- Open Access
Clinical effectiveness of fresh frozen plasma compared with fibrinogen concentrate: a systematic review
Critical Carevolume 15, Article number: R239 (2011)
Haemostatic therapy in surgical and/or massive trauma patients typically involves transfusion of fresh frozen plasma (FFP). Purified human fibrinogen concentrate may offer an alternative to FFP in some instances. In this systematic review, we investigated the current evidence for the use of FFP and fibrinogen concentrate in the perioperative or massive trauma setting.
Studies reporting the outcome (blood loss, transfusion requirement, length of stay, survival and plasma fibrinogen level) of FFP or fibrinogen concentrate administration to patients in a perioperative or massive trauma setting were identified in electronic databases (1995 to 2010). Studies were included regardless of type, patient age, sample size or duration of patient follow-up. Studies of patients with congenital clotting factor deficiencies or other haematological disorders were excluded. Studies were assessed for eligibility, and data were extracted and tabulated.
Ninety-one eligible studies (70 FFP and 21 fibrinogen concentrate) reported outcomes of interest. Few were high-quality prospective studies. Evidence for the efficacy of FFP was inconsistent across all assessed outcomes. Overall, FFP showed a positive effect for 28% of outcomes and a negative effect for 22% of outcomes. There was limited evidence that FFP reduced mortality: 50% of outcomes associated FFP with reduced mortality (typically trauma and/or massive bleeding), and 20% were associated with increased mortality (typically surgical and/or nonmassive bleeding). Five studies reported the outcome of fibrinogen concentrate versus a comparator. The evidence was consistently positive (70% of all outcomes), with no negative effects reported (0% of all outcomes). Fibrinogen concentrate was compared directly with FFP in three high-quality studies and was found to be superior for > 50% of outcomes in terms of reducing blood loss, allogeneic transfusion requirements, length of intensive care unit and hospital stay and increasing plasma fibrinogen levels. We found no fibrinogen concentrate comparator studies in patients with haemorrhage due to massive trauma, although efficacy across all assessed outcomes was reported in a number of noncomparator trauma studies.
The weight of evidence does not appear to support the clinical effectiveness of FFP for surgical and/or massive trauma patients and suggests it can be detrimental. Perioperatively, fibrinogen concentrate was generally associated with improved outcome measures, although more high-quality, prospective studies are required before any definitive conclusions can be drawn.
Surgery and massive trauma are frequently associated with significant derangement of haemostatic capacity caused by loss, consumption, endogenous inhibition (by the protein C pathway), dilution of coagulation factors (termed 'dilutional coagulopathy' or 'acute coagulopathy of shock and trauma') and increased clot breakdown (fibrinolysis). Most commonly, haemostatic therapy in patients without preexisting haemostatic disorders aims to substitute key components (clotting factors and other blood components) by transfusion of allogeneic blood products, including fresh frozen plasma (FFP), platelet concentrate (PC), packed red blood cells (RBC) and, in some countries, cryoprecipitate.
Clinical use of FFP in component therapy has increased over the past four decades . Reports of the success of high FFP:RBC ratios may be responsible for some of this rise [2–4]. The benefits of any intervention should outweigh the risks. FFP has been associated with increased risk of morbidity and mortality [5, 6], whilst the evidence to support the effectiveness of FFP in the perioperative setting or its appropriate dosing in the massive transfusion setting has been questioned [7–10].
Fibrinogen is a key protein in the new 'cell-based' model of haemostasis that involves four consecutive overlapping stages (initiation, amplification, propagation and stabilisation), in which the conversion of fibrinogen to a covalently linked fibrin network is the final stage [11, 12]. Of note, fibrinogen is the first coagulation factor to fall to a suboptimal level early during bleeding and dilutional coagulopathy . Fibrinogen supplementation is therefore recommended in patients with massive bleeding to maintain plasma fibrinogen levels above 1.5 to 2.0 g/L . Supplementation of fibrinogen may be most effective when performed as part of early goal-directed coagulation management . Typically, standard preparation FFP contains 2.0 g/L (range = 0.9 to 3.2 g/L) fibrinogen (equivalent to 0.6 g in a 300-ml unit), as well as other pro- and anticoagulant factors found in plasma, acute phase proteins (cytokines), electrolytes, immunoglobulins and albumin [9, 16]. Fibrinogen concentrate (from various manufacturers) is currently licensed for use in congenital bleeding in China, Japan, the USA and throughout Europe, and for use in acquired bleeding in > 15 countries globally. Pasteurised and lyophilised human fibrinogen concentrate is typically reconstituted in 50 ml of sterile water to a final concentration of 20 g/L. Each vial of fibrinogen concentrate contains 1.0 g (range = 0.9 to 1.3 g) of fibrinogen, as well as albumin, L-arginine hydrochloride, sodium chloride and sodium citrate . The concentrated dose of fibrinogen provided by fibrinogen concentrate (final concentration 10 times higher than FFP) might be preferable to FFP for restoring plasma fibrinogen levels because of its rapid availability (no thawing), reduced volume (faster infusion time) and increased safety, and it has recently been suggested to be more effective than administration of FFP . However, despite growing evidence based on both preclinical and clinical studies to support its efficacy and safety [17–20], fibrinogen concentrate is not yet a standard component of many transfusion protocols.
This systematic review was performed to investigate the evidence base for the use of FFP and fibrinogen concentrate in the perioperative and/or massive trauma setting. We have included observational studies and case series in addition to randomised, controlled trials (RCTs) to provide a comprehensive overview of the current clinical situation.
Materials and methods
Study concept and administrative structure
The initial rationale behind this systematic review was formulated by the lead author (SKL), who subsequently recruited the coauthors, arranged for an unrestricted educational grant from CSL Behring (Marburg, Germany), a manufacturer of fibrinogen concentrate, and liaised closely with Fishawack Communications (Oxford, UK), which provided editorial support. Within this structure, we had full control of the ideas, data, reporting and conclusions of the research and were not influenced by any commercial activities. Our study did not require ethical approval.
Studies reporting the administration of FFP or fibrinogen concentrate in a perioperative or massive trauma setting were identified in MEDLINE and EMBASE (1 January 1995 to 31 December 2010). The reference lists of identified studies and relevant reviews were checked for additional citations and to identify key FFP RCTs conducted prior to 1995.
In the electronic database search, we used 'perioperative', 'surgery', 'h(a)emostasis', 'bleeding', 'traumatic injuries', 'blood component transfusion' as both input words and subject headings. The FFP search also included 'fresh frozen plasma', 'FFP', 'plasma' and 'therapeutic plasma', and the fibrinogen concentrate search comprised 'fibrinogen/therapeutic use', 'fibrinogen concentrate', 'fibrinogen concentrates'. Additional limits were added: (1) language: English or German; (2) date range: 1 January 1995 to 31 December 2010; and (3) article type: clinical trial, meta-analysis, RCTrandomized controlled trial, case reports, clinical trial phases I to IV, comparative study, controlled clinical trial and journal article. Titles and abstracts were screened for relevance, and full publications of the potentially relevant studies were assessed against the formal eligibility criteria.
Studies were eligible for inclusion in the systematic review if they reported a predefined outcome of the administration of FFP or fibrinogen concentrate specifically within the perioperative or massive trauma setting. All preparations of FFP ('standard' as well as 'pathogen-reduced') were eligible for inclusion. Abstracts of work presented at congresses were excluded.
Outcomes of interest included blood loss, allogeneic transfusion requirements, survival, hospital and/or ICU length of stay (LOS), plasma fibrinogen levels, thrombotic events, acute lung injury (ALI), transfusion-associated circulatory overload (TACO), infections (bacterial contamination and viral transmission) and multiple organ failure (MOF). A meta-analysis of the effect of FFP on morbidity was recently published by Murad and colleagues . To avoid redundancy, outcomes related to morbidity (thrombotic events, ALI, TACO, infections [bacterial contamination and viral transmission] and MOF) were not extracted and tabulated for FFP studies.
All study types were included (RCTs, non-RCTs, prospective comparator studies, retrospective comparator studies, prospective and retrospective noncomparator studies, and case reports). Study design and quality of evidence were captured at the data extraction stage.
Studies were included regardless of patient age, sample size or duration of patient follow-up. We excluded preclinical studies, studies which included patients with congenital clotting factor deficiencies or other haematological disorders and studies reporting the prophylactic administration of FFP or fibrinogen concentrate in the absence of surgery. Studies reporting mixed populations were included only if > 50% of the cases were surgical and/or trauma patients. Studies reporting the administration of FFP for liver disease or reversal of vitamin K anticoagulation were excluded if there was no surgical intervention. Studies in which control groups received autologous platelet-rich plasma were also excluded. For assessment of the effect of each intervention on survival, studies that reported no deaths in either study arm were excluded from the survival outcome but included in all other applicable outcomes of interest.
Data from eligible studies were extracted according to the population, intervention, comparison and outcome (PICO) method into a standard form and included study size, study type, number of study arms (including the presence of a control group), the number and age (paediatric or adult) of patients in each arm, indication for and nature of the intervention (including the control group where applicable), the presence of chronic liver disease, treatment with anticoagulants, methods for measuring (where applicable) blood loss and fibrinogen levels, and relevant outcome data. Where possible, blood loss and transfusion requirements were recorded as intra-, peri- or postoperative (where perioperative was the intra- and postoperative periods combined), and survival rates were recorded by the time period reported (6 hours, 24 hours, 30 days, in-hospital, and so on). Consequently, in some instances, multiple outcomes from a single study were included.
Studies were categorised by type, then assessed by the effect of the intervention on each applicable outcome criterion. Each intervention (FFP or fibrinogen concentrate) could show a positive, negative or null effect against the comparator group or against absolute values where no comparator group was available. As such, data from the observational and case studies were generally descriptive in nature and were only included as supportive evidence. Studies without comparator groups were not included in any formal calculations of the efficacy of the intervention. Where outcome measures were compared between groups within a study, these comparisons were assessed on the basis of a difference in group averages (mean or median as available). The primary purpose of this review was achieved by describing the numbers and the quality of studies identified in relation to the effect of FFP or fibrinogen concentrate on the stated outcome measures. To avoid redundancy and the inclusion of multiple instances of data from the same study, meta-analyses were not intended to be formally included in the analysis (that is, outcomes from meta-analyses were not counted towards the number of studies reporting the effect of an intervention for each outcome). Instead, meta-analyses were included descriptively as supportive evidence. Meta-analysis was not a stated aim of this review, and analysis of the data extracted from the eligible trials formed the basis of the conclusions reached.
The selection process and study flow are depicted in Figure 1. The majority of identified citations were easily excluded at the level of title or abstract on the basis of no relevance to this review. After screening, there were 91 studies that fulfilled our eligibility criteria, reported outcomes of interest and were formally included in the analysis (Tables 1, 2 and 3). There was also one meta-analysis that was used as supportive evidence. Only a minority of selected studies (n = 18) were high-quality prospective studies with randomisation procedures and a control arm (Table 4). A further 39 nonrandomised and observational studies with a comparator group were included. The majority (62%) of FFP studies involved the comparison of the intervention group against a different dosage (typically by assessing the effect of different FFP:RBC ratios), formulation (various kinds of 'pathogen-reduced' plasmas) or blood product (for example, cryoprecipitate or whole blood). There were only 20 studies in which FFP was compared with no FFP or with a non blood product (for example, colloid or crystalloid). There were five fibrinogen concentrate comparator studies, two comparing fibrinogen concentrate with no fibrinogen concentrate or with a non blood product and, importantly, three studies comparing the effect of fibrinogen concentrate directly with FFP (administered in combination with other allogeneic products).
The average amount of FFP administered in each study varied greatly, ranging from a nominal prophylactic dose to tens of units (typically in the massive transfusion studies). Several studies did not report the FFP dose administered. The dosage of fibrinogen concentrate typically ranged from 2 to 8 g. In studies of massive transfusion, the intervention group was classified as those patients receiving the highest FFP:RBC ratio (typically 1:1), whereas the control groups comprised those patients who received lower FFP:RBC ratios. Control groups from studies in which the effect of FFP:RBC ratios was not assessed typically received various forms of colloid or crystalloid, apart from those studies directly comparing the administration of fibrinogen concentrate with that of FFP (in addition to other allogeneic components).
Articles and studies excluded because of overlapping and duplicate data
Studies containing overlapping or duplicate populations were excluded prior to the completion of the data tables. Two articles reported the same data comparing the outcomes of liver transplant patients who were administered either standard FFP or solvent/detergent-treated FFP (SD-FFP) [21, 22]. Data from the more recent publication were used . The same study of infants undergoing craniofacial surgery was published in two articles [23, 24]. Where the same outcome data were reported in both articles, the earlier publication was used . Two articles also reported data from the same trial of patients undergoing cardiovascular (CV) surgery [25, 26]. The article reporting the greater number of outcomes of interest was retained .
Three massive transfusion studies reported data from an overlapping population [2, 27, 28]; however, two of these publications compared cohorts of patients pre- and postimplementation of a massive transfusion protocol. The publication that specifically compared different FFP:RBC ratios was used in this review . Overlapping data were reported in another three massive transfusion studies [4, 29, 30]. One reported the results from the first year of a prospective study assessing the effect of the FFP:RBC ratio on survival and compared these with matched historical cases , the second reported the results from the entire prospective study only  and the entire prospective data set was analysed against matched historical cases in the third . Survival data were taken from the most recent publication in which the entire prospective data set was compared against matched historical cases . Additional outcomes of interest were found in the earliest publication, so they were included where appropriate . There were overlapping populations in another three massive transfusion publications [31–33]. For the purposes of this review, they were classified as a single study because subsets of patients were analysed in each publication.
Fresh frozen plasma
Of the comparator studies reporting the effect of FFP on blood loss, one reported lower blood loss as a result of FFP . The investigators in this massive trauma study compared high, medium and low FFP:RBC ratios. Patients receiving a high ratio (1:1.4) of FFP:RBC were less likely than patients in the low ratio group to have uncontrolled early haemorrhage (1:8).
In total, 18 of 20 outcomes indicated no reduction in blood loss (primarily reported as postoperative blood loss) for the FFP group in relation to the comparator group [23, 35–50] (Table 5). In one study, 2 of 52 patients who received FFP had 'significant bleeding' > 1,100 ml) versus 0 of 48 in the group that received 5% albumin, though there was no significant difference between the groups in mean blood loss . In another study, the researchers reported a (nonsignificant) trend towards increased chest tube drainage (CTD) in the FFP group compared with the control group that received prothrombin complex concentrates . In addition, in one study of paediatric cardiopulmonary bypass surgery patients, patients who weighed > 8 kg showed significantly greater 24-hour CTD volume following administration of FFP than those who did not receive FFP .
All three noncomparator trials that were identified reported no reduction in blood loss following administration of FFP [51–53]. Two studies, one block-RCT  (evaluating the effectiveness of FFP versus 'pathogen-reduced' plasma) and one prospective observational study , showed mixed results following administration of FFP. In the RCT, the efficacy of FFP was reported as 'good' (defined as the infusion causing arrest or > 50% reduction in CTD within a six-hour period) in 42% of patients; however, it was judged to have had no influence on the amount of blood lost in 23% of patients . There was no significant difference between the FFP and 'pathogen-reduced' plasma groups. In the observational study, 37% of patients continued to bleed after FFP administration . Interestingly, the plasma fibrinogen level, as well as its increase, after transfusion was markedly lower in patients with ongoing bleeding than in those who stopped bleeding, suggesting that the amount of fibrinogen delivered by the administration of FFP (mean ± SD = 780 ± 280 ml) was not sufficient to achieve haemostasis in a subset of patients.
Four comparator studies reported the effect of fibrinogen concentrate on blood loss (Table 5). Three of these studies involved adults, of which one was an RCT involving the prophylactic administration of 2 g of fibrinogen concentrate prior to surgery . The other two were comparator trials evaluating the post cardiopulmonary bypass administration of 7.8 ± 2.7 g  and 5.7 ± 0.9 g  fibrinogen concentrate compared with approximately 8 U of FFP (+PC) in patients with ongoing bleeding. All three studies showed a positive effect of fibrinogen concentrate administration, which reduced postoperative blood loss by 32 to 59% compared with the control group, which received 'standard' allogeneic transfusion therapy in two cases [26, 54, 55]. Another RCT investigated the effect of fibrinogen concentrate administration and transfusion therapy guided by thromboelastography compared with 'standard allogeneic transfusion therapy' in children undergoing complex CV surgery . Postoperative blood loss at 1, 6 and 24 hours by CTD was similar in both groups.
Researchers in another seven noncomparator articles (one retrospective observational study and six case studies) observed a beneficial effect of fibrinogen concentrate on blood loss, with haemostasis frequently achieved after allogeneic transfusion therapies had failed [57–63]. The retrospective observational study of 43 patients (comprising 39 adults, 8 of whom were excluded from analysis because of early death, and 4 newborns) reported a significant decrease in median blood loss (from 4,000 to 50 ml) in the adult patients following administration of fibrinogen concentrate during serious haemorrhage . A case report of a trauma patient suggested that 15 U of FFP would have been required to achieve haemostasis in place of the 5-g fibrinogen concentrate administered, which would have exposed the patient to the risk of volume overload as well as the risks associated with administration of any allogeneic blood product .
Allogeneic transfusion requirements
Fresh frozen plasma
A total of 19 comparator studies reported 22 outcomes of the effect of FFP on allogeneic transfusion requirements [22, 23, 30, 35–37, 39, 41, 43, 44, 47, 49, 50, 64–69]. These requirements were reported as intraoperative, postoperative or total (studies in which the requirements were reported for the whole perioperative period). Of these studies, only five showed some benefit for FFP over the comparator group, with the majority of the studies finding no effect and two studies reporting an increase in allogeneic transfusion requirements in the groups receiving FFP (Table 6).
Seven studies investigated the effect of FFP compared with a non blood product (for example, colloid and/or crystalloid). Six of these showed no difference in the intraoperative , postoperative [23, 35, 36, 47] or total [41, 49] requirements (requirements were measured as either RBC or any allogeneic product and excluded the study dose of FFP). A block-RCT of coronary artery bypass graft surgery patients compared those who received 4 U of FFP intraoperatively with controls who received hydroxyethyl starch (HES) . The study showed that transfusion requirements for RBC were significantly higher (both intra- and postoperatively) among those patients receiving FFP compared with patients administered HES. A further (paediatric) study also found that a greater proportion of patients in the FFP group required postoperative transfusions compared with those not receiving FFP . Two studies that compared FFP with 'pathogen-reduced' plasma showed no differences between groups in the total requirements for allogeneic transfusion [22, 65].
There were six articles in which the effect of the FFP:RBC ratio on transfusion requirements was assessed. Three found reduced RBC requirements at higher FFP:RBC ratios (typically 1:1 to 1:1.5) [66–68]. At FFP:RBC ratios ≥ 1:2 versus < 1:2, there was no difference in RBC requirements over the initial 6 or 24 hours; however, the longer-term > 24 hours) transfusion requirements for both RBC and FFP were lower in the higher ratio group . One further study (of low sample size) also demonstrated that postoperative RBC, FFP and PC requirements were reduced by increasing the amount of FFP administered intraoperatively to achieve a FFP:RBC ratio closer to 1:1 .
There were another two noncomparator studies (one prospective and one retrospective) reporting the effect of FFP on allogeneic transfusion requirements [53, 70]. The volume of intraoperatively transfused FFP was inversely associated with the postoperative administration of allogeneic products in one (paediatric) study . There was a mixed response to FFP in the other study; 2 U were sufficient to achieve haemostasis in 63% of patients, while the remaining 37% received additional transfusions .
The effect of fibrinogen concentrate on allogeneic transfusions was assessed in five comparator trials, four of which showed a reduction in requirements as a result of the intervention [26, 54–56, 71] (Table 6). Notably, the exposure to all allogeneic products (RBCs, FFP and PC) transfused postoperatively was reduced in two of these studies [26, 55]. In the control groups (treated with approximately 8 U of FFP), 100% of patients received postoperative transfusions compared with only 20%  and 44%  of patients who received fibrinogen concentrate. A third study reported lower postoperative RBC requirements in the fibrinogen concentrate group compared with the control group (that received saline), with no difference found for intraoperative RBC requirements . The fourth study, a RCT of children undergoing CV surgery, found a significant reduction in postoperative and total FFP requirements in the fibrinogen concentrate group compared with the control group . The intervention group received less than half the amount of FFP than the control group (10.6 ± 6.5 ml/kg versus 22.5 ± 13.1 ml/kg). No differences were seen in the amount of intra-, post- or perioperative RBC administered. A fifth study reported no difference in the amount of postoperative allogeneic products administered to the group that had received a prophylactic dose of 2 g of fibrinogen concentrate prior to surgery compared with the control group (no fibrinogen concentrate) .
Four retrospective noncomparator studies provided evidence for a reduction in allogeneic transfusion requirements following administration of fibrinogen concentrate, with a further five case studies also suggesting a reduction as a result of the intervention [57–62, 72–74]. One of the noncomparator studies that presented data derived from CV surgery patients reported that 35 of 39 patients did not receive any further intraoperative FFP or PC after administration of fibrinogen concentrate (the remaining four patients received PC) . In addition, in the postoperative period, only 11 of 39 patients required additional transfusions, whereas in another sizable study of trauma patients, only 6 of the 123 patients who received fibrinogen concentrate were administered intraoperative FFP, and only 12 of 128 received FFP in the first 24 hours after admission to the emergency room . The other two noncomparator studies demonstrated a reduction in allogeneic transfusions, with one reporting a drop in transfusion of RBC from 6 U to 3 U after administration of fibrinogen concentrate  and the other reporting significantly fewer allogeneic transfusions in the 24 hours after administration of the fibrinogen concentrate than in the 24 hours prior to administration .
Fresh frozen plasma
We found 32 comparator studies involving FFP reporting results from 40 time points over periods ranging from 6 hours to 10 years [3, 4, 28, 31–34, 38–40, 42, 66–69, 75–93] (Table 7). Eight studies compared the effect of FFP with no FFP, of which, three showed no effect of the intervention on survival (trauma with nonmassive transfusion , hepatectomy for hepatocellular carcinoma  and CV surgery ), and five reported reduced survival for patients receiving FFP (trauma , traumatic brain injury , liver transplantation , liver resection for colorectal metastases  and hepatectomy for hepatocellular carcinoma ). In the trauma study, the investigators found a dose-dependent correlation between FFP transfusion and mortality, with each unit of FFP given increasing the risk of death by 3.5% .
