Iron chelation in 1998

被引:4
作者
de Montalembert, M [1 ]
机构
[1] Etablissement Transfus Sanguine AP HP, F-75015 Paris, France
关键词
deferiprone; Desferal (R); hemochromatosis; L1;
D O I
10.1016/S1246-7820(98)85006-4
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Chronic transfusion regimens lead inevitably to iron overload, causing progressive organ dysfunctions and limiting life expectancy, so that iron chelation is needed in multiple-transfused patients to reduce iron accumulation and toxicity. Desferal(R) is still the most used and the most efficacious chelator. It must be, however, administered through subcutaneous infusion over 8-12 hours. Difficulties with compliance have prompted an ongoing search for alternatives, and in particular for molecules active after oral administration. The only drug available today is L1. This drug is less active than Desferal(R), and is responsible for rare agranulocytosis. Its indications are still to be discussed. (C) 1998 Elsevier, Paris.
引用
收藏
页码:353 / 356
页数:4
相关论文
共 7 条
[1]
A novel delivery system for continuous desferrioxamine infusion in transfusional iron overload [J].
Araujo, A ;
Kosaryan, M ;
MacDowell, A ;
Wickens, D ;
Puri, S ;
Wonke, B ;
Hoffbrand, AV .
BRITISH JOURNAL OF HAEMATOLOGY, 1996, 93 (04) :835-837
[2]
Evaluation of a new method of administration of the iron chelating agent deferoxamine [J].
BorgnaPignatti, C ;
Cohen, A .
JOURNAL OF PEDIATRICS, 1997, 130 (01) :86-88
[3]
GABUTTI V, 1994, BAIL CL HAE, V7, P919, DOI 10.1016/S0950-3536(05)80131-3
[4]
Iron chelators for thalassaemia [J].
Hershko, C ;
Konijn, AM ;
Link, G .
BRITISH JOURNAL OF HAEMATOLOGY, 1998, 101 (03) :399-406
[5]
Long-term trial of deferiprone in 51 transfusion-dependent iron overloaded patients [J].
Hoffbrand, AV ;
Al-Refaie, F ;
Davis, B ;
Siritanakatkul, N ;
Jackson, BFA ;
Cochrane, J ;
Prescott, E ;
Wonke, B .
BLOOD, 1998, 91 (01) :295-300
[6]
Iron-chelating therapy and the treatment of thalassemia [J].
Olivieri, NF ;
Brittenham, GM .
BLOOD, 1997, 89 (03) :739-761
[7]
SURVIVAL IN MEDICALLY TREATED PATIENTS WITH HOMOZYGOUS BETA-THALASSEMIA [J].
OLIVIERI, NF ;
NATHAN, DG ;
MACMILLAN, JH ;
WAYNE, AS ;
LIU, PP ;
MCGEE, A ;
MARTIN, M ;
KOREN, G ;
COHEN, AR .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (09) :574-578