Observational study to evaluate discontinuation of monotherapy with cobicistat-boosted darunavir in patients with human immunodeficiency virus.
Antonio Solana-AltabellaEmilio Monte-BoquetMarta MonteroPablo Pérez-HuertasMaria Jesús Cuéllar-MonrealMiguel SalavertJosé Luis Poveda-AndrésPublished in: Medicine (2023)
To evaluate the reasons for changing to monotherapy with protease inhibitors, together with the proportion and reasons for the interruption to treatment, in patients who have been treated at some point with cobicistat-boosted darunavir (DRV/c). Outpatients in a tertiary hospital. Observational retrospective study to evaluate monotherapy with DRV/c (800 mg/150 mg) in adult patients with human immunodeficiency virus infection, from December 2014 to July 2022. Demographic variables, viral load, cluster of differentiation 4 lymphocyte lymphocyte count, and antiretroviral therapy were assessed. 42 patients were included. 36% of the patients were undergoing monotherapy at the time of the analysis. The main reason for discontinuation was poor adherence. At time of analysis, 80% of the patients in monotherapy had an undetectable viral load. Antiretroviral therapy recommendations advise against exposing the patient to functional monotherapy with a single drug due to the high risk of virological failure and the onset of resistance to a single drug. Following the analysis of the results, DRV/c in monotherapy is not an effective strategy in the medium and long term due to factors such as lack of adherence or virological failure, although it can be maintained in specific circumstances. Therefore, patients undergoing monotherapy require close monitoring.
Keyphrases
- antiretroviral therapy
- human immunodeficiency virus
- end stage renal disease
- combination therapy
- hiv infected
- hiv infected patients
- newly diagnosed
- open label
- chronic kidney disease
- ejection fraction
- patients undergoing
- prognostic factors
- hiv aids
- hepatitis c virus
- endothelial cells
- emergency department
- type diabetes
- metabolic syndrome
- patient reported
- south africa
- insulin resistance
- skeletal muscle
- weight loss
- adverse drug
- pluripotent stem cells