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1.
Mil Med ; 180(1): 111-7, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25562866

ABSTRACT

The Veterans Health Administration (VHA) provides care to over 8 million Veterans and operates over 1,700 sites of care across 21 regional networks in the United States. Health care providers within VHA report large seasonal variation in the demand for services, especially in the southern United States because of arrival of "snowbirds" during the winter. Because resource allocation activities are primarily carried out through an annual budgeting process, the seasonal load imposed by "traveling Veterans"-Veterans that seek care at VHA sites outside of their home network-make providing high-quality services more challenging. This work constitutes the first major effort within VHA to understand the impact of traveling Veterans. We discovered strong seasonal fluctuations in demand at a clinic located in the southeastern United States and developed a seasonal autoregressive integrated moving average model to help the clinic forecast demand for its services with significantly less error than historical averaging. Monte Carlo simulation of the clinic revealed that physicians are overutilized, suggesting the need to re-evaluate how the clinic is currently staffed. More broadly, this study demonstrates how operations management methods can assist operational decision making at other clinics and medical centers both within and outside VHA.


Subject(s)
Ambulatory Care Facilities/statistics & numerical data , Health Resources/statistics & numerical data , Health Services Needs and Demand/trends , Models, Statistical , Seasons , Veterans , Ambulatory Care Facilities/supply & distribution , Computer Simulation , Forecasting/methods , Health Resources/supply & distribution , Human Migration/trends , Humans , Monte Carlo Method , Southeastern United States , Travel/trends , United States , United States Department of Veterans Affairs/organization & administration , Workforce
2.
Macromol Biosci ; 12(10): 1342-53, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22927323

ABSTRACT

Previous studies demonstrated the importance of substrate stiffness and topography on the phenotype of many different cell types including fibroblasts. Yet the interaction of these two physical parameters remains insufficiently characterized, in particular for cardiac fibroblasts. Most studies focusing on contact guidance use rigid patterned substrates. It is not known how the ability of cardiac fibroblasts to follow grooves and ridges changes as the substrate stiffness is decreased to match the range of stiffness found in native heart tissues. This report demonstrates a significant interactive effect of substrate stiffness and topography on cardiac fibroblast elongation and orientation using polyacrylamide substrates of different stiffness and topography.


Subject(s)
Acrylic Resins/chemical synthesis , Biocompatible Materials/chemical synthesis , Collagen/chemistry , Fibroblasts/cytology , Acrylic Resins/pharmacology , Animals , Animals, Newborn , Biocompatible Materials/pharmacology , Cell Survival/drug effects , Cells, Cultured , Elasticity , Fibroblasts/drug effects , Fibroblasts/physiology , Heterocyclic Compounds, 4 or More Rings/pharmacology , Hydrogels , Microscopy, Electron, Scanning , Myocardium/cytology , Rats , Surface Properties , Tissue Engineering , Tissue Scaffolds
3.
Tissue Eng Part A ; 17(13-14): 1713-23, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21306293

ABSTRACT

Poly(ethylene glycol) (PEG) hydrogels are popular for cell culture and tissue-engineering applications because they are nontoxic and exhibit favorable hydration and nutrient transport properties. However, cells cannot adhere to, remodel, proliferate within, or degrade PEG hydrogels. Methacrylated gelatin (GelMA), derived from denatured collagen, yields an enzymatically degradable, photocrosslinkable hydrogel that cells can degrade, adhere to and spread within. To combine the desirable features of each of these materials we synthesized PEG-GelMA composite hydrogels, hypothesizing that copolymerization would enable adjustable cell binding, mechanical, and degradation properties. The addition of GelMA to PEG resulted in a composite hydrogel that exhibited tunable mechanical and biological profiles. Adding GelMA (5%-15% w/v) to PEG (5% and 10% w/v) proportionally increased fibroblast surface binding and spreading as compared to PEG hydrogels (p<0.05). Encapsulated fibroblasts were also able to form 3D cellular networks 7 days after photoencapsulation only within composite hydrogels as compared to PEG alone. Additionally, PEG-GelMA hydrogels displayed tunable enzymatic degradation and stiffness profiles. PEG-GelMA composite hydrogels show great promise as tunable, cell-responsive hydrogels for 3D cell culture and regenerative medicine applications.


Subject(s)
Gelatin/pharmacology , Methacrylates/pharmacology , Polyethylene Glycols/chemical synthesis , Polyethylene Glycols/pharmacology , Animals , Cell Adhesion/drug effects , Cell Survival/drug effects , Fibroblasts/cytology , Fibroblasts/drug effects , Hydrogels , Mechanical Phenomena/drug effects , Mice , NIH 3T3 Cells , Surface Properties/drug effects , Water
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