The effect of FFP on patient mortality has largely been reported in the form of articles exploring the impact of different FFP:RBC ratios, of which we found 19 such studies. Sixteen studies reported the impact of FFP:RBC ratios in trauma patients, typically by comparing a prospective cohort that received a 'transfusion protocol' with a historical cohort that received treatment prior to implementation of the protocol [3, 4, 28, 31–34, 66–68, 80, 81, 85–87, 89–91]. In general, outcomes were favourable for patients who received more FFP than for those who received less FFP, though the exact ratio needed to achieve an improvement in the survival rate was not consistent. In fact, one study suggested that the survival rate followed a U-shaped curve and that the lowest predicted mortality was associated with a FFP:RBC ratio of 1:2 to 1:3, with a FFP:RBC ratio of 1:1 resulting in reduced survival .
Murad and colleagues  conducted a meta-analysis of studies reporting of the effect of FFP on mortality compared with a control group and found that, for patients undergoing massive transfusion > 10 U of RBC), FFP:RBC ratios in the range of 1:2.5 to 1:1 were associated with a significant reduction in mortality risk (OR = 0.38). However, this improvement in survival was reversed in surgical patients who did not receive massive transfusions, where FFP was associated with a trend towards increased mortality (OR = 1.22).
Ten noncomparator studies also reported on the effect of FFP on survival [94–103]. Both studies of CV surgery patients showed a significant association between FFP and reduced in-hospital survival (OR = 2.51 and OR = 12.6) [94, 98]. In one trauma study, FFP was shown to have no effect on mortality when early deaths < 48 hours) were excluded. Furthermore, FFP administration was associated with a 2.9% decreased risk of mortality for every unit transfused when the early deaths were included . Higher levels of FFP were also reported to improve survival in two trauma studies [97, 99]. Another study found no significant association between FFP administered in the ICU and in-hospital survival rates (OR = 1.03) .
Only three fibrinogen concentrate studies, one retrospective comparator study and two retrospective noncomparator studies [26, 73, 104] (Table 7), were suitable for inclusion in this section of the review. There were no deaths reported in either arm of the fibrinogen concentrate studies included elsewhere in this review. In the retrospective comparator study, there was no significant difference in 30-day mortality between groups. In the 'standard therapy' group, 2 (17%) of 12 patients died within 30 days of surgery compared with 0 (0%) of 6 patients in the fibrinogen concentrate group, although this difference was nonsignificant (P > 0.05).
Analysis by logistic regression of data from patients with acquired acute afibrinogenaemia (due to surgery and/or trauma) in one retrospective noncomparator study indicated a statistically significant association between the higher plasma fibrinogen levels measured after fibrinogen concentrate administration and 7 day patient survival . The other study, which reported the effect of fibrinogen concentrate administration to trauma patients, observed significantly reduced mortality compared with the mortality predicted by Trauma Injury Severity Score (TRISS) and by revised injury severity classification (RISC) .
Length of stay
Fresh frozen plasma
The impact of FFP on LOS for patients in the ICU was reported in 14 comparator studies [3, 24, 32, 33, 39, 50, 66, 67, 69, 77, 79, 81, 83, 87, 105] (Table 8). Of these, over half reported an increased ICU LOS for patients in the (high) FFP group compared with controls [39, 66, 67, 69, 77, 81, 83, 105], with two studies reporting ICU stays were over 50% longer for patients administered FFP compared with the nontransfused controls [77, 105]. Conversely, in one study, a 1:1 FFP:RBC ratio was associated with an approximately 50% reduction in ICU LOS compared with a 1:4 ratio [32, 33]. Three studies found no difference in ICU LOS between the group that received FFP and a control group that did not [24, 50, 79].
Eleven comparator studies reported the effect of FFP on patients' hospital LOS [3, 24, 39, 40, 66, 67, 69, 77, 79, 81, 87], with only one reporting a benefit for FFP  (Table 8). Of the three retrospective noncomparator studies involving FFP, administration was significantly associated with an increased or prolonged ICU stay in two [98, 106], but it was not correlated with LOS in the third . Hospital LOS was reported in one noncomparator study in which surgical patients were analysed. That study found that, as with ICU LOS, FFP use was not correlated with hospital LOS .
All three fibrinogen concentrate studies reporting LOS showed significant reductions in the time spent in the ICU of 11 hours , 78 hours  and 36 hours  for patients in the intervention group compared with those in the control (FFP) group. Hospital LOS was also reported in these three studies. One observed a significantly reduced hospital LOS for patients in the fibrinogen concentrate group compared with the control group (21 days versus 32 days, respectively) . The other two studies found no difference in hospital LOS between patients in the intervention and control groups [26, 55].
Plasma fibrinogen levels
Fresh frozen plasma
Eleven FFP comparator studies reported plasma fibrinogen levels pre- and postadministration or in relation to a control [22, 23, 30, 38, 41, 43, 44, 49, 64, 108, 109] (Table 9). It is difficult to compare most of the results directly because they differ widely in the way in which they were reported. For instance, some studies compared plasma fibrinogen levels pre- and postadministration, whereas others compared the difference in levels between groups at certain time points. To further complicate matters, many comparisons were made between groups of patients receiving different doses or formulations of FFP and did not compare the effect of FFP against a non plasma product. A positive effect was seen for the FFP group in five studies [23, 30, 38, 41, 43] whereas the control group had higher levels in two [44, 108].
Four studies assessed the effect of FFP versus a non blood product. Two found significantly higher plasma fibrinogen levels postadministration in the FFP group than in the control group [23, 41]. Intraoperative plasma fibrinogen levels were maintained at the preoperative level of 2.0 g/L in the FFP group compared with a decline to an intraoperative value of 1.3 g/L in the albumin group in the study involving infants undergoing craniofacial surgery . In the study of adults undergoing CV surgery, plasma fibrinogen levels fell from a baseline value of 2.7 g/L to a postadministration value of 1.8 g/L in the FFP group compared with a fall from 2.9 g/L to 1.3 g/L in the HES group, at which point plasma fibrinogen levels were significantly higher in the FFP group than in the control group . A third study reported significantly reduced levels from baseline values throughout the operative period, with no significant differences between the two study groups at any point despite the administration of 600 ml of FFP to one group . The fourth study reported significantly lower plasma fibrinogen levels compared with baseline in the FFP group, but not in the control group .
Chowdhury and colleagues  reported the effect on plasma fibrinogen levels of two different doses of FFP (12.2 ml/kg and 30 ml/kg) in a prospective, observational study of a consecutive cohort of patients with haemorrhage in the ICU. The first 10 patients received the lower dose, and the next 12 patients received the higher dose. There was no significant difference between the two groups postadministration, and plasma fibrinogen levels were not significantly higher postadministration than preadministration in either group.
Five noncomparator studies reported the effect of FFP on plasma fibrinogen levels. Two indicated a benefit from FFP [53, 70], whilst three found that FFP was associated with lower plasma fibrinogen levels [51, 110, 111]. Of note, one study reporting the effect of FFP on plasma fibrinogen levels in a cohort of paediatric surgery patients found the volume of FFP was inversely associated with a postoperative plasma fibrinogen level < 1.0 g/L .
Plasma fibrinogen levels following administration of fibrinogen concentrate were reported in four comparator studies [26, 54, 55, 71] (Table 9). In all studies, plasma fibrinogen levels were significantly higher postadministration in the fibrinogen concentrate group than in the control group (which received FFP in two studies). Increases in plasma fibrinogen levels postadministration ranged from 0.6 g/L following a preoperative 2-g prophylactic dose  to 2.0 g/L following a mean intraoperative dose of 7.8 g . Importantly, plasma fibrinogen levels were not significantly higher in the fibrinogen concentrate group than in the control group at the next assessment point (6 to 24 hours later).
A further 13 noncomparator studies presented data on the effect of fibrinogen concentrate on plasma fibrinogen levels, all of which also showed an increase in plasma fibrinogen levels after the intervention [59–62, 72–74, 104, 112–116]. Six retrospective observational studies showed mean increases in plasma fibrinogen levels, ranging from 0.6 g/L after a median dose of 2 g  to 1.7 g/L after a mean dose of 6.5 g .
Quality of evidence
There is a relative paucity of high-quality evidence reporting the outcome of administration of FFP in a perioperative or massive trauma setting, despite the long period of its usage. Also, few high-quality trials were identified that reported the outcome of administration of fibrinogen concentrate perioperatively, and none assessed the intervention during massive trauma. Controlled trials with robust blinding and randomisation procedures are the gold standard when assessing the efficacy and safety of interventions. However, the low number of RCTs conducted for each intervention may reflect the difficulties in designing and implementing such trials in bleeding patients who are in potentially life-threatening situations.
Despite there being fewer fibrinogen concentrate comparator studies than FFP comparator studies (5 versus 52, respectively), the nature of the comparison must also be considered. Of the FFP comparator studies analysed, only 38% (20 of 52) compared FFP with no FFP or with a non blood product (for example, colloid or crystalloid). Many FFP studies assessed outcomes against a control group that received a different dosage or formulation of FFP reflecting the widely held assumption that 'standard' FFP is efficacious in these situations. In contrast, 40% (2 of 5) of fibrinogen concentrate studies compared the intervention with either no fibrinogen concentrate or a colloid or crystalloid control, and the other 60% (3 of 5) compared the use of fibrinogen concentrate with FFP. Therefore, the low number of comparator trials for fibrinogen concentrate still provided useful evidence and allowed valuable comparisons to be made between the intervention and a non blood control, as well as a direct comparison with FFP. Whilst observations can be made about the relative efficacies of FFP and fibrinogen concentrate in the perioperative setting, it is notable that, despite a number of noncomparator studies of fibrinogen concentrate in the trauma setting (with one recent study involving 128 patients), there are no comparator studies involving the use of fibrinogen concentrate in patients with haemorrhage due to massive trauma. This lack of evidence highlights a need for more research in this area so that the efficacy of fibrinogen concentrate can be assessed in this clinical setting.
Potential for bias
The majority of studies included in this review were observational in nature and as such could be subject to bias, particularly in studies in which researchers were looking for associations between outcomes and different dosages of an intervention. Most of the studies did not report whether they had performed an assessment of, or had controlled for, bias when calculating the effect of the intervention in question. Bias may have occurred by a number of mechanisms. First, a selection bias may have been in effect because the most resources were directed towards the patients deemed most likely to survive. Second, in other studies, the less-well patients may have received more of an intervention because they were more ill. Third, the studies may have had a survival bias where patients in the worst condition died too quickly to receive a high dose of the intervention, so, by default, the patients with a poor prognosis were preferentially included in the low-dose groups. In these instances, data suggesting that the intervention was responsible for a difference in morbidity and/or mortality between groups may not be reliable. It is possible that the intervention group had a prognosis different from that of the comparison group regardless of the amount of the intervention administered, post hoc ergo propter hoc.
The use of fibrinogen concentrate as a haemostatic intervention in the management of perioperative bleeding is still in its early years. Therefore, in the current literature, there may be a publication bias towards studies demonstrating the successful use of a product rather than those reporting failure.
