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Mexican-Americans at Risk
About half of 1,787 Mexican American adults, surveyed because they were obese, reported never receiving advice from a health care provider to eat less fatty food (52% informed) or exercise more (45% informed). “Given the seriousness of obesity-related health risks and the increasing prevalence of overweight status and obesity among Mexican Americans, it is vital that providers are involved in finding ways to effectively educate and/or treat overweight patients,” the authors wrote in the American Journal of Health Promotions. The survey showed that men, respondents with little education, those who preferred to speak Spanish at home, and nonmarried respondents were least likely to receive advice on exercise and diet. Respondents with comorbidities were more likely than others to have gotten diet and exercise advice (79% vs. 43%).
New Drug Reviews Expected
The largest pharmaceutical company in Japan, Takeda Pharmaceuticals, has resubmitted applications for two type 2 diabetes drugs to the U.S. Food and Drug Administration. The FDA is expected to review the drugs within the next 6 months, according to the company. The applications are for alogliptin and a combination of alogliptin and pioglitazone. Both therapies are for adults and intended as adjuncts to diet and exercise. Interim results from a study of possible cardiovascular risks from alogliptin, a selective dipeptidyl peptidase IV inhibitor (DPP-4i), should satisfy FDA concerns in that area, said Dr. David Recker, a senior vice president for research and development at Takeda, in a company news release. “If approved, alogliptin/pioglitazone will be the first type 2 diabetes treatment option in the U.S. to include both a DPP-4 inhibitor and a thiazolidinedione in a single tablet,” he added. Alogliptin was rejected by the FDA in 2009, which asked for more data on its cardiovascular effects.
Managers Face Challenges
Managers of group practices say that preparing for risk-based reimbursement and implementing electronic health records are their biggest challenges, according to a survey from the Medical Group Management Association. Dealing with rising operating costs and implementing an accountable care organization or a patient-centered medical home are also significant challenges, according to the MGMA survey. Electronic health records and other technologies are increasingly problematic, said MGMA President and CEO William Jessee. “The pressure to adopt technology and the morass our members face in determining the best systems for their practices, and then complying with the various government programs to receive incentives and avoid penalties, are proving to be of particular concern,” he said in a statement.
Food Makers Pan Guidelines
Food manufacturers charged that voluntary guidelines proposed by the federal government ignore the industry's progress on responsible marketing of food to children. The proposal from the Federal Trade Commission says that only foods that contribute to a healthful diet should be marketed to children and offers targets for saturated fat, trans fat, added sugars, and sodium in such food. In a letter to the FTC, the FDA, and other agencies, 150 state, regional, and national food groups and manufacturers argue that there's no evidence the proposed restrictions would contribute to long-term changes in eating behavior or solve childhood obesity. Separately, the National Restaurant Association called for the voluntary standards to be withdrawn because they could become mandatory.
FDA May Change Consumer Ads
The FDA is considering changing how it regulates direct-to-consumer drug ads to reflect results of agency studies of how patients perceive and recall ad information. hhe research found that people better understood the “brief summary” section of prescription drug ads that are presented in a format similar to the simpler labels on over-the-counter drugs. Prescription drug ads use densely packed, small-type paragraphs to describe risks. The studies also found that noting a serious risk or providing extra details on side effects didn't hinder consumers' understanding of overall risk information.
Mexican-Americans at Risk
About half of 1,787 Mexican American adults, surveyed because they were obese, reported never receiving advice from a health care provider to eat less fatty food (52% informed) or exercise more (45% informed). “Given the seriousness of obesity-related health risks and the increasing prevalence of overweight status and obesity among Mexican Americans, it is vital that providers are involved in finding ways to effectively educate and/or treat overweight patients,” the authors wrote in the American Journal of Health Promotions. The survey showed that men, respondents with little education, those who preferred to speak Spanish at home, and nonmarried respondents were least likely to receive advice on exercise and diet. Respondents with comorbidities were more likely than others to have gotten diet and exercise advice (79% vs. 43%).
New Drug Reviews Expected
The largest pharmaceutical company in Japan, Takeda Pharmaceuticals, has resubmitted applications for two type 2 diabetes drugs to the U.S. Food and Drug Administration. The FDA is expected to review the drugs within the next 6 months, according to the company. The applications are for alogliptin and a combination of alogliptin and pioglitazone. Both therapies are for adults and intended as adjuncts to diet and exercise. Interim results from a study of possible cardiovascular risks from alogliptin, a selective dipeptidyl peptidase IV inhibitor (DPP-4i), should satisfy FDA concerns in that area, said Dr. David Recker, a senior vice president for research and development at Takeda, in a company news release. “If approved, alogliptin/pioglitazone will be the first type 2 diabetes treatment option in the U.S. to include both a DPP-4 inhibitor and a thiazolidinedione in a single tablet,” he added. Alogliptin was rejected by the FDA in 2009, which asked for more data on its cardiovascular effects.
