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Featured researches published by D. Scott Batey.


Aids Research and Therapy | 2016

The HIV treatment cascade and care continuum: updates, goals, and recommendations for the future

Emma Sophia Kay; D. Scott Batey; Michael J. Mugavero

The HIV care continuum is a framework that models the dynamic stages of HIV care. The continuum consists of five main steps, which, at the population level, are depicted cross-sectionally as the HIV treatment cascade. These steps include diagnosis, linkage to care (LTC), retention in care (RiC), adherence to antiretroviral therapy (ART), and viral suppression. Although the HIV treatment cascade is represented as a linear, unidirectional framework, persons living with HIV (PLWH) often experience the care continuum in a less streamlined fashion, skip steps altogether, or even exit the continuum for a period of time and regress to an earlier stage. The proportion of PLWH decreases at each successive step of the cascade, beginning with an estimated 86% who are diagnosed and dropping dramatically to approximately 30% of PLWH who are virally suppressed in the United States (US). In this current issues review, we describe each step in the cascade, discuss targeted interventions that address weak points in the continuum, review domestic and international policies that help shape and direct HIV care strategies, and conclude with recommendations and future directions for HIV providers and policymakers. While we primarily examine issues related to domestic HIV care in the US, we also discuss international applications of the continuum in order to provide broader context.


Aids Care-psychological and Socio-medical Aspects of Aids\/hiv | 2015

Patient and provider priorities for self-reported domains of HIV clinical care.

Rob J. Fredericksen; Todd C. Edwards; Jessica S. Merlin; Laura E. Gibbons; Deepa Rao; D. Scott Batey; Lydia Dant; E. Paez; Anna E. Church; Paul K. Crane; Heidi M. Crane; Donald L. Patrick

We sought to understand how HIV-infected patients, their providers, and HIV care researchers prioritize self-reported domains of clinical care. Participants rank-ordered two lists of domains. A modified Delphi process was used for providers and researchers. Approximately 25% of patients were interviewed to discuss rationale for rank order choices. List 1 included anger, anxiety, depression, fatigue, physical function, pain, and sleep disturbance. List 2 included alcohol abuse, cognitive function, HIV stigma, HIV and treatment symptoms, medication adherence, positive affect, sexual risk behavior, sexual function, social roles, spirituality/meaning of life, and substance abuse. Seventy-four providers, 80 HIV care researchers, and 66 patients participated. Patients ranked context-based domains, such as HIV stigma, more highly than providers, while health behaviors, such as drug or alcohol use, ranked lower. Patients described a need to address wider-context challenges such as HIV stigma in order to positively impact health behaviors. Divergent patient and provider priorities highlight the importance of incorporating views from all stakeholders and suggests the need for a care approach that more effectively addresses contextual barriers to adverse health behaviors.


Journal of Acquired Immune Deficiency Syndromes | 2017

Experienced Hiv-Related Stigma in Healthcare and Community Settings: Mediated Associations With Psychosocial and Health Outcomes

Emma Sophia Kay; Whitney S. Rice; Kaylee B. Crockett; Ghislaine C. Atkins; D. Scott Batey; Bulent Turan

Introduction: There are multiple dimensions of HIV-related stigma that can compromise the mental and physical health of people living with HIV. We focused on the dimension of experienced stigma, defined as exposure to acts of discrimination, devaluation, and prejudice, and investigated its relationship with HIV health and psychosocial outcomes. Methods: We examined associations between experienced stigma in the community and health care settings and psychosocial and health outcomes for people living with HIV (N = 203) receiving care at an urban HIV clinic in the Southeastern United States. We also investigated whether those effects are unique to experienced stigma or are mediated by other dimensions of HIV-related stigma. Results: Experienced stigma was associated with suboptimal clinical outcomes such as viral nonsuppression, as well as poor affective, cognitive, and mental health outcomes (self-esteem, depressive symptoms, avoidance coping, and blame coping) and interpersonal outcomes such as social support and physician trust. Furthermore, serial mediation models suggested significant indirect effects of experienced stigma through internalized stigma and anticipated stigma from various theoretically expected sources of stigma (eg, community members, friends and family, and health care workers), with varying effects depending on the source. Conclusions: These findings suggest nuanced mechanisms for the effects of experienced HIV-related stigma, especially in health care settings, and may be used to inform stigma-reduction interventions. Interventions designed to address experienced stigma in health care settings might be more tailored to specific outcomes, such as depression and physician trust, than interventions designed to address experienced stigma in the community.


