- Open Access
Trauma-induced coagulopathy and critical bleeding: the role of plasma and platelet transfusion
Journal of Intensive Care volume 5, Article number: 2 (2017)
Hemorrhage is responsible for 30 to 40% of all trauma-related mortality. Among adult trauma patients, 94% of hemorrhage-related deaths occur within 24 h and approximately 60% of these deaths within 3 h of hospital admission. Therefore, appropriate initial fluid resuscitation for bleeding is crucial to avoid preventable trauma-related death. In particular, the resuscitation strategy must be designed to complement prompt correction of anemia, coagulopathies, and thrombocytopenia. Conventional damage control resuscitation (DCR) of patients with severe trauma and massive hemorrhage is usually begun with rapid infusion of 1000 to 2000 mL of crystalloid fluids with subsequent transfusion of type O or uncross-matched red blood cells (RBCs) without plasma such as fresh frozen plasma (FFP) or platelets (PLTs). However, this DCR technique often leads to several adverse events such as abdominal compartment syndrome, acute respiratory distress syndrome, multiple organ failure, and dilutional coagulopathy. Simultaneous transfusion of FFP and PLTs along with the first units of RBCs while minimizing crystalloid infusion was recently recommended as a renewed DCR strategy. This aggressive RBC transfusion with FFP and PLTs is not only essential for the correction of coagulopathies and thrombocytopenia but also has the potential to ensure a good outcome in trauma patients. Additionally, it is important to maintain the resuscitation ratios of FFP/RBC and PLT/RBC. Most recently, DCR has been advocated for rapid hemorrhage control through early administration of a mixture of FFP, PLTs, and RBCs in a balanced ratio of 1:1:1.
Trauma is a major health care issue that results in the annual death of 5–8 million people worldwide . It is the sixth most common cause of death in Japan and the third most common in the USA. Hemorrhage is responsible for 30–40% of total trauma-related mortality . Among adult trauma patients, 94% of hemorrhagic deaths occur within 24 h and ~60% of these deaths within 3 h of hospital admission .
Bleeding in trauma is due to vascular damage, but in 25–30% of patients, it is also due to trauma-induced coagulopathy [1, 4–6]. It was long presumed that the main causative factor in traumatic coagulopathy was iatrogenic hemodilution. However, traumatic coagulopathy was recently shown to already develop at the trauma scene, before any medical intervention . This finding is of particular relevance given that traumatic coagulopathy results in considerably increased mortality [4, 5, 8, 9].
In the early phase of injury, rapid surgical or angiographic hemostasis is the first priority in avoiding trauma-related death. Preventable trauma death (PTD) may be attributable to the absence of appropriate initial resuscitation for bleeding. Therefore, any effective resuscitation strategy must be designed to complement the appropriate and prompt correction of anemia, coagulopathy, and abnormalities in fibrinolysis.
The damage control resuscitation (DCR) strategy, which is focused on halting and/or preventing the lethal triad of coagulopathy, acidosis, and hypothermia, has challenged traditional thinking on early resuscitation strategies . In DCR, transfusion is carried out during the early stage of patient management. It involves the use of increased amounts of plasma and platelets (PLTs) along with the first units of red blood cells (RBCs), while simultaneously minimizing crystalloid administration in patients who are predicted to require massive transfusion (defined as >10 units of RBCs in 24 h) [10–13].
Coagulopathy during the pre-hospital stage
Our understanding of major hemorrhage in trauma has dramatically changed over the past decade, mainly due to the recognition that patients who are bleeding when they present to the hospital already have an established coagulopathy, before the dilutional effects of fluid resuscitation. This has led to the use of a new terminology: acute traumatic coagulopathy (ATC) or acute coagulopathy of trauma shock, or trauma-induced coagulopathy (TIC). ATC/TIC quickly follows severe and profound injury and is present in one quarter to one third of these patients at the time of hospital admission [14, 15].
The importance of ATC/TIC is that its presence is a prognostic indicator, based on its association with a poor clinical outcome. In traumatic hemorrhage patients, a prolonged prothrombin time (PT) and/or activated partial thromboplastin time (aPTT) at hospital admission, before resuscitation, is associated with a three- to fourfold higher mortality and independently associated with increased transfusion requirements, organ dysfunction, and critical care length of stay [16, 17].
ATC/TIC is a multifactorial, global failure of the coagulation system to sustain adequate hemostasis after major trauma. Its pathophysiology is thought to be due to the massive stimulation of thrombin generation, PLT consumption, and fibrinolysis by damaged tissues [18, 19]. Tissue damage exposes tissue factor, which drives thrombin generation and activation of the coagulation cascade. Thrombin activates PLTs, leukocytes, tissue plasminogen activator (t-PA), and the endothelium. Other factors that activate t-PA include hypoxia and vasopressors .
The development of coagulopathy in the emergency department
In the 1970s and 1980s, resuscitation of the most severely injured and massively hemorrhaging patients usually began with the rapid administration of 1000–2000 mL of crystalloid fluids, followed by type O or uncross-matched RBCs. However, the administration of significant amounts of crystalloid leads to abdominal compartment syndrome, acute respiratory distress syndrome (ARDS), and multiple organ failure . Ley et al.  determined that the replacement of ≥1.5 L of intravenous crystalloids in the emergency department is an independent risk factor for mortality. High volumes of crystalloids (>3 L) are associated with a high mortality rate, particularly in elderly trauma patients. Additionally, in this setting, low blood volume, insensible losses and/or consumption, and resuscitation with plasma-poor RBCs rapidly lead to plasma coagulation factor concentrations of <40%, even before 10 units of RBCs have been transfused. However, the early initiation of plasma therapy is often delayed by its lack of immediate availability in the trauma center. Additionally, while PLT concentrations usually fall to 50–100 × 109/L (=50,000–100,000/μL) after 10–20 units of RBCs have been administered, in individual patients, they are quite variable and larger decreases are possible . Consequently, delays in the early initiation of PLT therapy are typically greater than those in plasma administration.
Situation of dilutional coagulopathy and thrombocytopenia according to differences in blood components
Kornblith et al.  obtained 23 units of fresh frozen plasma (FFP), PLT concentrate, and RBCs from a regional blood collection center and mixed them to create 23 units of 1:1:1 and 1:1:2 reconstituted whole blood (RWB) (Fig. 1). They then measured the international normalized ratio (INR)/partial thromboplastin time (PTT) and performed a complete blood cell count, functional studies, and an extensive panel of procoagulant and anticoagulant factor assays using these products. The hemoglobin (Hgb) and hematocrit (Hct) were significantly lower in patients administered 1:1:1 RWB than 1:1:2 RWB, but the former had a higher PLT count. Moreover, the PLT counts were typically only 70% of the transfused circulating PLTs. Notably, 1:1:1 RWB patients had a significantly lower INR and PTT than did 1:1:2 RWB patients and a significantly higher fibrinogen level (Table 1). Previous studies [24, 25] showed that an INR or PTT ratio >1.5 and low PLT counts were strongly associated with uncontrolled microvascular bleeding and hemorrhage-related mortality . Therefore, caution is warranted regarding the use of therapy with blood components, as an inappropriate unit ratio will lead to dilutional coagulopathy and thrombocytopenia.
Colloid or crystalloid in DCR?
The overuse of crystalloids before the administration of any blood product as a primary initial resuscitative solution in patients with hemorrhagic shock leads to dilutional coagulopathy, pulmonary edema (ARDS), and severe interstitial edema (abdominal compartment syndrome). Furthermore, because crystalloid- or colloid-based resuscitation causes acidosis, and a steady decline in oxygen delivery, the underlying coagulation and metabolic disorders that evolve after injury and blood loss are further aggravated .
However, for the last four decades, most trauma resuscitations have consisted of an initial 2000 mL of crystalloid given according to the early protocols of the American College of Surgeons’ Advanced Trauma Life Support course. During the same period, there was little argument about PLT administration. However, this resulted in unintentional hemodilution, which led to a vicious circle of coagulopathy, acidosis, and hypothermia, the “lethal triad of trauma” .
Importance of FFP transfusion and the FFP/RBC ratio
Cinat et al.  reported that early aggressive transfusion with FFP is essential to the correction of coagulopathy and results in a good outcome in trauma patients. According to Hirshberg et al. , prolongation of the PT to >1.8 times normal is the sentinel event of dilutional coagulopathy and the key to preventing coagulopathy is plasma infusion before the PT becomes subhemostatic. Based on a computer simulation, those authors concluded that the optimal replacement FFP/RBC and PLT/RBC ratios were 2:3 for plasma and 8:10 for PLTs to minimize dilutional coagulopathy. In the early 2000s, the two-part DCR concept was proposed for severely injured patients. The strategy is initiated within minutes of the arrival of these patients in the emergency department, with resuscitation initially limited to maintaining blood pressure at ~90 mmHg; this so-called permissive hypotension prevents renewed bleeding from recently clotted vessels. In the second step, intravascular volume restoration is accomplished using plasma as the primary resuscitation fluid in at least a 1:1 or 1:2 ratio of FFP/RBC .
Many studies have evaluated the effects of the FFP/RBC on mortality in massive transfusion after trauma (Table 2). Most of them demonstrated a survival advantage of an increased plasma ratio, with the majority suggesting an optimal FFP/RBC ratio of ≥1:2.
However, this approach has not been tested in prospective randomized controlled trials.
The Prospective, Observational, Multicenter, Major Trauma Transfusion (PROMMTT) Study Group, a highly publicized prospective cohort study, documented the timing of transfusions during active resuscitation and the respective patient outcomes . In the first 6 h after admission, patients with an FFP/RBC ratio of <1:2 were three to four times more likely to die than patients with ratios of ≥1:1. Higher plasma ratios early in resuscitation were associated with a decreased mortality in patients who received transfusions of at least three total units of RBCs, FFP, or PLTs during the first 24 h after admission. In a multivariable time-dependent Cox model, an increased FFP/RBC ratio was independently associated with a decrease in 6-h post-admission mortality (adjusted hazard ratio = 0.31; 95% confidence interval, 0.16–0.58), when hemorrhagic death predominates. Hagiwara et al.  also reported that in severe blunt trauma patients (injury severity score ≥16), the transfusion of an FFP/RBC ratio of ≥1 within the first 6 h was related to outcome. These results provide strong support for the early and high-dose administration of FFP in DRC blood transfusion therapy.
In severe trauma patients, massive transfusions of RBCs and FFP and other intravenous fluids give rise to dilutional thrombocytopenia. However, many studies have shown that in the early stages of trauma hemorrhage thrombocytes are maintained at levels not expected to contribute to a clinically significant coagulopathy . Thus, while PLT transfusion may not be essential for the correction of ATC/TIC, together with the combined effects of shock, hypothermia, etc., ATC theoretically produces aberrant PLT function by disrupting activation and adhesion pathways.
Starting time of platelet transfusion
In Japan, there are no clear criteria regarding the starting time of PLT transfusion for trauma patients, whereas in Europe, there is a guideline for the management of bleeding and coagulopathy following major trauma. According to the European guideline, in grade 1C patients, PLTs should be administered to maintain a concentration of >50 × 109/L. In grade 2C patients, the maintenance of a PLT count of >100 × 109/L is recommended for patients with ongoing bleeding and/or traumatic brain injury, with an initial dose of four to eight single PLTs units or one apheresis pack . The guideline for the administration of PLTs, however, is based mainly on observational studies and opinions.
Ciavarella et al.  reported that the most sensitive laboratory predictors of diffuse non-mechanical microvascular bleeding (MVB) were a PLT count <50 × 109/L (=50,000/μL) or a fibrinogen level of <0.5 g/L. Accordingly, a PLT count of <50 × 109/L (=50,000/μL) may serve as one of the criteria for the starting time of PLT administration in severe trauma patients, even in the absence of MVB. This starting time is consistent with the study by Johansson et al.  of patients with a ruptured abdominal aortic aneurysm, in whom 30-day survival was related to the PLT count determined upon arrival at the intensive care unit (ICU); this PLT count in the analyzed patients was well above the recommended 50 × 109/L.