Our systematic literature search identified 70 FFP and 21 fibrinogen concentrate publications reporting the effects of the intervention on a number of outcomes of interest. However, although 74% of identified FFP studies had a comparator group, many involved different doses or formulations of FFP rather than a non FFP arm. Furthermore, the majority of fibrinogen concentrate studies (76%) were of low quality and did not report the effect of the intervention in relation to a comparator group. Figure 2 summarises the results of all studies in our review with a comparator group for each intervention by reported outcome and also as a combined total of all outcomes. Figure 2a reinforces the doubt about the efficacy of FFP, assessed across a range of outcomes, with no single outcome reflecting a benefit for FFP in > 50% of extracted measures. When all outcomes were added together, a benefit of FFP administration was found in only 28% of measures, only slightly more than those reporting a negative effect of FFP (22%). If only those studies comparing FFP with a non FFP group are considered, the picture is even less convincing, because only 7% of reported outcomes supported a beneficial effect of FFP (Figure 2c). In contrast, the evidence for the efficacy of fibrinogen concentrate was far more consistent, with no negative outcomes reported for any measure (Figure 2b). Fibrinogen concentrate was shown to reduce blood loss, reduce allogeneic transfusion requirements, reduce ICU and hospital LOS and increase plasma fibrinogen levels in over two-thirds of reported outcomes. In the five comparator trials, 70% of outcomes showed a benefit of fibrinogen concentrate over the control. Importantly, the control was FFP in three of the studies, thus providing some evidence that fibrinogen concentrate is more efficacious than FFP across a range of clinical outcomes in the perioperative setting.
The strongest support for a benefit for FFP derives from studies reporting survival, where 50% suggested that FFP (typically at higher FFP:RBC ratios) reduces mortality; however, FFP was associated with increased mortality in 20% of studies. In general, studies reporting an association of higher doses of FFP with improved survival assessed the effect of FFP:RBC ratios during massive transfusion. This finding is in agreement with the meta-analysis performed by Murad and colleagues . Many studies targeting higher FFP:RBC ratios did so by increasing the amount of FFP administered in the early phase of massive haemorrhage. This temporal aspect of FFP administration was highlighted in a recent publication which found that patients who received an early high FFP:RBC ratio were in less severe shock and less likely to die early from uncontrollable haemorrhage than were those patients in the low FFP:RBC ratio group, who never achieved a high ratio . The survival advantage associated with the higher FFP:RBC ratios currently being lauded in the literature may be due partly to selection, whereby patients in such studies die with a low FFP:RBC ratio, not because of a low ratio. Fibrinogen deficiency manifests early in bleeding patients. It is possible that an improvement in survival rates at higher FFP:RBC ratios was due in part to earlier supplementation of plasma fibrinogen in the resuscitation effort and not to a benefit of FFP per se. The fibrinogen concentrate studies identified were typically small, with a mean of only 10 patients per arm. Consequently, there were almost no deaths reported in either group, making a robust assessment of any survival benefit following the administration of fibrinogen concentrate (early or late) virtually impossible.
In this review, we examined relevant outcomes of interest by analysing the literature regarding one of two interventions: FFP and fibrinogen concentrate. However, haemostatic support during surgery or massive trauma is rarely achieved by the administration of one product alone; therefore, the majority of the studies included in this review involved the administration of other products, particularly RBC, but also PC, cryoprecipitate, prothrombin complex concentrate, tranexamic acid, aprotinin and others. The influence of coadministered products on the outcomes of interest was not studied in this review, though the potential for an impact should be considered when drawing any conclusions regarding the impact of each intervention on these outcomes, particularly in studies where cryoprecipitate was administered, as this would provide a more concentrated dose of fibrinogen than FFP alone.
Risk versus benefit
The benefits of any intervention should outweigh the risks. In this review, we found inconsistent and contradictory evidence concerning the efficacy of FFP. Furthermore, the findings of this review are in line with other published work, where FFP has particularly been associated with an increased risk of mortality when used during nonmassive transfusion . In terms of risks, Murad and colleagues examined the incidence of ALI and MOF in their meta-analysis , in which they reported that FFP significantly increased the risk of pulmonary complications (OR = 2.92). Contrary to researchers in other studies [103, 118], however, they reported a significant reduction in the risk of MOF with FFP administration (OR = 0.40). Although the risk of viral and bacterial transmission by FFP exists, it is very low. The introduction of nucleic acid screening for known infectious diseases has led to the transmission of infectious diseases being rare . Other adverse events (AEs) are associated with the use of FFP, such as allergic and haemolytic transfusion reactions, but these are infrequent ≤ 1 event per 100,000 blood components issued ). Furthermore, several strategies have been employed successfully to reduce many of the risks associated with 'standard' FFP, such as the introduction of different formulations of plasma (for example, SD-FFP and photochemical treatment FFP, lyophilised and others), the use of leucocyte-depleted plasma and restricting the use of FFP from female donors . Half of all outcomes analysed in this review indicated that FFP had no effect, positive or negative, and it could be argued that administration of FFP is worthwhile on the basis of the possibility that it might be efficacious and at worst will effect no change in clinical parameters. Nonetheless, when the potential risks associated with FFP, however rare, are considered in the context of the efficacy findings in this study, in which fewer than one-third of the reported outcomes favoured FFP over the comparator, the continued use of the product should be questioned in an approach that weighs risk versus benefit.
There was consistent evidence that fibrinogen concentrate improved the outcomes studied in this review. More than two-thirds (16 of 23) of all outcomes showed a benefit of fibrinogen concentrate over any comparator, notably 72% (13 of 18) of the outcomes were favourable for fibrinogen concentrate over FFP. Furthermore, no study reported a negative effect versus a comparator on any outcome measure included in this review. In terms of the risks involved with fibrinogen concentrate, there is a low risk of AEs such as allergic reactions, and, in rare cases, administration of fibrinogen concentrate has been associated with thromboembolic events [120, 121]. A number of preclinical studies have provided evidence supporting the safety and tolerability of fibrinogen concentrate, and preclinical models, including one of venous stasis, have shown no evidence of thrombosis formation in treated animals, demonstrating the low thrombogenic potential of the product [120, 122–125]. In addition, a pharmacosurveillance report and systematic review of thrombotic events in clinical studies (of patients with both congenital and acquired afibrinogenaemia) showed no significant safety concerns associated with fibrinogen concentrate (Haemocomplettan P; CSL Behring, Marburg, Germany) use in perioperative bleeding situations with regard to thrombogenicity . Over a 22-year pharmacosurveillance period, nine thrombotic events possibly related to the administration of fibrinogen concentrate were reported (seven of which were in patients with congenital fibrinogen deficiency) at an incidence of 3.48 per 100,000 treatment episodes. However, further safety studies employing rigorous methods intended to detect conditions such as deep vein thrombosis are still required to confirm the findings from the preclinical and pharmacosurveillance studies.
Among the trials included in this review [26, 54–63, 71–74, 104, 112–116], there was a low incidence of the predefined safety outcomes (thrombotic events, ALI, TACO, infections [bacterial contamination and viral transmission] and MOF). Furthermore, there was a low frequency of AEs of any nature in the 17 fibrinogen concentrate studies in which AEs were reported (Table 10). Of the trials with a comparator group, an AE (postoperative atrial fibrillation) was reported for 1 of 36 (3%) patients receiving fibrinogen concentrate compared with 7 of 37 (19%) of patients in the comparator groups [26, 54, 55, 71]. There were another seven AEs reported in the noncomparator trials and case reports of 240 patients receiving fibrinogen concentrate (3%) [57–61, 63, 72, 74, 104, 112, 113, 115, 116]. Four of the AEs (all arterial ischaemic events) occurred between 4 and 12 days (median = 7.5 days) after fibrinogen concentrate administration in postoperative surgical patients who had massive perioperative haemorrhage and required more than 12 U of RBC . Of the remaining three AEs, one case of 'jitter and snoring respiration' was reported by nursing staff, though the patient was judged to be alert with normal respiration upon the arrival of the attending physician; one patient complained of attacks of shivering 24 hours after fibrinogen concentrate administration ; and one patient who received massive transfusion of a variety of haemostatic products had subsequent acute renal failure .
This review presents a consistent picture of the efficacy of fibrinogen concentrate and supports the safety of the product, with a low incidence of thrombotic events reported in the included studies. However, this evidence was derived from a small number of studies with a low number of patients in each arm. Whilst published studies support the efficacy and safety of fibrinogen concentrate during surgical procedures, more trials reporting outcomes from a greater number of patients are needed to reinforce these findings.
Fresh frozen plasma and fibrinogen concentrate during surgery and massive trauma
The use of haemostatic products often occurs in response to a 'trigger', and for FFP, historically, this was based on the percentage of blood volume lost. However, there are many difficulties inherent in estimating the volume of blood lost in a patient with a life-threatening massive haemorrhage, for whom resuscitation efforts may continue for some time. Though primarily used during massive trauma bleeding, a ratio-based approach, often integrated into a massive transfusion protocol which aims to coordinate the activities of the various necessary departments and personnel, is steadily replacing the volume of blood loss as the trigger for FFP administration. This approach appears simple and practical, though concerns remain, not the least of which is that the optimum FFP:RBC ratio has yet to be determined , an observation highlighted in recent evidence-based guidelines . In addition to uncertainty over the optimum FFP:RBC ratio, there are a number of logistical considerations, such as potential issues with the availability of thawed FFP, the waste that could be created by immediately thawing large quantities of FFP (because of the short shelf-life of thawed FFP) and the need for ABO-compatible plasma early on. Interestingly, three studies prompt questions regarding the survival benefits reported for increased FFP:RBC ratios in massive trauma patients. Snyder and colleagues  suggested that the reduction in mortality reported in many studies of this type is due to survival bias brought about by the exclusion from the analyses of patients who died during the early phase of the study. To test this hypothesis, they performed an analysis adjusted for survival bias and found that an FFP:RBC ratio ≥ 1:2 no longer had any effect on in-hospital mortality rates compared with < 1:2. Furthermore, both Riskin and colleagues  and Gunter and colleagues  found a significant improvement in survival after implementation of a massive transfusion protocol despite unchanged FFP:RBC ratios. This suggests that simply increasing the amount of FFP administered during a massive transfusion is not the key factor in improving survival and that other factors inherent in a transfusion protocol also have a substantial impact. The survival benefit of FFP may be due more to the focus on 'haemostasis' and the timely delivery of blood products rather than to the increase in FFP, which was reinforced in a recent review of the impact of the introduction of goal-directed haemostatic resuscitation on surgical and trauma patients .
When a ratio-based approach is not considered appropriate, such as during routine surgical procedures, a laboratory test-based approach is often employed to guide the administration of FFP on the basis of the prothrombin time and International Normalised Ratio. However, only the initiation phase of haemostasis is monitored by conventional coagulation tests. Screening may not indicate abnormalities, such as the presence of critically low fibrinogen levels, if the coagulopathy occurs in the amplification, propagation or stabilisation phase. The change in plasma fibrinogen levels reported in relevant studies in response to different doses of FFP and fibrinogen concentrate indicate that a good response was achieved in all studies in which fibrinogen concentrate was used, with 2 to 4 g typically raising plasma fibrinogen levels by around 1 g/L [26, 54, 55, 59, 71, 72, 104, 113, 115]. The increases in levels were generally more variable and less predictable for FFP [22, 23, 30, 38, 41, 49, 53, 64, 108–110]. According to recent measurements, because 1 L of FFP provides an average of 2.0 g of fibrinogen  and the same amount of fibrinogen can be found in just 100 ml of fibrinogen concentrate , the use of fibrinogen concentrate over FFP for substitution of fibrinogen may be more favourable. This reduced infusion volume may help avoid dilutional coagulopathy and the risk of volume overload associated with FFP use in patients with nonmassive bleeding. Conversely, in situations where a patient has experienced massive blood loss, the greater infusion volume of FFP may better restore some of the lost volume (though FFP should never be used solely as a volume expander [9, 119]).
A goal-directed approach using low fibrinogen levels as a trigger for intervention could improve outcomes. The efficacy of fibrinogen concentrate to improve haemostasis has been demonstrated in a number of in vitro and animal models of haemodilution and severe bleeding [120, 122–125, 129, 130]. These efficacious findings in preclinical studies are supported by the safety record of fibrinogen concentrate, such as the low thrombogenic potential demonstrated in animal models [120, 124, 125], and that reported in published trials. In our experience, fibrinogen concentrate has some clear advantages over FFP. The preparation method carries a reduced risk of immunological side effects, reduced risk of viral transmission, reduced transfusion volume and a known factor content . In addition to the low risk of the product, its low volume facilitates faster infusion times. Furthermore, rapid administration is possible because there is no need to blood-type, thaw or warm fibrinogen concentrate.
The evidence for the efficacy of FFP in our review was inconsistent across all assessed outcomes. The weight of the evidence does not appear to support the clinical effectiveness of FFP in many situations, and even suggests that it can be detrimental. The evidence was typically not of high quality, and, combined with nonstandard reporting of outcomes, drawing definitive conclusions about the benefits of FFP in the perioperative and/or massive trauma setting is difficult. In contrast, despite a low number of studies reporting outcomes associated with the perioperative administration of fibrinogen concentrate, there was a much more consistent message showing a benefit of fibrinogen concentrate over both FFP and crystalloid and colloid on a number of outcome measures, including reduction of blood loss and allogeneic transfusions. Perioperatively, the use of fibrinogen concentrate in an early goal-directed coagulation management strategy may be preferable to FFP in terms of clinical effectiveness. However, there is currently insufficient evidence in the literature to draw any definitive conclusions. More high-quality prospective studies, particularly studies directly comparing fibrinogen concentrate with FFP, are required.
◆ There is a relative paucity of high-quality prospective studies reporting the outcome of FFP administration in a perioperative or massive trauma setting, despite having been in use for many years.
◆ There is inconsistent and contradictory evidence concerning the efficacy of FFP. No single outcome has shown a benefit of FFP in > 50% of extracted measures.
◆ The use of fibrinogen concentrate as a haemostatic intervention in the management of perioperative bleeding is still in its early years, which is reflected by the low number of published studies that we identified.
◆ Evidence for the efficacy of fibrinogen concentrate was consistent, with no negative outcome reported for any measure.
◆ There appears to be some promise in the use of fibrinogen concentrate instead of FFP for the treatment of acquired bleeding, although there is insufficient evidence currently available in the literature to draw any definitive conclusions. More high-quality prospective studies are needed, particularly studies directly comparing fibrinogen concentrate with FFP.
acute lung injury
chest tube drainage
fresh frozen plasma
length of stay
multiple organ failure
packed red blood cells
randomised, controlled trial
solvent/detergent-treated fresh frozen plasma
transfusion-associated circulatory overload
transfusion-associated acute lung injury.
Holcomb JB, Spinella PC: Optimal use of blood in trauma patients. Biologicals 2010, 38: 72-77. 10.1016/j.biologicals.2009.10.007
Cotton BA, Au BK, Nunez TC, Gunter OL, Robertson AM, Young PP: Predefined massive transfusion protocols are associated with a reduction in organ failure and postinjury complications. J Trauma 2009, 66: 41-49. 10.1097/TA.0b013e31819313bb
Holcomb JB, Wade CE, Michalek JE, Chisholm GB, Zarzabal LA, Schreiber MA, Gonzalez EA, Pomper GJ, Perkins JG, Spinella PC, Williams KL, Park MS: Increased plasma and platelet to red blood cell ratios improves outcome in 466 massively transfused civilian trauma patients. Ann Surg 2008, 248: 447-458.
Shaz BH, Dente CJ, Nicholas J, MacLeod JB, Young AN, Easley K, Ling Q, Harris RS, Hillyer CD: Increased number of coagulation products in relationship to red blood cell products transfused improves mortality in trauma patients. Transfusion 2010, 50: 493-500. 10.1111/j.1537-2995.2009.02414.x
Murad MH, Stubbs JR, Gandhi MJ, Wang AT, Paul A, Erwin PJ, Montori VM, Roback JD: The effect of plasma transfusion on morbidity and mortality: a systematic review and meta-analysis. Transfusion 2010, 50: 1370-1383. 10.1111/j.1537-2995.2010.02630.x
Stainsby D, Jones H, Asher D, Atterbury C, Boncinelli A, Brant L, Chapman CE, Davison K, Gerrard R, Gray A, Knowles S, Love EM, Milkins C, McClelland DB, Norfolk DR, Soldan K, Taylor C, Revill J, Williamson LM, Cohen H, SHOT Steering Group: Serious hazards of transfusion: a decade of hemovigilance in the UK. Transfus Med Rev 2006, 20: 273-282. 10.1016/j.tmrv.2006.05.002
Practice guidelines for blood component therapy: a report by the American Society of Anesthesiologists Task Force on Blood Component Therapy Anesthesiology 1996, 84: 732-747. 10.1097/00000542-199603000-00032
Ho AM, Karmakar MK, Dion PW: Are we giving enough coagulation factors during major trauma resuscitation? Am J Surg 2005, 190: 479-484. 10.1016/j.amjsurg.2005.03.034
O'Shaughnessy DF, Atterbury C, Bolton Maggs P, Murphy M, Thomas D, Yates S, Williamson LM: Guidelines for the use of fresh-frozen plasma, cryoprecipitate and cryosupernatant. Br J Haematol 2004, 126: 11-28.
Stanworth SJ, Brunskill SJ, Hyde CJ, McClelland DB, Murphy MF: Is fresh frozen plasma clinically effective? A systematic review of randomized controlled trials. Br J Haematol 2004, 126: 139-152. 10.1111/j.1365-2141.2004.04973.x
Hoffman M, Monroe DM: Coagulation 2006: a modern view of hemostasis. Hematol Oncol Clin North Am 2007, 21: 1-11. 10.1016/j.hoc.2006.11.004
Monroe DM, Hoffman M: What does it take to make the perfect clot? Arterioscler Thromb Vasc Biol 2006, 26: 41-48. 10.1161/01.ATV.0000193624.28251.83
Hiippala ST, Myllylä GJ, Vahtera EM: Hemostatic factors and replacement of major blood loss with plasma-poor red cell concentrates. Anesth Analg 1995, 81: 360-365.
Rossaint R, Bouillon B, Cerny V, Coats TJ, Duranteau J, Fernández-Mondéjar E, Hunt BJ, Komadina R, Nardi G, Neugebauer E, Ozier Y, Riddez L, Schultz A, Stahel PF, Vincent JL, Spahn DR, Task Force for Advanced Bleeding Care in Trauma: Management of bleeding following major trauma: an updated European guideline. Crit Care 2010, 14: R52. 10.1186/cc8943
Schöchl H, Nienaber U, Maegele M, Hochleitner G, Primavesi F, Steitz B, Arndt C, Hanke A, Voelckel W, Solomon C: Transfusion in trauma: thromboelastometry-guided coagulation factor concentrate-based therapy versus standard fresh frozen plasma-based therapy. Crit Care 2011, 15: R83. 10.1186/cc10078
Theusinger OM, Baulig W, Seifert B, Emmert MY, Spahn DR, Asmis LM: Relative concentrations of haemostatic factors and cytokines in solvent/detergent-treated and fresh-frozen plasma. Br J Anaesth 2011, 106: 505-511. 10.1093/bja/aer003
Fenger-Eriksen C, Ingerslev J, Sørensen B: Fibrinogen concentrate: a potential universal hemostatic agent. Expert Opin Biol Ther 2009, 9: 1325-1333. 10.1517/14712590903193051
Sørensen B, Bevan D: A critical evaluation of cryoprecipitate for replacement of fibrinogen. Br J Haematol 2010, 149: 834-843. 10.1111/j.1365-2141.2010.08208.x
Fries D, Martini WZ: Role of fibrinogen in trauma-induced coagulopathy. Br J Anaesth 2010, 105: 116-121. 10.1093/bja/aeq161
Spannagl M, Joch C, Heindl B: [Safety of plasma-derived factor concentrates: an example of pharmacovigilance with fibrinogen and factor XIII-concentrate] [in German]. Hamostaseologie 2006,26(3 Suppl 1):S36-S40.
Freeman JW, Williamson LM, Llewelyn C, Fisher N, Allain JP, Bellamy M, Baglin TP, Klinc J, Ala FA, Smith N, Neuberger J, Wreghitt T: A randomized trial of solvent/detergent and standard fresh frozen plasma in the treatment of the coagulopathy seen during orthotopic liver transplantation. Vox Sang 1998,74(Suppl 1):225-229.
Williamson LM, Llewelyn CA, Fisher NC, Allain JP, Bellamy MC, Baglin TP, Freeman J, Klinck JR, Ala FA, Smith N, Neuberger J, Wreghitt TG: A randomized trial of solvent/detergent-treated and standard fresh-frozen plasma in the coagulopathy of liver disease and liver transplantation. Transfusion 1999, 39: 1227-1234. 10.1046/j.1537-2995.1999.39111227.x
Hildebrandt B, Machotta A, Riess H, Kerner S, Ahlers O, Haberl H, Dörken B, Kerner T: Intraoperative fresh-frozen plasma versus human albumin in craniofacial surgery: a pilot study comparing coagulation profiles in infants younger than 12 months. Thromb Haemost 2007, 98: 172-177.
Kerner T, Machotta A, Kerner S, Ahlers O, Haberl H, Riess H, Hildebrandt B: A clinical pilot study of fresh frozen plasma versus human albumin in paediatric craniofacial repair. J Int Med Res 2008, 36: 171-177.
Rahe-Meyer N, Solomon C, Winterhalter M, Gras C, Piepenbrock S, Pichlmaier M: Treatment of intra-operative bleeding in thoracoabdominal aortic surgery with fibrinogen concentrate. Appl Cardiopulm Pathophysiol 2007, 11: 52-53.
