Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Más filtros










Base de datos
Intervalo de año de publicación
1.
Nurs Outlook ; 63(5): 585-92, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26183661

RESUMEN

BACKGROUND: With looming provider shortages and increased demand for health care, many states are looking for low-cost ways to alleviate the shortages. PURPOSE: The purpose of this study was to assess the economic impact of less restrictive regulations for advanced practice registered nurses (APRNs) in North Carolina. METHOD: We use economic impact analysis to demonstrate the economic impacts of making state scope-of-practice regulations on APRNs less restrictive in North Carolina. Outcomes include economic output, value-added, payroll compensation, employment, and tax revenue for North Carolina and for various subregions. DISCUSSION: If North Carolina adopted the same approach to APRN regulation as the least restrictive states, its economy will benefit from substantial increases in economic output and employment. The state will also see increases in tax revenue. CONCLUSIONS: In addition to substantially shrinking the size of projected physician shortages, allowing full scope-of-practice for APRNs will bring significant economic benefits to the state of North Carolina. Our analysis should be helpful to policy makers considering ways to deal with provider shortages.


Asunto(s)
Enfermería de Práctica Avanzada/economía , Enfermería de Práctica Avanzada/legislación & jurisprudencia , Regulación Gubernamental , Gobierno Estatal , Empleo , Reforma de la Atención de Salud/economía , Necesidades y Demandas de Servicios de Salud , Humanos , Licencia en Enfermería , North Carolina , Médicos/provisión & distribución , Formulación de Políticas , Impuestos
2.
Genet Med ; 12(4 Suppl): S194-211, 2010 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-20393308

RESUMEN

Cystic fibrosis is one of the most commonly tested autosomal recessive disorders in the United States. Clinical cystic fibrosis is associated with mutations in the CFTR gene, of which the most common mutation among Caucasians, DeltaF508, was identified in 1989. The University of Michigan, Johns Hopkins University, and the Hospital for Sick Children, where much of the initial research occurred, hold key patents on cystic fibrosis genetic sequences, mutations, and methods for detecting them. Several patents, including the one that covers detection of the DeltaF508 mutation, are jointly held by the University of Michigan and the Hospital for Sick Children in Toronto, with Michigan administering patent licensing in the United States. The University of Michigan broadly licenses the DeltaF508 patent for genetic testing with >60 providers of genetic testing to date. Genetic testing is now used in newborn screening, diagnosis, and for carrier screening. Interviews with key researchers and intellectual property managers, a survey of laboratories' prices for cystic fibrosis genetic testing, a review of literature on cystic fibrosis tests' cost-effectiveness, and a review of the developing market for cystic fibrosis testing provide no evidence that patents have significantly hindered access to genetic tests for cystic fibrosis or prevented financially cost-effective screening. Current licensing practices for cystic fibrosis genetic testing seem to facilitate both academic research and commercial testing. More than 1000 different CFTR mutations have been identified, and research continues to determine their clinical significance. Patents have been nonexclusively licensed for diagnostic use and have been variably licensed for gene transfer and other therapeutic applications. The Cystic Fibrosis Foundation has been engaged in licensing decisions, making cystic fibrosis a model of collaborative and cooperative patenting and licensing practice.


Asunto(s)
Fibrosis Quística/diagnóstico , Genes , Pruebas Genéticas , Accesibilidad a los Servicios de Salud , Concesión de Licencias , Patentes como Asunto , Análisis Costo-Beneficio , Fibrosis Quística/genética , Femenino , Costos de la Atención en Salud , Humanos , Recién Nacido , Masculino , Mutación , Embarazo , Diagnóstico Preimplantación
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA
...