Is fibrin sealant effective and safe in total knee arthroplasty? A meta-analysis of randomized trials
© Wang et al.; licensee BioMed Central Ltd. 2014
Received: 10 March 2014
Accepted: 28 April 2014
Published: 16 May 2014
The objective of this study was to evaluate the efficacy and safety of fibrin sealant in patients following total knee arthroplasty (TKA). A comprehensive literature search of the electronic databases PubMed, MEDLINE, Web of Science, and Cochrane Library for published randomized controlled trials (RCTs) was undertaken. The evidence base was critically appraised using a tool from the Cochrane Bone, Joint and Muscle Trauma Group. Eight RCTs involving 641 patients were included. The use of fibrin sealant significantly reduced postoperative drainage (weighted mean difference (WMD) −346, 95% confidence interval (CI) −496.29 to −197.54, P < 0.00001) and blood transfusions (risk ratio (RR) 0.47, 95% CI 0.35 to 0.63, P < 0.00001) and led to a significant improvement in the range of motion (WMD 16.59, 95% CI 6.92 to 26.25, P = 0.0008). However, using fibrin sealant did not significantly reduced total blood loss (WMD −305.25, 95% CI −679.44 to 68.95, P = 0.11). Regarding complications, there were no significant differences in any adverse events, fever, infection, or hematoma among the study groups. In conclusion, the present meta-analysis indicates that the use of fibrin sealant was effective and safe as a hemostatic therapy for patients with TKA.
KeywordsTotal knee arthroplasty (TKA) Fibrin sealant Meta-analysis Efficacy and safety
Total knee arthroplasty (TKA) is a safe and effective treatment for alleviation of pain and restoration of function for end-stage knee diseases. However, TKA is associated with significant blood loss because of extensive dissections through bony and fibrotic tissue [1, 2]. Blood loss is a common problem during and after TKA, which can result in the need for transfusions, postoperative anemia, and increased costs for health care . In addition, blood transfusions may also increase the patient’s risk for postoperative infection . Various technologies have been employed to minimize the need for allogeneic blood transfusion. Perioperative strategies include the use of autologous blood donation and administration of erythropoietin [5, 6]; intraoperative measures include acute normovolemic hemodilution, hypotensive anesthesia, intraoperative blood salvage, specialized cautery, topical hemostatic agents, and pharmacologic agents .
The use of fibrin sealant (i.e., fibrin glues, fibrin tissue adhesives) could be a promising approach to reduce bleeding and consequently lead to lower transfusion rates . Fibrin sealants have been increasingly used as adjunctive surgical and hemostatic agents for over 20 years . A number of systematic reviews have examined the efficacy and safety in cardiac surgery , thoracic surgery , plastic and reconstructive surgery , and orthopedic surgery settings . The main components of the sealant are fibrinogen, factor XIII, thrombin, and antifibrinolytic agents, such as aprotinin or tranexamic acid. Fibrin sealants achieve their local hemostatic effects by reproducing the last step of the coagulation cascade, thereby facilitating formation of a stable fibrin clot and subsequent hemostasis .
To date, several randomized controlled trials (RCTs) have been done to examine the efficacy of fibrin sealants for TKA. Results from these trials have indicated that fibrin sealants were efficacious and promising agents in TKA. However, at least two studies found that fibrin sealants had no effect on drain output or functional recovery following TKA [15, 16]. The aim of this review is to evaluate the effectiveness of fibrin sealant treatment in reducing postoperative blood loss and transfusion for patients undergoing TKA.
Method and material
A systematic search of literature was conducted on PubMed, Web of Science, MEDLINE, and Cochrane Library databases for relevant articles published until 27 June 2013. Articles were identified using the following search terms: ‘fibrin sealant’ OR ‘fibrin glues’ OR ‘fibrin tissue adhesives’ AND ‘total knee arthroplasty’ OR ‘total knee replacement’. The language of the publications was limited to English. The title and abstract of studies identified in the search were scanned to exclude any clearly irrelevant studies. Furthermore, references of identified articles were also searched manually. A search for unpublished literature was not performed.
To minimize any possible selection bias, the following criteria were used: (i) the study should be a randomized controlled trial, (ii) the study should compare the use of fibrin sealant (fibrin glue, fibrin tissue adhesive) with no sealant or placebo or standard method of hemostasis or other hemostatic agents, and (iii) the study should report the clinical outcome of the fibrin sealant in TKA. We excluded articles of studies on animals, reviews, editorial letters, case reports, poster sessions, or studies with insufficient data. Firstly, we screened the title and abstract to see whether they met the inclusion criteria. Then, based on the initial screening, we scrutinized the full manuscript of studies that needed further examination.
In order to assess the methodological quality of included studies, two authors used a modification of the generic evaluation tool used by the Cochrane Bone, Joint and Muscle Trauma Group . The methodological quality of each trial was scored and ranged from 0 to 24. Any controversy was cross-checked and resolved by a third author to reach a final consensus.
Two authors extracted independently all relevant data in the specially predesigned data form; any disagreements during the extraction process were resolved by consulting the first author until a final consensus was achieved. For each trial, the following data were collected: the author details; year of publication; country in which the study was performed; study design; general characteristics of patients, interventions, and control treatment; outcome data; and definitions of outcomes from studies.
The primary outcome measures included in this review were postoperative drainage, total blood loss, blood transfusion, hemoglobin (Hb) drop, range of motion, and length of hospital stay. Secondary outcome measures were data about safety, including any adverse events (AEs), fever, infection, and hematoma.
Statistical analysis was performed with Review Manager version 5.1. For dichotomous data, the risk ratio (RR) and 95% confidence interval (CI) were calculated. Weighted mean difference (WMD) was used to report continuous outcomes. Clinical heterogeneity was evaluated by considering the design of each trial. If clinical heterogeneity did not exist, the statistical heterogeneity was assessed using the chi-square test (P < 0.1 indicating significance) and quantified using the I2 statistic (I2 value > 50% means significant heterogeneity). When there was a significant heterogeneity across the included trials, a random effects model was used for analysis. If no heterogeneity was present among studies, the fixed effects model was performed. Funnel plot was performed to identify the possibility of publication bias.
Study characteristics and quality assessment
Characteristics of randomized controlled trials included in the meta-analysis
Number of patients (FS/control)
Heyse et al. 
Fibrin sealant 10 ml before tourniquet release
TBL: FS 1,441 ml vs. control 1,409 ml
Control: no fibrin sealant
24 h postoperative blood drainage: FS 780 ml vs. control 673 ml
48 h postoperative Hb drop: FS 3.47 g/l vs. control 3.84 g/l
Kluba et al. 
Single-center, prospective, RCT
Fibrin sealant 2 ml before closing the wound
Postoperative blood drainage: FS 475.4 ml vs. control 813.3 ml
Control: no fibrin sealant
8 days postoperative ROM: FS 90.8 vs. control 85.4
Length of hospital stay: FS 12.67 days vs. control 13.67 days
Levy et al. 
Multicenter, prospective, RCT
Fibrin sealant 10–20 ml before closing the wound
TBL: FS 1,063 ml vs. control 1,768 ml
Control: no fibrin sealant
Postoperative blood loss: FS 360 ml vs. control 878 ml
Postoperative Hb drop: FS 25 g/l vs. control 37 g/l
Blood transfusion rate: FS 5 patients vs. control 16 patients
Molloy et al. 
Northern Ireland, 2007
Fibrin sealant 6 ml before the prosthesis is inserted, then 4 ml after placement of the prosthesis
TBL: FS 1,190 ml vs. control 1,415 ml
Control: no pharmacological intervention
Postoperative Hb drop: FS 2.68 g/dl vs. control 3.20 g/dl
Blood transfusion rate: FS 7 patients vs. control 11 patients
Notarnicola et al. 
Fibrin sealant (5 and 10 ml) before closing the wound and releasing the tourniquet
3 days postoperative blood drainage: FS (5 ml) 415 ml vs. FS (10 ml) 228.3 ml vs. control 815 ml
Control: no fibrin sealant
Postoperative Hb drop: FS (5 ml) 2.6 mg/dl vs. FS (10 ml) 2.5 mg/dl vs. control 3.7 mg/dl
Blood transfusion rate: FS (5 ml) 10 patients vs. FS (10 ml) 7 patients vs. control 19 patients
7 days postoperative ROM: FS (5 ml) 96.5 vs. FS (10 ml) 98.8 vs. control 75.5
Length of hospital stay: FS (5 ml) 10 days vs. FS (10 ml) 9.2 days vs. control 13.6 days
Sabatini et al. 
