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Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_35_библиотеки_им_акад_М_И_Перельмана

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C. L. Riley and J. Dean
anesthesiologist) or emergency medicine physician. The team provides hospital level care to patients in ight after recover­ing them from the battleeld in potentially non- permissive areas (hostile) while transporting them to more denitive care [3]. Anesthesiologists in France have been part of the disaster response system for several decades and are a key element of the French emergency medical service, Service d’Aide Medicale Urgente (SAMU) [2]. Anesthesiologists are often the lead clinician sent with SAMU to mass casualty events to provide an advanced level of care near the site of the disaster and coordinate with re and police. In this arrangement, pre­hospital disaster management and hospital disaster manage­ment are integrated [2].
Hemorrhage is the leading cause of potentially prevent­able mortality in MCEs [1, 47]. Mortality from terrorist attacks increased 500% between 2000 and 2014. Although mortality from terrorist attacks has dropped to 27% since 2014, terrorism is more widespread affecting more countries than in 2014 [8]. While only modest numbers of patients fol­lowing MCEs require transfusion, a small number of patients with critical injuries and polytrauma will require immediate transfusion as part of damage control resuscitation (DCR). Damage control resuscitation is a resuscitation strategy to prevent death from catastrophic hemorrhage and refers to US military guidelines developed for combat casualties with massive bleeding in Iraq and Afghanistan. DCR is well described throughout trauma and resuscitation literature and involves multiple interventions including earlier and bal­anced transfusion of plasma and platelets with initial red blood cell (RBC) transfusion. DCR evolved from the earlier concept of damage control surgery (DCS), the practice of
rapid and abbreviated surgery after initial resuscitation to control bleeding and reduce infection risk by removing debris, fecal matter, and body uids followed by continued resuscitation and physiological stabilization in the intensive care unit (ICU) [9]. Denitive surgical repair could be deferred for several days as DCS emphasized avoiding the lethal triad of acidosis, hypothermia, and coagulopathy. However, direct treatment of coagulopathy was not a pri­mary focus of DCS because coagulopathy had been pre­sumed to be due primarily to initial resuscitation, hemodilution, and hypothermia rather than the physiological response to trauma and hemorrhage [10]. Damage control resuscitation is a comprehensive approach (incorporating DCS) from the point of trauma to denitive treatment to min­imize blood loss, maintain tissue oxygenation, and correct the lethal triad at the earliest moment after the occurrence of trauma [9, 10]. Intravascular treatment of bleeding and coag­ulopathy are integral to damage control resuscitation, and more recent DCR research has shown that prehospital initia­tion of resuscitation, including transfusion of packed RBCs, thawed plasma, and platelets, decreases morbidity and mor­tality in trauma patients at risk of shock [1115] (Fig.18.1).
The surge in demand for blood products during a mass casualty event and the earlier and higher number of blood products required for DCR demand that transfusion emer­gency preparedness be integrated into the medical emer­gency preparedness planning process [16, 17]. Effective and timely deployment of blood products during natural and man-made disasters and in military conict requires the inte­gration of research from multiple specialties including indus­trial engineering and operations research, emergency
Fig. 18.1 Mass casualty
event at Bagram air base 2011– single operating room used for two simultaneous surgeries after a mass casualty event (Photograph from author’s private collection)
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preparedness, blood banking, transfusion medicine, as well as emergency and trauma medicine. As anesthesiologists assume larger roles in hospital and community emergency preparedness, a basic understanding of blood transfusion emergency preparedness across the continuum of care is valuable.
The USBlood Supply System andCurrent Challenges toSustainability andResiliency
Organization
The US blood supply system is comprised of many organiza­tions with different structures and philosophies and all func­tion to meet the nation’s blood needs for component therapy and plasma. This chapter focuses on the collection of whole blood for processing into component therapy (RBCs, plasma, platelets, cryoprecipitate) used in transfusion because these components are the primary therapies required in MCEs. Although plasma collected by plasmapheresis can be used for transfusion, this collection process is separate, and the plasma collected is generally used as raw material to manufacture plasma derivatives such as brinogen, Factor IX, anti-throm­bin III, etc. The blood collection system in the USA is hetero­geneous because it developed on the free market without consideration of patient referral patterns [18]. Blood collec­tion is performed by a network of federally regulated nonprot organizations and supplied by donors that are all nancially uncompensated volunteers. Nearly half of all blood is col­lected by the American Red Cross (ARC) collection centers. The remainder of blood collection in areas not represented by the ARC is performed by independent nonprot community blood centers and hospital blood banks. Most geographical areas are served by only one blood collection organization. Although blood is collected from volunteers by nonprot col­lections centers, blood and its fractionated products are com­modities with processing and distribution costs as well as a uctuating “market price” depending on supply and demand. Areas with high supply and low demand can export their over­supply to areas with high demand and lower supply through blood resource sharing. “Spot” markets exist for urgent pur­chases where prices are based on current market supply and immediate delivery. Blood collection centers compete on blood component price for contracts to supply hospitals and other health-care organizations [18].
Regulation
Blood centers are licensed and regulated by the USFood and Drug Agency (FDA). Other Federal organizations involved in maintaining the health and safety of the blood supply
include the Department of Health and Human Services (DHHS), the Public Health Service (PHS), and the Centers for Disease Control (CDC) providing direction, oversight, and surveillance. The American Association of Blood Banks (AABB) is a nonprot association that performs inspections and accreditation of blood banks and blood centers; estab­lishes standards for blood collection, processing, and stor­age; and participates in the National Blood Exchange Program, facilitating movement of blood products from sur­plus areas to shortage areas.
Challenges intheUSBlood Supply System
Over the last decade, the demand for blood products has decreased signicantly. Between 2009 and 2016, the number of units of blood collected and distributed by the American Red Cross decreased by >25% [19]. This decline is largely due to several advances in clinical medical practice and hos­pital cost-containment efforts. Less invasive surgeries, phar­macological alternatives to transfusion, non-myeloablative treatment of malignancies, and comprehensive patient blood management strategies have reduced the demand for blood [20]. Patient blood management has been motivated by the need to improve blood safety and patient outcomes, preserve the blood inventory, and constrain escalating hospital costs [21]. Blood management strategies promote appropriate use of blood components with the goal of minimizing their use and promote transfusion alternatives.
Despite the decreased demand for blood products, the number of blood centers collecting, processing, and distrib­uting blood has remained nearly the same. Costs for these blood centers have remained constant or increased. New test­ing for specic diseases and broader pathogen-reduction technologies add production and testing costs to the blood centers that are difcult to pass on to hospitals [22]. For example, the emergence of the Zika virus in Puerto Rico required development and implementation of additional test­ing at additional cost to blood centers. Additionally, blood products from non-affected areas had to be transported to Puerto Rico to maintain a safe blood supply prior to develop­ment of Zika testing. Other blood center cost increases include more selective donor criteria, expensive information systems for data analysis, and leukocyte reduction of RBCs. All of this has made blood transfusion safer but also more expensive. Hospital consolidation has shifted negotiating power away from blood centers and kept blood component prices low. Private and government insurers do not treat blood as a distinct reimbursable product or service in hospi­talized patients resulting in no direct linkage between hospi­tal reimbursement and the true cost of providing blood components. Approximately 80% of all transfusions occur in hospitals.
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The blood center response to these challenges has been predictable but concerning for the ability of the US blood supply system to remain resilient especially in the face of a prolonged disaster. Many blood centers have removed excess capacity by reducing collections to a minimum, reducing staff, limiting availability of specialty blood products, and reducing or eliminating uncompensated services like surveil­lance and education [23]. In response to the changing eco­nomic landscape of blood centers, the Department of Health and Human Services (DHHS) contracted the RAND Corporation to study the sustainability of the blood supply in the United States.The RAND (Research ANd Development) Corporation is an American nonprot global policy think tank created in 1948 by Douglas Aircraft Company to offer research and analysis to the USArmed Forces. Their report
Toward a Sustainable Blood Supply in the United States: An Analysis of the Current System and Alternatives for the Future [22] concluded that the current blood supply system
is robust, operating efciently most of the time, but that con­tinued market contraction will likely result in more wide­spread shortages in the future. Recommendations for improving the resiliency of the US blood supply include both market solutions and government intervention. Their conclu­sions include the following:
1. Separate payments for blood products may mitigate pres-
sures on the blood system.
