
In emergent
cases, rapid loss of circulating blood volume results
in a sharp drop in blood pressure, increase in heart rate, tissue hypoxia and weakness. If not treated
promptly, it inevitably leads to haemorrhagic shock, as in cases with ruptured ectopic
pregnancy accounting for about 9 % to 13 % of
pregnancy-related deaths [3,7]. Urgent surgical haemostasis and rapid blood volume replacement are the primary measures to
save the trauma and obstetric patients
[7].
Various methods and devices have been described
for the collection of shed blood in open or closed systems
and transfusing it to the same patient,
having certain points in common, from very simple and improvised (i.e. ,on war fields) to highly
sophisticated commercial ones [2,4, 8-11]. Blood is harvested
into canisters/bags or reservoirs pre-, peri-, or directly post-operatively, by suctions, aspirators,
drains or chest tubes (for haemothorax),
from a body cavity (thoracic or abdominal) or a wounded extremity [2-5]. At present,
there are three main methods
of ABT, namely Cell Salvage
(CS), Preoperative Autologous Donation (PAD), and Acute Normovolaemic Haemodilution (ANH) [3-5, 12]. CS is emerging as the preferred method for recovery
type ABT, and an increasing amount of evidence is accumulating with respect to
its safety and efficacy; PAD and ANH
could be useful in some elective high blood loss procedures and rare blood groups
[4,12,13].
The best auto transfusion technique
for unstable patients
in resource-limited conditions should be simple,
safe and cheap,
requiring no power supply and only minimal human resources [3,4]. The simpler
method is generating unprocessed blood, which is crude shed blood collected promptly
into a sterile container, filtered
through multiple layers of gauze (6-8) or compresses
(generally, one for the chest, two for the abdomen or limps), and
returned directly to the patient
[2,4,14]. Coverage with wide-spectrum antibiotics is always required, although
experience has shown that infection after ABT (in the absence of cell-salvage technology) of even enteric-contaminated blood, filtered
twice, is rare [2,14].
The need for anticoagulants (citrate phosphate dextrose adenine, CPDA) or heparin (500-1000 U per unit
blood) when transfusing non-processed blood has been a subject
of controversy [2]. However, it is accepted
that, for blood retrieved from a haemothorax, which does not form clots because it is defibrinogenerated unless the haemorrhage is from the great vessels,
the use of anticoagulant or heparin is probably not required; instead,
for shed blood from large vessels, it is theoretically warranted, although
clinically this has not always been
proved [2,6]. In the peritoneal cavity, coagulopathy results from microaggregates of platelets, red
blood cells (RBCs) and debris.
Heparin as a better anticoagulant has been proposed in cases with activated coagulation cascade leading to disseminated intravascular coagulation (DIC). In blood
collected from rupture of an ectopic
pregnancy, the trophoblastic products could cause DIC [2]. In blood recuperated from fractured limbs, the microaggregates include fat globules
that theoretically can cause fat embolism [2,5]. Of course, performing controlled clinical trials under circumstances with limited resources
would be difficult.
Electively, processed blood is aspirated by the
suction machine into an apparatus that adds an anticoagulant, then filters, and complementary
provides a cell-washing stage and centrifugation, that dramatically eliminate
all serum proteins,
free haemoglobulin, platelets,
clots, cell debris and the anticoagulant [2-4].
Only a concentrated RBC mass with a haematocrit of 50 % to 70 % returns to the patient [2,3,8]. These mechanical systems require
specialised personnel. On the other hand, in case of ongoing
massive abdominal haemorrhage (i.e., ruptured spleen or liver, ectopic pregnancy), intraoperative haemostasis from the surgeon comes first, while the abdominal
cavity is cleared with a laparotomy suction
of low pressure (or a “sump aspiration” device) to avoid
haemolysis, handled by an operating
assistant; the sterile
collection bottle contains
anticoagulant and normal
saline to avoid clotting [2]. Otherwise, blood can be scooped into a
basin or kidney dish with a sterile soup ladle, but this is time- consuming; this open method is usually
used in case of haemorrhage from limbs. The recuperated
blood is immediately filtered twice
before transfusion. Specifically , the autotransfusion system in massive haemothorax (> 2000 ml) uses the
intercostal chest tube that is connected to a re-sterilizeable chest bottle containing 100 ml saline (or, “in
extremis”, a urine collection bag without
saline), which, after filtering the
blood, is inverted to become the administration set [2].
ABT is placed in the setting of a surgical
approach to the haemorrhagic
patient, which includes timely control of bleeding and meticulous haemostasis [9,15]. Based on the ICRC recommendations [2], in most bleeding patients
whose evacuation is delayed
and total blood loss is 1000 ml or more, but
arrive in a relatively stable hypovolaemic condition, initial treatment requires
basic resuscitation with I.V. crystalloids, plasma, and plasma expanders (if available) prior to surgery. In patients
with acute and massive haemorrhage, the degree of urgency,
the desperate need for blood transfusion to save them, and the lack of any other source of blood appears to define the deadline for ABT more than anything else
[2,6,15]. In these cases, the rapid
loss of over 20 % of estimated blood volume (i.e. ,1000 ml blood), or a haematocrit value of less than 35 % on admission with expected crystalloid requirements of
more than 2000 ml, should alert the
surgeon and anaesthetist for the need for possible autotransfusion [2,15]. The most common use has been for ectopic
pregnancy and massive haemothorax. Other indications for ABT concern
cases with substantial blood loss occurring
either when the operation commences
(usually, a laparotomy with ruptured spleen and packed liver ,and the bleeding control
of wounded limps) or in the postoperative setting [2,3,12,14].
ABT lacks some important disadvantages of the allogenic blood transfusion, such as immunosuppression,
transmission of diseases (including
viral, such as hepatitis and human immunodeficiency, but also bacterial
or parasitic), haemolytic reactions/technical errors
in histocompatibility, scarcity of resources and uncertainty in patients with rare blood groups and
multiple auto-antibodies [3,4,13,15]. On the other hand, autotransfusion may cause transient
haematological abnormalities (i.e., coagulopathies, especially when more than three liters of
unprocessed blood are given) and possibly febrile
reactions that disappear
within 72 hours [2,11]. One should also not forget
that laboratory results (i.e.,
hematocrit) are influenced through the haemodilution from the synchronous rapid infusion of crystalloids.
Clinically, ABT has proven safe and effective
as it has not resulted in significant increase of
infectious complications, even with
blood harvested from war wounds, which is obviously not sterile [2]. Other potential complications of ABT, reported but rarely causing significant risks, are
haemolysis/haemoglobinuria with transient
deterioration of renal function (treatment with aggressive hydration
and urine alkalinization), electrolyte disorders, pulmonary
hypertension and Acute Respiratory Distress Syndrome (ARDS) [3,4]. In the
setting of the patient massively bleeding,
with little or no blood available for homologous
transfusion, the great benefits of ABT have proven to outweigh by far the possible
risks, even of multiple organ dysfunction/
failure [2,15]. Finally, there are only a small number of studies indicating that reinfusion of fetal cells in salvage
blood during caesarian section can be
used without the complications of amniotic fluid embolism and rhesus sensitization [4]. Larger cohort-studies are certainly required.
Conclusively, in circumstances where blood for transfusion is scarce, recovery
ABT for massive haemorrhage is time and lifesaving. ABT, as a simple method of blood replacement requiring
no specific equipment, is
placed in the setting of the emergency
approach to the haemorrhagic patient ,which includes timely control of bleeding and haemostasis .