Increased Aripiprazole Concentrations in an HIV-Positive Male Concurrently Taking Duloxetine, Darunavir, and Ritonavir

被引:15
|
作者
Aung, Gregory L. [1 ]
O'Brien, John G.
Tien, Pamela G. [1 ]
Kawamoto, Laura S. [1 ]
机构
[1] Univ Pacific, Santa Clara Valley Med Ctr, PACE Clin, Thomas J Long Sch Pharm & Hlth Sci, Stockton, CA 95211 USA
关键词
aripiprazole; darunavir; duloxetine; interaction; ritonavir; NEUROLEPTIC MALIGNANT SYNDROME; SERUM CONCENTRATIONS; OVERDOSE; SAFETY;
D O I
10.1345/aph.1P139
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OBJECTIVE: To report a case of increased aripiprazole concentrations during coadministration with darunavir, ritonavir, and duloxetine. CASE SUMMARY: A 43-year-old HIV-positive Hispanic man received darunavir/ ritonavir-based antiretroviral therapy (ART) in addition to aripiprazole and duloxetine for depression and anxiety. A month after the aripiprazole dosage was increased to 50 mg daily, the patient developed confusion and loss of coordination. Weeks later, he presented to the emergency department with fever, cough, headache, neck stiffness, back pain, and blurred vision and was admitted for possible meningitis. Because symptoms improved with pain control and intravenous fluids during hospitalization, he was discharged within a couple days after admission. One month later he was readmitted for worsening symptoms, and the resulting diagnostic workup showed unremarkable findings except for lymphadenopathy (LAD). This finding was attributed to discontinuing ARTs after his first admission. He was discharged on aripiprazole 50 mg daily, darunavir 800 mg daily, ritonavir 100 mg daily, and duloxetine 60 mg daily. A random steady-state concentration of aripiprazole was 1100 ng/mL (therapeutic concentration 100-200 ng/mL) obtained 49 days after discharge. DISCUSSION: The Horn Drug Interaction Probability Scale demonstrated a possible relationship between the increased aripiprazole concentration and coadministration of darunavir/ritonavir and duloxetine, which inhibit CYP3A4 and 2D6. Potential confounders to the increased concentration include duloxetine inhibition of CYP2D6 polymorphism, possible 2D6 polymorphism, and exceeding aripiprazole's maximum dose. The initial presentation of confusion and loss of coordination may have been early signs of aripiprazole toxicity, which relapsed as shown by his symptoms prior to admission. CONCLUSIONS: The interaction between aripiprazole and darunavir, ritonavir, and duloxetine may be significant. Clinicians should be cognizant of increased risk of aripiprazole toxicity in HIV-positive patients concurrently taking ritonavir-boosted ART and other cytochrome P450 inhibitors like duloxetine. Dose adjustments or monitoring parameters should be an area of research and discussion.
引用
收藏
页码:1850 / 1854
页数:5
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