Dilated cardiomyopathy (DCM) is characterized by dilatation and impaired systolic function of one or both ventricles. Five to eight people per 100,000 develop this disorder each year. It is more common in men. Malignant arrhythmias are the most common cause of death in DCM1. Around 50 % of cases of nonischaemic dilated cardiomyopathy are idiopathic. Other causes are familial, infectious, infiltrative and connective tissue diseases. This is a report of successful anesthetic management of a patient with severe DCM undergoing a surgical procedure using combined thoracic epidural analgesia (TEA) and general anesthesia (GA)
Dilated cardiomyopathy (DCM) is a clinical diagnosis characterized by left ventricular or biventricu...
Hypertrophic obstructive cardiomyopathy (HOCM) is a rare genetic disorder characterized by left vent...
This review highlights some essential concepts in the medical diagnosis of DCM patients, etiology an...
Dilated cardiomyopathy (DCM) is a form of cardiomyopathy characterized by left ventricular or bivent...
Dilated cardiomyopathy (DCM) describes a group of diseases involving the myocardium. Anesthesia mana...
We report a case of a 37 year old man, with history of rhabdomyosarcoma as a child. Patient develope...
AbstractDilated cardiomyopathy (DCM) is a form of cardiomyopathy characterized by left ventricular o...
Dilated cardiomyopathy with decreased contractility of left or both ventricles impose a serious risk...
Perioperative management of a patient with dilated cardiomyopathy (DCM) is challenging for an anesth...
AbstractIntroductionTakotsubo cardiomyopathy (TCM) is a stress-induced cardiomyopathy. It is charact...
Abstract Introduction: Takotsubo cardiomyopathy (TCM) is a stress-induced cardiomyopathy. It is cha...
Hypertrophic obstructive cardiomyopathy (HOCM) is a genetically mediated disease causing left ventri...
Hypertrophic cardiomyopathy (HCM) is the most common genetic cardiovascular disorder, characterized ...
This study focuses on some key issues in the medical diagnosis of DCM patients, such as etiology and...
Abstract Background and objectives: Dilated cardiomyopathy is a state of progressive enlargement of...
Dilated cardiomyopathy (DCM) is a clinical diagnosis characterized by left ventricular or biventricu...
Hypertrophic obstructive cardiomyopathy (HOCM) is a rare genetic disorder characterized by left vent...
This review highlights some essential concepts in the medical diagnosis of DCM patients, etiology an...
Dilated cardiomyopathy (DCM) is a form of cardiomyopathy characterized by left ventricular or bivent...
Dilated cardiomyopathy (DCM) describes a group of diseases involving the myocardium. Anesthesia mana...
We report a case of a 37 year old man, with history of rhabdomyosarcoma as a child. Patient develope...
AbstractDilated cardiomyopathy (DCM) is a form of cardiomyopathy characterized by left ventricular o...
Dilated cardiomyopathy with decreased contractility of left or both ventricles impose a serious risk...
Perioperative management of a patient with dilated cardiomyopathy (DCM) is challenging for an anesth...
AbstractIntroductionTakotsubo cardiomyopathy (TCM) is a stress-induced cardiomyopathy. It is charact...
Abstract Introduction: Takotsubo cardiomyopathy (TCM) is a stress-induced cardiomyopathy. It is cha...
Hypertrophic obstructive cardiomyopathy (HOCM) is a genetically mediated disease causing left ventri...
Hypertrophic cardiomyopathy (HCM) is the most common genetic cardiovascular disorder, characterized ...
This study focuses on some key issues in the medical diagnosis of DCM patients, such as etiology and...
Abstract Background and objectives: Dilated cardiomyopathy is a state of progressive enlargement of...
Dilated cardiomyopathy (DCM) is a clinical diagnosis characterized by left ventricular or biventricu...
Hypertrophic obstructive cardiomyopathy (HOCM) is a rare genetic disorder characterized by left vent...
This review highlights some essential concepts in the medical diagnosis of DCM patients, etiology an...