Nora V. Hirschler
Blood Centers of the Pacific
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Publication
Featured researches published by Nora V. Hirschler.
Blood | 2012
Pearl Toy; Ognjen Gajic; Peter Bacchetti; Mark R. Looney; Michael A. Gropper; Rolf D. Hubmayr; Clifford A. Lowell; Philip J. Norris; Edward L. Murphy; Richard B. Weiskopf; Gregory A. Wilson; Monique Koenigsberg; Deanna Lee; Randy M. Schuller; Ping Wu; Barbara Grimes; Manish J. Gandhi; Jeffrey L. Winters; David C. Mair; Nora V. Hirschler; Rosa Sanchez Rosen; Michael A. Matthay
Transfusion-related acute lung injury (TRALI) is the leading cause of transfusion-related mortality. To determine TRALI incidence by prospective, active surveillance and to identify risk factors by a case-control study, 2 academic medical centers enrolled 89 cases and 164 transfused controls. Recipient risk factors identified by multivariate analysis were higher IL-8 levels, liver surgery, chronic alcohol abuse, shock, higher peak airway pressure while being mechanically ventilated, current smoking, and positive fluid balance. Transfusion risk factors were receipt of plasma or whole blood from female donors (odds ratio = 4.5, 95% confidence interval [CI], 1.85-11.2, P = .001), volume of HLA class II antibody with normalized background ratio more than 27.5 (OR = 1.92/100 mL, 95% CI, 1.08-3.4, P = .03), and volume of anti-human neutrophil antigen positive by granulocyte immunofluoresence test (OR = 1.71/100 mL, 95% CI, 1.18-2.5, P = .004). Little or no risk was associated with older red blood cell units, noncognate or weak cognate class II antibody, or class I antibody. Reduced transfusion of plasma from female donors was concurrent with reduced TRALI incidence: 2.57 (95% CI, 1.72-3.86) in 2006 versus 0.81 (95% CI, 0.44-1.49) in 2009 per 10 000 transfused units (P = .002). The identified risk factors provide potential targets for reducing residual TRALI.
Transfusion | 2007
Brian Custer; Artina Chinn; Nora V. Hirschler; Michael P. Busch; Edward L. Murphy
BACKGROUND: The consequences of temporary deferral are not well understood. This study sought to investigate blood donor return after deferral expiration.
Transfusion | 2008
Dorothy D. Nguyen; Deborah DeVita; Nora V. Hirschler; Edward L. Murphy
BACKGROUND: New regulatory requirements for donor eligibility challenge blood centers to recruit and retain enough donors. This study evaluated correlations between overall satisfaction with the donation process and donor demographics and the effect of both on a donors intent to return.
Transfusion | 2004
Brian Custer; Eric S. Johnson; Sean D. Sullivan; Tom K. Hazlet; Scott D. Ramsey; Nora V. Hirschler; Edward L. Murphy; Michael P. Busch
BACKGROUND: Donors are deferred for multiple reasons. Losses related to disease marker rates are well established. Donor and donation losses for other reasons, however, have not been extensively quantified.
Transfusion | 2005
Ana M. Sanchez; George B. Schreiber; Catharie C. Nass; Simone A. Glynn; Debra Kessler; Nora V. Hirschler; Joy Fridey; James Bethel; Edward L. Murphy; Michael P. Busch
BACKGROUND: Men who have had sex with men (MSM) since 1977 are permanently deferred from donating blood. Excluding only men who engaged in male‐to‐male sex within either the prior 12 months or 5 years has been proposed. Little is known about infectious disease risks of MSM who donate blood.
Transfusion | 2006
Pascale Reich; Paula Roberts; Nancy Laabs; Artina Chinn; Patrick McEvoy; Nora V. Hirschler; Edward L. Murphy
BACKGROUND: Improvement in donor return rates, especially among first‐time donors, may significantly improve the blood supply. There are few rigorous studies of the effectiveness of various approaches to donor recruitment, however.
Transfusion | 2009
Edward L. Murphy; Beth H. Shaz; Christopher D. Hillyer; Patricia M. Carey; Brian Custer; Nora V. Hirschler; Junyong Fang; George B. Schreiber
BACKGROUND: Historically, minority populations have represented only a small proportion of US blood donors, but recent trends in immigration and potential blood shortages emphasize the need for recruitment strategies to increase minority donations.
Critical Care Medicine | 2006
David C. Mair; Nora V. Hirschler; Ted Eastlund
Objective:Discuss the pros and cons of using donor and blood product-management strategies to prevent transfusion-related acute lung injury (TRALI). Data Source:A review of the literature was performed. Results:Despite therapeutic advances in pulmonary and critical care medicine, TRALI is now considered to be one of the leading causes of transfusion-associated mortality, and thus determining how to prevent TRALI is extremely important. Donor and product-management strategies to prevent this life-threatening condition have been suggested, but because of gaps in our understanding of TRALI, blood-bankers do not know how beneficial these interventions will be, nor the amount of potential harm—such as decreasing the availability of blood—that could arise if they were implemented. This article discusses the advantages and disadvantages of the various preventive measures that have been described in the literature. Conclusions:Preventing TRALI poses a difficult challenge for blood-banking experts, because it is unknown which measures will be effective in decreasing the incidence of TRALI and which could have significant drawbacks. Only additional research into TRALI prevention will provide the answers on how to best protect patients from this potentially fatal reaction.
Transfusion | 2008
Jed B. Gorlin; Susan N. Rossmann; Gene Robertson; Fred Stallone; Nora V. Hirschler; Kim-Anh Nguyen; Ronald O. Gilcher; Helen Fernandes; Stacey Alvey; Patience Ajongwen; Paul Contestable; Harold Warren
BACKGROUND: This multicenter prospective study was designed to evaluate the performance characteristics of a new commercially available enzyme‐linked immunosorbent assay (ELISA) for the detection of antibodies to Trypanosoma cruzi in blood donors, the ORTHO T. cruzi ELISA Test System (Ortho‐Clinical Diagnostics).
Critical Care Medicine | 2014
Mark R. Looney; Nareg Roubinian; Ognjen Gajic; Michael A. Gropper; Rolf D. Hubmayr; Clifford A. Lowell; Peter Bacchetti; Gregory A. Wilson; Monique Koenigsberg; Deanna C. Lee; Ping Wu; Barbara Grimes; Philip J. Norris; Edward L. Murphy; Manish J. Gandhi; Jeffrey L. Winters; David C. Mair; Randy M. Schuller; Nora V. Hirschler; Rosa Sanchez Rosen; Michael A. Matthay; Pearl Toy
Objective:Transfusion-related acute lung injury is the leading cause of transfusion-related mortality. A prospective study using electronic surveillance was conducted at two academic medical centers in the United States with the objective to define the clinical course and outcomes in transfusion-related acute lung injury cases. Design:Prospective case study with controls. Setting:University of California, San Francisco and Mayo Clinic, Rochester. Patients:We prospectively enrolled 89 patients with transfusion-related acute lung injury, 164 transfused controls, and 145 patients with possible transfusion-related acute lung injury. Interventions:None. Measurements and Main Results:Patients with transfusion-related acute lung injury had fever, tachycardia, tachypnea, hypotension, and prolonged hypoxemia compared with controls. Of the patients with transfusion-related acute lung injury, 29 of 37 patients (78%) required initiation of mechanical ventilation and 13 of 53 (25%) required initiation of vasopressors. Patients with transfusion-related acute lung injury and possible transfusion-related acute lung injury had an increased duration of mechanical ventilation and increased days in the ICU and hospital compared with controls. There were 15 of 89 patients with transfusion-related acute lung injury (17%) who died, whereas 61 of 145 patients with possible transfusion-related acute lung injury (42%) died and 7 of 164 of controls (4%) died. Patients with transfusion-related acute lung injury had evidence of more systemic inflammation with increases in circulating neutrophils and a decrease in platelets compared with controls. Patients with transfusion-related acute lung injury and possible transfusion-related acute lung injury also had a statistically significant increase in plasma interleukin-8, interleukin-10, and interleukin-1 receptor antagonist posttransfusion compared with controls. Conclusions:In conclusion, transfusion-related acute lung injury produced a condition resembling the systemic inflammatory response syndrome and was associated with substantial in-hospital morbidity and mortality in patients with transfusion-related acute lung injury compared with transfused controls. Patients with possible transfusion-related acute lung injury had even higher in-hospital morbidity and mortality, suggesting that clinical outcomes in this group are mainly influenced by the underlying acute lung injury risk factor(s).