONS: A lower virological efficacy should be expected for experienced or naive patients with plasma trough lopinavir concentrations<3 mg/L at the beginning of treatment.
Authors: Imke H Bartelink; Rada M Savic; Grant Dorsey; Theodore Ruel; David Gingrich; Henriette J Scherpbier; Edmund Capparelli; Vincent Jullien; Sera L Young; Jane Achan; Albert Plenty; Edwin Charlebois; Moses Kamya; Diane Havlir; Francesca Aweeka Journal: Pediatr Infect Dis J Date: 2015-03 Impact factor: 2.129
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Authors: Imke H Bartelink; Rada M Savic; Julia Mwesigwa; Jane Achan; Tamara Clark; Albert Plenty; Edwin Charlebois; Moses Kamya; Sera L Young; Monica Gandhi; Diane Havlir; Deborah Cohan; Francesca Aweeka Journal: J Clin Pharmacol Date: 2013-09-21 Impact factor: 3.126
Authors: Natella Rakhmanina; John van den Anker; Aline Baghdassarian; Steven Soldin; Keetra Williams; Michael N Neely Journal: Antimicrob Agents Chemother Date: 2009-03-02 Impact factor: 5.191
Authors: William E Cunningham; Robin M Nance; Carol E Golin; Patrick Flynn; Kevin Knight; Curt G Beckwith; Irene Kuo; Anne Spaulding; Faye S Taxman; Fredrick Altice; Joseph A Delaney; Heidi M Crane; Sandra A Springer Journal: BMC Infect Dis Date: 2019-10-29 Impact factor: 3.090