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1.
Clin Chest Med ; 44(3): 501-508, 2023 09.
Article in English | MEDLINE | ID: mdl-37517830

ABSTRACT

Rural populations experience significant pulmonary health disparities compared with urban populations. Patients in rural communities experience health determinants including high smoking prevalence, worse nutrition, lower educational attainment, specific occupational exposures, decreased health-care access, as well as unique cultural and political drivers of health. This article describes social determinants of pulmonary health relevant in rural communities, describes examples of existing pulmonary disparities in rural populations, and highlights health policies with potential to mitigate disparities.


Subject(s)
Rural Population , Humans , Risk Factors , Urban Population
2.
Clin Chest Med ; 44(3): 651-660, 2023 09.
Article in English | MEDLINE | ID: mdl-37517842

ABSTRACT

Expansion of telehealth services has the potential to attenuate health inequities in pulmonary medicine, by improving access to care and health outcomes in patients with lung disease. These telehealth services include remote patient monitoring, synchronous telemedicine, and remote pulmonary rehabilitation. Currently, patients who are White, well-educated, wealthy, and from urban areas are the most likely to benefit from telehealth services. Without clear policy decisions and planning to overcome the "Digital Divide," telehealth services will only exacerbate existing disparities within the pulmonary disease. We describe the benefits and limitations of these new technologies and their impact on improving equity in pulmonary medicine.


Subject(s)
Pulmonary Medicine , Telemedicine , Humans , Outcome Assessment, Health Care , Health Services Accessibility
4.
Yale J Biol Med ; 94(3): 477-486, 2021 09.
Article in English | MEDLINE | ID: mdl-34602885

ABSTRACT

The population living in Central Appalachia is disproportionately impacted by lung disease. This is driven, in part, by occupational hazards and environmental exposures. However, it is more than coal dust that is driving the ongoing disparity of lung disease in the region. This review describes how the decline of the coal mine industry and subsequent rise of unemployment, poverty, and educational disparities have increased risk for worse pulmonary health outcomes in the region. Additional challenges related to healthcare access, substance use, cultural characteristics, and social capital are highlighted in their relation to pulmonary health within Central Appalachia. Lastly, the review describes strategies that hold promise to reduce regional health disparities. Several healthcare and community-centered initiatives are highlighted as successful examples of collaborative efforts working towards improving pulmonary health outcomes in the region. However, significant challenges related to social, economic, and environmental factors remain. Addressing these social determinants of health must be a paramount concern for healthcare, community and political leaders seeking to impact change and improve the health and well-being of this vulnerable population.


Subject(s)
Coal , Lung Diseases , Appalachian Region/epidemiology , Dust , Environmental Exposure , Humans
5.
Clin Chest Med ; 42(3): 407-415, 2021 09.
Article in English | MEDLINE | ID: mdl-34353447

ABSTRACT

Gender is the centerpiece to an individual's understanding of self and encompasses many behavioral, social, and cultural arenas; its broad scope means that it also intersects many social determinants of health. Multiple examples of social determinants highlighted in this article, including income, education, occupation, domestic exposures, and cultural norms such as sexual identity, are critical factors that contribute to ongoing respiratory disparities between genders. Each of these social factors can have disparate impact on patients of differing genders. Understanding and addressing social determinants of health between genders is an essential first step toward achieving respiratory health equity.


Subject(s)
Health Equity , Pulmonary Medicine , Female , Gender Identity , Humans , Male , Social Determinants of Health
6.
Clin Transplant ; 35(5): e14275, 2021 05.
Article in English | MEDLINE | ID: mdl-33682171

ABSTRACT

Post-operative delirium after lung transplantation is common. Its associations with health-related quality of life (HRQL), depression, and mortality remains unknown. In 236 lung transplant recipients, HRQL and depressive symptoms were assessed as part of a structured survey battery before and after transplantation. Surveys included the Geriatric Depressive Scale (GDS) and Short Form 12 (SF12). Delirium was assessed throughout the post-operative intensive care unit (ICU) stay with Confusion Assessment Method for ICU. Delirium and mortality data were extracted from electronic medical records. We examined associations between delirium and changes in depressive symptoms and HRQL using linear mixed effects models and association between delirium and mortality with Cox-proportional hazard models. Post-operative delirium occurred in 34 participants (14%). Delirium was associated with attenuated improvements in SF12-PCS (difference ₋4.0; 95%CI: -7.4, -0.7) but not SF12-MCS (difference 2.2; 95%CI: -0.7,5.7) or GDS (difference ₋0.4; 95%CI: -1.5,0.7). Thirty-two participants died during the study period. Delirium was associated with increased adjusted hazard risk of mortality (HR 17.9, 95%CI: 4.4,72.5). Delirium after lung transplantation identifies a group at increased risk for poorer HRQL and death within the first post-operative year. Further studies should investigate potential causal links between delirium, and poorer HRQL and mortality risk after lung transplantation.


