Donate Help Contact The AHA Sign In Home
American Heart Association
Stroke
Search: search_blue_button Advanced Search
Stroke. 2004;35:2762-2763
Published online before print October 28, 2004, doi: 10.1161/01.STR.0000146841.05980.a1
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
35/12/2762    most recent
01.STR.0000146841.05980.a1v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Bruno, A.
Right arrow Articles by Dechavanne, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bruno, A.
Right arrow Articles by Dechavanne, M.

(Stroke. 2004;35:2762.)
© 2004 American Heart Association, Inc.


Letters to the Editor

Predicting rtPA Associated ICH in Acute Stroke

Askiel Bruno, MD

Department of Neurology, Stroke Program, Indiana University School of Medicine, Indianapolis, Indiana


An extract of the first 250 words of the full text is provided, because this article has no abstract.
 

To the Editor:

I read with interest the study by Trouillas et al from Lyon, France,1 describing a plasma marker associated with parenchymal brain hemorrhage in patients treated with intravenous recombinant tissue plasminogen activator (rtPA) for acute stroke. Unusually high D-dimer levels measured at 2 hours after beginning rtPA were associated with increased risk of parenchymal hemorrhage within 24 hours. This is useful information that could be translated to patients treated elsewhere with a similar protocol. However, the currently adopted protocol for intravenous rtPA treatment of acute stroke in the United States and many other countries is according to the American Stroke Association (ASA)2 and the American Academy of Neurology (AAN)3 guidelines, and these guidelines differ in 2 important ways from the protocol used in Lyon. I would like to point out that because of these differences, the findings from Lyon may not translate to centers that follow the ASA/AAN guidelines.

First, the ASA/AAN guidelines do not recommend treatment beyond 3 hours after symptom onset, compared with up to 7 hours in Lyon. The mean delay to starting intravenous rtPA in Lyon was nearly 4 hours (based on a previous publication from that center),4 which is approximately 90 minutes later than in the United States. This difference may be important as longer exposure to brain ischemia, with greater injury to the blood vessels and surrounding tissue, may predispose to hemorrhagic complications more than shorter exposure.

Second, the ASA/AAN guidelines advise against anticoagulation within 24 hours after rtPA treatment, compared with . . . [Full Text of this Article]

Paul Trouillas, MD, PhD; Laurent Derex, MD; Fréderic Philippeau, MD; Norbert Nighoghossian, MD Jerome Honnorat, MD

Cerebrovascular Unit, Neurological Hospital, Lyon, France

Michel Hanss, MD Patrick French, MD

Hemostasis Department, Cardiological Hospital, Lyon, France

Patrice Adeleine, PhD

Biostatistical Laboratory, Lyon, France

Marc Dechavanne, MD

Hemostasis Laboratory, Lyon, France