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1.
Prog Transplant ; 30(2): 144-146, 2020 06.
Artículo en Inglés | MEDLINE | ID: mdl-32238046

RESUMEN

The purpose of this article is to describe palliative care incorporation within the care of heart transplant patients. Palliative care is a holistic approach to care that includes symptom management and goal setting to improve patients' quality of life. Palliative care is designed to be used with patients who have chronic illness that impacts quality of life and should be incorporated early in the disease. All providers have a responsibility to be knowledgeable in palliative care approaches and to know when to refer a patient for specialty palliative care services. This article will describe palliative care, research study findings, and current professional guideline recommendations for patients. The article also describes challenges and barriers to the use of palliative care in heart transplant patients and strategies to address these challenges and barriers.


Asunto(s)
Trasplante de Corazón , Cuidados Paliativos , Calidad de Vida , Humanos
2.
J Am Assoc Nurse Pract ; 33(2): 158-166, 2019 Nov 13.
Artículo en Inglés | MEDLINE | ID: mdl-31738276

RESUMEN

BACKGROUND: The growing number of homeless persons in the United States demonstrates greater morbidity and mortality than the population as a whole. Homeless persons are often without a regular source of primary care. Homeless persons use emergency departments and are hospitalized at higher rates than nonhomeless persons. In 2010, the enactment of the Affordable Care Act expanded access to primary care services. Nurse practitioners were at the forefront of its subsequent implementation. PURPOSE: The purpose of this qualitative study was to explore the factors that influence establishing and maintaining a regular source of primary care among homeless persons. METHODOLOGICAL ORIENTATION: In 2017, semistructured interviews were conducted in a federally qualified health center that serves predominately homeless persons. SAMPLE: A purposive convenience sample included adult health center users (N = 20). The majority of participants were insured (90%), African American (70%), and male (65%). CONCLUSIONS: Thematic analysis revealed five facilitators: sense of community, mutual patient-provider respect, financial assurance, integrated health services, and patient care teams. To establish and maintain use of a regular primary care source, homeless persons desire to experience a sense of community, feel respected by their provider/staff, and have certainty that costs will not exceed their capacity to pay. Integrated care models that leverage a multidisciplinary team approach support the use of a regular primary care source. IMPLICATIONS FOR PRACTICE: Actualizing achievable strategies that promote the consistent use of a regular primary care source can reduce use of avoidable emergency and hospital-based services, thereby improving health outcomes among homeless persons.


Asunto(s)
Personas con Mala Vivienda/psicología , Cobertura del Seguro/normas , Atención Primaria de Salud/métodos , Adulto , Femenino , Promoción de la Salud/métodos , Promoción de la Salud/normas , Promoción de la Salud/estadística & datos numéricos , Accesibilidad a los Servicios de Salud/normas , Accesibilidad a los Servicios de Salud/estadística & datos numéricos , Personas con Mala Vivienda/estadística & datos numéricos , Humanos , Cobertura del Seguro/tendencias , Masculino , Persona de Mediana Edad , Patient Protection and Affordable Care Act/estadística & datos numéricos , Atención Primaria de Salud/estadística & datos numéricos , Investigación Cualitativa
3.
Circulation ; 138(11): 1155-1165, 2018 09 11.
Artículo en Inglés | MEDLINE | ID: mdl-30354384

RESUMEN

Heart Centers for Women (HCW) developed as a response to the need for improved outcomes for women with cardiovascular disease (CVD). From 1984 until 2012, more women died of CVD every single year in comparison with men. Initially, there was limited awareness and sex-specific research regarding mortality or outcomes in women. HCW played an active role in addressing these disparities, provided focused care for women, and contributed to improvements in these gaps. In 2014 and 2015, death from CVD in women had declined below the level of death from CVD in comparison with men. Even though awareness of CVD in women has increased among the public and healthcare providers and both sex- and gender-specific research is currently required in all research trials, not all women have benefitted equally in mortality reduction. New strategies for HCW need to be developed to address these disparities and expand the current HCW model. The HCW care team needs to direct academic curricula on sex- and gender-specific research and care; expand to include other healthcare professionals and other subspecialties; provide new care models; address diversity; and include more male providers.


Asunto(s)
Instituciones de Atención Ambulatoria/organización & administración , Enfermedades Cardiovasculares/terapia , Prestación Integrada de Atención de Salud/organización & administración , Servicios de Salud para Mujeres/organización & administración , Salud de la Mujer , Anciano , Enfermedades Cardiovasculares/diagnóstico , Enfermedades Cardiovasculares/mortalidad , Femenino , Disparidades en el Estado de Salud , Disparidades en Atención de Salud , Humanos , Persona de Mediana Edad , Pronóstico , Medición de Riesgo , Factores de Riesgo
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