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      Routine HIV Screening in Two Health-Care Settings — New York City and New Orleans, 2011–2013

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          Abstract

          Approximately 16% of the estimated 1.1 million persons living with human immunodeficiency virus (HIV) in the United States are unaware of their infection and thus unable to benefit from effective treatment that improves health and reduces transmission risk (1,2). Since 2006, CDC has recommended that health-care providers screen for HIV all patients aged 13–64 years unless prevalence of undiagnosed HIV infection in their patients has been documented to be <0.1% (3). This report describes novel HIV screening programs at the Urban Health Plan (UHP), Inc. in New York City and the Interim Louisiana Hospital (ILH) in New Orleans. Data were provided by the two programs. UHP screened a monthly average of 986 patients for HIV during January 2011–September 2013. Of the 32,534 patients screened, 148 (0.45%) tested HIV-positive, of whom 147 (99%) received their test result and 43 (29%) were newly diagnosed. None of the 148 patients with HIV infection were previously receiving medical care, and 120 (81%) were linked to HIV medical care. The ILH emergency department (ED) and the urgent-care center (UCC) screened a monthly average of 1,323 patients from mid-March to December 2013. Of the 12,568 patients screened, 102 (0.81%) tested HIV-positive, of whom 100 (98%) received their test result, 77 (75%) were newly diagnosed, and five (5%) had acute HIV infection. Linkage to HIV medical care was successful for 67 (74%) of 91 patients not already in care. Routine HIV screening identified patients with new and previously diagnosed HIV infection and facilitated their linkage to medical care. The two HIV screening programs highlighted in this report can serve as models that could be adapted by other health-care settings. UHP, a federally qualified health center network of eight practice sites and eight school-based health centers, serves approximately 60,000 unique patients each year. ILH, a public hospital, serves approximately 76,000 unique patients in its ED and UCC each year. Both received startup funding from Gilead Sciences’ HIV on the Frontlines of Communities in the United States (FOCUS)* program to implement routine HIV screening based on four principles: 1) institutional policy change reflecting an organization-wide commitment to routine HIV testing and diagnosis; 2) integration of HIV testing into existing clinical workflows to promote its normalization and sustainability; 3) use of electronic health records (EHR) to prompt testing, automate laboratory orders, and track performance; and 4) required staff education on best HIV testing practices and outcomes. Before FOCUS, UHP counselors conducted risk-based, point-of-care rapid or laboratory HIV tests. With the new routine supported by FOCUS at UHP from January 2011 to September 2013, a medical assistant provides HIV information required by New York state, offers an HIV test to all patients aged 13–64 years with no documented HIV test within 12 months, and documents the offer in the EHR. The EHR prompts the health-care provider to confirm the patient’s agreement, and the health-care provider orders an HIV laboratory test. Negative test results are provided at the patient’s next visit or by letter. The program coordinator contacts patients who test positive and schedules an appointment to receive their test results and follow-up at the center that provides primary HIV medical care. The UHP commercial laboratory uses an HIV antibody assay and Western blot that detects established but not acute HIV infection, the highly infectious stage before antibodies to HIV develop that contributes disproportionately to HIV transmission (4). Before March 2013, when support from FOCUS began, ILH conducted opt-in HIV screening with point-of-care rapid tests 70 hours a week using staff dedicated only to HIV testing and counseling. Now the EHR prompts an HIV test offer at triage to all ED and UCC patients aged ≥13 years who have had no documented HIV test within 6 months. Unless the patient declines, the HIV test is ordered and processed in the hospital laboratory 24 hours a day, 7 days a week. Test results are delivered during the same visit. Patients who test positive receive CD4+ T-lymphocyte cell count and HIV viral load tests, meet with a navigator, and are linked to local HIV care facilities. The ILH laboratory uses an HIV antigen/antibody combination assay and, if necessary, a nucleic acid test to detect acute or established HIV infection. Each program provided data on the testing outcomes before and after the new screening programs, which were collected from EHRs (last updated in March 2014). At UHP, new diagnosis and linkage to care† were based on patient report and chart review. ILH defined a new HIV diagnosis as one not previously reported to the HIV surveillance system; linkage to care was based on chart review. At UHP, the percentage of patients tested for HIV increased from 8% during calendar year 2010 to 56% during January 2011–September 2013. The monthly average number of patients screened increased from 188 during 2007–2010 to 986 during the routine screening period. Of the 3,358 patients screened in 2010, 19 (0.57%) tested HIV-positive, of whom three (16%) were newly diagnosed. Of the 32,534 patients screened during January 2011–September 2013, 148 (0.45%) tested HIV-positive, of whom 147 (99%) received their test result and 43 (29%) were newly diagnosed. The prevalence of newly diagnosed HIV infection was higher among males (0.25%) than females (0.08%), non-Hispanics (0.23%) than Hispanics (0.12%), and persons aged ≥31 years (0.18%–0.19%) than persons aged ≤30 years (0.08%) (Table 1). None of the 148 patients diagnosed with HIV were previously receiving medical care, and 120 (81%) were subsequently linked to HIV medical care. At ILH, the HIV screening program increased the percentage of patients tested from 17% (ED) and 3% (UCC) during calendar year 2012 to 26% (ED) and 17% (UCC) from mid-March to December 2013. The monthly average number of patients screened increased from 821 during 2010–2012 to 1,323 in the 2013 period. Of the 11,257 patients screened in 2012, 106 (0.94%) tested HIV-positive, of whom 54 (51%) were newly diagnosed. Of the 12,568 patients screened from mid-March to December 2013, 102 (0.81%) tested HIV-positive, of whom 100 (98%) received their test result, 77 (75%) were newly diagnosed, and five (5%) had acute HIV infection. The prevalence of newly diagnosed HIV infection was higher among males (0.89%) than females (0.28%), blacks (0.63%) than whites (0.49%), Hispanics (1.00%) than non-Hispanics (0.60%), and persons aged 23–30 years (0.92%) than in age groups <23 (0.68%) and >30 years (0.32%–0.71%) (Table 2). Among the 102 patients testing HIV-positive, 91 (89%) were not previously receiving medical care; 67 (74%) of these 91 patients, including the five patients with acute HIV infection, were linked to HIV medical care. Discussion The findings of both FOCUS programs demonstrate that routine HIV screening using existing clinical staff increased the numbers of patients tested and diagnosed with HIV infection. The prevalence of undiagnosed HIV infection at both programs exceeded CDC’s recommended threshold (≥0.1%) for routine screening (3), and most persons previously diagnosed with HIV infection at both programs were not receiving medical care. UHP and ILH identified patients with undiagnosed and previously diagnosed HIV infections and successfully linked the majority to HIV medical care. Active linkage is an essential element of a routine screening program to ensure that HIV-infected persons receive HIV care and services. These integrated routine HIV screening programs can serve as models for other emergency and primary health-care settings. Several factors associated with the FOCUS principles, including supportive institutional policy changes, EHR prompts, staff education, and conventional laboratory testing for HIV, contributed to these sustainable and scalable routine HIV screening programs. Similar EHR prompts, provider training, and periodic feedback led to immediate and sustained increases in HIV testing in Veterans Healthcare Administration facilities during 2009–2011 (5). New laboratory testing methods can reduce turnaround time for test results, are more sensitive during early infection, and can detect acute HIV infections. The transition from point-of-care rapid testing to laboratory testing reduced staff time (6) and costs (7), increased feasibility to test larger numbers of patients, and allowed ILH to detect acute HIV infections. Almost all patients who tested HIV-positive received their test results. UHP received FOCUS support in the first 2 years but has continued the HIV screening program without external funding. Replication of the FOCUS model has begun; UHP staff trained five federally qualified health centers in New York City in 2013 to implement routine HIV screening. The findings in this report are subject to at least four limitations. First, it was not possible to assess how much each factor of the new screening strategy individually contributed to the increase in screening. Second, the findings from this study might not be generalizable to other clinic settings with different HIV prevalence. Third, UHP might have underestimated HIV infections because its laboratory testing was unable to detect acute HIV infection. Finally, linkage to care might be underreported if it occurred at a different care facility. Routine HIV screening with an active linkage element reduces the number of persons unaware of their HIV infection and links patients to medical care. These patients are then able to benefit from effective treatment to improve health and reduce transmission risk (2). The two programs highlighted in this report screened more patients for HIV by using EHR prompts, conventional laboratory testing, and provider training and feedback. Combined, these techniques identified more patients with HIV infection and linked them to care by adopting practices that other health-care settings might choose to replicate. What is already known on this topic? In 2006, CDC issued recommendations for routine human immunodeficiency virus (HIV) screening of adults, adolescents, and pregnant women in health-care settings. However, many clinical settings have not adopted routine screening. Routine screening promotes the linkage of HIV-infected persons into medical care. This allows them to benefit from effective treatment, which improves their health and reduces HIV transmission. What is added by this report? Electronic health record prompts, staff education, and shift from point-of-care rapid testing to laboratory testing were features that made routine HIV screening programs successful at the Urban Health Plan in New York City and the Interim Louisiana Hospital in New Orleans. This allowed integration of HIV screening into clinic workflow, scalability (i.e., the ability to expand the number of patients screened), and sustainability. In addition to identifying patients newly diagnosed with HIV infection, routine screening also identified patients previously diagnosed but not in care, and actively linked these patients to care. What are the implications for public health practice? These programs made HIV screening more scalable, and linked patients to HIV care. The design is being sustained without external support at the Urban Health Plan and is being replicated in other clinics. These two programs can serve as models that could be adapted by other health-care settings.

