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Prolonged Corrected QT Interval as a Predictor of Clinical Outcome in Acute Ischemic Stroke
M. Hromádka, J. Seidlerová, V. Rohan, J. Baxa, J. Šedivý, D. Rajdl, I. Ulč, P. Ševčík, J. Polívka, R. Rokyta,
Language English Country United States
Document type Journal Article
- MeSH
- Action Potentials MeSH
- Biomarkers blood MeSH
- Time Factors MeSH
- Stroke diagnosis mortality physiopathology therapy MeSH
- Computed Tomography Angiography MeSH
- Adult MeSH
- Electrocardiography * MeSH
- Brain Ischemia diagnosis mortality physiopathology therapy MeSH
- Intensive Care Units MeSH
- Middle Aged MeSH
- Humans MeSH
- Logistic Models MeSH
- Hospital Mortality MeSH
- Cerebral Angiography methods MeSH
- Multivariate Analysis MeSH
- Natriuretic Peptide, Brain blood MeSH
- Neurologic Examination MeSH
- Recovery of Function MeSH
- Odds Ratio MeSH
- Disability Evaluation MeSH
- Predictive Value of Tests MeSH
- Heart Conduction System physiopathology MeSH
- Patient Admission MeSH
- Risk Factors MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Heart Rate * MeSH
- Troponin I blood MeSH
- Treatment Outcome MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
BACKGROUND: This study aimed to investigate changes of corrected QT (QTc) interval during acute ischemic stroke and its correlation with high-sensitivity troponin I (hsTnI), brain natriuretic peptide (BNP), neurological outcome, and 1-year mortality. METHODS: We registered electrocardiogram in 69 patients immediately after admission to the intensive care unit and then after 24 and 48 hours. Computed tomography was performed on admission to determine brain infarct size and localization. Neurological outcome was assessed by modified Rankin scale (mRS) at discharge. RESULTS: Forty-five (65.2%) patients had prolonged QTc at baseline; only 18 (26.1%) patients had prolonged QTc after 48 hours. Baseline QTc was not associated with neurological outcome (P = .27). However, prolonged QTc after 48 hours was associated with worse mRS at discharge (4.5 [4.0-6.0] versus 2.0 [1.0-3.0]; P < .0001). Patients who deceased during hospitalization (n = 7 [10.1%]) as compared with survivors had more frequently prolonged QTc after 48 hours (38.9 versus 0%; P < .0001), higher level of hsTnI (48.4 [36.1-75.0] versus 8.6 [3.4-26.5]; P = .003), and BNP (334 [224-866] versus 109 [30-190]; P = .014). In univariate analysis, 1-year mortality was associated with prolonged QTc after 48 hours, hsTnI, and BNP. In multivariate analysis, only BNP remained to be associated with 1-year mortality (odds ratio 3.41, 95% confidence interval 1.06-11.03). CONCLUSIONS: QTc interval in patients with acute ischemic stroke is a dynamic parameter. Prolonged QTc after 48 hours, but not baseline QTc, correlated with neurological outcome and 1-year mortality. Patients with prolonged QTc had higher level of hsTnI.
Biomedical Centre Faculty of Medicine in Pilsen Charles University Czech Republic
Department of Clinical Biochemistry and Hematology Faculty Hospital in Pilsen Czech Republic
Department of Imaging Methods Faculty of Medicine in Pilsen Charles University Czech Republic
Internal Department 2 Faculty of Medicine in Pilsen Charles University Czech Republic
Neurology Department Faculty of Medicine in Pilsen Charles University Czech Republic
References provided by Crossref.org
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- $a BACKGROUND: This study aimed to investigate changes of corrected QT (QTc) interval during acute ischemic stroke and its correlation with high-sensitivity troponin I (hsTnI), brain natriuretic peptide (BNP), neurological outcome, and 1-year mortality. METHODS: We registered electrocardiogram in 69 patients immediately after admission to the intensive care unit and then after 24 and 48 hours. Computed tomography was performed on admission to determine brain infarct size and localization. Neurological outcome was assessed by modified Rankin scale (mRS) at discharge. RESULTS: Forty-five (65.2%) patients had prolonged QTc at baseline; only 18 (26.1%) patients had prolonged QTc after 48 hours. Baseline QTc was not associated with neurological outcome (P = .27). However, prolonged QTc after 48 hours was associated with worse mRS at discharge (4.5 [4.0-6.0] versus 2.0 [1.0-3.0]; P < .0001). Patients who deceased during hospitalization (n = 7 [10.1%]) as compared with survivors had more frequently prolonged QTc after 48 hours (38.9 versus 0%; P < .0001), higher level of hsTnI (48.4 [36.1-75.0] versus 8.6 [3.4-26.5]; P = .003), and BNP (334 [224-866] versus 109 [30-190]; P = .014). In univariate analysis, 1-year mortality was associated with prolonged QTc after 48 hours, hsTnI, and BNP. In multivariate analysis, only BNP remained to be associated with 1-year mortality (odds ratio 3.41, 95% confidence interval 1.06-11.03). CONCLUSIONS: QTc interval in patients with acute ischemic stroke is a dynamic parameter. Prolonged QTc after 48 hours, but not baseline QTc, correlated with neurological outcome and 1-year mortality. Patients with prolonged QTc had higher level of hsTnI.
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