Browsing by Author "Potpara, Tatjana S. (57216792589)"
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Publication A 12-year follow-up study of patients with newly diagnosed lone atrial fibrillation. Implications of arrhythmia progression on prognosis: The Belgrade atrial fibrillation study(2012) ;Potpara, Tatjana S. (57216792589) ;Stankovic, Goran R. (59150945500) ;Beleslin, Branko D. (6701355424) ;Polovina, Marija M. (35273422300) ;Marinkovic, Jelena M. (7004611210) ;Ostojic, Miodrag C. (34572650500)Lip, Gregory Y. H. (57216675273)Background: Lone atrial fibrillation (AF) has been suggested to have a favorable long-term prognosis. Significant interest has been directed at factors predicting arrhythmia progression, and the HATCH score (hypertension, age ≥ 75 years, transient ischemic attack or stroke [2 points], COPD, and heart failure [2 points]) recently has been proposed as a predictive score for AF progression. We investigated long-term outcomes in a large cohort of newly diagnosed lone AF and whether progression from paroxysmal to permanent AF confers an adverse impact on outcomes, including stroke and thromboembolism. Methods: The study was an observational cohort of 346 patients with newly diagnosed lone AF with a mean follow-up of 12.1 ± 7.3 years. Results: Baseline paroxysmal AF was confirmed in 242 patients, and of these, 65 (26.9%) subsequently experienced progression to permanent AF. Older age and development of congestive heart failure during follow-up were the multivariate predictors of AF progression (both P<.01), which was documented in 19.8% of patients with a HATCH score of 0 vs 63.2% with a score of 2 ( P<.001), although the predictive validity of the HATCH score per se was modest (C statistic, 0.6). The annual rate of thromboembolism and heart failure during follow-up were low (0.4% each), and five patients (1.4%) died. AF progression, development of cardiac diseases, and older age were multivariate predictors of adverse outcomes, including thromboembolism (all P<.05). Baseline CHADS2 (congestive heart failure, hypertension, age ≥75, diabetes mellitus, prior stroke or transient ischemic attack) score was not predictive for thromboembolism (C statistic, 0.50; 95% CI, 0.31-0.69). Conclusions: This 12-year follow-up study provides confirmatory evidence of a generally favorable prognosis of lone AF, but adverse outcomes (including stroke and thromboembolism) are significantly infl uenced by age and the (new) development of underlying heart disease. Arrhythmia progression in lone AF is a marker of increased risk for adverse cardiovascular events. © 2012 American College of Chest Physicians. - Some of the metrics are blocked by yourconsent settings
Publication A comparison of clinical characteristics and long-term prognosis in asymptomatic and symptomatic patients with first-diagnosed atrial fibrillation: The Belgrade Atrial Fibrillation Study(2013) ;Potpara, Tatjana S. (57216792589) ;Polovina, Marija M. (35273422300) ;Marinkovic, Jelena M. (7004611210)Lip, Gregory Y.H. (57216675273)Background To investigate baseline characteristics and long-term prognosis of carefully characterized asymptomatic and symptomatic patients with atrial fibrillation (AF) in a 'real-world' cohort of first-diagnosed non-valvular AF over a 10-year follow-up period. Methods and results We conducted an observational, non-interventional, and single-centre registry-based study of consecutive first-diagnosed AF patients. Of 1100 patients (mean age 52.7 ± 12.2 years and mean follow-up 9.9 ± 6.1 years), 146 (13.3%) had asymptomatic AF. Persistent or permanent AF, slower ventricular rate during AF (< 100/min), CHA2DS2-VASc score of 0, history of diabetes mellitus and male gender were independent baseline risk factors for asymptomatic AF presentation (all p < 0.01) with a good predictive ability of the multivariable model (c-statistic 0.86, p < 0.001). Kaplan-Meier 10-year estimates of survival free of progression of AF (log-rank test = 33.4, p < 0.001) and ischemic stroke (log-rank test = 6.2, p = 0.013) were significantly worse for patients with asymptomatic AF compared to those with symptomatic arrhythmia. In the multivariable Cox regression analysis, intermittent asymptomatic AF was significantly associated with progression to permanent AF (Hazard Ratio 1.6; 95% CI, 1.1-2.2; p = 0.009). Conclusions In a 'real-world' setting, patients with asymptomatic presentation of their first-diagnosed AF could have different risk profile and long-term outcomes compared to those with symptomatic AF. Whether more intensive monitoring and comprehensive AF management including AF ablation at early stage following the incident episode of AF and increased quality of oral anticoagulation could alter the long-term prognosis of these patients requires further investigation. © 2013 Elsevier Ireland Ltd. - Some of the metrics are blocked by yourconsent settings
Publication A square root pattern of changes in heart rate variability during the first year after circumferential pulmonary vein isolation for paroxysmal atrial fibrillation and their relation with long‑term arrhythmia recurrence(2020) ;Marinković, Milan (56160715300) ;Mujović, Nebojša (16234090000) ;Vučićević, Vera (55550927000) ;Steffel, Jan (8882159100)Potpara, Tatjana S. (57216792589)BACKGROUND An incidental lesion of the parasympathetic ganglia during circumferential pulmonary vein isolation (CPVI) may affect heart rate variability (HRV). AIMS We studied the pattern of changes in HRV parameters and the relationship between the 1‑year HRV change following CPVI and the recurrence of atrial fibrillation (AF). METHODS A total of 100 consecutive patients undergoing CPVI for paroxysmal AF were enrolled (mean [SD] age, 56 [11.2] years; 61 men). We measured HRV on the day before and after CPVI, and then at 1 month as well as 3, 6, and 12 months after CPVI using 24‑hour Holter monitoring. RESULTS During the median follow‑up of 33 months, 38 patients experienced the late recurrence of AF (LRAF). Compared with the pre‑CPVI values, HRV was significantly attenuated on day 1 after CPVI in all patients. However, at 3 to 6 months after CPVI, all HRV parameters remained significantly decreased in LRAF‑free patients but not in those with LRAF. The multivariate Cox analysis showed that early AF recurrence within the blanking period (hazard ratio [HR], 4.87; 95% CI, 2.44–9.69; P <0.001) and a change in the standard deviation of normal‑to‑normal intervals (SDNN) observed 3 months after ablation (HR, 0.99; 95% CI, 0.98–1; P= 0.01) were associated with LRAF. The cumulative LRAF freedom after CPVI was greater in patients with an SDNN reduction of more than 25 ms reported 3 months after ablation than in those with a reduction of 25 ms or lower (log‑rank P = 0.004). CONCLUSIONS Sustained parasympathetic denervation during 12 months after CPVI was a marker of successful CPVI, whereas a 3‑month post‑CPVI SDNN reduction of 25 ms or lower predicted LRAF. Copyright by the Author(s), 2020. - Some of the metrics are blocked by yourconsent settings
Publication Adherence to the “Atrial fibrillation Better Care” (ABC) pathway in patients with atrial fibrillation and cancer: A report from the ESC-EHRA EURObservational Research Programme in atrial fibrillation (EORP-AF) General Long-Term Registry(2022) ;Vitolo, Marco (57204323320) ;Proietti, Marco (57202956034) ;Malavasi, Vincenzo L. (6508266512) ;Bonini, Niccolo’ (57203751290) ;Romiti, Giulio Francesco (56678539100) ;Imberti, Jacopo F. (57212103023) ;Fauchier, Laurent (7005282545) ;Marin, Francisco (57212539524) ;Nabauer, Michael (7004310943) ;Potpara, Tatjana S. (57216792589) ;Dan, Gheorghe-Andrei (57222706010) ;Kalarus, Zbigniew (56266442700) ;Maggioni, Aldo Pietro (57203255222) ;Lane, Deirdre A. (57203229915) ;Lip, Gregory Y H (57216675273) ;Boriani, Giuseppe (57675336900) ;Tavazzi, L. (58091986000) ;Marin, F. (59820237400) ;Goda, A. (23049970100) ;Mairesse, G. (7003921830) ;Shalganov, T. (58558219800) ;Antoniades, L. (6602084348) ;Taborsky, M. (7004445570) ;Riahi, S. (57739037000) ;Muda, P. (6603274130) ;Bolao, I. García (59037308600) ;Piot, O. (7006174412) ;Etsadashvili, K. (26026305500) ;Simantirakis, E.N. (6603927258) ;Haim, M. (7004459681) ;Azhari, A. (56185098900) ;Najafian, J. (14060714800) ;Santini, M. (7103044873) ;Mirrakhimov, E. (57216202888) ;Kulzida, K. (57311698200) ;Erglis, A. (6602259794) ;Poposka, L. (23498648800) ;Burg, M.R. (57205667025) ;Crijns, H. (58302709000) ;Erküner, Ö. (57191578368) ;Atar, D. (7005111567) ;Lenarczyk, R. (6603516741) ;Oliveira, M. Martins (35509269800) ;Shah, D. (7402371395) ;Serdechnaya, E. (57188719922) ;Diker, E. (59811913000)Lane, D. (7403211608)Background: Implementation of the Atrial fibrillation Better Care (ABC) pathway is recommended by guidelines on atrial fibrillation (AF), but the impact of adherence to ABC pathway in patients with cancer is unknown. Objectives: To investigate the adherence to ABC pathway and its impact on adverse outcomes in AF patients with cancer. Methods: Patients enrolled in the EORP-AF General Long-Term Registry were analyzed according to (i) No Cancer; and (ii) Prior or active cancer and stratified in relation to adherence to the ABC pathway. The composite Net Clinical Outcome (NCO) of all-cause death, major adverse cardiovascular events and major bleeding was the primary endpoint. Results: Among 6550 patients (median age 69 years, females 40.1%), 6005 (91.7%) had no cancer, while 545 (8.3%) had a diagnosis of active or prior cancer at baseline, with the proportions of full adherence to ABC pathway of 30.6% and 25.7%, respectively. Adherence to the ABC pathway was associated with a significantly lower occurrence of the primary outcome vs. non-adherence, both in ‘no cancer’ and ‘cancer’ patients [adjusted Hazard Ratio (aHR) 0.78, 95% confidence interval (CI): 0.66–0.92 and aHR 0.59, 95% CI 0.37–0.96, respectively]. Adherence to a higher number of ABC criteria was associated with a lower risk of the primary outcome, being lowest when 3 ABC criteria were fulfilled (no cancer: aHR 0.54, 95%CI: 0.36–0.81; with cancer: aHR 0.32, 95% CI 0.13–0.78). Conclusion: In AF patients with cancer enrolled in the EORP-AF General Long-Term Registry, adherence to ABC pathway was sub-optimal. Full adherence to ABC-pathway was associated with a lower risk of adverse events © 2022 - Some of the metrics are blocked by yourconsent settings
Publication Adherence to the 4S-AF Scheme in the Balkan region: Insights from the BALKAN-AF survey(2022) ;Kozieł-Siołkowska, Monika (56723727500) ;Mihajlovic, Miroslav (57207498211) ;Nedeljkovic, Milan (7004488186) ;Pavlovic, Nikola (23486720000) ;Paparisto, Vilma (57115549700) ;Music, Ljilja (25936440400) ;Trendafilova, Elina (55396473400) ;Dan, Anca Rodica (55986915200) ;Kusljugic, Zumreta (6508231417) ;Dan, Gheorghe-Andrei (57222706010) ;Lip, Gregory Y.H. (57216675273)Potpara, Tatjana S. (57216792589)Background: The 4S-AF scheme includes stroke risk, symptoms, severity of burden, and substrate severity domain. Aim: We aimed to assess the adherence to the 4S-AF scheme in patients classified according to stroke risk in post hoc analysis of the BALKAN-AF dataset. Methods: A 14-week prospective enrolment of consecutive patients with electrocardiographically documented atrial fibrillation (AF) was performed in seven Balkan countries from 2014 to 2015. Results: Low stroke risk (CHA2DS2-VASc score, 0 in males or 1 in females) was present in 162 (6.0%) patients. 2 099 (77.4%) patients had CHA2DS2-VASc score ≥3 in females or ≥2 in males (high stroke risk), and 613 (22.6%) had CHA2DS2-VASc score <3 in females or <2 in males. Seventy-five (46.3%) patients with low stroke risk and 1555 (74.1%) patients with high stroke risk were prescribed oral anticoagulants (OAC). Two thousand six hundred and seventy-seven (98.6%) had data on European Heart Rhythm Association (EHRA) class. Among 2099 patients with high stroke risk, 703 (33.4%) had EHRA class ≥3. Two hundred and seven (29.4%) patients with EHRA class ≥3 and high stroke risk were offered rhythm control; 620 (55.2%) of individuals with first-diagnosed or paroxysmal AF with high stroke risk were offered rhythm control. Two or more comorbidities occurred in 1927 (91.8%) patients with high stroke risk. Conclusions: OAC overuse was observed in patients with low stroke risk, whilst OAC underuse was evident in those with high risk of stroke. The percentage of highly symptomatic patients with high risk of stroke who were offered a rhythm control strategy was low. © the Author(s), 2022. - Some of the metrics are blocked by yourconsent settings
Publication Adherence to the ABC (Atrial fibrillation Better Care) pathway in the Balkan region: The BALKAN-AF survey(2020) ;Kozieł, Monika (56723727500) ;Simovic, Stefan (57219778293) ;Pavlovic, Nikola (23486720000) ;Kocijancic, Aleksandar (36016706900) ;Paparisto, Vilma (57115549700) ;Music, Ljilja (25936440400) ;Trendafilova, Elina (55396473400) ;Dan, Anca R. (55986915200) ;Kusljugic, Zumreta (6508231417) ;Dan, Gheorghe Andrei (6701679438) ;Lip, Gregory Y.H. (57216675273)Potpara, Tatjana S. (57216792589)INTRODUCTION The Atrial fibrillation Better Care (ABC) pathway provides a useful way of simplifying decision-making considerations in a holistic approach to atrial fibrillation management. OBJECTIVES To evaluate adherence to the ABC pathway and to determine major gaps in adherence in patients in the BALKAN-AF survey. PATIENTS AND METHODS In this ancillary analysis, patients from the BALKAN-AF survey were divided into the following groups: A (avoid stroke) + B (better symptom control) + C (cardiovascular and co- morbidity risk management)-adherent and -nonadherent management. RESULTS Among 2712 enrolled patients, 1013 (43.8%) patients with mean (SD) age of 68.8 (10.2) years and mean CHA2DS2-VASc score of 3.4 (1.8) had A+B+C-adherent management and 1299 (56.2%) had A+B+C-nonadherent management. Independent predictors of increased A+B+C-adherent manage- ment were: capital city (odds ratio [OR], 1.23; 95% CI, 1.03-1.46; P = 0.02), treatment by cardiologist (OR, 1.34; 95% CI, 1.08-1.66; P = 0.01), hypertension (OR, 2.2; 95% CI, 1.74-2.77; P <0.001), dia- betes mellitus (OR, 1.28; 95% CI, 1.05-1.57; P = 0.01), and multimorbidity (the presence of 2 or more long-term conditions) (OR, 1.85; 95% CI, 1.43-2.38; P <0.001). Independent predictors of decreased A+B+C-adherent management were: age 80 years or older (OR, 0.61; 95% CI, 0.48-0.76; P <0.001) and history of bleeding (OR, 0.5; 95% CI, 0.33-0.75; P = 0.001). CONCLUSIONS Physicians' adherence to integrated AF management based on the ABC pathway was suboptimal. Addressing the identified clinical and system-related factors associated with A+B+C-nonadherent manage- ment using targeted approaches is needed to optimize treatment of patients with AF in the Balkan region. © by Medycyna Praktyczna, Kraków 2020 - Some of the metrics are blocked by yourconsent settings
Publication Antithrombotic therapy in patients with atrial fibrillation and acute coronary syndrome and / or undergoing percutaneous coronary intervention(2020) ;Mihajlovi, Miroslav (57218694239) ;Marinkovi, Milan (56575143300) ;Kozie, Monika (57219611719) ;aMujovi, Neboj (57219606791) ;Lip, Gregory Y.H. (57216675273)Potpara, Tatjana S. (57216792589)The use of triple antithrombotic therapy (TAT) consisting of an oral anticoagulant (OAC), aspirin, and a P2Y12 inhibitor in patients with atrial fibrillation (AF) and acute coronary syndrome (ACS) and / or undergoing percutaneous coronary intervention (PCI) is associated with a high risk of bleeding. Recently, several randomized clinical trials tested the hypothesis as to whether dual antithrombotic therapy (DAT) regimens (consisting of an OAC and a single antiplatelet drug) may be safer in terms of bleeding events as compared with TAT. They also investigated the role of non–vitamin K antagonist oral anticoagulants (NOACs) as a part of DAT and TAT. The purpose of this review is to provide an overview of available evidence regarding the safety and efficacy of DAT compared with TAT regimens, international guidelines recommendations, knowledge gaps, and unmet needs in the management of patients with AF and ACS and / or undergoing PCI. © 2020 Medycyna Praktyczna Cholerzyn. All rights reserved. - Some of the metrics are blocked by yourconsent settings
Publication Antithrombotic Therapy in Patients with Atrial Fibrillation and Acute Coronary Syndrome Treated Medically or with Percutaneous Coronary Intervention or Undergoing Elective Percutaneous Coronary Intervention: Insights from the AUGUSTUS Trial(2019) ;Windecker, Stephan (7003473419) ;Lopes, Renato D. (57203183974) ;Massaro, Tyler (57220358144) ;Jones-Burton, Charlotte (9337741100) ;Granger, Christopher B. (7202019383) ;Aronson, Ronald (59425124700) ;Heizer, Gretchen (42561352300) ;Goodman, Shaun G. (7402115222) ;Darius, Harald (35416880900) ;Jones, W. Schuyler (57212876373) ;Aschermann, Michael (7005976448) ;Brieger, David (7004107910) ;Cura, Fernando (6603543967) ;Engstrøm, Thomas (7004069840) ;Fridrich, Viliam (6602656890) ;Halvorsen, Sigrun (9039942100) ;Huber, Kurt (35376715600) ;Kang, Hyun-Jae (27171630200) ;Leiva-Pons, Jose L. (13604803900) ;Lewis, Basil S. (7401867678) ;Malaga, German (56481406300) ;Meneveau, Nicolas (55820664600) ;Merkely, Bela (7004434435) ;Milicic, Davor (56503365500) ;Morais, Joaõ (57210400438) ;Potpara, Tatjana S. (57216792589) ;Raev, Dimitar (57192352050) ;Sabaté, Manel (57193753144) ;De Waha-Thiele, Suzanne (36189558700) ;Welsh, Robert C. (35239007400) ;Xavier, Denis (55403963100) ;Mehran, Roxana (7004992409)Alexander, John H. (57218960656)Background: The safety and efficacy of antithrombotic regimens may differ between patients with atrial fibrillation who have acute coronary syndromes (ACS), treated medically or with percutaneous coronary intervention (PCI), and those undergoing elective PCI. Methods: Using a 2×2 factorial design, we compared apixaban with vitamin K antagonists and aspirin with placebo in patients with atrial fibrillation who had ACS or were undergoing PCI and were receiving a P2Y12 inhibitor. We explored bleeding, death and hospitalization, as well as death and ischemic events, by antithrombotic strategy in 3 prespecified subgroups: Patients with ACS treated medically, patients with ACS treated with PCI, and those undergoing elective PCI. Results: Of 4614 patients enrolled, 1097 (23.9%) had ACS treated medically, 1714 (37.3%) had ACS treated with PCI, and 1784 (38.8%) had elective PCI. Apixaban compared with vitamin K antagonist reduced International Society on Thrombosis and Haemostasis major or clinically relevant nonmajor bleeding in patients with ACS treated medically (hazard ratio [HR], 0.44 [95% CI, 0.28-0.68]), patients with ACS treated with PCI (HR, 0.68 [95% CI, 0.52-0.89]), and patients undergoing elective PCI (HR, 0.82 [95% CI, 0.64-1.04]; Pinteraction=0.052) and reduced death or hospitalization in the ACS treated medically (HR, 0.71 [95% CI, 0.54-0.92]), ACS treated with PCI (HR, 0.88 [95% CI, 0.74-1.06]), and elective PCI (HR, 0.87 [95% CI, 0.72-1.04]; Pinteraction=0.345) groups. Compared with vitamin K antagonists, apixaban resulted in a similar effect on death and ischemic events in the ACS treated medically, ACS treated with PCI, and elective PCI groups (Pinteraction=0.356). Aspirin had a higher rate of bleeding than did placebo in patients with ACS treated medically (HR, 1.49 [95% CI, 0.98-2.26]), those with ACS treated with PCI (HR, 2.02 [95% CI, 1.53-2.67]), and those undergoing elective PCI (HR, 1.91 [95% CI, 1.48-2.47]; Pinteraction=0.479). For the same comparison, there was no difference in outcomes among the 3 groups for the composite of death or hospitalization (Pinteraction=0.787) and death and ischemic events (Pinteraction=0.710). Conclusions: An antithrombotic regimen consisting of apixaban and a P2Y12 inhibitor without aspirin provides superior safety and similar efficacy in patients with atrial fibrillation who have ACS, whether managed medically or with PCI, and those undergoing elective PCI compared with regimens that include vitamin K antagonists, aspirin, or both. © 2019 American Heart Association, Inc. - Some of the metrics are blocked by yourconsent settings
Publication Approach to cardio-oncologic patients with special focus on patients with cardiac implantable electronic devices planned for radiotherapy: Results of the European Heart Rhythm Association survey(2017) ;Lenarczyk, Radosław (6603516741) ;Potpara, Tatjana S. (57216792589) ;Haugaa, Kristina H. (24733615600) ;Deharo, Jean-Claude (7004231392) ;Hernandez-Madrid, Antonio (57208118344) ;Del Carmen Exposito Pineda, Maria (57195964856) ;Kiliszek, Marek (24332191600)Dagres, Nikolaos (7003639393)The aim of this European Heart Rhythm Association (EHRA) survey was to evaluate clinical practice regarding cardio-oncologic patients, with special focus on patients with cardiac implantable electronic devices (CIEDs) planned for anticancer radiotherapy (RT), among members of the EHRA electrophysiology research network. Of the 36 responding centres, 89% managed patients who were diagnosed or treated oncologically, and this diagnosis affected 1-5% of cardiovascular patients in majority of centres (57%). The main side effects of anticancer therapy in patients treated by cardiologists were thromboembolic complications and left ventricular dysfunction (both reported as 'frequent' by 43% of the centres). The main agents associated with complications were anthracyclines, RT, and monoclonal antibodies. Echocardiography was the most common method of screening for cardiovascular complications (93%), and 10% of the centres did not routinely screen for treatment-induced cardiotoxicity. Opinions on the safe radiation dose, methods of device shielding, and risk calculation prior to RT in CIED patients differed among centres. Precaution measures in high-risk CIED patients were very heterogeneous among centres. Our survey has shown that the awareness of cardiac consequences of anticancer therapy is high, despite relatively low proportion of patients treated oncologically among all cardiovascular patients. There is a consensus of which screening methods should be used for cardiotoxicity of anticancer treatment, but the apprehension of screening necessity is low. Methods of risk assessment and safety measures in CIED patients undergoing RT are very heterogeneous among the European centres, underscoring the need for standardization of the approach to cardio-oncologic patients. © 2017 The Author. - Some of the metrics are blocked by yourconsent settings
Publication Assessment of patient-reported treatment burden in patients with coronary artery disease(2024) ;Nedeljkovic, Milan (7004488186) ;Mihajlovic, Miroslav (57207498211) ;Mujovic, Nebojsa (16234090000) ;Lip, Gregory Y.H. (57216675273)Potpara, Tatjana S. (57216792589)Introduction: Patient-reported treatment burden (TBN) refers to the patient’s time and effort invested in the management of their chronic health conditions. The aim of this research was to explore TBN in patients with coronary artery disease (CAD). Methods: Consecutive patients with chronic medical condition(s) were invited to complete the study questionnaires (TBN and EQ-5D). Results: Of 514 enrolled patients, 116 (22.6%) patients had CAD. The mean TBN score for CAD vs. non-CAD was 40.49 ±21.54 and 46.17 ±21.44 (p = 0.023), respectively. Conclusions: Patients with CAD could have a lower TBN in comparison to patients with other chronic medical conditions. © 2024 Termedia & Banach. - Some of the metrics are blocked by yourconsent settings
Publication Atrial Fibrillation(2022) ;Kozieł Siołkowska, Monika (56723727500) ;Potpara, Tatjana S. (57216792589)Lip, Gregory Y. (57802425600)Atrial fibrillation (AF) is the most prevalent sustained cardiac arrhythmia, affecting approximately 3% of adults worldwide. Its prevalence and incidence is rising continuously with the increasingly aging population. AF is associated with impaired prognosis, increased risk of all-cause mortality, stroke, heart failure, and hospital admissions, in addition to poor quality of life. Importantly, AF should not be considered in isolation regarding the process of prevention, detection, and management. Rather, a more holistic approach and integrated care is needed to take into account underlying comorbidities and cross-disease sequelae of AF. In this chapter, we present a brief overview of the overall aspects of AF, with particular focus on the issues relating to stroke and systemic embolism (SSE). © 2023 by Elsevier Inc. All rights reserved. - Some of the metrics are blocked by yourconsent settings
Publication ATRIAL FIBRILLATION: IMPORTANCE OF REAL WORLD DATA FROM REGIONAL REGISTRIES. A FOCUS ON THE BALKAN-AF REGISTRY(2020) ;Kozieł, Monika (56723727500) ;Lip, Gregory Y. H. (57216675273)Potpara, Tatjana S. (57216792589)[No abstract available] - Some of the metrics are blocked by yourconsent settings