2. Assess emerging technologies for maximum benet and
incentivize the adoption of these technologies.
3. Develop a vision of appropriate levels of surge capacity.
4. Distinguish between the costs of maintaining a surge
capacity and the normal costs of doing business and
nance the surge capacity.
5. Build relationships across blood brokerages (ARC,
Armed Services Blood Program) to address short-term
and local shortages.
6. Implement emergency use authorizations by DHHS for
replacement supplies in the event of a shortage.
products require careful temperature control, and therefore shipping blood products is costly with added weight of insu­lation and ice.
Armed Services Blood Program
Organization andRegulation
The US military maintains its own blood supply under the Armed Services Blood Program (ASBP). The ASBP repre­sents all three branches of military, and its components col­lect, process, store, transport, and transfuse blood to service members and their families worldwide. Like civilian blood centers, the ASBP is governed by the FDA guidelines for maintaining safety and quality of blood products. The ASBP also follows the standards, procedures, recommendations, and guidelines of the AABB.Any service member receiving blood or blood products in a combat area will receive blood through the ASBP.Although the ASBP does work with the ARC and other blood centers during civilian emergencies, the two blood supplies are usually distinct. The ASBP sends all blood collected at military blood donation centers (on military bases and civilian locations) to two Armed Services Whole Blood Processing Laboratories (ASWBPLs). Blood reaches combat theater either by pre-positioning frozen blood at Blood Product Depots or by sending blood and blood components to Expeditionary Blood Transshipment Systems which move the blood products to Blood Supply Units in theater. From there, blood is moved in theater to forward deployed surgical units, theater hospitals, USNavy ships, and Allied/Coalition hospitals. Forward surgical units and theater hospitals provide blood and blood products to rst responders at the individual unit level [26].
Challenges intheJoint Service Blood Supply Chain
Review of the literature also suggests that international blood product sharing agreements could support longer-term blood supply challenges such as infectious disease emergen­cies like Zika virus outbreak [24].
Other ongoing challenges to the blood supply include donor dependence, perishability of blood products, and costly transit. The size of the donor pool is dwindling due to increased donor exclusions and the aging population. Minorities are also underrepresented in the donor pool due to higher donor deferral rates, mistrust of the medical commu­nity, and lack of awareness of the blood donation process and the need for rare blood [25]. The shelf life of blood products is short, and therefore there is great potential for waste which further burdens the cost of producing the product. Blood
The military blood supply chain faces different challenges especially in some operating environments. Large-scale combat operations can potentially result in a signicant demand surge for blood products while simultaneously reducing freedom of movement for US forces and limiting the capacity to transport blood products to forward operating locations. A sustained conict successful at targeting critical military infrastructure such as command centers, runways, and fuel depots could limit the movement of blood into the­ater from donation centers. Blood stored in medical treat­ment facilities (MTFs) would become depleted interrupting care to combat casualties [27]. The Defense Advanced Research Projects Agency (DARPA) has focused on devel­oping approaches to augment operational resiliency. Three
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principles of operational resiliency have been integrated in the joint service blood supply chain. Fractionation enables the scaling of elements within the supply chain to deploy downrange as needs require. For example, a small expedi­tionary blood collection center could be deployed until a larger capability was established or restored. Composition enables tailoring capabilities to best suit the needs down­range. Although a deploying Army brigade may not have the capability to thaw and process frozen blood, the Air Force has a small deployable capability that offers these services. The Air Force capability can be tasked to deploy with the Army. Functional substitution enables amending current capabilities with substitutes better suited for operational needs such as stocking frozen packed red blood cells that have a longer shelf life than packed red blood cells [27].
Transfusion Disaster Preparedness
Transfusion Disaster Plan
Transfusion support is critical in the health-care response to MCEs, and every hospital should include transfusion disas­ter preparedness in its overall emergency planning. The over­all goals of transfusion disaster preparedness should be holistic and include the following aims [28]:
1. To protect the delivery of key products and services
2. To manage the incident within regulatory requirements
3. To strive for recovery of normal business as soon as
possible
4. To safeguard the health, safety, and welfare of staff and
donors
After September 11, 2001, the American Society of Anesthesiologists (ASA) formed the Committee on Trauma and Emergency Preparedness (COTEP). Recognizing the unique skill set anesthesiologists have, COTEP collaborated with different organizations to create a resource center for anesthesiologists to learn about emergency preparedness. COTEP developed the Emergency Preparedness Manual for Anesthesia Department Organization and Management that emphasizes the importance of care coordination within the hospital in order to successfully manage the surge of patients requiring intervention. Core concepts of any hospital emer­gency preparedness plan should include the following:
1. Integration– It is of private and public medical capabili-
ties with public health systems.
2. Medical preparedness– Increase the response capabilities
and surge capacities.
3. At-risk populations – Identify populations most at-risk
after an event and determine their needs.
4. Continuity of operations – Maintain adequate public health and medical services.
More specic details should include process and outcome
objectives with identication of surveillance methods. Chain of command and expected ow of information should be determined including methods for communicating with the public. Personnel response timing and phasing should be established including clinical and administrative leaders. Equipment needs should be identied. Anesthesiologists can provide airway and resuscitation expertise in a rst responder role in the emergency department as well as liaison with staff in the operating room to facilitate appropriate operating room utilization. Figure18.2 details a general checklist for operating room readiness in a mass casualty event.
The AABB has developed a disaster operations handbook
to help blood centers, hospital blood banks, and transfusion services respond to disasters affecting the blood supply or the distribution of blood products [ intended to facilitate coordination among blood centers, hos­pital transfusion services, national blood organizations, and government ofcials to determine the medical need for blood, to establish transportation of blood from one facility to another, and to communicate a common message to the national blood community and the public about the status of the blood supply in the disaster-affected area. The AABB denes a disaster as any event that:
1. Suddenly requires a much larger amount of blood than usual
2. Temporarily restricts/eliminates a blood collector’s abil­ity to collect, test, process, and distribute blood
3. Temporarily restricts/prevents local population from donating blood
4. Temporarily restricts/prevents use of available inventory of blood products requiring immediate replacement
5. Creates a sudden inux of donors requiring accelerated drawing of blood to meet an emergent need elsewhere
This denition of disaster is broad and focuses attention
on any disruption however brief to the blood supply chain. The broad denition encourages early communication between all points in the blood supply chain to ensure early response to interruptions in blood product supply. Communication up and down the blood supply chain is prob­ably the single most important component of any transfusion disaster preparedness plan and should include hospital phy­sicians involved in emergency response. See Fig.18.3.
Another important element in any transfusion disaster pre-
paredness plan is a business continuity plan to prevent loss of function if routine infrastructure is disrupted (computer net­works, blood processing centers), maintain services through event, and initiate disaster recovery [30]. Disaster plans should
29]. The handbook is
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Fig. 18.2 Operating room
procedures for mass casualty– management step by step (Reprinted with permission of the American Society of Anesthesiologists, 1061 American Lane, Schaumburg, Illinois 60,173–4973)
C. L. Riley and J. Dean
be rehearsed [28, 29] regularly. Exercises can be simple table­top exercises and do not require extensive simulation equip­ment. Low delity exercises can challenge current assumptions and reveal inadequate or inefcient processes [28]. Previous assumptions are based on past data and do not reect future
challenges so transfusion emergency planning should be viewed as dynamic and iterative. For example, the last decade has seen both a change in resuscitation and transfusion prac­tice and increased lethality in many events including terrorist attacks and mass shootings [1, 31].
R
DISASTER OPERATIONS HANDBOOK • OCTOBER 2008
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Fig. 18.3 Response plan
ow chart– this owchart shows the bidirectional communication ow for transfusion response during a disaster. ARC American Red Cross, CDC Centers for Disease Control, HHS Health and Human Services, AABB American Association of Blood Banks, BCA Blood Centers of America, ABC America’s Blood Centers, ASBP Armed Services Blood Program, FDA Food and Drug Administration
e
L
ABC
BCA
Assist
Affected
Blood
Collector
EVENT
Affected
Blood
Collector
AABB
F
k
s
a
T
1
l
e
v
ARC CDC
AABB
ASBP
HHS
o
r
c
e
Message to Blood Community
and Donors
Message to Public
HHS
FDA
Level 2
Task
Force
ESPONSE PLAN FLOW CHART
Step 1.
Affected Blood Collector (BC) Assesses Medical Need for Blood
Contact local hospital customers and emergency services to determine impact of event, including:
Hospitals
Nature of emergency (e.g., disaster, terrorism)
Number of current and expected hospital admissions
• Types of expected injuries
• Potential effect on local donor base
Gather information on local blood inventory levels from both BC and hospital customers.
Calculate the medical need for blood for a nonbiological event based on three units of type O RBCs per current and expected hospital admissions resulting from the event (see Event Assessment Form).
Step 2.
Affected BC Contacts AABB (ideally within 1 hour of event)
Contact AABB (use redundant communication channels in order listed below):
Land line: (800) 458-9388
1.
Cell phone: (240) 994-6700
2.
E-mail: nbe@aabb.org
3.
Text message: (240) 994-6700
4.
Satellite phone: (254) 377-3726
5.
Report medical need and local blood inventories.
Step 3.
Step 4.
Interorganizational Task Force (TF) Conference Call
AABB convenes a conference call with Level 1 TF members (Level 2 TF members included if necessary–see page 42 for a list of Level 1 and Level 2 TF member organizations).
TF determines national strategy and coordination efforts, including:
Message to blood community/donors
1.
Transpor tation and coordination of blood to affected BC
2.
Next steps until event is resolved
3.
AABB communicates decisions to Level 2 TF members.
Implementation of Task Force Recommendation
TF representatives communicate recommendations to their respective constituencies.
TF distributes unified message to blood community and donors
(e.g., joint press releases).
TF coordinates message to the public with Department of
Health and Human Services (HHS).
Blood Supply Chain Management (BSCM)
Glasgow et al. [1] showed that there are relationships between casualty statistics and RBC use but that reporting of blood use is often inconsistent and incomplete. Understanding how the blood supply chain operates during the surge condi­tions of an MCE is challenging because data collection and experimentation are low priority during an event. Furthermore, the blood supply chain is dynamic with irregu­lar supply, stochastic demand, perishable commodities, expensive and technical processing, and costly transporta­tion. Operational research techniques offer an approach to investigate this complex system as these techniques provide models that can interact and experiment with the numerous
variables involved in the delivery of transfusion services dur­ing an MCE [32]. Operational research models can evaluate BSCM along each of the four main processes: procurement, production, inventory, and distribution [33]. Other models can evaluate for efciency (minimize cost) and effectiveness (minimize delivery time) and effects of pandemics on blood supply regionally [34, 35]. Dynamic supply chain modeling can consider adjustments inlocation and capacity of facili­ties at different time periods representing different periods of an MCE. In-hospital MCE response modeling has shown perceived hospital ability to manage MCEs to be overly opti­mistic and specically identied blood resources as a limit­ing factor in event response time [36] and recommend early automatic restocking during an MCE to preserve red cell
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supply. BSCM modeling offers additional techniques to pre­pare for MCEs that do not interrupt patient care and can con­sider the large number of variables that impact the complex blood supply chain. This area of research is promising as resuscitation and transfusion practices evolve, and MCE planning must include supply of coagulation components both in the hospital and prehospital response.
