Emergency administration of fibrinogen concentrate for haemorrhage: systematic review and meta-analysis

doi:10.21203/rs.3.rs-2480451/v1

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Emergency administration of fibrinogen concentrate for haemorrhage: systematic review and meta-analysis

https://doi.org/10.21203/rs.3.rs-2480451/v1

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published 30 Mar, 2023

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Introduction:

The occurrence of massive haemorrhages in various emergency situations increases the need for blood transfusions and increases the risk of mortality. Fibrinogen concentrate (FC) use may increase plasma fibrinogen levels more rapidly than fresh-frozen product or cryoprecipitate use. Previous several systematic reviews and meta-analyses have not effectively demonstrated FC efficacy in significantly improving the risk of mortality and reducing transfusion requirements. In this study, we investigated the use of FC for haemorrhages in emergency situations.

Methods and analysis:

In this systematic review and meta-analysis, we included controlled trials, but excluded randomized controlled trials (RCTs) in elective surgeries. The study population consisted of patients with haemorrhages in emergency situations, and the intervention was emergency supplementation of FC. The control group was administered with ordinal transfusion or placebo. The primary and secondary outcomes were in-hospital mortality and the amount of transfusion and thrombotic events, respectively. The electronic databases searched included MEDLINE (PubMed), Web of Science, and the Cochrane Central Register of Controlled Trials.

Results

Nine RCTs in the qualitative synthesis with a total of 701 patients were included. Results showed a slight increase in in-hospital mortality with FC treatment (RR 1.24, 95% CI: 0.64–2.39, p = 0.52) with very low certainty of the evidence. There was no reduction in the use of red blood cells (RBC) transfusion in the first 24 h after admission with FC treatment (mean difference [MD] 0.0 Unit in the FC group, 95% CI: -0.99–0.98, p = 0.99) with very low certainty of the evidence. However, the use of fresh frozen plasma (FFP) transfusion significantly increased in the first 24 h after admission with FC treatment (MD 2.61 Unit higher in the FC group, 95% CI: 0.07–5.16, p = 0.04). The occurrence of thrombotic events did not significantly differ with FC treatment.

Conclusions

The present study indicates that the use of FC may result in a slight increase in in-hospital mortality. While FC did not appear to reduce the use of RBC transfusion, it likely increased the use of FFP transfusion and may result in a large increase in platelet concentrate (PC) transfusion. However, the results should be interpreted cautiously due to the unbalanced severity in the patient population, high heterogeneity, and risk of bias.

coagulopathy

fibrinogen concentrate

haemorrhage

transfusion

The occurrence of massive haemorrhages in various emergency situations, such as severe trauma, major surgeries, and postpartum, increases the need for blood transfusions and the risk of mortality [1–3]. Fibrinogen levels tend to deteriorate faster than other coagulation factors in conditions such as severe trauma, surgical bleeding, and postpartum [4–7], highlighting the importance of aggressively supplementing fibrinogen haemostasis [8, 9]. Fibrinogen can be supplemented with fresh frozen plasma (FFP), cryoprecipitate, or fibrinogen concentrate (FC). FC has several advantages over these alternatives, including the fact that it does not require a thawing process or ABO compatibility confirmation [10]. Furthermore, FC may increase plasma fibrinogen levels more rapidly than FFP or cryoprecipitate [11] and reduce transfusion volume and the risk of immunogenic or infectious complications [12]. These features make FC a promising option for the management of haemorrhage.

Several systematic reviews and meta-analyses of randomized controlled trials (RCTs) examining the use of major surgery have been published [13–16]. However, these reviews primarily focused on elective surgeries and did not consider emergency settings. The use of FC has been shown to rapidly supplement fibrinogen levels [17], making it a potential option in emergency situations. In 2017, Innerhofer et al. conducted an RCT that demonstrated the superiority of FC supplementation with other coagulation factor concentrates, compared to FFP in reducing the need for massive transfusion [18]. However, a meta-analysis by Stabler et al. in 2020 found that FC did not significantly improve mortality rates or reduce transfusion requirements in trauma-related RCTs [19]. This meta-analysis should be interpreted with caution due to the small sample sizes and low quality of the included evidence.

