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CP-127 Incidence and risk factors for tenofovir-associated renal toxicity in HIV-infected patients
  1. P Rodríguez-Quesada,
  2. L López-Esteban,
  3. J Ramón,
  4. R Vázquez-Sánchez,
  5. J Sánchez-Rubio,
  6. T Molina-García
  1. Hospital Universitario de Getafe, Pharmacy, Madrid (Getafe), Spain


Background Tenofovir (TNF) is one of the most used antiretroviral drugs for treatment of HIV infection worldwide. Although well tolerated, effects of TNF on renal function are still of concern.

Purpose To assess the incidence of tenofovir-associated renal toxicity in HIV-infected patients and which factors may contribute to this adverse effect.

Materials and methods Retrospective observational study in HIV-infected adult patients treated with TNF (January 2010–December 2012). Inclusion criteria: baseline normal creatinine clearance (CrCl), more than six months on TNF treatment and three CrCl determinations. Incidence of moderate (CrCl <60 ml/min) and severe (CrCl <30 ml/min) renal toxicity was calculated. Potential risk factors analysed were: age, gender, baseline CD4 and HIV-RNA, hepatitis, hypertension, diabetes, cardiovascular disease (CVD), AIDS, previous treatments and concomitant antiretroviral drugs. Continuous variables were compared by univariate analysis: T-Student or Mann-Whitney test and with Chi-square test for categorical variables. Multivariate analysis was performed on parameters with p < 0.10 in univariate models. p-values <0.05 were regarded as significant.

Results 232 patients were included (72% male, mean age 42.5 ± 8.7 years). At baseline, comorbidity rates were: 8% diabetes, 17% dyslipidaemia, 9% CVD, 14% hypertension, 7% hepatitis B and 61% hepatitis C co-infection. 30% of patients had AIDS. Mean number of treatment lines prior to TNF was 2.4 ± 2.1 and 22% of patients were treatment-naïve. The incidence of moderate renal insufficiency was 23.9 per 1000 patient-years (IC95%:33.3–14.5) and 1.9 per 1000 patient-years (IC95%:0.0–4.5) for severe renal insufficiency.

In the univariate analysis, variables related to toxicity were age, baseline creatinine, hypertension, and boosted protease inhibitor (PI) treatment. Treatment with non-analogues and treatment-naïve status were protective factors. In multivariate analysis, independent risk factors were age (OR = 1.1; IC95%1.5–7.7; p < 0.01), hypertension (OR = 2.8; IC95%1.2–6.8; p = 0.03), PI (OR = 3.2; IC95%1.3–6.9; p < 0.01) and baseline creatinine (OR = 37.9; IC95%3.5–410; p < 0.01).

Conclusions Renal toxicity among tenofovir-treated patients is common although severe cases are scarce. Caution should be observed in older patients and those with hypertension, PI and higher baseline creatinine even within the normal range.

No conflict of interest.

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