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Thoracoscopic ablation of atrial fibrillation – Should we still be concerned about periprocedural complications

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064173%3A_____%2F17%3AN0000009" target="_blank" >RIV/00064173:_____/17:N0000009 - isvavai.cz</a>

  • Nalezeny alternativní kódy

    RIV/00216208:11120/17:43913456

  • Výsledek na webu

    <a href="http://dx.doi.org/10.1016/j.crvasa.2017.06.004" target="_blank" >http://dx.doi.org/10.1016/j.crvasa.2017.06.004</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.crvasa.2017.06.004" target="_blank" >10.1016/j.crvasa.2017.06.004</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Thoracoscopic ablation of atrial fibrillation – Should we still be concerned about periprocedural complications

  • Popis výsledku v původním jazyce

    Introduction: Minimally invasive surgical ablations are becoming an interesting treatment option for patients with stand-alone atrial fibrillation (AF). However, they are in general connected with higher rates of perioperative complications. The aim of this study was to summarize the complications of all such procedures performed in our center and compare them with similar recent papers. Material and methods: All perioperative and 30-days complications of thoracoscopic ablations of AF performed in our center were collected and analyzed. Recent literature was searched for studies describing the outcomes of thoracoscopic and hybrid ablations. Rates of complications were then compared with our outcomes and also with catheter ablations. Results: A total of 112 patients underwent a thoracoscopic ablation of AF in our center between 2006 and 2017, with use of three different devices. Mean age was 61.4. ±. 8.8 years, 66% were males and 53% of patients had long-standing persistent AF. A life-threatening complications occurred in 2 (1.8%) patients, including 1 conversion to sternotomy and 1 stroke. Severe complications occurred in 6 (5.4%) patients including 2 re-explorations for bleeding, 3 cases of phrenic nerve palsy and 1 respiratory failure. A minor od moderate complications occurred in 17 (15.2%) patients. Twenty-seven suitable papers were identified in recent literature for comparison (total of 1869 patients). The rates of significant complications varied between 0 and 16% over different centers, mean rate was 4.8%. Regarding the catheter ablation studies, 5-7% of patients suffer from some severe complication after ablation of AF. Conclusions: Rates of 30-days, life-threatening and severe complications are comparable between mini-invasive surgical and catheter ablations of AF. Rates of minor complications appear to be higher in surgical ablations. To keep the rates low or even to decrease them, those surgical or hybrid procedures should be performed in experienced centers.

  • Název v anglickém jazyce

    Thoracoscopic ablation of atrial fibrillation – Should we still be concerned about periprocedural complications

  • Popis výsledku anglicky

    Introduction: Minimally invasive surgical ablations are becoming an interesting treatment option for patients with stand-alone atrial fibrillation (AF). However, they are in general connected with higher rates of perioperative complications. The aim of this study was to summarize the complications of all such procedures performed in our center and compare them with similar recent papers. Material and methods: All perioperative and 30-days complications of thoracoscopic ablations of AF performed in our center were collected and analyzed. Recent literature was searched for studies describing the outcomes of thoracoscopic and hybrid ablations. Rates of complications were then compared with our outcomes and also with catheter ablations. Results: A total of 112 patients underwent a thoracoscopic ablation of AF in our center between 2006 and 2017, with use of three different devices. Mean age was 61.4. ±. 8.8 years, 66% were males and 53% of patients had long-standing persistent AF. A life-threatening complications occurred in 2 (1.8%) patients, including 1 conversion to sternotomy and 1 stroke. Severe complications occurred in 6 (5.4%) patients including 2 re-explorations for bleeding, 3 cases of phrenic nerve palsy and 1 respiratory failure. A minor od moderate complications occurred in 17 (15.2%) patients. Twenty-seven suitable papers were identified in recent literature for comparison (total of 1869 patients). The rates of significant complications varied between 0 and 16% over different centers, mean rate was 4.8%. Regarding the catheter ablation studies, 5-7% of patients suffer from some severe complication after ablation of AF. Conclusions: Rates of 30-days, life-threatening and severe complications are comparable between mini-invasive surgical and catheter ablations of AF. Rates of minor complications appear to be higher in surgical ablations. To keep the rates low or even to decrease them, those surgical or hybrid procedures should be performed in experienced centers.

Klasifikace

  • Druh

    J<sub>SC</sub> - Článek v periodiku v databázi SCOPUS

  • CEP obor

  • OECD FORD obor

    30201 - Cardiac and Cardiovascular systems

Návaznosti výsledku

  • Projekt

    <a href="/cs/project/NV16-32478A" target="_blank" >NV16-32478A: Projekt EndoMaze HYBRID- podrobné zhodnocení bezpečnosti a efektivity hybridní ablace perzistentní a dlouhodobě perzistentní fibrilace síní</a><br>

  • Návaznosti

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Ostatní

  • Rok uplatnění

    2017

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    Cor et Vasa

  • ISSN

    0010-8650

  • e-ISSN

    1803-7712

  • Svazek periodika

    59

  • Číslo periodika v rámci svazku

    4

  • Stát vydavatele periodika

    NL - Nizozemsko

  • Počet stran výsledku

    8

  • Strana od-do

    e317-e324

  • Kód UT WoS článku

    000410033600007

  • EID výsledku v databázi Scopus

    2-s2.0-85023631234