Listing 1 - 10 of 11 | << page >> |
Sort by
|
Choose an application
Le but de cette étude est d'analyser le pronostic vital à court et à long terme des patients ayant bénéficié d'une chirurgie de remplacement de la valve aortique (RVAo) par une prothèse mécanique. Dans un but de contrôle de qualité, nous souhaitons comparer les événements observés à ceux prédits par des scores validés pour la mortalité et les autres complications à court et à long terme. Une évaluation du pouvoir de prédiction des différents scores pour la prédiction de la mortalité à 1 an est réalisée.Matériel et méthodes : Une série consécutive de 690 patients (63 ans d'âge moyen) ayant bénéficié d'un RVAo par une prothèse mécanique de janvier 1998 à décembre 2012. L'implantation a été associée à un pontage coronarien chez 214 patients (31,0 %), à un BENTALL chez 80 patients (11,6 %), à une buse/plastie chez 14 patients (2,0 %), à une myomectomie septale chez 23 patients (3,3 %), à une endartériectomie carotidienne chez 15 patients (2,2 %), à un MAZE chez 9 patients (1,3 %) et à une fermeture d'un foramen ovale perméable chez 10 patients (1,4 %). Le devenir à court et à long terme fut analysé rétrospectivement et comparé à des scores prédictifs (l'EuroSCORE I, l'EuroSCORE II et le STS).Résultats: La mortalité opératoire est de 4,3%. Les complications post-opératoires sont : un infarctus du myocarde chez 17 patients (2,5%), un AVC chez 12 patients (1,7%), une dialyse chez 25 patients (3,6%), une implantation d'un pacemaker chez 37 patients (5,4%) et de la FA chez 279 patients (40,4%). Les complications à long terme sur une durée de 3,4 années de suivi moyen, sont : 39 événements hémorragiques (5,7%), 24 AVC (3,5%), 8 reprise de plaie sternale (1 ,2%), 6 redo (0,9%), 4 dysfonctions valvulaires (0,6%), 2 endocardites (0,3%) et 2 embolies périphérique s (0,3%). Le taux de survie global, estimé par la méthode de KAPLAN-MEIER, à 5 et 10 ans étaient respectivement de 84% et 60%. Pour la prédiction de la mortalité à 1 an, l'EuroSCORE 1 a la meilleure courbe ROC avec une AUC à 0,77.Conclusion : Le taux de mortalité observé est similaire aux valeurs prédites par l'EuroSCORE I et l'EuroSCORE Il. Les taux de complications procédurales correspondent aux valeurs prédites par le STS, sauf pour la ventilation prolongée et la réopération où nous avons obtenu un résultat inférieur, c'est-à-dire meilleur dans ce cas-ci. The purpose of this study is to analyze the short and long-term prognosis of patients who underwent aortic valve replacement surgery by a mechanical prosthesis. For quality control purposes, we wanted to compare the events observed against predicted scores validated for mortality and other short and long-term complications. An evaluation of the predictive power of the different scores for the prediction of 1-year mortality is carried out.Material and methods: A consecutive series of 690 patients (average age 63 years) having benefited an aortic valve replacement by a mechanical prosthesis from January 1998 to December 2012. The implantation was associated with coronary artery bypass grafting for 214 patients (31,0%), with a BENTALL for 80 patients (11,6%), with a Buse / plasty for 14 patients (2,0%), with a septal myomectomy for 23 patients (3,3%), with a carotid endarterectomy for 15 patients (2,2%), with a MAZE in 9 patients (1,3%) and with a closure of a patent foramen ovale for 10 patients (1,4%). The short and long term future was retrospectively analyzed and compared with predictive scores (the EuroSCORE I, II and STS).Results: Operative mortality was 4,3%. Postoperative complications were: a myocardial infarction for 17 patients (2,5%), a stroke for 12 patients (1,7%), a dialysis for 25 patients (3,6%), the implantation of a pacemaker for 37 patients (5,4%) and FA for 279 patients (40,4%). Long term complications over an average follow-up period of 3.4 years are: 39 bleeding events (5,7%), 24 strokes (3,5%), 8 resumption of sternal wound (1,2%), redo 6 (0,9%), 4 valvular dysfunction (0,6%), 2 endocarditis (0,3%) and 2 peripheral embolism (0,3%). The overall survival rate, estimated by the Kaplan-Meier method, to 5 and 10 years were 84% and 60% respectively. For the prediction of 1-year mortality, the EuroSCORE I has the best curve with a ROC AUC 0,77. Conclusions: The observed mo1tality rate is similar to the values predicted by the EuroSCORE 1 and II. The rates of procedural complications correspond to the values assessed by the STS, except for prolonged ventilation and reoperation where we obtained a lower (better) result.
Choose an application
Introduction. The elderly population is on the increase and many are affected by aortic stenosis. Several alternatives to conventional aortic valve replacement exist, including the transapical TAVI (TA). However, adverse effects exist. It would therefore be interesting to resect the native aortic valve before implantation of a new valve. The work aims to assess the feasibility of percutaneous resection of the stenotic native aortic valve before implantation of an endovalve by TA in inoperable patients. Methods. To achieve this assessment, first, we have completed a database for TA without resection for comparison with what has already been done and, in the near future, comparison with TA with resection. We included in this monocentric prospective study, 82 patients operated by TA at the Cliniques Universitaires Saint-Luc from 9/4/2008 until 15/1/2016. We closed the database on 31/5/2016. Then we have developed in collaboration with engineers, a resection tool that has been clinically tested. Results. Mean age was 83.45 years (+-6.12; n=82), we counted 59.76% men and 40.24% women. Mean logistic euroSCORE and euroSCORE II were respectively 36.76% (+-18.17; n=56) and 6.29 (+-5.13; n=26). Mean length of hospital stay was 12.93 days (+-4.95; n=82). 10 patients died during hospitalization (12.20%), 14 at 30 days (17.07%), 24 at 1 year (29.27%) and a total of 39 known deaths (47.56%). We noted a survival rate of 50% at 3.20 years (see Kaplan Meier curve). The maximum clinical follow-up was 5 years and 4 months. The mean clinical follow-up was 16.57 months. The maximum survival was 6 years and 10 months. We identified perioperative and early postoperative complications: repoerations (4.88%), cardiac (65.85%), vascular (18.29%), pulmonary (35.37%), infectious (20.73%), gastrointestinal (3.66%) complications, stroke (9.76%), AKF (23.17%). At the ultrasound control, there was no statistically significant difference in the left ventricular ejection function. There was a statistically significant difference in the aortic valve area, the maximum and the mean gradient preoperatively compared to postoperatively until 4 years. Patients with moderate or severe paravalvular leaks died faster. Concomitantly, the resection tool has been tested on 10 patients during open heart operations, with an excellent cutting result. The miniaturization phase to reach the TA resection has just started. Discussion. We confirmed with this study that the TA without resection is feasible but several side effects exits. We look forward to the resection of the native aortic valve by the transapical way to compare our results. Introduction. La population âgée est croissante et nombreux sont ceux touché par une sténose aortique. Plusieurs alternatives au remplacement valvulaire aortique conventionnel existent, notamment le TAVI transapical (TA). Néanmoins, celui-ci n’est pas sans conséquence. Il serait dès lors intéressant de réséquer la valve aortique native avant l’implantation d’une nouvelle valve. Ainsi, le travail effectué a pour but d’évaluer la faisabilité d’une résection percutanée de la valve aortique native sténosée avant implantation d’une endovalve TA chez les malades inopérables. Matériel et méthodes. Pour réaliser cette évulation, nous avons, tout d’abord, complété une base de données pour les TA sans résection pour la comparer à ce qui a déjà été fait, et dans un futur proche, la comparer avec les TA avec résection. Nous avons inclus, dans cette étude prospective monocentrique, 82 patients après par TA aux Cliniques Universitaires Saint-Luc du 9/4/2008 au 15/1/12016. Nous avons clôturé la base de donnes le 31/5/2016. Ensuite, nous avons développé en collaboration avec des ingénieurs, un outil de résection qui a déjà été testé cliniquement. Résultats. La moyenne d’êge était de 83.45 ans (+-6.12 ; n=82) ; nous comptions 59.76 d’hommes et 40.24% de femmes. Les moyennes du logistic euroSCORE et de l’euroSCORE II étaient respectivement 36.76% (+-18.17 ; n=56) et 6.29% (+-5.13 ; n=26). La durée de l’hospitalisation était en moyenne de 12.93 jours (+-4.95 ; n=82). 10 patients sont décédés durant l’hospitalisation (12.20%), 14 dans les 30 jours (17.07%), 24 à 1 an (29.27%) et nous comptions un total de 39 décès (47.56%). Nous notions un taux de survie de 50% 3 0.20 ans (cfr courbe Kaplan Meier). Le suivi clinique maximal était de 5 ans et 4 mois. Le suivi clinique moyen était de 16.57 mois. La survie maximale était de 6 ans et 10 mois. Nous avons relevé les complications périopératoires et postopératoires précoces : réopérations (4.88%), complications cardiaques (65.58%), vasculaire (18.29%), pulmonaires (35.37%), infectieuses (20.73%), gastro-intestinales (3.66%), AVC (9.76%), IRA (23.17%). Lors du suivi échographique, il n’y avait pas de différence statistiquement significative entre la fonction d’éjection ventriculaire gauche en pré- et postopératoire. Il existait une différence statistiquement significative entre les valeurs préopératoires et postopératoires jusqu’à 4 ans pour la surface valvulaire aortique, le gradient maximal et le gradient moyen. Les patients atteints d’une fuite paravalvulaire modérée à sévère décédaient plus rapidement. En parallèle, l’outil de résection a été testé sur 10 patients, durant des opérations à cœur ouvert, avec un excellent résultat de découpe. La phase de miniaturisation pour aboutir à la résection TA vient de démarrer. Discussion. Nous avons confirmé avec cette étude que le TA sans résection est faisable mais qu’il existe certains effets indésirables. Nous attendons avec impatience la résection de valves aortiques natives par voie transapicale pour comparer nos résultats.
Catheter Ablation --- Aortic Valve Stenosis --- Transcatheter Aortic Valve Replacement
Choose an application
Structural heart disease encompasses a wide range of abnormalities involving noncoronary structures like the heart's valves, walls, and chambers. The last decade emphasized the burden of the disease and revolutionized the treatment strategies. The number of percutaneous structural heart interventions constantly increases worldwide. While some parts of the world acquire experience with various intervention treatments, techniques, and devices, others are paving their first steps. Complex Cases in Structural Heart Interventions provide a descriptive and highly illustrative insight into unique clinical situations managed by one of the world's most experienced and innovative teams. Each case study contains a clinical presentation, imaging analysis, procedural dilemmas, and resulting outcome. A detailed explanation of the technique used, key points and tips were highlighted, and a literature review covered broad knowledge on each topic. The authors shared their knowledge and distinctive solutions from over a decade of experience to ensure an educational adventure for the medical community and a roadmap for interventional heart teams.
Heart --- Diseases --- Treatment. --- Transcatheter Aortic Valve Replacement --- Heart Valve Diseases --- Balloon Valvuloplasty --- surgery --- Balloon Valvotomy --- Balloon Valvotomies --- Balloon Valvuloplasties --- Valvotomies, Balloon --- Valvotomy, Balloon --- Valvuloplasties, Balloon --- Valvuloplasty, Balloon --- Transcatheter Aortic Valve Implantation --- Transcatheter Aortic Valve Replacement. --- Balloon Valvuloplasty.
Choose an application
Advances in structural heart disease (SHD) is occurring at a rapid rate, and the Mayo Clinic is at the forefront of developing procedural techniques in this fast-changing field. Handbook of Structural Heart Interventions provides practical, focused coverage of SHD, bringing you up to date with today's evidence-based techniques and approaches for common and uncommon SHD procedures. Ideal for both SHD trainees and established practitioners, attendings, and fellows in interventional cardiology, this easy-to-use handbook is a unique educational and clinical resource in a quickly expanding field. -- Publisher
Heart --- Cardiac Catheterization --- Cardiac Surgical Procedures --- Transcatheter Aortic Valve Replacement --- Heart Diseases --- Heart Defects, Congenital --- Abnormalities. --- Diseases --- Treatment. --- methods. --- surgery. --- Heart defects --- Abnormities and deformities --- methods --- surgery
Choose an application
"With the dramatic reduction of rheumatic disease and the increase in life expectancy, valvular diseases are now mostly degenerative in industrialized countries(1). Calcific aortic stenosis (AS) is the most common heart valve anomaly, with a largely age-dependent prevalence, a calculated annual incidence rate in the range of 4-5% in general populations and a marked increase up to 6% in patients greater than or equal to 75 years of age(2,3). Surgical aortic valve replacement (SAVR) was previously the only option available to patients with symptomatic, severe aortic stenosis, without which a median survival of 2 years was to be expected(4). After the first-in-human transcatheter aortic valve implantation (TAVI) performed by Alain Cribier in 2002(5), the treatment strategy for patients with symptomatic aortic stenosis has been revolutionized. In over 15 years, penetration of TAVI has grown exponentially, as a result of accruing evidence demonstrating safety and efficacy, and reduced invasiveness compared with SAVR"--
Aortic valve --- Cardiac catheterization --- Aortic Valve Stenosis --- Transcatheter Aortic Valve Replacement --- Intraoperative Complications --- Stenosis --- Surgery. --- Complications --- surgery --- adverse effects --- prevention & control --- therapy
Choose an application
This reprint focuses on the transcatheter treatment of the main structural heart diseases covering the latest innovations and hot topics on this subject. All the technological developments witnessed in recent decades have made structural heart disease interventions a growing field and have contributed to offering patients less invasive, more effective, and safe alternative approaches.
Medicine --- Cardiovascular medicine --- cerebral protection device --- transcatheter aortic valve replacement --- stroke --- cerebrovascular events --- bovine aortic arch --- TAVR --- percutaneous access --- vascular complications --- surgical cut-down --- transfemoral approach --- aortic stenosis --- transcatheter aortic valve implantation --- valvular heart disease --- congestion --- plasma volume --- risk stratification --- TAVI --- SAVR --- young --- balloon aortic valvuloplasty --- bridge therapy --- destination therapy --- heart failure --- transradial coronaro-angiography --- single-catheter technique --- coronary artery disease --- futility --- transfemoral --- transcatheter --- aortic valve --- vascular --- complications --- BASILICA --- coronary artery obstruction --- structural heart intervention --- transcatheter mitral valve replacement --- mitral regurgitation --- transoesophageal echocardiography --- cardiac computed tomography --- TAVI degeneration --- SAVR after TAVI --- long-term outcome of TAVI --- tricuspid regurgitation --- atrial functional tricuspid regurgitation --- transcatheter tricuspid valve interventions --- echocardiography --- three-dimensional echocardiography --- multimodality imaging --- sizing --- planning --- MDCT --- 3D echocardiography --- MRI --- n/a
Choose an application
Hereditary hemorrhagic telangiectasia (HHT) is an inherited disease that affects the blood vessels, and is characterized by direct connections between arteries and veins with no intervening capillaries. These abnormal vessels may appear in the skin as tiny red dilated blood vessels in the mouth, lips, fingers and toes. The presence of these vascular lesions in the mucosa can lead to spontaneous and recurrent nose bleeding, typically beginning in mid-childhood, and this is the most common clinical manifestation of HHT, occurring in over 90% of patients. Gastrointestinal bleeding, derived from mucocutaneous vascular lesions, affects approximately 25% of patients, almost always presenting after the age of 50. Chronic nasal and gastrointestinal bleeding can cause iron-deficiency anemia, and current therapeutic strategies are trying to minimize iron and blood transfusions. HHT patients also present large vascular lesions, known as arteriovenous malformations, that occur in internal organs like lungs, liver, and brain, and may result in life-threatening complications often related to the shunting of blood. This book not only highlights the current knowledge regarding diagnosis and treatment of HHT, but also the newest insights in the molecular basis of HHT, the understanding of which is essential for the development of new medicines or therapeutic strategies.
Research & information: general --- hereditary hemorrhagic telangiectasia --- rare diseases --- telangiectasis --- transforming growth factor-beta (TGF-β) --- Smad pathway --- gastrointestinal bleeding --- epistaxis --- nosebleeds --- tacrolimus --- nasal ointment --- genetic disease --- rare disease --- hereditary hemorrhagic telangiectasia (HHT) --- telangiectases --- mechanical damage --- sun-induced trauma --- vascular malformations --- Endoglin --- activin-receptor-like kinase 1 --- Hereditary Hemorrhagic Telangiectasia --- antithrombotic therapy --- anticoagulants --- antiplatelets --- bleeding --- safety --- HHT --- ALK1 --- endoglin --- raloxifene --- bazedoxifene --- tranexamic acid --- propranolol --- FK506 --- etamsylate --- N-acetylcysteine --- pulmonary arteriovenous malformations --- transcatheter embolotherapy --- screening --- guidelines --- Hereditary hemorrhagic telangiectasia --- pediatrics --- genotype–phenotype correlation --- arteriovenous malformation --- ENG --- ACVRL1 --- SMAD4 --- microRNA --- biomarker --- plasma --- arteriovenous malformations (AVMs) --- angiogenesis --- activin receptor-like kinase 1 (ALK1) --- transforming growth factor beta (TGF-β) --- bone morphogenetic protein (BMP) --- propranolol gel --- epistaxis severity score --- nasal endoscopy --- antiangiogenic properties --- non-coding RNAs --- microRNAs --- long non-coding RNAs --- biomarkers --- endothelial cells --- hereditary hemorrhagic telangiectasia (HHT), second-hit --- arteriovenous malformation (AVM) --- Smad4 --- inflammation --- shear stress --- vascular injury --- somatic mutation --- cell adhesion --- vascular endothelial growth factor (VEGF) --- telangiectasia --- hereditary hemorrhagic --- survival --- life expectancy --- pulmonary arteriovenous malformation --- contrast enhanced magnetic resonance angiography --- liver --- MRI --- ultrasound --- AVM --- bevacizumab --- Osler–Weber–Rendu --- hereditary hemorrhagic telangiectasia/HHT/osler’s disease --- cerebral ischemic lesions --- catheter based embolization therapy
Choose an application
There has been significant progress in the field of interventional cardiology, from the development of newer devices to newer applications of technology, resulting in improved cardiovascular outcomes. The goal of this Special Issue is to update practicing clinicians and provide a comprehensive collection of original articles, reviews, and editorials. To this end, we invited state-of-the-art reviews, including reviews of new technology and therapeutics, as well as original research in this area to be considered for inclusion in this issue. Examples include the history and evolution of interventional techniques, reviews of specific devices and technologies for coronary artery disease (i.e., stent technology, atherectomy devices, coronary physiology, intracoronary imaging, and robotics), structural heart diseases (i.e., ASD: atrial septal defect; LAAC: left atrial appendage closure; MC: MitraClip; PFO: patent foramen ovale; TAVI: transcatheter aortic valve implantation), advances in the management of challenging coronary anatomy, new biomarkers of cardiovascular disease (noncoding RNAs, etc.), and interventional techniques in the management of heart failure, peripheral arterial diseases, and pulmonary embolism. This Special Issue presents the most recent advances in the field of coronary and structural heart diseases as well as their implications for future patient care.
left atrial appendage --- WATCHMAN occlusive device --- 2D transesophageal echocardiography --- 3D transesophageal echocardiography --- computerized tomography --- atherosclerosis --- cholesterol --- FDG --- inflammation --- PET --- statins --- coronary artery bypass --- on-pump coronary artery bypass --- off-pump coronary artery bypass --- young patients --- severe aortic stenosis --- longitudinal axis strain --- late gadolinium enhancement --- cardiac magnetic resonance imaging --- optical coherence tomography --- percutaneous coronary interventions --- borderline lesions --- nonsignificant lesions --- left main --- bifurcations --- bilateral internal mammary artery --- coronary artery disease --- coronary artery bypass grafting --- da Vinci --- sternotomy --- outcome --- stent thrombosis --- bioresorbable scaffold --- drug eluting stents --- stent bioresorbable --- congenital heart disease --- cardiac surgery --- open heart --- progenitor cells --- regeneration --- stem cells --- subclinical coronary artery disease --- accelerated atherosclerosis --- HIV infection --- carotid intima-media thickness --- coronary calcium scoring --- coronary CT angiography --- magnetic resonance angiography --- fluorodeoxyglucose positron emission tomography --- mechanical circulatory support --- percutaneous coronary intervention --- cardiogenic shock --- acute myocardial infarction --- patient selection --- right heart catheterization --- pulmonary hypertension --- heart failure --- diagnosis --- prognostic evaluation --- clinical implications --- systemic disease --- cardiac computed tomography --- cardiac magnetic resonance --- feature tracking --- tagging --- myocardial deformation --- strain --- radial --- ulnar --- distal radial --- snuffbox --- aortic valvuloplasty --- dual antiplatelet therapy --- antiplatelet --- structural heart disease --- bioresorbable vascular scaffold --- drug-eluting stent --- angioplasty --- acute coronary syndrome --- chronic total occlusion --- target vessel failure --- re-occlusion --- surveillance coronary angiography --- meta-analysis --- ACURATE neo --- SAPIEN 3 --- transcatheter aortic valve replacement --- TAVR --- TAVI --- low risk --- STS --- aortic stenosis --- SAVR
Choose an application
Hereditary hemorrhagic telangiectasia (HHT) is an inherited disease that affects the blood vessels, and is characterized by direct connections between arteries and veins with no intervening capillaries. These abnormal vessels may appear in the skin as tiny red dilated blood vessels in the mouth, lips, fingers and toes. The presence of these vascular lesions in the mucosa can lead to spontaneous and recurrent nose bleeding, typically beginning in mid-childhood, and this is the most common clinical manifestation of HHT, occurring in over 90% of patients. Gastrointestinal bleeding, derived from mucocutaneous vascular lesions, affects approximately 25% of patients, almost always presenting after the age of 50. Chronic nasal and gastrointestinal bleeding can cause iron-deficiency anemia, and current therapeutic strategies are trying to minimize iron and blood transfusions. HHT patients also present large vascular lesions, known as arteriovenous malformations, that occur in internal organs like lungs, liver, and brain, and may result in life-threatening complications often related to the shunting of blood. This book not only highlights the current knowledge regarding diagnosis and treatment of HHT, but also the newest insights in the molecular basis of HHT, the understanding of which is essential for the development of new medicines or therapeutic strategies.
hereditary hemorrhagic telangiectasia --- rare diseases --- telangiectasis --- transforming growth factor-beta (TGF-β) --- Smad pathway --- gastrointestinal bleeding --- epistaxis --- nosebleeds --- tacrolimus --- nasal ointment --- genetic disease --- rare disease --- hereditary hemorrhagic telangiectasia (HHT) --- telangiectases --- mechanical damage --- sun-induced trauma --- vascular malformations --- Endoglin --- activin-receptor-like kinase 1 --- Hereditary Hemorrhagic Telangiectasia --- antithrombotic therapy --- anticoagulants --- antiplatelets --- bleeding --- safety --- HHT --- ALK1 --- endoglin --- raloxifene --- bazedoxifene --- tranexamic acid --- propranolol --- FK506 --- etamsylate --- N-acetylcysteine --- pulmonary arteriovenous malformations --- transcatheter embolotherapy --- screening --- guidelines --- Hereditary hemorrhagic telangiectasia --- pediatrics --- genotype–phenotype correlation --- arteriovenous malformation --- ENG --- ACVRL1 --- SMAD4 --- microRNA --- biomarker --- plasma --- arteriovenous malformations (AVMs) --- angiogenesis --- activin receptor-like kinase 1 (ALK1) --- transforming growth factor beta (TGF-β) --- bone morphogenetic protein (BMP) --- propranolol gel --- epistaxis severity score --- nasal endoscopy --- antiangiogenic properties --- non-coding RNAs --- microRNAs --- long non-coding RNAs --- biomarkers --- endothelial cells --- hereditary hemorrhagic telangiectasia (HHT), second-hit --- arteriovenous malformation (AVM) --- Smad4 --- inflammation --- shear stress --- vascular injury --- somatic mutation --- cell adhesion --- vascular endothelial growth factor (VEGF) --- telangiectasia --- hereditary hemorrhagic --- survival --- life expectancy --- pulmonary arteriovenous malformation --- contrast enhanced magnetic resonance angiography --- liver --- MRI --- ultrasound --- AVM --- bevacizumab --- Osler–Weber–Rendu --- hereditary hemorrhagic telangiectasia/HHT/osler’s disease --- cerebral ischemic lesions --- catheter based embolization therapy
Choose an application
There has been significant progress in the field of interventional cardiology, from the development of newer devices to newer applications of technology, resulting in improved cardiovascular outcomes. The goal of this Special Issue is to update practicing clinicians and provide a comprehensive collection of original articles, reviews, and editorials. To this end, we invited state-of-the-art reviews, including reviews of new technology and therapeutics, as well as original research in this area to be considered for inclusion in this issue. Examples include the history and evolution of interventional techniques, reviews of specific devices and technologies for coronary artery disease (i.e., stent technology, atherectomy devices, coronary physiology, intracoronary imaging, and robotics), structural heart diseases (i.e., ASD: atrial septal defect; LAAC: left atrial appendage closure; MC: MitraClip; PFO: patent foramen ovale; TAVI: transcatheter aortic valve implantation), advances in the management of challenging coronary anatomy, new biomarkers of cardiovascular disease (noncoding RNAs, etc.), and interventional techniques in the management of heart failure, peripheral arterial diseases, and pulmonary embolism. This Special Issue presents the most recent advances in the field of coronary and structural heart diseases as well as their implications for future patient care.
Medicine --- left atrial appendage --- WATCHMAN occlusive device --- 2D transesophageal echocardiography --- 3D transesophageal echocardiography --- computerized tomography --- atherosclerosis --- cholesterol --- FDG --- inflammation --- PET --- statins --- coronary artery bypass --- on-pump coronary artery bypass --- off-pump coronary artery bypass --- young patients --- severe aortic stenosis --- longitudinal axis strain --- late gadolinium enhancement --- cardiac magnetic resonance imaging --- optical coherence tomography --- percutaneous coronary interventions --- borderline lesions --- nonsignificant lesions --- left main --- bifurcations --- bilateral internal mammary artery --- coronary artery disease --- coronary artery bypass grafting --- da Vinci --- sternotomy --- outcome --- stent thrombosis --- bioresorbable scaffold --- drug eluting stents --- stent bioresorbable --- congenital heart disease --- cardiac surgery --- open heart --- progenitor cells --- regeneration --- stem cells --- subclinical coronary artery disease --- accelerated atherosclerosis --- HIV infection --- carotid intima-media thickness --- coronary calcium scoring --- coronary CT angiography --- magnetic resonance angiography --- fluorodeoxyglucose positron emission tomography --- mechanical circulatory support --- percutaneous coronary intervention --- cardiogenic shock --- acute myocardial infarction --- patient selection --- right heart catheterization --- pulmonary hypertension --- heart failure --- diagnosis --- prognostic evaluation --- clinical implications --- systemic disease --- cardiac computed tomography --- cardiac magnetic resonance --- feature tracking --- tagging --- myocardial deformation --- strain --- radial --- ulnar --- distal radial --- snuffbox --- aortic valvuloplasty --- dual antiplatelet therapy --- antiplatelet --- structural heart disease --- bioresorbable vascular scaffold --- drug-eluting stent --- angioplasty --- acute coronary syndrome --- chronic total occlusion --- target vessel failure --- re-occlusion --- surveillance coronary angiography --- meta-analysis --- ACURATE neo --- SAPIEN 3 --- transcatheter aortic valve replacement --- TAVR --- TAVI --- low risk --- STS --- aortic stenosis --- SAVR
Listing 1 - 10 of 11 | << page >> |
Sort by
|