CEREBROVASCULAR ACCIDENTS IN SICKLE-CELL DISEASE - RISK-FACTORS AND BLOOD-TRANSFUSION INFLUENCE

被引:26
作者
DEMONTALEMBERT, M
BEAUVAIS, P
BACHIR, D
GALACTEROS, F
GIROT, R
BADOUAL, J
BATAILLE, H
BEAUVAIS, P
BEGUE, P
BELLOY, M
VILMER, E
BENICHOU, JJ
BOCCARA, F
CYNOBER, T
ELION, J
FEINGOLD, J
GUILLOUDBATAILLE, M
GALACTEROS, F
GIROT, R
BOUZID, K
LABIE, D
LAMBILLIOTTE, A
LEMERLE, S
MALOU, M
MONTALEMBERT, M
NATHANSON, M
NOSEDA, G
OLIVIER, C
QUESTIAUX, E
QUINET, B
REINERT, P
ROSA, J
TCHERNIA, G
VANHAEKE, D
VIGNES, B
ZAMET, P
机构
[1] HOP HENRI MONDOR,F-94000 CRETEIL,FRANCE
[2] HOP TROUSSEAU,F-75571 PARIS 12,FRANCE
关键词
SICKLE CELL DISEASE; CEREBROVASCULAR ACCIDENT; STROKE; TRANSFUSION; MENINGITIS;
D O I
10.1007/BF01956144
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
This study presents a series of 34 sickle cell patients with one or more cerebrovascular accidents (CVA). Risk factors were studied in a subgroup of 19 patients whose clinical and biological characteristics were compared to those of a group of 444 sickle cell patients without CVA. The only risk factor discovered was a past history of purulent meningitis, which was significantly more frequent in sickle cell patients than in those without CVA (P < 0.0001). No biological or radiological factor affecting the risk of recurrence was found. The risk of recurrence, neurological defects or death after subsequent CVA justify long-term transfusion treatment in patients presenting with a second CVA. However our study shows that 10 patients who were not transfused after their first CVA had no recurrences, (median follow up = 7.9 years; 2-18 years), providing a basis for discussion on the indications of long-term transfusion therapy for sickle cell patients presenting with their first CVA.
引用
收藏
页码:201 / 204
页数:4
相关论文
共 16 条
[1]   CEREBRAL INFARCTION IN SICKLE-CELL ANEMIA - MECHANISM BASED ON CT AND MRI [J].
ADAMS, RJ ;
NICHOLS, FT ;
MCKIE, V ;
MCKIE, K ;
MILNER, P ;
GAMMAL, TE .
NEUROLOGY, 1988, 38 (07) :1012-1017
[2]   RECURRENT CEREBRAL-ISCHEMIA DURING HYPER-TRANSFUSION THERAPY IN SICKLE-CELL-ANEMIA [J].
BUCHANAN, GR ;
BOWMAN, WP ;
SMITH, SJ .
JOURNAL OF PEDIATRICS, 1983, 103 (06) :921-923
[3]   SUBARACHNOID HEMORRHAGE IN SICKLE-CELL DISEASE [J].
CAREY, J ;
NUMAGUCHI, Y ;
NADELL, J .
CHILDS NERVOUS SYSTEM, 1990, 6 (01) :47-50
[4]  
DAVIES SC, 1989, LANCET, V2, P283
[5]  
HUTTENLOCHER PR, 1984, PEDIATRICS, V73, P615
[6]   CEREBROVASCULAR ACCIDENTS IN CHILDREN WITH SICKLE-CELL DISEASE AND ALPHA-THALASSEMIA [J].
MILLER, ST ;
RIEDER, RF ;
RAO, SP ;
BROWN, AK .
JOURNAL OF PEDIATRICS, 1988, 113 (05) :847-849
[7]  
PIOMELLI S, 1986, PEDIATR RES, V20, P285
[8]   NATURAL-HISTORY OF STROKE IN SICKLE-CELL DISEASE [J].
POWARS, D ;
WILSON, B ;
IMBUS, C ;
PEGELOW, C ;
ALLEN, J .
AMERICAN JOURNAL OF MEDICINE, 1978, 65 (03) :461-471
[9]   STROKE ASSOCIATED WITH OBSTRUCTIVE SLEEP-APNEA IN A CHILD WITH SICKLE-CELL ANEMIA [J].
ROBERTSON, PL ;
ALDRICH, MS ;
HANASH, SM ;
GOLDSTEIN, GW .
ANNALS OF NEUROLOGY, 1988, 23 (06) :614-616
[10]   SICKLE-CELL-ANEMIA AND CENTRAL-NERVOUS-SYSTEM INFARCTION - A NEUROPATHOLOGICAL STUDY [J].
ROTHMAN, SM ;
FULLING, KH ;
NELSON, JS .
ANNALS OF NEUROLOGY, 1986, 20 (06) :684-690