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Dive into the research topics where Mark A. Popovsky is active.

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Featured researches published by Mark A. Popovsky.


Transfusion | 2001

HLA class II antibodies in transfusion‐related acute lung injury

Patricia M. Kopko; Mark A. Popovsky; Malcolm R. MacKenzie; Teresa Paglieroni; Kathryn N. Muto; Paul V. Holland

BACKGROUND: Transfusion‐related acute lung injury (TRALI) is a serious, sometimes fatal, complication of transfusion. Granulocyte and HLA class I antibodies present in blood donors have been associated with TRALI. HLA class II antibodies have recently been described in a few cases of TRALI.


Bone Marrow Transplantation | 2001

Bigger is better: maternal and neonatal predictors of hematopoietic potential of umbilical cord blood units

Karen K. Ballen; M Wilson; J Wuu; Am Ceredona; C Hsieh; Fm Stewart; Mark A. Popovsky; Peter J. Quesenberry

Umbilical cord blood (CB) is a useful stem cell source for patients without matched family donors. CB banking is expensive, however, because only a small percentage of the cord units stored are used for transplantation. In this study, we determined whether maternal factors, such as race, age, and smoking status have an effect on laboratory parameters of hematopoietic potential, such as viability, cell counts, CD34+ cell counts, and CFU-GM. We studied the effect of neonatal characteristics such as birth order, birth weight, gestational age, and sex of the baby on the same laboratory parameters. Race and maternal age had no effect on these laboratory parameters. In multivariate analysis, babies of longer gestational age had higher cell counts, but lower CD34+ cell counts and CFU-GM. Bigger babies had higher cell counts, more CD34+ cells, and more CFU-GM. Women with fewer previous live births also produced cord units with higher cell counts, CFU-GM, and CD34+ cell counts. Specifically, each 500 g increase in birth weight contributed to a 28% increase in CD34+ cell counts, each week of gestation contributed to a 9% decrease in CD34+cell counts, and each previous birth contributed to a 17% decrease in CD34+ cell counts (all P < 0.05). These data may be used to select the optimal cord blood donors and allow CB banks efficient resource allocation. Bone Marrow Transplantation (2001) 27, 7–14.


Transfusion | 2003

TRALI: correlation of antigen-antibody and monocyte activation in donor-recipient pairs.

Patricia M. Kopko; Teresa Paglieroni; Mark A. Popovsky; Kathryn N. Muto; Malcolm R. MacKenzie; Paul V. Holland

BACKGROUND : TRALI may be a severe reaction associated with transfusion of plasma‐containing blood components. TRALI has usually been associated with antibodies against granulocytes and HLA class I antigens, but more recently with antibodies against HLA class II and monocytes. TRALI cases were investigated to determine correlation between antigen and antibody. Additionally, activation of monocytes by TRALI serums was studied.


Transfusion | 1999

A case-controlled multicenter study of vasovagal reactions in blood donors: influence of sex, age, donation status, weight, blood pressure, and pulse.

Jonathan Trouern‐Trend; Ritchard G. Cable; Stanley J. Badon; Bruce Newman; Mark A. Popovsky

BACKGROUND: Vasovagal reactions occur in a small, but significant number of blood donors. These reactions may decrease return donation and disrupt blood collection activities. The purpose of this study was to define the contributory role of sex, age, weight, blood pressure, and pulse in vasovagal reactions with syncope in blood donors.


Transfusion | 1995

Prophylactic versus therapeutic platelet transfusion practices in hematology and/or oncology patients

Patricia T. Pisciotto; K. Benson; Heather Hume; Armand B. Glassman; Harold A. Oberman; Mark A. Popovsky; Deanna Hines; Kenneth C. Anderson

BACKGROUND: Platelet utilization has steadily increased throughout the past three decades. At the same time, there has been very little study of the current transfusion practices. STUDY DESIGN AND METHODS: A survey was conducted of institutional members of the American Association of Blood Banks (hospitals) that were actively involved in the care of pediatric and/or adult hematology and/or oncology patients. Inquiries were made relating to the extent of prophylactic versus therapeutic use of platelets, criteria used for prophylactic transfusion of platelets and type, and dose of platelets used. Data were analyzed according to patient age and type of hospital. RESULTS: Of 786 responding hospitals, 630 (80.2%) provided sufficient data for analysis; 126 of that 630 provided care for pediatric patients. The majority (60.9%) of responding hospitals had a minimum of four hematologists and/or oncologists. Eighty‐four percent of hospitals reported transfusing some apheresis platelets. The dose of platelet concentrates most frequently used for adults ranged from 6 to 10, with pools of 10 more commonly used in community hospitals. More than 70 percent of hospitals reported transfusing platelets primarily for prophylaxis: 60 percent of hospitals set the threshold platelet count for prophylactic platelet transfusion at 20,000 per microL, with approximately 20 percent each transfusing at higher and lower levels. A platelet count of 50,000 per microL was most frequently required for performance of a minor invasive procedure. CONCLUSION: The data from this study show that the majority of institutions use prophylactic platelet transfusion in both pediatric and adult hematology and/or oncology patients. However, there is considerable variation in platelet transfusion practice.


