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1.
J Palliat Med ; 23(1): 60-66, 2020 01.
Artículo en Inglés | MEDLINE | ID: mdl-31298605

RESUMEN

Background: The End of Life Option Act (EOLOA) legalized physician aid in dying for competent, terminally ill Californians in 2016. The law allows clinicians, hospitals, and health systems to decide whether to participate. About 4 in 10 California hospitals permit the EOLOA, but little is known about their approaches and concerns. Objective: Describe hospital EOLOA policies and challenges. Design and Measurements: Survey study of hospitals in California, administered September 2017 to March 2018. We describe hospital policies concerning the EOLOA and perform thematic analysis of open-ended questions about challenges, including availability of providers, process of implementing EOLOA, experiences of distress by providers and patients, and questions about medications. Results: Of 315 hospitals surveyed, 270 (86%) responded. Every surveyed hospital had established a position on the EOLOA. Among hospitals permitting EOLOA, 38% required safeguards not required in the law, 87% provided for referral to another provider if the patient's physician did not participate, and 65% counseled staff, if needed. Among hospitals not permitting the EOLOA, nearly all allowed providers to follow patients choosing to pursue the EOLOA elsewhere and most permitted a provider to refer to another provider or system. Most hospitals expressed concerns about implementation of the EOLOA and interest in sharing promising practices. Conclusions: This survey of California hospitals demonstrates considerable heterogeneity in implementing the EOLOA. For many Californians, access to the EOLOA depends on where one receives medical care. Implementation would be improved by hospitals and health systems sharing promising practices.


Asunto(s)
Hospitales , Enfermo Terminal , California , Muerte , Política de Salud , Humanos
4.
J Pain Symptom Manage ; 53(5): 821-832.e1, 2017 05.
Artículo en Inglés | MEDLINE | ID: mdl-28062339

RESUMEN

CONTEXT: Despite increasing interest in advance care planning (ACP) and previous ACP descriptions, a consensus definition does not yet exist to guide clinical, research, and policy initiatives. OBJECTIVE: The aim of this study was to develop a consensus definition of ACP for adults. METHODS: We convened a Delphi panel of multidisciplinary, international ACP experts consisting of 52 clinicians, researchers, and policy leaders from four countries and a patient/surrogate advisory committee. We conducted 10 rounds using a modified Delphi method and qualitatively analyzed panelists' input. Panelists identified several themes lacking consensus and iteratively discussed and developed a final consensus definition. RESULTS: Panelists identified several tensions concerning ACP concepts such as whether the definition should focus on conversations vs. written advance directives; patients' values vs. treatment preferences; current shared decision making vs. future medical decisions; and who should be included in the process. The panel achieved a final consensus one-sentence definition and accompanying goals statement: "Advance care planning is a process that supports adults at any age or stage of health in understanding and sharing their personal values, life goals, and preferences regarding future medical care. The goal of advance care planning is to help ensure that people receive medical care that is consistent with their values, goals and preferences during serious and chronic illness." The panel also described strategies to best support adults in ACP. CONCLUSIONS: A multidisciplinary Delphi panel developed a consensus definition for ACP for adults that can be used to inform implementation and measurement of ACP clinical, research, and policy initiatives.


Asunto(s)
Planificación Anticipada de Atención/clasificación , Planificación Anticipada de Atención/normas , Enfermedad Crónica/clasificación , Enfermedad Crónica/terapia , Técnica Delphi , Guías de Práctica Clínica como Asunto , Terminología como Asunto , Adulto , Toma de Decisiones , Femenino , Humanos , Investigación Interdisciplinaria/normas , Internacionalidad , Masculino
5.
J Gen Intern Med ; 31(10): 1119-26, 2016 10.
Artículo en Inglés | MEDLINE | ID: mdl-27188700