Fibrin sealant 5 ml before the prosthesis is inserted
3 days postoperative blood drainage: FS 910 ml vs. control 1,250 ml
Control: no fibrin sealant
24 h postoperative Hb drop: FS 2.6 g/dl vs. control 3 g/dl
Blood transfusion rate: FS 5 patients vs. control 15 patients
Skovgaard et al. 
Double-blind, prospective, RCT
Fibrin sealant 10 ml after the prosthesis is inserted
24 h postoperative blood drainage: FS 582 ml vs. control 576 ml
7 days postoperative ROM: FS 88 vs. control 86
Wang et al. 
Multicenter, prospective, RCT
Fibrin sealant 10 ml before closing the wound and releasing the tourniquet
12 h postoperative blood drainage: FS 184.5 ml vs. control 408.3
24 h postoperative Hb drop: FS 20.1 g/l vs. control 27.3 g/l
Control: no placebo
Blood transfusion rate: FS 9 patients vs. control 14 patients
Meta-analysis of efficacy
Range of motion
Length of hospital stay
Meta-analysis of safety
Summary of adverse events in randomized controlled trials included in the meta-analysis
Fibrin sealant events/total
Heterogeneity (P, I 2 )
Any adverse events
Risk ratio (M-H, fixed, 95% CI)
1.21 (0.63, 2.31)
Risk ratio (M-H, fixed, 95% CI)
1.06 (0.79, 1.44)
Risk ratio (M-H, fixed, 95% CI)
1.50 (0.26, 8.72)
Risk ratio (M-H, fixed, 95% CI)
0.31 (0.09, 1.08)
The benefit of using fibrin sealant has been demonstrated in several clinical studies, most of which show reduced blood loss, lower transfusion rate, improved range of motion, and shorter hospital stay. Similarly, the results of our meta-analysis demonstrated a statistically significant benefit in using fibrin sealant in patients following TKA as well. However, these results must be interpreted with caution because of the significant heterogeneity in trial findings.
Most of the observed heterogeneity seemed to be from clinical practice or trial methodology. First, for time of evaluation, the outcome measures were different. To avoid a possible bias, the time of evaluation period was considered ‘short term’ (ranging 12 to 72 h). For example, drainage output at 24 h in the Skovgaard et al. study was around 580 ml, as compared to 878 ml in the Levy et al. study  and 408 ml in the Wang et al. study  after 12 h. Besides, the amount of fibrin sealant used may influence the blood drainage: Levy et al.  used 10–20 ml, Kluba et al.  used 2 ml, and Notarnicola et al.  assessed the efficacy of two different doses (5 and 10 ml). However, the dose of fibrin sealant did not appear to have any bearing on the results. Furthermore, tourniquet time and tourniquet pressure should be kept short and low, and differences in these trials may also influence the outcome. Also, fibrin sealant may contain tranexamic acid, which has been demonstrated to be effective on its own in reducing blood loss. Finally, the control group in this review consisted of a variety of interventions including no fibrin sealant, placebo, and standard method of treatments, resulting in clinical and methodological heterogeneity. Subgroup analysis by the evaluation time and dose of fibrin sealant was constrained by the small number of trials.
Bleeding remains an ongoing concern after TKA. Fibrin sealants are topically applied hemostatic agents that reduce the time required to achieve hemostasis as well as the volume of blood loss. Wang et al.  found that there was a statistically significant reduction in blood loss 12 h postoperatively (184.5 ml in the fibrin sealant group vs. 408.3 ml in the control group), as well as a minor Hb reduction on the first postoperative day as compared with baseline (14.9% vs. 20.7%). However, in the Heyse et al. study , it was found that the use of topical fibrinogen did not lead to a relevant reduction in blood loss or transfusions in primary TKA. They considered that suction drainage may have affected the impact of topically applied fibrinogen. Molloy et al.  reported that the main cause was they did not spray the prepared bone surfaces before placement of the cementless components. Additionally, the amount of blood loss after TKA is often underestimated because measuring blood loss is a complex science in a controlled clinical trial environment. This may be one reason why the use of fibrin sealant did not significantly reduce total blood loss compared with the control group.
