Alma Mater Studiorum - Forlì


Home page
Le collezioni
La scuola
Il progetto
I collaboratori
Gli sponsor
Il laboratorio
Regole e normative
Per contattarci
Copyright


login
password
ho dimenticato la password
mi voglio iscrivere

ceci n'est pas une pomme
 
previous myocardiopathy - collezione «Medicina: Ematologia: Talassemie e trapianto del midollo osseo» - Deborah Olmi next
Cerca   nella collezione  

Medicina: Ematologia: Talassemie e trapianto del midollo osseo

English
myocardiopathy clicca per ingrandire
Attestation 3
Part of speech Noun
Grammatical label Countable
Definition The high prevalence of cardiac and endocrine disorders cush as miocardiopathy in the older thalassemic patients, as well as the increasing number of patients affected by cardiac disease, is alarming and requires special attention. As a result, the particular problems of preventing and treating siderotic complications in these patients require more and more attention. The difficulty of insufficient compliance with chelation therapy, discussed repeatedly, seems to be particularly important for adolescents. An important factor might be the increasing need for self-responsibility, which is not met by the patients, in connection with particular aspects of psychological development during this period of life. Transfusional iron overload leading to miocardiopathy and other severe complications continues to be a major problem in chronically transfused homozygous b-thalassaemia patients. It is well known that young red cells (neocytes) survive longer after transfusion and therefore may contribute to the extension of the intervals between transfusions.
Definition source Spanos, T., et al. (1996). ‘The impact of neocyte transfusion in the management of thalassaemia’. Vox Sanguinis 70(4):217-23.
Context The long-term effects of BMT in thalassemia are being monitored in patients transplanted between 1987-1995 and compared with those subjects matched for age and treated during the same period with conventional therapy. The incidences of fulminant sepsis and growth impairment are significantly higher in transplanted patients, whereas the-occurrence of hypothyroidism, hypogonadism, and myocardiopathy are higher in the other group of patients. Non-significant differences are observed in the incidences of diabetes, liver disease, and severe infections.
Context source Barth, E., et al. (2000). ‘Allogeneic bone marrow transplantation in hematologic disorders of childhood: new trends and controversies’. Haematologica 85(11 Suppl):2-8. Review. (RISCEN28)
Subject field Haemopoiesis
Specific concept Myocardiosclerosis
Related concept Hemosiderosis, iron-chelation therapy, iron overload
it Miocardiopatia
Reliability code 3



SSLMIT - Scuola Superiore di Lingue Moderne per Interpreti e Traduttori  &  MIT - Management Innovative Tools S.p.A. - Powered by : Powered by DynaMIT