Donate Help Contact The AHA Sign In Home
American Heart Association
Stroke
Search: search_blue_button Advanced Search
Stroke. 2007;38:e131
Published online before print September 13, 2007, doi: 10.1161/STROKEAHA.107.485508
This Article
Right arrow Extract Freely available
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
38/11/e131    most recent
STROKEAHA.107.485508v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
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 den Hertog, H. M.
Right arrow Articles by Dippel, D. W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by den Hertog, H. M.
Right arrow Articles by Dippel, D. W.
Right arrowPubmed/NCBI databases
*Compound via MeSH
*Substance via MeSH
Hazardous Substances DB
*ACETAMINOPHEN
Medline Plus Health Information
*Fever
*Pain Relievers
*Stroke

(Stroke. 2007;38:e131.)
© 2007 American Heart Association, Inc.


Letters to the Editor

Acetaminophen for Temperature Reduction in Acute Stroke: Potential but Unproven Benefits

Heleen M. den Hertog, MD

Erasmus MC University Medical Center, Rotterdam, The Netherlands

H. Bart van der Worp, MD, PhD

University Medical Center, Utrecht, The Netherlands

H. Maarten van Gemert, MD, PhD

Meander Medical Center, Amersfoort, The Netherlands

Diederik W. Dippel, MD, PhD

Erasmus MC University Medical Center, Rotterdam, The Netherlands

To the Editor:

We read with interest the review by Hemmen and Lyden on induced hypothermia for acute ischemic stroke.1 The review focuses on physical cooling methods in acute stroke. Some points, however, deserve in our opinion a more extensive discussion.

The authors state that controlling body temperature below 36.5°C has been proven to correlate with good clinical outcome. They do not cite controlled clinical trials to support their point, but refer to 2 observational studies instead.

Indeed, well-designed studies have shown a consistent relationship between increased body temperature measured within 12 to 24 hours after onset of stroke, and outcome, but not beyond that interval.2 These studies suggest that reductions in body temperature of 0.5°C might lead to a relative risk reduction in poor outcome of 10%. Reductions in body temperature of this magnitude have been proven feasible in 2 pilot studies of high-dose acetaminophen.3,4

In our view, the uncontrolled studies and small randomized trials in acute ischemic stroke that have been conducted so far have not provided sufficient evidence of safety and feasibility of physical cooling methods. We need more randomized phase II studies with several cooling devices. These studies should explore the relationship between intensity of treatment, temperature reduction, and adverse events, such as arterial hypotension, infections, and cardiac arrhythmias. On the other hand, the risk of complications, the high costs of this mode of treatment, and other logistical barriers imply that there is a need for a simple medical intervention that may reduce body temperature to lesser extent, but is cheap and safe.

Although several national and international guidelines recommend the use of acetaminophen in patients with fever after stroke, it is recognized that there is no evidence available of a therapeutic effect.5 Moreover, most patients develop fever after the first 24 hours, and it appears unlikely that late treatment will have an effect on outcome.

Why not treat all patients early with high-dose acetaminophen? The main reason is that this treatment strategy has not yet been proven to improve functional outcome after stroke. In addition, acetaminophen can be dangerous in high doses and cause liver failure. Use of acetaminophen may delay the recognition of pneumonia and urinary tract infections, and thus lead to delayed treatment and poor outcome.

We conclude that a large pragmatic placebo-controlled randomized clinical trial of acetaminophen in acute ischemic stroke is needed. Exactly such a trial is underway in the Netherlands, PAIS: Paracetamol (Acetaminophen) In Stroke. More than 1100 patients have been included in the trial as of January 2007. We expect to be able to present the trial’s results in 2008.6

Acknowledgments

Disclosures

None.

References

1. Hemmen TM, Lyden PD. Induced hypothermia for acute stroke. Stroke. 2007; 38: 794–799.[Abstract/Free Full Text]

2. Reith J, Jorgensen HS, Pedersen PM, Nakayama H, Raaschou HO, Jeppesen LL, Olsen TS. Body temperature in acute stroke: relation to stroke severity, infarct size, mortality, and outcome. Lancet. 1996; 347: 422–425.[CrossRef][Medline] [Order article via Infotrieve]

3. Dippel DW, van Breda EJ, van Gemert HM, van der Worp HB, Meijer RJ, Kappelle LJ, Koudstaal PJ. Effect of paracetamol (acetaminophen) on body temperature in acute ischemic stroke: a double-blind, randomized phase II clinical trial. Stroke. 2001; 32: 1607–1612.[Abstract/Free Full Text]

4. Dippel DW, van Breda EJ, van Gemert HM, van der Worp HB, Meijer RJ, Kappelle LJ, Koudstaal PJ. Effect of paracetamol (acetaminophen) and ibuprofen on body temperature in acute ischemic stroke PISA, a phase II double-blind, randomized, placebo-controlled trial. BMC Cardiovasc Disord. 2003; 3: 2.[CrossRef][Medline] [Order article via Infotrieve]

5. Adams H, Adams R, Del Zoppo G, MD, Goldstein LB. Guidelines for the early management of patients with ischemic stroke. 2005 guidelines update. A scientific statement from the Stroke Council of the American Heart Association/American Stroke Association. Stroke. 2005; 36: 916–923.[Free Full Text]

6. Van Breda EJ, van der Worp HB, van Gemert HM, Algra A, Kapelle LJ, Gijn J, Koudstaal PJ, Dippel DWJ. PAIS: paracetamol (acetaminophen) in stroke; protocol for a randomized, double blind clinical trial [ISCRTN 74418480] BMC Cardiovasc Disord. 2005; 5: 24.[CrossRef]





This Article
Right arrow Extract Freely available
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
38/11/e131    most recent
STROKEAHA.107.485508v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
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 den Hertog, H. M.
Right arrow Articles by Dippel, D. W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by den Hertog, H. M.
Right arrow Articles by Dippel, D. W.
Right arrowPubmed/NCBI databases
*Compound via MeSH
*Substance via MeSH
Hazardous Substances DB
*ACETAMINOPHEN
Medline Plus Health Information
*Fever
*Pain Relievers
*Stroke