J-1 ECONOMIC EVALUATION OF MONITORING VIROLOGIC RESPONSES TO ANTIRETROVIRAL THERAPY IN HIV-INFECTED CHILDREN IN RESOURCE-LIMITED SETTINGS

Tuesday, October 26, 2010: 1:00 PM
Grand Ballroom Centre (Sheraton Centre Toronto Hotel)
Karen Schneider1, Thanyawee Puthanakit2, June Ohata2, Stephen Kerr3, Matthew Law1, David Cooper1, Basil Donovan1, Nittaya Phanuphak4, Jintanat Ananworanich5 and David Wilson1, (1)National Centre in HIV Epidemiology and Clinical Research, Sydney, Australia, (2)The HIV Netherlands Australia Thailand Research Collaboration, Bangkok, Thailand, (3)National Centre in HIV Epidemiology & Clinical Research, Sydney, Australia, (4)The Thai Red Cross Aids Research Centre, Bangkok, Thailand, (5)South East Asia Research Collaboration with Hawaii, Bangkok, Thailand

Purpose:    This study aimed to assess the cost-effectiveness and -utility of different frequencies of monitoring viral load of HIV-positive children initiating antiretroviral treatment (ART) in a resource-limited setting.

Method:    An agent-based simulation model of virological and immunological outcomes of HIV-infected children on ART was built and directly informed by a longitudinal cohort study of 304 HIV-infected children starting ART in Thailand between October 2001 and May 2009. Rates of virological failure, suppression, and rebound, as well as CD4 progression, on first- and second-line ART were captured in the cohort and represented by the model. The model simulated expected clinical outcomes of CD4 percentage (CD4%) and viral load over time among children on ART according to different frequencies of viral load monitoring and initiation of second-line therapies where appropriate. Cost-utility, expressed as cost per quality adjusted life-years (QALYs) saved, and cost-effectiveness, expressed as cost per year of virological failure averted was calculated across 11 monitoring frequencies.  

Result:      Compared with the status quo, of no viral load monitoring, all frequencies of monitoring and access to second-line ART led to significant reductions in the number of children failing ART after 10 years. A single screening during the first year of ART led to an estimated 43.9% reduction in ART failures after 10 years, with repeated viral load monitoring leading to an average 75.1% reduction. The cost per year of virological failure averted, including antiretroviral drug costs, ranged from US$2,332 (IQR: US$2,311−US$2,365) for a one-off screening 30 weeks after the initiation of ART to US$4,098 (IQR: US$4,057−US$4,134) for screening children every 6 months.    Most individuals initiated first-line treatment with a low CD4% and recovered immunologically regardless of monitoring frequency; therefore only a modest gain in QALYs was observed. The incremental cost per QALY gained, attributed to monitoring alone, ranged from US$1,109 (IQR: US$859−US$1,557) for a one-off screening during the first year of ART to US$15,817 (IQR: US$13,961−US$19,855) for screening children every 6 months.

Conclusion:    Even very infrequent viral load monitoring is likely to provide substantial clinical benefit to HIV-infected children on ART and be moderately cost-effective. Without access to second-line drugs and regular viral load monitoring the current efficiency of first-line therapies is likely to be compromised, ultimately leading to a reduction in future drug options for Thailand’s population.

Candidate for the Lee B. Lusted Student Prize Competition