Neeta Rugg
University of Cincinnati
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Publication
Featured researches published by Neeta Rugg.
Transfusion | 2003
John R. Hess; Heather R. Hill; Cindy K. Oliver; Lloyd E. Lippert; Neeta Rugg; Amy D. Joines; Jennifer F. Gormas; P. Gayle Pratt; Edward B. Silverstein; Tibor J. Greenwalt
BACKGROUND: Better storage can improve RBC availability and safety. Optimizing RBC ATP production and minimizing hemolysis has allowed progressively longer storage.
Transfusion | 2006
John R. Hess; Neeta Rugg; Amy D. Joines; Jennifer F. Gormas; P.G. Pratt; Edward B. Silberstein; T.J. Greenwalt
BACKGROUND: Red blood cell (RBC) storage solutions work in a narrow pH range between 7.2 and 6.4. While keeping RBC within that pH range, ATP production can be increased by buffering or dilution.
Transfusion | 2000
John R. Hess; Neeta Rugg; Amy D. Knapp; Jennifer F. Gormas; Edward B. Silberstein; T.J. Greenwalt
BACKGROUND: This study explored the effect of storing packed RBCs suspended in 200 mL of an alkaline, hypotonic, experimental additive solution (EAS 61).
Transfusion | 2013
Larry J. Dumont; Jose A. Cancelas; Deborah F. Dumont; Alan Siegel; Zbigniew M. Szczepiorkowski; Neeta Rugg; P. Gayle Pratt; D. Nicole Worsham; Elizabeth L. Hartman; Susan K. Dunn; Margaret O'Leary; Janet H. Ransom; Rodney A. Michael; Victor W. Macdonald
BACKGROUND: Availability of platelets (PLTs) is severely limited by shelf life in some settings. Our objective was to determine and compare to Food and Drug Administration (FDA) criteria the PLT recovery and survival of autologous PLTs cryopreserved at −65°C or less in 6% dimethyl sulfoxide (DMSO) reconstituted with a no‐wash method (cryopreserved PLTs [CPPs]) compared to autologous fresh PLTs.
Transfusion | 2000
John R. Hess; Lloyd E. Lippert; C.P. Derse‐Anthony; Heather R. Hill; Cynthia K. Oliver; Neeta Rugg; Amy D. Knapp; Jennifer F. Gormas; T.J. Greenwalt
BACKGROUND: RBC ATP concentrations are the most important correlate of RBC viability. Tests were performed to determine whether increased AS volume, pH, and phosphate content increased stored RBC ATP concentrations.
Transfusion | 2011
Jose A. Cancelas; Neeta Rugg; Dana Fletcher; P. Gayle Pratt; D. Nicole Worsham; Susan K. Dunn; Susanne Marschner; Heather L. Reddy; Raymond P. Goodrich
BACKGROUND: A novel system using ultraviolet (UV) light and riboflavin (Mirasol System, CaridianBCT Biotechnologies) to fragment nucleic acids has been developed to treat whole blood (WB), aiming at the reduction of potential pathogen load and white blood cell inactivation. We evaluated stored red blood cell (RBC) metabolic status and viability, in vitro and in vivo, of riboflavin/UV light–treated WB (IMPROVE study).
Transfusion | 2003
Edward L. Snyder; M. Dean Elfath; Harry Taylor; Neeta Rugg; Tibor J. Greenwalt; Laurene L. Baril; Pamela Whitley; Barbara Brantigan; Ken Story
BACKGROUND: A portable automated component collection system that produces double (2) units of leukoreduced RBCs (DRBCs) from a single donation was evaluated. This study analyzed quality of the collected and final products, the efficacy of automated leukoreduction, and donor safety.
Transfusion | 2015
Jose A. Cancelas; Larry J. Dumont; Lou Ann Maes; Neeta Rugg; Louise Herschel; Pamela Whitley; Zbigniew M. Szczepiokowski; Alan Siegel; John R. Hess; Majid Zia
Transfusion of long‐stored red blood cells (RBCs) is associated with decreased in vivo RBC recovery, delivery of RBC breakdown products, and increased morbidity and mortality. Reducing the burden of this RBC “storage lesion” is a major challenge in transfusion medicine. Additive solution‐7 (AS‐7) is a new RBC storage solution designed to improve RBC metabolism by providing phosphate and increasing buffering capacity.
Transfusion | 2001
John R. Hess; Neeta Rugg; Jenny K. Gormas; Amy D. Knapp; Heather R. Hill; Cynthia K. Oliver; Lloyd E. Lippert; Edward B. Silberstein; Tibor J. Greenwalt
BACKGROUND: Increasing the length of RBC storage can increase both RBC availability and quality. This work addresses 11‐week RBC storage in experimental ASs (EASs).
Transfusion | 2011
Jose A. Cancelas; Larry J. Dumont; Neeta Rugg; Zbigniew M. Szczepiorkowski; Louis Herschel; Alan Siegel; P. Gayle Pratt; D. Nicole Worsham; Anne Erickson; Meisa Propst; Anne North; Claire D. Sherman; Nina Mufti; William Reed; Laurence Corash
BACKGROUND: Transfusion‐transmitted infections and immunologic effects of viable residual lymphocytes remain a concern in red blood cell (RBC) transfusion. Pathogen reduction technologies for RBC components are under development to further improve transfusion safety. S‐303 is a frangible anchor‐linker‐effector with labile alkylating activity and a robust pathogen reduction profile. This study characterized the viability of RBCs prepared with a second‐generation S‐303 process and stored for 35 days.