Original contributionEmergency Provider Attitudes and Barriers to Universal HIV Testing in the Emergency Department
Introduction
In 2006, the Centers for Disease Control and Prevention (CDC) published recommendations for routine, voluntary human immunodeficiency virus (HIV) testing of persons 13–64 years of age in all health care settings, including the emergency department (ED) (1). In settings like the ED, the rapid pace of patient flow, coupled with substantial disease severity, may lead providers to focus preferentially on acute patient care over HIV screening. The successful implementation of any HIV testing program in the ED setting depends upon the willingness and commitment of ED providers to adopt such a program.
In April 2007, the American College of Emergency Physicians responded to the new CDC guidelines with a policy statement suggesting criteria under which EDs would embrace HIV testing. The criteria include requirements that ED-based HIV testing be feasible, practical, and based on local needs. The requirements also require that testing have adequate funding and not interfere with the acute care mission of Emergency Medicine (2). The implementation of an HIV testing program requires the provision of ED resources in addition to those required to meet the acute care mission. A more detailed understanding of emergency provider knowledge, attitudes, perceptions, and barriers toward HIV testing is needed for successful implementation of such a program.
The Universal Screening for HIV-infection in the Emergency Room (USHER) Trial is a National Institutes of Health-funded study examining alternative strategies for implementing routine HIV testing in the ED at the Brigham and Women's Hospital, Boston, Massachusetts. Before and after trial initiation, ED providers were surveyed to examine their attitudes and perceived barriers to HIV testing. The objective was to identify these barriers and then to see if they changed over time. The data collected may help inform further HIV testing programs so that these barriers can be addressed early and long term, thereby facilitating program success.
Section snippets
Study Design
The USHER Trial is a randomized, prospective clinical trial designed to evaluate alternative approaches to routine HIV testing in the ED. For this study, a survey was distributed to ED health care providers before (T0, December 2006) and 6 months after (T1, July 2007) clinical trial initiation. To be eligible for survey inclusion in this analysis, providers had to be full-time ED staff at both time points.
The analysis was focused on ED providers' knowledge and attitudes toward routine HIV
Characteristics of Study Subjects
At T0 (baseline), 357 emergency providers were employed in the Brigham and Women's Hospital ED, and 161 were excluded based on their part-time or per-diem status. Among the 196 eligible full-time ED providers, 159 (81%) completed the survey before USHER Trial initiation (Figure 1). At T1 (6 months), 358 emergency providers were employed and 151 were excluded for the same reasons. Among the 207 eligible providers, 141 (68%) completed the survey 6 months after program initiation. The intersection
Discussion
This study reports results from a survey of providers in an urban ED before and after the implementation of an HIV testing program. The results suggest that emergency providers generally favor the implementation of a large-scale HIV testing program in accordance with the CDC recommendations, but due to several major barriers, they are still generally unwilling to offer the test (1). Whereas some of the perceived barriers to testing were improved over time, other barriers were reported at an
Conclusion
ED health care providers are generally supportive of the recent CDC guidelines recommending routine HIV testing in the ED setting (1). Results of this study emphasize the importance of understanding provider barriers to HIV testing, as these perceived barriers highly correlate with providers' support of testing programs. These results have significant implications for EDs trying to implement routine testing efforts, and suggest the need to collect data specific to individual institutions,
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This research was funded by the National Institute of Mental Health (R01 MH0735445, R01 MH65869) and the Doris Duke Charitable Foundation (Clinical Scientist Development Award to Rochelle P. Walensky, md, mph), ClinicalTrials.Gov: #NCT00502944.