Transfusion Demand Forecasting andPlanning
The greatest challenge in transfusion disaster preparedness is balancing demand and supply especially the demand for uni­versal components such as group O RBCs in an MCE.Transfusion services must assess the event and predict the likelihood for extensive use of blood components and rapidly obtain more components if necessary. Transfusion demand planning is increasingly important for MCE plan­ning, and the literature is evolving. Transfusion demand planning has been informed by civilian MCEs globally as well as by changing trends in trauma care. Evidence from these global MCEs suggests only a modest number of MCE victims admitted to the hospital require transfusion. The mean blood use per patient is consistently calculated at 2–3units PRBC per patient or 6–7 units PRBC per moder­ately and severely injured patient. Most of that product is transfused within the rst 6–12h [1, 28, 37, 38]. Blood use reporting however is inconsistent following MCEs, and reporting standardization would improve data validation. Additionally, much of the data used to derive the above esti­mates was gathered before the introduction of damage con­trol resuscitation. Blood use has changed over the last decade with the increased use of hemostatic components [1] includ­ing in the prehospital period. While this may reduce the demand on RBCs, there will likely be strain on supplies of plasma, platelets, and cryoprecipitate in the future. A recent attempt to correlate transfusion needs with injury mecha­nisms and severity found that while the demand for compo­nents correlated with the number of casualties, injury mechanism was less useful in prediction of blood require­ments [28, 31] possibly because response and evacuation times for events were very different.
Early Blood Grouping andTransfusion Triage
Massive transfusion protocol use in treatment of hemorrhage has led to increased demand for group O Rh negative RBCs and AB plasma. Activation of massive transfusion protocols for multiple patients in an MCE can quickly lead to a demand that exceeds supply of universal components and hemostatic components if these practices are not incorporated into local demand planning. Transfusion triage of patients by age and
gender can identify patients that are able to receive alterna­tive universal blood products (O Rh positive RBCs for all men and women over 50years old). Use of anti-D immuno­globulin can also reduce the risk from alternative universal blood products. The use of group A plasma in patients with unknown blood type instead of group AB plasma has not been shown to increase morbidity and mortality in patients with group B blood [ have been used in lieu of group O platelets in patients with unknown blood types. Although red cell contamination can increase the risk of alloimmunization, platelet additive solu­tions may reduce the risk of hemolysis [40, 41]. Transfusion triage also can identify patients in whom transfusion is not immediately required. Early blood grouping of these less acute patients can help preserve the supply of universal com­ponents [28]. It is important to mention that blood grouping during an MCE increases the risk of ABO blood group incompatible transfusion and any blood grouping plan should include a clear emergency plan for identifying, sampling, and labeling patients and their blood group. Glasgow etal.
32] described simulation modeling of deliberate RBC, and
[ emergency group O blood transfusion restriction during an MCE increased overall patient treatment rates. Red blood cell transfusion restriction especially in combination with hemorrhage control, early use of tranexamic acid, and pre­hospital plasma transfusion offers another potential tool to extend blood supply in an MCE.
39]. Similarly, group A and B platelets
Management ofBlood Donation andStock
Management of blood stock and blood donation during an MCE is critical to disaster preparedness. Maintaining large stock holdings leads to wastage due to perishability, but insufcient stock may interrupt the ability to provide clinical care to patients. Immediate demand for blood should be met by existing stocks although this may require movement of stock. Shortages should be expected during any unplanned event, and blood shortage plans should be prepared. More rural areas may not be able to depend on immediate stock. In a prolonged MCE or an event with large numbers of casual­ties or an event in remote areas, replacement will be required. Blood collection agencies should work closely with donors to ensure continued supply of blood but also not overwhelm the collection system during a disaster. After the World Trade Center and Pentagon attacks on September 11, 2001, over 475,000 units of blood were collected of which only 258 were used [42]. Blood collection centers need to appeal to that altruism during non-disaster periods to meet collection targets that will ensure capacity when emergency events occur. Most blood services prefer to hold sufcient replace­ment stock rather than accept emergency donations, but a prolonged MCE may require a variety of approaches to
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restocking supplies including stock movement, use of an emergency/high-readiness donor pool, increase collection targets, adjustments in testing and processing, and support from other blood services [16]. Transportation should also be a consideration in blood stock planning. Interruption of usual transportation modes and routes must be considered in con­tingency plans for continued re-supply. Emerging technolo­gies such as aerial drone technology offer transportation alternatives for delivery of blood products to austere or remote locations. Any transportation alternative must con­sider the cold chain management required for blood products to ensure safe use. Widespread use of aerial drones for a vari­ety of tasks is accelerating the development of improved drone capability with an associated reduction in cost. This includes increased speed and increased payload capacity. This technology holds promise for blood stock resupply in a disaster [43].
Emergency Donors andWhole Blood
Development of blood component therapy focused primarily on medical indications for transfusion therapy for specic patient groups. Component therapy enables targeted treat­ment for patients with a single blood cell or factor deciency as in sickle cell disease or hemophilia. Component therapy also optimizes storage of a limited resource that is dependent on volunteers for sourcing. In contrast to medical patients, hemorrhaging patients become decient in all components of blood, and our current balanced mass transfusion practice attempts to replace all of these components.
The US military has been using whole blood transfusion in resuscitation of severe traumatic hemorrhage since World War I [44, 45]. Whole blood (WB) transfusion can provide oxygen-carrying capacity to military personnel injured in austere environments and has been used extensively during the wars in Iraq and Afghanistan by the US military and NATO Coalition Forces [44, 4648]. The current US military Joint Trauma System Clinical Practice Guideline (JTS CPG) for whole blood transfusion provides guidelines for both cold-stored whole blood (SWB) and fresh whole blood (FWB) transfusion [49]. Whole blood in one of the antico­agulant citrate solutions is an FDA-approved product when it is collected, stored, and tested for transfusion-transmitted disease (TTD). It can be stored for 21–35days depending on the citrate solution at 1–6°C and is referred to as SWB. The hemostatic function of SWB is adequate and stable for the rst 2weeks after collection but may require supplementa­tion with other blood components (platelets, FFP) for ade­quate hemostasis after 2weeks. FWB refers to whole blood collected on an emergency basis from a “walking blood bank” (WBB), a group of pre-screened donors that respond to an emergency call from the military treatment facility
(MTF). FWB can be stored at room temperature for up to 24h before it must be discarded. If refrigerated within 8h of collection and submitted for complete transfusion-transmit­ted disease testing, FWB becomes SWB. FWB has full hemostatic function and usually does not undergo full FDA­approved TTD testing prior to transfusion. For this reason, FWB transfusion is not FDA­when tested blood products are unavailable and the need for transfusion is urgent [49]. See Fig.18.4 for a sample emer­gency donor panel questionnaire for FWB donor.
The most important safety factor when transfusing WB is donor RBC compatibility with the recipient’s pre-formed anti-A or anti-B antibodies. WB from group O donors con­tain RBCs compatible with all recipients, but the plasma in group O WB may cause hemolysis if the anti-A or anti-B antibody titers are high. This challenge can be addressed by transfusing only same-group WB (A to A, B to B, AB to AB, and O to O) or using low titer anti-A and anti-B group O WB (LTOWB) [ donor WB, and low titer SWB is the preferred resuscitation product for the prehospital treatment of patients in hemor­rhagic shock [52]. If the situation permits, rapid infectious disease testing (HIV, HBV, HCV) is performed on donor specimens prior to transfusion, and retrospective samples on all donors are sent for FDA-approved TTD testing.