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          Most cited references4

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          Revised recommendations for HIV testing of adults, adolescents, and pregnant women in health-care settings.

          These recommendations for human immunodeficiency virus (HIV) testing are intended for all health-care providers in the public and private sectors, including those working in hospital emergency departments, urgent care clinics, inpatient services, substance abuse treatment clinics, public health clinics, community clinics, correctional health-care facilities, and primary care settings. The recommendations address HIV testing in health-care settings only. They do not modify existing guidelines concerning HIV counseling, testing, and referral for persons at high risk for HIV who seek or receive HIV testing in nonclinical settings (e.g., community-based organizations, outreach settings, or mobile vans). The objectives of these recommendations are to increase HIV screening of patients, including pregnant women, in health-care settings; foster earlier detection of HIV infection; identify and counsel persons with unrecognized HIV infection and link them to clinical and prevention services; and further reduce perinatal transmission of HIV in the United States. These revised recommendations update previous recommendations for HIV testing in health-care settings and for screening of pregnant women (CDC. Recommendations for HIV testing services for inpatients and outpatients in acute-care hospital settings. MMWR 1993;42[No. RR-2]:1-10; CDC. Revised guidelines for HIV counseling, testing, and referral. MMWR 2001;50[No. RR-19]:1-62; and CDC. Revised recommendations for HIV screening of pregnant women. MMWR 2001;50[No. RR-19]:63-85). Major revisions from previously published guidelines are as follows: For patients in all health-care settings HIV screening is recommended for patients in all health-care settings after the patient is notified that testing will be performed unless the patient declines (opt-out screening). Persons at high risk for HIV infection should be screened for HIV at least annually. Separate written consent for HIV testing should not be required; general consent for medical care should be considered sufficient to encompass consent for HIV testing. Prevention counseling should not be required with HIV diagnostic testing or as part of HIV screening programs in health-care settings. For pregnant women HIV screening should be included in the routine panel of prenatal screening tests for all pregnant women. HIV screening is recommended after the patient is notified that testing will be performed unless the patient declines (opt-out screening). Separate written consent for HIV testing should not be required; general consent for medical care should be considered sufficient to encompass consent for HIV testing. Repeat screening in the third trimester is recommended in certain jurisdictions with elevated rates of HIV infection among pregnant women.
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            Comparing the costs of HIV screening strategies and technologies in health-care settings.

