Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 7 de 7
Filtrar
1.
Eur J Case Rep Intern Med ; 7(8): 001811, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-32789144

RESUMEN

The SARS-CoV-2 virus is a newly emergent pathogen first identified in Wuhan, China, and responsible for the COVID-19 global pandemic. In this case report we describe a manifestation of non-bacterial thrombotic endocarditis with continuous peripheral embolization in a COVID-19-positive patient. The patient responded well to high-dose LMWH treatment with cessation of the embolic process. LEARNING POINTS: Raising awareness of possible complications of COVID-19.To highlight the importance of the careful consideration of and dosage of anticoagulation in non-bacterial thrombotic endocarditis.

2.
Cardiol Res Pract ; 2013: 895215, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23476886

RESUMEN

Background. Although our comprehension of nonrheumatic aortic stenosis (NRAS) has increased substantially during the last decade, less is known about the histopathology of rheumatic aortic stenosis (RAS). The aim of this study was to investigate rheumatic aortic stenosis by means of analyses previously used in nonrheumatic stenosis. Material and Methods. Valve specimens were obtained from 39 patients referred to hospital due to significant aortic stenosis. According to established macroscopic criteria the valves were divided into two groups consisting of 29 NRAS and 10 RAS valves. Mononuclear inflammatory cells and apolipoproteins were investigated using immunohistochemical analyses. Results. The localisation of calcification differed in tricuspid nonrheumatic valves when compared to bicuspid nonrheumatic and rheumatic valves. The RAS valves revealed a lower degree of T lymphocyte infiltration compared with the NRAS valves. Infiltration of macrophages was seen in all valves and there were no differences regarding deposition of apolipoprotein. Conclusion. Rheumatic and nonrheumatic aortic stenotic valves show a similar and significant chronic inflammation. The similarities regarding the localisation of calcification indicate that the valve anomaly/morphology can influence the pathogenesis of aortic stenosis. Finally, our findings highlight the question of a postinflammatory valvular disease of other causes than rheumatic fever.

3.
JACC Cardiovasc Imaging ; 2(1): 48-55, 2009 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-19356532

RESUMEN

OBJECTIVES: Ejection fraction (EF) reaction upon exercise by radionuclide ventriculography and standard echocardiographic parameters was evaluated as predictors for post-operative left ventricular (LV) function in chronic aortic regurgitation (AR). BACKGROUND: The optimal timing of surgery for chronic AR is when the left ventricle is still compensating for the volume and pressure overload without irreversible dysfunction. For asymptomatic patients when EF is normal and LV diameters are borderline, exercise testing is recommended by present guidelines. However, only a limited number of studies have been performed, and data are scarce on this subject. METHODS: Radionuclide ventriculography with multiple gated acquisition at rest and during exercise was performed in 29 consecutive patients with severe chronic aortic regurgitation pre-operatively and 6 months post-operatively. Patient subgroups were formed based on pre-operative EF exercise response (DeltaEF) and were categorized as decreasing (DeltaEF <-5%), unaltered (-5% 5%). A 5% or higher increase was considered normal. The LV diameters and mass were measured by echocardiography. RESULTS: Pre-operative LV diameters were markedly elevated before surgery and diminished significantly after surgery. Left ventricular diameters, LV mass, EF at rest (EF(rest)), and EF change from rest to exercise (DeltaEF) were independent of New York Heart Association functional class. Pre-operative end-diastolic diameter proved to be a predictor for pre- and post-operative DeltaEF (p = 0.003; p = 0.04) but not for the nature of the exercise response post-operatively. Patients with decreasing and unaltered EF pre-operatively presented a significantly higher but still abnormal DeltaEF post-operatively. Those with increasing EF pre-operatively had a similar response and a normal DeltaEF post-operatively. Pre-operative DeltaEF was not only a predictor for post-operative DeltaEF (p = 0.02) but also classified patients into post-operative subgroups (EF decreasing, p = 0.03; unaltered, p = 0.02; increasing, p = 0.0008). CONCLUSIONS: An abnormal EF response to exercise may also occur in patients who do not fulfill criteria for surgery based on LV dimensions or EF. A follow-up of exercise LV function and adjusting the timing of surgery according to the nature of exercise response could, therefore, be beneficial.


