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Dive into the research topics where Lawrence Williams is active.

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Featured researches published by Lawrence Williams.


The New England Journal of Medicine | 2002

Cost Effectiveness of Aspirin, Clopidogrel, or Both for Secondary Prevention of Coronary Heart Disease

Jean Michel Gaspoz; Pamela G. Coxson; Paula A. Goldman; Lawrence Williams; Karen M. Kuntz; M. G. Myriam Hunink; Lee Goldman

BACKGROUND Both aspirin and clopidogrel reduce the rate of cardiovascular events in patients with coronary heart disease. We estimated the cost effectiveness of the increased use of aspirin, clopidogrel, or both for secondary prevention in patients with coronary heart disease. METHODS We used the Coronary Heart Disease Policy Model, a computer simulation of the U.S. population, to estimate the incremental cost effectiveness (in dollars per quality-adjusted years of life gained) of four strategies in patients over 35 years of age with coronary disease from 2003 to 2027: aspirin for all eligible patients (i.e., those who were not allergic to or intolerant of aspirin), aspirin for all eligible patients plus clopidogrel for patients who were ineligible for aspirin, clopidogrel for all patients, and the combination of aspirin for all eligible patients plus clopidogrel for all patients. RESULTS The extension of aspirin therapy from the current levels of use to all eligible patients for 25 years would have an estimated cost-effectiveness ratio of about


Annals of Internal Medicine | 2000

Cost-Effectiveness of Cholesterol-Lowering Therapies according to Selected Patient Characteristics

Lisa A. Prosser; Aaron A. Stinnett; Paula A. Goldman; Lawrence Williams; M. G. Myriam Hunink; Lee Goldman; Milton C. Weinstein

11,000 per quality-adjusted year of life gained. The addition of clopidogrel for the 5 percent of patients who are ineligible for aspirin would cost about


Neurology | 1999

Cost-effectiveness of donepezil in the treatment of mild or moderate Alzheimer’s disease

Peter J. Neumann; Richard C. Hermann; Karen M. Kuntz; Sally S. Araki; S. B. Duff; Joel Leon; P. A. Berenbaum; Paula A. Goldman; Lawrence Williams; Milton C. Weinstein

31,000 per quality-adjusted year of life gained. Clopidogrel alone in all patients or in routine combination with aspirin had an incremental cost of more than


Annals of Internal Medicine | 2009

Comparing Impact and Cost-Effectiveness of Primary Prevention Strategies for Lipid-Lowering

Mark J. Pletcher; Lawrence D. Lazar; Kirsten Bibbins-Domingo; Andrew E. Moran; Nicolas Rodondi; Pamela G. Coxson; James Lightwood; Lawrence Williams; Lee Goldman

130,000 per quality-adjusted year of life gained and remained financially unattractive across a wide range of assumptions. However, clopidogrel alone or in combination with aspirin would cost less than


The New England Journal of Medicine | 2015

Cost-Effectiveness of Hypertension Therapy According to 2014 Guidelines

Andrew E. Moran; Michelle C. Odden; Anusorn Thanataveerat; Keane Y. Tzong; Petra W. Rasmussen; David Guzman; Lawrence Williams; Kirsten Bibbins-Domingo; Pamela G. Coxson; Lee Goldman; Abstr Act

50,000 per quality-adjusted year of life gained if its price were reduced by 70 to 82 percent, to


American Journal of Public Health | 2009

Forecasting the future economic burden of current adolescent overweight: an estimate of the coronary heart disease policy model.

James Lightwood; Kirsten Bibbins-Domingo; Pamela G. Coxson; Y. Claire Wang; Lawrence Williams; Lee Goldman

1.00 and


Circulation | 1997

Cost-Effectiveness of Populationwide Educational Approaches to Reduce Serum Cholesterol Levels

Anna N. A. Tosteson; Milton C. Weinstein; M. G. Myriam Hunink; Murray A. Mittleman; Lawrence Williams; Paula A. Goldman; Lee Goldman

0.60 per day, respectively. CONCLUSIONS Increased prescription of aspirin for secondary prevention of coronary heart disease is attractive from a cost-effectiveness perspective. Because clopidogrel is more costly, its incremental cost effectiveness is currently unattractive, unless its use is restricted to patients who are ineligible for aspirin.


Journal of the American College of Cardiology | 2001

The effect of risk factor reductions between 1981 and 1990 on coronary heart disease incidence, prevalence, mortality and cost☆

Lee Goldman; Kathryn A. Phillips; Pamela G. Coxson; Paula A. Goldman; Lawrence Williams; M. G. Myriam Hunink; Milton C. Weinstein