Publication Atrial fibrillation: stroke prevention(2024) ;Chao, Tze-Fan (35335897300) ;Potpara, Tatjana S. (57216792589)Lip, Gregory Y.H. (57216675273)Stroke prevention is central to the management of patients with atrial fibrillation (AF) which has moved towards a more holistic or integrative care approach. The published evidence suggests that management of AF patients following such a holistic approach based on the Atrial fibrillation Better Care (ABC) pathway is associated with a lower risk of stroke and adverse events. Risk assessment, re-assessment and use of direct oral anticoagulants (DOACs) are important for stroke prevention in AF. The stroke and bleeding risks of AF patients are not static and should be re-assessed regularly. Bleeding risk assessment is to address and mitigate modifiable bleeding risk factors, and to identify high bleeding risk patients for early review and follow-up. Well-controlled comorbidities and healthy lifestyles also play an important role to achieve a better clinical outcome. Digital health solutions are increasingly relevant in the diagnosis and management of patients with AF, with the potential to improve stroke prevention. In this review, we provide an update on stroke prevention in AF, including importance of holistic management, risk assessment/re-assessment, and stroke prevention for special AF populations. Evidence-based and structured management of AF patients would reduce the risk of stroke and other adverse events. © 2023 The Author(s) - Some of the metrics are blocked by yourconsent settings
Publication Authors' reply(2020) ;Mujovic, Nebojsa (16234090000) ;Marinkovi, Milan (56575143300) ;Mihajlovi, Miroslav (57218694239) ;Mujovic, Nata (22941523800)Potpara, Tatjana S. (57216792589)[No abstract available] - Some of the metrics are blocked by yourconsent settings
Publication Brugada syndrome: A general cardiologist's perspective(2017) ;Polovina, Marija M. (35273422300) ;Vukicevic, Milica (57194569272) ;Banko, Bojan (35809871900) ;Lip, Gregory Y.H. (57216675273)Potpara, Tatjana S. (57216792589)Brugada syndrome (BrS) is one of the commonest inherited primary arrhythmia syndromes typically presenting with arrhythmic syncope or sudden cardiac death (SCD) due to polymorphic ventricular tachycardia and ventricular fibrillation precipitated by vagotonia or fever in apparently healthy adults, less frequently in children. The prevalence of the syndrome (0.01%–0.3%) varies among regions and ethnicities, being the highest in Southeast Asia. BrS is diagnosed by the “coved type” ST-segment elevation ≥ 2 mm followed by a negative T-wave in ≥ 1 of the right precordial leads V 1 –V 2 . The typical electrocardiogram in BrS is often concealed by fluctuations between normal, non-diagnostic and diagnostic ST-segment pattern in the same patient, thus hindering the diagnosis. Presently, the majority of BrS patients is incidentally diagnosed, and may remain asymptomatic for their lifetime. However, BrS is responsible for 4–12% of all SCDs and for ~ 20% of SCDs in patients with structurally normal hearts. Arrhythmic risk is the highest in SCD survivors and in patients with spontaneous BrS electrocardiogram and arrhythmic syncope, but risk stratification for SCD in asymptomatic subjects has not yet been fully defined. Recent achievements have expanded our understanding of the genetics and electrophysiological mechanisms underlying BrS, while radiofrequency catheter ablation may be an effective new approach to treat ventricular tachyarrhythmias in BrS patients with arrhythmic storms. The present review summarizes our contemporary understanding and recent advances in the inheritance, pathophysiology, clinical assessment and treatment of BrS patients. © 2017 - Some of the metrics are blocked by yourconsent settings
Publication Cardiac troponins and adverse outcomes in European patients with atrial fibrillation: A report from the ESC-EHRA EORP atrial fibrillation general long-term registry(2022) ;Vitolo, Marco (57204323320) ;Malavasi, Vincenzo L. (6508266512) ;Proietti, Marco (57202956034) ;Diemberger, Igor (8070601200) ;Fauchier, Laurent (7005282545) ;Marin, Francisco (57212539524) ;Nabauer, Michael (7004310943) ;Potpara, Tatjana S. (57216792589) ;Dan, Gheorghe-Andrei (57222706010) ;Kalarus, Zbigniew (56266442700) ;Tavazzi, Luigi (7102746954) ;Maggioni, Aldo Pietro (57203255222) ;Lane, Deirdre A. (57203229915) ;Lip, Gregory Y.H. (57216675273) ;Boriani, Giuseppe (57675336900) ;Tavazzi, L. (58091986000) ;Marin, F. (57211248449) ;Goda, A. (23049970100) ;Mairesse, G. (7003921830) ;Shalganov, T. (58558219800) ;Antoniades, L. (6602084348) ;Taborsky, M. (7004445570) ;Riahi, S. (57739037000) ;Muda, P. (6506246174) ;García Bolao, I. (6603274130) ;Piot, O. (7006174412) ;Etsadashvili, K. 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(57200407716) ;Borowiec, A. (57507508000) ;Majos, E. (40261795700) ;Dabrowski, R. (7102754191) ;Szwed, H. (7007183538) ;Musialik-Lydka, A. (6603331952) ;Leopold-Jadczyk, A. (57189096335) ;Jedrzejczyk-Patej, E. (55482785200) ;Koziel, M. (56723727500) ;Mazurek, M. (26641934600) ;Krzemien-Wolska, K. (55753414900) ;Starosta, P. (57312809300) ;Nowalany-Kozielska, E. (6603172943) ;Orzechowska, A. (57312372000) ;Szpot, M. (57311704300) ;Staszel, M. (57312809400) ;Almeida, S. (57685569600) ;Pereira, H. (7103250994) ;Brandão Alves, L. (57312809500) ;Miranda, R. (57201151329) ;Ribeiro, L. (57685506900) ;Costa, F. (57220845858) ;Morgado, F. (8116194300) ;Carmo, P. (58441529100) ;Galvao Santos, P. (56659450400) ;Bernardo, R. (57684303400) ;Adragão, P. (7003991651) ;Ferreira da Silva, G. (8846412000) ;Peres, M. (8846411400) ;Alves, M. (57930438600) ;Leal, M. (57200589120) ;Cordeiro, A. (57209226653) ;Magalhães, P. (55874294400) ;Fontes, P. (57312809600) ;Leão, S. (56236068400) ;Delgado, A. (57089792300) ;Costa, A. (56392129000) ;Marmelo, B. (55878029900) ;Rodrigues, B. (59120645400) ;Moreira, D. (59579190100) ;Santos, J. (59276251300) ;Santos, L. (8689428100) ;Terchet, A. (57312372200) ;Darabantiu, D. (8203870500) ;Mercea, S. (57218281354) ;Turcin Halka, V. (57313031300) ;Pop Moldovan, A. (57193484230) ;Gabor, A. (57312593500) ;Doka, B. (57205664757) ;Catanescu, G. (57311704500) ;Rus, H. (57193428053) ;Oboroceanu, L. (57313031400) ;Bobescu, E. (8285538300) ;Popescu, R. (7006780050) ;Dan, A. (55986915200) ;Buzea, A. (55344454500) ;Daha, I. (6508302107) ;Neuhoff, I. (57191268038) ;Baluta, M. (57065729500) ;Ploesteanu, R. (56046728700) ;Dumitrache, N. (57205665174) ;Vintila, M. (6603430988) ;Daraban, A. (54887342600) ;Japie, C. (56595615200) ;Badila, E. (56783170700) ;Tewelde, H. (57312372300) ;Hostiuc, M. (57793115600) ;Frunza, S. (57312372400) ;Tintea, E. (57311925800) ;Bartos, D. (7004077704) ;Ciobanu, A. (57213857415) ;Popescu, I. (57205665546) ;Toma, N. (57312593700) ;Gherghinescu, C. (36918134700) ;Cretu, D. (57193256201) ;Patrascu, N. (59890381300) ;Stoicescu, C. (58326975500) ;Udroiu, C. (57222189673) ;Bicescu, G. (36473047100) ;Vintila, V. (14023742900) ;Vinereanu, D. (6603080279) ;Cinteza, M. (6604034145) ;Rimbas, R. (55096937100) ;Grecu, M. (6701669740) ;Cozma, A. (8251934500) ;Boros, F. (57312593800) ;Ille, M. (57312372500) ;Tica, O. (57211508952) ;Tor, R. (57311925900) ;Corina, A. (57945991100) ;Jeewooth, A. (57313031500) ;Maria, B. (57507008000) ;Georgiana, C. (57312809700) ;Natalia, C. (57220079021) ;Alin, D. (57313258700) ;Dinu-Andrei, D. (57311926000) ;Livia, M. (57229768200) ;Daniela, R. (57611492700) ;Larisa, R. (57739000000) ;Umaar, S. (57312151000) ;Tamara, T. (57591094200) ;Ioachim