Results 181 to 190 of about 44,165 (267)

Wide QRS Tachycardia in WPW: When Antidromic AVRT Imitates VT

open access: yesClinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Atrioventricular Re‐entry Tachycardia (AVRT) occurs in patients with accessory pathways (AP) via a re‐entry circuit between the AV node and the AP. Anterograde conduction through the AP causes antidromic AVRT with wide QRS complexes, which may mimic ventricular tachycardia (VT). We report a 59‐year‐old male with ischemic cardiomyopathy (EF 35%)
Aleksandra Grbović   +7 more
wiley   +1 more source

From Thrombolysis to Transplant: Navigating the Storm of Delayed STEMI and Cardiogenic Shock

open access: yesClinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Delayed STEMI presentation can cause extensive myocardial necrosis, left ventricular thrombus, cardiogenic shock, and progression to end‐stage heart failure despite reperfusion. Early recognition and timely transfer to specialized shock centers are critical.
Syed Rafay Hussain Zaidi   +8 more
wiley   +1 more source

Poland Syndrome With Dextrocardia: A Rare Association Leading to Complex Cardiopulmonary Challenges

open access: yesClinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Patients with Poland syndrome, especially those with left‐sided defects accompanied by dextrocardia, may be predisposed to significant respiratory and cardiac complications. This case underscores the importance of early recognition, thorough cardiopulmonary assessment, and proactive planning for airway management and ventilatory support to ...
Sai Kommineni   +4 more
wiley   +1 more source

Adaptive immune response to the autoantigen LL‐37 differentiates atherosclerotic cardiovascular disease phenotypes

open access: yesClinical &Translational Immunology, Volume 15, Issue 3, 2026.
The study provides evidence that the immune response to the antimicrobial peptide LL‐37 differentiates atherosclerotic cardiovascular disease phenotypes. Stable MI patients had a distinct CD4+ T cell response to LL‐37 with a differential LL‐37 IgG immune complex subclass compared to stroke.
Paul C. Dimayuga   +6 more
wiley   +1 more source

Wolf Creek XVIII Part 3: Innovations in Defibrillation Science. [PDF]

open access: yesResusc Plus
Koster RW   +4 more
europepmc   +1 more source

The Effects of Nitrate on Brown Fat Fraction and Activation in Older Adults With Type 2 Diabetes: A Randomised, Double‐Blind and Placebo‐Controlled Crossover Trial

open access: yesEuropean Journal of Sport Science, Volume 26, Issue 3, March 2026.
ABSTRACT Type 2 diabetes mellitus (T2DM) is a metabolic disease characterised by chronic hyperglycaemia, whereas obesity is a major risk factor which increases morbidity and mortality. Treatments that alter white adipose tissue to express a metabolically active brown adipose phenotype in rats may offer adjunct treatment in people with T2DM.
Rebecca A. Neal   +13 more
wiley   +1 more source

Impact of remote biometric sensing on readmission risk and mortality after hospital discharge: Insights from a systematic review and meta‐analysis

open access: yesJournal of Hospital Medicine, Volume 21, Issue 3, Page 298-307, March 2026.
Abstract Introduction Unplanned hospital readmissions are associated with higher morbidity, mortality, and financial burden. This study evaluated the association between the use of remote biometric sensing devices (RBS) and all‐cause readmission and mortality rates among adult patients discharged from the hospital.
Parisa Farahani   +15 more
wiley   +1 more source

Protocol of the RADIO-STAR trial: a phase 1 safety and dose finding study of hypofractionated radiotherapy to the stellate ganglia for the treatment of ventricular arrhythmia. [PDF]

open access: yesBMJ Open
Bussmann BM   +11 more
europepmc   +1 more source

A Meta‐Analysis to Unveil the Diagnostic Gaps in Anderson–Fabry Disease in Women

open access: yesJournal of Inherited Metabolic Disease, Volume 49, Issue 2, March 2026.
ABSTRACT Anderson–Fabry disease (AFD) is an X‐linked lysosomal storage disorder caused by mutations in the GLA gene, leading to deficient α‐galactosidase A activity. Although historically considered a male disease, it is now recognized that heterozygous women can present with a wide range of symptoms. However, diagnosis in women remains challenging, as
L. Lenzini   +6 more
wiley   +1 more source

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