Can the time window for administration of thrombolytics in stroke be increased?

被引:18
作者
Donnan, GA
Howells, DW
Markus, R
Toni, D
Davis, SM
机构
[1] Natl Stroke Res Inst, Austin & Repatriat Med Ctr, Heidelberg West, Vic 3081, Australia
[2] Univ Melbourne, Dept Med, Austin & Repatriat Med Ctr, Heidelberg, Vic, Australia
[3] Univ Roma La Sapienza, Stroke Unit, Dept Neurol Sci, Rome, Italy
[4] Royal Melbourne Hosp, Dept Neurol, Parkville, Vic 3050, Australia
基金
英国医学研究理事会; 美国国家卫生研究院;
关键词
D O I
10.2165/00023210-200317140-00001
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Level 1 evidence now shows that thrombolysis in cases of acute ischaemic stroke is effective if administered within 3 hours of stroke onset. This benefit has been shown to be time dependent and potentially extends beyond 3 hours, with evidence that potentially viable penumbral tissue may be present in a significant proportion of cases well beyond 3-6 hours and, in isolated cases, perhaps up to 48 hours. This exposes a 'stroke recovery gap', the difference observed between the clinical response to thrombolytic therapy in a given population of patients presenting with ischaemic stroke and the potential clinical recovery if all of the penumbra were salvaged under ideal circumstances. The means of bridging this 'stroke recovery gap' using thrombolysis must involve extending the therapeutic time window (i.e. the time between stroke onset and administration of thrombolytics). Approaches to do this include the use of: (i) improved patient selection with modem neuroimaging techniques, particularly magnetic resonance imaging using perfusion-weighted image/diffusion-weighted image mismatch; (ii) newer thrombolytic agents; (iii) lower doses of these agents; (iv) varied methods of administration of thrombolytic therapy including combined intravenous and intra-arterial approaches; and (v) adjunctive therapies such as neuroprotectants. Should these means of extending the time window for thrombolysis prove successful, a more widespread use of this form of acute stroke therapy will be possible.
引用
收藏
页码:995 / 1011
页数:17
相关论文
共 111 条
[1]
Effects of citicoline combined with thrombolytic therapy in a rat embolic stroke model [J].
Andersen, M ;
Overgaard, K ;
Meden, P ;
Boysen, G .
STROKE, 1999, 30 (07) :1464-1470
[2]
THRESHOLDS IN CEREBRAL-ISCHEMIA - THE ISCHEMIC PENUMBRA [J].
ASTRUP, J ;
SIESJO, BK ;
SYMON, L .
STROKE, 1981, 12 (06) :723-725
[3]
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
[4]
TREATMENT OF ACUTE ISCHEMIC STROKE - CHALLENGING THE CONCEPT OF A RIGID AND UNIVERSAL TIME WINDOW [J].
BARON, JC ;
VONKUMMER, R ;
DELZOPPO, GJ .
STROKE, 1995, 26 (12) :2219-2221
[5]
BELL WR, 1968, LANCET, V1, P490
[6]
Regulation of fibrinolytic activity by localization of inhibitors to fibrin(ogen) [J].
Booth, NA .
FIBRINOLYSIS & PROTEOLYSIS, 2000, 14 (2-3) :206-213
[7]
MONOCLONAL-ANTIBODIES PREVENTING LEUKOCYTE ACTIVATION REDUCE EXPERIMENTAL NEUROLOGIC INJURY AND ENHANCE EFFICACY OF THROMBOLYTIC THERAPY [J].
BOWES, MP ;
ROTHLEIN, R ;
FAGAN, SC ;
ZIVIN, JA .
NEUROLOGY, 1995, 45 (04) :815-819
[8]
Reperfusion after thrombolytic therapy of embolic stroke in the rat:: Magnetic resonance and biochemical imaging [J].
Busch, E ;
Krüger, K ;
Allegrini, PR ;
Kerskens, CM ;
Gyngell, ML ;
Hoehn-Berlage, M ;
Hossmann, KA .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1998, 18 (04) :407-418
[9]
TNK tissue plasminogen activator compared with front-loaded alteplase in acute myocardial infarction - Results of the TIMI 10B trial [J].
Cannon, CP ;
Gibson, CM ;
McCabe, CH ;
Adgey, AAJ ;
Schweiger, MJ ;
Sequeira, RF ;
Grollier, G ;
Giugliano, RP ;
Frey, M ;
Mueller, HS ;
Steingart, RM ;
Weaver, WD ;
Van de Werf, F ;
Braunwald, E .
CIRCULATION, 1998, 98 (25) :2805-2814
[10]
Cannon CP, 1997, CIRCULATION, V95, P351