Sameh M. Said

ORCID: 0000-0003-2193-0314
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Congenital Heart Disease Studies
  • Cardiac Valve Diseases and Treatments
  • Cardiac Structural Anomalies and Repair
  • Aortic Disease and Treatment Approaches
  • Infective Endocarditis Diagnosis and Management
  • Coronary Artery Anomalies
  • Tracheal and airway disorders
  • Cardiac Arrhythmias and Treatments
  • Vascular anomalies and interventions
  • Congenital Diaphragmatic Hernia Studies
  • Cardiovascular Issues in Pregnancy
  • Cardiovascular and Diving-Related Complications
  • Cardiomyopathy and Myosin Studies
  • Cardiac tumors and thrombi
  • Cardiac and Coronary Surgery Techniques
  • Cardiovascular Function and Risk Factors
  • Mechanical Circulatory Support Devices
  • Cardiac pacing and defibrillation studies
  • Pulmonary Hypertension Research and Treatments
  • Cardiac, Anesthesia and Surgical Outcomes
  • Trauma Management and Diagnosis
  • Congenital Anomalies and Fetal Surgery
  • Transplantation: Methods and Outcomes
  • Aortic aneurysm repair treatments
  • Cardiovascular Effects of Exercise

Maria Fareri Children's Hospital
2022-2025

New York Medical College
2022-2025

Westchester Medical Center
2022-2025

Alexandria University
2003-2025

Karachi Medical and Dental College
2024

National Centre for Nuclear Energy, Science and Technology
2024

University of Minnesota
2020-2023

University of Minnesota Children's Hospital
2019-2023

Zagazig University
2008-2023

Federal University Dutsin-Ma
2022

Hypertrophic cardiomyopathy (HCM) is a primary myocardial disease characterized by left ventricular hypertrophy in the absence of other etiologies. Clinical presentation may vary from asymptomatic to sudden cardiac death. Medical treatment first-line therapy for symptomatic patients. Extended septal myectomy procedure choice if medical unsuccessful or intolerable.More than 3,000 patients have had HCM at Mayo Clinic (MN, USA) 1993 2016. Risk hospital death after isolated obstructive <1% and...

10.21037/acs.2017.07.03 article EN Annals of Cardiothoracic Surgery 2017-07-01

Physiologic dead space was determined in the supine and upright postures by simultaneous sampling subsequent analysis of arterial blood expired gas for Pco2. In seven normal men there invariably a higher than position. The difference averaged 83 ml statistically significant (S.E. 25 P &lt; 0.01). ratio to tidal volume also increased on assuming posture. Evidence is presented believing that most change physiologic resulted from alveolar space. Estimated changes suggest approximately one...

10.1152/jappl.1959.14.3.339 article EN Journal of Applied Physiology 1959-05-01

Abstract Background: Apical and midventricular hypertrophic cardiomyopathy (HCM) are rare variants of HCM, in which the hypertrophy is located mainly at to apical levels. Heart transplantation was only possible surgical solution for many these patients; however, transapical myectomy represents another good alternative. We present our technique ventriculotomy myectomy. Technique: A 6-cm incision made apex heart lateral left anterior descending coronary artery. The provides excellent exposure...

10.1111/j.1540-8191.2012.01475.x article EN Journal of Cardiac Surgery 2012-05-29

Background Stenosis of the venous connections and conduits is a well-known late complication Fontan procedure. Currently, data on outcomes percutaneous intervention for treatment extra- or intracardiac lateral tunnel baffles obstruction are limited. In an attempt to better define nature severity stenosis results catheter interventional management, we reviewed patients with obstructed baffles. Methods Retrospective review all who had cardiac catheterization from January 2002 October 2018 was...

10.1111/chd.12757 article EN cc-by-nc-nd Congenital Heart Disease 2019-02-25

Objective Valve repair for pediatric patients with Ebstein anomaly has historically yielded varied results. The cone reconstruction (CR) first described by Da Silva revolutionized the surgical approach to these patients. This study reports our recent experience CR in children and young adults anomaly. Design Electronic medical records were reviewed all < 21 years old who had surgery at Mayo Clinic Rochester between June 2007 December 2012. Clinical data including preoperative demographics,...

10.1111/chd.12155 article EN Congenital Heart Disease 2013-12-23

10.1053/j.optechstcvs.2012.04.002 article EN publisher-specific-oa Operative Techniques in Thoracic and Cardiovascular Surgery 2012-01-01

Mitral annular calcifications have been known to increase complexity during mitral valve replacement (MVR). Standard procedure requires decalcification followed by reconstruction of the annulus prior placing prosthesis. While this is ideal technique, it not feasible in every patient due associated risks. The mere attempt at without proper has with a high incidence periprosthetic leak which complicates postoperative course and increased morbidity mortality. With advances transcatheter...

10.5761/atcs.nm.24-00081 article EN Annals of Thoracic and Cardiovascular Surgery 2025-01-01

An 8-week-old, 3.4-kg infant, who was diagnosed prenatally with tetralogy of Fallot and absent pulmonary valve syndrome, intubated after birth failed extubation due to severe tracheobronchomalacia. He deemed inoperable prior being transferred our institution. The left artery severely aneurysmal the point occupying almost entire upper lobe. Standard repair performed together bilateral reduction arterioplasties a modified Lecompte manoeuvre. No interventions were done directly airways. In this...

10.1510/mmcts.2024.124 article EN Multimedia Manual of Cardio-Thoracic Surgery 2025-01-20

A 3-month-old, 5.2-kg infant with Williams syndrome presented failure to thrive and a systolic murmur. He was taken the cardiac catheterization laboratory for planned pulmonary valvotomy based on findings of severe stenosis transthoracic echocardiogram. However, he suffered arrest had be resuscitated; procedure aborted. Cardiac revealed suprasystemic right ventricular pressure bilateral branch artery hypoplasia. The decision made proceed surgical relief obstruction.

10.1510/mmcts.2024.117 article EN Multimedia Manual of Cardio-Thoracic Surgery 2025-02-03

Background Minimally invasive thoracotomies to repair selected congenital heart defects are considered only a cosmetic alternative approach by many; however, they represent the routine in centers of expertise. Methods Pooled institutional data from European Congenital Heart Surgeons Association using mini-thoracotomy approaches were analyzed since beginning their respective experiences until an inclusion surgical date January 31, 2024, allowing at least six months postoperative follow-up....

10.1177/21501351251322155 article EN cc-by World Journal for Pediatric and Congenital Heart Surgery 2025-03-25

An 18-year-old female presented with cyanosis and clubbing. She was diagnosed late congenitally corrected transposition of the great arteries a ventricular septal defect severe left outflow tract obstruction. had no history prior interventions. Anatomical repair performed, she is doing well as most recent follow-up.

10.1510/mmcts.2024.141 article EN Multimedia Manual of Cardio-Thoracic Surgery 2025-04-01
Coming Soon ...