The New England Journal of Medicine | 1990

Prevalence of Human Immunodeficiency Virus Type 1 p24 Antigen in U.S. Blood Donors — An Assessment of the Efficacy of Testing in Donor Screening

Harvey J. Alter; Jay S. Epstein; Sally G. Swenson; Mark J. VanRaden; John W. Ward; Richard A. Kaslow; Jay E. Menitove; Harvey G. Klein; S. Gerald Sandler; Merlin H. Sayers; Indira Hewlett; Amoz I. Chernoff; Mark A. Popovsky; Hilda McDonald; Jay H. Herman; William Sherwood; Jan Forey; Kate Rothko; Paul C. Van Ness; Sandy Ellisor; Gerald I. Shulman; Alfred J. Grindon; Steven H. Kleinman; Bruce A. Lenes; Peter Tomasulo; Ron Gilcher; Linda Chandler; Linda Belcher; Pablo Fortes; David Fortenberry

Abstract Background. We performed a multicenter study in 1989 to determine whether screening whole-blood donors for human immunodeficiency virus type 1 (HIV-1) p24 antigen would improve transfusion safety by identifying carriers of the virus who are seronegative for HIV-1 antibody. Methods. More than 500,000 donations were tested at 13 U.S. blood centers with test kits from two manufacturers. Units found repeatedly reactive were retested in a central laboratory; if the results were positive, they were confirmed by a neutralization assay. A subgroup of units was also tested for HIV-1 by the polymerase chain reaction. Selected donors confirmed or not confirmed as having p24 antigen were contacted for follow-up interviews to identify risk factors and undergo retesting for HIV-1 markers. Results. Positive tests for p24 antigen were confirmed by neutralization in five donors (0.001 percent of all donations tested), all of whom were also positive for HIV-1 antibody and HIV-1 by polymerase chain reaction. Three ...


Vox Sanguinis | 2004

Transfusion and the lung: circulatory overload and acute lung injury.

Mark A. Popovsky

Transfusion associated circulatory overload (TACO) and transfusion-related acute lung injury (TRALI) are increasingly recognized as important complications of haemotherapy. Circulatory overload refers to transfusion-triggered congestive heart failure. It is most frequently seen in the very young or those over 60 and it can be life-threatening. While its incidence is 1–8% in certain populations, it is frequently underrecognized. Circulatory overload is associated with both allogeneic and autologous transfusion. TRALI is a syndrome with several presentations, ranging from mild to life-threatening. The sine qua non is respiratory distress. Pulmonary oedema, hypoxaemia and hypotension frequently accompany the more severe form of TRALI, and, in these cases, death occurs in 5–14%. The true frequency is unknown. Symptoms present within 2 h of transfusion of any plasmacontaining blood product. While both immunological and non-immunological mechanisms of injury have been proposed, the preponderance of evidence implicates a role for passively transfused HLA, granulocyte or monocyte antibodies. There are no definitive laboratory diagnostic tools. Therapy is directed toward relief of symptoms.


Transfusion | 1996

Hypotensive reactions : a previously uncharacterized complication of platelet transfusion ?

Heather Hume; Mark A. Popovsky; K. Benson; Glassman Ab; Deanna Hines; Harold A. Oberman; Patricia T. Pisciotto; Kenneth C. Anderson

Background: In 1993, the American Association of Blood Banks (AABB) received reports of severe hypotensive reactions associated with platelet transfusions. The question arose as to whether these reports were indicative of a previously uncharacterized platelet transfusion reaction.


Transfusion | 2000

Transfusion to blood group A and O patients of group B RBCs that have been enzymatically converted to group O.

Margot S. Kruskall; James P. AuBuchon; Kathleen Y. Anthony; Louise Herschel; Connie Pickard; Ruth Biehl; Marilyn S. Horowitz; Donald Brambilla; Mark A. Popovsky

BACKGROUND: The transfusion of ABO‐incompatible RBCs is the leading cause of fatal transfusion reactions. Group O RBCs, lacking terminal immunodominant A and B sugars to which humans are immunized, are safe for transfusion to persons of any ABO blood group. With the use of a recombinant α‐galactosidase to remove terminal galactose from group B RBCs, the safety and efficacy of enzyme‐converted group‐B‐to‐group‐O (ECO) RBC components were studied in transfusion‐dependent patients.


Transfusion | 2002

Racial and ethnic composition of volunteer cord blood donors: comparison with volunteer unrelated marrow donors

Karen K. Ballen; Julie Hicks; Bernie Dharan; Daniel R. Ambruso; Kenneth C. Anderson; Celso Bianco; Lynn Bemiller; William C. Dickey; Richard Lottenberg; Mary O'Neill; Mark A. Popovsky; Donna Skerrett; Irena Sniecinski; John R. Wingard

BACKGROUND : Umbilical cord blood is an alternative peripheral blood progenitor cell source for patients who need transplantation. A presumed advantage of cord blood is the ability to increase minority recruitment.

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Karen K. Ballen

University of Massachusetts Medical School

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Margot S. Kruskall

Beth Israel Deaconess Medical Center

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