1. Which of the following patients would not be a good candidate for the single-tablet regimen of dolutegravir/lamivudine (DTG/3TC)?

2. Your patient, a 54-year-old man with HIV, diabetes mellitus, hypertension, moderate renal insufficiency, chronic hepatitis B, and obesity is seen for follow-up. His HIV history is notable for previously having advanced HIV disease when he was first diagnosed 4 years ago, which was complicated by Pneumocystis pneumonia and oral and esophageal candidiasis. At that time, his CD4 cell count was 10 cells/mm3, and his HIV viral load was 720,000 copies/mL. However, he has been stable for the past several years and currently is receiving tenofovir alafenamide/emtricitabine/bictegravir. His most recent CD4 cell count was 380 cells/mm3, with a viral load <20 copies/mL. If you consider switching his regimen to dolutegravir/lamivudine, which of the following findings would be an absolute contraindication to making this change?

3. Which of the following is true regarding weight gain and the use of antiretroviral therapy (ART)?

4. The VIKING study evaluated patients with HIV who had integrase inhibitor (INI) resistance. As demonstrated in that study, which of the following therapies had activity in highly treatment-experienced patients with INI-resistant virus?

5. Which of the following studies is evaluating long-acting (LA) rilpivirine (RPV) and LA cabotegravir (CAB) in persons living with HIV who have had evidence of nonadherence for at least 6 months?

6. The HPTN 083 trial, comparing injectable long-acting cabotegravir (CAB LA) every 8 weeks with daily tenofovir disoproxil fumarate/emtricitabine (TDF/FTC) for pre-exposure prophylaxis, demonstrated that:

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