- Research Article
- Open Access
The efficacy and safety of topical administration of tranexamic acid in spine surgery: a meta-analysis
Journal of Orthopaedic Surgery and Researchvolume 13, Article number: 96 (2018)
We conducted a meta-analysis from randomized controlled trials (RCTs) and non-RCTs to assess the efficacy and safety of tranexamic acid (TXA) in spine surgery.
Potentially relevant academic articles were identified from the Cochrane Library, MEDLINE (1966–2017.11), PubMed (1966–2017.11), Embase (1980–2017.11), and ScienceDirect (1985–2017.11). Secondary sources were identified from the references of the included literature. The pooled data were analyzed using RevMan 5.1.
Three RCTs and one non-RCT met the inclusion criteria. There were significant differences in total blood loss (MD = − 267.53, 95% CI − 373.04 to − 106.02, P < 0.00001), drainage volume (MD = − 157.00, 95% CI − 191.17 to − 122.84, P < 0.00001), postoperative hemoglobin level (MD = 0.95, 95% CI 0.44 to 1.47, P = 0.0003), and length of hospital stay (MD = − 1.42, 95% CI − 1.92 to − 0.93, P < 0.00001). No significant differences were found regarding transfusion requirement, deep vein thrombosis (DVT), pulmonary embolism (PE), wound hematoma, and infection between the two groups.
The present meta-analysis indicated that the topical application of TXA in spinal surgery decreases the total blood loss and drainage volume and preserves higher postoperative hemoglobin level without increasing the risk of DVT infection, hematoma, DVT, and PE.
Spinal surgery is associated with significant perioperative blood loss that may lead to acute anemia and lead to serious complications . Blood transfusions are often required to correct acute anemia and carry their own risks, such as inducing disease transmission, hemolysis, and anaphylactic reactions [2, 3]. In addition, blood transfusions increase the economic burden. Multiple blood conserving interventions  have been utilized to minimize the blood loss, such as normovolemic hemodilution, blood salvage, hypotensive anesthesia, bipolar electrocautery, and hemostatic agents. However, many patients still require blood transfusions.
Tranexamic acid (TXA), an antifibrinolytic drug, competitively blocks the lysine-binding site of plasminogen and has been used to reduce blood loss in spine surgery for many years . Various studies have reported that intravenous application of TXA reduces blood loss and allogenic blood transfusions in spinal surgery without increasing related complications [6,7,8]. In theory, there remains an unresolved concern about the potential thrombogenicity of intravenous TXA . Topical application of TXA would decrease systemic absorption and result in lower risk of adverse reactions. Recently, several studies [10,11,12] have reported topical application of TXA in spinal surgery. However, there is still no consensus whether to use topical application of TXA during spinal surgery or not. Moreover, some limitations exist in previous studies such as small sample size and inconclusive results. Therefore, we conducted a large sample meta-analysis to evaluate the efficacy and safety of topical application of TXA in spinal surgery from randomized controlled trials (RCTs) and non-RCTs.
Electronic databases were searched, including Cochrane Library, MEDLINE (1966–2017.11), PubMed (1966–2017.11), Embase (1980–2017.11), and ScienceDirect (1985–2017.11). In addition, the same search terms were manually searched for the reference lists of all included studies, relevant books, review articles, and meeting proceedings to identify trials that might have been missed in the electronic search. The search process was conducted as follows in Fig. 1. The key words “tranexamic acid,” “topical,” “spine,” and “surgery” were used in combination with the Boolean operators AND or OR.
Studies were considered eligible for inclusion if they met the following criteria: (1) patients treated with spine surgery; (2) the intervention used TXA and studies contained a control group; (3) the outcomes included blood loss, blood transfusion, post-operative Hb level, length of hospital stay, peri-operative outcomes, and complications; and (4) the study was a published or unpublished comparative trial (RCTs or non-RCTs).
We excluded articles that were (1) studies without controlled groups, (2) articles without available full-text versions, and (3) no available outcomes data.
Two reviewers independently screened the titles and abstracts for eligibility criteria. Subsequently, the full text of the studies that potentially met the inclusion criteria were read, and the literature was reviewed to determine the final inclusion. Disagreement was resolved by consulting a third reviewer.
