Paul G. Barnett
VA Palo Alto Healthcare System
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The New England Journal of Medicine | 2008
William S. Weintraub; John A. Spertus; Paul Kolm; David J. Maron; Zefeng Zhang; Claudine Jurkovitz; Wei Zhang; Pamela Hartigan; Cheryl Lewis; Emir Veledar; Jim Bowen; Sandra B. Dunbar; Christi Deaton; Stanley Kaufman; Robert A. O'Rourke; Ron Goeree; Paul G. Barnett; Koon K. Teo; William E. Boden
BACKGROUND It has not been clearly established whether percutaneous coronary intervention (PCI) can provide an incremental benefit in quality of life over that provided by optimal medical therapy among patients with chronic coronary artery disease. METHODS We randomly assigned 2287 patients with stable coronary disease to PCI plus optimal medical therapy or to optimal medical therapy alone. We assessed angina-specific health status (with the use of the Seattle Angina Questionnaire) and overall physical and mental function (with the use of the RAND 36-item health survey [RAND-36]). RESULTS At baseline, 22% of the patients were free of angina. At 3 months, 53% of the patients in the PCI group and 42% in the medical-therapy group were angina-free (P<0.001). Baseline mean (+/-SD) Seattle Angina Questionnaire scores (which range from 0 to 100, with higher scores indicating better health status) were 66+/-25 for physical limitations, 54+/-32 for angina stability, 69+/-26 for angina frequency, 87+/-16 for treatment satisfaction, and 51+/-25 for quality of life. By 3 months, these scores had increased in the PCI group, as compared with the medical-therapy group, to 76+/-24 versus 72+/-23 for physical limitation (P=0.004), 77+/-28 versus 73+/-27 for angina stability (P=0.002), 85+/-22 versus 80+/-23 for angina frequency (P<0.001), 92+/-12 versus 90+/-14 for treatment satisfaction (P<0.001), and 73+/-22 versus 68+/-23 for quality of life (P<0.001). In general, patients had an incremental benefit from PCI for 6 to 24 months; patients with more severe angina had a greater benefit from PCI. Similar incremental benefits from PCI were seen in some but not all RAND-36 domains. By 36 months, there was no significant difference in health status between the treatment groups. CONCLUSIONS Among patients with stable angina, both those treated with PCI and those treated with optimal medical therapy alone had marked improvements in health status during follow-up. The PCI group had small, but significant, incremental benefits that disappeared by 36 months. (ClinicalTrials.gov number, NCT00007657.)
Medical Care Research and Review | 2003
Wei Yu; Arliene Ravelo; Todd H. Wagner; Ciaran S. Phibbs; Aman Bhandari; Shuo Chen; Paul G. Barnett
Chronic conditions are among the most common causes of death and disability in the United States. Patients with such conditions receive disproportionate amounts of health care services and therefore cost more per capita than the average patient. This study assesses the prevalence among the Department of Veterans Affairs (VA) health care users and VA expenditures (costs) of 29 common chronic conditions. The authors used regression to identify the marginal impact of these conditions on total, inpatient, outpatient, and pharmacy costs. Excluding costs of contracted medical services at non-VA facilities, total VA health care expenditures in fiscal year 1999 (FY1999) were
Circulation | 2014
Jeffrey L. Anderson; Paul A. Heidenreich; Paul G. Barnett; Mark A. Creager; Gregg C. Fonarow; Raymond J. Gibbons; Jonathan L. Halperin; Mark A. Hlatky; Alice K. Jacobs; Daniel B. Mark; Frederick A. Masoudi; Eric D. Peterson; Leslee J. Shaw
14.3 billion. Among the 3.4 million VA patients in FY1999, 72 percent had 1 or more of the 29 chronic conditions, and these patients accounted for 96 percent of the total costs (
The New England Journal of Medicine | 2011
Robert A. Rosenheck; John H. Krystal; Robert A. Lew; Paul G. Barnett; Louis D. Fiore; Danielle Valley; Soe Soe Thwin; Julia E. Vertrees; Matthew H. Liang
13.7 billion). In addition, 35 percent (1.2 million) of VA health care users had 3 or more of the 29 chronic conditions. These individuals accounted for 73 percent of the total cost. Overall, VA health care users have more chronic diseases than the general population.
