Aims: Androgen deprivation therapy (ADT), usually achieved with luteinising hormone releasing hormone analogues (LHRHa), is central to prostate cancer management. LHRHa reduce both testosterone and oestrogen and are associated with significant long-term toxicity. Previous use of oral oestrogens as ADT was curtailed because of cardiovascular toxicity.
View Article and Find Full Text PDFBackground: Routinely-collected healthcare systems data (HSD) are proposed to improve the efficiency of clinical trials. A comparison was undertaken between cardiovascular (CVS) data from a clinical trial database with two HSD resources.
Methods: Protocol-defined and clinically reviewed CVS events (heart failure (HF), acute coronary syndrome (ACS), thromboembolic stroke, venous and arterial thromboembolism) were identified within the trial data.
Sixteen cirrhotic patients with ascites and HBs antigen (HBsAg), were chosen for this study. Serum and ascitic fluid samples were tested for Ag, total proteins, electrophoretic pattern and immunoglobulin IgG, IgA, IgM and IgE. Transmission of HBsAg through the peritoneal membrane was confirmed.
View Article and Find Full Text PDFA 10-month-old female infant with purpura fulminans is reported. The patient had clotting abnormality compatible with consumption coagulopathy. Histopathological examination revealed the presence of microthrombi.
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