51. Experience of dolutegravir in HIV-infected treatment-naive patients from a tertiary care University Hospital in Ireland
- Author
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Gerard Sheehan, Anjali Patel, Sarmad Waqas, John S. Lambert, Ciara Levey, Gordana Avramovic, Mairead O’Connor, and Paddy Mallon
- Subjects
0301 basic medicine ,Pediatrics ,medicine.medical_specialty ,Integrase inhibitor ,Tertiary care ,Therapy naive ,03 medical and health sciences ,chemistry.chemical_compound ,0302 clinical medicine ,Pharmacoepidemiology/drug safety ,Medicine ,030212 general & internal medicine ,tolerability ,lcsh:R5-920 ,biology ,business.industry ,HIV ,integrase inhibitor ,General Medicine ,University hospital ,030112 virology ,Integrase ,dolutegravir ,viral load ,chemistry ,Tolerability ,naive ,Dolutegravir ,biology.protein ,Original Article ,lcsh:Medicine (General) ,business ,Viral load - Abstract
Objective: Dolutegravir, an HIV integrase inhibitor, is a relatively new treatment option. To assess the tolerability, side effects, and time to viral decline to non-detectable in patients newly started on dolutegravir. Methods: Retrospective health care record of 61 consecutive HIV treatment-naive patients started on dolutegravir was reviewed and analysed on SPSS. Results: The mean initial viral load was 160826.05 copies/mL (range, 79–1,126,617 copies/mL). HIV viral load became non-detectable in 63.9% of patients on dolutegravir within 3 months. In all, 60.7% of patients reported no side effects on dolutegravir; 98.4% of the patients claimed full compliance to their antiretrovirals. Conclusion: Dolutegravir was found to be efficacious and well tolerated in HIV-infected treatment-naive patients.
- Published
- 2016