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1.
J Cardiovasc Med (Hagerstown) ; 9(3): 239-44, 2008 Mar.
Article in English | MEDLINE | ID: mdl-18301139

ABSTRACT

BACKGROUND: Takotsubo cardiomyopathy consists of reversible systolic left ventricular apical ballooning associated with chest pain. Electrocardiographic abnormalities and the minimal rise of serum cardiac markers are similar to those in acute myocardial infarction, but without evidence of myocardial ischemia or injury. To date, many reports concerning this kind of acute reversible heart failure have been published, but the information available about the management of affected patients is scarce and the clinical data are incomplete. AIMS: In the present study, we report a collection of 40 patients who were affected by Takotsubo cardiomyopathy obtained in a multicentric international study, aiming to investigate the origins, and the clinical and instrumental patterns, and to establish the best diagnostic criteria for this syndrome. METHODS AND RESULTS: In the analysed group, the mean age was 68 years, of whom 85% were women. On admission to hospital, 68% of patients reported chest pain. An electrocardiogram (ECG) showed anterolateral (34%) or anterior (36%) ST segment elevation. The ECG demonstrated hyperkinesis of the basal segments with a severe hypokinesis of the other segments. Mean ejection fraction was 42.53%. Three patients died within the first 24 h from acute heart failure. The remaining 37 patients showed a complete resolution of symptoms and a complete normalization of the kinesis deficiency. Sixteen patients underwent myocardial scintigraphy, nine cases underwent myocardial biopsy and two patients received an ergonovine test. CONCLUSION: Our results demonstrate a good course of Takotsubo cardiomioathy, after the initial phase. An echocardiogram is an important tool for improving the diagnosis.


Subject(s)
Echocardiography/methods , Electrocardiography/methods , Gated Blood-Pool Imaging/methods , Takotsubo Cardiomyopathy/diagnosis , Aged , Coronary Angiography , Diagnosis, Differential , Exercise Test , Female , Follow-Up Studies , Humans , Male , Myocardial Contraction/physiology , Prognosis , Severity of Illness Index , Stroke Volume/physiology , Takotsubo Cardiomyopathy/physiopathology , Time Factors
2.
Int J Cardiol ; 127(1): 121-3, 2008 Jun 23.
Article in English | MEDLINE | ID: mdl-17544159

ABSTRACT

BACKGROUND: Takotsubo cardiomyopathy is a disorder that has been appreciated only recently. In most of reported cases, this syndrome mimes an acute myocardial infarction. Till this moment no data are available from literature about the treatment in the acute phase of this disease. AIM OF THE STUDY: In our multicentric experience we have retrospectively looked at the benefits of a treatment with ACE-inhibitors, beta-blockers, Aspirin and calcium channels blockers, started until the early phases of the disease and continued for 30 days, in 36 patients affected by Takotsubo cardiomyopathy. We chose as endpoint of the study the efficacy of the used drug in improving left ventricular myocardial function and the rapidity of the effects of the same drug.bethods: from an international registry about the Takotsubo cardiomiopathy, co-ordinate by our research group, we evaluated the long term efficacy of some drugs, administrated like single treatment in some patients. RESULTS: Obtained data did not show any statistically significant difference in the percentages of improvement in the left ventricle ejection fraction evaluated at the admission to the hospital, before the discharge and after 30 days of treatment between each treated group and the control group of non-treated patients. No significant differences were found in hospitalization times between treated patients and controls. None of our patients experienced during the observation period a relapse of the disease. CONCLUSIONS: The results of our survey suggest that a chronic treatment with beta-blockers, ACE-inhibitors, calcium channels blockers and aspirin does not provide any benefit in patients with Takotsubo cardiomyopathy. Thus, it seem to be important an early correct differential diagnosis to avoid any chronic treatment in these patients.


