Abstract

BackgroundThe Centers for Disease Control and Prevention recommends nontargeted opt-out HIV screening in healthcare settings. Cost effectiveness is critical when considering potential screening methods. Our goal was to compare programmatic costs of nontargeted opt-out rapid HIV screening with physician-directed diagnostic rapid HIV testing in an urban emergency department (ED) as part of the Denver ED HIV Opt-Out Trial.MethodsThis was a prospective cohort study nested in a larger quasi-experiment. Over 16 months, nontargeted rapid HIV screening (intervention) and diagnostic rapid HIV testing (control) were alternated in 4-month time blocks. During the intervention phase, patients were offered HIV testing using an opt-out approach during registration; during the control phase, physicians used a diagnostic approach to offer HIV testing to patients. Each method was fully integrated into ED operations. Direct program costs were determined using the perspective of the ED. Time-motion methodology was used to estimate personnel activity costs. Costs per patient newly-diagnosed with HIV infection by intervention phase, and incremental cost effectiveness ratios were calculated.ResultsDuring the intervention phase, 28,043 eligible patients were included, 6,933 (25%) completed testing, and 15 (0.2%, 95% CI: 0.1%–0.4%) were newly-diagnosed with HIV infection. During the control phase, 29,925 eligible patients were included, 243 (0.8%) completed testing, and 4 (1.7%, 95% CI: 0.4%–4.2%) were newly-diagnosed with HIV infection. Total annualized costs for nontargeted screening were $148,997, whereas total annualized costs for diagnostic HIV testing were $31,355. The average costs per HIV diagnosis were $9,932 and $7,839, respectively. Nontargeted HIV screening identified 11 more HIV infections at an incremental cost of $10,693 per additional infection.ConclusionsCompared to diagnostic testing, nontargeted HIV screening was more costly but identified more HIV infections. More effective and less costly testing strategies may be required to improve the identification of patients with undiagnosed HIV infection in the ED.

Highlights

  • Over 1.1 million individuals are infected with HIV in the United States, while approximately 230,000 remain undiagnosed and 50,000 new infections occur annually [1,2]

  • To better inform operational considerations among emergency physicians and administrators, we proposed the following objectives as part of the Denver emergency department (ED) HIV Opt-Out Study: [21] (1) to estimate total direct costs associated with performing nontargeted opt-out rapid HIV screening in the ED per newly-identified HIV-infected patient; and (2) to compare such costs to those associated with diagnostic rapid HIV testing

  • During the two-year study period, 65,163 patients presented to the ED, of which, 28,043 eligible patients were included in the intervention phase and 29,925 eligible patients were included in the control phase

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Summary

Introduction

Over 1.1 million individuals are infected with HIV in the United States, while approximately 230,000 remain undiagnosed and 50,000 new infections occur annually [1,2]. In 2006 the Centers for Disease Control and Prevention (CDC) dramatically shifted its HIV testing paradigm to recommend nontargeted opt-out HIV screening in settings where the undiagnosed HIV prevalence was 0.1% or greater [6]. In 2013, the U.S Preventive Services Task Force (USPSTF) published Grade A recommendations supporting routine HIV screening [7]. Both recommendations are congruent with the 2010 National HIV/AIDS Strategy and align with HIV testing proposed as part of the Patient Protection and Affordable Care Act [8]. The Centers for Disease Control and Prevention recommends nontargeted opt-out HIV screening in healthcare settings.

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