Subject(s)
Delirium , Lung Transplantation , Aged , Humans , Intensive Care Units , Patient Reported Outcome Measures , Quality of Life
7.
AIDS Res Hum Retroviruses ; 35(8): 734-745, 2019 08.
Article in English | MEDLINE | ID: mdl-31146536

ABSTRACT

Many AIDS drug assistance programs (ADAPs) purchased Affordable Care Act (ACA) qualified health plans (QHPs) for low-income people living with HIV. To date, little has been written about this from the client perspective. The study's objective was to gain information about the experience of Virginia ADAP-funded QHP enrollment and the impact of this change. English-speaking clients who were eligible for ADAP-funded QHPs were recruited at three HIV clinics in Virginia. The goal was to enroll ≥5% of those who were eligible for ADAP-funded QHPs in two Virginia Department of Health planning districts. Participants were surveyed about demographic characteristics, and semi-structured interviews were performed. Descriptive analyses were performed for cohort characteristics. Using an open coding strategy, codebooks were generated for the interviews and themes were identified. The cohort (n = 53) met our recruitment goal. Two-thirds gained their ACA knowledge at HIV clinics from case managers and social workers. Many barriers to enrollment were identified, including internet access/literacy. Almost 9 out of 10 participants had concerns about privacy, which centered on QHP's mandated use of mail-order pharmacies. Except for medication concerns, most participants had positive perceptions of the impact of QHP enrollment on their health care. HIV clinic case managers and social workers are often the primary source of knowledge for patients about insurance options and their assistance is crucial for QHP enrollment. Our findings indicate that reducing identified barriers and addressing privacy concerns by allowing people to opt out of mail order pharmacies may encourage QHP enrollment.


Subject(s)
Acquired Immunodeficiency Syndrome/drug therapy , Anti-HIV Agents/economics , Health Services Accessibility/statistics & numerical data , Medical Assistance/statistics & numerical data , Patient Protection and Affordable Care Act , Adult , Anti-HIV Agents/therapeutic use , Confidentiality/psychology , Female , Humans , Insurance, Health , Male , Patient Medication Knowledge , Pharmacies/classification , Postal Service , Poverty/psychology , Surveys and Questionnaires , United States , Virginia
8.
JMIR Form Res ; 3(1): e11578, 2019 Mar 20.
Article in English | MEDLINE | ID: mdl-30892269

ABSTRACT

BACKGROUND: Linkage to and retention in HIV care are challenging, especially in the Southeastern United States. The rise in mobile phone app use and the potential for an app to deliver just in time messaging provides a new opportunity to improve linkage and retention among people living with HIV (PLWH). OBJECTIVE: This study aimed to develop an app to engage, link, and retain people in care. We evaluated the acceptability, feasibility, and impact of the app among users. METHODS: App development was informed by principles of chronic disease self-management and formative interviews with PLWH. Once developed, the app was distributed among participants, and usability feedback was incorporated in subsequent iterations. We interviewed app users after 3 weeks to identify usability issues, need for training on the phone or app, and to assess acceptability. We tracked and analyzed usage of app features for the cohort over 2 years. RESULTS: A total of 77 participants used the app during the pilot study. The query response rate for the first 2 years was 47.7%. Query response declined at a rate of 0.67% per month. The community message board was the most popular feature, and 77.9% (60/77) of users posted on the board at least once during the 2 years. CONCLUSIONS: The PositiveLinks app was feasible and acceptable among nonurban PLWH. High participation on the community message board suggests that social support from peers is important for people recently diagnosed with or returning to care for HIV.

9.
AIDS Behav ; 22(10): 3395-3406, 2018 Oct.
Article in English | MEDLINE | ID: mdl-29882048

ABSTRACT

Stigma has negative consequences for quality of life and HIV care outcomes. PositiveLinks is a mobile health intervention that includes a secure anonymous community message board (CMB). We investigated discussion of stigma and changes in stigma scores. Of 77 participants in our pilot, 63% were male, 49% Black, and 72% had incomes below the federal poverty level. Twenty-one percent of CMB posts (394/1834) contained stigma-related content including negative (experiencing stigma) and positive (overcoming stigma) posts addressing intrapersonal and interpersonal stigma. Higher baseline stigma was positively correlated with stress and negatively correlated with HIV care self-efficacy. 12-month data showed a trend toward more improved stigma scores for posters on the CMB versus non-posters (- 4.5 vs - 0.63) and for posters of stigma-related content versus other content (- 5.1 vs - 3.3). Preliminary evidence suggests that a supportive virtual community, accessed through a clinic-affiliated smartphone app, can help people living with HIV to address stigma.


Subject(s)
HIV Infections/psychology , Mobile Applications , Quality of Life , Social Stigma , Telemedicine , Adult , Ambulatory Care Facilities , Female , Humans , Male , Middle Aged , Pilot Projects , Smartphone
10.
AIDS Behav ; 21(11): 3087-3099, 2017 Nov.
Article in English | MEDLINE | ID: mdl-27766448

ABSTRACT

Social support can improve outcomes for people living with HIV (PLWH) and could be provided through online support groups. The Positive Links smartphone app is a multicomponent intervention that allows users to interact in a clinic-affiliated anonymous online support group. We investigated how social support was exchanged in a group of 55 participants over 8 months, using an adaptation of the Social Support Behavior Code. Participant interviews assessed their experiences and perceptions of the app. Of 840 posts analyzed, 115 (14 %) were coded as eliciting social support and 433 (52 %) as providing social support. Messages providing support were predominantly emotional (41 %), followed by network (27 %), esteem (24 %), informational (18 %), and instrumental (2 %) support. Participants perceived connection and support as key benefits of the app. Technical issues and interpersonal barriers limited some participants in fully using the app. Mobile technology offers a useful tool to reach populations with barriers to in-person support and may improve care for PLWH.


Subject(s)
Ambulatory Care Facilities/organization & administration , HIV Infections/psychology , Self-Help Groups , Social Support , Acquired Immunodeficiency Syndrome/psychology , Adult , Emotions , Female , Humans , Male , Middle Aged , Smartphone
11.
Clin Transplant ; 30(11): 1473-1479, 2016 11.
Article in English | MEDLINE | ID: mdl-27623240

ABSTRACT

OBJECTIVE: The purpose of this study was to determine whether bacterial contamination of islets affects graft success after total pancreatectomy with islet autotransplantation (TPIAT). BACKGROUND: Factors associated with insulin independence after TPIAT are inconclusive. Although bacterial contamination does not preclude transplantation, the impact of bacterial contamination on graft success is unknown. METHODS: Patients who received TPIAT at the University of Virginia between January 2007 and January 2016 were reviewed. Patient charts were reviewed for bacterial contamination and patients were prospectively contacted to assess rates of insulin independence. RESULTS: There was no significant difference in demographic or perioperative data between patients who achieved insulin independence and those who did not. However, six of 27 patients analyzed (22.2%) grew bacterial contaminants from culture of the final islet preparations. These patients had significantly lower islet yield and C-peptide at most recent follow-up (P<.05), and none of these patients achieved insulin independence. CONCLUSIONS: Islet transplant solutions are often culture positive, likely secondary to preprocurement pancreatic manipulation and introduction of enteric flora. Although autotransplantation of culture-positive islets is safe, it is associated with higher rates of graft failure and poor islet yield. Consideration should be given to identify patients who may develop refractory chronic pancreatitis and offer early operative management to prevent bacterial colonization.


Subject(s)
Diabetes Mellitus, Type 1/drug therapy , Insulin/therapeutic use , Islets of Langerhans Transplantation , Islets of Langerhans/microbiology , Pancreatectomy , Pancreatitis, Chronic/surgery , Postoperative Complications/drug therapy , Adolescent , Adult , Diabetes Mellitus, Type 1/etiology , Diabetes Mellitus, Type 1/prevention & control , Female , Follow-Up Studies , Humans , Male , Middle Aged , Postoperative Complications/prevention & control , Prospective Studies , Retrospective Studies , Transplantation, Autologous , Treatment Outcome , Young Adult
12.
Telemed J E Health ; 22(9): 746-54, 2016 09.
Article in English | MEDLINE | ID: mdl-27002956

ABSTRACT

BACKGROUND: Although there is growing interest in mobile applications and online support groups to enhance chronic disease self-management, little is known about their potential impact for people living with HIV (PLWH). INTRODUCTION: We developed an innovative online support group delivered through a community message board (CMB) within a clinic-affiliated smartphone application Positive Links (PL). We analyzed characteristics of posters and nonposters to the CMB and evaluated content posted to the CMB. MATERIALS AND METHODS: For this study, 38 HIV-infected patients received cell phones with the PL application that included the opportunity to interact with other users on a CMB. Logistic regressions investigated associations between participant characteristics and posting. CMB messages were downloaded and analyzed qualitatively. RESULTS: 24 participants posted to the CMB; 14 did not. Participants had lower odds of posting if they were white (p = 0.028) and had private insurance (p = 0.003). Participants had higher odds of posting if they had unsuppressed viral loads (p = 0.034). Of the 840 CMB messages over 8 months, 62% had psychosocial content, followed by community chat (29%), and biomedical content (10%). DISCUSSION: Psychosocial content was most prevalent on this CMB, in contrast to other online forums dominated by informational content. Participants who posted expressed support for each other, appreciation for the community, and a perception that the app played a positive role in their HIV self-management. CONCLUSIONS: This CMB on a clinic-affiliated mobile application may reach vulnerable populations, including racial/ethnic minorities and those of lower socioeconomic status, and provide psychosocial support to PLWH.


Subject(s)
HIV Infections/psychology , Internet , Mobile Applications , Self-Help Groups/organization & administration , Adult , Female , Humans , Male , Middle Aged , Patient Education as Topic , Smartphone , Socioeconomic Factors
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