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1.
Clin Radiol ; 78(12): e941-e949, 2023 12.
Article in English | MEDLINE | ID: mdl-37788968

ABSTRACT

AIM: To investigate how magnetic resonance imaging (MRI) examinations are protocolled in tertiary paediatric neuroradiology centres around the UK for some of the more common presentations encountered in paediatric neuroradiology, and to identify any variations of note. MATERIALS AND METHODS: All 19 UK tertiary paediatric neuroradiology centres registered with the British Society of Neuroradiologists-Paediatric Group were contacted and asked if they could provide a copy of their standard MRI protocols. Twelve responded (63%) and 10 of the more common presentations were selected and the standard acquired sequences obtained at each participating centre were compared. Where available the collated protocols were also compared against current published guidance. RESULTS: The basic sequences carried out by centres around the UK are similar; however, there are lots of variations overall. The only standardised protocol currently being implemented nationally in paediatric imaging is that for brain tumours. Otherwise, chosen protocols are generally dependent on the preferences and technical capabilities of individual centres. Suggested published protocols also exist for non-accidental injury (NAI), multiple sclerosis, epilepsy, and head and neck imaging. CONCLUSIONS: The differences in MRI protocolling depend in part on technical capabilities and in part on the experience and preferences of the paediatric neuroradiologists at each centre. For most presentations, there is no consensus as to what constitutes the perfect protocol. The present results will be useful for specialist centres who may wish to review their current protocols, and for more generalist centres to use as a reference to guide their MRI protocolling.


Subject(s)
Brain Neoplasms , Hospitals, Pediatric , Child , Humans , Brain Neoplasms/diagnostic imaging , Magnetic Resonance Imaging/methods , Tertiary Care Centers , United Kingdom
2.
J Cardiovasc Surg (Torino) ; 52(2): 251-9, 2011 Apr.
Article in English | MEDLINE | ID: mdl-21460776

ABSTRACT

AIM: Coronary artery bypass grafting (CABG) is a standard procedure for treatment of coronary heart disease. Eighty percent of all CABGs are performed with venous grafts which then get exposed to an arterial pressure after surgery. This widely used procedure, however, is complicated by the development of alterations in the vein graft wall, leading to a decreased patency rate and graft failure. This study enlightens the influence of an even moderate arterial pressure on the gene expression of adhesion molecules in venous grafts which play a decisive role for the early induction of atherogenesis. METHODS: Segments of porcine vena jugularis and arteria carotis were mounted in a simulated bypass circuit and subjected to pulsatile flow. Vessel segments were examined for adhesion molecule expression with quantitative real-time - polymerase chain reaction (qRT-PCR) and adherence of leukocytes was observed by confocal laser scanning microscopy and scanning electron microscopy. RESULTS: Veins grafts subjected to an even moderate arterial pressure showed a 14-fold increase of ICAM-1 expression already after 4 hours. An arterial pressure of around 100/80 mmHg was enough to stimulate the adhesion molecule expression Furthermore it led to a 9-fold increase of leukocyte adhesion to the venous endothelium, but, in contrast this was not the case in arteries. CONCLUSION: This study showed, that already 100 mmHg upregulates the expression of several adhesion molecules in pig veins followed by increased adhesion of leukocytes. Therefore, our data demonstrate the advantage of arteries for CABG, and that new therapeutic strategies are urgently necessary to protect vein grafts either physically or pharmacologically if arteries are not available for CABG.


Subject(s)
Blood Pressure , Carotid Arteries/immunology , Cell Adhesion Molecules/metabolism , Coronary Artery Bypass/adverse effects , Jugular Veins/immunology , Animals , Cell Adhesion , Cell Adhesion Molecules/genetics , E-Selectin/metabolism , Female , Gene Expression Regulation , In Vitro Techniques , Intercellular Adhesion Molecule-1/metabolism , Jugular Veins/transplantation , Leukocytes/immunology , Microscopy, Confocal , Microscopy, Electron, Scanning , Perfusion , Pulsatile Flow , Reverse Transcriptase Polymerase Chain Reaction , Swine , Time Factors , Vascular Cell Adhesion Molecule-1/metabolism
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