Abstract:SYNOPSISObjective. The present study examined the scope of rapid human immunodeficiency virus (HIV) testing in urban U.S. hospitals.Methods. In a multistage national probability sample, 12 primary metropolitan statistical areas (three per region) were sampled randomly, with weights proportionate to acquired immunodeficiency syndrome (AIDS) populations. All 671 eligible hospitals within areas were selected. Laboratory staff from 584 hospitals (87%) were interviewed by telephone in 2005.Results. About 52% report… Show more
“…Despite recent moves to increase implementation of these guidelines by individual states, and an increase in ED‐based HIV testing programs, there are few empirical data on ED patients' knowledge, beliefs, attitudes, and acceptance toward these revised HIV testing strategies . Studies that have examined patients' acceptance of revised HIV testing strategies tend to focus on the number of patients who accept or refuse an offer of HIV testing, but do not always delve deeply into the reasons behind these decisions .…”
Objectives
The objective of this study was to explore emergency department (EDs) patient’s knowledge, beliefs, attitudes, and acceptability towards revised human immunodeficiency virus (HIV) testing recommendations.
Methods
Participants were recruited in proportion to the racial, sex, and ethnic makeup of the study ED. Interviewers presented participants with a stimulus followed by questions about opt-out consent, elimination of separate written consent, and curtailed counseling. Three investigators coded all transcripts using an iterative coding strategy until thematic saturation was achieved.
Results
Thirty-four semi-structured, in-depth, individual interviews were conducted, including five with patients ages 13 to 17 years, and five with Spanish-speaking patients. Nineteen (56%) participants were women. The mean age was 31 years (SD ±12 years). Most were Hispanic (38%), or African American/black (44%). Only one (2.9%) participant knew about the revised testing recommendations. Participants believed opt-out consent would result in increased testing, but this was confounded by misunderstanding of the consent process: “so the opt-out is, you basically don’t have a choice.” Participants thought eliminating separate written consent was a positive change but that it could result in people being tested without their knowledge. Attitudes diverged over curtailed counseling, but participants felt patients “should have options” for counseling because “everybody isn’t the same.”
Conclusions
Emergency department patients were unaware of revised HIV testing recommendations. Most felt opt-out consent and elimination of separate written consent were positive changes but could result in a patient being tested without his or her knowledge. The response to curtailed counseling was polarized but participants agreed on the need to accommodate personal preferences. This information may be useful to when designing ED-based HIV testing programs.
“…Despite recent moves to increase implementation of these guidelines by individual states, and an increase in ED‐based HIV testing programs, there are few empirical data on ED patients' knowledge, beliefs, attitudes, and acceptance toward these revised HIV testing strategies . Studies that have examined patients' acceptance of revised HIV testing strategies tend to focus on the number of patients who accept or refuse an offer of HIV testing, but do not always delve deeply into the reasons behind these decisions .…”
Objectives
The objective of this study was to explore emergency department (EDs) patient’s knowledge, beliefs, attitudes, and acceptability towards revised human immunodeficiency virus (HIV) testing recommendations.
Methods
Participants were recruited in proportion to the racial, sex, and ethnic makeup of the study ED. Interviewers presented participants with a stimulus followed by questions about opt-out consent, elimination of separate written consent, and curtailed counseling. Three investigators coded all transcripts using an iterative coding strategy until thematic saturation was achieved.
Results
Thirty-four semi-structured, in-depth, individual interviews were conducted, including five with patients ages 13 to 17 years, and five with Spanish-speaking patients. Nineteen (56%) participants were women. The mean age was 31 years (SD ±12 years). Most were Hispanic (38%), or African American/black (44%). Only one (2.9%) participant knew about the revised testing recommendations. Participants believed opt-out consent would result in increased testing, but this was confounded by misunderstanding of the consent process: “so the opt-out is, you basically don’t have a choice.” Participants thought eliminating separate written consent was a positive change but that it could result in people being tested without their knowledge. Attitudes diverged over curtailed counseling, but participants felt patients “should have options” for counseling because “everybody isn’t the same.”
