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A PHYSICIANS GUIDE TO TRANSFUSION OPTIONS
New York State Council on Human Blood and Transfusion Services
New York State Department of Health
Council Members
February 1994
Adapted from materials prepared by the New York Blood Center
TABLE OF CONTENTS
Disclaimer: The New York State Council on Human Blood
and Transfusion Services has attempted to provide you with the most current
information on the use of autologous and directed blood services. The circular
of information for the use of human blood and blood components should be
consulted for current information.
INTRODUCTION
The mission of the New York State Council on Human Blood and Transfusion Services is to set
standards and develop guidelines for transfusion-related products and services
in New York State.
This booklet is provided to assist you in your discussions
with your patients regarding their transfusion options, particularly to
emphasize autologous transfusion possibilities.
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TRANSFUSION OPTIONS SUMMARY
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| OPTION
Pre-operative
Autologous
Donation
Perioperative
Autologous Blood
Recovery
Volunteer
Homologous (Allogeneic)
Blood Donation
Directed Donor
Blood Donation
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DEFINITION
A patient's blood is collected and stored until needed
Blood is collected during or near the time of surgery*
Blood voluntarily donated to a community blood center
Patient selects blood donor
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ADVANTAGE
Disease transmission and allergic reactions are eliminated
Disease transmission and allergic reactions are eliminated
Availability in emergencies
Patient feels safe with donors selected
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DISADVANTAGE
Must be planned in advance
May delay surgery
Certain medical conditions disqualify the patient as donor
Hemodilution - may cause fluid overload
Intraoperative or postoperative recovery - cannot be used
if cancer or infection is present, risk of air embolism
Small, but possible, risk of disease transmission and
allergic reaction
May carry higher risk of disease transmission and allergic
reaction
Blood group must be compatible
Must be planned in advance
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*Blood may be collected from the patient immediately preoperatively,
or collected intraoperatively from the operative site or from extracorporeal
circuit. Under postoperative and posttraumatic situations, shed blood may
be collected from body cavities, joint spaces and other closed operative
or trauma sites. Preoperative hemodilution - Blood is collected preoperatively
with isovolemic fluid replacement and blood is reinfused at the end of
surgery. Intraoperative and postoperative recovery - Blood is collected
from surgical or trauma sites, processed and returned after surgery.
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ALL BLOOD IS TESTED
New York State regulations require testing of homologous
(allogeneic) blood donors for eight markers associated with an increased
risk for transmissible disease, in addition to blood group determinations.
When autologous donations are not possible or are insufficient, blood for
your patient's transfusion can be provided by homologous blood donors who
meet strict medical eligibility guidelines. Blood from such donors found
positive for any of these markers may not be used for transfusion.
THE TESTS
All allogeneic donations are tested for:
- ABO group
- Rh type
- Antibody to human immunodeficiency virus, type 1 and
type 2 (HIV-1/HIV-2)
- Hepatitis B surface antigen (HBsAg)
- Antibody to Hepatitis C (HCV)
- Antibody to human T-cell lymphotropic virus, type I (HTLV-I)
Syphilis
- Antibody to hepatitis B core antigen (anti HBc)
- Acceptable level of alanine aminotransferase (ALT)
- Tests for unexpected antibodies against red cell antigens.
Careful Donor Screening
Before giving blood, all homologous (allogeneic) blood
donors must answer extensive questions concerning their health histories.
The questions are designed to identify and eliminate prospective donors
who may be at risk of transmitting infectious diseases.
All the materials used for donation (including the needle)
are new, sterile, disposable, used only once and discarded.
Autologous Donations
For autologous (autogeneic) blood collected by blood centers,
donors undergo the same tests as for community donations. Such testing
must be performed at 30-day intervals, at a minimum. You or the patient
will be informed if an autologous donation is found positive for any of
the standard tests. Authorization for release may be needed from you as
the attending physician and from the hospital's blood bank director. If
the blood is collected by a blood center, the hospital blood bank director
may be notified. Once a unit is found to be positive for any of the tests,
the patient may be ineligible for further autologous donations. Such testing
is not required by regulation for collections performed by hospitals for
use at that hospital, but may be performed voluntarily.