Several large-scale, long-term clinical trials evaluating statin drugs (3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors) have confirmed the beneficial effect of reducing cholesterol levels on coronary event rates and related mortality (1-5). Statin drugs are expensive, especially considering the large number of persons who could potentially benefit from cholesterol-lowering therapies. As a result, many analyses have focused on the costs, resource use, and cost-effectiveness of using statins to lower cholesterol levels (6-15). In this analysis, the cost-effectiveness of primary and secondary prevention with cholesterol-lowering therapies was evaluated in separate risk subgroups to assess how cost-effectiveness varies with individual patient characteristics. This analysis extends the results of previous analyses by examining a greater number of specific patient subgroups, particularly with respect to primary prevention. It improves on previous analyses by including updated costs and epidemiologic estimates and by following recommendations from the U.S. Panel on Cost-Effectiveness in Health and Medicine. The incremental cost-effectiveness of statins compared with diet therapy was explicitly modeled. Finally, we compared the cost-effectiveness results with the treatment guidelines recommended by the National Cholesterol Education Program Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel II) (16). Methods The analysis used a previously validated computer simulation model, the Coronary Heart Disease Policy Model (17-19), to estimate the effects and costs of each cholesterol-lowering strategy in each risk group. The assumptions and design of the Coronary Heart Disease Policy Model are described in detail elsewhere (17, 18). The model consists of three integrated submodels: the demographic-epidemiologic submodel, the bridge submodel, and the disease history submodel. The demographic-epidemiologic submodel predicts coronary heart disease incidence and noncoronary heart disease mortality among people 35 to 84 years of age without coronary heart disease. The risk function for incidence of coronary heart disease is based on age, sex, diastolic blood pressure, smoking status, low-density lipoprotein (LDL) cholesterol level, and high-density lipoprotein (HDL) cholesterol level. The risk function for noncoronary heart disease mortality includes age, sex, diastolic blood pressure, and smoking status. Noncoronary heart disease mortality is assumed to be unaffected by serum cholesterol levels (1, 2). After a person in the model develops coronary heart disease, he or she moves into the bridge submodel, which characterizes the initial coronary heart disease event (cardiac arrest, myocardial infarction, or angina) and the sequelae in the first 30 days after the event. The disease history submodel tracks the subsequent development of coronary heart disease events, revascularization procedures (coronary artery bypass grafting and angioplasty), coronary heart disease mortality, and noncoronary heart disease mortality among patients with coronary heart disease. Target Population The base-case analysis evaluated the cost-effectiveness of primary and secondary prevention in all persons with LDL cholesterol levels of 4.1 mmol/L or greater ( 160 mg/dL). Specific subgroup analyses examined how the cost-effectiveness changed according to patient age (35 to 44, 45 to 54, 55 to 64, 65 to 74, or 75 to 84 years), sex, smoking status (yes or no), diastolic blood pressure (<95 mm Hg or 95 mm Hg), HDL cholesterol level (<0.9, 0.9 to 1.3, or>1.3 mmol/L [<35, 35 to 49, or 50 mg/dL]), and LDL cholesterol level (4.2 to 4.9 or 4.9 mmol/L [160 to 189 or 190 mg/dL]). These risk factors closely correspond to but are not exactly the same as the National Cholesterol Education Program risk factor definitions (16). Effectiveness Lipid Levels Results from five studies were pooled to estimate the effects of a low-cholesterol diet (step I diet) on cholesterol levels (20-24). Data used to model the effectiveness of primary prevention with a statin came from three long-term studies of pravastatin, 40 mg/d, because the quality of effectiveness data was high for this dosage (2, 25, 26). Effectiveness estimates for secondary prevention with a statin was based on results from the Scandinavian Simvastatin Survival Study (Appendix Table 1) (1). A 2-year time lag between the start of treatment and the effects of treatment on coronary events was assumed (1, 2). Quality of Life Quality-of-life weights in the general population without coronary heart disease were based on data from the Beaver Dam Health Outcomes Study according to age and sex (27). Additional quality-of-life adjustments for coronary heart diseaserelated morbidity were made for persons in the disease history submodel; because community preferences were not available, these adjustments were based on a survey of Medicare patients with a history of coronary heart disease (28, 29). Costs In the Coronary Heart Disease Policy Model, total costs were calculated as the sum of intervention costs, costs of coronary heart disease care, and costs of noncoronary heart disease health care. All costs were converted to 1997 U.S. dollars by using the Medical Care Component of the Consumer Price Index. Intervention costs included the costs of medication, physician visits (including the associated patient time), and laboratory tests. National Cholesterol Education Program guidelines were used to guide estimates of the number of physician visits and laboratory tests each year (16). Medication Medication costs for primary and secondary prevention with statins were calculated by using the average wholesale prices of pravastatin and simvastatin, respectively (30). The base-case analysis does not include adjustment of future medication costs resulting from loss of patent protection for statin drugs. To adjust for compliance, it was assumed that patients receiving statins take 95% of the suggested regimen (31); this average compliance rate is reflected in the pool of studies from which the estimates of effectiveness were derived (Appendix Table 1). Primary Prevention Patients receiving diet therapy were assumed to have two physician visits per year. Patients receiving primary prevention with a statin were assumed to have five physician visits in the first year and two physician visits in each year after the first year. A cost of


American Journal of Cardiology | 1993

Cost-effectiveness considerations in the treatment of heterozygous familial hypercholesterolemia with medications.

Lee Goldman; Paula A. Goldman; Lawrence Williams; Milton C. Weinstein

34.34 was associated with each office visit (32, 33). In addition, the value of patient time associated with each visit was estimated by multiplying the average time per visit (including travel, waiting, and encounter times) by age- and sex-specific average hourly wages. These age- and sex-adjusted patient time costs range from approximately


Circulation | 1989

Relative impact of targeted versus populationwide cholesterol interventions on the incidence of coronary heart disease. Projections of the Coronary Heart Disease Policy Model.

Lee Goldman; Milton C. Weinstein; Lawrence Williams

12 to

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Lee Goldman

University of California

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M. G. Myriam Hunink

Erasmus University Rotterdam

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