Ability of patients with acute ischemic stroke to recall given information on intravenous thrombolysis: Results of a prospective multicenter study

Author:

Schuster Luzie1ORCID,Essig Fabian2,Daneshkhah Naeimeh2,Herm Juliane345,Hellwig Simon346,Endres Matthias34567,Dirnagl Ulrich38,Hoffmann Frank9,Michalski Dominik1,Pfeilschifter Waltraud1011,Urbanek Christian12,Petzold Gabor C1314,Rizos Timolaos15ORCID,Kraft Andrea9,Haeusler Karl Georg2

Affiliation:

1. Department of Neurology, University of Leipzig, Leipzig, Germany

2. Department of Neurology, Universitätsklinikum Würzburg, Würzburg, Germany

3. Klinik und Hochschulambulanz für Neurologie, Charité - Universitätsmedizin Berlin, Berlin, Germany

4. Center for Stroke Research Berlin, Charité - Universitätsmedizin Berlin, Berlin, Germany

5. German Center for Cardiovascular Diseases (DZHK), Partner Site Berlin, Germany

6. Berlin Institute of Health at Charité - Universitätsmedizin Berlin, Berlin, Germany

7. German Center for Neurodegenerative Diseases (DZNE), Partner Site Berlin, Germany

8. QUEST Center, Berlin Institute of Health (BIH), Berlin, Germany

9. Department of Neurology, Martha-Maria Hospital, Halle/Saale, Germany

10. Department of Neurology, University of Frankfurt, Frankfurt/Main, Germany

11. Department of Neurology, Hospital Lüneburg, Lüneburg, Germany

12. Department of Neurology, Hospital Ludwigshafen, Ludwigshafen am Rhein, Germany

13. Division of Vascular Neurology, Department of Neurology, University of Bonn, Bonn, Germany

14. German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany

15. Department of Neurology, University of Heidelberg, Heidelberg, Germany

Abstract

Introduction: Intravenous thrombolysis (IVT) is an on label treatment for selected patients with acute ischemic stroke (AIS). As major bleeding or allergic shock may occur, the need to ensure patients’ informed consent for IVT is a matter of debate. Patients and methods: Prospective investigator-initiated multi-center observational study to assess the ability of AIS patients to recall information, provided by a physician during a standardized educational talk (SET) on IVT use. The recall of 20 pre-defined items was assessed in AIS after 60–90 min ( n = 93) or 23–25 h ( n = 40) after SET. About 40 patients with subacute stroke, 40 non-stroke patients, and 23 relatives of AIS patients served as controls, and were surveyed 60–90 min after SET. Results: Within 60–90 min after SET, AIS patients (median age 70 years, 31% female, median NIHSS score on admission 3 points) who were considered capable to provide informed consent recalled 55% (IQR 40%–66.7%) of the provided SET items. In multivariable linear regression analysis recapitulation by AIS patients was associated with their educational level (β = 6.497, p < 0.001), self-reported excitement level (β = 1.879, p = 0.011) and NIHSS score on admission (β = −1.186, p = 0.001). Patients with subacute stroke (70 years, 40% female, median NIHSS = 2) recalled 70% (IQR 55.7%–83.6%), non-stroke patients (75 years, 40% female) 70% (IQR 60%–78.7%), and AIS relatives (58 years, 83% female) 70% (IQR 60%–85%). Compared to subacute stroke patients, AIS patients less often recalled the frequency of IVT-related bleeding (21% vs 43%), allergic shock (15% vs 39%), and bleeding-related morbidity and mortality (44% vs 78%). AIS patients recalled 50% (IQR 42.3%–67.5%) of the provided items 23–25 h after SET. Conclusion: AIS patients eligible for IVT remember about half of all SET-items after 60–90 min or 23–25 h, respectively. The fact that the recapitulation of IVT-associated risks is particularly poor should be given special consideration.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Neurology (clinical)

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