Setting | HIV Consent | Testing assay | HIV Testing Program | ||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
Year | Geographic location | ED volume (Visits/year) | Consent | Default assumption of patient willingness | Patient indication of willingness | Parental involvement | Assay | Additional test (Confirmatory test) | Hours of coverage | Program Staffing | Program details |
April 1995—March 1997 | Milwaukee, WI | 75,000 | Voluntary | Opt-in | Written Consent | No parental consent > 13 years | Phlebotomized samples for ELISA | Western blot | ED nurse | Program improvement initiative; follow-up pre- vs. post-program intervention evaluated | |
November 2003—May 2004 | Boston, MA | 25,000 | Voluntary | Opt-in | Written Consent > 18 years | Assent & parent/ guardian permission for 15–17 years | OraSure (Orasure Technologies, Inc.) oral fluid sampling; Testing performed by state laboratory after the patient visit | Western blot | Mondays-Fridays, noon-10 pm | One research assistant | |
September 2003—August 2006 | Philadelphia, PA | 70,000 | Voluntary | Opt-in | Verbal consent for sexual health counseling; written consent for HIV testing | Not required per state law | OraSure (Orasure Technologies, Inc.) oral fluid sampling; Testing performed by an offsite laboratory | 32 h/week | Health Educator | Program primarily provided sexual health counseling (30 min); testing offered after counseling. Patients presenting with possible sexually transmitted diseases and those referred by ED providers received priority for counseling | |
March 2008—October 2008 | Memphis, TN | 90,000 | Implied | Opt-out | General consent & information sheet on HIV | Oraquick Advance Rapid HIV Antibody 1/2 test (OraSure Technologies, Inc) using oral fluid sampling | Western blot | Nurses | |||
October 2009—December 2009 | Newark, NJ | 35,000 | Voluntary | Opt-in | Written Consent | Clearview HIV 1/2 STAT-PAK (Chembio Diagnostics Systems, Inc.) rapid HIV fingerstick testing | Western blot | Every day, 24 h / day | Offer testing: PED clinical providers and department of health HIV counselors; Perform testing: HIV counselors | ||
March 2009-February 2011 | Washington, DC | 126,000 combined (2 PEDs) | Voluntary | Opt-out | Verbal consent | Oraquick Advance Rapid HIV 1/2 Antibody Test (OraSure Technologies, Inc.) using oral fluid sampling | Western blot | Grant-funded personnel at ED1 and ED personnel at ED2 performed testing | |||
January 2012-December 2016 | Cincinnati, OH | 89,000 | Voluntary | Opt-out | Verbal consent | Oraquick Advance Rapid HIV 1/2 Antibody Test (OraSure Technologies, Inc) using oral fluid sampling | 4th generation antigen/antibody testing | Every day, 24 h / day | PED clinical providers | ||
June 2019-October 2019 | Atlanta, GA | 60,000 | Voluntary | Opt-out | Verbal consent | Architect HIV Ag/Ab Combo Test (Abbott Laboratories, Inc.); Fingerstick or phlebotomy sampling | 40–60 h per week | Study investigators |
Setting | Postresults Communication and Methods | Patient Selection Strategies and Criteria | HIV Testing and Yield | Result Notification/ Linkage | |||||||||||
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Year | Geographic location | ED volume (Visits/year) | Post results notification and referral | Age | Screening | Exclusion criteria | Population count (Eligible by age) | Eligible (by inclusion/exclusion criteria) | Offered | Accepting HIV testing | Tested (if different number than accepted) | Reactive | Confirmed positive (n/tested %) | Result notification | Linkage to HIV care |
April 1995—March 1997 | Milwaukee, WI | 75,000 | ED nurse was responsible for arranging follow-up of HIV test results | 12–18 years old | Targeted: presenting for possible STD | Pre-program: 490 STD visits; Post-program: 372 STD visits | Pre-program: 18% HIV tested Post-program: 27% HIV testing | 4 ELISA positive HIV tests; 3 indeterminate and 1 negative Western blot | Pre-program:8.1% notified of HIV test results Post-program: 57% notified of test results | 2 | |||||
November 2003—May 2004 | Boston, MA | 25,000 | Follow-up of testing results was scheduled two weeks post-testing at an urgent care facility. The appointments of those who did not follow-up were not rescheduled | 15–21 years old | Nontargeted | Tested for sexually transmitted diseases/HIV in past month; known HIV-positive status; non English- or Spanish-speaking; critically ill; intoxicated or presented with a psychiatric illness; university students or hospital employees; receiving care in common (open, less private) treatment areas of the ED; report being not “sexually experienced” if 15–17 years-old; presented to ED solely for HIV testing | 1,749 Age-eligible; 1,202 Approached | 791 | 765 Offered (96.7%) | 464 Accepted (60.7%) | 459 | 1 (0.2%) | 1 | ||
September 2003—August 2006 | Philadelphia, PA | 70,000 | Test results given within two weeks at a follow-up appointment | 14–24 years old | Nontargeted | Victims of child abuse; “significantly developmentally delayed”; medically “unstable” per ED treatment team | 32,121 | 1,287 Offered counseling (4%) | 318 Accepted HIV testing and Tested (49.4%) (643 Accepted counseling (50.0%)) | 2 (0.6%) | 2 | ||||
March 2008—October 2008 | Memphis, TN | 90,000 | Follow-up for testing appointment given 7–10 days post-testing at an adolescent HIV clinic | 13–18 years old | Nontargeted | Critically-ill or injured | 5,399 | 2,002 Approached (37.1%) | 1,735 Accepted and Tested (86.7%) | 1 (0.06%) | 1 | ||||
October 2009—December 2009 | Newark, NJ | 35,000 | 13–20 years old | Nontargeted | Critically ill; altered mental status; tested for HIV within past 3 months | 2,645 | 300 Offered (11.3%) | 224 Accepted (74.7%) | 213 | 0 (0.0%) | NA | ||||
March 2009-February 2011 | Washington, DC | 126,000 combined (2 PEDs) | Patients whose rapid HIV test was positive received individual counseling with the case manager in the ED and a follow-up appointment 48–72 h after their PED visit at the specialized adolescent HIV services in the same medical center | 13–24 years old | Nontargeted | Documented HIV test in the ED within the past six months (unless identified as high-risk) | 8,528 | 8,519 (visits) Offered (77.5%) | 6,184 Accepted (72.6%) | 5,764 | 12 | 8 (.14%) | 8 | ||
January 2012-December 2016 | Cincinnati, OH | 89,000 | Patients ≤ 18 years old were scheduled to follow up in 7–10 days at the HIV clinic or primary care, and patients older than 18 years old were scheduled for a follow-up at the adult HIV clinic | Targeted: presenting for possible STD | Denied ever being sexually active or were being evaluated for concerns of sexual assault/abuse | 4,378 Offered | 14 | 11 (0.25%) 8 newly positive; 3 previously positive | 11 | ||||||
June 2019-October 2019 | Atlanta, GA | 60,000 | 13–18 years old | Critically ill; unable to consent due to developmental delays or impaired mental status; deemed ineligible by their attending provider; previously diagnosed with HIV | 1,307 | 1,061 | 806 Offered (76%) | 344 Accepted (42.7%) | 1 (0.3%) | 1 |