Felipe Fernández-Vázquez

Dr. Felipe Fernández-Vázquez

Hospital Universitario de León, Spain
orcid

Research Focus & Metrics

Academic Career Length

39Years (1988-Present)

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

Representative Publications

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1 October 2013 in Circulation
Verified
Journal Article
Closed access
BIBorja Ibanez
Borja Ibanez
CMCarlos Macaya
Carlos Macaya
VSVicente Sánchez-Brunete
Vicente Sánchez-Brunete
GPGonzalo Pizarro
Gonzalo Pizarro
LFLeticia Fernández-Friera
Leticia Fernández-Friera
VFValentin Fuster
Valentin Fuster
Background—: The effect of β-blockers on infarct size when used in conjunction with primary percutaneous coronary intervention is unknown. We hypothesize that metoprolol reduces infarct size when administered early (intravenously before reperfusion). Methods and Results—: Patients with Killip class II or less anterior ST-segment–elevation myocardial infarction (STEMI) undergoing percutaneous coronary intervention within 6 hours of symptoms onset were randomized to receive intravenous metoprolol (n=131) or not (control, n=139) before reperfusion. All patients without contraindications received oral metoprolol within 24 hours. The predefined primary end point was infarct size on magnetic resonance imaging performed 5 to 7 days after STEMI. Magnetic resonance imaging was performed in 220 patients (81%). Mean±SD infarct size by magnetic resonance imaging was smaller after intravenous metoprolol compared with control (25.6±15.3 versus 32.0±22.2 g; adjusted difference, −6.52; 95% confidence interval, −11.39 to −1.78; P =0.012). In patients with pre–percutaneous coronary intervention Thrombolysis in Myocardial Infarction grade 0 to 1 flow, the adjusted treatment difference in infarct size was −8.13 (95% confidence interval, −13.10 to −3.16; P =0.0024). Infarct size estimated by peak and area under the curve creatine kinase release was measured in all study populations and was significantly reduced by intravenous metoprolol. Left ventricular ejection fraction was higher in the intravenous metoprolol group (adjusted difference, 2.67%; 95% confidence interval, 0.09–5.21; P =0.045). The composite of death, malignant ventricular arrhythmia, cardiogenic shock, atrioventricular block, and reinfarction at 24 hours in the intravenous metoprolol and control groups was 7.1% and 12.3%, respectively ( P =0.21). Conclusions—: In patients with anterior Killip class II or less ST-segment–elevation myocardial infarction undergoing primary percutaneous coronary intervention, early intravenous metoprolol before reperfusion reduced infarct size and increased left ventricular ejection fraction with no excess of adverse events during the first 24 hours after STEMI. Clinical Trial Registration—: URL: http://www.clinicaltrials.gov . Unique identifier: NCT01311700. EUDRACT number: 2010-019939-35.

1 September 2004 in The Lancet
Verified
Journal Article
Closed access
FFFrancisco Fernández-Avilés
Francisco Fernández-Avilés
JAJoaquín J Alonso
Joaquín J Alonso
ACAlfonso Castro-Beiras
Alfonso Castro-Beiras
NVNicolás Vázquez
Nicolás Vázquez
JBJesús Blanco
Jesús Blanco
BRBenigo Ramos
Benigo Ramos

1 March 2014 in JACC: Cardiovascular Interventions
Verified
Journal Article
Closed access
JHJose M. de la Torre Hernandez
Jose M. de la Torre Hernandez
JAJosé A. Baz Alonso
José A. Baz Alonso
JHJoan A. Gómez Hospital
Joan A. Gómez Hospital
FMFernando Alfonso Manterola
Fernando Alfonso Manterola
TCTamara Garcia Camarero
Tamara Garcia Camarero
JGJavier Zueco Gil
Javier Zueco Gil

1 August 2011 in JACC
Verified
Journal Article
Closed access
GEGeorgina M Ellison-Hughes
Georgina M Ellison-Hughes
DTDaniele Torella
Daniele Torella
SDSanto Dellegrottaglie
Santo Dellegrottaglie
CPClaudia C. Pérez-Martínez
Claudia C. Pérez-Martínez
APArmando Perez De Prado
Armando Perez De Prado
BNBernardo Nadal-Ginard
Bernardo Nadal-Ginard

1 March 2021 in Circulation: Arrhythmia and Electrophysiology
Verified
Journal Article
Closed access
PDF file
JCJames Coromilas
James Coromilas
SKStephanie Kochav
Stephanie Kochav
IGIsaac Goldenthal
Isaac Goldenthal
ABAngelo Biviano
Angelo Biviano
HGHasan Garan
Hasan Garan
EWElaine Y. Wan
Elaine Y. Wan
Background - COVID-19 has led to over 1 million deaths worldwide and has been associated with cardiac complications including cardiac arrhythmias. The incidence and pathophysiology of these manifestations remain elusive. In this worldwide survey of patients hospitalized with COVID-19 who developed cardiac arrhythmias, we describe clinical characteristics associated with various arrhythmias, as well as global differences in modulations of routine electrophysiology practice during the pandemic. Methods - We conducted a retrospective analysis of patients hospitalized with COVID-19 infection worldwide with and without incident cardiac arrhythmias. Patients with documented atrial fibrillation (AF), atrial flutter (AFL), supraventricular tachycardia (SVT), non-sustained or sustained ventricular tachycardia (VT), ventricular fibrillation (VF), atrioventricular block (AVB), or marked sinus bradycardia (HR<40bpm) were classified as having arrhythmia. De-identified data was provided by each institution and analyzed. Results - Data was collected for 4,526 patients across 4 continents and 12 countries, 827 of whom had an arrhythmia. Cardiac comorbidities were common in patients with arrhythmia: 69% had hypertension, 42% diabetes mellitus, 30% had heart failure and 24% coronary artery disease. Most had no prior history of arrhythmia. Of those who did develop an arrhythmia, the majority (81.8%) developed atrial arrhythmias, 20.7% developed ventricular arrhythmias, and 22.6% had bradyarrhythmia. Regional differences suggested a lower incidence of AF in Asia compared to other continents (34% vs. 63%). Most patients in in North America and Europe received hydroxychloroquine, though the frequency of hydroxychloroquine therapy was constant across arrhythmia types. Forty-three percent of patients who developed arrhythmia were mechanically ventilated and 51% survived to hospital discharge. Many institutions reported drastic decreases in electrophysiology procedures performed. Conclusions - Cardiac arrhythmias are common and associated with high morbidity and mortality among patients hospitalized with COVID-19 infection. There were significant regional variations in the types of arrhythmias and treatment approaches.

1 February 2012 in Circulation: Arrhythmia and Electrophysiology
Verified
Journal Article
Open access
PDF file
LNLuis Nombela
Luis Nombela
CMCristina D. Mitroi
Cristina D. Mitroi
IFIgnacio Fernández-Lozano
Ignacio Fernández-Lozano
AGArturo García-Touchard
Arturo García-Touchard
JTJorge Toquero
Jorge Toquero
ALAlonso-Pulpón Luis
Alonso-Pulpón Luis
Background—: An implantable cardioverter-defibrillator (ICD) is the therapy of choice for primary prevention in patients with ischemia who are at risk for sudden cardiac death (SCD). One third of patients with significant coronary disease have chronic total coronary occlusion (CTO), which is associated with long-term mortality in patients with previous myocardial infarction. However, the impact of CTO on the occurrence of ventricular arrhythmias and long-term mortality in ICD recipients remains unknown. Methods and Results—: All consecutive patients with coronary artery disease receiving ICD therapy for the prevention of SCD were included in the study. Among other characteristics, the existence of CTO was assessed. During follow-up, the occurrence of appropriate device delivery because of ventricular arrhythmias as well as mortality were noted. A total of 162 patients (mean age, 62±9 years; 93% men) with an ICD were included and followed for a median of 26 months (interquartile range, 12–42). At least 1 CTO was present in 71 (44%) patients. Appropriate device therapy was detected in 18% of the patients during the follow-up. The presence of CTO was associated with higher ventricular arrhythmia and mortality rates (log-rank test, <0.01). Multivariable analysis revealed that CTO was independently associated with appropriate ICD intervention (hazard ratio, 3.5; P =0.003). Conclusions—: In patients with ischemic heart disease receiving ICDs for primary prevention of SCD, CTO is an independent predictor for the occurrence of ventricular arrhythmias and has an adverse impact on long-term mortality.