Intraoperative Autologous Transfusion and Post-operative
Cell Recovery
Blood recovered through these procedures do not require
testing provided it is collected, processed and returned during or within
six hours of the patient's surgery.
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PREPARING YOUR PATIENT FOR AN AUTOLOGOUS DONATION
Informing Your Patient
Discuss with your patient how transfusion needs
can be met, the advantages and risks. See Transfusion Options Summary and
Summary Chart of Blood Components, pages 1 and 6.
Share any available pamphlets on blood transfusion
options with your patients who may need blood.
Make an appointment: Most transfusion options and
services begin with an appointment for blood donation.
Pre-donation interview: It is advisable to instruct
your patient to call the blood collection facility as soon as possible.
Staff will interview your patient, usually over the phone, to gather pre-donation
information needed to ensure your patient's comfort and safety during the
autologous donation. Staff will answer any questions your patient may have
and provide guidance through the donation process.
Notify hospital blood bank: If blood is to be collected
by a blood center, it is advisable to notify the hospital's blood bank
that autologous blood will be delivered for your patient.
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AUTOLOGOUS BLOOD DONATION
A Physician's Order Form Is Required.
Your careful attention in completing and signing this prescription will
help ensure the most efficient and comfortable donation experience, and
the safest blood possible for your patient. Regulations require a completed
and signed form on file.
The Form: Critical Points
Most blood banks require that the patient submit completed forms before
the first donation appointment.
If the patient has a history of:
- cardiovascular disease, especially history of angina,
myocardial infarction, bypass surgery
- cerebrovascular disease, especially history of stroke
- cardiac valvular disease, especially aortic stenosis
- seizure disorders, especially if not well-controlled
by medication, or
- any other medical condition for which a prolonged vasovagal
reaction or rapid (within 5 minutes) loss of 500 ml of blood would be dangerous
for the patient,
the patient's attending specialist or personal physician
must describe details of the medical problem and must certify that the
patient may safely undergo phlebotomy.
To ensure proper labelling of the unit, the order form
should be complete with:
- patient's full legal name
- patient's social security number
- date of birth
- date of anticipated transfusion
- full name and address of hospital where transfusion
will be performed.
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AUTOLOGOUS DONOR ELIGIBILITY
Autologous blood donors do not need to meet the standard
eligibility guidelines set for community volunteer donors. However, certain
criteria must be reviewed:
Cardiac Fitness
The patient's physician should be sure the patient's cardiovascular status
can tolerate the withdrawal of up to 500 ml of whole blood (for adults)
within five minutes before requesting autologous blood collection.
Hemoglobin Concentration
Hemoglobin readings are measured before each donation to determine the
donor's continued eligibility. A minimum hemoglobin concentration of 11
g/dL is required for autologous donors unless otherwise approved by the
medical director of the blood collection facility.
Iron Supplements
Oral iron supplements are recommended for patients making more than one
autologous blood donation. The usual adult dosage is ferrous sulfate, 325
mg, three times daily beginning one week before the first donation.
History of Hepatitis, HIV or AIDS
Patients with positive test results may be ineligible for autologous blood
donation at some blood banks; such units may not be acceptable for use
in certain hospitals.
Patients with known histories of HIV or AIDS are ineligible
for autologous donation at most blood banks.
Is the Patient Under 17 Years Of Age?
Special arrangements may be required. The blood bank should be notified
so that special arrangements may be made. A parent or legal guardian must
accompany the minor. If the child weighs less than 110 pounds, less than
a full unit may be collected at one time.
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BLOOD DONATION PROCEDURE
The patient should send the completed and signed physician's order form
to the blood collecting facility before the first appointment.
The patient will be asked to complete a medical history
questionnaire, and have temperature, blood pressure, pulse, and hemoglobin
readings measured. Should any of these values fall outside standard autologous
criteria ranges, the patient will be ineligible for donation at that visit.
