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      B-Type Natriuretic Peptides and Cardiac Troponins for Diagnosis and Risk-Stratification of Syncope

      1 , 2 , 1 , 2 , 3 , 1 , 2 , 1 , 2 , 2 , 4 , 2 , 4 , 5 , 6 , 2 , 7 , 8 , 2 , 9 , 2 , 10 , 2 , 11 , 2 , 12 , 1 , 2 , 1 , 2 , 13 , 1 , 2 , 1 , 2 , 1 , 2 , 1 , 2 , 14 , 1 , 2 , 15 , 1 , 1 , 1 , 1 , 16 , 1 , , , , , , , , , , , , , , , , , , , , , , , , , , , For the BASEL IX Investigators
      Circulation
      Ovid Technologies (Wolters Kluwer Health)

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          Estimating and comparing time-dependent areas under receiver operating characteristic curves for censored event times with competing risks.

          The area under the time-dependent ROC curve (AUC) may be used to quantify the ability of a marker to predict the onset of a clinical outcome in the future. For survival analysis with competing risks, two alternative definitions of the specificity may be proposed depending of the way to deal with subjects who undergo the competing events. In this work, we propose nonparametric inverse probability of censoring weighting estimators of the AUC corresponding to these two definitions, and we study their asymptotic properties. We derive confidence intervals and test statistics for the equality of the AUCs obtained with two markers measured on the same subjects. A simulation study is performed to investigate the finite sample behaviour of the test and the confidence intervals. The method is applied to the French cohort PAQUID to compare the abilities of two psychometric tests to predict dementia onset in the elderly accounting for death without dementia competing risk. The 'timeROC' R package is provided to make the methodology easily usable. Copyright © 2013 John Wiley & Sons, Ltd.
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            Incidence and prognosis of syncope.

            Little is known about the epidemiology and prognosis of syncope in the general population. We evaluated the incidence, specific causes, and prognosis of syncope among women and men participating in the Framingham Heart Study from 1971 to 1998. Of 7814 study participants followed for an average of 17 years, 822 reported syncope. The incidence of a first report of syncope was 6.2 per 1000 person-years. The most frequently identified causes were vasovagal (21.2 percent), cardiac (9.5 percent), and orthostatic (9.4 percent); for 36.6 percent the cause was unknown. The multivariable-adjusted hazard ratios among participants with syncope from any cause, as compared with those who did not have syncope, were 1.31 (95 percent confidence interval, 1.14 to 1.51) for death from any cause, 1.27 (95 percent confidence interval, 0.99 to 1.64) for myocardial infarction or death from coronary heart disease, and 1.06 (95 percent confidence interval, 0.77 to 1.45) for fatal or nonfatal stroke. The corresponding hazard ratios among participants with cardiac syncope were 2.01 (95 percent confidence interval, 1.48 to 2.73), 2.66 (95 percent confidence interval, 1.69 to 4.19), and 2.01 (95 percent confidence interval, 1.06 to 3.80). Participants with syncope of unknown cause and those with neurologic syncope had increased risks of death from any cause, with multivariable-adjusted hazard ratios of 1.32 (95 percent confidence interval, 1.09 to 1.60) and 1.54 (95 percent confidence interval, 1.12 to 2.12), respectively. There was no increased risk of cardiovascular morbidity or mortality associated with vasovagal (including orthostatic and medication-related) syncope. Persons with cardiac syncope are at increased risk for death from any cause and cardiovascular events, and persons with syncope of unknown cause are at increased risk for death from any cause. Vasovagal syncope appears to have a benign prognosis. Copyright 2002 Massachusetts Medical Society
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              State of the art: using natriuretic peptide levels in clinical practice.

              Natriuretic peptide (NP) levels (B-type natriuretic peptide (BNP) and N-terminal proBNP) are now widely used in clinical practice and cardiovascular research throughout the world and have been incorporated into most national and international cardiovascular guidelines for heart failure. The role of NP levels in state-of-the-art clinical practice is evolving rapidly. This paper reviews and highlights ten key messages to clinicians: 1) NP levels are quantitative plasma biomarkers of heart failure (HF). 2) NP levels are accurate in the diagnosis of HF. 3) NP levels may help risk stratify emergency department (ED) patients with regard to the need for hospital admission or direct ED discharge. 4) NP levels help improve patient management and reduce total treatment costs in patients with acute dyspnoea. 5) NP levels at the time of admission are powerful predictors of outcome in predicting death and re-hospitalisation in HF patients. 6) NP levels at discharge aid in risk stratification of the HF patient. 7) NP-guided therapy may improve morbidity and/or mortality in chronic HF. 8) The combination of NP levels together with symptoms, signs and weight gain assists in the assessment of clinical decompensation in HF. 9) NP levels can accelerate accurate diagnosis of heart failure presenting in primary care. 10) NP levels may be helpful to screen for asymptomatic left ventricular dysfunction in high-risk patients.
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                Author and article information

                Journal
                Circulation
                Circulation
                Ovid Technologies (Wolters Kluwer Health)
                0009-7322
                1524-4539
                May 21 2019
                May 21 2019
                : 139
                : 21
                : 2403-2418
                Affiliations
                [1 ]Cardiovascular Research Institute Basel (CRIB) and Department of Cardiology, University Hospital Basel, University of Basel, Switzerland (J.d.F.d.L., P.B., T.N., T.Z., J.W., R.T., C.P., D.W., J.B., L.K., I.S., J.L., E.M., M.K., T.R.).
                [2 ]GREAT Network, Roma, Italy (J.d.F.d.L., P.B., T.N., T.Z., O.M., E.S., L.C., M.F., F.J.M.-S., S.D.S., W.F.P., B.M., J.W., R.T., C.P., D.W., J.B., L.K., I.S.).
                [3 ]Division of Cardiology, University of Illinois at Chicago, IL (P.B.).
                [4 ]Hospital Clinic, Barcelona, Catalonia, Spain (O.M., E.S.).
                [5 ]Department of Emergency Medicine, Kantonsspital Luzern, Switzerland (M.C.).
                [6 ]Department of Emergency Medicine, Hospital of Liestal, Switzerland (N.G.).
                [7 ]Royal Brisbane & Women’s Hospital, Herston, Australia (L.C.).
                [8 ]Christchurch Hospital, Christchurch, New Zealand (M.T.).
                [9 ]Servicio de Urgencias, Hospital Clínico San Carlos, Madrid, Spain (F.J.M.S.).
                [10 ]Emergency Medicine, Department of Medical-Surgery Sciences and Translational Medicine, University Sapienza Rome, Sant’Andrea Hospital, Italy (S.D.S.).
                [11 ]Baylor College of Medicine, Department of Emergency Medicine, Houston, TX (W.F.P.).
                [12 ]2nd Department of Cardiology, School of Medicine with the Division of Dentistry in Zabrze, Medical University of Silesia, Katowice, Poland (B.M.).
                [13 ]Department of General and Interventional Cardiology, University Heart Center Hamburg, University Hospital Hamburg-Eppendorf, Hamburg, Germany (R.T.).
                [14 ]Department of Heart Surgery, University Hospital Basel, Switzerland (L.K.).
                [15 ]Emergency Department, University Hospital Zurich, Switzerland (D.I.K.).
                [16 ]Department of Cardiology, Inselspital, Bern, University Hospital, University of Bern, Switzerland (T.R.).
                Article
                10.1161/CIRCULATIONAHA.118.038358
                20395153-2243-4c38-af3d-5f87e652a373
                © 2019
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