Popescu, M. (57739623000) ;Nistor, D. (57223384717) ;Sus, I. (55858381900) ;Coborosanu, O. (57313259000) ;Alina-Ramona, N. (57312372600) ;Dan, R. (57313259100) ;Petrescu, L. (56653730000) ;Ionescu, G. (57312151100) ;Vacarescu, C. (58020633800) ;Goanta, E. (57202020271) ;Mangea, M. (57313259200) ;Ionac, A. (24176655100) ;Mornos, C. (14045651100) ;Cozma, D. (55916552100) ;Pescariu, S. (57884285700) ;Solodovnicova, E. (57313031800) ;Soldatova, I. (57312809800) ;Shutova, J. (57312594000) ;Tjuleneva, L. (57311704700) ;Zubova, T. (57216440573) ;Uskov, V. (57311704800) ;Obukhov, D. (57312372700) ;Rusanova, G. (57312809900) ;Isakova, N. (57312594100) ;Odinsova, S. (57312151200) ;Arhipova, T. (57313031900) ;Kazakevich, E. (57739420500) ;Zavyalova, O. (56925554200) ;Novikova, T. (57190751817) ;Riabaia, I. (57312810000) ;Zhigalov, S. (57311698700) ;Drozdova, E. (57311704900) ;Luchkina, I. (57313259300) ;Monogarova, Y. (57313259400) ;Hegya, D. (57221846648) ;Rodionova, L. (57225763494) ;Nevzorova, V. (6603425593) ;Lusanova, O. (57312594300) ;Arandjelovic, A. (8603366600) ;Toncev, D. (57312810100) ;Vukmirovic, L. (57739623200) ;Radisavljevic, M. (57740038000) ;Milanov, M. (57195324235) ;Sekularac, N. (57945912100) ;Zdravkovic, M. (24924016800) ;Hinic, S. (55208518100) ;Dimkovic, S. (25642588400) ;Acimovic, T. (57807942100) ;Saric, J. (57311705000) ;Radovanovic, S. (24492602300) ;Kocijancic, A. (36016706900) ;Obrenovic-Kircanski, B. (18134195100) ;Kalimanovska Ostric, D. (6603414966) ;Simic, D. (57212512386) ;Jovanovic, I. (57223117334) ;Petrovic, I. (57526019000) ;Polovina, M. (35273422300) ;Vukicevic, M. (57194569272) ;Tomasevic, M. (59891899100) ;Mujovic, N. (16234090000) ;Radivojevic, N. (58242426500) ;Petrovic, O. (33467955000) ;Aleksandric, S. (35274271700) ;Kovacevic, V. (57190845395) ;Mijatovic, Z. (57740038200) ;Ivanovic, B. (24169010000) ;Tesic, M. (36197477200) ;Ristic, A. (7003835406) ;Vujisic-Tesic, B. (6508177183) ;Nedeljkovic, M. (7004488186) ;Karadzic, A. (10140305100) ;Uscumlic, A. (56807174000) ;Prodanovic, M. (57739761400) ;Zlatar, M. (57003172000) ;Asanin, M. (8603366900) ;Bisenic, B. (57739899100) ;Vasic, V. (57312594400) ;Popovic, Z. (59634174400) ;Djikic, D. (35798144600) ;Sipic, M. (57794789300) ;Peric, V. (9741677100) ;Dejanovic, B. (57739555900) ;Milosevic, N. (57685779400) ;Backovic, S. (57740038300) ;Stevanovic, A. (57195989683) ;Andric, A. (57078860800) ;Pencic, B. (12773061100) ;Pavlovic-Kleut, M. (55515527600) ;Celic, V. (57132602400) ;Pavlovic, M. (57195322261) ;Petrovic, M. (56595474600) ;Vuleta, M. (57313033500) ;Petrovic, N. (57685696100) ;Simovic, S. (57219778293) ;Savovic, Z. (57189442420) ;Milanov, S. (57198090480) ;Davidovic, G. (14008112400) ;Iric-Cupic, V. (57220206415) ;Djordjevic, D. (57739077800) ;Damjanovic, M. (24801926700) ;Zdravkovic, S. (22236158500) ;Topic, V. (57794228100) ;Stanojevic, D. (55596857900) ;Randjelovic, M. (57191951207) ;Jankovic-Tomasevic, R. (55246100200) ;Atanaskovic, V. (57202073374) ;Antic, S. (59264735100) ;Simonovic, D. (36633326900) ;Stojanovic, M. (57188923072) ;Stojanovic, S. (57313033600) ;Mitic, V. (55874230000) ;Ilic, V. (57313260900) ;Petrovic, D. (57209495976) ;Deljanin Ilic, M. (24922632600) ;Ilic, S. (58806191700) ;Stoickov, V. (22954494800) ;Markovic, S. (57195327212) ;Mijatovic, A. (57739899200) ;Tanasic, D. (57745495800) ;Radakovic, G. (57792840100) ;Peranovic, J. (57739761500) ;Panic-Jelic, N. (57739899400) ;Vujadinovic, O. (57208350695) ;Pajic, P. (57739220100) ;Bekic, S. (58021110200) ;Kovacevic, S. (57195323936) ;García Fernandez, A. (7004201866) ;Perez Cabeza, A. (16639169700) ;Anguita, M. (59572041200) ;Tercedor Sanchez, L. (6603579058) ;Mau, E. (57794241800) ;Loayssa, J. (57739000700) ;Ayarra, M. (57311706700) ;Carpintero, M. (57313261000) ;Roldán Rabadan, I. (7801463733) ;Gil Ortega, M. (58040560600) ;Tello Montoliu, A. (12902661100) ;Orenes Piñero, E. (6503955410) ;Manzano Fernández, S. (23095070000) ;Marín, F. (59820237400) ;Romero Aniorte, A. (55314347300) ;Veliz Martínez, A. (57197825845) ;Quintana Giner, M. (56540040500) ;Ballesteros, G. (57159722500) ;Palacio, M. (57508447300) ;Alcalde, O. (6507322945) ;García-Bolao, I. (58403332700) ;Bertomeu Gonzalez, V. (55967422500) ;Otero-Raviña, F. (12785964500) ;García Seara, J. (6508344902) ;Gonzalez Juanatey, J. (7005529659) ;Dayal, N. (57312595600) ;Maziarski, P. (57202831385) ;Gentil-Baron, P. (8902856200) ;Koç, M. (57535812300) ;Onrat, E. (59273005100) ;Dural, I.E. (57217126546) ;Yilmaz, K. (57311927500) ;Özin, B. (6701872987) ;Tan Kurklu, S. (57312374700) ;Atmaca, Y. (6602732981) ;Canpolat, U. (34767873500) ;Tokgozoglu, L. (7004724917) ;Dolu, A.K. (57883521500) ;Demirtas, B. (57945912300) ;Sahin, D. (56692378900) ;Ozcan Celebi, O. (24478640000) ;Gagirci, G. (57312595700) ;Turk, U.O. (12774004400) ;Ari, H. (58286721400) ;Polat, N. (57313033900) ;Toprak, N. (57312595800) ;Sucu, M. (59798099900) ;Akin Serdar, O. (35091141700) ;Taha