Patients at Risk for Significant CMV Infection

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Transcript Patients at Risk for Significant CMV Infection

Salwa Hindawi MSc, FRCPath, CTM
Director of Blood Transfusion Services
kAUH, Jeddah
Saudi Arabia
ESPHO Cairo 2008
Salwa Hindawi

Despite general measures to ensure transfusion
safety, there still an added risk to infants and
children with underlying hematological,
oncologic and immunologic disorders.

Transfusion reaction may be caused by both
infectious or non infectious processes.

Special products are blood components
collected, processed, and selected specifically
to minimize these complications.
Salwa Hindawi

CMV is transmitted by leucocytes.

The use of CMV-seronegative blood components
has been shown to reduce the incidence of CMV
infection to 1-3%.
Salwa Hindawi
Patients with congenital immunodeficiency disorders
 AIDS (human immunodeficiency virus infection) patients
 Hematopoietic progenitor cell transplant recipients
 Organ allograft transplant recipients
 Premature infants during infancy
 Cancer patients undergoing intense chemotherapy
 Recipients of intrauterine transfusions

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
Leucocytes in the blood components can lead to
many complications

Universal Leucodepletion verses specific
indications.
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
Nonhemolytic transfusion reactions (commonly called
“febrile nonhemolytic transfusion reactions”)

Alloimmunization to HLA Class I antigens

Cytomegalovirus infections

Immune modulation

Graft-vs-host disease
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WHY?
 To Prevent Graft verses Host Disease mediated by T
lymphocytes in units of Packed RBCs, Platelets, and
Granulocytes.

Blood components that contain viable lymphocytes
may be irradiated to prevent proliferation of T
lymphocytes, which is the immediate cause of GVHD.

The standard dose of gamma irradiation is 2500 cGy ,
maximum allowable dose is 5000cGy.
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
Patients with congenital immunodeficiency disorders
of cellular immunity.

Intrauterine transfusion and neonatal exchange
transfusion recipients.

Hematopoietic progenitor cell transplant recipients.

Recipients of blood components from 1st & 2nd
degree relatives.
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 Patients
receiving HLA-matched cellular blood
components.
 Patients
with hematologic malignancies and
Cancer patients
undergoing intense chemotherapy or Hodgkin’s
disease receiving fludarabine.
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Sickle cell trait:
Hb A = 60%
Hb S = 40%


Hypoxia and acidosis can lead to sickle crisis.

Can donate blood.
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Define patients populations who should receive red
blood cells known to lack hemoglobin S.
1- infants with small blood volume or massive
transfusion in neonates.
2- Sickle cell patients
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The risk of:
Bacterial contamination
Emerging pathogens
are still a major concerns which lead to the need for
better techniques.
PI for platelet concentrates have been in routine use
since 2002 and for plasma in 2006 (INTERCEPT blood
system).
A noval PI approach to blood safety (the Mirasol PRT
System).

Salwa Hindawi

Nucleic acid targeted pathogen inactivation
technologies offer the potential to protect from
infectious and non infectious processes through
prevention of cell replication and transcription.

To accurately assess the true value of a pathogen
reduction system it is essential to weigh its cost against
the saving it offers in terms of quality of life and
reduced cost to society.
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MIRASOL PRT system for platelets
and plasma – Concept
+
Platelet or
plasma product
+
Riboflavin
(Vitamin B2)
UV Light
Reduction of viruses, bacteria, parasites 
Inactivation of residual white cells 
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The MIRASOL PRT process:
1
2
3
Transfer platelet
product to MIRASOL
Illumination bag
Add 35 mL
Riboflavin Solution
(500 uM)
Illuminate
product for
6-10 min.*
* Illumination time depends on product volume
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 delayed
clamping of the umbilical cord;
 restricting
blood sampling
 using
recombinant human erythropoietin to
stimulate erythropoiesis
 using
iron supplementation or vitamins to
minimize the severity of anemia
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 using
appropriately collected and stored
multipack RBC units
 using
appropriately screened and handled
RBCs from regular or designated donors; and
 collecting
and transfusing umbilical cord
blood (autologous blood transfusion).
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
The use of special products is a must for specific
patients in pediatric age group to ensure safety.

The use of PI procedures are recommended to ensure
better safety.

Training for the staff, policies, and guidelines in
pediatric age group are important issues to be
considered.
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Pediatric Transfusion, A Physician’s handbook
 2nd Edition, 2006.
 Prenatal and childhood transfusion, Practical
Transfusion Medicine 2001.
 A novel Approach to blood safety, Gambro BCT 2007.
 Impact of Pathogen activation on platelets utilization
during 3 years of routine use, AABB October 2007.
 Pathogen Inactivation making decisions about new
technologies preliminary reports of a consensus
conference, Vox Sanguinis 2007.

Salwa Hindawi
Salwa Hindawi