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1.
Gerontol Geriatr Educ ; 40(1): 121-131, 2019.
Article in English | MEDLINE | ID: mdl-29630470

ABSTRACT

There is a well-described need to increase the competence of the primary care workforce in the principles of geriatrics and palliative care, and as value-based payment models proliferate, there is increased incentive for the acquisition of these skills. Through a Geriatric Workforce Enhancement Program grant, we developed an adaptable curriculum around commonly encountered topics in palliative care and geriatrics that can be delivered to multidisciplinary clinicians in primary care settings. All participants in this training were part of an Accountable Care Organization (ACO) and were motivated to improve to care for complex older adults. A needs assessment was performed on each practice or group of learners and the curriculum was adapted accordingly. With the use of patient education and screening tools with strong validity evidence, the participants were trained in the principals of geriatrics and palliative care with a focus on advance care planning and assessing for frailty and functional decline. Comparison of pre- and post-test scores demonstrated increased confidence and knowledge in goals of care and basic geriatric assessment. Participants described feeling more able to address needs, have conversations around goals of care, and more able to recognize patients who would benefit from collaboration with geriatrics and palliative care.


Subject(s)
Geriatrics/education , Interprofessional Relations , Palliative Care/organization & administration , Patient Care Team/organization & administration , Primary Health Care/organization & administration , Accountable Care Organizations/organization & administration , Aged , Aged, 80 and over , Cooperative Behavior , Curriculum , Geriatric Assessment , Humans , Patient Care Planning , Patient Education as Topic/organization & administration , Program Evaluation , Quality Improvement/organization & administration
2.
Addict Sci Clin Pract ; 12(1): 24, 2017 10 02.
Article in English | MEDLINE | ID: mdl-28965489

ABSTRACT

BACKGROUND: Contemporary studies about HIV care continuum (HCC) outcomes within substance using populations primarily focus on individual risk factors rather than provider- or systems-level influences. Over 25% of people living with HIV (PLWH) have substance use disorders that can alter their path through the HCC. As part of a study of HCC outcomes in nine small cities in Southern New England (population 100,000-200,000 and relatively high HIV prevalence particularly among substance users), this qualitative analysis sought to understand public health staff and HIV service providers' perspectives on how substance use may influence HCC outcomes. METHODS: Interviews with 49 participants, collected between November 2015 and June 2016, were analyzed thematically using a modified social ecological model as the conceptual framework and codes for substance use, HCC barriers and facilitators, successes and failures of initiatives targeting the HCC, and criminal justice issues. RESULTS: Eight themes were identified concerning the impact of substance use on HCC outcomes. At the individual level, these included coping and satisfying basic needs and could influence all HCC steps (i.e., testing, treatment linkage, adherence, and retention, and viral load suppression). The interpersonal level themes included stigma issues and providers' cultural competence and treatment attitudes and primarily influenced treatment linkage, retention, and viral load suppression. These same HCC steps were influenced at the health care systems level by organizations' physical environment and resources as well as intra-/inter-agency communication. Testing and retention were the most likely steps to affect at the policy/society level, and the themes included opposition within an organization or community, and activities with unintended consequences. CONCLUSIONS: The most substantial HCC challenges for PLWH with substance use problems included linking and retaining in treatment those with multiple co-morbidities and meeting their basic living needs. Recommendations to improve HCC outcomes for PLWH with substance use problems include increasing easy access to effective drug and mental health treatment, expanding case management and peer navigation services, training staff about harm reduction, de-stigmatizing, and culturally competent approaches to interacting with patients, and increasing information-sharing and service coordination among service providers and the social service and criminal justice systems.


Subject(s)
HIV Infections/drug therapy , Health Services Accessibility , Medication Adherence/statistics & numerical data , Patient Acceptance of Health Care/psychology , Substance-Related Disorders/complications , Continuity of Patient Care , Female , HIV Infections/complications , Health Behavior , Humans , Male , Middle Aged , New England , Socioeconomic Factors
3.
J Int AIDS Soc ; 20(1): 21290, 2017 01 17.
Article in English | MEDLINE | ID: mdl-28364562

ABSTRACT

INTRODUCTION: Acceptability and willingness to both take and pay for HIV self-tests (HIVSTs) in US neighbourhoods with high rates of HIV infection are not well understood. METHODS: We surveyed 1,535 individuals about acceptability and willingness to take and pay for an HIVST in a predominately African American neighbourhood with 3% HIV seroprevalence. We recruited individuals presenting for HIV screening services in a community-based programme. Latent class analysis (LCA) grouped individuals with similar patterns of HIV-risk behaviours and determined which groups would be most willing to use and buy HIVSTs. RESULTS: Nearly 90% of respondents were willing to use an HIVST; 55% were willing to buy HIVSTs, but only 23% were willing to pay the market price of US $40. Four distinct groups emerged and were characterized by risk behaviours: (1) low risk (N = 324); (2) concurrent partnerships (N = 346); (3) incarceration and substance use (N = 293); and (4) condomless sex/multiple partners (N = 538). Individuals in the low-risk class were less willing to self-test compared to concurrent sexual partners (OR = 0.39, p = .003) and incarceration and substance use (OR = 0.46, p = .011) classes. There were no significant differences across classes in the amount individuals were willing to pay for an HIVST. CONCLUSION: HIVSTs were overwhelmingly acceptable but cost prohibitive; most participants were unwilling to pay the market rate of US $40. Subsidizing and implementing HIVST programmes in communities with high rates of infection present a public health opportunity, particularly among individuals reporting condomless sex with multiple partners, concurrent sexual partnerships and those with incarceration and substance use histories.


Subject(s)
AIDS Serodiagnosis/methods , HIV Infections/diagnosis , Self Care/methods , Serologic Tests/economics , AIDS Serodiagnosis/economics , Adolescent , Adult , Black or African American , Cities , Data Collection , Female , HIV Infections/epidemiology , Humans , Male , Risk Factors , Self Care/economics , United States/epidemiology
4.
Public Health Rep ; 131(2): 264-71, 2016.
Article in English | MEDLINE | ID: mdl-26957661

ABSTRACT

Frequent use of websites and mobile telephone applications (apps) by men who have sex with men (MSM) to meet sexual partners, commonly referred to as "hookup" sites, make them ideal platforms for HIV prevention messaging. This Rhode Island case study demonstrated widespread use of hookup sites among MSM recently diagnosed with HIV. We present the advertising prices and corporate social responsibility (CSR) programs of the top five sites used by newly diagnosed HIV-positive MSM to meet sexual partners: Grindr, Adam4Adam, Manhunt, Scruff, and Craigslist. Craigslist offered universal free advertising. Scruff offered free online advertising to selected nonprofit organizations. Grindr and Manhunt offered reduced, but widely varying, pricing for nonprofit advertisers. More than half (60%, 26/43) of newly diagnosed MSM reported meeting sexual partners online in the 12 months prior to their diagnosis. Opportunities for public health agencies to promote HIV-related health messaging on these sites were limited. Partnering with hookup sites to reach high-risk MSM for HIV prevention and treatment messaging is an important public health opportunity for reducing disease transmission risks in Rhode Island and across the United States.


Subject(s)
Consumer Health Information/organization & administration , HIV Infections/prevention & control , Health Promotion/organization & administration , Homosexuality, Male , Marketing of Health Services/organization & administration , Sexual Partners , Social Networking , Substance Abuse, Intravenous/complications , Adolescent , Adult , Consumer Health Information/economics , Consumer Health Information/methods , Female , HIV Infections/epidemiology , HIV Infections/transmission , Health Promotion/economics , Health Promotion/methods , Humans , Internet , Interviews as Topic , Male , Marketing of Health Services/economics , Marketing of Health Services/methods , Middle Aged , Mobile Applications , Organizational Case Studies , Rhode Island/epidemiology , Risk Assessment , Risk-Taking , Sexual Behavior/statistics & numerical data , Substance Abuse, Intravenous/epidemiology , Young Adult
5.
Public Health Rep ; 131 Suppl 1: 30-40, 2016.
Article in English | MEDLINE | ID: mdl-26862228

ABSTRACT

OBJECTIVE: CDC has recommended routine HIV screening since 2006. However, few community health centers (CHCs) routinely offer HIV screening. Research is needed to understand how to implement routine HIV screening programs, particularly in medically underserved neighborhoods with high rates of HIV infection. A routine HIV screening program was implemented and evaluated in a Philadelphia, Pennsylvania, neighborhood with high rates of HIV infection. METHODS: Implementation science is the study of methods to promote the integration of research findings and evidence into health-care policy and practice. Using an implementation science approach, the results of the program were evaluated by measuring acceptability, adoption, and penetration of routine HIV screening. RESULTS: A total of 5,878 individuals were screened during the program. HIV screening was highly accepted among clinic patients. In an initial needs assessment of 516 patients, 362 (70.2%) patients reported that they would accept testing if offered. Routine screening policies were adopted clinic-wide. Staff trainings, new electronic medical records that prompted staff members to offer screening and evaluate screening rates, and other continuing quality-improvement policies helped promote screenings. HIV screening offer rates improved from an estimated 5.0% of eligible patients at baseline in March 2012 to an estimated 59.3% of eligible patients in December 2014. However, only 5,878 of 13,827 (42.5%) patients who were offered screening accepted it, culminating in a 25.2% overall screening rate. Seventeen of the 5,878 patients tested positive, for a seropositivity rate of 0.3%. CONCLUSION: Routine HIV screening at CHCs in neighborhoods with high rates of HIV infection is feasible. Routine screening is an important tool to improve HIV care continuum outcomes and to address racial and geographic disparities in HIV infection.


Subject(s)
AIDS Serodiagnosis , Community Health Centers , Mass Screening , AIDS Serodiagnosis/methods , Adolescent , Adult , Aged , Community Health Centers/organization & administration , Female , HIV Infections/diagnosis , HIV Infections/epidemiology , Health Services Needs and Demand , Humans , Male , Mass Screening/methods , Mass Screening/organization & administration , Middle Aged , Philadelphia/epidemiology , Program Development , Urban Health Services/organization & administration , Young Adult
6.
AIDS Behav ; 20(6): 1334-42, 2016 06.
Article in English | MEDLINE | ID: mdl-26683032

ABSTRACT

The US HIV/AIDS epidemic is concentrated in the Deep South, yet factors contributing to HIV transmission are not fully understood. We examined relationships between substance use, sexual partnership characteristics, and condom non-use in an African American sample of STI clinic attendees in Jackson, Mississippi. We assessed condom non-use at last intercourse with up to three recent sexual partners reported by participants between January and June 2011. Participant- and partner-level correlates of condom non-use were examined using generalized estimating equations. The 1295 participants reported 2880 intercourse events, of which 1490 (51.7 %) involved condom non-use. Older age, lower educational attainment, reporting financial or material dependence on a sex partner, sex with a primary partner, and higher frequency of sex were associated with increased odds of condomless sex. HIV prevention efforts in the South should address underlying socioeconomic disparities and structural determinants that result in partner dependency and sexual risk behavior.


Subject(s)
Black or African American/psychology , Condoms/statistics & numerical data , HIV Infections/prevention & control , Sexual Behavior , Sexual Partners , Acquired Immunodeficiency Syndrome/prevention & control , Adult , Black or African American/statistics & numerical data , Ambulatory Care Facilities , Data Collection , Female , HIV Infections/epidemiology , Humans , Male , Mississippi/epidemiology , Risk Factors , Risk-Taking , Safe Sex/statistics & numerical data , Substance-Related Disorders/epidemiology , Substance-Related Disorders/psychology , Unsafe Sex/statistics & numerical data
7.
J Gen Intern Med ; 30(7): 950-7, 2015 Jul.
Article in English | MEDLINE | ID: mdl-25680353

ABSTRACT

BACKGROUND: Many of the five million Americans chronically infected with hepatitis C (HCV) are unaware of their infection and are not in care. OBJECTIVE: We implemented and evaluated HCV screening and linkage-to-care interventions in a community setting. DESIGN: We developed a comprehensive, community-based HCV screening and linkage-to-care program in a medically underserved neighborhood with high rates of HCV infection in Philadelphia, Pennsylvania. We provided patient navigation services to enroll uninsured patients in insurance programs, facilitate referrals from primary care physicians and link patients to an HCV infectious disease specialist with intention to treat and cure. PATIENTS: Philadelphia residents were recruited through street outreach. MAIN MEASURES: We measured anti-HCV seroprevalence and diagnosis, linkage and retention in care outcomes for chronically infected patients. KEY RESULTS: We screened 1,301 participants for HCV; anti-HCV seroprevalence was 3.9 % and 2.8% of all patients were chronically infected. Half of chronically infected patients were newly diagnosed; the remaining patients were aware of infection but not in care. We provided confirmatory RNA testing and results, assisted patients with attaining insurance and linked most chronically infected patients to a primary care provider. The biggest barrier to retaining patients in care was obtaining referrals for subspecialty providers; however, we obtained referrals for 64% of chronically infected participants and have retained most in subspecialty HCV care. Several have commenced treatment. CONCLUSIONS: Non-clinical screening programs with patient navigator services are an effective means to diagnose, link, retain and re-engage patients in HCV care. Eliminating referral requirements for subspecialty care might further enhance retention in care for patients chronically infected with HCV.


Subject(s)
Community Health Services/organization & administration , Hepatitis C, Chronic/diagnosis , Patient Navigation/organization & administration , Adult , Aged , Case Management/organization & administration , Female , Health Services Research/methods , Humans , Insurance, Health/statistics & numerical data , Male , Mass Screening/organization & administration , Medically Underserved Area , Middle Aged , Pennsylvania , Primary Health Care/organization & administration , Program Evaluation , Referral and Consultation/organization & administration , Risk-Taking , Socioeconomic Factors
8.
Health Promot Pract ; 16(1): 91-100, 2015 Jan.
Article in English | MEDLINE | ID: mdl-24879446

ABSTRACT

African Americans account for 45% of new HIV infections in the United States. Little empirical research investigates African American community leaders' normative recommendations for addressing these disparities. Philadelphia's HIV infection rate is 5 times the national average, nearly 70% of new infections are among African Americans, and 2% of African Americans in Philadelphia are living with HIV/AIDS. Using a community-based participatory research approach, we convened focus groups among 52 African American community leaders from diverse backgrounds to solicit normative recommendations for reducing Philadelphia's racial disparities in HIV infection. Leaders recommended that (a) Philadelphia's city government should raise awareness about HIV/AIDS with media campaigns featuring local leaders, (b) local HIV-prevention interventions should address social and structural factors influencing HIV risks rather than focus exclusively on mode of HIV transmission, (c) resources should be distributed to the most heavily affected neighborhoods of Philadelphia, and (d) faith institutions should play a critical role in HIV testing, treatment, and prevention efforts. We developed a policy memo highlighting these normative recommendations for how to enhance local HIV prevention policy. This policy memo led to Philadelphia City Council hearings about HIV/AIDS in October 2010 and subsequently informed local HIV/AIDS prevention policy and development of local HIV prevention interventions. This community-based participatory research case study offers important lessons for effectively engaging community leaders in research to promote HIV/AIDS policy change.


Subject(s)
Black or African American , HIV Infections/ethnology , HIV Infections/therapy , Acquired Immunodeficiency Syndrome/ethnology , Acquired Immunodeficiency Syndrome/therapy , Community-Based Participatory Research , Focus Groups , HIV Infections/prevention & control , Health Knowledge, Attitudes, Practice , Health Status Disparities , Humans , Philadelphia , Religion , United States
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