Publications by authors named "Andrew Gaballa"

Background: Mavacamten is commercially approved for use in symptomatic obstructive hypertrophic cardiomyopathy (oHCM) patients. This study evaluated its real-world impact on symptoms, echocardiographic changes, and the need for septal reduction therapy (SRT) in oHCM patients treated at a multi-hospital referral center.

Methods: We included 244 oHCM patients (mean age 64 years, 57% female, 21% with atrial fibrillation, 51% New York Heart Association [NYHA] Class III, 82% on beta-blockers) treated with mavacamten for ≥3 months (171 for ≥12 months).

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Introduction Clostridioides difficile infection (CDI) leads to significant morbidity and mortality in hospitalized patients. We aim to investigate whether chronic kidney disease (CKD) or end-stage renal disease (ESRD) are predictors of mortality in admitted patients with CDI, and whether the presence of inflammatory bowel disease (IBD) has any impact on the mortality rate.  Methods The data of 133,099 hospitalized patients with CDI were analyzed from the National Inpatient Sample (NIS) database from 2016 to 2018.

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Calcium supplement intake, with or without vitamin D supplementation, has risen amongst the older population, who are more likely to have deficiencies. Our aim was to investigate how the supplementation of calcium and vitamin D is associated with survival in patients with moderate concomitant aortic and mitral valve disease. A total of 3,257 patients (mean age of 71.

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Background: There is an emerging interest in artificial intelligence-enhanced 12-lead electrocardiogram (AI-ECG) in detection of hypertrophic cardiomyopathy (HCM).

Objectives: This study describes the initial real-world experience of using AI-ECG (Viz-HCM, developed using a convolutional neural network trained algorithm) in our center.

Methods: All patients undergoing 12-lead electrocardiograms at Cleveland Clinic, Cleveland, Ohio, between February 19, 2024, and November 1, 2024, were prospectively analyzed for potential HCM using AI-ECG.

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Article Synopsis
  • AI-ECG can effectively detect hypertrophic cardiomyopathy (HCM) and track treatment responses using 12-lead ECGs.
  • The study analyzed data from patients undergoing surgical reduction and those receiving mavacamten at multiple healthcare centers, finding no improvement in HCM scores after surgery, but a significant decrease in scores among patients taking mavacamten.
  • This highlights AI-ECG's potential for ongoing monitoring of heart condition improvements following medication rather than surgical interventions.
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Background: In hypertrophic cardiomyopathy, histologic findings like myocyte hypertrophy and disarray, interstitial fibrosis (IF), and small intramural coronary artery dysplasia (SICAD) result in left ventricular hypertrophy, diastolic dysfunction, arrhythmogenicity, and microvascular ischemia.

Objectives: The authors sought to evaluate the association between histology and outcomes in obstructive hypertrophic cardiomyopathy (oHCM) patients undergoing surgical myectomy (SM).

Methods: The study included 1,722 symptomatic oHCM patients (mean age: 56 ± 14 years; 948 [55%] men) who underwent SM at a tertiary center between 2005 and 2018.

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Background: Apical hypertrophic cardiomyopathy (aHCM) is a distinct variant characterized by predominant hypertrophy of the left ventricle apex.

Objectives: This study sought to describe aHCM patients' characteristics and develop a risk score for aHCM patients.

Methods: A total of 462 patients (age 58 ± 15 years, 68% male) diagnosed with aHCM were included.

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Background: In severely symptomatic patients with obstructive hypertrophic cardiomyopathy, VALOR-HCM (A Study to Evaluate Mavacamten in Adults With Symptomatic Obstructive Hypertrophic Cardiomyopathy Who Are Eligible for Septal Reduction Therapy) demonstrated that mavacamten reduces the need for septal reduction therapy with sustained improvement in left ventricular (LV) outflow tract gradients and symptoms. Global longitudinal strain (GLS), a measure of regional myocardial function, is a more sensitive marker of systolic function. In VALOR-HCM, we assessed serial changes in LV and right ventricular (RV) strain.

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Introduction: Hypertrophic cardiomyopathy (HCM) is a heterogeneous genetic heart disease with an estimated prevalence in the general population of 0.2% to 0.6%.

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Article Synopsis
  • Mavacamten is approved for treating symptomatic obstructive hypertrophic cardiomyopathy (oHCM) and aims to improve left ventricular outflow tract gradients and reduce the need for septal reduction therapy (SRT).
  • A study of 150 patients showed significant improvements in New York Heart Association (NYHA) class and reduced LVOT gradients after 12 weeks of mavacamten treatment, with 46% of patients showing at least one class improvement.
  • Although there was a slight decline in left ventricular ejection fraction (LVEF), no patients required SRT or experienced severe heart failure complications during the study period.
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Article Synopsis
  • Artificial intelligence-enhanced electrocardiography (AI-ECG) can detect hypertrophic cardiomyopathy (HCM) and monitor treatment responses through ECGs, presenting a modern alternative to surgical options like septal reduction therapy (SRT) and oral treatments like mavacamten.
  • A study involving patients from multiple health systems showed no significant change in AI-ECG HCM scores after SRT, indicating that this surgical method may not effectively improve HCM scores.
  • In contrast, patients on mavacamten therapy showed a significant decrease in their AI-ECG scores over a median follow-up period, suggesting that AI-ECG could be useful for regularly tracking improvements in HCM
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