TRANSFUSION REQUIREMENTS AND EFFECTS IN PATIENTS WITH THALASSEMIA MAJOR

被引:62
作者
REBULLA, P [1 ]
MODELL, B [1 ]
机构
[1] UNIV COLL & MIDDLESEX SCH MED,CTR PERINATAL,LONDON,ENGLAND
关键词
D O I
10.1016/0140-6736(91)90881-O
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Analysis of data available in 1985 on 3468 Italian and Greek patients registered in Cooleycare, an international cooperative programme of quality assessment of treatment delivery in thalassaemia, gave the following picture of treatment requirements and effects. The proportion of patients undergoing splenectomy has progressively decreased, and age at splenectomy has increased with time over the past 20 years. Age at first transfusion exceeds 4 years in a small but important group of patients, which indicates that a milder form of thalassaemia exists in this group. Children receiving modern treatment remain of near-normal stature until age 11 but later tend to e stunted. The mean blood requirement is 35% higher in non-splenectomised than in splenectomised patients. Differences in transfusion interval of 2 to 4 weeks have no measurable effect on measurable effect on blood requirement. Mean blood requirement rises gradually with mean haemoglobin concentration, possibly in a non-linear fashion. The prevalence of red cell alloimmunisation rises with delay in start on transfusion. Transfusion reactions were reported in 1% of transfusions (90% of which were leucocyte-depleted), from 17% of patients.
引用
收藏
页码:277 / 280
页数:4
相关论文
共 11 条
[1]  
CAO A, 1987, THALASSEMIA TODAY ME, P633
[2]   HEMOGLOBIN LEVELS AND BLOOD REQUIREMENT IN THALASSEMIA [J].
GABUTTI, V ;
PIGA, A ;
NICOLA, P ;
VULLO, C ;
CAPRA, L ;
DIPALMA, A ;
MASERA, G ;
TERZOLI, S ;
MAURI, R .
ARCHIVES OF DISEASE IN CHILDHOOD, 1982, 57 (02) :156-158
[3]   ALLOIMMUNIZATION TO RED-CELL ANTIGENS IN THALASSEMIA - COMPARATIVE-STUDY OF USUAL VERSUS BETTER-MATCH TRANSFUSION PROGRAMS [J].
MICHAILMERIANOU, V ;
PAMPHILIPANOUSOPOULOU, L ;
PIPERILOWES, L ;
PELEGRINIS, E ;
KARAKLIS, A .
VOX SANGUINIS, 1987, 52 (1-2) :95-98
[4]   TOTAL MANAGEMENT OF THALASSEMIA MAJOR [J].
MODELL, B .
ARCHIVES OF DISEASE IN CHILDHOOD, 1977, 52 (06) :489-500
[5]  
Modell B., 1984, CLIN APPROACH THALAS
[6]  
PIGA A, 1982, RIV ITAL PED, V8, P823
[7]   HYPERTRANSFUSION REGIMEN IN PATIENTS WITH COOLEYS ANEMIA [J].
PIOMELLI, S ;
KARPATKIN, MH ;
ARZANIAN, M ;
ZAMANI, M ;
BECKER, MH ;
GENEISER, N ;
DANOFF, SJ ;
KUHNS, WJ .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1974, 232 (MAY24) :186-192
[8]  
PROPPER RD, 1980, BLOOD, V55, P55
[9]  
REBULLA P, 1987, THALASSAEMIA TODAY M, P31
[10]  
WOLMAN IJ, 1964, ANN NY ACAD SCI, V119, P736