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Progress of Hemophilia A Therapeutics in Korea / 임상소아혈액종양
Clinical Pediatric Hematology-Oncology ; : 17-22, 2018.
Artigo em Inglês | WPRIM | ID: wpr-714203
ABSTRACT
Over the past several decades, hemophilia treatment in Korea has progressed dramatically. It has become possible to prevent hemophilia complications by maintenance treatment as well as on-demand treatment with the help of the National Health Insurance program. Treatment and prevention of hemorrhage, prevention of joint complications, treatment and prevention of infectious complications have greatly improved the quality of life and life expectancy of hemophilia patients. However, the development of inhibitor is the most serious and challenging complication of clotting factor replacement therapy, although immune tolerance regimens and bypassing agents have shown some efficacy in countering this complication. The development of novel methods of therapy, including the use of extended half-life factors and gene therapy, will further improve the outcome of hemophilia patients. Administering the right drug to the right patients with the right dose at the right time will be necessary for treating the patient. Achievement of optimal therapeutic goals will require continued cooperation between patients and medical staff.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Qualidade de Vida / Fator VIII / Terapia Genética / Expectativa de Vida / Meia-Vida / Hemofilia A / Hemorragia / Tolerância Imunológica / Articulações / Coreia (Geográfico) Limite: Humanos País/Região como assunto: Ásia Idioma: Inglês Revista: Clinical Pediatric Hematology-Oncology Ano de publicação: 2018 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Qualidade de Vida / Fator VIII / Terapia Genética / Expectativa de Vida / Meia-Vida / Hemofilia A / Hemorragia / Tolerância Imunológica / Articulações / Coreia (Geográfico) Limite: Humanos País/Região como assunto: Ásia Idioma: Inglês Revista: Clinical Pediatric Hematology-Oncology Ano de publicação: 2018 Tipo de documento: Artigo