9 results match your criteria: "St Vincent's Hospital and the Victor Chang Cardiac Research Institute[Affiliation]"
Biomed J
October 2022
Critical Care Research Group, Level 3, Clinical Sciences Building, The Prince Charles Hospital, Rode Road, Brisbane, Australia. Electronic address:
Introduction: Organs procured following brain stem death (BSD) are the main source of organ grafts for transplantation. However, BSD is associated with inflammatory responses that may damage the organ and affect both the quantity and quality of organs available for transplant. Therefore, we aimed to investigate plasma and bronchoalveolar lavage (BAL) pro-inflammatory cytokine profiles and cardiovascular physiology in a clinically relevant 6-h ovine model of BSD.
View Article and Find Full Text PDFJ Biomed Sci
October 2020
Critical Care Research Group, Level 3, Clinical Sciences Building, The Prince Charles Hospital, Rode Road, Brisbane, Australia.
Background: A lung transplant is the last resort treatment for many patients with advanced lung disease. The majority of donated lungs come from donors following brain death (BD). The endothelin axis is upregulated in the blood and lung of the donor after BD resulting in systemic inflammation, lung damage and poor lung graft outcomes in the recipient.
View Article and Find Full Text PDFCirc Cardiovasc Imaging
December 2015
From the Department of Cardiovascular Imaging (R.H., N.V., N.C., B.G., T.R., E.A.U., C.C., G.C.-W., E.N., V.O.P.) and Division of Cardiovascular Sciences (S.K.), King's College London, London, United Kingdom; Cardiovascular Department, University Hospital Ramón y Cajal, Madrid, Spain (R.H.); Department of Cardiology, St. Vincent's Hospital and The Victor Chang Cardiac Research Institute, Sydney, New South Wales, Australia (A.J., C.-Y.Y.); German Heart Institute Berlin, Berlin, Germany (R.G., A.D., S.K.); and Division of Internal Medicine III, Department of Cardiology (V.O.P.) and Institute for Experimental and Translational Cardiovascular Imaging, DZHK Centre for Cardiovascular Imaging (E.N.), Goethe University Frankfurt, Frankfurt, Germany.
Background: The differential diagnosis of left ventricular (LV) hypertrophy remains challenging in clinical practice, in particular, between hypertrophic cardiomyopathy (HCM) and increased LV wall thickness because of systemic hypertension. Diffuse myocardial disease is a characteristic feature in HCM, and an early manifestation of sarcomere-gene mutations in subexpressed family members (G+P- subjects). This study aimed to investigate whether detecting diffuse myocardial disease by T1 mapping can discriminate between HCM versus hypertensive heart disease as well as to detect genetically driven interstitial changes in the G+P- subjects.
View Article and Find Full Text PDFJACC Cardiovasc Imaging
January 2015
Cardiovascular Imaging Department, Division of Imaging Sciences, King's College London, London, United Kingdom. Electronic address:
Objectives: This study investigated whether T1 mapping by cardiac magnetic resonance (CMR) reflects the clinical evolution of disease in myocarditis and supports its diagnosis independently of the disease stages.
Background: Acute viral myocarditis is characterized by a range of intracellular changes due to viral replication and extracellular spill of debris within days of viral infection. Convalescence may be characterized by a chronic low-grade inflammation leading to ventricular remodelling, but also a complete resolution of myocardial changes.
Heart Lung Circ
October 2000
St Vincent's Hospital and the Victor Chang Cardiac Research Institute, Victoria Street, Darlinghurst, New South Wales, Australia.
Background: We aimed to develop a large animal model of orthotopic cardiac transplantation, incorporating donor brain death, to assess new methods of preservation of the donor heart.
Methods: Brain death was achieved in the donor pig by inflation of a 20 cc subdural balloon 1 h prior to harvest. The donor heart was stored for 6 h with conventional hypothermic ischaemic preservation.
J Heart Lung Transplant
August 2003
Heart and Lung Transplant Unit, St. Vincent's Hospital and the Victor Chang Cardiac Research Institute, Sydney, NSW, Australia.
Background: Acute brain death from increased intracranial pressure results in a transient increase in myocardial adenosine and lactate, which indicates that oxygen demand exceeds oxygen delivery during the sympathetic "storm". The aim of this study was to determine the functional significance of this period of ischemia.
Methods: Brain death was inflicted on 40 Westran pigs (36.
Eur J Cardiothorac Surg
June 2003
Heart and Lung Transplant Unit, St. Vincent's Hospital and the Victor Chang Cardiac Research Institute, Sydney, Australia.
Objective: To determine if the initial rate of troponin I release post-reperfusion reflects the effectiveness of myocardial protection during cardiac allograft preservation.
Methods: A porcine model of orthotopic heart transplantation was used. Data from two control groups (CON(4) and CON(14)) and two treatment groups (CAR(4) and CAR(14)) were analysed.
J Heart Lung Transplant
March 2003
Heart and Lung Transplant Unit, St Vincent's Hospital and the Victor Chang Cardiac Research Institute, Sydney, Australia
Eur J Cardiothorac Surg
November 2002
Cardiac Mechanics Research Laboratory, St Vincent's Hospital and the Victor Chang Cardiac Research Institute, Victoria Street, Darlinghurst, Sydney, NSW 2061, Australia.
Objective: Paradoxically, it has been reported that after 1.5-4 h of hypothermic ischaemic preservation there is complete recovery of contractile function in canine cardiac allografts, as assessed by the preload recruitable stroke work (PRSW) relationship. This raises questions about the suitability of the canine heart as a model for preservation research and the PRSW relationship as an end-point.
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