299556
Universal "Test and Treat" for All HIV+ People In Ethiopia Is Feasible
Methods: We examined the feasibility of 'test and treat' in Ethiopia, with an estimated overall HIV prevalence of 1.5% (1.9% for women, 1.0% for men). Using current data on the volume of HIV patients, the distribution of CD4 counts, and the price of ARVs and CD4 testing, we calculated the increase in resources required if Ethiopia moves to treat all HIV+ people regardless of CD4 count.
Results: Switching to 'test and treat' regardless of CD4 count will increase ART patients by 29% and decrease CD4 testing. The current policy for ARVs only at a CD4 count of 500 costs $100,667,400. If CD4 testing is not required to start patients on ART, the total annual cost of a universal treatment policy of al HIV+s would be $113,890,200. Adopting "test and treat" will result in an extra cost of $13,222,800 per year, i.e. a 13% increase. This additional cost is not excessive, considering that 'test and treat' would extend the life of current HIV patients and prevent many new infections, thus reducing future health care costs as fewer patients will be infected.
Conclusions: Implementing 'test and treat' is clearly the most ethical and economically feasible approach and is a reasonable next step for resource poor countries like Ethiopia. There is no reason why Africa should lag behind.
Learning Areas:
Public health or related laws, regulations, standards, or guidelinesLearning Objectives:
Identify the factors that influence cost-effectiveness of a test and treat policy in Ethiopia.
Describe the value added of moving to a test and treat policy in Ethiopia, as a model for other resource constrained countries.
Keyword(s): HIV Interventions, Accessibility
Qualified on the content I am responsible for because: I supervise the project director and was involved in the concept development and the research presented here.
Any relevant financial relationships? No
I agree to comply with the American Public Health Association Conflict of Interest and Commercial Support Guidelines, and to disclose to the participants any off-label or experimental uses of a commercial product or service discussed in my presentation.