Rahe-Meyer N, Solomon C, Winterhalter M, Piepenbrock S, Tanaka K, Haverich A, Pichlmaier M: Thromboelastometry-guided administration of fibrinogen concentrate for the treatment of excessive intraoperative bleeding in thoracoabdominal aortic aneurysm surgery. J Thorac Cardiovasc Surg 2009, 138: 694-702. 10.1016/j.jtcvs.2008.11.065
Cotton BA, Gunter OL, Isbell J, Au BK, Robertson AM, Morris JA Jr, St Jacques P, Young PP: Damage control hematology: the impact of a trauma exsanguination protocol on survival and blood product utilization. J Trauma 2008, 64: 1177-1183. 10.1097/TA.0b013e31816c5c80
Gunter OL Jr, Au BK, Isbell JM, Mowery NT, Young PP, Cotton BA: Optimizing outcomes in damage control resuscitation: identifying blood product ratios associated with improved survival. J Trauma 2008, 65: 527-534. 10.1097/TA.0b013e3181826ddf
Dente CJ, Shaz BH, Nicholas JM, Harris RS, Wyrzykowski AD, Ficke BW, Vercruysse GA, Feliciano DV, Rozycki GS, Salomone JP, Ingram WL: Early predictors of massive transfusion in patients sustaining torso gunshot wounds in a civilian level I trauma center. J Trauma 2010, 68: 298-304. 10.1097/TA.0b013e3181cf7f2a
Dente CJ, Shaz BH, Nicholas JM, Harris RS, Wyrzykowski AD, Patel S, Shah A, Vercruysse GA, Feliciano DV, Rozycki GS, Salomone JP, Ingram WL: Improvements in early mortality and coagulopathy are sustained better in patients with blunt trauma after institution of a massive transfusion protocol in a civilian level I trauma center. J Trauma 2009, 66: 1616-1624. 10.1097/TA.0b013e3181a59ad5
Duchesne JC, Hunt JP, Wahl G, Marr AB, Wang YZ, Weintraub SE, Wright MJ, McSwain NE Jr: Review of current blood transfusions strategies in a mature level I trauma center: were we wrong for the last 60 years? J Trauma 2008, 65: 272-278. 10.1097/TA.0b013e31817e5166
Duchesne JC, Islam TM, Stuke L, Timmer JR, Barbeau JM, Marr AB, Hunt JP, Dellavolpe JD, Wahl G, Greiffenstein P, Steeb JE, McGinness C, Baker CC, McSwain NE Jr: Hemostatic resuscitation during surgery improves survival in patients with traumatic-induced coagulopathy. J Trauma 2009, 67: 33-39. 10.1097/TA.0b013e31819adb8e
Duchesne JC, Kimonis K, Marr AB, Rennie KV, Wahl G, Wells JE, Islam TM, Meade P, Stuke L, Barbeau JM, Hunt JP, Baker CC, McSwain NE Jr: Damage control resuscitation in combination with damage control laparotomy: a survival advantage. J Trauma 2010, 69: 46-52. 10.1097/TA.0b013e3181df91fa
Borgman MA, Spinella PC, Perkins JG, Grathwohl KW, Repine T, Beekley AC, Sebesta J, Jenkins D, Wade CE, Holcomb JB: The ratio of blood products transfused affects mortality in patients receiving massive transfusions at a combat support hospital. J Trauma 2007, 63: 805-813. 10.1097/TA.0b013e3181271ba3
Chong Sung K, Kum Suk P, Mi Ja Y, Kyoung Ok K: Effects of intravascular volume therapy using hydroxyethyl starch (130/0.4) on post-operative bleeding and transfusion requirements in children undergoing cardiac surgery: a randomized clinical trial. Acta Anaesthesiol Scand 2006, 50: 108-111. 10.1111/j.1399-6576.2005.00881.x
Consten EC, Henny CP, Eijsman L, Dongelmans DA, van Oers MH: The routine use of fresh frozen plasma in operations with cardiopulmonary bypass is not justified. J Thorac Cardiovasc Surg 1996, 112: 162-167. 10.1016/S0022-5223(96)70192-7
Demeyere R, Gillardin S, Arnout J, Strengers PF: Comparison of fresh frozen plasma and prothrombin complex concentrate for the reversal of oral anticoagulants in patients undergoing cardiopulmonary bypass surgery: a randomized study. Vox Sang 2010, 99: 251-260. 10.1111/j.1423-0410.2010.01339.x
Haubelt H, Blome M, Kiessling AH, Isgro F, Bach J, Saggau W, Hellstern P: Effects of solvent/detergent-treated plasma and fresh-frozen plasma on haemostasis and fibrinolysis in complex coagulopathy following open-heart surgery. Vox Sang 2002, 82: 9-14. 10.1046/j.1423-0410.2002.00129.x
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: 593-598. 10.1111/j.1537-2995.2007.01160.x
Kaibori M, Saito T, Matsui K, Yamaoka M, Kamiyama Y: Impact of fresh frozen plasma on hepatectomy for hepatocellular carcinoma. Anticancer Res 2008, 28: 1749-1755.
Kasper SM, Giesecke T, Limpers P, Sabatowski R, Mehlhorn U, Diefenbach C: Failure of autologous fresh frozen plasma to reduce blood loss and transfusion requirements in coronary artery bypass surgery. Anesthesiology 2001, 95: 81-86. 10.1097/00000542-200107000-00017
Mell MW, O'Neil AS, Callcut RA, Acher CW, Hoch JR, Tefera G, Turnipseed WD: Effect of early plasma transfusion on mortality in patients with ruptured abdominal aortic aneurysm. Surgery 2010, 148: 955-962. 10.1016/j.surg.2010.02.002
Menges T, Rupp D, van Lessen A, Hempelmann G: [Measures for reducing the use of homologous blood: effects on blood coagulation during total endoprosthesis] [in German]. Anaesthesist 1992, 41: 27-33.
Miller BE, Mochizuki T, Levy JH, Bailey JM, Tosone SR, Tam VK, Kanter KR: Predicting and treating coagulopathies after cardiopulmonary bypass in children. Anesth Analg 1997, 85: 1196-1202.
Noddeland H, Töllöfsrud S, Svennevig J, Bentsen G, Brosstad F, Solheim B: Universal solvent/detergent-treated fresh frozen plasma (Uniplas): rationale and clinical properties. Thromb Res 2002,107(Suppl 1):S33-S37.
Reed RL, Ciavarella D, Heimbach DM, Baron L, Pavlin E, Counts RB, Carrico CJ: Prophylactic platelet administration during massive transfusion: a prospective, randomized, double-blind clinical study. Ann Surg 1986, 203: 40-48. 10.1097/00000658-198601000-00008
Roy RC, Stafford MA, Hudspeth AS, Meredith JW: Failure of prophylaxis with fresh frozen plasma after cardiopulmonary bypass. Anesthesiology 1988, 69: 254-257. 10.1097/00000542-198808000-00017
Trimble AS, Osborn JJ, Kerth WJ, Gerbode F: The prophylactic use of fresh frozen plasma after extracorporeal circulation. J Thorac Cardiovasc Surg 1964, 48: 314-316.
von Sommoggy S, Fraunhofer J, Jelen-Esselborn S, Stemberger A: [Coagulation changes during aortofemoral bifurcation bypass: is volume and plasma substitution possible with hydroxyethyl starch alone?] [in German]. Anaesthesist 1990, 39: 353-360.
Wilhelmi M, Franke U, Cohnert T, Weber P, Kaukemüller J, Fischer S, Wahlers T, Haverich A: Coronary artery bypass grafting surgery without the routine application of blood products: is it feasible? Eur J Cardiothorac Surg 2001, 19: 657-661. 10.1016/S1010-7940(01)00648-0
Aiyagari V, Menendez JA, Diringer MN: Treatment of severe coagulopathy after gunshot injury to the head using recombinant activated factor VII. J Crit Care 2005, 20: 176-179. 10.1016/j.jcrc.2005.02.004
Fischer D, Schloesser R, Buxmann H, Veldman A: Recombinant activated factor VII as a hemostatic agent in very low birth weight preterms with gastrointestinal hemorrhage and disseminated intravascular coagulation. J Pediatr Hematol Oncol 2008, 30: 337-342. 10.1097/MPH.0b013e3181639b28
Schols SE, van der Meijden PE, van Oerle R, Curvers J, Heemskerk JW, van Pampus EC: Increased thrombin generation and fibrinogen level after therapeutic plasma transfusion: relation to bleeding. Thromb Haemost 2008, 99: 64-70.
Karlsson M, Ternström L, Hyllner M, Baghaei F, Flinck A, Skrtic S, Jeppsson A: Prophylactic fibrinogen infusion reduces bleeding after coronary artery bypass surgery: a prospective randomised pilot study. Thromb Haemost 2009, 102: 137-144.
Rahe-Meyer N, Pichlmaier M, Haverich A, Solomon C, Winterhalter M, Piepenbrock S, Tanaka KA: Bleeding management with fibrinogen concentrate targeting a high-normal plasma fibrinogen level: a pilot study. Br J Anaesth 2009, 102: 785-792. 10.1093/bja/aep089
Cui Y, Hei F, Long C, Feng Z, Zhao J, Yan F, Wang Y, Liu J: Perioperative monitoring of thromboelastograph on blood protection and recovery for severely cyanotic patients undergoing complex cardiac surgery. Artif Organs 2010, 34: 955-960. 10.1111/j.1525-1594.2010.01148.x
Böhrer H: Prothrombin complex concentrate substitution during liver transplantation. Thromb Res 1999,95(4 Suppl 1):S71-S74.
Brenni M, Worn M, Brüesch M, Spahn DR, Ganter MT: Successful rotational thromboelastometry-guided treatment of traumatic haemorrhage, hyperfibrinolysis and coagulopathy. Acta Anaesthesiol Scand 2010, 54: 111-117. 10.1111/j.1399-6576.2009.02132.x
Fenger-Eriksen C, Lindberg-Larsen M, Christensen AQ, Ingerslev J, Sørensen B: Fibrinogen concentrate substitution therapy in patients with massive haemorrhage and low plasma fibrinogen concentrations. Br J Anaesth 2008, 101: 769-773. 10.1093/bja/aen270
Innerhofer P: [Perioperative management of coagulation] [in German]. Hamostaseologie 2006,26(3 Suppl 1):S3-S14.