Conclusions
Emergency department patients were unaware of revised HIV testing recommendations. Most felt opt-out consent and elimination of separate written consent were positive changes but could result in a patient being tested without his or her knowledge. The response to curtailed counseling was polarized but participants agreed on the need to accommodate personal preferences. This information may be useful to when designing ED-based HIV testing programs.
“…The cost of an oral or serum rapid HIV test is relatively inexpensive ranging from approximately $8 to $25, not including the cost of the control packs (CDC, 2008). While use of rapid HIV testing is increasing (Thornton, Delpech, Kall, & Nardone, 2012), limited availability of rapid HIV testing for sexual assault survivors continues in the United States (Bogart et al, 2008) and for any population in Canada (Lee, Plitt, Fenton, Preiksaitis, & Singh, 2011; Thornton et al, 2012). …”
This cross-sectional study describes Sexual Assault Nurse Examiner (SANE)/Forensic Nurse Examiner (FNE) program practices related to HIV testing, non-occupational post-exposure prophylaxis (nPEP), and common barriers to offering HIV testing and nPEP. A convenience sample of 174 SANE/FNE programs in the United States and Canada was drawn from the International Association of Forensic Nurses database, and program coordinators completed web-based surveys. Three quarters of programs had nPEP policies, 31% provided HIV testing; and 63% offered nPEP routinely or upon request. Using Chi-square and Fishers' exact tests a greater proportion of Canadian programs had an nPEP protocol (p = .010), provided HIV testing (p = .004), and offered nPEP (p = .0001) than U.S.-based programs. Program coordinators rated providing pre-/post-counseling and follow-up as the most important barrier to HIV testing and medication costs as the most important barrier to providing nPEP. Our results indicate HIV-related services are offered inconsistently across SANE/FNE programs.
“…(8) HIV testing, the foremost imperative for preventing further transmission and to caring for those infected, is traditionally performed outside of the clinical encounter in centralized laboratories. (9) Tested individuals are asked to return several weeks post-test to learn the results, and for treatment and prevention counseling, to reduce risky behaviors among those found to be infected. However, more than one third of those tested do not return for results, representing a missed prevention opportunity.…”
Section: The Case For Point-of-care Technologies (Poct)mentioning
confidence: 99%
“…POC testing for screening, diagnosis, treatment initiation, and the monitoring of HIVtreatment efficacy helps resolve these deficiencies by allowing infected individuals to learn their serostatus quickly and by connecting them to medical care. (9) Low cost, user-friendly, and accurate HIV diagnostic tests, patterned after home pregnancy tests, are particularly enabling for those individuals who may not otherwise test. Direct ways of measuring the amount of the HIV virus present (viral load) allows monitoring of how advanced the infection is and how well treatment is working.…”
Section: The Case For Point-of-care Technologies (Poct)mentioning
The expectations of point-of-care technologies (POCT) are being increasingly shaped by the patient-centric narrative of P5 (predictive, preventive, personalized, participatory, and populationbased) medicine. Shifting the focus of our healthcare system to a personalized and preemptive approach will depend partly on the availability of field-deployable measurement technologies that provide rapid biometric information to providers and patients. In order to respond to the changing healthcare paradigm and hasten the integration of emerging sensor materials into clinically useful point-of-care (POC) approaches, it is essential that the sensor materials community understand and appreciate the clinical context, expectations, and aspirations of the healthcare consumers. After reviewing the drivers of the P5 medicine initiative, we review the context within which the POCT will be used, and some of the challenges associated with delivering portable, fast response, and highly reliable measurement technologies that can be used with complex biofluids in a range of settings by a variety of users. We conclude by emphasizing the potential synergies of linking POCT's to the "connected health" model which integrates mobile technologies, low-cost hardware, healthcare IT systems, big data analytics, and the Internet of Things (IoT) to connect all stakeholders for a timely sharing of pertinent health information necessary for timely and personalized healthcare.
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