There is a lack of comprehensive research on the efficacy of FC administration in emergency situations, including trauma and massive haemorrhage. In order to address this gap in knowledge, we conducted a systematic review and meta-analysis of studies examining the safety and effectiveness of FC administration in emergency settings, compared to traditional transfusion strategies. Our aim was to assess the early supplementation of fibrinogen in emergent massive haemorrhage using FC.

Protocol registration

This study protocol has been published [20] and registered in the UMIN (UMIN registration number: UMIN0000415989, URL https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000047487). This systematic review and meta-analysis was reported according to The Preferred Reporting Items for Systematic Reviews and Meta-Analyses Protocols guidelines [21].

Database search

To retrieve relevant articles, we performed a literature search in the following major electronic bibliographic databases: MEDLINE (PubMed), Web of Science, and the Cochrane Central Register of Controlled Trials. The details of the search strategy are available in the protocol of this systematic review and meta-analysis [20].

Types of studies

In this systematic review and meta-analysis, we included controlled trials (including ongoing RCTs and other controlled trials) published until October 17, 2020. Studies were excluded if they did not clearly report the population, treatment, or outcomes of interest. We also excluded RCTs on elective surgeries and animal studies. No language restrictions were be applied. For non-English language publications, we utilized appropriate translation services. Our focus was on evaluating the effect of FC on uncontrolled bleeding in emergency situations.

Study population

This study included patients admitted to the hospital with emergency haemorrhage. The aetiologies of the haemorrhages included trauma, postpartum bleeding, cardiovascular diseases, and emergency surgery. Elective surgery patients were excluded from analysis. No geographical restrictions were placed on the study sample.

Intervention and control

The focus of this study was the use of emergency fibrinogen supplementation as an intervention for haemostasis. The control groups were administered standard transfusion treatments (i.e., FFP) or placebo. No restrictions were placed on the type, amount, or timing of FC administration in the review.

Outcomes

The primary outcome measure was all-cause in-hospital mortality. Secondary outcome measures included the volume of transfused blood within the first 24 h, blood loss within the first 24 h, thrombotic events (i.e., deep venous thromboses, pulmonary embolization, myocardial infarctions, strokes), multiple organ failure, length of intensive care unit (ICU) stay, and length of hospital stay.

Selection of studies

Citations were stored and duplicates were removed using EndNote X9.3.3 (Thomson Reuters, Toronto, Ontario, Canada). The systematic review process was conducted using Rayyan software [22]. Two reviewers (YI and YT) independently screened the titles and abstracts of retrieved studies using the search strategy to identify those that potentially met the inclusion criteria. The full texts of these potentially eligible studies were retrieved and independently assessed by the two reviewers (YI and YT). Any disagreement regarding study eligibility was resolved through consultation with a third reviewer (KY).

Data extraction

A standardized, pre-piloted form was used to extract data from the included studies in order to assess the quality of the studies and the methods of data synthesis. The extracted information included the following variables: study setting, study population, baseline characteristics of the participants, details of the interventions and control conditions, study methodology, outcomes, and assessments of risks bias. Two independent reviewers (YI and YT) extracted the data independently, and any discrepancies were resolved through discussion with the third author (KY).

Assessment of risk of bias in individual studies

The two independent reviewers (YI and YT) assessed the risk of bias and methodological quality of the articles, and any disagreements were resolved by discussion with a third reviewer (KY). The risk of bias in individual studies was evaluated using uniform criteria based on the tool for assessing the risk of bias in randomized trials (RoB2) [23]. This included assessment of (1) random sequence generation, (2) allocation concealment, (3) blinding of participants and personnel, (4) blinding of outcome assessment, (5) incomplete outcome data, (6) selective reporting, and (7) other bias for each study.

Data summary

A meta-analysis was performed when data were available in one or more trials, following the guidelines of the “Cochrane Handbook for Systematic Reviews of Interventions [24].” For binary variables, risk ratios or odds ratios were expressed as point estimates with 95% confidence intervals (CIs). Continuous variables, such as length of ICU stay, were expressed as mean differences with 95% CIs and p values. Mean and standard deviation were estimated from sample size, median, and interquartile range using appropriate methods [25, 26].

Data synthesis

Findings from the included studies were estimated using a random-effects model. This model considers statistical heterogeneity and provides a more conservative estimate of the pooled effect size than a fixed-effects model. No multiple imputations were performed for missing data, data synthesis, or analysis of randomized trials.

All statistical analyses, including assessment of risk of bias within and across studies were conducted using Review Manager, Version 5.4. (RevMan; The Cochrane Collaboration 2019, The Nordic Cochrane Centre, Copenhagen, Denmark) [27]. A p value of < 0.05 was considered statistically significant.

Assessment of heterogeneity

Statistical heterogeneity was assessed using the Mantel–Haenszel χ² test and the I² statistic (with I² values > 50% indicating significant heterogeneity) [28]. The presence of clinical heterogeneity was considered in the decision to conduct a quantitative synthesis of data or perform sensitivity analyses.

Sensitivity analysis

We examined the robustness of this meta-analysis by conducting sensitivity analysis according to the different components of the Cochrane risk of bias tool. We also conducted an analysis in which studies with a high overall risk of bias judgement were excluded.

Subgroup analysis

Subgroup analyses were performed according to the type of haemorrhage experienced by the patient.

Rating the strength of evidence using the GRADE approach

The two authors (YI and YT) assessed the strength of evidence independently, using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach [29]. The quality of evidence was assessed for each outcome and categorized as high, moderate, low, or very low according to the GRADE approach.

Patient and public involvement

Patients and the general public were not involved in the design of this systematic review and meta-analysis.

Search results and characteristics of included trials

After removing duplicates, 2265 records were identified during the search conducted in November 2020. Twenty-eight full-text articles were identified and assessed for their eligibility, and nine RCTs with a total of 701 patients were included in the qualitative synthesis (see Figure 1. For PRISMA flow chart). Table 1 summarizes the published studies included in the synthesis. Data from seven trials were analysed and are shown in Figure 2 and supplementary figures 1-4. The risk of bias assessment is summarized in Supplementary Figures 5. The summary of findings is shown in Table 2.

Primary outcomes

In-hospital mortality

Data from five trials indicated that FC as a treatment for emergency haemorrhagic events may result in a slight increase in in-hospital mortality (RR 1.21, 95% CI: 0.49–3.00, p = 0.68). However, due to the moderate weight of high risk of bias and low number of events, the certainty of this evidence is very low. Statistical heterogeneity was also observed (Tau² = 0.68; I² = 54%). In order to address this heterogeneity in in-hospital mortality, a sensitivity analysis was conducted (Supplementary Figure 2a.). When considering the high risk of bias, the risk ratio for in-hospital mortality was 1.21 (95% CI: 0.49–3.00, p = 0.68). Further details on risk of bias can be found in Supplementary Figure 5.

Secondary outcomes

RBC Transfusion in the first 24 h

The results from six clinical trials suggest that FC does not significantly reduce the need for RBC transfusion within the first 24 h after admission (MD 0.00 units lower in the FC group, 95% CI: -0.99–0.98, p = 0.99). However, the certainty of this evidence is very low due to moderate weight of high risk of bias, low number of events, and high levels of heterogeneity (Tau² = 1.02; I² = 77%). A sensitivity analysis was conducted with the removal of the high risk of bias study, resulting in a MD of 0.03 units for RBC transfusion in the first 24 hours (95% CI: -0.55–0.62, p = 0.001) (Supplementary Figure 2b). Subgroup analyses were also performed for each type of haemorrhage. Further details on risk of bias can be found in Supplementary Figure 5.

FFP Transfusion in the first 24 h

The results from five clinical trials suggest that FC may increase the need for FFP transfusion in the first 24 h after admission (MD 2.61 units higher in the FC group, 95% CI: 0.07–5.16, p = 0.04). The certainty of this evidence is low due to the low number of events. Statistical heterogeneity was also observed (Tau² = 3.43; I² = 71%) (see Figure 2c). A sensitivity analysis was conducted with the removal of the high risk of bias study, resulting in a mean difference of 1.21 units for FFP transfusion (95% CI: 0.76–1.67, p < 0.01) (see Supplementary figure 2c). Subgroup analyses were also performed for each type of haemorrhage.

PC transfusion in the first 24 h

The results of the study suggest that FC may result in a large increase in PC transfusion within the first 24 h after admission (MD 0.46 units higher in the FC group, 95% CI: 0.17–0.76, p = 0.002). The certainty of this evidence is moderate due to the moderate number of events. No statistical heterogeneity was observed (Tau² = 0.00; I² = 0%) (Figure 2d). Further details on risk of bias can be found in Supplementary Figure 5.

Blood loss within first 24 h after admission

The results of a clinical trial suggest that FC may result in little to no difference in blood loss within the first 24 h. The mean blood loss within the first 24 h was 392.88 mL (MD 171 mL lower in the FC group, 95% CI: -400.35–58.35, p= 0.14). The risk of bias was low due to the low number of events. Heterogeneity was not applicable (see Supplementary Figure 1a). Further details on risk of bias can be found in Supplementary Figure 5.

Thrombotic events

The results from five clinical trials suggest that FC may result in little to no difference in thrombotic events. The risk ratio was 0.71 (95% CI: 0.32–1.58, p = 0.4) with very low level of certainty due to the moderate weight of high risk of bias and low number of events. No statistical heterogeneity was observed (Tau² = 0.00; I² = 0%) (see Supplementary Figure 1b). Further details on Risk of bias can be found in Supplementary Figure 5.

Multiple organ failure

The results from two clinical trials suggest that FC may result in a slight reduction in the risk of multiple organ failure. The risk ratio was 0.54 (95% CI: 0.18–1.56, p=0.25) with a low risk of bias due to the moderate weight of high risk of bias and low number of events. Statistical heterogeneity was observed (Tau² = 0.40; I² = 57%) (see Supplementary Figure 1c). Further details on the risk of bias can be found in Supplementary Figure 5.

Length of ICU stay

The results from one clinical trial suggest that FC may result in little to no difference in the length of ICU stay. The mean length of ICU stay was lower in the FC group (MD, -2.22 days lower, 95% CI: -4.96–0.52, p = 0.11) with a very low risk of bias due to the moderate weight of high risk of bias and low number of events. Statistical heterogeneity was not applicable (see Supplementary Figure 1d). Further details on risk of bias can be found in Supplementary Figure 5.

Length of hospital stay

The results of two clinical trials suggest that FC may result in a slight reduction in the length of hospital day. The mean length of hospital stay was lower in the FC group (MD, -1.08 days lower, 95% CI: -3.35–1.19, p = 0.35) with a very low risk of bias due to the moderate weight of high risk of bias and low number of events. Statistical heterogeneity was not observed (Tau² = 3.11; I² = 50%) (see Supplementary Figure 1e). Further details on risk of bias can be found in Supplementary Figure 5.

Subgroup analysis: Trauma setting

The results of the study indicate that the risk ratio for in-hospital mortality was 1.08 (95% CI: 0.64–1.84, p = 0.77). The MD in RBC transfusion was – 0.35 units (95% CI: -0.76-0.05, p = 0.02). The MD in FFP transfusion was 1.24 units (95% CI: 0.79–1.69, p < 0.01). The mean difference of PC transfusion in the first 24 hours was 0.46 units (95% CI: 0.17–0.76, p = 0.002). The RR for the thrombotic events was 0.67 (95% CI: 0.30–1.51, p = 0.33) (Supplementary figure 3a-e).

Subgroup analysis: Obstetrics setting

In-hospital mortality was not analysed as the included RCTs reported no death. The MD of RBC transfusion was – 0.09 (95% CI: -0.87–-0.69, p = 0.82). The MD of the FFP transfusion was not estimable due to no demand of FFP in the included trial. The risk ratio of the thrombotic events was 0.96 (95% CI: 0.06–16.21, p = 0.98) (see Supplementary figure 4a-b).

In this systematic review and meta-analysis, a systematic search for RCTs in the emergency bleeding setting resulted in studies conducted in trauma and postpartum settings. FC did not significantly decrease in-hospital mortality or the amount of transfusion. However, FC may result in little to no difference in thrombotic events and a slight reduction in the risk multiple organ failure. It is important to note that due to the unbalanced severity of the patient population, high levels of heterogeneity, and risk of bias, these results should be interpreted cautiously.

In the present study, FC had no significant effect on reducing in-hospital mortality or RBC transfusion within the first 24 h after admission, though the evidence for this finding is very low. In the subgroup analysis for trauma patients, FC administration was associated with a slight decrease in the amount of RBC transfusion, but no significant difference in in-hospital mortality was observed. It is important to note that due to the high levels of heterogeneity among the studies and the short duration of treatment for the patients, the results may not be generalizable.