The entire process takes about an hour. The donation itself takes about
5 to 7 minutes.
Autologous donors may generally give blood twice each
week over the five-week period preceding the transfusion date. Donations
can generally be made up to three working days before transfusion. (Note:
If the blood is to be shipped out of state, the last donation generally
needs to be made no later than 10 working days before transfusion.)
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SUMMARY CHART OF BLOOD COMPONENTS
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| COMPONENT
Whole Blood
Red Blood Cells
Red Blood Cells,
Leukocytes
Removed
Red Blood Cells,
Adenine-Saline
Added
Fresh Frozen
Plasma
Liquid Plasma
and Plasma
Cryoprecipitated AHF
Platelets, Platelets
by Pheresis
Granulocytes
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MAJOR
INDICATIONS
Symptomatic
anemia with large
volume deficit
Symptomatic
anemia
Symptomatic
anemia; febrile
reactions from
leukocyte antibodies
Symptomatic
anemia with volume
deficit
Deficit of labile and
stable plasma
coagulation factors
and TTP
Deficit of stable
coagulation factors
Hemophilia A; von
Willebrand's disease;
hypofibrinogenemia;
factor XIII deficiency
Bleeding from
thrombocytopenia or
platelet function
abnormality
Neutropenia with
infection
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ACTION
Restoration of
oxygen-carrying
capacity, restoration
of blood volume
Restoration of
oxygen-carrying
capacity
Restoration of
oxygen-carrying
capacity
Restoration of
oxygen-carrying
capacity
Source of labile and
nonlabile plasma
factors
Source of nonlabile
factors
Provides factor VIII;
fibrinogen; von
Willebrand factor;
factor XIII
Improves
hemostasis
Provides
granulocytes
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NOT INDICATED
FOR*
Conditions
responsive
to specific
component
Pharmacologically
treatable anemia;
coagulation
deficiency
Pharmacologically
treatable anemia;
coagulation
deficiency
Pharmacologically
treatable anemia;
coagulation
deficiency
Conditions responsive
to volume
replacement
Deficit of labile
coagulation factors
or volume
replacement
Conditions not
deficient in
contained factors
Plasma coagulation
deficits and some
conditions with rapid
platelet destruction
(e.g. ITP)
Infections responsive
to antibiotics
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| *Applies to allogeneic blood. May not apply
to autologous blood. |
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SUMMARY CHART OF BLOOD COMPONENTS continued
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| COMPONENT
Whole Blood
Red Blood Cells
Red Blood Cells,
Leukocytes
Removed
Red Blood Cells,
Adenine-Saline
Added
Fresh Frozen
Plasma
Liquid Plasma
and Plasma
Cryoprecipitated AHF
Platelets, Platelets
by Pheresis
Granulocytes
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SPECIAL
PRECAUTIONS*
Must
be ABO-
identical; labile
coagulation factors
deteriorate within 24
hours after collection
Must be ABO
-compatible
Must be ABO
-compatible
Must be ABO
-compatible
Should be ABO
-compatible
Should be ABO
-compatible
Frequent repeat
doses may be
necessary
Should not use some
microaggregate
filters (check
manufacturer's
instructions)
Must be ABO
-compatible, do not
use depth-type micro-
aggregate filters
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HAZARDS*
Infectious diseases;
septic/toxic, allergic,
febrile reactions;
circulatory overload
Infectious diseases;
septic/toxic, allergic,
febrile reactions
Infectious diseases;
septic/toxic, allergic
reaction (unless
plasma is also
removed, eg., by
washing)
Infectious diseases;
septic/toxic, allergic,
febrile reactions;
circulatory overload
Infectious diseases;
allergic reactions;
circulatory overload
Infectious diseases;
allergic reactions
Infectious diseases;
allergic reactions
Infectious diseases;
septic/toxic, allergic,
febrile reactions
Infectious diseases;
allergic reactions;
febrile reactions
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RATE OF INFUSION
For massive loss, as
fast as patient can
tolerate
Generally 2 hours,
as tolerated by the
patient; no more
than 4 hours
Generally 2 hours,
as tolerated by the
patient; no more
than 4 hours
Generally 2 hours,
as tolerated by the
patient; no more
than 4 hours
Generally 2 hours
(no more than 4 hours)
Generally 2 hours
(no more than 4 hours)
Generally 2 hours
(no more than 4 hours)
Generally 2 hours
(no more than 4
hours)
(Set of platelet
concentrates or 1
pheresis unit)
One pheresis unit
over 2-4 hour period-
closely observe
recipient for
reactions
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*Applies to allogeneic blood. May not apply to autologous blood.
