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1.
Am J Public Health ; 112(12): 1757-1764, 2022 12.
Artículo en Inglés | MEDLINE | ID: mdl-36383931

RESUMEN

Objectives. To systematically identify and analyze US state-level legislation concerning people who were undocumented during the COVID-19 pandemic, from January 2020 through August 2021. Methods. Using standard public health law research methods, we searched Westlaw's online database between November 2021 and January 2022 to identify legislation addressing COVID-19 and people who were undocumented. We abstracted relevant information, analyzed the data, and identified primary themes for each bill and resolution. Results. Sixty-six bills and resolutions, from 13 states, met the inclusion criteria. Legislation addressed 5 primary themes: eligibility and access to health-related services (n = 16), health and personal information (n = 10), housing assistance (n = 13), job security and employment benefits (n = 14), and monetary assistance (n = 13). Conclusions. Approximately one quarter of state legislatures introduced bills or resolutions regarding people who were undocumented and COVID-19. State-level laws are an important tool to mitigate the disproportionate impact of public health emergencies on vulnerable groups. Public Health Implications. As states shift attention away from the exigencies of COVID-19, this research provides insight into how law might be used to protect those who are undocumented throughout the full cycle of future public health emergencies. (Am J Public Health. 2022;112(12):1757-1764. https://doi.org/10.2105/AJPH.2022.307090).


Asunto(s)
COVID-19 , Humanos , Estados Unidos/epidemiología , COVID-19/epidemiología , Urgencias Médicas , Pandemias , Salud Pública , Servicios de Salud
2.
J Prim Care Community Health ; 13: 21501319221112588, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-35847997

RESUMEN

BACKGROUND: The patient-centered medical home (PCMH) model, an important component of healthcare transformation in the United States, is an approach to primary care delivery with the goal of improving population health and the patient care experience while reducing costs. PCMH research most often focuses on system level indicators including healthcare use and cost; descriptions of patient and provider experience with PCMH are relatively sparse and commonly limited in scope. This study, part of a mixed-methods evaluation of a multi-year New York State initiative to refine and expand the PCMH model, describes patient and provider experience with New York State PCMH and its key components. METHODS: The qualitative component of the evaluation included focus groups with patients of PCMH practices in 5 New York State counties (n = 9 groups and 67 participants) and interviews with providers and practice administrators at New York State PCMH practices (n = 9 interviews with 10 participants). Through these focus groups and interviews, we elicited first-person descriptions of experiences with, as well as perspectives on, key components of the New York State PCMH model, including accessibility, expanded use of electronic health records, integration of behavioral health care, and care coordination. RESULTS: There was evident progress and some satisfaction with the PCMH model, particularly regarding integrated behavioral health and, to some extent, expanded use of electronic health records. There was less evident progress with respect to improved access and reasonable wait times, which caused patients to continue to use urgent care or the emergency department as substitutes for primary care. CONCLUSIONS: It is critical to understand the strengths and limitations of the PCMH model, so as to continue to improve upon and promote it. Strengths of the model were evident to participants in this study; however, challenges were also described. It is important to note that these challenges are difficult to separate from wider healthcare system issues, including inadequate incentives for value-based care, and carry implications for PCMH and other models of healthcare delivery.


Asunto(s)
Atención Primaria de Salud , Calidad de la Atención de Salud , Humanos , New York , Atención Dirigida al Paciente , Investigación Cualitativa , Estados Unidos
3.
AIDS Care ; 34(4): 440-445, 2022 04.
Artículo en Inglés | MEDLINE | ID: mdl-33719775

RESUMEN

ABSTRACTRates of opioid use disorder and associated deaths remain alarmingly high. Measures to address the epidemic have included reductions in opioid prescribing, in part guided by the Centers for Disease Control Opioid Prescribing Guideline (CDCG). While reductions in over-prescribing have occurred, these measures have also resulted in decreased access and adverse outcomes for some stable opioid-treated chronic pain patients. The TOWard SafER Opioid Prescribing (TOWER) intervention was designed to support HIV primary care providers in use of the CDCG and in decision-making and patient-provider communication regarding safe opioid prescribing. Eleven HIV primary care providers and 40 of their patients were randomized into intervention and control groups. Transcripts from 21 patient visits were analyzed, focusing on opioid and pain-related communications. Findings from this research indicate greater alignment with the CDCG among visits carried out with providers in the TOWER intervention group. However, control group visits were notably consistent with guideline recommendations in several key areas. Differences observed between the intervention and control group visits demonstrate intervention strengths, as well as areas where additional work needs to be done to ensure prescribing and communication consistent with the CDCG.


Asunto(s)
Dolor Crónico , Infecciones por VIH , Trastornos Relacionados con Opioides , Analgésicos Opioides/uso terapéutico , Dolor Crónico/complicaciones , Dolor Crónico/tratamiento farmacológico , Infecciones por VIH/complicaciones , Infecciones por VIH/tratamiento farmacológico , Humanos , Trastornos Relacionados con Opioides/tratamiento farmacológico , Pautas de la Práctica en Medicina
4.
Prog Community Health Partnersh ; 15(4): 525-532, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-34975034

RESUMEN

BACKGROUND: Community collaboratives have been shown to be effective in changing environments and systems to promote health by facilitating and coordinating programs, services, and practices. East Harlem, a New York City neighborhood, recently experienced a growth in bicycling infrastructure and resources. However, community concerns raised about safety, equity, and inclusion highlighted the need for a coordinated effort to reduce barriers to biking. OBJECTIVES: To describe the formation of and activities of El Barrio Bikes, a community biking collaborative by providing examples of community engagement strategies, evaluation methods, and lessons learned. METHODS: A values-driven community engagement framework was used to form a multi-sector community collaborative to reduce barriers to biking in East Harlem. El Barrio Bikes conducted monitoring and evaluation activities to evaluate community engagement strategies used, to ensure that the group's goals were being met, and to make improvements or adjustments when needed. RESULTS: The use of a community engagement framework was critical to the evolution of El Barrio Bikes from a group of individual partners to a model of shared leadership. Collaborative decision-making, extensive outreach efforts, and feedback surveys were time-intensive, but essential in in developing a sustainable and equitable partnership. CONCLUSIONS: Carefully selected community engagement strategies were integral to the success of creating a community biking collaborative to promote biking. Collaboration between community stakeholders can strengthen community ties and power, which are key to implementing an effective strategy to reducing barriers to biking in East Harlem.


Asunto(s)
Ciclismo , Promoción de la Salud , Investigación Participativa Basada en la Comunidad , Humanos , Liderazgo , Características de la Residencia
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