The demand of FFP and PC were controversial despite of FC administration. This may be in part due to the heterogeneity of the included studies. In the trauma setting, patients in the FC group had higher ISS scores [18, 30–32] and more severe haematological conditions than patients in the control group [32], which may have affected the amounts of FFP and PC transfusion. Additionally, the majority of the studies included in the meta-analysis were open-label RCTs, which may have resulted in more aggressive transfusion of these blood products in the FC group compared to the Control group [18, 33–35]. The RETIC trial by Innerhofer et al, found a significant reduction in FFP transfusion in the FC group compared to the control group [18] with a median 5 units in the FC group (IQR 5 to 5), versus 14 units in the control group (IQR 10 to 14) (p = 0.023). However, due to the similarity of the first and third quartiles of FFP administration, this trial could not be included in the meta-analysis. The lack of availability of this data may have impaired the quality of the meta-analysis.

The results of studies conducted in the trauma settings suggest that FC may slightly reduce the risk of multiple organ failure and the length of ICU and hospital stays. Despite the higher amount of transfusion in the FC group, these results may be due to the stabilizing effect of FC on the vital signs and organ damage of severely injured patients. However, as the amounts of crystalloids and measure of haemostasis were not obtained from the included studies, more information is needed to fully understand the mechanisms underlying these effects. Further investigation is warranted.

This study has several limitations. The types of bleeding included in the analysis were limited, and the obstetrics subgroup had a lower number of events, resulting in no significant differences. The number of eligible patients and the amount of high-quality randomized controlled data were insufficient [4, 30, 32]. Furthermore, the specific haemostasis procedures used in the trauma setting RCTs were not described, and the supplementation of tranexamic acid or other coagulation factors was not precisely investigated in this meta-analysis. The studies included in the meta-analyses varied in terms of risk of bias, and particularly in the emergency setting, it is difficult to include a sufficient number of patients and control for patient characteristics in RCTs. While some of the studies were conducted in a double-blinded setting, the overall certainty of the evidence was reduced due to the weight of high risk of bias, low number of events, and high levels of heterogeneity.

The present study indicates that FC administration in emergency settings may lead to a slight increase in in-hospital mortality. While there is low certainty of evidence to suggest that FC administration may reduce the need for RBC transfusions, it is probable that FC administration results in increased use of FFP transfusions, and is likely to result in a significant increase in PC transfusions with moderate certainty of the evidence. However, caution should be exercised in interpreting these findings due to the presence of imbalanced patient severity, high heterogeneity, and potential biases.

CI = confidence interval, FC = fibrinogen concentrate, FFP = fresh-frozen plasma, GRADE = Grading of Recommendations Assessment, Development and Evaluation, RCT = randomized controlled trial.

Ethical Approval and Consent to participate

Approval from the ethics board and patient consent were not required in our study since this was a systematic review and meta-analysis of publicly available data without any direct involvement of human participants. This study protocol has been funded through a protocol registry. The registry number is UMIN000041598.

Consent for publication

Not applicable.

Availability of data and materials

All relevant data are presented in the published manuscript.

Competing interests

The authors of this work have nothing to disclose.

Funding

Not applicable.

Authors' contributions

KY and MH were guarantors and contributed to the conception of the study. The manuscript was drafted by YI and was revised by KY, MH and SH. The search strategy was developed by YI, YT, KY and MH. YI and YT independently extracted data from the included studies, assess the risk of bias and complete the data synthesis. KY arbitrated in cases of disagreement and ensure the absence of errors.

Acknowledgments

We would like to thank Editage (www.editage.com) for English language editing.

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Emergency administration of fibrinogen concentrate for haemorrhage: systematic review and meta-analysis

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Introduction:

Methods and analysis:

Results

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Background

Methods

Protocol registration

Database search

Types of studies

Study population

Intervention and control

Outcomes

Selection of studies

Data extraction

Assessment of risk of bias in individual studies

Data summary

Data synthesis

Assessment of heterogeneity

Sensitivity analysis

Subgroup analysis

Rating the strength of evidence using the GRADE approach

Patient and public involvement

Results

Discussion

Conclusion

Abbreviations

Declarations

References

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Supplementary Files

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