Admission fibrinolytic profile is associated with symptomatic hemorrhagic transformation in stroke patients treated with tissue plasminogen activator

被引:116
作者
Ribo, M
Montaner, J
Molina, CA
Arenillas, JF
Santamarina, E
Quintana, M
Alvarez-Sabín, J
机构
[1] Hosp Gen Valle Hebron, Neurovasc Unit, Neurovasc Res Lab, Barcelona, Spain
[2] Univ Autonoma Barcelona, Barcelona, Spain
关键词
blood-brain barrier; complications; hemostasis; stroke; acute; thrombolysis;
D O I
10.1161/01.STR.0000137608.73660.4c
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-Symptomatic intracranial hemorrhage (SICH) is the most feared complication after tissue plasminogen activator (tPA) stroke treatment. Endogenous fibrinolysis inhibitors play an essential role in the coagulation/fibrinolysis balance and may be involved in the bleeding process. We aim to determine the predictive value of pretreatment levels of fibrinolysis inhibitors (PAI-1, lipoprotein(a), TAFI, and homocysteine) on SICH. Methods-Consecutive tPA-treated stroke patients with middle cerebral artery occlusion were studied. Baseline blood samples were obtained just before tPA administration and fibrinolysis inhibitors were determined. A second computed tomography (CT) scan was obtained at 24 hours or when a neurological worsening occurred to rule out SICH. Results-Seventy-seven patients (40% women, age 75 years) were studied. Median admission National Institutes of Health Stroke Scale was 17 (range, 7 to 22) and mean time to treatment was 160 minutes. Six patients (7.9%) presented with a SICH. In analyses based on clinical and CT variables, no relation could be found with SICH. When laboratory data were analyzed, patients who experienced SICH showed lower baseline PAI-1 (21.7+/-3.5 ng/mL versus 31.8+/-12.1 ng/mL; P<0.01) and higher TAFI (216.7 +/- 78.4% versus 162.1 +/- 54.2%; P=0.03). Homocysteine and lipoprotein(a) were not related to SICH. The only factors associated with SICH were TAFI>180% (OR, 12.9; CI, 1.41 to 118.8; P=0.02) and PAI-1<21.4 ng/mL (OR, 12.75; CI, 1.17 to 139.2; P=0.04). The combination of admission PAI-1<21.4 ng/mL and TAFI>180% had a sensibility of 75% and a specificity of 97.6% (P<0.01) predicting SICH, with a positive predictive value of 75% and negative predictive value of 97.6%. Conclusions-Baseline PAI-1 and TAFI levels predict SICH after stroke tPA therapy. In the future, these biomarkers could be used to improve thrombolysis safety.
引用
收藏
页码:2123 / 2127
页数:5
相关论文
共 26 条
[1]  
Adams HP, 1996, STROKE, V27, P1711
[2]   CLASSIFICATION OF SUBTYPE OF ACUTE ISCHEMIC STROKE - DEFINITIONS FOR USE IN A MULTICENTER CLINICAL-TRIAL [J].
ADAMS, HP ;
BENDIXEN, BH ;
KAPPELLE, LJ ;
BILLER, J ;
LOVE, BB ;
GORDON, DL ;
MARSH, EE ;
KASE, CS ;
WOLF, PA ;
BABIKIAN, VL ;
LICATAGEHR, EE ;
ALLEN, N ;
BRASS, LM ;
FAYAD, PB ;
PAVALKIS, FJ ;
WEINBERGER, JM ;
TUHRIM, S ;
RUDOLPH, SH ;
HOROWITZ, DR ;
BITTON, A ;
MOHR, JP ;
SACCO, RL ;
CLAVIJO, M ;
ROSENBAUM, DM ;
SPARR, SA ;
KATZ, P ;
KLONOWSKI, E ;
CULEBRAS, A ;
CAREY, G ;
MARTIR, NI ;
FICARRA, C ;
HOGAN, EL ;
CARTER, T ;
GURECKI, P ;
MUNTZ, BK ;
RAMIREZLASSEPAS, M ;
TULLOCH, JW ;
QUINONES, MR ;
MENDEZ, M ;
ZHANG, SM ;
ALA, T ;
JOHNSTON, KC ;
ANDERSON, DC ;
TARREL, RM ;
NANCE, MA ;
BUDLIE, SR ;
DIERICH, M ;
HELGASON, CM ;
HIER, DB ;
SHAPIRO, RA .
STROKE, 1993, 24 (01) :35-41
[3]   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
[4]  
Anglés-Cano E, 2001, ANN NY ACAD SCI, V936, P261
[5]   PURIFICATION AND CHARACTERIZATION OF TAFI, A THROMBIN-ACTIVABLE FIBRINOLYSIS INHIBITOR [J].
BAJZAR, L ;
MANUEL, R ;
NESHEIM, ME .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (24) :14477-14484
[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]   URGENT THERAPY FOR STROKE .1. PILOT-STUDY OF TISSUE PLASMINOGEN-ACTIVATOR ADMINISTERED WITHIN 90 MINUTES [J].
BROTT, TG ;
HALEY, EC ;
LEVY, DE ;
BARSAN, W ;
BRODERICK, J ;
SHEPPARD, GL ;
SPILKER, J ;
KONGABLE, GL ;
MASSEY, S ;
REED, R ;
MARLER, JR .
STROKE, 1992, 23 (05) :632-640
[8]   Acute release of plasminogen activator inhibitor-1 in ST-segment elevation myocardial infarction predicts mortality [J].
Collet, JP ;
Montalescot, G ;
Vicaut, E ;
Ankri, A ;
Walylo, F ;
Lesty, C ;
Choussat, R ;
Beygui, F ;
Borentain, M ;
Vignolles, N ;
Thomas, D .
CIRCULATION, 2003, 108 (04) :391-394
[9]  
Davalos A, 2003, STROKE, V34, P247
[10]   Predictors of good outcome after intravenous tPA for acute ischemic stroke [J].
Demchuk, AM ;
Tanne, D ;
Hill, MD ;
Kasner, SE ;
Hanson, S ;
Grond, M ;
Levine, SR .
NEUROLOGY, 2001, 57 (03) :474-480