Presenting Symptoms and Dysphagia Screen Predict Outcome in Mild and Rapidly Improving Acute Ischemic Stroke Patients

Objective There are limited data on which patients not treated with intravenous (IV) tissue-type plasminogen activator (tPA) due to mild and rapidly improving stroke symptoms (MaRISS) have unfavorable outcomes. Materials and Methods Acute ischemic stroke (AIS) patients not treated with IV tPA due to...

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Veröffentlicht in:Journal of stroke and cerebrovascular diseases 2016-12, Vol.25 (12), p.2876-2881
Hauptverfasser: Gadodia, Gaurav, BS, Rizk, Nibal, MD, Camp, Deborah, RN, MHA, CCM, SCRN, Bryant, Katja, MSN, RN, CNRN, Zimmerman, Susan, RN, MSN, CNRN, Brasher, Cynthia, RN, CNRN, SCRN, Connelly, Kerrin, RN, MSN, MPH, Dunn, Joshua, RN, MSN, CCRN, Frankel, Michael, MD, Ido, Moges Seymour, MD, MS, MPH, Lugtu, James, RN, FNP, MSN, Nahab, Fadi, MD
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Sprache:eng
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Zusammenfassung:Objective There are limited data on which patients not treated with intravenous (IV) tissue-type plasminogen activator (tPA) due to mild and rapidly improving stroke symptoms (MaRISS) have unfavorable outcomes. Materials and Methods Acute ischemic stroke (AIS) patients not treated with IV tPA due to MaRISS from January 1, 2009 to December 31, 2013 were identified as part of the Georgia Coverdell Acute Stroke Registry. Multivariable regression analysis was used to identify factors associated with a lower likelihood of favorable outcome, defined as discharge to home. Results There were 1614 AIS patients who did not receive IV tPA due to MaRISS (median National Institutes of Health stroke scale [NIHSS] 1], of which 305 (19%) did not have a favorable outcome. Factors associated with lower likelihood of favorable outcome included Medicare insurance status (odds ratio [OR]: .53, 95% confidence interval [CI]: .34-.84), arrival by emergency medical services (OR: .46, 95% CI: .29-.73), increasing NIHSS score (per unit OR: .89, 95% CI: .84-.93), weakness as the presenting symptom (OR: .50, 95% CI: .30-.84), and a failed dysphagia screen (OR: .43, 95% CI: .23-.80). During the study period,
ISSN:1052-3057
1532-8511
DOI:10.1016/j.jstrokecerebrovasdis.2016.07.049