Loni Calhoun
University of California, Los Angeles
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Transfusion | 2000
Lawrence D. Petz; George Garratty; Loni Calhoun; Bill Clark; Paul I. Terasaki; Christopher J. Gresens; Jeffrey Gornbein; Elliot M. Landaw; Randy Smith; J. Michael Cecka
BACKGROUND: Patients who are refractory to platelet transfusion as a result of HLA alloimmunization are generally given HLA‐matched or crossmatched platelets. However, HLA‐matched platelets that are matched at HLA‐A and ‐B loci (A‐matched) or those without any mismatched or cross‐reactive antigens (BU‐matched) are frequently unavailable. A disadvantage of crossmatching is that crossmatched platelets have a shelf life of only 5 days, so that crossmatch tests must be performed frequently for patients requiring long‐term platelet transfusions. An alternative method is the selection of platelets according to the patients HLA antibody specificity, called the antibody specificity prediction (ASP) method.
American Journal of Clinical Pathology | 2006
Priscilla Figueroa; Alyssa Ziman; Christine Wheeler; Jeffrey Gornbein; Michael Monson; Loni Calhoun
To detect miscollected (wrong blood in tube [WBIT]) samples, our institution requires a second independently drawn sample (check-type [CT]) on previously untyped, non-group O patients who are likely to require transfusion. During the 17-year period addressed by this report, 94 WBIT errors were detected: 57% by comparison with a historic blood type, 7% by the CT, and 35% by other means. The CT averted 5 potential ABO-incompatible transfusions. Our corrected WBIT error rate is 1 in 3,713 for verified samples tested between 2000 and 2003, the period for which actual number of CTs performed was available. The estimated rate of WBIT for the 17-year period is 1 in 2,262 samples. ABO-incompatible transfusions due to WBIT-type errors are avoided by comparison of current blood type results with a historic type, and the CT is an effective way to create a historic type.
Transfusion | 1995
Ritchard G. Cable; Sara E. Thal; Arlene Fink; Loni Calhoun; Lawrence D. Petz
BACKGROUND: The Transfusion Medicine Academic Awards (TMAA) program, sponsored by the National Heart, Lung, and Blood Institute, has provided grants to medical schools to help them develop comprehensive curricula in transfusion medicine. In 1989, the TMAA Group published a set of comprehensive curricular goals for teaching transfusion medicine. The medical student portion of this curriculum has now been revised to reflect new developments in transfusion medicine and recent trends in medical school education. STUDY DESIGN AND METHODS: Two medical schools independently revised the 1989 curriculum for their students. Because significant similarities were noted between curricula of the two institutions, the two revisions were combined and submitted to all TMAA institutions for comment. As a result, a revised medical school curriculum was developed and approved by the TMAA Group. RESULTS: The revised curriculum consists of 28 objectives in six major areas of transfusion medicine. It is presented in its entirety in this article. CONCLUSION: The TMAA transfusion medicine curriculum should provide to medical schools a valuable resource for evaluating their teaching of transfusion medicine and should provide to medical school deans and curriculum committees an authoritative source of transfusion medicine expertise.
Transfusion | 2003
Edward P. Laine; Randolph H. Steadman; Loni Calhoun; Douglas P. Blackall; Philip Levin; Michelle Braunfeld; Hamid Nourmand; Gundappa Neelakanta; Lena Ting; Jeffrey Gornbein; Ronald W. Busuttil; Lawrence D. Petz
BACKGROUND : Component therapy has become the accepted standard of care in transfusion medicine. In instances of large blood loss, the transfusion of whole blood rather than the combination of RBCs and FFP is rational and may be preferred.
Transfusion | 2000
Edward P. Laine; Regina M. Leger; Patricia A. Arndt; Loni Calhoun; George Garratty; Lawrence D. Petz
BACKGROUND: In a patient with warm autoantibodies who has recently received a transfusion, it is not recommended to perform adsorptions using autologous RBCs to detect alloantibodies. Although not scientifically documented, this position is based on the theory that transfused RBCs in the patient′s circulation would be capable of adsorbing alloantibodies that may be present. This in vitro study was designed to determine what percentage of transfused RBCs might completely remove alloantibodies in vivo.
Transfusion | 1999
Patricia M. Kopko; Loni Calhoun; Lawrence D. Petz
BACKGROUND: There are seven reports of “immunosilent AIDS” in which there was a lack of development of anti‐HIV for more than 6 months. Thus, when a frequent blood donor presented with clinical findings highly suggestive of overt AIDS, there was concern that he may have had a prolonged immunosilent infection.
The New England Journal of Medicine | 1992
Lawrence D. Petz; Loni Calhoun
CHANGES in blood type have been described in a variety of illnesses, usually acute infections or neoplasms.1 With the advent of transplantation of bone marrow and solid organs, a growing number of ...
Blood | 1992
James Gajewski; Lawrence D. Petz; Loni Calhoun; Sheryl O'Rourke; Elliot M. Landaw; Nancy R. Lyddane; Lynne Hunt; Gary J. Schiller; Winston G. Ho; Richard E. Champlin
American Journal of Clinical Pathology | 2004
Christine A. Wheeler; Loni Calhoun; Douglas P. Blackall
Obstetrical & Gynecological Survey | 1995
Jeff Etchason; Lawrence D. Petz; Emmett B. Keeler; Loni Calhoun; Steven H. Kleinman; Cynthia J. Snider; Arlene Fink; Robert H. Brook