In the study by Kluba et al. , fibrin sealant patients showed a slightly better range of motion and functional knee recovery compared with the control group of patients with a maximum flexion 8 days after surgery, but the difference missed statistical significance (P = 0.052). Similarly, Heyse et al.  had shown that there was no difference between the two groups at 6 weeks follow-up. However, in the Notarnicola et al.  study, functional recovery was quicker in patients administered the fibrin sealant. They believed that fibrin sealant use allowed an immediate control of bleeding, which may have a beneficial effect on the achievement of early and better postoperative rehabilitation. The pooled data showed that the difference was not significant between the groups. However, it is important to state that the range of motion include only a few trials (less than 2) and have a small sample size (less than 144). Further randomized prospective studies will be needed to clarify the relationship between the use of fibrin sealant in TKA and the functional results.
Postoperative thromboembolism is one of the most serious and potentially fatal complications after TKA . The Italian Agency of Drugs (AIFA) had informed that the use of a spray device to apply fibrin sealant can produce massive embolism. They recommend to use a spray device with pressure of less than 2.0–2.5 bar, to apply fibrin sealant (Quixil, a commercial fibrin sealant; OMRIX Biopharmaceuticals, Ltd., Kiryat-Ono, Israel) from a minimal distance of 10–15 cm, and to monitor patient spray application. Sabatini et al.  did not find any clinical signs of pulmonary embolism with application of these recommendations. Levy et al.  believed that the use of fibrin sealant may allow the use of full-dose preoperative thromboprophylaxis with low molecular weight heparin, thereby reducing the risk of deep vein thrombosis without increasing the risk of postoperative bleeding in patients following TKA. Additionally, our pooled results showed that there were no significant differences on complications in the fibrin sealant compared with the control group, including AEs, infection, fever, and hematoma.
The cost of fibrin sealant also warrants discussion. The beneficial effects of using fibrin sealant are associated with reduced blood loss and decreased rates of allogeneic red blood cell (RBC) transfusion . In the study by Molloy et al. , the cost of the pharmaceutical intervention involved in the topical fibrin group was £380, which did not justify its additional cost. However, in the trial by Kluba et al. , results showed that in daily clinical practice, a routine application of fibrin sealant adds costs to TKA treatment without reducing the number of transfused RBC. Steuten et al.  performed a simple cost model to compare the cost of using a commercial fibrin sealant. Their conclusion is that whether using fibrin sealant is cost saving strongly depends on the amount used, the achieved reduction in hospital length of stay, and the price of fibrin sealant.
There are several limitations to our meta-analysis. First, we only included the study in English, and some relevant studies might not be included in the review. The few numbers of studies included in our analysis would limit the statistical power. Additionally, most of the studies did not report the results of all outcomes selected; each outcome measure was assessed in a variable number of studies and in different studies which could make comparison difficult between different domains. Furthermore, the methodological quality of the trials was poor, with only two trials judged to be double-blind. Nevertheless, our meta-analysis has several strengths. First, this review combined relevant literature published up to June 2013, with eight RCTs included in our meta-analysis. Furthermore, the present study is the first systematic review assessing the efficacy and safety of fibrin sealant treatment in patients with TKA.
This meta-analysis investigated the efficacy and safety of fibrin sealant in terms of blood loss, Hb level, range of motion, length of hospital stay, and complications. Based on our findings, the use of fibrin sealant was effective and safe as a hemostatic therapy for patients with TKA. Given the limitation in this study, fibrin sealant treatment should be carefully considered for each patient. Further well-designed and large-scale clinical trials and systemic reviews are required to confirm these findings.
HW and LS are co-first authors.
This work was supported by NSFC (81202115), the Key Project of Basic Research of Shanghai (11JC1410101), the Shanghai Pujiang Program (12PJ1407100), and the excellent young talent program of Shanghai Municipal Commission of Health and Family Planning (XYQ2013108).
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