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.
Haemophilia ; 30(3): 609-616, 2024 May.
Artículo en Inglés | MEDLINE | ID: mdl-38523289

RESUMEN

BACKGROUND: The healthcare systems in Asia vary greatly due to the socio-economic and cultural diversities which impact haemophilia management. METHODS: An advisory board meeting was conducted with experts in haemophilia care from Asia to understand the heterogeneity in clinical practices and care provision in the region. FINDINGS: The overall prevalence of haemophilia in Asia ranges between 3 and 8.58/100,000 patients. Haemophilia A was more prevalent as compared to haemophilia B with a ratio of around 5:1. There is under-diagnosis in the region due to lack of diagnosis, registries and/or lack of appropriate facilities in suburban areas. Most patients are referred to the haematologists by their families or primary care physicians, while some are identified during bleeding episodes. Genetic testing faces obstacles like resource constraints, services available at limited centres and unwillingness of patients to participate. Prophylaxis is offered for people with haemophilia (PWH) with a severe bleeding phenotype. Recombinant factors are approved in most countries across the region and are the preferred therapy. The challenges highlighted for not receiving a high standard of care include patients' reluctance to use an intravenous treatment, poor patient compliance due to frequency of infusions, budget constraints and lack of funding, insurance, availability and accessibility of factor concentrates. Prevalence of neutralizing antibodies ranged from 5% to 20% in the region. Use of immune tolerance induction and bypassing agents to treat inhibitors depends on their cost and availability. CONCLUSION: Haemophilia care in Asia has evolved to a great extent. However, some challenges remain for which a strategic approach along with multi-stakeholder involvement are needed.


Asunto(s)
Hemofilia A , Humanos , Hemofilia A/terapia , Hemofilia A/epidemiología , Asia/epidemiología , Prevalencia , Atención a la Salud , Hemofilia B/terapia , Hemofilia B/epidemiología
2.
Bioethics ; 19(3): 290-303, 2005 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-16167408

RESUMEN

With the controversial ethical issues on the creation of human embryos through cloning for therapeutic research, which holds more promise of medical breakthroughs that the world could ever imagine and the acknowledgement by many scientists that this technology may not lead in the near future to therapies; this country report discusses the approach Singapore takes on human stem cell research, interjected with the authors' own arguments and suggestions especially on research compensation injuries, an often neglected important issue. International comparative viewpoints taken by the major countries in the world are also included in the appendix.


Asunto(s)
Clonación de Organismos , Investigaciones con Embriones , Política Pública , Control Social Formal , Células Madre , Feto Abortado/citología , Adulto , Comités Consultivos , Clonación de Organismos/ética , Clonación de Organismos/legislación & jurisprudencia , Destinación del Embrión/ética , Investigaciones con Embriones/ética , Investigaciones con Embriones/legislación & jurisprudencia , Embrión de Mamíferos/citología , Fertilización In Vitro , Regulación Gubernamental , Guías como Asunto , Humanos , Consentimiento Informado , Internacionalidad , Legislación como Asunto , Singapur , Donantes de Tejidos
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA