Mostrando entradas con la etiqueta Cardiomyopathies. Mostrar todas las entradas
Mostrando entradas con la etiqueta Cardiomyopathies. Mostrar todas las entradas

miércoles, 12 de septiembre de 2018

Libro sobre Cardiomiopatias / Book on Cardiomyopathies

Septiembre  11, 2018. No. 3183
Cardiomiopatías. Tipos y manejos
Cardiomyopathies Types and Treatments
Sakarya University, Turkey
Cardiomyopathies are the most featured cardiac pathologies in the twenty-first century, that threaten public health and burden healthcare budgets. This book is composed of the main topics on pathophysiology, general forms and specific types of cardiomyopathies and it also introduces new research in the field. Specific forms with or without genetic inheritance are discussed separately to attract the readers' attention on these topics. Well-known medical follow-up strategies occur ineffective at the end-stage heart failure, however, new surgical approaches can be an alternative for these patients to get a chance at the last crossroad and to improve their life quality and survival and also to gain or prolong time until possible heart transplantation.
Cardiomiopatías y anestesia
Cardiomyopathies and anaesthesia.
Indian J Anaesth. 2017 Sep;61(9):728-735. doi: 10.4103/ija.IJA_385_17.
Abstract
Cardiomyopathy is considered as a heart muscle disease of multiple aetiologies, unlike other cardiac diseases related to a definitive pathophysiology. With more and more research and with the advent of genetic analysis pin pointing the disease causing mutations, causative factors have been defined and classifications and definitions have changed over time. Patients with these conditions present to anaesthesiologists in elective and emergency situations, placement of automated internal cardioverter defibrillator (AICD) devices or biventricular pacing but may also be diagnosed at anaesthetic pre-assessment. We describe cardiomyopathies such as dilated cardiomyopathy, hypertrophic cardiomyopathy, post-partum cardiomyopathy and Takotsubo cardiomyopathy in brief and their anaesthetic management.
KEYWORDS: Anaesthesiologist; cardiomyopathy; hypertrophic cardiomyopathy
Anestesia en pacientes con cardiomiopatía dilatada para cirugía no cardiaca
Anesthetic management of patients with dilated cardiomyopathy for noncardiac surgery.
Eur Rev Med Pharmacol Sci. 2017 Feb;21(3):627-634.Abstract
Anesthetic management of patients with dilated cardiomyopathy (DCM) is a challenge to the anesthesiologist, due to poor left systolic function, ventricular enlargement, risk of malignant arrhythmias and sudden cardiac death. Therefore, preoperative assessment and appropriate anesthetic management are important in patients with DCM. This review describes the preoperative evaluation and anesthesiaconsiderations of patients with DCM undergoing non-cardiac surgery. Patient pathophysiology and clinical status, such as ventricular function, degree of myocardial fibrosis, resting heart rate and high-sensitivity C-reactive protein can affect survival rates. Advanced monitoring devices, such as transesophageal echocardiography and cardiac resynchronization therapy can be used to assess ventricular function and myocardial fibrosis. Thoracic epidural blockade can improve ventricular function. In summary, the optimal anesthetic management of patients with dilated cardiomyopathy requires good preoperative assessment, close perioperative monitoring, suitable anesthetic, optimization fluid management, and stable hemodynamic status.

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