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2.
J Electrocardiol ; 76: 79-84, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-36512934

RESUMEN

BACKGROUNDS: Study concerning the clinical features, electrocardiogram (ECG) findings and outcomes in patients presenting with acute total occlusion of left main coronary artery (LM) without collateral circulation is limited. METHODS: 25 patients with acute total LM occlusion without collateral circulation by emergency coronary angiography, from muti-center registry, were retrospectively studied. The clinical and angiographic characteristics, ECG and in-hospital mortality were reviewed. RESULTS: Nineteen patients (76%) presented with cardiogenic shock. Twelve (60%, 12/20) patients had coronary slow flow or no reflow phenomenon after primary percutaneous coronary intervention (PCI). The in-hospital mortality rate was 88% (n = 22). All the patients presented with ST-segment elevation myocardial ischemia (STEMI) pattern, mostly involving leads I, aVL, V2, V3, V4, V5 and ST-segment depression in leads II, III and aVF. CONCLUSIONS: Acute total LM occlusion without collateral circulation portends high in-hospital mortality. Anterior ST elevation in the precordial leads from V2 to V4 through V6, and ST elevation in leads I and aVL, accompanying with ST depression in the inferior leads is associated with acute total LM occlusion without collateral circulation.


Asunto(s)
Oclusión Coronaria , Intervención Coronaria Percutánea , Infarto del Miocardio con Elevación del ST , Humanos , Infarto del Miocardio con Elevación del ST/complicaciones , Estudios Retrospectivos , Vasos Coronarios , Circulación Colateral , Electrocardiografía , Oclusión Coronaria/diagnóstico , Oclusión Coronaria/cirugía , Oclusión Coronaria/complicaciones , Angiografía Coronaria , Arritmias Cardíacas
5.
Am J Emerg Med ; 35(4): 664.e1-664.e2, 2017 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-27839841

RESUMEN

Negative T waves in electrocardiography have been widely studied. We presents a case of Wellens' syndrome which is a pattern of global inverted T waves with QT prolongation on ECG due to transient proximal LAD occlusion and pointed out other differential diagnosis.


Asunto(s)
Síndrome de Brugada/diagnóstico , Estenosis Coronaria/diagnóstico , Electrocardiografía , Síndrome de Brugada/etiología , Trastorno del Sistema de Conducción Cardíaco , Dolor en el Pecho/etiología , Angiografía Coronaria , Estenosis Coronaria/sangre , Estenosis Coronaria/complicaciones , Estenosis Coronaria/diagnóstico por imagen , Diagnóstico Diferencial , Humanos , Masculino , Persona de Mediana Edad , Troponina I/sangre
6.
Heart ; 102(10): e3, 2016 05 15.
Artículo en Inglés | MEDLINE | ID: mdl-26715569

RESUMEN

CLINICAL INTRODUCTION: An 88-year-old man, admitted to the emergency room (ER) after three episodes of syncope within 1 day, reported a precursory of syndrome of light-headedness with rapid palpitations that led to an abrupt loss of consciousness. After undergoing percutaneous and surgical revascularisation, he started complaining of chest and back discomfort for the past 20 years and searching for help from Chinese medicine, Fuzi. He had history of chronic renal failure and heart failure, but denied neither taking digitalis nor having family history related to sudden death.On arrival, heart rate was 150 bpm and blood pressure (BP) by cuff was 91/81 mm Hg (non-invasive BP could not be accurately obtained during tachycardia) plus oedema on both lower extremities. There were diffuse crackles and indistinct heart sounds on auscultation.The admission ECG was performed in the ER (figure 1). His serum creatinine was 139.7 mmol/L, serum K(+) was 4.7 mmol/L, N-terminal of the prohormone brain natriuretic peptide was highly elevated (12 000 pg/mL) and troponin I was negative. QUESTION: What is the most likely diagnosis suggested based on the patient's ECG and history? Aconite poisoningDigitalis toxicityCatecholaminergic polymorphic ventricular tachycardia (CPVT)Andersen-Tawil syndrome (ATS).


Asunto(s)
Aconitum/envenenamiento , Diterpenos/envenenamiento , Medicamentos Herbarios Chinos/envenenamiento , Sistema de Conducción Cardíaco/efectos de los fármacos , Síncope/inducido químicamente , Taquicardia/inducido químicamente , Potenciales de Acción/efectos de los fármacos , Anciano de 80 o más Años , Electrocardiografía , Sistema de Conducción Cardíaco/fisiopatología , Frecuencia Cardíaca/efectos de los fármacos , Humanos , Masculino , Síncope/diagnóstico , Síncope/fisiopatología , Taquicardia/diagnóstico , Taquicardia/fisiopatología
8.
FEBS Lett ; 588(1): 58-64, 2014 Jan 03.
Artículo en Inglés | MEDLINE | ID: mdl-24239537

RESUMEN

Reelin is an extracellular glycoprotein that is highly conserved in mammals. In addition to its expression in the nervous system, Reelin is present in erythroid cells but its function there is unknown. We report in this study that Reelin is up-regulated during erythroid differentiation of human erythroleukemic K562 cells and is expressed in the erythroid progenitors of murine bone marrow. Reelin deficiency promotes erythroid differentiation of K562 cells and augments erythroid production in murine bone marrow. In accordance with these findings, Reelin deficiency attenuates AKT phosphorylation of the Ter119(+)CD71(+) erythroid progenitors and alters the cell number and frequency of the progenitors at different erythroid differentiation stages. A regulatory role of Reelin in erythroid differentiation is thus defined.


Asunto(s)
Moléculas de Adhesión Celular Neuronal/metabolismo , Diferenciación Celular , Células Eritroides/metabolismo , Proteínas de la Matriz Extracelular/metabolismo , Proteínas del Tejido Nervioso/metabolismo , Serina Endopeptidasas/metabolismo , Animales , Western Blotting , Células de la Médula Ósea/metabolismo , Moléculas de Adhesión Celular Neuronal/genética , Linaje de la Célula/genética , Células Precursoras Eritroides/metabolismo , Proteínas de la Matriz Extracelular/genética , Regulación Leucémica de la Expresión Génica , Homocigoto , Humanos , Células K562 , Leucemia Eritroblástica Aguda/genética , Leucemia Eritroblástica Aguda/metabolismo , Ratones , Ratones Mutantes Neurológicos , Proteínas del Tejido Nervioso/genética , Fosforilación , Proteínas Proto-Oncogénicas c-akt/metabolismo , Interferencia de ARN , Proteína Reelina , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Serina Endopeptidasas/genética , Regulación hacia Arriba
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