Jonathan B. Brown
Kaiser Permanente
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Featured researches published by Jonathan B. Brown.
Diabetes Research and Clinical Practice | 2010
Ping Zhang; Xinzhi Zhang; Jonathan B. Brown; Dorte Vistisen; Richard Sicree; Jonathan E. Shaw; Gregory A. Nichols
AIMS To estimate the global health expenditure on diabetes among people aged 20-79 years for the years 2010 and 2030. METHODS Country-by-country expenditures for 193 countries, expressed in United States Dollars (USD) and in International Dollars (ID), were estimated based on the countrys age-sex specific diabetes prevalence and population estimates, per capita health expenditures, and health expenditure ratios per person with and without diabetes. Diabetes prevalence was estimated from studies in 91 countries. Population estimates and health expenditures were from the United Nations and the World Health Organization. The health expenditure ratios were estimated based on utilization and cost data of a large health plan in the U.S. Diabetes expenditures for the year 2030 were projected by considering future changes in demographics and urbanization. RESULTS The global health expenditure on diabetes is expected to total at least USD 376 billion or ID 418 billion in 2010 and USD 490 billion or ID 561 billion in 2030. Globally, 12% of the health expenditures and USD 1330 (ID 1478) per person are anticipated to be spent on diabetes in 2010. The expenditure varies by region, age group, gender, and countrys income level. CONCLUSIONS Diabetes imposes an increasing economic burden on national health care systems worldwide. More prevention efforts are needed to reduce this burden. Meanwhile, the very low expenditures per capita in poor countries indicate that more resources are required to provide basic diabetes care in such settings.
Diabetes Care | 1998
Jonathan B. Brown; Kathryn L. Pedula; Joshua I. Barzilay; Michael K Herson; Peggy Latare
OBJECTIVE To provide a context for the interpretation of lactic acidosis risk among patients using metformin, we measured rates of lactic acidosis in patients with type 2 diabetes before metformin was approved for use in the U.S. RESEARCH DESIGN AND METHODS Using electronic databases of hospital discharge diagnoses and laboratory results maintained by a large, nonprofit health maintenance organization (HMO), we identified possible lactic acidosis events in three geographically and racially diverse populations with type 2 diabetes. We then reviewed hard-copy clinical records to confirm and describe each event and determine its likely cause(s). RESULTS From <41,000 person-years of experience, we found four confirmed, three possible, and three borderline cases of lactic acidosis. In each case, we identified at least one severe medical condition that could have caused the acidosis. The annual confirmed event rate is similar to published rates of metformin-associated lactic acidosis. CONCLUSIONS Lactic acidosis occurs regularly, although infrequently, among persons with type 2 diabetes, at rates similar to its occurrence among metformin users. The medical conditions with which both metformin-associated and naturally occurring lactic acidosis cooccur are also its potential causes. The observed association between metformin and lactic acidosis may be coincidental rather than causal. This possibility merits further study.
Journal of The American Society of Nephrology | 2004
David H. Smith; Christina M. Gullion; Gregory A. Nichols; Douglas S. Keith; Jonathan B. Brown
Chronic kidney disease (CKD) afflicts up to 20 million people in the United States, but little is known about their health care costs. The authors analyzed costs and resource use associated with CKD by using National Kidney Foundation staging definitions. Patients insured through a large health maintenance organization with a laboratory finding of CKD (defined as estimated GFR between 15 and 90 ml/min per 1.73 m(2) in 1996 followed by a second GFR below 90 at the next creatinine measurement occurring at least 90 d later) were followed from 1996 for up to 66 mo. The final cohort included 13,796 persons with CKD and their age- and gender-matched controls; 1741 in stage 2; 11,278 in stage 3; and 777 in stage 4. Depending on stage, cases had 1.9 to 2.5 times more prescriptions, 1.3 to 1.9 times more outpatient visits, were 1.6 to 2.2 times more likely to have had an inpatient stay, and had 1.8 to 3.1 more stays than did controls. Total per patient follow-up costs were [
Diabetes Care | 2010
Jonathan B. Brown; Christopher Conner; Gregory A. Nichols
total, (95% CI) cases and controls, respectively]
The American Journal of Medicine | 2008
Gregory A. Nichols; Teresa A. Hillier; Jonathan B. Brown
38,764 (95% CI, 37,033 to
Pharmacogenomics | 2010
Shany Blum; Moshe Vardi; Jonathan B. Brown; Allen Russell; Uzi Milman; Chen Shapira; Nina S. Levy; Rachel Miller-Lotan; Rabea Asleh; Andrew P. Levy
40,496) and
Diabetes-metabolism Research and Reviews | 2005
Gregory A. Nichols; Carol E. Koro; Christina M. Gullion; Sara A. Ephross; Jonathan B. Brown
16,212 (95% CI,
Diabetes Research and Clinical Practice | 2000
Jonathan B. Brown; Allen Russell; Wiley Chan; Kathryn L. Pedula; Mikel Aickin
15,644 to
The Joint Commission journal on quality improvement | 2000
Jonathan B. Brown; Diana Shye; Bentson H. McFarland; Gregory A. Nichols; John P. Mullooly; Richard E. Johnson
16,780) in stage 2;
Journal of General Internal Medicine | 1999
Jonathan B. Brown; Arne Beck; Myde Boles; Paul Barrett
33,144 (95% CI,