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Similar Publications

Ventricular activation pattern of left ventricular septal pacing in a canine model.

J Interv Card Electrophysiol

August 2024

Department of Cardiology, The First People's Hospital of Yunnan Province, The Affiliated Hospital of Kunming University of Science and Technology, 157 Jinbi Road, 650032, Kunming, Yunnan Province, People's Republic of China.

Background: Left bundle branch pacing (LBBP) is a feasible and effective physiological pacing technique. The QRS morphology of left ventricular septal pacing (LVSP) is similar to that of LBBP. The ventricular activation pattern of LBBP is well-known, whereas the pattern of LVSP still needs further investigation.

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Due to low compliance by bedside nursing with a central line-associated bloodstream infection (CLABSI) prevention bundle and increased CLABSI rates, a mandatory re-education initiative at a 1200-bed university-affiliated hospital was undertaken. Despite this, 2 units, housing high-risk immunocompromised patients, continued to experience increased CLABSI rates. A quality improvement before-after project design in these units replaced bedside nursing staff with 2 nurses from the vascular access team (VAT) to perform central vascular access device (CVAD) dressing changes routinely every 7 days or earlier if needed.

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Sudden unexpected intrapartum death and left ventricular noncompaction involving the right ventricle.

Cardiovasc Pathol

May 2024

Department of Pathology and Laboratory Medicine, University of Texas Health Science Center at Houston (UTHealth), McGovern Medical School, Houston, TX 77030, USA.

Article Synopsis
  • Left ventricular noncompaction (LVNC) is a rare congenital heart disorder that primarily affects the right ventricle, showing a spongy myocardial appearance due to incomplete compression of the heart muscle.
  • A case is reported involving a 41-week female fetus who experienced sudden unexpected death during labor, where the right ventricular wall showed significant thickening and hypertrabeculation characteristic of LVNC.
  • The investigation revealed that the cause of death was linked to electrical conduction dysfunction due to LVNC, emphasizing the importance of comprehensive post-mortem examinations for unexpected fetal deaths, though standard guidelines are lacking.
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[Seroprevalence of Chagas disease at the Instituto Nacional de Cardiología Ignacio Chávez from 2004 to 2010].

Arch Cardiol Mex

March 2024

Departamento de Inmunología, Instituto Nacional de Cardiología Ignacio Chávez, Tlalpan, Ciudad de México, México.

Background: Different pathogens can cause dilated cardiomyopathy, one of them is Trypanosoma cruzi protozoan. T.cruzi-chronic infection causes chronic Chagasic cardiomyopathy and affects the sinus node and the conduction systembelow the bundle of His; besides, it shows excellent arrhythmogenic potential because of ventricular arrhythmias.

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Introduction: Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare inherited disorder usually affecting the right ventricle (RV), characterized by fibro-fatty tissue replacement of the healthy ventricular myocardium. It often predisposes young patients to ventricular tachycardia, heart failure, and/or sudden cardiac death. However, recent studies have suggested predominantly left ventricle (LV) involvement with variable and/or atypical manifestations.

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