However, some patients are able to maintain high PLT counts despite ongoing blood loss by recruiting PLTs from the spleen and possibly mobilizing new ones from bone marrow. Thus, when >220% of blood volume has been replaced, PLT counts will usually have fallen to around 50 × 109/L and frank coagulopathy will ensue .
Based on their small prospective study of 27 patients requiring massive transfusion, Counts et al.  concluded that the most useful parameter for estimating the need for PLT transfusions was the PLT count, with a count as high as 100 × 109/L potentially required to control bleeding from surgical wounds and serving as the threshold level for starting PLT transfusion.
A PLT count of <100 × 109/L is a possible risk factor for mortality, and a PLT count of <50 × 109/L leads to lethal coagulopathy. Therefore, PLT administration should be started when the PLT count is <100 × 109/L, and it should be maintained at >50 × 109/L in patients with severe trauma and/or ongoing bleeding. However, in one study, only 3% of trauma patients had a PLT count of <100 × 109/L at ICU admission , so a delay in the start of platelet administration should be avoided.
Ratio of the platelet transfusion
In massive transfusions (>10 units of RBCs within 24 h of admission), the resuscitation ratios of both FFP/RBC and PLT/RBC are undoubtedly important in reducing hemorrhagic mortality. However, neither civilian nor military practice has yielded a consensus on optimal PLT transfusions.
Inaba et al.  evaluated the impact of PLT transfusion in trauma patients receiving massive transfusion. With a decreasing PLT/RBC ratio, mortality at 24 h increased in a stepwise fashion. Compared with the group with the highest ratio (>1:6), the adjusted relative risk of death was 1.67 (adjusted p = 0.054) in the high-ratio group (≥1:12 and <1:6), 2.28 (adjusted p = 0.013) in the medium-ratio group (≥1:18 and <1:12), and 5.51 (adjusted p < 0.001) in the low-ratio group (<1:18). A similar stepwise increase in mortality with a decreasing PLT/RBC ratio was observed at 12 h after admission. After stepwise logistic regression, a high PLT/RBC ratio was independently associated with improved survival at 24 h (adjusted p < 0.001) (Fig. 2). Holcomb et al.  also determined the effect of the blood component ratio in massive transfusion. Patients with a high PLT/RBC ratio (≥1:2) had a significantly higher 30-day survival than those with a low PLT/RBC ratio (<1:2) (high 59.9% vs. low 40.1%, p < 0.01) as did those with a high (≥1:2) vs. low (<1:2) FFP/RBC ratio (high 59.6% vs. low 40.4%, p < 0.01). The authors concluded that not only a PLT/RBC ratio of ≥1:2 but also an FFP/RBC ratio of ≥1:2 was shown to be optimal and that both ratios were independent predictors of death at 6 and 24 h and at 30 days. These two treatment groups were then expanded to four in a 2 × 2 factorial layout (group 1: high FFP and PLT ratio; group 2: high FFP and low PLT ratio; group 3: low FFP and high PLT ratio; and group 4; low FFP and low PLT ratio). Kaplan–Meier analysis showed a significant separation of the groups within 6 and 24 h (p < 0.001) and that survival was higher in group 1 than in the other groups, at both 6 and 24 h (p < 0.001) (Fig. 3a). The overall 24-h difference was sustained for 30 days (p < 0.001) (Fig. 3b). These results suggest that in severe trauma patients the survival rate depends on a high PLT/RBC ratio rather than a high FFP/RBC ratio. Additionally, Holcomb et al.  retrospectively investigated the relationship between the PLT/RBC ratio and outcome based on 643 trauma patients who received massive transfusion. The patients were divided into three groups: a low-ratio group (>1:20), a medium-ratio group (1:2), and a high-ratio group (1:1). A propensity-adjusted Kaplan–Meier survival plot showed that higher PLT ratios were associated with improved survival at 24 h and 30 days (p < 0.001 for both) (Fig. 4).