RESUMEN

BACKGROUND: Physician Orders for Life-Sustaining Treatment (POLST) is a tool that facilitates the elicitation and continuity of life-sustaining care preferences. POLST was implemented in California in 2009, but how well it disseminated across a large, racially diverse population is not known and has implications for end-of-life care. OBJECTIVE: To evaluate the use of POLST among California nursing home residents, including variation by resident characteristics and by nursing home facility. DESIGN: Observational study using California Minimum Data Set Section S. PARTICIPANTS: A total of 296,276 people with a stay in 1,220 California nursing homes in 2011. MAIN MEASURES: The proportion of residents with a completed POLST (containing a resuscitation status order and resident/proxy and physician signatures) and relationship to resident characteristics; change in POLST use during 2011; and POLST completion and unsigned forms within nursing homes. KEY RESULTS: During 2011, POLST completion increased from 33 to 49 % of California nursing home residents. Adjusting for age and gender using a mixed-effects logistic model, long-stay residents were more likely than short-stay residents to have a completed POLST [OR = 2.36 (95 % CI 2.30, 2.42)]; severely cognitively impaired residents were less likely than unimpaired to have a completed POLST [OR = 0.89 (95 % CI 0.87, 0.92)]; and there was little difference by functional status. There was no difference in POLST completion among White non-Hispanic, Black, and Hispanic residents. Variation in POLST completion among nursing homes far exceeded that attributable to resident characteristics with 40 % of facilities having ≥80 % of long-stay residents with a completed POLST, while 20 % of facilities had ≤10 % of long-stay residents with a completed POLST. Thirteen percent of nursing home residents had a POLST containing a resuscitation preference but lacked a signature, rendering the POLST invalid. CONCLUSIONS: Statewide nursing home data show broad uptake of POLST in California without racial disparity. However, variation in POLST completion among nursing homes identifies potential areas for quality improvement.


Asunto(s)
Planificación Anticipada de Atención/organización & administración , Directivas Anticipadas , Casas de Salud/organización & administración , Cuidado Terminal/organización & administración , Actividades Cotidianas , Anciano , Anciano de 80 o más Años , California , Femenino , Humanos , Tiempo de Internación/estadística & datos numéricos , Cuidados a Largo Plazo/organización & administración , Masculino , Persona de Mediana Edad , Prioridad del Paciente , Mejoramiento de la Calidad , Órdenes de Resucitación
6.
Muscle Nerve ; 38(5): 1515-1517, 2008 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-18816629

RESUMEN

This case report describes a young man referred for electrodiagnostic evaluation for hand stiffness and intermittent numbness. His needle electromyography revealed diffusely increased insertional and spontaneous motor activity in the form of myotonic discharges. Given the finding of symptomatic myotonia also in his mother, Thomsen myotonia was suspected. Investigations not only confirmed Thomsen myotonia, but also led to the identification of a previously reported heterozygous Becker mutation in both the proband and his mother.


Asunto(s)
Canales de Cloruro/genética , Genes Recesivos , Mutación/genética , Miotonía Congénita/genética , Adolescente , Análisis Mutacional de ADN , Humanos , Masculino , Miotonía Congénita/fisiopatología
7.
Clin Immunol ; 119(3): 346-50, 2006 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-16542878

RESUMEN

To test whether MHC alleles associated with common variable immune deficiency (CVID) might also be over-represented in patients with normal serum immunoglobulin levels who suffer with recurrent sinopulmonary infections (RESPI), we identified 62 consecutive RESPI patients and compared their HLA-B and HLA-DR antigen frequencies to those of 60 consecutive patients with CVID, 1627 Alabama Caucasian bone marrow donors, and 997,230 published US Caucasians. Either HLA-B44, -B8, -DR3(17), or -DR7 was present in 74% of the RESPI and 85% of the CVID patients. HLA-B44 prevalence in particular proved identical between RESPI and CVID. When compared to US Caucasians, the increased prevalence of the four HLA alleles proved significant at P < 0.0001, P < 0.0001, P = 0.0005, and P = 0.02, respectively. When compared to Alabama Caucasians, only the increased prevalence of HLA-B44 achieved statistical significance (P = 0.0001). Inheritance of HLA-B44 may yield susceptibility to recurrent sinopulmonary infection even in the presence of normal serum immunoglobulin levels.


Asunto(s)
Inmunodeficiencia Variable Común/genética , Antígenos HLA-B/genética , Antígenos HLA-DR/genética , Infecciones del Sistema Respiratorio/genética , Adolescente , Adulto , Inmunodeficiencia Variable Común/sangre , Inmunodeficiencia Variable Común/inmunología , Femenino , Frecuencia de los Genes , Antígenos HLA-B/inmunología , Antígeno HLA-B44 , Antígenos HLA-DR/inmunología , Haplotipos , Humanos , Inmunoglobulinas/sangre , Masculino , Persona de Mediana Edad , Infecciones del Sistema Respiratorio/sangre , Infecciones del Sistema Respiratorio/inmunología , Factores Sexuales , Población Blanca/genética
9.
Clin Transplant ; 17(2): 77-88, 2003 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-12709071

RESUMEN

Each year, 55 000 organ transplants are performed worldwide. Cumulatively, the number of living organ recipients is now estimated to be over 300 000. Most of these transplant recipients will remain on immunosuppressive drugs for the remainder of their lives to prevent rejection episodes. Controlled doses of these drugs are required to prevent over-medication, which may leave the patient susceptible to opportunistic infection and drug toxicity effects, or under-dosing, which may lead to shortened graft survival because of rejection episodes. This paper describes the result of a multicenter study conducted at the Universities of Pittsburgh, Alabama and Maryland to evaluate an in vitro assay (CylexTM Immune Cell Function Assay) for the measurement of global immune response in transplant patients receiving immunosuppressive therapy. The assay uses a whole blood sample to maintain the presence of the drug during incubation. Following overnight incubation of blood with phytohemagglutinin (PHA), CD4 cells are selected using paramagnetic particles coated with a monoclonal antibody to the CD4 epitope. The CD4-positive cells are targeted as major immunosuppressive drugs are designed to specifically inhibit T-cell activation which has been implicated in rejection. The data generated at these three sites were submitted in support of an Food and Drug Association (FDA) application for the use of this assay in the detection of cell-mediated immunity in an immunosuppressed population. The assay was cleared by the FDA on April 2, 2002. This cross-sectional study was designed to establish ranges for reactivity of this bioassay in the assessment of functional immunity for an individual solid organ recipient at any point in time.


Asunto(s)
Monitoreo de Drogas , Inmunidad Celular , Inmunoensayo/métodos , Inmunología del Trasplante , Adulto , Recuento de Linfocito CD4 , Estudios de Casos y Controles , Estudios Transversales , Ciclosporina/sangre , Femenino , Citometría de Flujo , Humanos , Inmunosupresores/sangre , Activación de Linfocitos/efectos de los fármacos , Masculino , Persona de Mediana Edad , Fitohemaglutininas/farmacología , Linfocitos T/efectos de los fármacos , Tacrolimus/sangre
11.
Hum Immunol ; 63(2): 108-20, 2002 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-11821158

RESUMEN

Rhesus monkeys are relevant models for tolerance induction. Hematopoetic chimerism is believed to be one of these strategies. The purpose of this study was to detect donor class I A locus allele specific mRNA in Rhesus monkey kidney recipient. We report here for the first time the results of frequency resonance energy transfer (FRET) hybridization technology in frozen tissues. Frequency resonance energy transfer hybridization was performed by using two Mamu-A*05 allele specific oligonucleotides: a donor probe labeled with FITC and acceptor probe conjugated to Texas Red. The PCR-SSP microchimerism analysis method produced 0.05% and 0.5% of donor DNA for Mamu-DRB1*1002 and Mamu-DRBw301/3 alleles, respectively. The donor cells were detected in mesenteric and/or inguinal lymph nodes, spleen, and liver, where the signal was the strongest. The results of FRET hybridization demonstrated the identical staining pattern in the recipient frozen tissues to that determined by PCR-SSP. Following FRET hybridization, the sections underwent immunohistochemical analysis, which revealed that donor cells had CD8+ phenotype. We demonstrate here for the first time that FRET in situ hybridization technique can be utilized for microchimerism analysis in frozen tissues. We conclude that using two donor mRNA specific oligonucleotide probes, rather than one, produce higher specificity.


Asunto(s)
Hibridación in Situ/métodos , Quimera por Trasplante , Tolerancia al Trasplante , Alelos , Animales , Antígenos HLA-A , Inmunohistoquímica , Trasplante de Riñón , Macaca mulatta , Reacción en Cadena de la Polimerasa , ARN Mensajero/análisis , Sensibilidad y Especificidad , Espectrometría de Fluorescencia
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