Hemorrhagic transformation in acute ischemic stroke - The MAST-E study

被引:186
作者
Jaillard, A
Cornu, C
Durieux, A
Moulin, T
Boutitie, F
Lees, KR
Hommel, M
机构
[1] Univ Hosp, INSERM U438, Dept Clin & Biol Neurosci, Stroke Unit, Grenoble, France
[2] Univ Lyon 1, Serv Pharmacol, Clin EA 643, F-69365 Lyon, France
[3] Univ Hosp, Neurol Serv, Clermont Ferrand, France
[4] Univ Hosp, Neurol Serv, Besancon, France
[5] Univ Glasgow, Dept Med & Therapeut, Acute Stroke Unit, Glasgow, Lanark, Scotland
关键词
cerebral hemorrhage; clinical trials; streptokinase; stroke; acute;
D O I
10.1161/01.STR.30.7.1326
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose-Hemorrhagic transformation (HT) is the most critical complication of thrombolytics in clinical trials in acute stroke. The aim of this study was to determine the rates and the predictors of HT in the Multicenter Acute Stroke Trial-Europe (MAST-E) study. Methods-We performed a post hoc analysis of MAST-E data designed to assess the safety and efficacy of streptokinase administered intravenously within 6 hours of stroke onset. HT included all intracerebral hemorrhages and symptomatic hemorrhages (SHT) associated with clinical worsening. The predictors of PIT and SHT were determined using multivariate modeling. Results-Among the 310 patients included, 159 patients had HT and 37 SHT (97 and 33 in the streptokinase group and 62 and 4 in the placebo group, respectively). Patients with SPIT had significantly more atrial fibrillation, diabetes mellitus, no heparin use, streptokinase treatment, and early CT signs. In the multivariate analysis, HT was predicted by early CT signs and streptokinase treatment. SPIT was predicted by diabetes mellitus, early CT signs, streptokinase treatment, and the interaction between streptokinase treatment and decreased level of consciousness, Among the streptokinase-treated patients, the same predictors remained. Conclusions-The relative risks of HT after streptokinase were in the same range in MAST-E as in other streptokinase and tPA trials. Early CT signs were strong predictors of both HT and SHT, stressing that these patients are at high risk of bleeding. In our study, the predictors of HT and SHT were similar to those of tPA trials in acute stroke.
引用
收藏
页码:1326 / 1332
页数:7
相关论文
共 47 条
[1]   Predictors of hemorrhagic transformation occurring spontaneously and on anticoagulants in patients with acute ischemic stroke [J].
Alexandrov, AV ;
Black, SE ;
Ehrlich, LE ;
Caldwell, CB ;
Norris, JW .
STROKE, 1997, 28 (06) :1198-1202
[2]  
[Anonymous], 1998, JAMA, V279, P1265
[3]   INTRACEREBRAL HEMORRHAGE IN STROKE PATIENTS ANTICOAGULATED WITH HEPARIN [J].
BABIKIAN, VL ;
KASE, CS ;
PESSIN, MS ;
NORRVING, B ;
GORELICK, PB .
STROKE, 1989, 20 (11) :1500-1503
[4]  
BESSON G, 1998, ACTA NEUROL SCAND, V98, P292
[5]  
BOZZAO L, 1989, AM J NEURORADIOL, V10, P1215
[6]   Intracerebral hemorrhage after intravenous t-PA therapy for ischemic stroke [J].
Brott, T ;
Broderick, J ;
Kothari, R ;
ODonoghue, M ;
Barsan, W ;
Tomsick, T ;
Spilker, J ;
Miller, R ;
Sauerbeck, L ;
Farrell, J ;
Kelly, J ;
Perkins, T ;
Miller, R ;
McDonald, T ;
Rorick, M ;
Hickey, C ;
Armitage, J ;
Perry, C ;
Thalinger, K ;
Rhude, R ;
Schill, J ;
Becker, PS ;
Heath, RS ;
Adams, D ;
Reed, R ;
Klei, M ;
Hughes, A ;
Anthony, J ;
Baudendistel, D ;
Zadicoff, C ;
Rymer, M ;
Bettinger, I ;
Laubinger, P ;
Schmerler, M ;
Meiros, G ;
Lyden, P ;
Dunford, J ;
Zivin, J ;
Rapp, K ;
Babcock, T ;
Daum, P ;
Persona, D ;
Brody, M ;
Jackson, C ;
Lewis, S ;
Liss, J ;
Mahdavi, Z ;
Rothrock, J ;
Tom, T ;
Zweifler, R .
STROKE, 1997, 28 (11) :2109-2118
[7]  
BRYAN RN, 1991, AM J NEURORADIOL, V12, P611
[8]  
CANDELISE L, 1995, LANCET, V346, P1509
[9]   Intravenous tissue plasminogen activator for acute ischemic stroke: Feasibility, safety, and efficacy in the first year of clinical practice [J].
Chiu, D ;
Krieger, D ;
Villar-Cordova, C ;
Kasner, SE ;
Morgenstern, B ;
Bratina, PL ;
Yatsu, FM ;
Grotta, JC .
STROKE, 1998, 29 (01) :303-303
[10]   RECOMBINANT TISSUE PLASMINOGEN-ACTIVATOR IN ACUTE THROMBOTIC AND EMBOLIC STROKE [J].
DELZOPPO, GJ ;
POECK, K ;
PESSIN, MS ;
WOLPERT, SM ;
FURLAN, AJ ;
FERBERT, A ;
ALBERTS, MJ ;
ZIVIN, JA ;
WECHSLER, L ;
BUSSE, O ;
GREENLEE, R ;
BRASS, L ;
MOHR, JP ;
FELDMANN, E ;
HACKE, W ;
KASE, CS ;
BILLER, J ;
GRESS, D ;
OTIS, SM .
ANNALS OF NEUROLOGY, 1992, 32 (01) :78-86