Alper, A. (56079792600) ;Kepez, A. (13205139200) ;Yuksel, Y. (57311706800) ;Uzunselvi, A. (57312811500) ;Yuksel, S. (57685433800) ;Sahin, M. (57566430100) ;Kayapinar, O. (36084223000) ;Ozcan, T. (12647371900) ;Kaya, H. (57684507500) ;Yilmaz, M.B. (7202595585) ;Kutlu, M. (58338614400) ;Demir, M. (7004457669) ;Gibbs, C. (57531805500) ;Kaminskiene, S. (57311706900) ;Bryce, M. (57312152900) ;Skinner, A. (57311707000) ;Belcher, G. (57493387300) ;Hunt, J. (57685015200) ;Stancombe, L. (58040464300) ;Holbrook, B. (57312811600) ;Peters, C. (57650559900) ;Tettersell, S. (57311927800) ;Shantsila, A. (35079373300) ;Lane, D. (7403211608) ;Senoo, K. (55142173500) ;Russell, K. (57222071677) ;Domingos, P. (57517020100) ;Hussain, S. (57685661600) ;Partridge, J. (57203934997) ;Haynes, R. (57207752364) ;Bahadur, S. (57525514500) ;Brown, R. (55980533200) ;McMahon, S. (57684467000) ;McDonald, J. (57193498447) ;Balachandran, K. (7005369842) ;Singh, R. (55545408200) ;Garg, S. (13104177600) ;Desai, H. (57193275138) ;Davies, K. (57201005789) ;Goddard, W. (57204666991) ;Galasko, G. (6701497614) ;Rahman, I. (34873371900) ;Chua, Y. (57313261300) ;Payne, O. (57739420600) ;Preston, S. (59876054900) ;Brennan, O. (57216956497) ;Pedley, L. (57211331026) ;Whiteside, C. (57311707300) ;Dickinson, C. (57534507700) ;Brown, J. (58728413600) ;Jones, K. (57203296687) ;Benham, L. (59782401300) ;Brady, R. (59584340000) ;Buchanan, L. (57313261400) ;Ashton, A. (57206936864) ;Crowther, H. (59827973200) ;Fairlamb, H. (57794789100) ;Thornthwaite, S. (58020794200) ;Relph, C. (57211331700) ;McSkeane, A. (59511159800) ;Poultney, U. (57201077252) ;Kelsall, N. (57793671100) ;Rice, P. (57312595900) ;Wilson, T. (57685365300) ;Wrigley, M. (57311707400) ;Kaba, R. (6506113296) ;Patel, T. (59103651500) ;Young, E. (59872313000) ;Law, J. (57684598100) ;Runnett, C. (36180108200) ;Thomas, H. (57215339243) ;McKie, H. (57208499847) ;Fuller, J. (57685535600) ;Pick, S. (57312596000) ;Sharp, A. (16307611000) ;Hunt, A. (57685166000) ;Thorpe, K. (35425239000) ;Hardman, C. (57312596100) ;Cusack, E. (57311707600) ;Adams, L. (57685506000) ;Hough, M. (57311707700) ;Keenan, S. (57195550820) ;Bowring, A. (57201067591) ;Watts, J. (57311927900) ;Zaman, J. (56377827600) ;Goffin, K. (57312812000) ;Nutt, H. (57792837000) ;Beerachee, Y. (57213070710) ;Featherstone, J. (57313261500) ;Mills, C. (57313034300) ;Pearson, J. (57312587200) ;Stephenson, L. (57204249332) ;Grant, S. (57198160185) ;Wilson, A. (59631031000) ;Hawksworth, C. (57207304570) ;Alam, I. (57205493251) ;Robinson, M. (56844297100) ;Ryan, S. (57216331250) ;Egdell, R. (57312153200) ;Gibson, E. (57684451600) ;Holland, M. (36155539400) ;Leonard, D. (57313261600) ;Mishra, B. (57684210100) ;Ahmad, S. (59608270300) ;Randall, H. (57313034400) ;Hill, J. (59624291600) ;Reid, L. (57312153300) ;George, M. (57685637500) ;McKinley, S. (57685156900) ;Brockway, L. (57312153400) ;Milligan, W. (57313034600) ;Sobolewska, J. (57738999900) ;Muir, J. (57312375400) ;Tuckis, L. (57313034700) ;Winstanley, L. (57793117300) ;Jacob, P. (57685711800) ;Kaye, S. (57313261700) ;Morby, L. (57312812100) ;Jan, A. (57311707900) ;Sewell, T. (57208491277) ;Boos, C. (57215186525) ;Wadams, B. (57794228400) ;Cope, C. (57311928000) ;Jefferey, P. (57312812200) ;Andrews, N. (57685092800) ;Getty, A. (57311708000) ;Suttling, A. (57201075548) ;Turner, C. (59862902900) ;Hudson, K. (59797009200) ;Austin, R. (57313034800) ;Howe, S. (57226613839) ;Iqbal, R. (59428732300) ;Gandhi, N. (57312153600) ;Brophy, K. (57312153700) ;Mirza, P. (57312596200) ;Willard, E. (57312153800) ;Collins, S. (59587979100) ;Ndlovu, N. (57312596300) ;Subkovas, E. (36115255500) ;Karthikeyan, V. (12140159700) ;Waggett, L. (57311708100) ;Wood, A. (58927922500) ;Bolger, A. (7006577623) ;Stockport, J. (57500095300) ;Evans, L. (57197584258) ;Harman, E. (57200679402) ;Starling, J. (57312812300) ;Williams, L. (57199194899) ;Saul, V. (57739419900) ;Sinha, M. (57684496300) ;Bell, L. (57203044610) ;Tudgay, S. (57216471691) ;Kemp, S. (57311928100) ;Frost, L. (57193662333) ;Ingram, T. (57201068640) ;Loughlin, A. (59429441300) ;Adams, C. (57685038400) ;Adams, M. (57684291800) ;Hurford, F. (57201070687) ;Owen, C. (25951447600) ;Miller, C. (59597559600) ;Donaldson, D. (57205488172) ;Tivenan, H. (58770665200) ;Button, H. (57221937088) ;Nasser, A. (57312154000) ;Jhagra, O. (57311708300) ;Stidolph, B. (57739684300) ;Brown, C. (56504280400) ;Livingstone, C. (57311932100) ;Duffy, M. (57685038300) ;Madgwick, P. (57221928366) ;Roberts, P. (58927922000) ;Greenwood, E. (57312379600) ;Fletcher, L. (57313038700) ;Beveridge, M. (58579722500) ;Earles, S. (57312600000) ;McKenzie, D. (57312600100) ;Beacock, D. (57945752600) ;Dayer, M. (6603156411) ;Seddon, M. (57312158100) ;Greenwell, D. (57204981820) ;Luxton, F. (57205753334) ;Venn, F. (57312815800) ;Mills, H. (59853262200) ;Rewbury, J. (57739555000) ;James, K. (57685301300) ;Roberts, K. (57685753200) ;Tonks, L. (57192948586) ;Felmeden, D. (6701819995) ;Taggu, W. (23487337100) ;Summerhayes, A. (57210509872) ;Hughes, D. (35570067600) ;Sutton, J. (57217268183) ;Felmeden, L. (57210511714) ;Khan, M. (55808731000) ;Walker, E. (57206562395) ;Norris, L. (57312816000) ;O'Donohoe, L. (56868573300) ;Mozid, A. (57910839900) ;Dymond, H. (57193398283) ;Lloyd-Jones, H. (57312379700) ;Saunders, G. (57313266900) ;Simmons, D. (57684496200) ;Coles, D. (57312600200) ;Cotterill, D. (56868610400) ;Beech, S. (57311932300) ;Kidd, S. (57312379800) ;Wrigley, B. (35199378200) ;Petkar, S. (8958429800) ;Smallwood, A. (57312158300) ;Jones, R. (10042286500) ;Radford, E. (57311711100) ;Milgate, S. (57793669400) ;Metherell, S. (58203479200) ;Cottam, V. (55340845700) ;Buckley, C. (7202815244) ;Broadley, A. (57223976576) ;Wood, D. (58763955500) ;Allison, J. (57684920100) ;Rennie, K. (7004000843) ;Balian, L. (6506569497) ;Howard, L. (57612639400) ;Pippard, L. (58284678100) ;Board, S. (57201075413)Pitt-Kerby, T. (57195551123)Background: Cardiac troponins (cTn) have been reported to be predictors for adverse outcomes in atrial fibrillation (AF), patients, but their actual use is still unclear. Aim: To assess the factors associated with cTn testing in routine practice and evaluate the association with outcomes. Methods: Patients enrolled in the ESC-EHRA EORP-AF General Long-Term Registry were stratified into 3 groups according to cTn levels as (i) cTn not tested, (ii) cTn in range (≤99th percentile), (iii) cTn elevated (>99th percentile). The composite outcome of any thromboembolism /any acute coronary syndrome/cardiovascular (CV) death, defined as Major Adverse Cardiovascular Events (MACE) and all-cause death were the main endpoints. Results: Among 10 445 AF patients (median age 71 years, 40.3% females) cTn were tested in 2834 (27.1%). cTn was elevated in 904/2834 (31.9%) and in-range in 1930/2834 (68.1%) patients. Female sex, in-hospital enrollment, first-detected AF, CV risk factors, history of coronary artery disease, and atypical AF symptoms were independently associated with cTn testing. Elevated cTn were independently associated with a higher risk for MACE (Model 1, hazard ratio [HR] 1.74, 95% confidence interval [CI] 1.40–2.16, Model 2, HR 1.62, 95% CI 1.28–2.05; Model 3 HR 1.76, 95% CI 1.37–2.26) and all-cause death (Model 1, HR 1.45, 95% CI 1.21–1.74; Model 2, HR 1.36, 95% CI 1.12–1.66; Model 3, HR 1.38, 95% CI 1.12–1.71). Conclusions: Elevated cTn levels were associated with an increased risk of all-cause mortality and adverse CV events. Clinical factors that might enhance the need to rule out CAD were associated with cTn testing. © 2022 European Federation of Internal Medicine - Some of the metrics are blocked by yourconsent settings
