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Author's personal copy

BOOK REVIEWS

TRALI: Mechanisms, Management, and


Prevention. Edited by Kleinman S, Popovsky MA,
2008, AABB Press, Bethesda (Md), (196 pages)

HIS IS AN up-to-date text on transfusion- or related peptides that have been described; (c) the
T related acute lung injury (TRALI) by 2 indi-
viduals well versed in the field, Dr Steven Kleinman
reason why only the lungs appear to be affected
during TRALI-related events; (d) why only the
and Dr Mark Popovsky. They have assembled a transplanted lung was affected in the case reported
number of transfusion medicine specialists to author by Dykes et al (Br J Haematol 2000;109:674-676) is
most of the chapters and provide a comprehensive not explained; (e) possible approaches to reducing
overview of TRALI. The chapters tend to be well the risk of TRALI should have been more
referenced and are nicely illustrated; however, there thoroughly covered, especially for platelets and
is some duplication between chapters. Especially RBC transfusions; (f) the use of platelet additive
useful is a table, in chapter 2, on the differential solutions, RBC additive solutions, leukoreduction,
diagnosis of pulmonary transfusion reactions. pathogen reduction processes, and pooling plasma
Although the 2 proposed mechanisms for TRALI before viral inactivation processes should also have
are carefully evaluated, the evidence for leukocyte been mentioned; and most importantly, (g) commu-
antibodies as the main cause of TRALI is most nication with implicated donors, for example,
compelling. Thus, various studies cited that 61% to sample letters and a discussion of their impact on
90% of blood components implicated in TRALI donors, should have been presented.
events have detectable leukocyte antibodies. When Overall, TRALI: Mechanisms, Management, and
not found in the donors, they are sometimes detected Prevention is a good review and summary of this
in patients reacting with the leukocytes present in a important topic. With the publication of this book,
nonleukoreduced transfused component. Further, much current information on TRALI is now
TRALI has been elicited in healthy volunteers available in a single volume.
infused with leukocyte antibody–containing com-
Paul V. Holland
ponents, showing that this is sufficient to cause a
UC Davis Medical Center
TRALI event without invoking some underlying
Sacramento, CA
disease or associated clinical condition. Bioactive
Delta Blood Bank
lipids in a “2-hit” model of TRALI may explain
Stockton, CA
some cases of TRALI where red blood cell (RBC)
E-mail address: pvh@abotogo.com
concentrates near their outdate are implicated and no
leukocyte antibodies can be identified in the blood Judd's Methods in Immunohematology. Edited by
component associated with that TRALI event. This W. John Judd, Susan T. Johnson, Jill R. Storry, 3rd ed,
mechanism however does not explain cases wherein 2008, AABB Press, Bethesda (Md)
plasma-only or plasma-rich components alone
appear to cause a TRALI event. This occurs even HE TOPIC OF immunohematological meth-
if leukocyte antibodies are not found; assuming a
thorough search had been made for the latter.
T ods deserves a prominent place among the
concerns of blood bankers because of the plethora of
There are some flaws and missing items in this methods that exist and the fact that adequate training
otherwise authoritative work. These include (a) a for many bench technologists who might be faced
critical assessment as to why TRALI does not result with serological incompatibilities is not as common
when leukocyte antibodies are transfused to a blood as it once was. Thus, books that clearly indicate
component recipient whose leukocytes bear the
cognate antigen; (b) a discussion of the relevance of 0887-7963/09/$ - see front matter
the brain natriuretic peptide, which is now referred © 2009 Published by Elsevier Inc.
to as B or beta natriuretic peptide and other similar doi:10.1016/j.tmrv.2009.03.005

