Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Mais filtros








Base de dados
Intervalo de ano de publicação
1.
Eur J Haematol ; 97 Suppl 83: 3-18, 2016 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-27272000

RESUMO

Haemophilia remains a complex disorder to diagnose and manage, requiring close cooperation between multidisciplinary healthcare professionals. There are still many unmet challenges in haemophilia care. The first Team Haemophilia Education (THE) meeting, held on 7-8 May 2015 in Amsterdam, The Netherlands, aimed to promote the optimal care of haemophilia patients through education of the multidisciplinary treatment team. This was achieved by reviewing the latest developments in haemophilia management, considering how these can be implemented in the clinic to improve patient care and providing a platform for networking and debate for all haemophilia treatment team members. Haemophilia treatment centres from several countries were asked to complete a premeeting online questionnaire to establish the biggest challenges that they face when managing patients. The concerns expressed were used to develop the agenda, which comprised a combination of formal presentations, case studies and informal workshops covering such topics as pharmacokinetics, laboratory assays and tailoring of treatment to individual patients. This report is a summary of the key developments in haemophilia care presented by various investigators and healthcare professionals at THE meeting 2015.


Assuntos
Hemofilia A/terapia , Hemofilia B/terapia , Atenção à Saúde , Gerenciamento Clínico , Educação Médica Continuada , Custos de Cuidados de Saúde , Hemofilia A/prevenção & controle , Hemofilia B/prevenção & controle , Humanos , Países Baixos , Equipe de Assistência ao Paciente , Pré-Medicação , Resultado do Tratamento
2.
Medicine (Baltimore) ; 95(8): e2933, 2016 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-26937941

RESUMO

Mucormycosis is an aggressive fungal infection, which invades endothelial cells of blood vessels. This condition might lead to destruction of endothelium and release of heparin-like substances to the bloodstream and cause life-threatening bleeding, which is not well described in the literature.We present a patient with mucormycosis who experienced life-threatening bleeding, although no standard laboratory test could detect any coagulopathy.The cause of bleeding-coagulopathy was detected only by nonactivated thromboelastometry (NATEM), which revealed the presence of heparin-like substances. After treatment with recombinant activated FVII rotational thromboelastometry, results improved and the patient stopped bleeding. Regular application of the drug was necessary during acute phase of infection to prevent further bleeding.In this case report, we show that NATEM can detect the presence of heparin-like substances in bleeding patient with mucormycosis infection and that recombinant activated FVII can be used to stop and prevent bleeding until infection resolves.


Assuntos
Testes de Coagulação Sanguínea , Fator VIIa/uso terapêutico , Hemorragia/terapia , Heparinoides/metabolismo , Mucormicose/tratamento farmacológico , Antifúngicos/uso terapêutico , Criança , Drenagem/efeitos adversos , Feminino , Hemorragia/etiologia , Humanos , Doença Iatrogênica , Mucormicose/metabolismo , Proteínas Recombinantes/uso terapêutico , Baço/lesões , Baço/cirurgia , Esplenectomia
3.
Ann Transplant ; 19: 214-24, 2014 May 09.
Artigo em Inglês | MEDLINE | ID: mdl-24811685

RESUMO

BACKGROUND: Series of observations indicate PK/PD variability challenging the accuracy of the body-weight based busulfan (Bu) dosing schedule for (HSCT) conditioning therapy. The purpose of this communication is to describe the frequency of dose changes in initially body-weight-based fixed IV Bu dose and to emphasize the importance of TDM. MATERIAL AND METHODS: Sixty-two children (ages 2 months-18 years) were treated with IV busulfan doses based on body weight for myeloablation. TDM utilizing a limited sample strategy (trough concentration immediately before the 5th dose, followed by samples immediately after the end of the 2-h infusion peak, 4 h, and 6 h from initiation of the infusion) was performed in 46 of 62 subjects. Busulfan concentrations were determined by high-performance liquid chromatography (HPLC). AUC was calculated according to the trapezoidal rule. RESULTS: We observed trough levels of 25-1244 µg/L, peak levels of 849-4586 µg/L, and AUC of 2225-12818 µg/L·h following body weight-based high-dose busulfan. The doses were changed in 54% of cases. AUC in 5 of 9 patients with VOD were within target, in 3 patients AUS was higher, and in 1 patient AUC was lower. One of the 2 patients with neurotoxicity had higher AUC. Engraftment was 100%, but relapse occurred in 25% of cases. CONCLUSIONS: Our results demonstrate that even with IV busulfan, intra-individual PK/PD variability is challenging. Although AUC does not necessarily correspond with outcomes (due to the role of other factors the fact that doses were changed in 54% of cases underlines the importance of TDM.


Assuntos
Bussulfano/administração & dosagem , Monitoramento de Medicamentos/métodos , Transplante de Células-Tronco Hematopoéticas/métodos , Agonistas Mieloablativos/administração & dosagem , Condicionamento Pré-Transplante/métodos , Adjuvantes Imunológicos/administração & dosagem , Adolescente , Peso Corporal , Bussulfano/efeitos adversos , Bussulfano/farmacocinética , Criança , Pré-Escolar , Cromatografia Líquida de Alta Pressão , Ditiocarb/administração & dosagem , Relação Dose-Resposta a Droga , Humanos , Lactente , Infusões Intravenosas , Agonistas Mieloablativos/efeitos adversos , Agonistas Mieloablativos/farmacocinética , Condicionamento Pré-Transplante/efeitos adversos
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA