Impact of SARS-Cov-2 infection in patients with hypertrophic cardiomyopathy : results of an international multicentre registry

To describe the natural history of SARS-CoV-2 infection in patients with hypertrophic cardiomyopathy (HCM) compared with a control group and to identify predictors of adverse events. Three hundred and five patients [age 56.6 ± 16.9 years old, 191 (62.6%) male patients] with HCM and SARS-Cov-2 infection were enrolled. The control group consisted of 91 131 infected individuals. Endpoints were (i) SARS-CoV-2 related mortality and (ii) severe clinical course [death or intensive care unit (ICU) admission]. New onset of atrial fibrillation, ventricular arrhythmias, shock, stroke, and cardiac arrest were also recorded. Sixty-nine (22.9%) HCM patients were hospitalized for non-ICU level care, and 21 (7.0%) required ICU care. Seventeen (5.6%) died: eight (2.6%) of respiratory failure, four (1.3%) of heart failure, two (0.7%) suddenly, and three (1.0%) due to other SARS-CoV-2-related complications. Covariates associated with mortality in the multivariable were age {odds ratio (OR) per 10 year increase 2.25 [95% confidence interval (CI): 1.12-4.51], P = 0.0229}, baseline New York Heart Association class [OR per one-unit increase 4.01 (95%CI: 1.75-9.20), P = 0.0011], presence of left ventricular outflow tract obstruction [OR 5.59 (95%CI: 1.16-26.92), P = 0.0317], and left ventricular systolic impairment [OR 7.72 (95%CI: 1.20-49.79), P = 0.0316]. Controlling for age and sex and comparing HCM patients with a community-based SARS-CoV-2 cohort, the presence of HCM was associated with a borderline significant increased risk of mortality OR 1.70 (95%CI: 0.98-2.91, P = 0.0600). Over one-fourth of HCM patients infected with SARS-Cov-2 required hospitalization, including 6% in an ICU setting. Age and cardiac features related to HCM, including baseline functional class, left ventricular outflow tract obstruction, and systolic impairment, conveyed increased risk of mortality

Natural History of MYH7-Related Dilated Cardiomyopathy

BACKGROUND Variants in myosin heavy chain 7 (MYH7) are responsible for disease in 1% to 5% of patients with dilated cardiomyopathy (DCM); however, the clinical characteristics and natural history of MYH7-related DCM are poorly described. OBJECTIVES We sought to determine the phenotype and prognosis of MYH7-related DCM. We also evaluated the influence of variant location on phenotypic expression. METHODS We studied clinical data from 147 individuals with DCM-causing MYH7 variants (47.6% female; 35.6 +/- 19.2 years) recruited from 29 international centers. RESULTS At initial evaluation, 106 (72.1%) patients had DCM (left ventricular ejection fraction: 34.5% +/- 11.7%). Median follow-up was 4.5 years (IQR: 1.7-8.0 years), and 23.7% of carriers who were initially phenotype-negative developed DCM. Phenotypic expression by 40 and 60 years was 46% and 88%, respectively, with 18 patients (16%) first diagnosed at <18 years of age. Thirty-six percent of patients with DCM met imaging criteria for LV noncompaction. During follow-up, 28% showed left ventricular reverse remodeling. Incidence of adverse cardiac events among patients with DCM at 5 years was 11.6%, with 5 (4.6%) deaths caused by end-stage heart failure (ESHF) and 5 patients (4.6%) requiring heart transplantation. The major ventricular arrhythmia rate was low (1.0% and 2.1% at 5 years in patients with DCM and in those with LVEF of <= 35%, respectively). ESHF and major ventricular arrhythmia were significantly lower compared with LMNA-related DCM and similar to DCM caused by TTN truncating variants. CONCLUSIONS MYH7-related DCM is characterized by early age of onset, high phenotypic expression, low left ventricular reverse remodeling, and frequent progression to ESHF. Heart failure complications predominate over ventricular arrhythmias, which are rare. (C) 2022 The Authors. Published by Elsevier on behalf of the American College of Cardiology Foundation

Alteraciones de la estructura y función cardiaca en pacientes con enfermedad de Parkinson. Estudio con ecocardiografía y grupo control

Parkinson’s disease (PD) patients have most frequentlyheart failure regardless of the existence of cardiomyopathies or cardiovascular risk factors. However, the cause of this increased prevalence is not known. There are several pathophysiological hypotheses but they have not been studied in clinical practice. Thus, we designed a study to assess the cardiac function and structure in patients with PD compared with a control group. Methods: Cross-sectional study with 50 PD patients and 50 healthy matched controls. We excluded patients with known cardiopathy and valvular disease. We performed electroand echocardiograms to all patients and the measurements were blind. In addition, we performed a neurological assessment of patients with PD. Results: PD patients had higher left ventricular mass index (114.2± 38.4 g / m2 vs 94.1 ± 26.4 g / m2; p = 0.003), higher left atrial volumen (30.1 ± 7.9 ml/m2 vs 26.7 ± 6.2 ml/m2; p=0.01) and E / E' ratio (9.6 ± 3.1 vs 7.8 ± 1.7; p=0.001).They, also presented worse NYHA functional class due to diastolic dysfunction and the PD was an independent risk factor for elevated left ventricular filling pressures (OR=2.7, CI 95% 2.2-6.3; p=0.004). Concentric remodelling and left ventricular hypertrophy was associated with more advanced Hoehn and Yahr stages. Conclusions: Parkinson's disease is significantly associated with increased concentric left ventricular hypertrophy, atrial volume and diastolic dysfunction. Advanced stages of PDare associated with a more severe cardiac affection. Thesefindings can explain the increase of heart failure in PDpatients

Endoscopic Ultrasound for the Detection of Left Atrial Appendage Thrombus: A Useful Technique in Patients with Transesophageal Echocardiography Contraindication

Endoscopic ultrasound is a diagnostic and therapeutic technique used in specialized centers for patients that have undergone digestive procedures. This technique enables highly precise real-time imaging of the digestive tract wall and surrounding organs. Endoscopic ultrasound is also useful in patients with cardiovascular diseases such as atrial fibrillation. In patients with contraindication for transesophageal echocardiography due to high risk of esophageal bleeding or complications that may require immediate intervention, endoscopic ultrasound may be a safer option for visualizing atrial chambers to rule out the presence of left atrial appendage thrombi before cardioversion.S

Afectación cardiopulmonar por Citomegalovirus en individuos inmunocompetentes

Resumen: La infección por Citomegalovirus en adultos sanos suele cursar de forma asintomática o como un cuadro de mononucleosis. La afectación cardiopulmonar en individuos inmunocompetentes es infrecuente y se asocia a mal pronóstico. Su diagnóstico exige una elevada sospecha clínica. Se presenta el caso clínico de un paciente joven que debutó con clínica de neumonía atípica y en el estudio posterior se descubrió miocardiopatía dilatada con disminución de la contractilidad miocárdica. La serología para citomegalovirus fue positiva y el paciente recibió terapia antiviral específica con excelente resultado. Abstract: Cytomegalovirus infection in healthy adults is usually asymptomatic or as signs and symptoms of a mononucleosis. Cardiopulmonary involvement in immunocompetent individuals is uncommon and is associated with a poor prognosis. Its diagnosis requires a high clinical suspicion. The case is presented of a young patient in whom the first clinical sign was an atypical pneumonia, and in the subsequent study a dilated cardiomyopathy with a decrease in myocardial contractility was discovered. The serology for cytomegalovirus was positive, and the patient received specific antiviral therapy, with an excellent outcome. Palabras clave: Miocarditis, Virus, Infección, Insuficiencia cardíaca, Keywords: Myocarditis, Virus, Infection, Heart failur