Thursday, July 20, 2023

The use of alteplase, although safe, does not offer clear clinical advantages when mild stroke is non-disabling

Did you ask your patients if your definition of non-disabling matches theirs?   I thought not.

There are NO strokes that are too good to treat. Do you ever talk to stroke survivors about leaving them disabled because you did NOTHING?

The use of alteplase, although safe, does not offer clear clinical advantages when mild stroke is non-disabling

Giovanni Merlino1,2*, Lorenzo Nesi2, Pietro Vergobbi2, Marco Domenico Scanni2, Sara Pez2, Alessandro Marziali2, Yan Tereshko2, Giuseppe Sportelli2, Simone Lorenzut1, Francesco Janes1,2, Gian Luigi Gigli3 and Mariarosaria Valente2,3
  • 1Stroke Unit, Department of Head-Neck and Neuroscience, Udine University Hospital, Udine, Italy
  • 2Clinical Neurology, Udine University Hospital, Udine, Italy
  • 3Dipartimento di Area Medica (DAME), University of Udine, Udine, Italy

Introduction: It is unknown whether alteplase is effective and safe in patients with mild acute ischemic stroke (AIS). Determining whether symptoms are “disabling” or not is a crucial factor in the management of these patients. This study aimed to investigate the efficacy and safety of alteplase in patients with mild, non-disabling AIS.

Methods: We included all consecutive patients admitted for AIS at our institution from January 2015 to May 2022 who presented a baseline NIHSS score of 0–5 and fit the criteria to receive intravenous thrombolysis. In order to select only subjects with non-disabling AIS, we excluded patients who scored more than 1 point in the following NIHSS single items: vision, language, neglect, and single limb. Patients who scored at least 1 point in the NIHSS consciousness item were excluded as well. This study is a retrospective analysis of a prospectively collected database.

Results: After the application of the exclusion criteria, we included 319 patients, stratified into patients receiving and not receiving alteplase based on non-disabling symptoms. The two groups were comparable regarding demographic and clinical data. Rates of a 3-month favorable outcome, defined as a 3-month mRS score of 0–1, were similar, being 82.3% and 86.1% in the treated and untreated patients, respectively. Hemorrhagic complications and mortality occurred infrequently and were not affected by alteplase treatment.

Discussion: This observational study suggests that the use of alteplase, although safe, is not associated with a better outcome in highly selected patients with non-disabling AIS.

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