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BLOOD COMPONENTS AND PRODUCTS
Blood May Be Stored up to 42 Days
Whole blood is collected in one of several approved anticoagulant solutions.
Depending on solution used, blood may be stored in liquid form from 21
to 42 days. The most common solution allows liquid-packed red blood cells
to be stored 42 days before expiration.
If surgery is postponed, frozen storage may be available.
Other Autologous Blood Components and Products
Autologous blood components and products are presenting
new possibilities for improving patient care. Options available in some
areas include autologous cryoprecipitate. When used with thrombin, autologous
cryoprecipitate creates a hemostatic agent or "fibrin glue."
Services needed to prepare autologous platelets and autologous plasma may
also be available.
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PERIOPERATIVE CELL RECOVERY SERVICES
Perioperative Cell Recovery
Collection of autologous blood in the perioperative period is
a safe transfusion alternative for patients who may require a volume of
blood not possible to provide by autologous donation or for those who cannot
donate autologous blood prior to surgery. This blood may be collected using
perioperative blood recovery techniques or isovolemic hemodilution.
Pre (or Intra-)operative Hemodilution
Acute isovolemic hemodilution is the
withdrawal of one or more units of blood from the patient at the beginning
of the surgical procedure, for reinfusion at the end. The patient's blood
volume is maintained isovolemically with crystalloid or colloid solutions.
Hemodilution lowers autologous red cell loss by lowering the patient's
hematocrit; therefore the patient suffers a loss of fewer red cells in
a given volume of surgical blood loss. In addition, the autologous units
collected contain viable platelets and coagulation factors which may improve
postoperative hemostasis.
Careful management of fluid balance and cardiac
status is essential during this procedure. Detailed procedures and monitoring
of the patient are necessary during the procedure. The patient must have
an adequate hemoglobin at the beginning of the procedure and the use of
hemodilution usually results in a lower hematocrit than that found in control
patients during surgery.
Perioperative Blood Recovery
Perioperative blood recovery or blood salvage is the collection and reinfusion of blood lost
during and immediately after surgery. Patients most likely to be candidates
for intraoperative blood recovery are those in which substantial surgical
blood loss is anticipated, as in cardiac, vascular, orthopedic, neurosurgical
and complex gynecologic procedures. Blood recovery may reduce the use of
homologous (allogeneic) blood in trauma and in liver transplantation. Intraoperative
collection is usually contraindicated if the operative field is contaminated
with bacteria, such as with spilled intestinal contents or osteomyelitis,
or by malignant cells.
Blood recovered intraoperatively may be transfused
directly after collection (unwashed blood) using a disposable suction system,
often a canister system, or may be processed (washed) prior to infusion
using a semiautomated cell washer. Procedures which include the washing
step are more complex, requiring specialized equipment and training, and
careful coordination of operating room personnel. Return of washed products
may enable the red cells to be more concentrated, and eliminates contaminants
and procoagulants. Because of the lack of clotting factors in the washed
product, use of recovered blood may not reduce donor exposure to plasma
and platelets. Reinfusion of unwashed recovered blood is less complex and
costly, but usually has a much lower hematocrit and may include contaminants,
so that most hospitals limit the quantity of collected blood that can be
reinfused without washing.
Intraoperative blood recovery requires the anticipated
loss of a significant amount of blood, but the processing time is only
3 to 5 minutes so that the procedure does not prolong surgery or anesthesia
time and does not intrude on the surgical team's tasks.
