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Liraglutide Case Study

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Title: 3.0 mg of Liraglutide, in Addition to Diet and Exercise, is Associated with Weight Loss and Improved Metabolic Control. Obesity is a weight disorder that affects more people every year and poses serious health risks. Obesity can give way to further health conditions such as stroke, heart disease, type 2 diabetes and some forms of cancer. In the United States more than 78.6 million adults are obese; and in 2008, the estimated medical costs of obesity in the United States totaled $147 billion (USD), according to the Centers for Disease Control and Prevention. As the rising costs and consequences of obesity continue to expand, more alternatives to aid in weight loss could help to improve patient outcomes. Does 3.0 mg of once-daily …show more content…

Patients received counseling for lifestyle modifications and were randomly assigned in a 2:1 ratio to receive subcutaneous injections of Liraglutide once-daily (2487 patients) or placebo (1244 patients). Inclusion criteria included patients who did not have type 2 diabetes and who had a body mass index (BMI) of at least 30 or a BMI of at least 27 with concurrent dyslipidemia or hypertension. No statistical baseline differences occurred between the Liraglutide and placebo group; however, the study did enroll predominately Caucasian females which could impact the external validity of the results. Primary endpoints were the change in body weight and the proportion of patients that lost at least 5% and over 10% of their initial body weight. The study was conducted from June 1, 2011 through March 18, 2013 at 191 sites in 27 countries. After 56 weeks, the patients in the Liraglutide group were then randomly assigned in a 1:1 ratio to continue Liraglutide or receive placebo for an additional 12 weeks to assess for efficacy and safety after discontinuation. Patients who were originally placed in the placebo group continued to receive placebo after reassignment. Patient evaluation occurred at weeks 2, 4, 6, and 8 then every 4 weeks through week 44, and then again at weeks 50, 56, 58, 60, 64, 68, and 70. Patients that were not able to finish the study were asked to return at week 56 for the recording of measurement, weight and adverse

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