Asunto(s)
Insuficiencia de la Válvula Aórtica/diagnóstico por imagen , Procedimientos Quirúrgicos Cardíacos , Ecocardiografía de Estrés , Prueba de Esfuerzo , Ventriculografía con Radionúclidos , Volumen Sistólico , Disfunción Ventricular Izquierda/diagnóstico por imagen , Función Ventricular Izquierda , Anciano , Insuficiencia de la Válvula Aórtica/fisiopatología , Insuficiencia de la Válvula Aórtica/cirugía , Procedimientos Quirúrgicos Cardíacos/efectos adversos , Enfermedad Crónica , Progresión de la Enfermedad , Femenino , Implantación de Prótesis de Válvulas Cardíacas , Humanos , Masculino , Persona de Mediana Edad , Selección de Paciente , Valor Predictivo de las Pruebas , Reproducibilidad de los Resultados , Índice de Severidad de la Enfermedad , Factores de Tiempo , Resultado del Tratamiento , Disfunción Ventricular Izquierda/fisiopatología , Disfunción Ventricular Izquierda/cirugía
5.
Cardiovasc Pathol ; 16(3): 171-8, 2007.
Artículo en Inglés | MEDLINE | ID: mdl-17502247

RESUMEN

BACKGROUND: Nonrheumatic aortic stenosis is the predominant cause of heart valve surgery in the Western world. Aortic and mitral regurgitation account for a lesser amount of the heart valve surgery. During the 1990s, inflammatory cell infiltrates have been demonstrated in nonrheumatic stenotic aortic valves. These findings suggest an inflammatory component in the pathogenesis of nonrheumatic aortic valve stenosis. However, nonrheumatic regurgitant aortic and mitral valves have not been investigated in this respect. The aim of this study was to compare nonrheumatic regurgitant aortic and mitral valves with stenotic aortic valves regarding the presence of T lymphocytes, macrophages, apolipoprotein B, and apolipoprotein A-I. METHODS: Valve specimens were obtained from 42 patients referred to hospital for surgery because of significant heart valve disease. From these patients, 29 aortic stenotic valves, 9 aortic regurgitant, and 6 mitral regurgitant valves, all nonrheumatic, were obtained for the study. Fourteen valves collected from subjects undergoing clinical/medicolegal autopsy were used as control. In order to identify mononuclear inflammatory cells and apolipoproteins, sections were investigated with immunohistochemical analyses and then categorized semiquantitatively. RESULTS: Regurgitant and control valves showed a significantly lower degree of inflammatory cell infiltrate and a lower degree of apolipoprotein deposition as compared to stenotic aortic valves. CONCLUSIONS: The signs of inflammation seen in nonrheumatic aortic stenosis are not prominent features in the nonrheumatic, regurgitant valves. This is consistent with the multi-factorial pathogenesis of these conditions.


Asunto(s)
Insuficiencia de la Válvula Aórtica/patología , Estenosis de la Válvula Aórtica/patología , Enfermedades de las Válvulas Cardíacas/patología , Inflamación/patología , Adulto , Anciano , Insuficiencia de la Válvula Aórtica/metabolismo , Estenosis de la Válvula Aórtica/metabolismo , Apolipoproteína A-I/metabolismo , Apolipoproteínas B/metabolismo , Calcio/metabolismo , Femenino , Enfermedades de las Válvulas Cardíacas/metabolismo , Humanos , Inmunohistoquímica , Inflamación/metabolismo , Macrófagos/metabolismo , Macrófagos/patología , Masculino , Persona de Mediana Edad , Linfocitos T/metabolismo , Linfocitos T/patología
6.
Lakartidningen ; 103(11): 845-6, 848, 2006.
Artículo en Sueco | MEDLINE | ID: mdl-16613113
7.
Scand J Infect Dis ; 34(10): 759-62, 2002.
Artículo en Inglés | MEDLINE | ID: mdl-12477328

RESUMEN

The embedding of bacteria in the vegetation of infective endocarditis impedes the penetration of phagocytic cells. IL-8 has a stimulating effect on the immune system, particularly with respect to chemotaxis and activation of granulocytes. Tumor necrosis factor alpha (TNF-alpha) is 1 of the major proinflammatory cytokines. IL-8 and TNF-alpha were visualized by means of immunohistochemistry in paraffin-embedded heart valve biopsies from 6 patients with infective endocarditis who required cardiac surgery during the active phase of the infection. In 5/6 patients there were signs of inflammation, and in these patients IL-8- and TNF-alpha-containing cells were visualized in the heart valve stromas or vegetations. The largest numbers of IL-8-containing cells, and the greatest amount of inflammation, were seen in patients with short preoperative treatment courses. No such relationships were seen with respect to TNF-alpha-containing cells. These observations may suggest that the occurrence of IL-8-containing cells in infected heart valves could be used as a marker of disease activity.


Asunto(s)
Infecciones Bacterianas/inmunología , Endocarditis Bacteriana/inmunología , Enfermedades de las Válvulas Cardíacas/inmunología , Válvulas Cardíacas/patología , Interleucina-8/análisis , Factor de Necrosis Tumoral alfa/análisis , Adulto , Anciano , Infecciones Bacterianas/patología , Biomarcadores/análisis , Biopsia con Aguja , Endocarditis Bacteriana/patología , Femenino , Bacterias Gramnegativas/aislamiento & purificación , Bacterias Grampositivas/aislamiento & purificación , Enfermedades de las Válvulas Cardíacas/patología , Humanos , Inmunohistoquímica , Masculino , Persona de Mediana Edad , Estudios Prospectivos , Sensibilidad y Especificidad , Índice de Severidad de la Enfermedad
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA