13 research outputs found

    Pharmacological and Non-pharmacological Treatments for Stroke Prevention in Patients with Atrial Fibrillation

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    <p><strong>Article full text</strong></p> <br> The full text of this article can be found <a href="https://link.springer.com/article/10.1007/s12325-017-0616-6"><b>here</b>.</a><br> <br> <strong>Provide enhanced digital features for this article</strong><br> If you are an author of this publication and would like to provide additional enhanced digital features for your article then please contact <u>[email protected]</u>.<br> <br> The journal offers a range of additional features designed to increase visibility and readership. All features will be thoroughly peer reviewed to ensure the content is of the highest scientific standard and all features are marked as ‘peer reviewed’ to ensure readers are aware that the content has been reviewed to the same level as the articles they are being presented alongside. Moreover, all sponsorship and disclosure information is included to provide complete transparency and adherence to good publication practices. This ensures that however the content is reached the reader has a full understanding of its origin. No fees are charged for hosting additional open access content.<br> <br> Other enhanced features include, but are not limited to:<br> • Slide decks<br> • Videos and animations<br> • Audio abstracts<br> • Audio slide

    Catheter Ablation of Atrial Fibrillation: An Overview for Clinicians

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    <p><strong>Article full text</strong></p> <br> The full text of this article can be found <a href="https://link.springer.com/article/10.1007/s12325-017-0590-z"><b>here</b>.</a><br> <br> <strong>Provide enhanced digital features for this article</strong><br> If you are an author of this publication and would like to provide additional enhanced digital features for your article then please contact <u>[email protected]</u>.<br> <br> The journal offers a range of additional features designed to increase visibility and readership. All features will be thoroughly peer reviewed to ensure the content is of the highest scientific standard and all features are marked as ‘peer reviewed’ to ensure readers are aware that the content has been reviewed to the same level as the articles they are being presented alongside. Moreover, all sponsorship and disclosure information is included to provide complete transparency and adherence to good publication practices. This ensures that however the content is reached the reader has a full understanding of its origin. No fees are charged for hosting additional open access content.<br> <br> Other enhanced features include, but are not limited to:<br> • Slide decks<br> • Videos and animations<br> • Audio abstracts<br> • Audio slide

    Receiver-operator characteristic analyses of the biomarkers and stroke risk scores predictive ability for unfavourable 30-day outcome of ischemic stroke and pairwise comparisons (Table 2).

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    <p>Receiver-operator characteristic analyses of the biomarkers and stroke risk scores predictive ability for unfavourable 30-day outcome of ischemic stroke and pairwise comparisons (<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0106439#pone-0106439-t002" target="_blank">Table 2</a>).</p

    Crude associations of biomarkers and the CHADS<sub>2</sub>, CHA<sub>2</sub>DS<sub>2</sub>-VASc and HAS-BLED score with unfavourable 30-day outcome of ischemic stroke, predictive ability of each biomarker or score, and pairwise comparisons of each biomarker and stroke risk score predictive ability.

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    <p>OR, Odds Ratio; CI, Confidence Interval.</p><p>Only biomarkers with p<0.01 regarding unfavourable 30-day functional stroke outcome are shown.</p><p>CRP, C-reactive protein; WBC, white blood cell count; CrCl, creatinine clearance; CHA<sub>2</sub>DS<sub>2</sub>-VASc, congestive heart failure or left ventricular ejection fraction ≤40%, hypertension, age ≥75 years, diabetes mellitus, prior stroke or TIA, vascular disease (including myocardial infarction and peripheral artery disease), age >65 years, female gender (1 point each, age ≥75 years and prior stroke/TIA 2 points each); CHADS<sub>2</sub>, congestive heart failure, hypertension, age ≥75 years, diabetes mellitus, prior stroke or TIA (1 point each, prior stroke/TIA 2 points); HAS-BLED, hypertension, abnormal renal or liver function, prior stroke, labile INRs (International Normalized Ratio), elderly (>65 years), concomitant drugs or alcohol use.</p><p>Crude associations of biomarkers and the CHADS<sub>2</sub>, CHA<sub>2</sub>DS<sub>2</sub>-VASc and HAS-BLED score with unfavourable 30-day outcome of ischemic stroke, predictive ability of each biomarker or score, and pairwise comparisons of each biomarker and stroke risk score predictive ability.</p

    Baseline characteristic of patients with acute ischemic stroke according to favourable (mRS<3) or unfavourable 30-day functional stroke outcome (mRS≥3), including in-hospital death.

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    <p>Values are presented as n (%) or mean ± standard deviation or median with interquartile range (IQR).</p><p>mRS, modified Rankin Scale (patients who died were assigned a mRS of 6); NYHA, New York Heart Association; TIA, transient ischemic attack; CHADS<sub>2</sub>, congestive heart failure, hypertension, age ≥75 years, diabetes mellitus, prior stroke or TIA; CHA<sub>2</sub>DS<sub>2</sub>-VASc, congestive heart failure or left ventricular ejection fraction ≤40%, hypertension, age ≥75 years, diabetes mellitus, prior stroke or TIA, vascular disease (including myocardial infarction and peripheral artery disease), age >65 years, female gender; HAS-BLED, hypertension, abnormal renal or liver function, prior stroke, labile INRs (International Normalized Ratio), elderly (>65 years), concomitant drugs or alcohol use; MAC, mitral annulus calcification; ACEI, angiotensin converting enzyme inhibitor; ARB, angiotensin receptor blocker.</p><p>Baseline characteristic of patients with acute ischemic stroke according to favourable (mRS<3) or unfavourable 30-day functional stroke outcome (mRS≥3), including in-hospital death.</p

    Pairwise comparison of Receiver-operator characteristic of fully adjusted TnI, ‘classic’ and composed scores for unfavourable 30-day functional outcome of ischemic stroke.