Subject(s)
Takotsubo Cardiomyopathy/drug therapy , Adrenergic beta-Antagonists/therapeutic use , Aged , Angiotensin-Converting Enzyme Inhibitors/therapeutic use , Aspirin/therapeutic use , Calcium Channel Blockers/therapeutic use , Female , Humans , Male , Retrospective Studies , Treatment Outcome
3.
Int J Cardiol ; 127(2): 255-6, 2008 Jul 04.
Article in English | MEDLINE | ID: mdl-17467827

ABSTRACT

BACKGROUND: Isolated left ventricular noncompaction is the result of incomplete myocardial morphogenesis, leading to persistence of the embryonic myocardium. The condition is recognised by an excessively prominent trabecular meshwork and deep intertrabecular recesses of the left ventricle. Whether these intertrabecular recesses are a favorable substrate for supraventricular arrhythmias is unclear, even if the incidence of chronic heart failure seems to be high. RESULTS: We evaluated a continuous series of 238 patients affected by noncompaction. In 4 cases the patients reported palpitations and in 4 an episode of syncope. Periodic holter monitoring was performed every 6 months for 4 years. Only 9 patients had documented atrial fibrillation. In no cases we observed supraventricular tachycardia. CONCLUSIONS: Noncompaction alone does not seem to be a risk factor for supraventricular arrhythmias.


Subject(s)
Heart Defects, Congenital/complications , Tachycardia, Supraventricular/etiology , Adult , Aged , Aged, 80 and over , Electrocardiography , Female , Heart Defects, Congenital/physiopathology , Humans , Italy/epidemiology , Male , Middle Aged , Registries , Retrospective Studies , Risk Factors , Tachycardia, Supraventricular/epidemiology , Tachycardia, Supraventricular/physiopathology
4.
G Ital Cardiol (Rome) ; 8(2): 129-32, 2007 Feb.
Article in Italian | MEDLINE | ID: mdl-17402358

ABSTRACT

Isolated noncompaction of left ventricular myocardium is a rare congenital heart disease, characterized by an excessive prominence of trabecular meshwork, spaced out by deep intertrabecular recesses, consequent to the arrest of the normal myocardial embryogenesis. Although there are numerous descriptions, the pathophysiological effects of the structural alterations, like the clinical spectrum and the evolution of the disease, are not fully clarified. In this paper we evaluated the natural history of the disease, the family incidence and the alterations of the systolic and diastolic function. An interesting case report is described concerning a patient affected by noncompaction and atrial fibrillation.


Subject(s)
Atrial Fibrillation/etiology , Heart Defects, Congenital , Heart Failure/etiology , Heart Ventricles/abnormalities , Adult , Atrial Fibrillation/drug therapy , Atrial Fibrillation/surgery , Atrial Fibrillation/therapy , Catheter Ablation , Echocardiography , Electrocardiography , Follow-Up Studies , Heart Defects, Congenital/complications , Heart Defects, Congenital/diagnosis , Heart Failure/drug therapy , Humans , Magnetic Resonance Imaging , Male , Pacemaker, Artificial , Time Factors , Treatment Outcome
5.
Pacing Clin Electrophysiol ; 30(4): 544-6, 2007 Apr.
Article in English | MEDLINE | ID: mdl-17437580

ABSTRACT

BACKGROUND: Isolated left ventricular non-compaction is the result of incomplete myocardial morphogenesis, leading to persistence of the embryonic myocardium. The condition is recognized by an excessively prominent trabecular meshwork and deep intertrabecular recesses of the left ventricle. Whether these intertrabecular recesses are a favorable substrate for ventricular arrhythmias is unclear. Some reports have found that the fatal ventricular arrhythmias may occur in approximately half of the patients. In this report we investigated about this association. METHODS AND RESULTS: In total we evaluated a continuous series of 238 patients affected by non-compaction. Periodic Holter monitoring was performed every 6 months for 4 years. Only 11 patients had documented ventricular tachycardia, which was sustained in two cases and non-sustained in nine. In no cases we observed ventricular fibrillation. CONCLUSIONS: Non-compaction alone does not seem to be a risk factor for malignant ventricular arrhythmias.


Subject(s)
Heart Defects, Congenital/complications , Tachycardia, Ventricular/etiology , Adult , Child, Preschool , Electrocardiography , Female , Humans , Italy/epidemiology , Male , Middle Aged , Registries , Retrospective Studies , Risk Factors , Tachycardia, Ventricular/epidemiology
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