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1.
Int Heart J ; 52(6): 401-5, 2011.
Article in English | MEDLINE | ID: mdl-22188717

ABSTRACT

Nemaline myopathy is a representative form of congenital myopathy, and is characterized by nemaline bodies in muscle fibers. Here we report a 47-year-old man with congenital nemaline myopathy complicated with dilated cardiomyopathy-related heart failure, and restrictive respiratory failure. The complication of dilated cardiomyopathy in nemaline myopathy has rarely been reported. In this case, nemaline bodies were detected in the cardiac muscle fibers, demonstrating the presence of underlying disease-related myocardial degeneration. The patient responded to the combination of conventional therapy for heart failure including ß-blocker and noninvasive continuous positive-pressure ventilation for respiratory failure. His general condition has been stable during a 10-month follow up period.


Subject(s)
Cardiomyopathy, Dilated/complications , Myopathies, Nemaline/complications , Positive-Pressure Respiration , Respiratory Insufficiency/etiology , Cardiomyopathy, Dilated/physiopathology , Disease Progression , Echocardiography , Follow-Up Studies , Humans , Male , Middle Aged , Respiratory Insufficiency/physiopathology , Respiratory Insufficiency/therapy
2.
J Cardiol Cases ; 3(2): e62-e64, 2011 Apr.
Article in English | MEDLINE | ID: mdl-30532838

ABSTRACT

An 86-year-old woman was admitted to the hospital for syncope and convulsion 4 days after starting antibiotic therapy for pneumonia with oral garenoxacin 400 mg/day. She had a VDD pacemaker for complete atrioventricular (AV) block. Her electrocardiogram showed marked QT prolongation and during pacemaker interrogation pacing failure probably due to battery depletion induced torsades de pointes. After cessation of garenoxacin, QTc returned to normal range subsequently and a new pacemaker was implanted. In patients with risks of QT prolongation, garenoxacin should be used cautiously with QT interval monitoring.

3.
Circ J ; 70(4): 442-6, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16565562

ABSTRACT

BACKGROUND: Although nifekalant is a class III antiarrhythmic agent without negative inotropic activity, its effect in patients with shock-refractory ventricular fibrillation remains unclear. METHODS AND RESULTS: Patients who had an out-of-hospital cardiac arrest with ventricular fibrillation that persisted after 3 shocks from an external defibrillator, intravenous epinephrine, and another shock were retrospectively studied. The patients received lidocaine from January 1997 through June 2001 and nifekalant from July 2001 through December 2004. Short-term survival rates (survival to hospital admission and 24-h survival) were compared between the groups. The study group comprised 120 patients (mean age: 62+/-16 years): 55 received nifekalant and 65 received lidocaine. Age, sex, history of ischemic heart disease, whether arrest was witnessed or not and time to arrival at the hospital did not differ significantly between the groups. As compared with lidocaine, nifekalant was associated with significantly higher rates of survival to hospital admission (67% vs 37%, p<0.001) and 24-h survival (53% vs 31%, p=0.01). Multivariate analysis showed that treatment with nifekalant and early initiation of cardiopulmonary resuscitation were independent predictors of 24-h survival. CONCLUSIONS: As compared with lidocaine, nifekalant may improve short-term survival in patients with out-of-hospital cardiac arrest due to shock-refractory ventricular fibrillation.


Subject(s)
Anti-Arrhythmia Agents/therapeutic use , Cardiopulmonary Resuscitation , Lidocaine/therapeutic use , Pyrimidinones/therapeutic use , Ventricular Fibrillation/drug therapy , Aged , Epinephrine/therapeutic use , Female , Heart Arrest/drug therapy , Heart Arrest/mortality , Heart Arrest/physiopathology , Humans , Male , Middle Aged , Multivariate Analysis , Retrospective Studies , Survival Rate , Time Factors , Ventricular Fibrillation/etiology , Ventricular Fibrillation/mortality
4.
Ann Thorac Cardiovasc Surg ; 10(1): 64-6, 2004 Feb.
Article in English | MEDLINE | ID: mdl-15008705

ABSTRACT

It remains unclear whether or not the infarcted brain caused by aortic dissection should be reperfused when an emergency operation is needed for aortic arch dissection. A 64-year-old woman presented with severe back pain and syncope with a sudden left hemiplegia. CT scan demonstrated an aortic dissection of the entire aorta, obstruction of the right common carotid artery by extended aortic dissection, cerebral infarction of the right middle cerebral artery territory, brain edema and pericardial effusion. Though she was unable to communicate with us, she underwent an emergent aortic arch replacement and ligature of the right common carotid artery nine hours after the onset of stroke, when massive cerebral infarction was established. She survived the operation and regained full consciousness. When brain infarction was established by extended aortic dissection in emergent aortic surgery, concomitant ligature of the responsible artery to the brain infarction may be allowed for avoiding cerebral damage leading to brain death.


Subject(s)
Aorta, Thoracic/surgery , Aortic Rupture/complications , Aortic Rupture/surgery , Carotid Artery, Common/surgery , Infarction, Middle Cerebral Artery/etiology , Brain Edema/prevention & control , Female , Humans , Intracranial Hemorrhages/prevention & control , Ligation , Middle Aged
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