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    <p>Pairwise comparison of Receiver-operator characteristic of fully adjusted TnI, ‘classic’ and composed scores for unfavourable 30-day functional outcome of ischemic stroke.</p

    C-reactive protein, fibrinogen, TnI and D-dimer sensitivity, specificity and associated criterion for unfavourable 30-day outcome of ischemic stroke.

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    <p>C-reactive protein, fibrinogen, TnI and D-dimer sensitivity, specificity and associated criterion for unfavourable 30-day outcome of ischemic stroke.</p

    Crude associations of the CHA<sub>2</sub>DS<sub>2</sub>-VASc score and combinations of the score plus C-reactive protein, fibrinogen or TnI, or the CHA<sub>2</sub>DS<sub>2</sub>-VASc score plus all three biomarkers with unfavourable 30-day functional outcome of ischemic stroke and pairwise comparisons of the scores.

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    <p>CHA<sub>2</sub>DS<sub>2</sub>-VASc, congestive heart failure or left ventricular ejection fraction ≤40%, hypertension, age ≥75 years, diabetes mellitus, prior stroke or TIA, vascular disease (including myocardial infarction and peripheral artery disease), age >65 years, female gender (1 point each, age ≥75 years and prior stroke/TIA 2 points each); CHA<sub>2</sub>DS<sub>2</sub>-VASc-CRP, 1 additional point if C-reactive protein was >4 mg/L; CHA<sub>2</sub>DS<sub>2</sub>-VASc-F, 1 additional point if fibrinogen was >3.7 g/L; CHA<sub>2</sub>DS<sub>2</sub>-VASc-T, 1 additional point if TnI was >0.09µg/L; CHA<sub>2</sub>DS<sub>2</sub>-VASc-CRPFT, 1 additional point for each of three biomarkers if above the correspondent cut-off level.</p><p>Crude associations of the CHA<sub>2</sub>DS<sub>2</sub>-VASc score and combinations of the score plus C-reactive protein, fibrinogen or TnI, or the CHA<sub>2</sub>DS<sub>2</sub>-VASc score plus all three biomarkers with unfavourable 30-day functional outcome of ischemic stroke and pairwise comparisons of the scores.</p

    Baseline blood biomarkers levels in patients with acute ischemic stroke according to favourable (mRS<3) or unfavourable 30-day functional stroke outcome, including in-hospital death (mRS≥3).

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    <p>Values are presented as n (%) or mean ± standard deviation or median with interquartile range (IQR). C-reactive protein is given in mg/L, fibrinogen in g/L, TnI in μg/L and D-dimer in μg/mL.</p><p>mRS, modified Rankin Scale (patients who died were assigned a mRS of 6); WBC, white blood cell count; CrCl, creatinine clearance; HDL, high density lipoprotein; LDL, low density lipoprotein.</p><p>Baseline blood biomarkers levels in patients with acute ischemic stroke according to favourable (mRS<3) or unfavourable 30-day functional stroke outcome, including in-hospital death (mRS≥3).</p

    The adjusted associations of biomarkers, ‘classic’ scores and ‘composed’ scores with unfavourable 30-day functional outcome of ischemic stroke, with model discriminatory ability and goodness of model fit, and pairwise comparison of each model.

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    <p>OR, Odds Ratio; CI, Confidence Interval; ROC, Receiver Operating Characteristic; IDI – integrated discrimination index.</p><p>Only biomarkers or scores with significant association with unfavourable 30-day functional stroke outcome following adjustment are shown.</p><p>Cardiac TnI and fibrinogen adjusted for other biomarkers (white blood cell count, haemoglobin, haematocrit, C-reactive protein, D-dimer, creatinine clearance, total cholesterol, high-density lipoprotein and low-density lipoprotein), age, gender, body mass index, smoking status, alcohol consumption, NYHA class, atrial fibrillation, history of hypertension, heart failure, diabetes mellitus, chronic kidney disease, prior stroke/TIA, left atrial volume, left ventricular ejection fraction, the presence of mitral annular calcification and symptomatic haemorrhagic transformation of ischemic stroke.</p><p>The CHA<sub>2</sub>DS<sub>2</sub>-VASc score adjusted for CHADS<sub>2</sub> and HAS-BLED score, all biomarkers, gender, body mass index, smoking status, alcohol consumption, NYHA class, atrial fibrillation, chronic kidney disease, left atrial volume, left ventricular ejection fraction, the presence of mitral annular calcification and symptomatic haemorrhagic transformation of ischemic stroke.</p><p>The CHA<sub>2</sub>DS<sub>2</sub>-VASc-T and CHA<sub>2</sub>DS<sub>2</sub>-VASc-CRPFT scores adjusted for all blood biomarkers, gender, body mass index, smoking status, alcohol consumption, NYHA class, atrial fibrillation, chronic kidney disease, left atrial volume, left ventricular ejection fraction, the presence of mitral annulus calcification and symptomatic haemorrhagic transformation of ischemic stroke.</p><p>The adjusted associations of biomarkers, ‘classic’ scores and ‘composed’ scores with unfavourable 30-day functional outcome of ischemic stroke, with model discriminatory ability and goodness of model fit, and pairwise comparison of each model.</p
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