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Delayed Hepatic Veno-Occlusive Disease after Haploidentical Hematopoietic Stem Cell Transplantation:A Report of Six Cases / 中国实验血液学杂志
Journal of Experimental Hematology ; (6): 1149-1154, 2016.
Article en Zh | WPRIM | ID: wpr-246800
Biblioteca responsable: WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To evaluate the morbidity, risk factors, clinical characterisitics, treatments and prognosis of delayed hepatic veno-occlusive disease(HVOD) after haploidentical hematopoietic stem cell transplantation (hi-HSCT).</p><p><b>METHODS</b>The clinical data of 208 patients undergoing hi-HSCT were retrospectively analyzed.</p><p><b>RESULTS</b>Six patients were diagnosed with delayed VOD, among them 4 patients were moderate VOD and 2 patients were severe VOD. The incidence of VOD after hi-HSCT was 2.88%, the median onset time was 44.5(30-57) days after transplant, 2 patients died of multiple organ failure (MOF) due to rapid progress of disease. With intravenous administration of defibrotide, 4 patients displayed encouraging response, but 2 patients died of hepatic acute graft-versus-host disease (aGVHD), 1 had bone marrow relapse and the other one was cured.</p><p><b>CONCLUSION</b>Norethindrone is one of the high risk factors, while sex, age and disease status are irrelevant to the occurrence of VOD. Unfractionated heparin (UH) can effectively decrease the morbidity. Pretransplant hepatic function reserve, high dose preconditioning regimens and pharmacotherapy may result in delayed VOD onset. The delayed VOD has the same clinical features and treatment-response as early VOD, but a poorer prognosis is usually observed. A larger amount of samples (patients) is needed to research the relationship of the delayed VOD with hi-HSCT. Defibrotide can effectively increase the survival rate of VOD patients.</p>
Asunto(s)
Texto completo: 1 Base de datos: WPRIM Asunto principal: Polidesoxirribonucleótidos / Enfermedad Veno-Oclusiva Hepática / Heparina / Incidencia / Estudios Retrospectivos / Factores de Riesgo / Trasplante de Células Madre Hematopoyéticas / Enfermedad Injerto contra Huésped / Haploidia Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: Zh Revista: Journal of Experimental Hematology Año: 2016 Tipo del documento: Article
Texto completo: 1 Base de datos: WPRIM Asunto principal: Polidesoxirribonucleótidos / Enfermedad Veno-Oclusiva Hepática / Heparina / Incidencia / Estudios Retrospectivos / Factores de Riesgo / Trasplante de Células Madre Hematopoyéticas / Enfermedad Injerto contra Huésped / Haploidia Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: Zh Revista: Journal of Experimental Hematology Año: 2016 Tipo del documento: Article