6 results match your criteria: "Flinders Medical Centre and The Flinders University[Affiliation]"
Heart Lung Circ
April 2012
Cardiac and Thoracic Surgical Unit, Department of Medicine, Flinders Medical Centre and The Flinders University, Adelaide, South Australia, Australia.
Background: No Australian study has reported the association between selective-serotonin reuptake inhibitor (SSRI) and serotonin noradrenaline reuptake inhibitor (SNRI) with coronary artery bypass graft (CABG) surgery morbidity and mortality.
Methods: 4136 patients underwent CABG surgery between January 1996 and December 2008 and 105 (2.5%) were SSRI/SNRI users.
J Health Psychol
May 2011
Cardiac and Thoracic Surgical Unit, Department of Medicine, Flinders Medical Centre and The Flinders University, Adelaide, South Australia, Australia.
This study examined the Beck Depression Inventory-II (BDI-II) with Confirmatory Factor Analysis and followed up cardiac morbidity and mortality for a median of 4.9 years among 226 coronary artery bypass graft patients. Cardiac morbidity and mortality events (n = 65, 28.
View Article and Find Full Text PDFArch Clin Neuropsychol
December 2009
Cardiothoracic Surgery Unit and Cardiac Surgery Research, Flinders Medical Centre and The Flinders University, Adelaide, South Australia, Australia.
Research has shown conflicting results with regard to the influence of depression and anxiety on neuropsychological performance following coronary artery bypass graft (CABG) surgery. Notably, the independent effects of depression and anxiety have not been examined among CABG candidates in the longer term where it is has been suggested that these patients show marked cognitive deterioration. A neuropsychological test battery and measures of psychological distress were completed by 86 CABG patients and 50 nonsurgical control participants at baseline and 6 months, whereas 75 patients and 36 controls, respectively, completed a 5-year follow-up.
View Article and Find Full Text PDFJ Gastroenterol Hepatol
November 2000
Department of Anesthesia, Flinders Medical Centre and The Flinders University of South Australia, Australia.
Background And Aims: The gut flora play a significant role in the disposition of many foreign substances, as well as producing nutrients and toxins that may be absorbed and reach the liver. This study examines the influence of antibiotic-induced alterations in gut flora on the development of hepatic fibrosis in a rat model.
Methods: Thirty-six male Porton rats were fed alcohol (3.
Clin Sci (Lond)
April 2000
Department of Surgery, Flinders Medical Centre and the Flinders University of South Australia, Bedford Park, South Australia 5042, Australia.
The bikunin peptide chain of the protease inhibitor inter-alpha-inhibitor (IalphaI) has been reported to be an inhibitor of calcium oxalate (CaOx) crystallization, and hence has been proposed as having a role in CaOx kidney stone formation. However, further experimental evidence is required to assess if fragments of IalphaI other than bikunin may play a role in the regulation of crystallization events in stone formation. The aim of the present study was to assess the effects of IalphaI and several of its derivatives on CaOx crystallization in a seeded inorganic system and to compare these effects with those of a known inhibitor of crystallization, prothrombin.
View Article and Find Full Text PDFEur J Pain
August 2004
Pain Management Unit, Flinders Medical Centre and The Flinders University of South Australia, Bedford Park, Australia.
With increasing interest in the application of dextromethorphan in pain control, it is probable that patients will receive this drug in combination with analgesics such as opioids, giving rise to the potential for previously unobserved drug interactions. The interaction between dextromethorphan, and its pharmacologically active metabolite dextrorphan, and norpethidine, a toxic metabolite of pethidine, was examined in rats. Rats were assigned to receive dextromethorphan (0, 20 or 40 mg/kg) or dextrorphan (0, 15 or 30 mg/kg) combined with norpethidine (0, 28 or 42 mg/kg).
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