Clinical Infectious Diseases | 2018

The North-South Divide: Substance Use Risk, Care Engagement, and Viral Suppression Among Hospitalized Human Immunodeficiency Virus–Infected Patients in 11 US Cities

Morgan M. Philbin; Daniel J. Feaster; Lauren Gooden; Rui Duan; Moupali Das; Petra Jacobs; Gregory M. Lucas; D. Scott Batey; Ank E. Nijhawan; Jeffrey M. Jacobson; Raul N. Mandler; Eric S. Daar; Deborah McMahon; Wendy S. Armstrong; Carlos del Rio; Lisa R. Metsch

Regional variability in human immunodeficiency virus (HIV) care engagement remains underexplored. Multiple logistic models compared HIV outcomes for participants from 5 Southern (n = 557) and 6 non-Southern (n = 670) sites. Southern participants were less likely to experience viral suppression (adjusted odds ratio [aOR], 0.52; 95% confidence interval [CI], .37-.72) and had a higher likelihood of a CD4+ count <200 cells/µL (aOR, 1.53; 95% CI, 1.17-2.00). HIV intervention and social safety net programs should be expanded. Clinical Trials Registration NCT01612169.


Aids and Behavior | 2018

Suboptimal Retention in Care Among Recently Released Prisoners: Implications for Social Workers in HIV Primary Care

Jill Murphree; D. Scott Batey; Emma Sophia Kay; Andrew O. Westfall; Michael J. Mugavero

Certain populations of people living with HIV (PLWH) are at greater risk for falling out of care, including PLWH with a history of incarceration. This is associated with increased risk of morbidity and mortality. In the current retrospective cohort study, we examined patient-level information for 340 PLWH who had transferred HIV care services from prison or from other community-based or private HIV primary care providers to a large urban HIV clinic in the southeastern United States. Results indicated that, compared to those transferring care from another community-based or private medical provider, PLWH transferring care from prison were significantly less likely to be retained in care than PLWH transferring care from other providers, even after controlling for other factors. HIV primary care social workers, who are trained to provide case management services, can help provide PLWH with a coordinated continuum of care that addresses the complex issues faced post-release.


Journal of Public Health Management and Practice | 2017

The Fragile Balance of Community-Based Health Care: One Communityʼs United Response When the HIV/AIDS Primary Care Safety Net Failed

Matthew Fifolt; D. Scott Batey; James L. Raper; Jane E. Mobley; Lisa C. McCormick

After more than 20 years of continuous service to people living with HIV (PLWH), the doors of St Georges Clinic (St Georges), an ambulatory facility in Jefferson County, Alabama, were irrevocably closed on December 31, 2012. Despite serving an indigent patient population of more than 800 P


Clinical Infectious Diseases | 2010

Routine, Self-Administered, Touch-Screen, Computer- Based Suicidal Ideation Assessment Linked to Automated Response Team Notification in an HIV Primary Care Setting

Sarah T. Lawrence; James H. Willig; Heidi M. Crane; Jiatao Ye; Inmaculada Aban; William B. Lober; Christa R. Nevin; D. Scott Batey; Michael J. Mugavero; Cheryl McCullumsmith; Charles Wright; Mari M. Kitahata; James L. Raper; Micheal S. Saag; Joseph E. Schumacher


Aids and Behavior | 2013

Routine depression screening in an HIV clinic cohort identifies patients with complex psychiatric co-morbidities who show significant response to treatment.

Joseph E. Schumacher; Cheryl McCullumsmith; Michael J. Mugavero; Paige E. Ingle-Pang; James L. Raper; James H. Willig; Zhiying You; D. Scott Batey; Heidi M. Crane; Sarah T. Lawrence; Charles Wright; Glenn J. Treisman; Michael S. Saag


Social Work | 2013

Technology Use among Emerging Adult Homeless in Two U.S. Cities

David E. Pollio; D. Scott Batey; Kimberly Bender; Kristin M. Ferguson; Sanna J. Thompson


AIDS Research and Human Retroviruses | 2012

Short Communication Routine HIV Testing in the Emergency Department: Assessment of Patient Perceptions

D. Scott Batey; Victoria L. Hogan; Ryan Cantor; Christopher M. Hamlin; Kelly Ross-Davis; Christa R. Nevin; Cindy Zimmerman; Shakira Thomas; Michael J. Mugavero; James H. Willig

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Michael J. Mugavero

University of Alabama at Birmingham

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James L. Raper

University of Alabama at Birmingham

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Heidi M. Crane

University of Washington

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James H. Willig

University of Alabama at Birmingham

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Andrew O. Westfall

University of Alabama at Birmingham

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Anne Zinski

University of Alabama at Birmingham

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Ashutosh Tamhane

University of Alabama at Birmingham

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Bulent Turan

University of Alabama at Birmingham

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Charles Wright

University of Alabama at Birmingham

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