Post-operative Cell Recovery
Post-operative cell recovery may use the same procedures
and equipment as intraoperative recovery in the immediate postoperative
period. Use of a semiautomated cell washer may be appropriate if postoperative
drainage is expected to be brisk. More often, postoperative blood recovery
uses simpler equipment which does not process (wash) the blood. Blood is
collected directly from surgical drains, especially chest tubes, then filtered
and returned to the patient. Postoperatively recovered blood must be infused
within six hours of collection, whereas washed intraoperatively collected
blood may be stored up to 24 hours prior to transfusion.
The availability of any of these options may depend on the type of surgery being performed,
the hospital policies and procedures, and the availability of staff and
equipment.
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DIRECTED BLOOD DONATIONS
No Safer
Your patients may want to meet their transfusion needs with blood donations made by relatives and
friends. However, there is some evidence that directed donations are less
safe than those of volunteer blood donors.
Directed donors under pressure and in response to a desire to "help" may give inaccurate information
about their health. Often, directed donors are first-time donors. The risk
of diseases that cannot be detected by laboratory tests can be higher in
first-time donors. There are times when use of blood from close relatives
is not advised, especially if the patient is facing a future bone marrow
transplant, and husband-to-wife donations are not advisable during the
child-bearing years because of the risk of immunization. Opportunities
for such donations are, however, available in New York State.
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FEES
Why Are Fees Charged?
Processing fees are generally charged whether the patient
receives blood from autologous, volunteer or directed donations. The processing
fee covers the expenses incurred to prepare blood for transfusion and is
customarily charged directly to the hospital and passed on to the patient.
Special Handling Fees
In addition, autologous and directed blood donations
require special handling. Each unit is labelled specifically for the patient's
use and tracked through processing and test procedures. The units are packed
and shipped with special instructions to the hospital. Because of this,
processing fees are ordinarily charged whether or not the patient's autologous
or directed blood is transfused.
QUESTIONS
Any questions should be directed
to the blood bank of the hospital where the blood will be transfused.
Requests for copies of this publication may be directed to:
Blood Resources Program
Wadsworth Center for Laboratories and Research
New York State Department of Health
P.O. Box 509
Albany, New York 12201-0509
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NEW YORK STATE DEPARTMENT OF HEALTH
COUNCIL ON HUMAN BLOOD AND TRANSFUSION SERVICES
James Mohn, M.D., Chairperson
Buffalo General Hospital
Somerset Laboratories, Inc.
Buffalo, NY
Celso Bianco, M.D.
Greater New York Blood Program
New York, NY
Shelley Brown, M.D.
Lenox Hill Hospital
New York, NY
Robert Dracker, M.D.
State University of New York Health Science Center
Syracuse, NY
Neville Harper, M.D.
Rome Hospital and Murphy Memorial Hospital
Rome, NY
Thomas Harrington
Hemophilia Association of New York, Inc.
New York, NY
Klaus Mayer, M.D.
Memorial Sloan-Kettering Cancer Center
New York, NY
Judith Woll, M.D.
American Red Cross Blood Services
Rochester, NY
Mark R. Chassin, M.D., M.P.P., M.P.H. (Ex-officio)
Commissioner
New York State Department of Health
Albany, NY
Jeanne Linden, M.D., M.P.H., Executive Secretary
Wadsworth Center for Laboratories and Research
New York State Department of Health
Albany, NY
BLOOD SERVICES COMMITTEE
Klaus Mayer, M.D., Chairperson
Memorial Sloan-Kettering Cancer Center
New York, NY
John Gorman, M.D.
New York University Medical Center
New York, NY
Joanna Heal, M.D.
American Red Cross Blood Services
Rochester, NY
Helen Richards, M.D.
Harlem Hospital
New York, NY
Annie Strupp, M.D.
New York Blood Services
New York, NY
Joan Uehlinger, M.D.
Montefiore Medical Center
New York, NY
Jeanne Linden, M.D., M.P.H.
New York State Department of Health
Albany, NY
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