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Presentation Abstract
Session Number:
103
Monday, Sep 10, 2012, 11:15 AM - 1:15 PM
Presentation Title:
H-888 - High Incidence of Renal Stones in HIV-infected Patients on Ritonavir-boosted Atazanavir- than in Those on Other Protease Inhibitors-containing Antiretroviral Therapy
Location:
Halls A-C
Presentation Number:
H-888
Pres. Time:
Monday, Sep 10, 2012, 11:15 AM - 1:15 PM
Category:
H1
Keywords:
HIV infections/complications; atazanavir; protease inhibitor
Author(s):
Y. Hamada, MD -
fellow
1
, T. Nishijima, MD -
fellow
1
, K. Watanabe, MD -
staff doctor
1
, H. Komatsu, MD -
director
2
, K. Tsukada, MD -
director
1
, H. Gatanaga, MD -
director
1
, Y. Kikuchi, MD -
director
1
, S. Oka, MD -
director general
1
;
1
AIDS clinical Cetr., Natl. Cetr. for Global Hlth. and Med., Tokyo, Japan,
2
Saku Central Hosp., Nagano, Japan.
Financial Disclosures:
Y. Hamada,
None..
T. Nishijima,
None..
K. Watanabe,
None..
H. Komatsu,
None..
K. Tsukada,
None..
H. Gatanaga,
None..
Y. Kikuchi,
None.
S. Oka,
MSD KK
Role(s):
Research Contractor.
Roche Daiagnostics KK
Role(s):
Research Contractor.
AbbottJapan Co
Role(s):
Research Contractor.
Janssen Pharmaceutical Co
Role(s):
Research Contractor.
Pfizer Co
Role(s):
Research Contractor.
Abstract:
Background:
Little information is available on the incidence of renal stones (RS) with ritonavir-boosted atazanavir (ATV/r) use.
Methods:
The incidence of RS was compared between patients who commenced ATV/r-containing antiretroviral therapy (ART) and those on other protease inhibitors (other PIs). The effects of ATV/r were estimated by univariate and multivariate Cox hazards models. Other possible risk factors were evaluated by univariate analysis and those found significant were entered into multivariate analysis.
Results:
RS were diagnosed in 31 patients (23.7 per 1000 person-years) of the ATV/r (n=465), and 4 (2.2 per 1000 person-years) of the other PIs (n=775). ATV/r use was significantly associated with RS by uni- and multivariate analyses (adjusted HR=10.4; 95% CI, 3.69-29.6; p<0.01). ATV/r remained a significant risk for RS in all subgroups stratified by the median values of baseline variables. In the 31 patients on ATV/r who developed RS, the median time from commencement of ATV/r to diagnosis was 24.5 months (IQR, 14.7-34.6 months). Of the 18 patients who continued ATV/r despite the diagnosis of RS, 6 (33.3%) experienced recurrence. No patient who discontinued ATV/r had recurrence during the observation period (250.6 person-months).
Conclusions:
The incidence of RS was substantially higher in patients on ATV/r than those on other PIs. Continuation of ATV/r after diagnosis of RS was associated with high rate of recurrence. Switching ATV/r to other ART is warranted in patients who develop RS.
Multivariate analysis to estimate the risk of ATV/r- over other PIs-containing ART
Model 1 crude (n=1,240)
Model 2 adjusted (n=1,115)
Model 3 adjusted (n=1,115)
ATV/r use
HR (95%CI)
HR (95%CI)
HR (95%CI)
ATV/r use
10.44 (3.685-29.59)
9.339 (3.254-26.80)
10.08 (3.487-29.12)
Age per 1 year
1.012 (0.980-1.046)
1.002 (0.965-1.040)
Weight per 1 kg increment
0.980 (0.944-1.018)
0.965 (0.927-1.004)
Baseline eGFR per 10 ml/min/1.73m2 decrement
1.157 (0.968-1.382)
Baseline serum uric acid per 1mg/dl increment
1.423 (1.091-1.856)
Past exposure to indinavir
1.265 (0.415-3.859)
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