Schöchl H, Forster L, Woidke R, Solomon C, Voelckel W: Use of rotation thromboelastometry (ROTEM) to achieve successful treatment of polytrauma with fibrinogen concentrate and prothrombin complex concentrate. Anaesthesia 2010, 65: 199-203. 10.1111/j.1365-2044.2009.06188.x
Schöchl H, Posch A, Hanke A, Voelckel W, Solomon C: High-dose fibrinogen concentrate for haemostatic therapy of a major trauma patient with recent clopidogrel and aspirin intake. Scand J Clin Lab Invest 2010, 70: 453-457. 10.3109/00365513.2010.500396
Glover NJ, Collis RE, Collins P: Fibrinogen concentrate use during major obstetric haemorrhage. Anaesthesia 2010, 65: 1229-1230. 10.1111/j.1365-2044.2010.06548.x
Laine E, Steadman R, Calhoun L, Blackall D, Levin P, Braunfeld M, Nourmand H, Neelakanta G, Ting L, Gornbein J, Busuttil R, Petz L: Comparison of RBCs and FFP with whole blood during liver transplant surgery. Transfusion 2003, 43: 322-327. 10.1046/j.1537-2995.2003.00305.x
Mintz PD, Bass NM, Petz LD, Steadman R, Streiff M, McCullough J, Burks S, Wages D, Van Doren S, Corash L: Photochemically treated fresh frozen plasma for transfusion of patients with acquired coagulopathy of liver disease. Blood 2006, 107: 3753-3760. 10.1182/blood-2004-03-0930
Mitra B, Mori A, Cameron PA, Fitzgerald M, Paul E, Street A: Fresh frozen plasma (FFP) use during massive blood transfusion in trauma resuscitation. Injury 2010, 41: 35-39. 10.1016/j.injury.2009.09.029
Sperry JL, Ochoa JB, Gunn SR, Alarcon LH, Minei JP, Cuschieri J, Rosengart MR, Maier RV, Billiar TR, Peitzman AB, Moore EE, Inflammation the Host Response to Injury Investigators: An FFP:PRBC transfusion ratio ≥ 1:1.5 is associated with a lower risk of mortality after massive transfusion. J Trauma 2008, 65: 986-993. 10.1097/TA.0b013e3181878028
Zink KA, Sambasivan CN, Holcomb JB, Chisholm G, Schreiber MA: A high ratio of plasma and platelets to packed red blood cells in the first 6 hours of massive transfusion improves outcomes in a large multicenter study. Am J Surg 2009, 197: 565-570. 10.1016/j.amjsurg.2008.12.014
Johansson PI, Stensballe J: Effect of Haemostatic Control Resuscitation on mortality in massively bleeding patients: a before and after study. Vox Sang 2009, 96: 111-118. 10.1111/j.1423-0410.2008.01130.x
Stricker PA, Shaw TL, Desouza DG, Hernandez SV, Bartlett SP, Friedman DF, Sesok-Pizzini DA, Jobes DR: Blood loss, replacement, and associated morbidity in infants and children undergoing craniofacial surgery. Paediatr Anaesth 2010, 20: 150-159. 10.1111/j.1460-9592.2009.03227.x
Fenger-Eriksen C, Jensen TM, Kristensen BS, Jensen KM, Tønnesen E, Ingerslev J, Sørensen B: Fibrinogen substitution improves whole blood clot firmness after dilution with hydroxyethyl starch in bleeding patients undergoing radical cystectomy: a randomized, placebo-controlled clinical trial. J Thromb Haemost 2009, 7: 795-802. 10.1111/j.1538-7836.2009.03331.x
Solomon C, Pichlmaier U, Schoechl H, Hagl C, Raymondos K, Scheinichen D, Koppert W, Rahe-Meyer N: Recovery of fibrinogen after administration of fibrinogen concentrate to patients with severe bleeding after cardiopulmonary bypass surgery. Br J Anaesth 2010, 104: 555-562. 10.1093/bja/aeq058
Schöchl H, Nienaber U, Hofer G, Voelckel W, Jambor C, Scharbert G, Kozek-Langenecker S, Solomon C: Goal-directed coagulation management of major trauma patients using thromboelastometry (ROTEM)-guided administration of fibrinogen concentrate and prothrombin complex concentrate. Crit Care 2010, 14: R55. 10.1186/cc8948
Thorarinsdottir HR, Sigurbjornsson FT, Hreinsson K, Onundarson PT, Gudbjartsson T, Sigurdsson GH: Effects of fibrinogen concentrate administration during severe hemorrhage. Acta Anaesthesiol Scand 2010, 54: 1077-1082. 10.1111/j.1399-6576.2010.02289.x
Antolovic D, Koch M, Hinz U, Schöttler D, Schmidt T, Heger U, Schmidt J, Büchler MW, Weitz J: Ischemic colitis: analysis of risk factors for postoperative mortality. Langenbecks Arch Surg 2008, 393: 507-512. 10.1007/s00423-008-0300-z
Apaydin AZ, Posacioglu H, Islamoglu F, Calkavur T, Yagdi T, Buket S, Durmaz I: Analysis of perioperative risk factors in mortality and morbidity after modified Bentall operation. Jpn Heart J 2002, 43: 151-157. 10.1536/jhj.43.151
Bochicchio GV, Napolitano L, Joshi M, Bochicchio K, Meyer W, Scalea TM: Outcome analysis of blood product transfusion in trauma patients: a prospective, risk-adjusted study. World J Surg 2008, 32: 2185-2189. 10.1007/s00268-008-9655-0
Etemadrezaie H, Baharvahdat H, Shariati Z, Lari SM, Shakeri MT, Ganjeifar B: The effect of fresh frozen plasma in severe closed head injury. Clin Neurol Neurosurg 2007, 109: 166-171. 10.1016/j.clineuro.2006.09.001
Inaba K, Branco BC, Rhee P, Blackbourne LH, Holcomb JB, Teixeira PG, Shulman I, Nelson J, Demetriades D: Impact of plasma transfusion in trauma patients who do not require massive transfusion. J Am Coll Surg 2010, 210: 957-965. 10.1016/j.jamcollsurg.2010.01.031
Kashuk JL, Moore EE, Johnson JL, Haenel J, Wilson M, Moore JB, Cothren CC, Biffl WL, Banerjee A, Sauaia A: Postinjury life threatening coagulopathy: is 1:1 fresh frozen plasma:packed red blood cells the answer? J Trauma 2008, 65: 261-271. 10.1097/TA.0b013e31817de3e1
Maegele M, Lefering R, Paffrath T, Tjardes T, Simanski C, Bouillon B, Working Group on Polytrauma of the German Society of Trauma Surgery (DGU): Red-blood-cell to plasma ratios transfused during massive transfusion are associated with mortality in severe multiple injury: a retrospective analysis from the Trauma Registry of the Deutsche Gesellschaft für Unfallchirurgie. Vox Sang 2008, 95: 112-119. 10.1111/j.1423-0410.2008.01074.x
Massicotte L, Sassine MP, Lenis S, Seal RF, Roy A: Survival rate changes with transfusion of blood products during liver transplantation. Can J Anaesth 2005, 52: 148-155. 10.1007/BF03027720
Oberkofler CE, Dutkowski P, Stocker R, Schuepbach RA, Stover JF, Clavien PA, Béchir M: Model of end stage liver disease (MELD) score greater than 23 predicts length of stay in the ICU but not mortality in liver transplant recipients. Crit Care 2010, 14: R117. 10.1186/cc9068
Ono M, Wolf RK, Angouras DC, Brown DA, Goldstein AH, Michler RE: Short- and long-term results of open heart surgery in patients with abdominal solid organ transplant. Eur J Cardiothorac Surg 2002, 21: 1061-1072. 10.1016/S1010-7940(02)00060-X
Riskin DJ, Tsai TC, Riskin L, Hernandez-Boussard T, Purtill M, Maggio PM, Spain DA, Brundage SI: Massive transfusion protocols: the role of aggressive resuscitation versus product ratio in mortality reduction. J Am Coll Surg 2009, 209: 198-205. 10.1016/j.jamcollsurg.2009.04.016
Rose AH, Kotzé A, Doolan D, Norfolk DR, Bellamy MC: Massive transfusion: evaluation of current clinical practice and outcome in two large teaching hospital trusts in Northern England. Vox Sang 2009, 97: 247-253. 10.1111/j.1423-0410.2009.01198.x
Scalea TM, Bochicchio KM, Lumpkins K, Hess JR, Dutton R, Pyle A, Bochicchio GV: Early aggressive use of fresh frozen plasma does not improve outcome in critically injured trauma patients. Ann Surg 2008, 248: 578-584.
Scheele J, Altendorf-Hofmann A, Grube T, Hohenberger W, Stangl R, Schmidt K: [Resection of colorectal liver metastases. What prognostic factors determine patient selection?] [in German]. Chirurg 2001, 72: 547-560. 10.1007/s001040051345
Snyder CW, Weinberg JA, McGwin G Jr, Melton SM, George RL, Reiff DA, Cross JM, Hubbard-Brown J, Rue LW, Kerby JD: The relationship of blood product ratio to mortality: survival benefit or survival bias? J Trauma 2009, 66: 358-364. 10.1097/TA.0b013e318196c3ac
Stinger HK, Spinella PC, Perkins JG, Grathwohl KW, Salinas J, Martini WZ, Hess JR, Dubick MA, Simon CD, Beekley AC, Wolf SE, Wade CE, Holcomb JB: The ratio of fibrinogen to red cells transfused affects survival in casualties receiving massive transfusions at an army combat support hospital. J Trauma 2008,64(2 Suppl):S79-S85.
Teixeira PG, Inaba K, Shulman I, Salim A, Demetriades D, Brown C, Browder T, Green D, Rhee P: Impact of plasma transfusion in massively transfused trauma patients. J Trauma 2009, 66: 693-697. 10.1097/TA.0b013e31817e5c77
Tomimaru Y, Wada H, Marubashi S, Kobayashi S, Eguchi H, Takeda Y, Tanemura M, Noda T, Umeshita K, Doki Y, Mori M, Nagano H: Fresh frozen plasma transfusion does not affect outcomes following hepatic resection for hepatocellular carcinoma. World J Gastroenterol 2010, 16: 5603-5610. 10.3748/wjg.v16.i44.5603
Wright SE, Snowden CP, Athey SC, Leaver AA, Clarkson JM, Chapman CE, Roberts DR, Wallis JP: Acute lung injury after ruptured abdominal aortic aneurysm repair: the effect of excluding donations from females from the production of fresh frozen plasma. Crit Care Med 2008, 36: 1796-1802. 10.1097/CCM.0b013e3181743c6e
Díaz-Gómez JL, Nutter B, Xu M, Sessler DI, Koch CG, Sabik J, Bashour CA: The effect of postoperative gastrointestinal complications in patients undergoing coronary artery bypass surgery. Ann Thorac Surg 2010, 90: 109-115. 10.1016/j.athoracsur.2010.03.062
Fan ST, Lo CM, Liu CL, Yong BH, Wong J: Determinants of hospital mortality of adult recipients of right lobe live donor liver transplantation. Ann Surg 2003, 238: 864-870. 10.1097/01.sla.0000098618.11382.77
Gonzalez EA, Moore FA, Holcomb JB, Miller CC, Kozar RA, Todd SR, Cocanour CS, Balldin BC, McKinley BA: Fresh frozen plasma should be given earlier to patients requiring massive transfusion. J Trauma 2007, 62: 112-119. 10.1097/01.ta.0000250497.08101.8b
Moore FA, Nelson T, McKinley BA, Moore EE, Nathens AB, Rhee P, Puyana JC, Beilman GJ, Cohn SM, StO2 Study Group: Is there a role for aggressive use of fresh frozen plasma in massive transfusion of civilian trauma patients? Am J Surg 2008, 196: 948-960. 10.1016/j.amjsurg.2008.07.043
Ranucci M, Pazzaglia A, Bianchini C, Bozzetti G, Isgro G: Body size, gender, and transfusions as determinants of outcome after coronary operations. Ann Thorac Surg 2008, 85: 481-486. 10.1016/j.athoracsur.2007.10.014
Spinella PC, Perkins JG, Grathwohl KW, Beekley AC, Niles SE, McLaughlin DF, Wade CE, Holcomb JB: Effect of plasma and red blood cell transfusions on survival in patients with combat related traumatic injuries. J Trauma 2008,64(2 Suppl):S69-S78.
Swisher SG, Holmes EC, Hunt KK, Gornbein JA, Zinner MJ, McFadden DW: Perioperative blood transfusions and decreased long-term survival in esophageal cancer. J Thorac Cardiovasc Surg 1996, 112: 341-348. 10.1016/S0022-5223(96)70260-X
Tenza E, Bernardo CG, Escudero D, Otero J, Quindós B, Miyar A, Vázquez L, Taboada F, Rodríguez M, González-Dìéguez L, González-Pinto I, Barneo L: Liver transplantation complications in the intensive care unit and at 6 months. Transplant Proc 2009, 41: 1050-1053. 10.1016/j.transproceed.2009.02.014
Wiederkehr JC, Igreja MR, Nogara MS, Goncalves NL, Wiederkehr BA, Nascimento VB, Coelho IM, Locatelli FP: Analysis of survival after primary liver transplantation: multivariate analysis of 155 cases in a single center. Transplant Proc 2010, 42: 511-512. 10.1016/j.transproceed.2010.01.014
Watson GA, Sperry JL, Rosengart MR, Minei JP, Harbrecht BG, Moore EE, Cuschieri J, Maier RV, Billiar TR, Peitzman AB, Inflammation and Host Response to Injury Investigators: Fresh frozen plasma is independently associated with a higher risk of multiple organ failure and acute respiratory distress syndrome. J Trauma 2009, 67: 221-230. 10.1097/TA.0b013e3181ad5957
Farriols Danés A, Gallur Cuenca L, Rodríguez Bueno S, Mendarte Barrenechea L, Montoro Ronsano JB: Efficacy and tolerability of human fibrinogen concentrate administration to patients with acquired fibrinogen deficiency and active or in high-risk severe bleeding. Vox Sang 2008, 94: 221-226. 10.1111/j.1423-0410.2007.01024.x
Koch C, Li L, Figueroa P, Mihaljevic T, Svensson L, Blackstone EH: Transfusion and pulmonary morbidity after cardiac surgery. Ann Thorac Surg 2009, 88: 1410-1418. 10.1016/j.athoracsur.2009.07.020
Lei Q, Chen L, Jin M, Ji H, Yu Q, Cheng W, Li L: Preoperative and intraoperative risk factors for prolonged intensive care unit stay after aortic arch surgery. J Cardiothorac Vasc Anesth 2009, 23: 789-794. 10.1053/j.jvca.2009.05.028
Pull ter Gunne AF, Skolasky RL, Ross H, van Laarhoven CJ, Cohen DB: Influence of perioperative resuscitation status on postoperative spine surgery complications. Spine J 2010, 10: 129-135. 10.1016/j.spinee.2009.10.002
Boyd GL, Diethelm AG, Gelman S, Langner R, Laskow D, Deierhoi M, Barber WH: Correcting prolonged bleeding during renal transplantation with estrogen or plasma. Arch Surg 1996, 131: 160-165. 10.1001/archsurg.1996.01430140050013
Chowdhury P, Saayman AG, Paulus U, Findlay GP, Collins PW: Efficacy of standard dose and 30 ml/kg fresh frozen plasma in correcting laboratory parameters of haemostasis in critically ill patients. Br J Haematol 2004, 125: 69-73. 10.1111/j.1365-2141.2004.04868.x
Dann EJ, Michaelson M, Barzelay M, Hoffman R, Bonstein L: Transfusion medicine during the summer of 2006: lessons learned in northern Israel. Transfus Med Rev 2008, 22: 70-76. 10.1016/j.tmrv.2007.09.005
Magner JJ, Crowley KJ, Boylan JF: Fatal fibrinolysis during orthotopic liver transplantation in patients receiving solvent/detergent-treated plasma (Octaplas). J Cardiothorac Vasc Anesth 2007, 21: 410-413. 10.1053/j.jvca.2006.09.002
Bell SF, Rayment R, Collins PW, Collis RE: The use of fibrinogen concentrate to correct hypofibrinogenaemia rapidly during obstetric haemorrhage. Int J Obstet Anesth 2010, 19: 218-223. 10.1016/j.ijoa.2009.08.004
Haas T, Fries D, Velik-Salchner C, Oswald E, Innerhofer P: Fibrinogen in craniosynostosis surgery. Anesth Analg 2008, 106: 725-731. 10.1213/ane.0b013e318163fb26
Peitsidou A, Peitsidis P, Tsekoura V, Spathi A, Tzaneti A, Samanta E, Siampalioti G, Kioses E: Amniotic fluid embolism managed with success during labour: report of a severe clinical case and review of literature. Arch Gynecol Obstet 2008, 277: 271-275. 10.1007/s00404-007-0489-z
Weinkove R, Rangarajan S: Fibrinogen concentrate for acquired hypofibrinogenaemic states. Transfus Med 2008, 18: 151-157. 10.1111/j.1365-3148.2008.00854.x
Heindl B, Delorenzo C, Spannagl M: [High dose fibrinogen administration for acute therapy of coagulopathy during massive perioperative transfusion] [in German]. Anaesthesist 2005, 54: 787-790. 10.1007/s00101-005-0865-7
Magnotti LJ, Zarzaur BL, Fischer PE, Williams RF, Myers AL, Bradburn EH, Fabian TC, Croce MA: Improved survival after hemostatic resuscitation: does the emperor have no clothes? J Trauma 2011, 70: 97-102. 10.1097/TA.0b013e3182051691
Johnson JL, Moore EE, Kashuk JL, Banerjee A, Cothren CC, Biffl WL, Sauaia A: Effect of blood products transfusion on the development of postinjury multiple organ failure. Arch Surg 2010, 145: 973-977. 10.1001/archsurg.2010.216
Practice guidelines for perioperative blood transfusion and adjuvant therapies: an updated report by the American Society of Anesthesiologists Task Force on Perioperative Blood Transfusion and Adjuvant Therapies Anesthesiology 2006, 105: 198-208. 10.1097/00000542-200607000-00030
Dickneite G, Pragst I, Joch C, Bergman GE: Animal model and clinical evidence indicating low thrombogenic potential of fibrinogen concentrate (Haemocomplettan P). Blood Coagul Fibrinolysis 2009, 20: 535-540. 10.1097/MBC.0b013e32832da1c5
Kreuz W, Meili E, Peter-Salonen K, Haertel S, Devay J, Krzensk U, Egbring R: Efficacy and tolerability of a pasteurised human fibrinogen concentrate in patients with congenital fibrinogen deficiency. Transfus Apher Sci 2005, 32: 247-253.
Fries D, Haas T, Klingler A, Streif W, Klima G, Martini J, Wagner-Berger H, Innerhofer P: Efficacy of fibrinogen and prothrombin complex concentrate used to reverse dilutional coagulopathy: a porcine model. Br J Anaesth 2006, 97: 460-467. 10.1093/bja/ael191
Fries D, Krismer A, Klingler A, Streif W, Klima G, Wenzel V, Haas T, Innerhofer P: Effect of fibrinogen on reversal of dilutional coagulopathy: a porcine model. Br J Anaesth 2005, 95: 172-177. 10.1093/bja/aei160
Grottke O, Braunschweig T, Henzler D, Coburn M, Tolba R, Rossaint R: Effects of different fibrinogen concentrations on blood loss and coagulation parameters in a pig model of coagulopathy with blunt liver injury. Crit Care 2010, 14: R62. 10.1186/cc8960
Velik-Salchner C, Haas T, Innerhofer P, Streif W, Nussbaumer W, Klingler A, Klima G, Martinowitz U, Fries D: The effect of fibrinogen concentrate on thrombocytopenia. J Thromb Haemost 2007, 5: 1019-1025. 10.1111/j.1538-7836.2007.02481.x
Stansbury LG, Dutton RP, Stein DM, Bochicchio GV, Scalea TM, Hess JR: Controversy in trauma resuscitation: do ratios of plasma to red blood cells matter? Transfus Med Rev 2009, 23: 255-265. 10.1016/j.tmrv.2009.06.002
Roback JD, Caldwell S, Carson J, Davenport R, Drew MJ, Eder A, Fung M, Hamilton M, Hess JR, Luban N, Perkins JG, Sachais BS, Shander A, Silverman T, Snyder E, Tormey C, Waters J, Djulbegovic B, American Association for the Study of Liver, American Academy of Pediatrics, United States Army, American Society of Anesthesiology, American Society of Hematology: Evidence-based practice guidelines for plasma transfusion. Transfusion 2010, 50: 1227-1239. 10.1111/j.1537-2995.2010.02632.x
Johansson PI: Goal-directed hemostatic resuscitation for massively bleeding patients: the Copenhagen concept. Transfus Apher Sci 2010, 43: 401-405. 10.1016/j.transci.2010.09.002
Fenger-Eriksen C, Anker-Moller E, Heslop J, Ingerslev J, Sørensen B: Thrombelastographic whole blood clot formation after ex vivo addition of plasma substitutes: improvements of the induced coagulopathy with fibrinogen concentrate. Br J Anaesth 2005, 94: 324-329. 10.1093/bja/aei052
Fries D, Innerhofer P, Reif C, Streif W, Klingler A, Schobersberger W, Velik-Salchner C, Friesenecker B: The effect of fibrinogen substitution on reversal of dilutional coagulopathy: an in vitro model. Anesth Analg 2006, 102: 347-351. 10.1213/01.ane.0000194359.06286.d4
Funding for this review was provided by an unrestricted educational grant from CSL Behring (Marburg, Germany). The funding body had no role in the design of the study; the collection, analysis and interpretation of data; the writing of the manuscript; or the decision to submit the manuscript for publication. Editorial assistance was funded by the unrestricted educational grant and provided by Dr Rianne Stacey (Fishawack Communications).
SKL has received travel reimbursement and speaker's fees from Biotest, Octapharma, Baxter, TEM Innovations and CSL Behring; travel reimbursement and honoraria for consulting on a Biotest advisory board; and an unrestricted educational grant for the e-learning, 'perioperative bleeding', from CSL Behring. BS has participated on advisory boards and/or received speaker's honoraria from Novo Nordisk, Baxter, CSL Behring, Bayer, Pentapharm and Swedish Orphan Biovitrum GmbH. The Haemostasis Research Unit receives unrestricted research support from Novo Nordisk, Grifols, CSL Behring, LFB, Baxter, Bayer and Octapharma. JRH received travel reimbursement and an honorarium for consulting with CSL Behring.
DRS's academic department receives grant support from CSL Behring and Vifor SA (no grant numbers are attributed). DRS was chairman of the ABC Faculty and a member of the ABC Trauma Faculty, which is managed by Thomson Physicians World GmbH and sponsored by an unrestricted educational grant from Novo Nordisk A/S. DRS has received travel reimbursement and/or honoraria for consulting or lecturing from Abbott AG, AstraZeneca AG, Bayer (Schweiz) AG, Baxter SpA, B Braun Melsungen AG, Boehringer Ingelheim (Schweiz) GmbH, Bristol-Myers Squibb, CSL Behring GmbH, Curacyte AG, Ethicon Biosurgery, Fresenius SE, Galenica AG (including Vifor SA), GlaxoSmithKline GmbH & Co KG, Janssen-Cilag AG, Novo Nordisk A/S, Octapharma AG, Organon AG, Oxygen Biotherapeutics, Pentapharm GmbH (now Tem International GmbH), Roche Pharma (Schweiz) AG and Schering-Plough International.
SKL contributed to the conception and design of the study, the acquisition of funding, the systematic literature search and the drafting of the manuscript. BS contributed to the conception of the study, the interpretation of data and the drafting of the manuscript. JH and DS contributed substantially to the interpretation of data and critical revision of the manuscript. All authors read and approved the final manuscript for publication.