Thomas J. Flottemesch
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Featured researches published by Thomas J. Flottemesch.
Health Affairs | 2010
Michael V. Maciosek; Ashley B. Coffield; Thomas J. Flottemesch; Nichol M. Edwards; Leif I. Solberg
There is broad debate over whether preventive health services save money or represent a good investment. This paper analyzes the estimated cost of adopting a package of twenty proven preventive services--including tobacco cessation screening, alcohol abuse screening, and daily aspirin use--against the estimated savings that could be generated. We find that greater use of proven clinical preventive services in the United States could avert the loss of more than two million life-years annually. Whats more, increasing the use of these services from current levels to 90 percent in 2006 would result in total savings of
Journal of the National Cancer Institute | 2012
Ajay S. Behl; Katrina A.B. Goddard; Thomas J. Flottemesch; David L. Veenstra; Richard T. Meenan; Jennifer Lin; Michael V Maciosek
3.7 billion, or 0.2 percent of U.S. personal health care spending. These findings suggest that policy makers should pursue options that move the nation toward greater use of proven preventive services.
Clinical Toxicology | 2007
Joel S. Holger; Kristin M. Engebretsen; Sandy J. Fritzlar; Lane C. Patten; Carson R. Harris; Thomas J. Flottemesch
BACKGROUND In 2009, the American Society of Clinical Oncology recommended that patients with metastatic colorectal cancer (mCRC) who are candidates for anti-epidermal growth factor receptor (EGFR) therapy have their tumors tested for KRAS mutations because tumors with such mutations do not respond to anti-EGFR therapy. Limiting anti-EGFR therapy to those without KRAS mutations will reserve treatment for those likely to benefit while avoiding unnecessary costs and harm to those who would not. Similarly, tumors with BRAF genetic mutations may not respond to anti-EGFR therapy, though this is less clear. Economic analyses of mutation testing have not fully explored the roles of alternative therapies and resection of metastases. METHODS This paper is based on a decision analytic framework that forms the basis of a cost-effectiveness analysis of screening for KRAS and BRAF mutations in mCRC in the context of treatment with cetuximab. A cohort of 50 000 patients with mCRC is simulated 10 000 times, with attributes randomly assigned on the basis of distributions from randomized controlled trials. RESULTS Screening for both KRAS and BRAF mutations compared with the base strategy (of no anti-EGFR therapy) increases expected overall survival by 0.034 years at a cost of
Annals of Family Medicine | 2011
Leif I. Solberg; Stephen E. Asche; Patricia Fontaine; Thomas J. Flottemesch; Louise H. Anderson
22 033, yielding an incremental cost-effectiveness ratio of approximately
Annals of Internal Medicine | 2016
Steven P. Dehmer; Michael V. Maciosek; Thomas J. Flottemesch; Amy B. LaFrance; Evelyn P. Whitlock
650 000 per additional year of life. Compared with anti-EGFR therapy without screening, adding KRAS testing saves approximately
Annual Review of Public Health | 2009
Michael V. Maciosek; Ashley B. Coffield; Nichol M. Edwards; Thomas J. Flottemesch; Leif I. Solberg
7500 per patient; adding BRAF testing saves another
Annals of Emergency Medicine | 2008
Bradley D. Gordon; Thomas J. Flottemesch; Brent R. Asplin
1023, with little reduction in expected survival. CONCLUSIONS Screening for KRAS and BFAF mutation improves the cost-effectiveness of anti-EGFR therapy, but the incremental cost effectiveness ratio remains above the generally accepted threshold for acceptable cost effectiveness ratio of
Academic Emergency Medicine | 2008
Emily Binstadt; Scott Donner; Jessie Nelson; Thomas J. Flottemesch; Cullen Hegarty
100 000/quality adjusted life year.
American Journal of Preventive Medicine | 2014
Alyson H. Kristensen; Thomas J. Flottemesch; Michael V. Maciosek; Jennifer Jenson; Gillian Barclay; Marice Ashe; Eduardo Sanchez; Mary Story; Steven M. Teutsch; Ross C. Brownson
Objective. We compared insulin and glucose (IN/G) to vasopressin plus epinephrine (V/E) in a pig model of β-blocker toxicity. Primary outcome was survival over four hours. Methods. Ten pigs received a 0.5 mg/kg bolus of propranolol IV followed by a continuous infusion. At the point of toxicity 20 ml/kg normal saline was rapidly infused and the propranolol drip continued at 0.125 mg/kg/min over four hours of resuscitation. Each pig was randomized to either IN/G or V/E. The V/E group began with epinephrine at 10 mcg/kg/min titrated up by 10 mcg/kg/min every 10 min to 50 mcg/kg/min or until baseline was obtained. Simultaneously, these pigs received vasopressin at 0.0028 units/kg/min, titrated upwards every 10 min to 0.014 units/kg/min or until baseline was obtained. The IN/G group began with a 2 units/kg/hr drip and increased by 2 units every 10 minutes to 10 units/kg/hr, or until baseline hemodynamics were obtained. CO, SVR, systolic blood pressure, HR, MAP, glucose, and potassium were monitored. Glucose was given for values <60 mg/dl. Results. The study was terminated early due to marked survival differences after five pigs were entered in each group. All IN/G group pigs survived four hours. All V/E group pigs died within 90 min. CO in the IN/G group increased throughout the four hours, rising above pre-propranolol levels, while MAP, SBP, and SVR all trended slightly downward. CO in the V/E group dropped until death, while MAP, SBP, and SVR rose precipitously until 30–60 minutes when these dropped abruptly until death. Glucose was required in the IN/G group. Conclusion. In this swine model, IN/G is superior to V/E to treat β-blocker toxicity. IN/G has marked inotropic properties while the vasopressor effects of V/E depress CO and contribute to death. Increasing SVR in this condition is detrimental to survival.
Academic Emergency Medicine | 2010
Joel S. Holger; David J. Dries; Kelly Barringer; Benjamin J. Peake; Thomas J. Flottemesch; John J. Marini
PURPOSE We describe changes over time in performance on measures of technical quality and patient experience as a group of primary care clinics transformed themselves into level III patient-centered medical homes. METHODS A group of 21 Minnesota primary care clinics achieving level III recognition as medical homes by the National Committee for Quality Assurance has been tracking a variety of quality and patient satisfaction measures for years. We analyzed trends in these measures and compared them with those of other medical groups in the community to estimate what we might expect as other primary care sites gear up to achieve medical home status. RESULTS The clinics in this group achieved a 1% to 3% increase per year in patient satisfaction and a 2% to 7% increase per year in performance on quality measures for diabetes, coronary artery disease, preventive services, and generic medication use. When compared with the average for other medical groups in the region, the rates of increase were greater for satisfaction, but similar for the quality measures. CONCLUSIONS Achieving medical home recognition was associated with improvements in quality and patient satisfaction for these clinics, but the rate of improvement is slow and does not always exceed levels in the surrounding community in Minnesota (which are also improving). Expectations for large and rapid change are probably unrealistic.