Early [ 11 C]Flumazenil/H 2 O Positron Emission Tomography Predicts Irreversible Ischemic Cortical Damage in Stroke Patients Receiving Acute Thrombolytic Therapy
Author(s) -
Wolf-Dieter Heiß,
Lutz Kracht,
Martin Grond,
Jobst Rudolf,
Bernd Bauer,
K. Wienhard,
G. Pawlik
Publication year - 2000
Publication title -
stroke
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.397
H-Index - 319
eISSN - 1524-4628
pISSN - 0039-2499
DOI - 10.1161/01.str.31.2.366
Subject(s) - medicine , flumazenil , thrombolysis , stroke (engine) , tissue plasminogen activator , positron emission tomography , brain ischemia , penumbra , cardiology , ischemia , anesthesia , nuclear medicine , benzodiazepine , receptor , myocardial infarction , mechanical engineering , engineering
Central benzodiazepine receptor ligands, such as [(11)C]flumazenil (FMZ), are markers of neuronal integrity and therefore might be useful in the differentiation of functionally and morphologically damaged tissue early in ischemic stroke. We sought to assess the value of a benzodiazepine receptor ligand for the early identification of irreversible ischemic damage to cortical areas that cannot benefit from reperfusion.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom