Metformin ppt

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  1. leenex2 User

    Metformin ppt

    The UK Prospective Diabetes Study, a large clinical trial performed in 1980-90s, provided evidence that metformin reduced the rate of adverse cardiovascular outcomes in overweight patients with type 2 diabetes relative to other antihyperglycemic agents. Treatment guidelines for major professional associations including the European Association for the Study of Diabetes, the European Society for Cardiology and the American Diabetes Association, now describe evidence for the cardiovascular benefits of metformin as equivocal. In 2017, the American College of Physicians's guidelines were updated to recognize metformin as the first-line treatment for type-2 diabetes. For example, a 2014 review found tentative evidence that people treated with sulfonylureas had a higher risk of severe low blood sugar events (RR 5.64), though their risk of non-fatal cardiovascular events was lower than the risk of those treated with metformin (RR 0.67). There was not enough data available at that time to determine the relative risk of death or of death from heart disease. study known as the Diabetes Prevention Program, participants were divided into groups and given either placebo, metformin, or lifestyle intervention and followed for an average of three years. Metformin treatment of people at a prediabetes stage of risk for type 2 diabetes may decrease their chances of developing the disease, although intensive physical exercise and dieting work significantly better for this purpose. The intensive program of lifestyle modifications included a 16-lesson training on dieting and exercise followed by monthly individualized sessions with the goals of decreasing weight by 7% and engaging in physical activity for at least 150 minutes per week. The incidence of diabetes was 58% lower in the lifestyle group and 31% lower in individuals given metformin. Among younger people with a higher body mass index, lifestyle modification was no more effective than metformin, and for older individuals with a lower body mass index, metformin was no better than placebo in preventing diabetes. The bladder is a hollow organ in your lower abdomen that stores urine. Bladder cancer occurs in the lining of the bladder. It is the sixth most common type of cancer in the United States. Symptoms include Risk factors for developing bladder cancer include smoking and exposure to certain chemicals in the workplace. People with a family history of bladder cancer or who are older, white, or male have a higher risk. Treatments for bladder cancer include surgery, radiation therapy, chemotherapy, and biologic therapy. Biologic therapy boosts your body's own ability to fight cancer.

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    Metformin. S U s. Glinides. DPP-4. inhibitors. GLP-1R. agonists. A G I s. Metformin; Sulfonylureas; Thiazolidinediones; DPP-4 inhibitors; SGLT-2 inhibitors. Metformin Revisited A comprehensive review by Dr. R. V. S. N. Sarma, M. D. Diabetes Mellitus Type 2 DM NIDDM Not merely SUGAR DISORDER Multi system. – A free PowerPoint PPT presentation displayed as a Flash slide show on - id 3be925-M2YxN Nov 12, 2015. Metformin PowerPoint. 1. By Meredith Ashley Metformin; 2. › Prevalence – Affects 24 million people in the United States › Pathophysiology.

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    Metformin ppt

    PowerPoint 프레젠테이션 - 2017 International Congress of Diabetes., Metformin by Dr Sarma - PowerPoint PPT Presentation

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    Metformin in Diabetes/IGT 1. Metformin is documented to reduce CV events and mortality in Diabetes. 1. Metformin is known to prevent CV events in diabetic patients with cardiac disease undergoing intervention 2. Metformin is known to prevent onset of diabetes in patients with IGT 26. Type 2 Diabetes Management Goals - 2179 PPT. Presentation Summary This atypical presentation has been seen with other antihyperglycemic agents long before the introduction of SGLT2 inhibitors. PowerPoint Presentation Metformin was first described in the scientific literature in 1922, by Emil Werner and James Bell. In 1929, Slotta and Tschesche discovered its sugar-lowering action in rabbits, noting it was the most potent of the biguanide analogs they studied.

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