Clinical data suggests that the use of WB to treat hemor­rhage results in outcomes at least as favorable as those with component therapy including RBCs, plasma, and platelets [14]. WB mitigates some of the challenges of adequate stored components and supplies hemostatic components with a smaller anticoagulant load [53]. Infection risk in a properly prescreened donor group appears to be low. The ASBP spon­sored an epidemiological study to characterize transfusion­transmitted infection associated with emergently collected blood product transfusion [54]. The study looked at 761 recipients of emergently collected blood product transfusion and found no HIV or HBV transmission. One HCV trans­mission was identied. The study estimated the transfusion­transmitted infection prevalence in potential walking blood bank donors to be 8 in 1000 for HCV and 4 in 1000 for HBV.This non-zero risk requires a risk-benet analysis prior to use of FWB by experienced clinicians capable of assess­ing risk of withholding transfusion. A robust “walking blood bank” (WBB) with practiced collection and testing can pro­vide a more agile and resilient emergency transfusion response to a major incident especially in isolated regions. The Immunology and Transfusion Medicine Department of Haukeland University Hospital in Bergen, Norway, in col­laboration with the Norwegian Naval Special Operation Commando establishes a WBB for military settings. The col­laboration led to a mass casualty event contingency plan for the hospital that includes the use of low titer anti-A and anti­B FWB from established or pre-tested blood group O donors
50, 51]. LTOWB is considered the universal
approved and is reserved for
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C. L. Riley and J. Dean
[55]. The contingency plan was exercised in July 2018 when a critically ill patient received over 200units of blood prod­ucts, exhausting the supply of stored LTOWB.Collection of FWB was considered the fastest way to obtain platelet-con­taining blood product for immediate transfusion [53]. Norway has geography and population density that pose numerous transportation challenges especially in the long winter periods. Blood transfusion programs are therefore regional rather than national. Blood banks are run by local and regional hospitals and blood stock is maintained to meet usual hospital needs. This decentralized management of the Norwegian blood supply is similar to the independent blood center management of much of the US blood supply system. Locally developed transfusion disaster preparedness plans that include the development of a walking blood bank will increase the resiliency and responsiveness of their blood sup­ply especially in a major incident.
Fig. 18.4 Proposed eld emergency
donor panel questionnaire (Reproduced with permission from Wiley)
Future ofTransfusion Disaster Preparedness: TheGolden Hour ofTrauma
Military trauma care has transformed civilian trauma care in the last decade. Military practice has also impacted mass casualty event planning in the civilian sector because current trauma care is dependent on networks of rst responders trained in damage control resuscitation, blood centers responsive to the need for massive transfusion for major hemorrhage, and experienced clinicians leading emergency and surgical teams in triage and resource allocation for maxi­mum treatment capability in a major incident. The develop­ment of trauma registries has facilitated collaborative translational research that has improved overall survival in trauma patients.
Emergency donor panels (EDPs) and whole blood, tourni­quets and hemostatic dressings, and early tranexamic acid
18 Blood Deployment inNatural Disasters andaMilitary inConict
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Fig. 18.4 (continued)
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and hemostatic components are trauma practices that have been incorporated into civilian trauma care in the last decade. Despite the changes in trauma care and improvement in overall trauma patient survival, the mortality for trauma patients undergoing laparotomy that arrive at the emergency department (ED) with hypotension has remained unchanged and is approximately 48% [56].
Efforts to reduce that mortality risk are now focused on early hemorrhage control in the prehospital period, some­times referred to as the golden hour of trauma. Controlling hemorrhage before a patient is in shock reduces the risk of the lethal triad of acidosis, hypothermia, and coagulopathy. Transfusion of pre-thawed plasma has been incorporated into many ED transfusion stocks because it reduces plasma thaw time and patients receive balanced transfusion ratio of 1:1 plasma to RBCs earlier. In 2018, the FDA granted emer­gency use authorization to the Department of Defense to use pathogen-reduced leukocyte-depleted freeze-dried plasma. Freeze-dried plasma, known as French FDP or French lyoph­ilized plasma (FLYP) because it is manufactured by the French Military Blood Institute, has been used in the European Union (EU) for almost two decades. FLYP can be stored at room temperature for 2years without deterioration of coagulation factors, and the hemostatic properties of
FLYP are comparable to those of fresh frozen plasma [57,
58]. The immediate availability of FLYP translates to earlier
balanced transfusion of plasma and RBCs and may reduce the need for massive transfusion in trauma patients [59]. The storage capabilities of this product could potentially simplify the supply chain challenges for plasma. Alternative storage methods for blood components and development of synthetic blood components (platelets and oxygen carrying molecules) continue to be researched [6062] with the goal of reducing mortality from traumatic hemorrhage.
Summary
Transfusion capability is critical to the health-care response to MCEs with the key challenge being to match supply and demand. Hospitals and the community health-care services should include transfusion planning in their emergency preparedness plans. Review of historical events can provide guidance for future planning, but each new event offers new insight for transfusion management. Transfusion emergency preparedness is necessary to provide a timely, safe, and sus­tainable blood supply. Transfusion emergency preparedness plans need to include modeling frameworks to understand