Review Article - (2024) Volume 14, Issue 1
Optimizing Trauma Care with Pre-Hospital Blood Transfusion
Ritcha Saxena1* and
Ljiljana V Vasovic2
*Correspondence:
Ritcha Saxena, Department of Biomedical Sciences, University of Minnesota Medical School, Duluth, Minnesota,
USA,
Email:
Author info »
Abstract
Trauma is the main cause of morbidity and mortality, accounting for 10% of all mortality globally. This is primarily due to the occurrence of hemorrhagic shock. Uncontrolled hemorrhage and its effects, including anemia, hypovolemia, and impaired organ perfusion, necessitate the use of appropriate transfusion and volume resuscitation. For many years, the mainstay of treating trauma-induced bleeding was replenishing lost coagulation factors. The logical belief that coagulopathy should be directly addressed throughout trauma resuscitation has recently been strengthened by a greater knowledge of the pathophysiology of coagulopathy in trauma patients. Crystalloid was originally considered the cornerstone in pre-hospital management of hemorrhagic shock but is now revealed to result in a multitude of complications that raise patient morbidity. The Damage Control Resuscitation (DCR) strategy includes balanced resuscitation, hemostatic resuscitation, and prevention of acidosis, hypothermia, and hypocalcemia for critical trauma patients. Fluid administration is limited during balanced resuscitation, and hypotension is maintained up until the start of definitive hemostatic treatments. The best preventive measure for trauma-induced coagulopathy, according to recent treatment standards, is permissive hypotension and controlled resuscitation. Even after studying randomized-controlled trials, systematic reviews and meta-analyses, the feasibility of permissive hypotension and similar strategies remains unclear. It is necessary to conduct additional research to determine massive transfusion protocols that would benefit all trauma patients, regardless of variables like age, injury mechanism, or the existence of hypotension.
Keywords
•Trauma •Pre-hospital transfusion •Fluid resuscitation • Dilutional coagulopathy •Damage Control Resuscitation (DCR) •Permissive hypotension •Controlled resuscitation delayed resuscitation
Introduction
Hemorrhage-related deaths account for a large proportion of lives lost and are a primary cause of mortality worldwide [1,2]. Over a hundred years ago, early transfusion of whole blood post-trauma was discovered to be a lifesaving measure [3-5]. Several resuscitation methods have been implemented over the years to deal with this issue. Fluid resuscitation started in the 1970s with regular saline solution and transitioned eventually to blood component therapy [6, 7]. This was done in accordance with the notion that correcting hypovolemia recovers organ perfusion. The total time to transfusion onset has been demonstrated to play a critical role in lowering mortality [8,9]. This is in addition to the early utilization of blood products in the resuscitation of trauma patients.
Depending on the clinical circumstances, the appropriate transfusion strategies to be used in emergency situations can vary greatly. The transfusion plan is established by the healthcare professionals based on their evaluation of the patient's clinical stability, the severity of the hemorrhage or blood loss volume, and the speed of the bleeding [10]. Early resuscitations with blood products is made possible by the ability to transfuse patients in the pre-hospital setting. This review examines the role of pre-hospital transfusion, its guiding principles, and developing approaches to fluid resuscitation.
Literature Review
Pre-hospital transfusion
Pre-hospital transfusion refers to the administration of blood or blood products to a patient outside of a hospital setting, typically in an Emergency Medical Service (EMS) setting. The purpose of prehospital transfusion is to provide critical intervention in the form of rapid and targeted treatment to patients who have suffered significant blood loss due to trauma or other medical conditions [11, 12]. Pre-hospital transfusion has gained increasing recognition in recent years as a potentially life-saving intervention for critically injured patients. Traditionally, pre-hospital care has focused on stabilizing patients and transporting them to a hospital for further treatment [13-15]. However, this approach can be ineffective for patients who are bleeding profusely and require immediate transfusion [16-19].
The use of pre-hospital transfusion was first introduced by the military to improve survival rates for soldiers wounded in combat [20,21]. Since then, it has been adopted by EMS agencies around the world to improve outcomes for civilian trauma patients. One of the most important factors in the success of pre-hospital transfusion is the ability to identify patients who are most likely to benefit from this intervention. In the pre-hospital setting, where resources are scarce and sufficient volumes of blood are not easily accessible, it is extremely challenging to accurately evaluate patients who need blood transfusions. Inappropriate transfusion practices entail avoidable hazards and resource waste, especially of rare O negative units [22-27]. The most common indication for pre-hospital transfusion is severe hemorrhage, which can occur as a result of trauma, surgery, or other medical conditions. Patients who are in shock or have significant hypotension may also be candidates for pre-hospital transfusion. Any defined criterion is not enough; the clinical judgment of pre-hospital healthcare practitioners should also be taken into account when determining if transfusion is the best course of treatment.
Modalities involved in pre-hospital transfusion
Prompt hemorrhage management is the primary goal of pre-hospital transfusion in order to prevent hypovolemic shock and the lethal triad threat of coagulopathy, hypothermia, and acidosis. There are several different types of pre-hospital transfusions that may be used depending on the patient's condition and the resources available. One common approach is to administer Packed Red Blood Cells (PRBCs), which contain oxygen-carrying hemoglobin and can help to restore the patient's blood volume and oxygenation levels. Other blood products that may be used include Fresh Frozen Plasma (FFP), which contains clotting factors and can help to prevent bleeding, and platelets, which are essential for clot formation. For instance, in patients with penetrating injuries, clinical practice in the recent times has been dominated by a resuscitation approach that resolves around aggressive use of crystalloid as the primary fluid [28]. Since organ ischemia and decreased perfusion has a serious impact on mortality rates, it was thought that early, large-volume fluid resuscitation was essential in the treatment of hypotensive shock in trauma patients. A 3:1 replacement of crystalloid fluid to the amount of blood lost was the norm. Aggressive fluid resuscitation therefore gained popularity even before its effectiveness was well-examined and established [29,30].
However, in the past few years, it has been shown through various retrospective studies that intensive resuscitation, frequently commenced in the pre-hospital setting, may be deleterious to trauma patients [28,31-33].
The changing paradigm of fluid resuscitation techniques
While crystalloids can be helpful in restoring blood volume and hydration levels, despite their widespread use, they have some limitations and potential risks associated with their use. Unfortunately, this approach has now been linked to negative side effects that include electrolyte imbalance in the form of acid-base disturbances, hypothermia, dilutional coagulopathy, and rapid blood loss [34]. It is widely known that the amount of pre-hospital crystalloid infusion correlates with acute traumatic coagulopathy at the time of arrival to the hospital [35]. The use of excessive crystalloid volumes in the treatment of trauma patients can also cause resuscitation injury, inflammation damage, digestive and cardiac dysfunction, Acute Respiratory Distress Syndrome (ARDS), elevated extremity compartment pressures, clotting disturbances, abdominal compartment syndrome, and Multiple Organ Dysfunction Syndrome (MODS). They can also lead to pulmonary edema, heart failure, and other complications, particularly in patients with pre-existing cardiac or renal dysfunction [36-44].
One of the main concerns with crystalloid use is the potential for fluid overload, which can occur when large volumes of crystalloid solutions are administered. In particular, large volumes of crystalloid solutions can dilute the patient's blood components and lead to complications such as decreased coagulation ability. Another potential risk associated with crystalloid use is the dilutional effect on blood components which include red blood cells and clotting factors. Dilutional coagulopathy can occur when large volumes of crystalloid solutions are administered, which can impair the patient's ability to form clots and increase the risk of bleeding [45]. This is particularly concerning in patients who require transfusions of blood products, as dilutional coagulopathy can worsen bleeding and make it more difficult to control. In addition to concerns related to fluid overload and dilutional coagulopathy, crystalloid use may also have other potential risks, including electrolyte imbalances and acidbase disturbances. For example, administration of large volumes of normal saline can lead to hyperchloremic metabolic acidosis, which can impair renal function and increase the risk of infection [46]. To address these concerns, several studies have examined the use of balanced crystalloid solutions, which contain electrolytes in ratios that more closely mimic those found in the body's extracellular fluid [47-49]. One such solution is Plasma Lyte A, which has been shown to have a lower incidence of hyperchloremic acidosis and lower rates of renal failure compared to normal saline [50].