Circulation | 2014
Jeffrey L. Anderson; Paul A. Heidenreich; Paul G. Barnett; Mark A. Creager; Gregg C. Fonarow; Raymond J. Gibbons; Jonathan L. Halperin; Mark A. Hlatky; Alice K. Jacobs; Daniel B. Mark; Frederick A. Masoudi; Eric D. Peterson; Leslee J. Shaw
Traditionally, resource utilization and value considerations have been explicitly excluded from practice guidelines and performance measures formulations, although they often are implicitly considered. This document challenges this historical policy. With accelerating healthcare costs and the desire to achieve the best value (health benefit for every dollar spent), there is growing recognition of the need for more explicit and transparent assessment of the value of health care. Thus, from a societal policy perspective, a critical healthcare …
Journal of Health Economics | 1996
Theodore E. Keeler; Teh-wei Hu; Paul G. Barnett; Willard G. Manning; Hai-Yen Sung
BACKGROUND Long-acting injectable risperidone, a second-generation antipsychotic agent, may improve adherence to treatment and outcomes in schizophrenia, but it has not been tested in a long-term randomized trial involving patients with unstable disease. METHODS We randomly assigned patients in the Veterans Affairs (VA) system who had schizophrenia or schizoaffective disorder and who had been hospitalized within the previous 2 years or were at imminent risk for hospitalization to 25 to 50 mg of long-acting injectable risperidone every two weeks or to a psychiatrists choice of an oral antipsychotic. All patients were followed for up to 2 years. The primary end point was hospitalization in a VA or non-VA psychiatric hospital. Symptoms, quality of life, and functioning were assessed in blinded videoconference interviews. RESULTS Of 369 participants, 40% were hospitalized at randomization, 55% were hospitalized within the previous 2 years, and 5% were at risk for hospitalization. The rate of hospitalization after randomization was not significantly lower among patients who received long-acting injectable risperidone than among those who received oral antipsychotics (39% after 10.8 months vs. 45% after 11.3 months; hazard ratio, 0.87; 95% confidence interval, 0.63 to 1.20). Psychiatric symptoms, quality of life, scores on the Personal and Social Performance scale of global functioning, and neurologic side effects were not significantly improved with long-acting injectable risperidone as compared with control treatments. Patients who received long-acting injectable risperidone reported more adverse events at the injection site and more extrapyramidal symptoms. CONCLUSIONS Long-acting injectable risperidone was not superior to a psychiatrists choice of oral treatment in patients with schizophrenia and schizoaffective disorder who were hospitalized or at high risk for hospitalization, and it was associated with more local injection-site and extrapyramidal adverse effects. (Supported by the VA Cooperative Studies Program and Ortho-McNeil Janssen Scientific Affairs; ClinicalTrials.gov number, NCT00132314.).
Journal of Public Economics | 1995
Paul G. Barnett; Theodore E. Keeler; Teh-wei Hu
Cardiology requests that this document be cited as nreich PA, Barnett PG, Creager MA, Fonarow GC, Hlatky MA, Jacobs AK, Mark DB, Masoudi FA, C/AHA statement on cost/value methodology in d performance measures: a report of the American ican Heart Association Task Force on Performance n Practice Guidelines. J Am Coll Cardiol 2014;63: Betwee peer revie This ar Copies College o (my.amer Reprint D Permis tribution American (http://ww Mark A. Hlatky, MD, FACC, FAHA Alice K. Jacobs, MD, FACC, FAHA Daniel B. Mark, MD, MPH, FACC, FAHA Frederick A. Masoudi, MD, MSPH, FACC, FAHA Eric D. Peterson, MD, MPH, FACC, FAHA Leslee J. Shaw, PHD, FACC, FAHA
Circulation-cardiovascular Quality and Outcomes | 2008
William S. Weintraub; William E. Boden; Zugui Zhang; Paul Kolm; Zefeng Zhang; John A. Spertus; Pamela Hartigan; Emir Veledar; Claudine Jurkovitz; Jim Bowen; David J. Maron; Robert A. O'Rourke; Marcin Dada; Koon K. Teo; Ron Goeree; Paul G. Barnett
This study analyzes the interactive effects of oligopoly pricing, state taxation, and anti-smoking regulations on retail cigarette prices by state, using panel data for the 50 US states between 1960 and 1990. The results indicate that cigarette producers do price-discriminate by state, though the effect is not large relative to the final retail price. There are two further results: (1) state taxes are more than passed on - a 1-cent state tax increase results in a price increase of 1.11 cents, and (2) sellers offset state and local anti-smoking laws with lower prices, thereby blunting effects of the regulations.
Medical Care Research and Review | 2003
Todd H. Wagner; Shuo Chen; Paul G. Barnett
The economic incidence of cigarette excise taxes in the United States is estimated for 1955-1989. The analysis simultaneously considers consumer demand and the reactions of manufacturers and the distribution industry, and contrasts the incidence of federal with state and local taxes. A cost function was estimated, and found that cigarette manufacture is subject to increasing returns to scale. The model of the market found a mean price elasticity of demand of -1.08. Price elasticity has been decreasing. The elimination of simultaneity bias may explain why this estimate is higher than that of other studies. The industry was found to be less competitive than a Cournot industry. Competition among manufacturers has decreased substantially since 1980. This may be because manufacturers have become less concerned about anti-trust scrutiny or the prospect of new competitors. A simulation shows that an increase in the federal excise tax causes a greater increase in price, and a greater decrease in consumption, than does the same increase in the average of state and local tax rates. This is consistent with the view that in the face of an increase in a state or local tax, some demand shifts to neighboring jurisdictions with lower taxes.
Circulation | 2006
Kevin T. Stroupe; Douglass A. Morrison; Mark A. Hlatky; Paul G. Barnett; Lishan Cao; Christopher Lyttle; Denise M. Hynes; William G. Henderson
Background—The COURAGE (Clinical Outcomes Utilizing Revascularization and Aggressive druG Evaluations) trial compared the effect of percutaneous coronary intervention (PCI) plus optimal medical therapy with optimal medical therapy alone on cardiovascular events in 2287 patients with stable coronary disease. After 4.6 years, there was no difference in the primary end point of death or myocardial infarction, although PCI improved quality of life. The present study evaluated the relative cost and cost-effectiveness of PCI in the COURAGE trial. Methods and Results—Resource use was assessed by diagnosis-related group for hospitalizations and by current procedural terminology code for outpatient visits and tests and then converted to costs by use of 2004 Medicare payments. Medication costs were assessed with the Red Book average wholesale price. Life expectancy beyond the trial was estimated from Framingham survival data. Utilities were assessed by the standard gamble method. The incremental cost-effectiveness ratio was expressed as cost per life-year and cost per quality-adjusted life-year gained. The added cost of PCI was approximately