            In 2006, the Centers for Disease Control and Prevention (CDC) recommended routine human immunodeficiency virus (HIV) screening for people aged 13 to 64 years in all U.S. health-care settings. Earlier recommendations focused on those at high risk for HIV and included more extensive pretest counseling. HIV screening may also involve either rapid or conventional testing. The purpose of this research was to estimate the costs of these different testing procedures and the cost per HIV-infected patient correctly receiving test results in three health-care scenarios that illustrated these policy differences. The study estimated the costs of rapid and conventional HIV testing in the following scenarios: (1) sexually transmitted disease (STD) clinic counseling and testing (CT), (2) STD clinic screening, and (3) emergency department (ED) screening. Costs were estimated from the provider perspective in 2006 dollars. A decision analytic model was developed to estimate the cost per HIV-infected patient notified of test results using the two testing procedures in the three scenarios. Although the complete rapid testing procedure was more expensive than conventional testing, the cost per HIV-infected patient receiving test results was lower for the rapid test compared with conventional testing in all scenarios. Per-patient costs of receiving results were lowest in the ED screening scenario and highest in the STD CT scenario. These costs were sensitive to changes in test costs, HIV prevalence, and return rates following conventional tests. HIV screening in general health-care settings is economically feasible, particularly with rapid tests that lower the cost of HIV-infected patients receiving their test results.
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              Central implementation strategies outperform local ones in improving HIV testing in Veterans Healthcare Administration facilities.

              Pilot data suggest that a multifaceted approach may increase HIV testing rates, but the scalability of this approach and the level of support needed for successful implementation remain unknown. To evaluate the effectiveness of a scaled-up multi-component intervention in increasing the rate of risk-based and routine HIV diagnostic testing in primary care clinics and the impact of differing levels of program support. Three arm, quasi-experimental implementation research study. Veterans Health Administration (VHA) facilities. Persons receiving primary care between June 2009 and September 2011 INTERVENTION: A multimodal program, including a real-time electronic clinical reminder to facilitate HIV testing, provider feedback reports and provider education, was implemented in Central and Local Arm Sites; sites in the Central Arm also received ongoing programmatic support. Control Arm sites had no intervention Frequency of performing HIV testing during the 6 months before and after implementation of a risk-based clinical reminder (phase I) or routine clinical reminder (phase II). The adjusted rate of risk-based testing increased by 0.4 %, 5.6 % and 10.1 % in the Control, Local and Central Arms, respectively (all comparisons, p < 0.01). During phase II, the adjusted rate of routine testing increased by 1.1 %, 6.3 % and 9.2 % in the Control, Local and Central Arms, respectively (all comparisons, p < 0.01). At study end, 70-80 % of patients had been offered an HIV test. Use of clinical reminders, provider feedback, education and social marketing significantly increased the frequency at which HIV testing is offered and performed in VHA facilities. These findings support a multimodal approach toward achieving the goal of having every American know their HIV status as a matter of routine clinical practice.
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                Author and article information

                Journal
                MMWR Morb Mortal Wkly Rep
                MMWR Morb. Mortal. Wkly. Rep
                MMWR
                MMWR. Morbidity and Mortality Weekly Report
                U.S. Centers for Disease Control
                0149-2195
                1545-861X
                27 June 2014
                27 June 2014
                : 63
                : 25
                : 537-541
                Affiliations
                [1 ]EIS officer, CDC
                [2 ]Division of HIV/AIDS Prevention, National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention, CDC
                [3 ]Urban Health Plan, Inc., New York, New York
                [4 ]Section of Emergency Medicine, Louisiana State University Health Sciences Center
                Author notes
                Corresponding author: Xia Lin, xmlin@ 123456cdc.gov , 404-639-5296
                Article
                537-541
                5779387
                24964879
                a23094c0-629a-4778-b9d1-9ca29c2d8b1e
                Copyright @ 2014

                All material in the MMWR Series is in the public domain and may be used and reprinted without permission; citation as to source, however, is appreciated.

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