Alternative strategies of fluid resuscitation
For patients with severe trauma to receive optimal fluid resuscitation, it is crucial to maintain an equilibrium between organ perfusion and hemostasis. Hemostatic resuscitation of bleeding trauma patients with early deployment of blood components is the current best practice, according to studies published in the past couple of decades [51-58]. More recent approaches for managing patients with severe hemorrhage has evolved from supportive, reactive care using crystalloids to proactive, urgent deployment of standardized procedures known as Massive Transfusion Protocols (MTPs) [59]. Newer resuscitation techniques, such as Damage Control Resuscitation (DCR), which underscore the importance of early application of blood products and concentrates on providing the patient with balanced resuscitation, have been developed as a result of an increased awareness of the risks involved with crystalloid use and the necessity for early inclusion of blood products [30, 60].
The DCR paradigm stipulates that blood component transfusions (consisting of fresh frozen plasma, packed red blood cells, and platelets) be administered in a 1:1:1 ratio, (thereby resembling whole blood); priority be given to prompt hemorrhage management; and that crystalloid infusion be restricted to allow for a lower blood pressure until bleeding is controlled. In critical trauma patients, this approach has been associated with improved survival rates [61,62]. Up until bleeding can be surgically managed, DCR, which avoids crystalloids while accepting some degree of hypotension, is increasingly preferred [63-67].
Damage Control Resuscitation (DCR)
The core tenets of DCR are the mitigation and management of hypothermia, acidosis, and hypocalcemia, as well as permissive hypotension and swift and definitive hemorrhage control. Damagecontrol resuscitation aims to achieve definitive hemostasis, reduce iatrogenic resuscitation injury, and to preempt the acute traumatic shock from exacerbating [68]. According to Morrison et al., coagulopathy is one of the key distinctions between hypotensive resuscitation and normotensive resuscitation. Their study revealed that although the overall rate of mortality was not statistically different, the group that received hypotensive group had a much lower rate of mortality from bleeding due to coagulopathy within the initial 24 hours following injury [69]. This is because there were no deaths from bleeding following surgical hemorrhage repair. Three approaches-permissive hypotension, in which fluid is administered to raise the systolic blood pressure short of achieving normotension; controlled resuscitation, where a fixed volume of fluid is transfused; and delayed resuscitation, in which fluid is administered after bleeding has been controlled have been suggested to prevent clot disintegration and dilutional coagulopathy.
Hypotensive resuscitation, also known as permissive hypotension, achieves and sustains low tissue perfusion by minimal volume fluid resuscitation, such that the blood pressure is maintained in the lowerthan-normal range, which is ideal for short time frames. Goal-directed resuscitation, where the systolic blood pressure or mean arterial pressure is targeted depending on individual patient profile, or controlled resuscitation, where preestablished rates are infused such that normotension is not reached, are two methods for achieving permissive hypotension [70].
During the early resuscitation of hypotensive trauma patients, controlled resuscitation defined as administering smaller crystalloid boluses for either a systolic pressure less than 70 mmHg or in the absence of a radial pulse is practicable and secure. Controlled resuscitation may be safer in pre-hospital transfusion for blunt trauma-patients and may even result in better prognosis, especially in patients with pre-hospital hypotension, according to two important clinical trials [71,72]. However, this approach carries the potential threat of tissue hypoperfusion even if it may prevent the negative consequences of early and high-dose fluid resuscitation [73].