Transfusion Medicine Reviews, Vol 23, No 3 (July), 2009: p 229-231 229


Author's personal copy

230 BOOK REVIEWS

appropriate methods to be used for specific serolo- clear and concise description for the evaluation of
gical problems are extremely valuable. This latest difficult immunohematological problems that will
edition of the previously titled Methods in Immuno- benefit both bench technologists and clinical
hematology provides the comprehensiveness and transfusion medicine doctors. New Appendices C
clarity for those individuals interested in serological and D have also been added to address the hazards
(immunohematological) investigations. It has been of, and how to respond to, various chemical spills.
16 years since the last (second) edition of this book, These appendices should be very useful and much
and this third edition has little resemblance to its appreciated by both laboratory personnel and
previous counterpart. For one thing, the page number occupational health and safety committees.
has increased in this edition from 476 pages to 667. The section on the investigation of drug-induced
Importantly, however, the printed paper used in this hemolysis has been totally reorganized and is very
edition has a much better contrast than the previous up to date. The most current procedures have been
editions, making it much more attractive and easier to added for testing drug-treated red blood cells as well
read. One major change from the previous edition is as testing patient serum in the presence of drug. The
the inclusion of 2 additional coauthors, Sue Johnson different categories of drug-induced hemolytic
and Jill Storry, who have complimentary areas of anemias have been updated to reflect current
expertise to that of John Judd. This combination of thinking of the mechanisms involved. Another
authors has allowed for an important evolution of this important addition to this section is the completely
valuable reference book. updated Table of Drugs that have been reported to
The format for all the procedures has been changed cause hemolysis and/or a positive DAT. This is the
to an information mapped style. Processes and most up-to-date table on drugs that can cause a
procedures are now described in separate documents positive DAT and/or hemolysis that currently exists.
as opposed to the standard operating procedure Some may believe that the references used in this
(SOP) format where process and procedure were all edition are somewhat outdated, but I would beg to
contained in 1 document. These procedures are also differ. Although not extensive for obvious reasons,
contained on a CD-ROM component supplied with I believe that the referencing used in this book is
this book, which will allow procedures to be appropriate. The authors have provided a balance
modified to fit the characteristics of each individual between the historical literature and more recent
laboratory. This brilliant addition allows blood bank publications. In most cases, the authors include a
transfusion services and immunohematology refer- citation to the current edition of the AABB
ence laboratories to modify them, if necessary, to fit Technical Manual, which has the advantage of
their laboratory's requirements as a procedure to be being updated continuously, thus allowing this
used in their in-house SOPs. edition to be, in a sense, always current. I found the
In addition, a new Appendix A is included, which inclusion of many ‘obsolete’ procedures again, as
lists reagent preparations in a step-by-step format for the references used, as providing some historical
that will benefit many transfusion service and significance to the resolution of complex serologi-
reference laboratory technologists. Another innova- cal problems. I also agree with the Preface, which
tion is the use of process documents that have been indicates that including these ‘historical’ proce-
added to the antibody identification section. This dures ensures that they are not lost and; indeed,
includes a basic approach to be taken when some of these methods could still be applicable,
evaluating initial antibody identification panel under certain circumstances, to resolve some very
results, including the crossing out and selecting of complex serological problem. One other innovation
cells. This is a nice innovative addition to the book to this edition of the book that stands out is the
because there are essentially no other written inclusion of “Limitations” for each of the methods
materials that provide a step-by-step procedure for described. This is not often found in other Methods
basic crossing out and evaluation of antibody books and provides information that is vital to the
investigation results. In addition, a written process understanding of the method being used and how to
and flow charts are provided for evaluating patients troubleshoot, if necessary.
with hemolysis and/or a positive DAT and patients Much has changed over the 16 years since the
with antibodies to high-prevalence and low-pre- appearance of the last edition of this Methods book.
valence antigens. This provides the reader with a All of the changes that have occurred, particularly
Author's personal copy

BOOK REVIEWS 231

the way that SOPs are written, have been superbly Donald R. Branch
addressed in this third edition. Overall, this book Associate Professor of Medicine,
offers comprehensive and detailed instructions for a Laboratory Medicine, and Pathobiology
range of serological investigations and problems University of Toronto
that will be very useful to its intended readership. It Toronto, Ontario, Canada
will also be useful for teaching new personnel and Division of Cell and Molecular Biology
refreshing seasoned personnel on the serological Toronto General Research Institute
problems that can appear at any time and how to Toronto, Ontario, Canada
resolve such problems. This book should be Research and Development
required reference material for blood bankers, Canadian Blood Services
immunohematology reference laboratories, as well Toronto, Ontario, Canada
as laboratory and clinical transfusion specialists. E-mail address: don.branch@utoronto.ca

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