Johansson et al.  performed a meta-analysis of the potential effect on survival of hemostatic resuscitation based on the proactive administration of PLTs rather than RBCs in trauma patients with massive bleeding. Two studies addressed the effect of high vs. low PLT transfusion rates in 641 massively bleeding trauma patients, of whom 333 received high PLT/RBC ratio [40, 41]. According to these two studies, patients receiving PLT/RBC in a high ratio had a significantly lower mortality (odds ratio 0.45, 95% confidence interval 0.37–0.55). This finding could not be attributed to the heterogeneity between the studies (I 2 = 0%). However, because no randomized studies evaluating the effect of different transfusion ratios were included in this report, the evidence level of this meta-analysis was low. Additionally, the absence of a relationship between the PLT/RBC ratio and overall mortality has been reported [42, 43].
After considering the above findings, the administration of at least one pool of PLTs (four to six individual donor units) for every five units of RBCs to trauma patients requiring massive transfusion seems reasonable .
Combined therapy with RBC, FFP, and PLT
Previous investigations of the FFP/RBC transfusion ratio supported a ratio of 1:1 or higher [10, 45]. However, in the management of ATC/TIC, the simultaneous administration of not only RBCs and FFP but also PLTs, in appropriate ratios, is recommended, with limited use of crystalloid or colloid solution.
The “optimal” ratio is the subject of ongoing debate because it may be complicated by the volumes of anticoagulant and RBC additive solution in modern blood components. In the abovementioned study by Kornblith et al. , the differences in the INR, PTT, and PLT counts obtained with whole blood vs. reconstituted blood composed of either 1:1:1 or 2:1:1 ratios of units of RBC, FFP, and PLT were investigated (Fig. 1). The results of the present study showed that the mean INR of 1:1:1 reconstituted blood was 1.31 and the mean PTT 42 s (1.4 times > normal), whereas the values for 2:1:1 reconstituted blood were 1.55 and 46 s (1.53 times > normal), respectively. Moreover, PLT counts were higher for 1:1:1 than for 2:1:1 blood components (129 × 109/L vs. 95 × 109/L, respectively), and typically, only 70% of the transfused PLTs circulated (Table 1). This simple physical consequence of mixing blood products suggests that treatment with 1:1:1 blood components has the greater potential to correct ATC/TIC .
The potential of FFP/PLT/RBC = 1:1:1
In the last decade, an alternative resuscitation strategy was developed based on providing only the conventional blood components FFP, PLT, and RBC in a 1:1:1 ratio to maintain the intravascular volume, oxygen-carrying capacity, plasma coagulation factors, and functioning platelets. The administration of crystalloid fluids was markedly limited, and other colloid-containing fluids given for massive bleeding were avoided. In severely injured patients, this strategy appears to not only save lives but also to reduce blood product consumption . In light of this result, many guidelines now recommend 1:1:1 ratios.
Nascimento et al.  reported a feasibility study based on a small randomized controlled trial that included trauma patients expected to require a massive transfusion. A fixed FFP/PLT/RBC ratio of 1:1:1 was compared with standard practice (laboratory result-guided transfusion protocol). The trial was able to achieve the 1:1:1 ratio in 57% (21 of 37) of the patients in the fixed ratio group compared with 6% (2 of 32) of those in the control group, thus demonstrating the feasibility of the intervention. While the study was not powered to detect a difference in mortality, the all-cause 28-day mortality by intention-to-treat analysis (relative risk for fixed ratio, 2.27; 95% confidence interval, 0.98–9.63) and by per-protocol analysis (relative risk for fixed ratio, 3.17; 95% confidence interval, 1.15–18.24) was consistent with a safe outcome.
The recent Pragmatic Randomized Optimal Plasma and Platelet Ratios (PROPPR) trial , a large, prospective, randomized, interventional trial in which patients with severe bleeding trauma were the focus compared the efficacy and safety of a 1:1:1 transfusion ratio of FFP/PLT/RBC to a 1:1:2 ratio. There was no difference in 24-h or 30-day mortality between the two groups. However, a 1:1:1 ratio did result in a significant reduction in mortality from bleeding within the first 24 h (9.2 vs. 14.6%; p = 0.03), with no increase for the 1:1:2 ratio group in ARDS, venous thromboembolism, or other transfusion-related complications. The absolute benefit was a 4% reduction in mortality among randomized patients, and the relative benefit a 15% reduction in total mortality, from 26 to 22% overall.