According to whether the study is a randomized or non-randomized trial, the methodological index for non-randomized studies (MINORS) form was used to assess retrospective controlled trials . Quality assessment for RCT was conducted according to a modification of the generic evaluation tool used by the Cochrane Bone, Joint and Muscle Trauma Group . Disagreements were resolved by consensus or consultation with the senior reviewer.
Two researchers independently extracted the data from the included literature. The corresponding author was consulted for details in the case of incomplete data. The following information was extracted: first author name, year of publication, intervening measures, comparable baseline, sample size, and outcome measures. Other relevant parameters were also extracted from individual studies.
Data analysis and statistical methods
Pooling of data was analyzed by RevMan 5.1 (The Cochrane Collaboration, Oxford, UK). Heterogeneity was estimated depending on the value of P and I2 using the standard chi-square test. When I2 > 50%, P < 0.1 was considered to be a significant heterogeneity. Therefore, a random-effects model was applied for data analysis. A fixed-effects model was used when no significant heterogeneity was found. Subgroup analysis was performed to investigate sources in the case of significant heterogeneity. Mean difference (MD) and 95% confidence interval (CI) were presented for continuous outcomes. Risk difference (RD) and 95% CIs were calculated for dichotomous data.
A total of 186 studies were identified as potentially relevant literature reports. By scanning title and abstract, 182 reports were excluded according to the eligibility criteria. No additional studies were obtained after the reference review. Ultimately, three RCT [11, 15, 16] and one non-RCT  were eligible for data extraction and meta-analysis. The search process is shown in Fig. 1.
Demographic characteristics and details concerning the literature type of the included studies are summarized in Table 1. Statistically similar baseline characteristics were observed between both groups.
Risk of bias assessment
RCT quality was assessed based on the Cochrane Handbook for Systematic Review of Interventions (Fig. 2). For the non-RCTs, the MINORS score is 20. The methodological quality assessment is illustrated in Table 2.
Outcomes of meta-analysis
It was possible to perform a meta-analysis with nine outcomes (Table 3). There were statistically significant differences between topical TXA and control groups for total blood loss (MD = − 267.53, P = 0.00001), drainage volume (MD = − 157, P = 0.00001), length of hospital stay (MD = − 1.42, P < 0.00001), and postoperative hemoglobin level (MD = 0.95, P = 0.0003). There were no statistically significant differences between topical TXA and control groups for blood transfusion rate (RD = − 0.18, P = 0.28), wound hematoma (RD = 0.00, P = 1.00), wound infection (RD = 0.00, P = 1.00), DVT (RD = 0.00, P = 1.00), and PE (RD = 0.00, P = 1.00).
The intravenous application of TXA has been confirmed as effectively decreasing blood loss and transfusion requirement in spinal surgery [6, 7]. Recently, topical TXA is widely established in hip and knee arthroplasty and successfully reduced postoperative blood loss and blood transfusion requirements [17, 18]. Astedt et al.  considered that TXA acts at the active bleeding and clot formation site and not within the circulation itself. But there have been limited studies reporting the efficacy of topical administration in spinal surgery. This is the first meta-analysis to evaluate the efficacy and safety of topical application of TXA in spinal surgery. The most important results of the present meta-analysis were that the topical application of TXA during spinal surgery decreased total blood loss, drainage volume, and length of hospital stay and preserved higher postoperative hemoglobin level. Moreover, no significant difference is noticeable regarding the occurrence of infection, hematoma, DVT, and PE.
Total calculated blood loss ranged from 650 to 2839 ml in adult spine fusion surgery, and transfusion requirements were 50 to 81% without plotting any strategy to reduce hemorrhage . Pooled results indicated that total blood loss and drainage volume in the topical TXA group were significantly lower than that in the control group. Total blood loss included intra-operative blood loss (IBL), post-operative blood loss (PBL), and hidden blood loss (HBL). Xu et al.  performed an RCT evaluating the efficacy of topical tranexamic acid in posterior spinal fusion surgeries. They reported that IBL showed no significant difference between two groups. Most of current studies calculated PBL by measuring the amount of “blood” by wound drainage. All included studies reported that topical TXA reduce post-operative drainage volume. These results were consistent with our meta-analysis. The mechanisms of HBL may be hemolysis [21, 22] and loss going into tissue compartments . Smorgick et al.  reported that hidden blood loss accounts for 45% of total blood loss. Ren et al.  reported that topical TXA effectively reduce HBL following posterior lumbar interbody fusion (PLIF).
The indications for blood transfusion were based on postoperative hemoglobin levels and clinical symptoms of anemia. Although present meta-analysis showed that blood transfusion rate in topical TXA group is lower, there was no significant difference found between the two groups. The reason could be that transfusions trigger varied from different studies. Length of hospital stay is another element in determining the effectiveness of THA and TKA. Recently, two RCTs [11, 15] have reported that topical administration of TXA reduces length of hospital stay in PLIF. This was consistent with our meta-analysis results. The decreased blood loss contributes to not only a lower risk of anemia but also better recovery and shorter hospitalization.
DVT is a common complication following spine surgery, may develop to PE and result in serious complications. In theory, the intravenous application of TXA may enhance the possibility of venous thromboembolism. Present meta-analysis showed that topical application of TXA did not increase the risk of DVT or PE. Bleeding may still occur after wound closed and result in wound hematoma or infection. Topical application of TXA is simple and provides a maximum concentration of TXA at the bleeding field. Present meta-analysis showed that topical TXA did not increase the risk of wound hematoma or infection. Taking these findings together, we conclude that topical TXA is safe in spine surgery.
Several potential limitations should be noted. (1) Only four studies with relatively small sample size were included; (2) subgroup analysis was not performed because of the limited number of included studies, and we could not determine the source of heterogeneity; (3) methodological weaknesses exist in studies; and (4) several outcome parameters were not fully described so that we failed to perform a meta-analysis.
The present meta-analysis indicated that the topical application of TXA in spinal surgery decreases the total blood loss and drainage volume and preserves higher postoperative hemoglobin level without increasing the risk of infection, hematoma, DVT, and PE. More high-quality randomized controlled trials are required due to the limited quality and data in the evidence currently available.
Deep vein thrombosis
Hidden blood loss
Intra-operative blood loss
Methodological index for non-randomized studies
Post-operative blood loss
Posterior lumbar interbody fusion
Randomized controlled trials
Total knee arthroplasty
Nuttall GA, Horlocker TT, Santrach PJ, Oliver WC Jr, Dekutoski MB, Bryant S. Predictors of blood transfusions in spinal instrumentation and fusion surgery. Spine (Phila Pa 1976). 2000;25(5):596–601.
Alter HJ, Klein HG. The hazards of blood transfusion in historical perspective. Blood. 2008;112(7):2617–26.
Sandler SG, Yu H, Rassai N. Risks of blood transfusion and their prevention. Clin Adv Hematol Oncol. 2003;1(5):307–13.
Lerman DM, Rapp TB. Minimizing blood loss in orthopaedic surgery the role of Antifibrinolytics. Bull Hosp Jt Dis (2013). 2015;73(2):83–9.
Dunn CJ, Goa KL. Tranexamic acid: a review of its use in surgery and other indications. Drugs. 1999;57(6):1005–32.
Shi H, Ou Y, Jiang D, Quan Z, Zhao Z, Zhu Y. Tranexamic acid reduces perioperative blood loss of posterior lumbar surgery for stenosis or spondylolisthesis: a randomized trial. Medicine (Baltimore). 2017;96(1):e5718.
Yu CC, Gao WJ, Yang JS, Gu H, Md MZ, Sun K, Hao DJ. Can tranexamic acid reduce blood loss in cervical laminectomy with lateral mass screw fixation and bone grafting: a retrospective observational study. Medicine (Baltimore). 2017;96(5):e6043.
Yuan QM, Zhao ZH, Xu BS. Efficacy and safety of tranexamic acid in reducing blood loss in scoliosis surgery: a systematic review and meta-analysis. Eur Spine J. 2017;26(1):131–9.
Foreman PM, Chua M, Harrigan MR, Fisher WS 3rd, Tubbs RS, Shoja MM, Griessenauer CJ. Antifibrinolytic therapy in aneurysmal subarachnoid hemorrhage increases the risk for deep venous thrombosis: a case-control study. Clin Neurol Neurosurg. 2015;139:66–9.
Ren Z, Li S, Sheng L, Zhuang Q, Li Z, Xu D, Chen X, Jiang P, Zhang X. Efficacy and safety of topical use of tranexamic acid in reducing blood loss during primary lumbar spinal surgery: a retrospective case control study. Spine (Phila Pa 1976). 2017;42(23):1779–84.
Liang J, Liu H, Huang X, Xiong W, Zhao H, Chua S, Li Z. Using tranexamic acid soaked absorbable gelatin sponge following complex posterior lumbar spine surgery: a randomized control trial. Clin Neurol Neurosurg. 2016;147:110–4.
Ren Z, Li S, Sheng L, Zhuang Q, Li Z, Xu D, Chen X, Jiang P, Zhang X. Topical use of tranexamic acid can effectively decrease hidden blood loss during posterior lumbar spinal fusion surgery: a retrospective study. Medicine (Baltimore). 2017;96(42):e8233.
Slim K, Nini E, Forestier D, Kwiatkowski F, Panis Y, Chipponi J. Methodological index for non-randomized studies (minors): development and validation of a new instrument. ANZ J Surg. 2003;73(9):712–6.
Handoll HH, Gillespie WJ, Gillespie LD, Madhok R. The Cochrane Collaboration: a leading role in producing reliable evidence to inform healthcare decisions in musculoskeletal trauma and disorders. Indian J Orthop. 2008;42(3):247–51.
Xu D, Zhuang Q, Li Z, Ren Z, Chen X, Li S. A randomized controlled trial on the effects of collagen sponge and topical tranexamic acid in posterior spinal fusion surgeries. J Orthop Surg Res. 2017;12(1):166.
Krohn CD, Sorensen R, Lange JE, Riise R, Bjornsen S, Brosstad F. Tranexamic acid given into the wound reduces postoperative blood loss by half in major orthopaedic surgery. Eur J Surg Suppl. 2003;588:57–61.
Chen Y, Chen Z, Cui S, Li Z, Yuan Z. Topical versus systemic tranexamic acid after total knee and hip arthroplasty: a meta-analysis of randomized controlled trials. Medicine (Baltimore). 2016;95(41):e4656.
Chen TP, Chen YM, Jiao JB, Wang YF, Qian LG, Guo Z, Ma Z, Han CY, Shi TH. Comparison of the effectiveness and safety of topical versus intravenous tranexamic acid in primary total knee arthroplasty: a meta-analysis of randomized controlled trials. J Orthop Surg Res. 2017;12(1):11.
Astedt B, Liedholm P, Wingerup L. The effect of tranexamic acid on the fibrinolytic activity of vein walls. Ann Chir Gynaecol. 1978;67(6):203–5.
Elgafy H, Bransford RJ, McGuire RA, Dettori JR, Fischer D. Blood loss in major spine surgery: are there effective measures to decrease massive hemorrhage in major spine fusion surgery? Spine (Phila Pa 1976). 2010;35(9 Suppl):S47–56.
Pattison E, Protheroe K, Pringle RM, Kennedy AC, Dick WC. Reduction in haemoglobin after knee joint surgery. Ann Rheum Dis. 1973;32(6):582–4.
Faris PM, Ritter MA, Keating EM, Valeri CR. Unwashed filtered shed blood collected after knee and hip arthroplasties. A source of autologous red blood cells. J Bone Joint Surg Am. 1991;73(8):1169–78.
Erskine JG, Fraser C, Simpson R, Protheroe K, Walker ID. Blood loss with knee joint replacement. J R Coll Surg Edinb. 1981;26(5):295–7.
Smorgick Y, Baker KC, Bachison CC, Herkowitz HN, Montgomery DM, Fischgrund JS. Hidden blood loss during posterior spine fusion surgery. Spine J. 2013;13(8):877–81.
We thank the authors of the included studies and Wen-qing Hu and Jian-xiong Ma for their helping.
Availability of data and materials
As this paper is a meta-analysis, there are no patient data sets. The search strategy for the study selection supports the conclusion of the meta-analysis.
Ethics approval and consent to participate
Not applicable. This meta-analysis does not involve research on humans.
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.