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2.
J Card Surg ; 34(9): 867-870, 2019 Sep.
Article in English | MEDLINE | ID: mdl-31233236

ABSTRACT

Thrombus straddling a patent foramen ovale and massive pulmonary embolism is a very rare and life-threatening condition. Optimal management can be controversial because different therapeutic options are available and individual approach based in individual risk is needed. We present a case of a thrombus straddling the patent foramen ovale with massive pulmonary embolism, hemodynamic instability, and upper extremity embolism. We performed surgical pulmonary embolectomy, and venous arterial extracorporeal membrane oxygenation was needed to successfully overcome severe right ventricular impairment and pulmonary injury.


Subject(s)
Cardiac Surgical Procedures/methods , Embolectomy/methods , Extracorporeal Membrane Oxygenation/methods , Foramen Ovale, Patent/complications , Heart Ventricles , Pulmonary Embolism/complications , Thrombosis/etiology , Echocardiography , Echocardiography, Transesophageal , Female , Foramen Ovale, Patent/diagnosis , Foramen Ovale, Patent/surgery , Heart Diseases/diagnosis , Heart Diseases/etiology , Heart Diseases/surgery , Humans , Middle Aged , Pulmonary Embolism/diagnosis , Pulmonary Embolism/surgery , Thrombosis/diagnosis , Thrombosis/surgery , Tomography, X-Ray Computed
4.
J Am Heart Assoc ; 7(2)2018 01 22.
Article in English | MEDLINE | ID: mdl-29358198

ABSTRACT

BACKGROUND: Transplantation of adventitial pericytes (APCs) promotes cardiac repair in murine models of myocardial infarction. The aim of present study was to confirm the benefit of APC therapy in a large animal model. METHODS AND RESULTS: We performed a blind, randomized, placebo-controlled APC therapy trial in a swine model of reperfused myocardial infarction. A first study used human APCs (hAPCs) from patients undergoing coronary artery bypass graft surgery. A second study used allogeneic swine APCs (sAPCs). Primary end points were (1) ejection fraction as assessed by cardiac magnetic resonance imaging and (2) myocardial vascularization and fibrosis as determined by immunohistochemistry. Transplantation of hAPCs reduced fibrosis but failed to improve the other efficacy end points. Incompatibility of the xenogeneic model was suggested by the occurrence of a cytotoxic response following in vitro challenge of hAPCs with swine spleen lymphocytes and the failure to retrieve hAPCs in transplanted hearts. We next considered sAPCs as an alternative. Flow cytometry, immunocytochemistry, and functional/cytotoxic assays indicate that sAPCs are a surrogate of hAPCs. Transplantation of allogeneic sAPCs benefited capillary density and fibrosis but did not improve cardiac magnetic resonance imaging indices of contractility. Transplanted cells were detected in the border zone. CONCLUSIONS: Immunologic barriers limit the applicability of a xenogeneic swine model to assess hAPC efficacy. On the other hand, we newly show that transplantation of allogeneic sAPCs is feasible, safe, and immunologically acceptable. The approach induces proangiogenic and antifibrotic benefits, though these effects were not enough to result in functional improvements.


Subject(s)
Cell- and Tissue-Based Therapy/methods , Myocardial Infarction/surgery , Myocardial Reperfusion Injury/surgery , Myocardium/pathology , Neovascularization, Physiologic , Pericytes/transplantation , Ventricular Function, Left , Ventricular Remodeling , Aged , Aged, 80 and over , Allogeneic Cells , Animals , Cells, Cultured , Disease Models, Animal , Female , Fibrosis , Heterografts , Humans , Male , Middle Aged , Myocardial Contraction , Myocardial Infarction/pathology , Myocardial Infarction/physiopathology , Myocardial Reperfusion Injury/pathology , Myocardial Reperfusion Injury/physiopathology , Recovery of Function , Stroke Volume , Sus scrofa , Transplantation, Homologous
7.
Eur J Cardiothorac Surg ; 50(4): 685-692, 2016 Oct.
Article in English | MEDLINE | ID: mdl-27222592

ABSTRACT

OBJECTIVES: The impact of systolic flow displacement on the development and progression of ascending aorta dilatation in aortic valve disease is a matter of controversy. Our objective was to study the association between rheological stimuli and development of aortic dilatation in a large animal model of supravalvular aortic stenosis and eccentric flow. METHODS: Twenty-four pigs weighing 10-14 kg were randomly allocated (ratio 2:1) to either restrictive ascending aortic banding or sham operation. Aortic diameter and systolic flow displacement were assessed by three-dimensional phase-contrast magnetic resonance imaging at 6 and 18 weeks after surgery. Twenty pigs (n = 14, banded vs n = 6, sham) completed full imaging protocol and were included in the analysis. After the last follow-up, a subset of 14 animals was sacrificed for histological analysis. RESULTS: All banded animals developed significant progressive aortic dilatation both at 6 and 18 weeks, compared with sham-operated pigs: 34.3 ± 4.8 vs 21.4 ± 2.7 mm at 6 weeks (P < 0.001); and 50.0 ± 8.4 vs 38.0 ± 8.3 mm at 18 weeks (P = 0.002). The peak gradient at 6 weeks showed a trend to positively correlate with aortic diameter at 18 weeks (R = 0.50, P = 0.06), whereas the systolic flow displacement at 6 weeks correlated better with aortic diameter at 18 weeks (R = 0.59, P = 0.02). The aortic wall thickness was significantly decreased in the anterior aortic section in banded, compared with sham-operated, pigs (1.5 ± 0.4 vs 2.0 ± 0.1 mm, respectively; P = 0.03). In addition, banded pigs showed a higher degree of cystic medial necrosis and elastin fibre fragmentation, compared with sham-operated animals. CONCLUSIONS: In this preclinical model of supravalvular aortic stenosis and eccentric flow, we found that systolic flow displacement at earlier stages is positively correlated with the degree of aortic dilatation during follow-up as assessed by three-dimensional phase-contrast magnetic resonance imaging. If our findings are confirmed in further studies, this imaging parameter might be useful to identify those subjects with aortic valve disease who are at risk of developing aortic dilatation at a later stage.


Subject(s)
Aortic Aneurysm/diagnostic imaging , Animals , Aortic Aneurysm/physiopathology , Aortic Aneurysm/surgery , Aortic Stenosis, Supravalvular/diagnostic imaging , Aortic Stenosis, Supravalvular/physiopathology , Aortic Stenosis, Supravalvular/surgery , Disease Models, Animal , Heart/physiopathology , Magnetic Resonance Imaging , Male , Rheology , Swine , Ventricular Function, Left/physiology
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