However, the prospective observational PROMMTT trial  emphasized anew the problems arising from bias in the blood product delivery time. Despite the fact that all 10 participating centers tried to deliver the products in a 1:1:1 ratio, the fraction that succeeded in achieving this ratio for plasma was 30% at 1 h, 40% at 2 h, and 50% at 6 h. The achieved ratios were even worse for PLTs .
Preventable trauma death may be attributable to the absence of appropriate initial resuscitation for bleeding. Therefore, any effective resuscitation strategy must be designed to complement the appropriate and prompt correction of anemia, coagulopathy, and abnormalities in fibrinolysis. In DCR, transfusion must be carried out during the early stage of patient management. It involves the use of increased amounts of plasma and PLTs along with the first units of RBCs, while simultaneously minimizing crystalloid administration (1000-2000 mL) in patients who are predicted to require massive transfusion. At the present time DCR is recommended for rapid hemorrhage control through early administration of a mixture of FFP, PLTs, and RBCs in a balanced ratio of 1:1:1.
Activated partial thromboplastin time
Acute traumatic coagulopathy
Damage control resuscitation
Fresh frozen plasma
Preventable trauma death
Red blood cell
Spahn DR, Bouillon B, Cerny V, Coats TJ, Duranteau J, Fernández-Mondéjar E, et al. Management of bleeding and coagulopathy following major trauma: an updated European guideline. Crit Care. 2013;17:R76.
Johansson PI, Oliveri RS, Ostrowski SR. Hemostatic resuscitation with plasma and platelets in trauma. J Emerg Trauma Shock. 2012;5:120–5.
Holcomb JB, del Junco DJ, Fox EE, Wade CE, Cohen MJ, Schreiber MA, et al. The Prospective, Observational, Multicenter, Major Trauma Transfusion (PROMMTT) study: comparative effectiveness of a time-varying treatment with competing risks. JAMA Surg. 2013;148:127–36.
Frith D, Goslings JC, Gaarder C, Maegele M, Cohen MJ, Allard S, et al. Definition and drivers of acute traumatic coagulopathy: clinical and experimental investigations. J Thromb Haemost. 2010;8:1919–25.
Brohi K, Cohen MJ, Ganter MT, Matthay MA, Mackersie RC, Pittet JF. Acute traumatic coagulopathy: initiated by hypoperfusion: modulated through the protein C pathway? Ann Surg. 2007;245:812–8.
Rezende-Neto JB, Rodrigues GP, Lisboa TA, Carvalho-Junior M, Silva MJ, Andrade MV, et al. Fresh frozen plasma: red blood cells (1:2) coagulation effect is equivalent to 1:1 and whole blood. J Surg Res. 2015;199:608–14.
Theusinger OM, Baulig W, Seifert B, Müller SM, Mariotti S, Spahn DR. Changes in coagulation in standard laboratory tests and ROTEM in trauma patients between on-scene and arrival in the emergency department. Anesth Analg. 2015;120:627–35.
Da Luz LT, Nascimento B, Shankarakutty AK, Rizoli S, Adhikari NK. Effect of thromboelastography (TEG®) and rotational thromboelastometry (ROTEM®) on diagnosis of coagulopathy, transfusion guidance and mortality in trauma: descriptive systematic review. Crit Care. 2014;18:518.
Spahn DR, Spahn GH, Stein P. Indications and risks of fibrinogen in surgery and trauma. Semin Thromb Hemost. 2016;42:147–54.
Holcomb JB, Wade CE, Michalek JE, Chisholm GB, Zarzabal LA, Schreiber MA, et al. Increased plasma and platelet to red blood cell ratios improves outcome in 466 massively transfused civilian trauma patients. Ann Surg. 2008;248:447–58.
McMullin NR, Holcomb JB, Sondeen JL. Hemostatic resuscitation. In: Vincent J, editor. Yearbook of intensive care and emergency medicine. New York: Springer; 2006. p. 265–78.
Hess JR, Holcomb JB, Hoyt DB. Damage control resuscitation: the need for specific blood products to treat the coagulopathy of trauma. Transfusion. 2006;46:685–6.
Holcomb JB, Jenkins D, Rhee P, Johannigman J, Mahoney P, Mehta S, et al. Damage control resuscitation: directly addressing the early coagulopathy of trauma. J Trauma. 2007;62:307–10.
Simmons JW, Pittet JF, Pierce B. Trauma-induced coagulopathy. Curr Anestheol Rep. 2014;4:189–99.
Cohen MJ. Acute traumatic coagulopathy: clinical characterization and mechanistic investigation. Thromb Res. 2014;133:525–7.
Cap A, Hunt B. The pathogenesis of traumatic coagulopathy. Anaesthesia. 2015;70 Suppl 1:96–101. e32-e34.
Shah A, McKechnie S, Stanworth S. Use of plasma for acquired coagulation factor deficiencies in critical care. Semin Thromb Hemost. 2016;42:95–101.
Brohi K, Cohen MJ, Ganter MT, Schultz MJ, Levi M, Mackersie RC, et al. Acute coagulopathy of trauma: hypoperfusion induces systemic anticoagulation and hyperfibrinolysis. J Trauma. 2008;64:1211–7.
Davenport R. Pathogenesis of acute traumatic coagulopathy. Transfusion. 2013;53 Suppl 1:23S–7S.
Moore FA, McKinley BA, Moore EE. The next generation in shock resuscitation. Lancet. 2004;363:1988–96.
Ley EJ, Clond MA, Srour MK, Barnajian M, Mirocha J, Margulies DR, et al. Emergency department crystalloid resuscitation of 1.5 L or more is associated with increased mortality in elderly and nonelderly trauma patients. J Trauma. 2011;70:398–400.
Ketchum L, Hess JR, Hippala S. Indications for early fresh frozen plasma, cryoprecipitate, and platelet transfusion in trauma. J Trauma. 2006;60(6 Suppl):S51–8.
Kornblith LZ, Howard BM, Cheung CK, Dayter Y, Pandey S, Busch MP, et al. The whole is greater than the sum of its parts: hemostatic profiles of whole blood variants. J Trauma Acute Care Surg. 2014;77:818–27.
Kutcher ME, Howard BM, Sperry JL, Hubbard AE, Decker AL, Cuschieri J, et al. Evolving beyond the vicious triad: differential mediation of traumatic coagulopathy by injury, shock, and resuscitation. J Trauma Acute Care Surg. 2015;78:516–23.
Peltan ID, Vande Vusse LK, Maier RV, Watkins TR. An international normalized ratio-based definition of acute traumatic coagulopathy is associated with mortality, venous thromboembolism, and multiple organ failure after injury. Crit Care Med. 2015;43:1429–38.
Murphy CH, Hess JR. Massive transfusion red blood cell to plasma and platelet unit ratios for resuscitation of massive hemorrhage. Curr Opin Hematol. 2015;22:533–9.
Spinella PC, Doctor A. Role of transfused red blood cells for shock and coagulopathy within remote damage control resuscitation. Shock. 2014;41 Suppl 1:30–4.
Miller TE. New evidence in trauma resuscitation—is 1:1:1 the answer? Perioper Med (Lond). 2013;2:13.
Cinat ME, Wallace WC, Nastanski F, West J, Sloan S, Ocariz J, et al. Improved survival following massive transfusion in patients who have undergone trauma. Arch Surg. 1999;134:964–8.
Hirshberg A, Dugas M, Banez EI, Scott BG, Wall Jr MJ, Mattox KL. Minimizing dilutional coagulopathy in exsanguinating hemorrhage: a computer simulation. J Trauma. 2003;54:454–63.
Hagiwara A, Kushimoto S, Kato H, Sasaki J, Ogura H, Matsuoka T, et al. Can early aggressive administration of fresh frozen plasma improve outcomes in patients with severe blunt trauma?—A report by the Japanese Association for the Surgery of Trauma. Shock. 2016;45:495–501.
Frith D, Davenport R, Brohi K. Acute traumatic coagulopathy. Curr Opin Anaesthesiol. 2012;25:229–34.
Ciavarella D, Reed RL, Counts RB, Baron L, Pavlin E, Heimbach DM, et al. Clotting factor levels and the risk of diffuse microvascular bleeding in the massively transfused patient. Br J Haematol. 1987;67:365–8.
Johansson PI, Stensballe J, Rosenberg I, Hilsløv TL, Jørgensen L, Secher NH. Proactive administration of platelets and plasma for patients with a ruptured abdominal aortic aneurysm: evaluating a change in transfusion practice. Transfusion. 2007;47:593–8.
Hiippala S. Replacement of massive blood loss. Vox Sang. 1998;74:399–407.
Counts RB, Haisch C, Simon TL, Maxwell NG, Heimbach DM, Carrico CJ. Hemostasis in massively transfused trauma patients. Ann Surg. 1979;190:91–9.
MacLeod JB, Lynn M, McKenney MG, Cohn SM, Murtha M. Early coagulopathy predicts mortality in trauma. J Trauma. 2003;55:39–44.
Inaba K, Lustenberger T, Peter Rhee P, Holcomb JB, Blackbourne LH, Shulman I, et al. The impact of platelet transfusion in massively transfused trauma patients. J Am Coll Surg. 2010;211:573–9.
Holcomb JB, Zarzabal LA, Michalek JE, Kozar RA, Spinella PC, Perkins JG, et al. Increased platelet:RBC ratios are associated with improved survival after massive transfusion. J Trauma. 2011;71(2 Suppl 3):S318–28.
Schnüriger B, Inaba K, Abdelsayed GA, Lustenberger T, Eberle BM, Barmparas G, et al. The impact of platelets on the progression of traumatic intracranial hemorrhage. J Trauma. 2010;68:881–5.
Perkins JG, Cap AP, Spinella PC, Blackbourne LH, Grathwohl KW, Repine TB, et al. An evaluation of the impact of apheresis platelets used in the setting of massively transfused trauma patients. J Trauma. 2009;66(4 Suppl):S77–85.
Dirks J, Jørgensen H, Jensen CH, Ostrowski SR, Johansson PI. Blood product ratio in acute traumatic coagulopathy—effect on mortality in a Scandinavian level 1 trauma centre. Scand J Trauma Resusc Emerg Med. 2010;18:65.
Simmons JW, White CE, Eastridge BJ, Mace JE, Wade CE, Blackbourne LH. Impact of policy change on US Army combat transfusion practices. J Trauma. 2010;69 Suppl 1:S75–80.
Jansen JO, Thomas R, Loudon MA, Brooks A. Damage control resuscitation for patients with major trauma. BMJ. 2009;338:b1778.
Schuster KM, Davis KA, Lui FY, Maerz LL, Kaplan LJ. The status of massive transfusion protocols in United States trauma centers: massive transfusion or massive confusion? Transfusion. 2010;50:1545–51.
Nascimento B, Callum J, Tien H, Rubenfeld G, Pinto R, Lin Y, et al. Effect of a fixed-ratio (1:1:1) transfusion protocol versus laboratory-results-guided transfusion in patients with severe trauma: a randomized feasibility trial. CMAJ. 2013;185:E583–9.
Holcomb JB, Tilley BC, Baraniuk S, PROPPR Study Group, et al. Transfusion of plasma, platelets, and red blood cells in a 1:1:1 vs a 1:1:2 ratio and mortality in patients with severe trauma: the PROPPR randomized clinical trial. JAMA. 2015;313:471–82.
Availability of data and materials
Since this article is a review article, the datasets supporting the conclusions are available in publicly published articles listed in the reference list.
HI contributed to the conception of the review, drafting of the manuscript, and critical revisions of the manuscript for intellectual content. TK provided intellectual input to the text and helped to draft the manuscript. Both authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
Since this article is a review article, this section is not applicable to this article. We do not include any specific data originally derived from our unpublished experiments or clinical study.
About this article
Cite this article
Ishikura, H., Kitamura, T. Trauma-induced coagulopathy and critical bleeding: the role of plasma and platelet transfusion. j intensive care 5, 2 (2017). https://doi.org/10.1186/s40560-016-0203-y
- Fresh frozen plasma
- Damage control resuscitation
- Acute traumatic coagulopathy
- Acute coagulopathy of trauma shock
- Trauma-induced coagulopathy