Managers Face Challenges
Managers of group practices say that preparing for risk-based reimbursement and implementing electronic health records are their biggest challenges, according to a survey from the Medical Group Management Association. Dealing with rising operating costs and implementing an accountable care organization or a patient-centered medical home are also significant challenges, according to the MGMA survey. Electronic health records and other technologies are increasingly problematic, said MGMA President and CEO William Jessee. “The pressure to adopt technology and the morass our members face in determining the best systems for their practices, and then complying with the various government programs to receive incentives and avoid penalties, are proving to be of particular concern,” he said in a statement.
Food Makers Pan Guidelines
Food manufacturers charged that voluntary guidelines proposed by the federal government ignore the industry's progress on responsible marketing of food to children. The proposal from the Federal Trade Commission says that only foods that contribute to a healthful diet should be marketed to children and offers targets for saturated fat, trans fat, added sugars, and sodium in such food. In a letter to the FTC, the FDA, and other agencies, 150 state, regional, and national food groups and manufacturers argue that there's no evidence the proposed restrictions would contribute to long-term changes in eating behavior or solve childhood obesity. Separately, the National Restaurant Association called for the voluntary standards to be withdrawn because they could become mandatory.
FDA May Change Consumer Ads
The FDA is considering changing how it regulates direct-to-consumer drug ads to reflect results of agency studies of how patients perceive and recall ad information. hhe research found that people better understood the “brief summary” section of prescription drug ads that are presented in a format similar to the simpler labels on over-the-counter drugs. Prescription drug ads use densely packed, small-type paragraphs to describe risks. The studies also found that noting a serious risk or providing extra details on side effects didn't hinder consumers' understanding of overall risk information.
Mexican-Americans at Risk
About half of 1,787 Mexican American adults, surveyed because they were obese, reported never receiving advice from a health care provider to eat less fatty food (52% informed) or exercise more (45% informed). “Given the seriousness of obesity-related health risks and the increasing prevalence of overweight status and obesity among Mexican Americans, it is vital that providers are involved in finding ways to effectively educate and/or treat overweight patients,” the authors wrote in the American Journal of Health Promotions. The survey showed that men, respondents with little education, those who preferred to speak Spanish at home, and nonmarried respondents were least likely to receive advice on exercise and diet. Respondents with comorbidities were more likely than others to have gotten diet and exercise advice (79% vs. 43%).
New Drug Reviews Expected
The largest pharmaceutical company in Japan, Takeda Pharmaceuticals, has resubmitted applications for two type 2 diabetes drugs to the U.S. Food and Drug Administration. The FDA is expected to review the drugs within the next 6 months, according to the company. The applications are for alogliptin and a combination of alogliptin and pioglitazone. Both therapies are for adults and intended as adjuncts to diet and exercise. Interim results from a study of possible cardiovascular risks from alogliptin, a selective dipeptidyl peptidase IV inhibitor (DPP-4i), should satisfy FDA concerns in that area, said Dr. David Recker, a senior vice president for research and development at Takeda, in a company news release. “If approved, alogliptin/pioglitazone will be the first type 2 diabetes treatment option in the U.S. to include both a DPP-4 inhibitor and a thiazolidinedione in a single tablet,” he added. Alogliptin was rejected by the FDA in 2009, which asked for more data on its cardiovascular effects.
Managers Face Challenges
Managers of group practices say that preparing for risk-based reimbursement and implementing electronic health records are their biggest challenges, according to a survey from the Medical Group Management Association. Dealing with rising operating costs and implementing an accountable care organization or a patient-centered medical home are also significant challenges, according to the MGMA survey. Electronic health records and other technologies are increasingly problematic, said MGMA President and CEO William Jessee. “The pressure to adopt technology and the morass our members face in determining the best systems for their practices, and then complying with the various government programs to receive incentives and avoid penalties, are proving to be of particular concern,” he said in a statement.
Food Makers Pan Guidelines
Food manufacturers charged that voluntary guidelines proposed by the federal government ignore the industry's progress on responsible marketing of food to children. The proposal from the Federal Trade Commission says that only foods that contribute to a healthful diet should be marketed to children and offers targets for saturated fat, trans fat, added sugars, and sodium in such food. In a letter to the FTC, the FDA, and other agencies, 150 state, regional, and national food groups and manufacturers argue that there's no evidence the proposed restrictions would contribute to long-term changes in eating behavior or solve childhood obesity. Separately, the National Restaurant Association called for the voluntary standards to be withdrawn because they could become mandatory.
FDA May Change Consumer Ads
The FDA is considering changing how it regulates direct-to-consumer drug ads to reflect results of agency studies of how patients perceive and recall ad information. hhe research found that people better understood the “brief summary” section of prescription drug ads that are presented in a format similar to the simpler labels on over-the-counter drugs. Prescription drug ads use densely packed, small-type paragraphs to describe risks. The studies also found that noting a serious risk or providing extra details on side effects didn't hinder consumers' understanding of overall risk information.