Delayed resuscitation results in lower mortality rates and shorter hospitalizations. Aggressive fluid administration prior to surgery and hemorrhage management is believed to escalate blood loss, dislodge clots, and even result in a secondary hemorrhage [30].
In patients with Traumatic Brain Injury (TBI) and/or spinal injury, neither permissive hypotension/hypotensive resuscitation nor restricted/ controlled resuscitation is recommended [74]. This is due to the fact that adequate perfusion must be sustained during resuscitation in so as to ensure tissue oxygenation of the compromised central nervous system and prevent secondary damage [65, 75,76]. To further understand the efficacy of these methods and to create treatment plans that examine the role of trauma-induced coagulopathy in the pathophysiology of trauma and pre-hospital transfusions, additional research is required.
Challenges and room for improvement
Protocols guiding the resuscitation with blood components, plasma protein, and associated products have emerged in the pre-hospital setting in accordance with the concept that the slightest delay can dramatically increase the mortality rate [77,78]. The need of the hour is to develop strategies that guarantee the safety of transfusion medicine procedures and accordingly meet the accreditation standards, thereby avoiding unnecessary waste and ensuring personnel competences.
Despite the potential benefits of pre-hospital transfusion, there are some challenges associated with this intervention. One of the biggest challenges is ensuring that blood products are administered safely and appropriately. Blood products must be stored and transported under specific conditions to maintain their efficacy and safety. Blood transfusions are also not able to be utilized routinely in the pre-hospital setting due to logistical and operational constraints [79]. Furthermore, there is also lack of information available on the pre-hospital indications for blood transfusions and evidence of the effectiveness of these practices is not widely available [80,81] When transit times are short, performing transfusion can be done to the detriment of drug administration, because transfusions need separate intravenous lines. Less patients received tranexamic acid as a result of these factors following the implementation of pre-hospital blood products in their service, according to Jenkins et al [82]. In addition, pre-hospital transfusion can be expensive and resource intensive.
Most randomized-controlled trials in pre-hospital transfusion are based on plasma transfusions, even though it is the red blood cells and tranexamic acid that are predominantly used in most pre-hospital transfusion programs [83-87]. Elements including prolonged arrival times to the trauma center, simultaneous delivery of red blood cells and plasma and blunt-trauma patients may result in favorable patient outcomes with pre-hospital transfusion, despite mixed evidence [88-94]. Most importantly, priority should be given to timely transfer of patients to appropriate facilities where standard-of-care is received, and definitive care is offered [95-98].
Conclusion
In conclusion, pre-hospital transfusion has emerged as an important intervention for patients with significant blood loss due to trauma or other medical conditions. With proper implementation, prehospital transfusion has the potential to save lives and improve outcomes for critically injured patients. In situations where transport time to definitive care is prompt, delayed resuscitation is preferable; while in slow transport circumstances, goaldirected resuscitation with low-volume crystalloid seems advisable. However, the impacts of pre-hospital transfusions are undoubtedly multifaceted, hence studying more complex outcomes in addition to just mortality statistics will be crucial for understanding their implications.
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Author Info
Ritcha Saxena1* and
Ljiljana V Vasovic2
1Department of Biomedical Sciences, University of Minnesota Medical School, Duluth, Minnesota, USA
2Department of Pathology, Weill Cornell Medicine, New York, New York, USA
Citation: Saxena, R. & Vasovic, L.V. Optimizing Trauma Care with Pre-Hospital Blood Transfusion. Prim Health Care, 2023, 13(3), 491.
Received: 06-Apr-2023, Manuscript No. JPHC-23-91029;
Editor assigned: 10-Apr-2023, Pre QC No. JPHC-23-91029 (PQ);
Reviewed: 24-Apr-2023, QC No. JPHC-23-91029 (Q);
Revised: 27-Apr-2023, Manuscript No. JPHC-23-91029 (R);
Published:
30-Apr-2023
Copyright: ©2023 Saxena, R. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.