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Institution

Wilford Hall Medical Center

HealthcareSan Antonio, Texas, United States
About: Wilford Hall Medical Center is a healthcare organization based out in San Antonio, Texas, United States. It is known for research contribution in the topics: Population & Poison control. The organization has 1998 authors who have published 2063 publications receiving 81040 citations.


Papers
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Journal ArticleDOI
TL;DR: Prevalence of nonalcoholic fatty liver disease and NASH is higher than estimated previously and Hispanics and patients with diabetes are at greatest risk for both NAFLD and NASh.

1,910 citations

Journal ArticleDOI
TL;DR: Demographic changes in the United States will result in a marked increase in the number of cancer diagnoses over the next 20 years, and continued efforts are needed to improve cancer care for older adults and minorities.
Abstract: Purpose By 2030, the United States' population will increase to approximately 365 million, including 72 million older adults (age ≥ 65 years) and 157 million minority individuals. Although cancer incidence varies by age and race, the impact of demographic changes on cancer incidence has not been fully characterized. We sought to estimate the number of cancer patients diagnosed in the United States through 2030 by age and race. Methods Current demographic-specific cancer incidence rates were calculated using the Surveillance Epidemiology and End Results database. Population projections from the Census Bureau were used to project future cancer incidence through 2030. Results From 2010 to 2030, the total projected cancer incidence will increase by approximately 45%, from 1.6 million in 2010 to 2.3 million in 2030. This increase is driven by cancer diagnosed in older adults and minorities. A 67% increase in cancer incidence is anticipated for older adults, compared with an 11% increase for younger adults. A 9...

1,484 citations

Journal ArticleDOI
01 Jun 2005-Spine
TL;DR: Clinicians can be confident that a 2-point change on the numerical pain rating scale (NPRS) represents clinically meaningful change that exceeds the bounds of measurement error.
Abstract: Study design Cohort study of patients with low back pain (LBP) receiving physical therapy. Objective To examine the responsiveness characteristics of the numerical pain rating scale (NPRS) in patients with LBP using a variety of methods. Summary of background data Although several studies have assessed the reliability and validity of the NPRS, few studies have characterized its responsiveness in patients with LBP. Methods Determination of change on the NPRS during 1 and 4 weeks was examined by calculating mean change, standardized effect size, Guyatt Responsiveness Index, area under a receiver operating characteristic curve, minimum clinically important difference, and minimum detectable change. Change in the NPRS from baseline to the 1 and 4-week follow-up was compared to the average of the patient and therapist's perceived improvement using the 15-point Global Rating of Change scale. Results The majority of patients had clinically meaningful improvement after both 1 and 4 weeks of rehabilitation. The standard error of measure was equal to 1.02, corresponding to a minimum detectable change of 2 points. The area under the curve at the 1 and 4-week follow-up was 0.72 (0.62, 0.81) and 0.92 (0.86, 0.97), respectively. The minimum clinically important difference at the 1 and 4-week follow-up corresponded to a change of 2.2 and 1.5 points, respectively. Conclusions Clinicians can be confident that a 2-point change on the NPRS represents clinically meaningful change that exceeds the bounds of measurement error.

1,132 citations

Journal ArticleDOI
TL;DR: It is demonstrated that surface roughness alters osteoblast proliferation, differentiation, and matrix production in vitro and suggests that implant surfaceroughness may play a role in determining phenotypic expression of cells in vivo.
Abstract: The effect of surface roughness on osteoblast proliferation, differentiation, and protein synthesis was examined. Human osteoblast-like cells (MG63) were cultured on titanium (Ti) disks that had been prepared by one of five different treatment regimens. All disks were pretreated with hydrofluoric acid-nitric acid and washed (PT). PT disks were also: washed, and then electropolished (EP); fine sandblasted, etched with HCl and H 2 SO 4 , and washed (FA); coarse sandblasted, etched with HCl and H 2 SO 4 , and washed (CA); or Ti plasma-sprayed (TPS). Standard tissue culture plastic was used as a control. Surface topography and profile were evaluated by brightfield and darkfield microscopy, cold field emission scanning electron microscopy, and laser confocal microscopy, while chemical composition was mapped using energy dispersion X-ray analysis and elemental distribution determined using Auger electron spectroscopy. The effect of surface roughness on the cells was evaluated by measuring cell number, [ 3 H]thymidine incorporation into DNA, alkaline phosphatase specific activity, [ 3 H]uridine incorporation into RNA, [ 3 H]proline incorporation into collagenase digestible protein (CDP) and noncollagenase-digestible protein (NCP), and [ 35 S]sulfate incorporation into proteoglycan. Based on surface analysis, the five different Ti surfaces were ranked in order of smoothest to roughest: EP, PT, FA, CA, and TPS. A TiO 2 layer was found on all surfaces that ranged in thickness from 100 A in the smoothest group to 300 A in the roughest. When compared to confluent cultures of cells on plastic, the number of cells was reduced on the TPS surfaces and increased on the EP surfaces, while the number of cells on the other surfaces was equivalent to plastic. [ 3 H]Thymidine incorporation was inversely related to surface roughness. Alkaline phosphatase specific activity in isolated cells was found to decrease with increasing surface roughness, except for those cells cultured on CA. In contrast, enzyme activity in the cell layer was only decreased in cultures grown on FA- and TPS-treated surfaces. A direct correlation between surface roughness and A and CDP production was found. Surface roughness had no apparent effect on NCP production. Proteoglycan synthesis by the cells was inhibited on all the surfaces studied, with the largest inhibition observed in the CA and EP groups. These results demonstrate that surface roughness alters osteoblast proliferation, differentiation, and matrix production in vitro. The results also suggest that implant surface roughness may play a role in determining phenotypic expression of cells in vivo

1,117 citations


Authors

Showing all 2007 results

NameH-indexPapersCitations
Robert Langer2812324326306
Jonathan I. Epstein138112180975
Peter T. Fox13162283369
Robert J. Kurman12739760277
Anthony A. Amato10591157881
Benjamin Smith10363146514
Ian M. Thompson9977146524
Louis R. Kavoussi9554431830
Philip A. Pizzo8336629870
Douglas B. Cines7939727792
Warren S. Alexander7825428414
Richard J. Barohn7832723499
Michael J. Yaszemski7737919116
Paul A. Gurbel7758928852
Jeffrey A. Cadeddu7557619510
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20235
20228
20215
20206
20194
20181