Publication Catheter ablation for atrial flutter: A survey by the European heart rhythm association and canadian heart rhythm society(2016) ;Glover, Benedict M. (9241879700) ;Chen, Jian (15769086600) ;Hong, Kathryn L. (57194019368) ;Boveda, Serge (6701478201) ;Baranchuk, Adrian (18036557700) ;Haugaa, Kristina H. (24733615600) ;Dorian, Paul (7005356417) ;Potpara, Tatjana S. (57216792589) ;Crystal, Eugene (35428230600) ;Mitchell, Brent (7203039142) ;Tilz, Roland (16065182300) ;Leong-Sit, Peter (6507351732)Dagres, Nikolaos (7003639393)The purpose of this EP wire survey was to examine current practice in the management of both cavotricuspid isthmus (CTI)-dependent and non-CTI-dependent atrial flutter (AFL) ablation amongst electrophysiologists in European and Canadian centres and to understand how current opinions vary from guidelines. The results of the survey were collected from a detailed questionnaire that was created by the European Heart Rhythm Association Research Network and the Canadian Heart Rhythm Society. Responses were received from 89 centres in 12 countries. The survey highlighted variability within certain aspects of the management of AFL ablation. The variability in opinion regarding other procedural details suggests a need for further research in this area and consideration of the development of guidelines specific to AFL. Overall, there is reasonable consensus regarding oral anticoagulation and the desired endpoints of ablation for patients with CTI-dependent AFL and for non-CTI-dependent AFL. © The Author 2016. - Some of the metrics are blocked by yourconsent settings
Publication Catheter Ablation of Atrial Fibrillation: An Overview for Clinicians(2017) ;Mujović, Nebojša (16234090000) ;Marinković, Milan (56160715300) ;Lenarczyk, Radoslaw (6603516741) ;Tilz, Roland (16065182300)Potpara, Tatjana S. (57216792589)Catheter ablation (CA) of atrial fibrillation (AF) is currently one of the most commonly performed electrophysiology procedures. Ablation of paroxysmal AF is based on the elimination of triggers by pulmonary vein isolation (PVI), while different strategies for additional AF substrate modification on top of PVI have been proposed for ablation of persistent AF. Nowadays, various technologies for AF ablation are available. The radiofrequency point-by-point ablation navigated by electro-anatomical mapping system and cryo-balloon technology are comparable in terms of the efficacy and safety of the PVI procedure. Long-term success of AF ablation including multiple procedures varies from 50 to 80%. Arrhythmia recurrences commonly occur, mostly due to PV reconnection. The recurrences are particularly common in patients with non-paroxysmal AF, dilated left atrium and the "early recurrence" of AF within the first 2–3 post-procedural months. In addition, this complex procedure can be accompanied by serious complications, such as cardiac tamponade, stroke, atrio-esophageal fistula and PV stenosis. Therefore, CA represents a second-line treatment option after a trial of antiarrhythmic drug(s). Good candidates for the procedure are relatively younger patients with symptomatic and frequent episodes of AF, with no significant structural heart disease and no significant left atrial enlargement. Randomized trials demonstrated the superiority of ablation compared to antiarrhythmic drugs in terms of improving the quality of life and symptoms in AF patients. However, nonrandomized studies reported additional clinical benefits from ablation over drug therapy in selected AF patients, such as the reduction of the mortality and stroke rates and the recovery of tachyarrhythmia-induced cardiomyopathy. Future research should enable the creation of more durable ablative lesions and the selection of the optimal lesion set in each patient according to the degree of atrial remodeling. This could provide better long-term CA success and expand indications for the procedure, especially among the patients with non-paroxysmal AF. © 2017, The Author(s). - Some of the metrics are blocked by yourconsent settings
Publication Challenges in clinical decision-making on concomitant drug therapies in patients with atrial fibrillation taking oral anticoagulants(2019) ;Steffel, Jan (8882159100)Potpara, Tatjana S. (57216792589)[No abstract available] - Some of the metrics are blocked by yourconsent settings
Publication Clinical approach to the patient with Brugada Syndrome: Risk stratification and optimal management(2019) ;Marinković, Milan M. (56160715300) ;Mujović, Nebojša M. (16234090000)Potpara, Tatjana S. (57216792589)The Brugada Syndrome (BrS) is an inherited cardiac ion channel disorder associated with increased risk of ventricular arrhythmias and mortality. Diagnosis is based on a characteristic electrocardiographic (EC G) pattern of coved type ST-segment elevation >2 mm followed by a negative T-wave in ≥1 of the right precordial leads V1 to V3. Since the first description of BrS, the definition of disease and underlying pathophysiological mechanisms have been significantly improved in recent years. Also, significant progress has been made in the field of genetic testing in these patients. Still, there are several open questions regarding the management and outcome of these patients. There is more information about patients who would need an implantable cardiac defibrillator for the primary prevention of sudden cardiac death (that is, those with spontaneous Type I Brugada EC G pattern and arrhythmia-related syncope), but currently published data concerning asymptomatic patients with Brugada EC G pattern and other less-well defined presentations are conflicting. Whereas the role of cardiac defibrillator in patients with Brugada Syndrome is clear, optimal use of catheter ablation and antiarrhythmic drug therapy needs to be further investigated. In this review, we summarize current evidence and contemporary management of patients with BrS. © 2019 EDIZIONI MINERVA MEDICA.
