Georgios Leventopoulos

Dr. Georgios Leventopoulos

cardiology, General University Hospital of Patras, Pátrai, Greece
orcid

Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 May 2009 in Pediatric Neurology
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Journal Article
Closed access
Georgios LeventopoulosGeorgios Leventopoulos
Georgios Leventopoulos
SKSophia Kitsiou-Tzeli
Sophia Kitsiou-Tzeli
KKKonstantinos Kritikos
Konstantinos Kritikos
SPStavroula Psoni
Stavroula Psoni
AMAriadni Mavrou
Ariadni Mavrou
HFHelen Fryssira
Helen Fryssira

25 May 2023 in Life
Verified
Journal Article
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Georgios LeventopoulosGeorgios Leventopoulos
Georgios Leventopoulos
RKRafail Koros
Rafail Koros
CTChristoforos K. Travlos
Christoforos K. Travlos
APAngelos Perperis
Angelos Perperis
PCPanagiotis Chronopoulos
Panagiotis Chronopoulos
Grigorios TsigkasGrigorios Tsigkas
Grigorios Tsigkas
Atrial fibrillation (AF) is a very common arrhythmia that mainly affects older individuals. The mechanism of atrial fibrillation is complex and is related to the pathogenesis of trigger activation and the perpetuation of arrhythmia. The pulmonary veins in the left atrium arei confirm that onfirm the most common triggers due to their distinct anatomical and electrophysiological properties. As a result, their electrical isolation by ablation is the cornerstone of invasive AF treatment. Multiple factors and comorbidities affect the atrial tissue and lead to myocardial stretch. Several neurohormonal and structural changes occur, leading to inflammation and oxidative stress and, consequently, a fibrotic substrate created by myofibroblasts, which encourages AF perpetuation. Several mechanisms are implemented into daily clinical practice in both interventions in and the medical treatment of atrial fibrillation.

5 December 2007 in European Journal of Pediatrics
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Journal Article
Closed access
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HFHelen Fryssira
Helen Fryssira
Georgios LeventopoulosGeorgios Leventopoulos
Georgios Leventopoulos
SPStavroula Psoni
Stavroula Psoni
SKSophia Kitsiou-Tzeli
Sophia Kitsiou-Tzeli
NSNikolaos Stavrianeas
Nikolaos Stavrianeas
EKEmmanuel Kanavakis
Emmanuel Kanavakis

30 July 2023 in International Journal of Cardiology
Verified
Journal Article
Closed access
Georgios LeventopoulosGeorgios Leventopoulos
Georgios Leventopoulos
CTChristoforos K. Travlos
Christoforos K. Travlos
KAKonstantinos N. Aronis
Konstantinos N. Aronis
VAVirginia Anagnostopoulou
Virginia Anagnostopoulou
PPPanagiotis Patrinos
Panagiotis Patrinos
PDPeriklis Davlouros
Periklis Davlouros

7 November 2024 in EP Europace
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Journal Article
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Christian-H HeegerChristian-H Heeger
Christian-H Heeger
AAAlexandre Almorad
Alexandre Almorad
USUniv.-Prof. Priv.-Doz. Dr.med.univ. Daniel Scherr
Univ.-Prof. Priv.-Doz. Dr.med.univ. Daniel Scherr
NSNándor Szegedi
Nándor Szegedi
SSSebastian Seidl
Sebastian Seidl
RTRoland Richard Tilz
Roland Richard Tilz
Aims: Temperature-controlled high-power short-duration (HPSD) radiofrequency catheter ablation for pulmonary vein isolation (PVI) utilizing a novel ablation catheter (QDOT Micro) with real-time assessment of catheter tip temperature aims for safer, more effective, and faster procedures. Methods and results: The peQasus study is a large European multicentre study set up to assess safety, acute efficacy, and outcomes of temperature-controlled HPSD-based PVI. The primary endpoints were safety, efficacy, and 12-month freedom from atrial tachyarrhythmias. Additionally, two strategies namely very HPSD (90 W for 4 s) only and a hybrid approach (HPSD with maximum of 50 W and vHPSD) were compared. A total of 1023 AF patients in 15 centres from nine European countries received PVI with the QDOT. Complete PVI was successfully achieved in all patients. In 699/1023 (68.3%), the vHPSD-only approach (vHPSD group) and in 324/ (31.7%) patients, the hybrid approach (hybrid group) was utilized. The mean procedure duration was 98.4 ± 37.4 min (vHPSD: 88.2 ± 34.9 min, hybrid: 117.4 ± 32.7 min, P < 0.001). The first-pass isolation rate of all PVs was 64% (vHPSD: 62.6%, hybrid: 67.1%, P = 0.187). Severe adverse events were observed in 1.7% (vHPSD: 1.6%, hybrid: 1.9%, P = 0.746). Twelve-month arrhythmia-recurrence-free survival was 77.1% (vHPSD: 76.8%, hybrid: 77.8%, P = 0.241). Conclusion: In this large multicentre study, temperature-controlled HPSD and vHPSD ablation via a novel ablation catheter provides safe and effective PVI with a relatively short procedure duration. Despite a shorter procedure time, no differences in terms of safety and freedom from arrhythmia recurrence were found irrespective of utilizing vHPSD or the hybrid approach.

9 November 2023 in Reviews in Cardiovascular Medicine
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Journal Article
Open access
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Georgios LeventopoulosGeorgios Leventopoulos
Georgios Leventopoulos
CTChristoforos K. Travlos
Christoforos K. Travlos
VAVirginia Anagnostopoulou
Virginia Anagnostopoulou
PPPanagiotis Patrinos
Panagiotis Patrinos
APAngeliki Papageorgiou
Angeliki Papageorgiou
PDPeriklis Davlouros
Periklis Davlouros
Background: Biventricular pacing (BVP) is recommended for patients with heart failure (HF) who require cardiac resynchronization therapy (CRT). Left bundle branch area pacing (LBBAP) is a novel pacing strategy that appears to ensure better electrical and mechanical synchrony in these patients. Our aim was to systematically review and meta-analyze the existing evidence regarding the clinical outcomes of LBBAP-CRT compared with BVP-CRT. Methods: Medline, Embase, Cochrane Central Register of Controlled Trials and Web of Science databases were searched for studies comparing LBBAP-CRT with BVP-CRT. Outcomes were all-cause mortality, heart failure hospitalizations (HFH) and New York Heart Association (NYHA) class improvement. We included randomized controlled trials (RCTs) and observational studies with participants that had left ventricular ejection fraction (LVEF) ≤40% and (i) symptomatic HF or (ii) expected ventricular pacing >40%. Random and fixed effects models pairwise meta-analysis was conducted. Cochrane Risk of Bias 2 assessment tool (ROB 2.0) and the Newcastle–Ottawa scale (NOS) were used to assess the quality of the studies. Results: Eleven studies (10 observational studies and 1 RCT) with 3141 patients were included in the analysis. Compared with BVP-CRT, LBBAP-CRT was associated with lower risk of all-cause mortality (risk ratio (RR): 0.71, 95% CI: 0.57 to 0.87; p = 0.001), lower risk of HFH (RR: 0.59, 95% CI: 0.50 to 0.71; p < 0.00001) and more improvement in NYHA class (weighed mean difference (WMD): –0.36, 95% CI: –0.59 to –0.13; p < 0.00001) compared with patients who received BVP-CRT. Conclusions: Compared with BVP-CRT, receipt of LBBAP-CRT in patients with HF is associated with a lower risk of mortality, and HFH and greater improvement in NHYA class.