Intraoperative thromboelastography-guided transfusion in a patient with factor XI deficiency: A case report

Abstract

BACKGROUND

Factor XI (FXI) deficiency, also known as hemophilia C, is a rare bleeding disorder of unpredictable severity that correlates poorly with FXI coagulation activity. This often poses great challenges in perioperative hemostatic management. Thromboelastography (TEG) is a method for testing blood coagulation using a viscoelastic hemostatic assay of whole blood to assess the overall coagulation status. Here, we present the successful application of intraoperative TEG monitoring in an FXI-deficient patient as an individualized blood transfusion strategy.

CASE SUMMARY

A 21-year-old male patient with FXI deficiency was scheduled to undergo reconstructive surgery for macrodactyly of the left foot under general anesthesia. To minimize his bleeding risk, he was scheduled to receive fresh frozen plasma (FFP) as an empirical prophylactic FXI replacement at a dose of 15-20 mL/kg body weight (900-1200 mL) before surgery. Subsequent FFP transfusion was to be adjusted according to surgical need. Instead, TEG assessment was used at the beginning and toward the end of his surgery. According to intraoperative TEG results, the normalization of coagulation function was achieved with an infusion of only 800 mL FFP, and blood loss was minimal. The patient showed an uneventful postoperative course and was discharged on postoperative day 8.

CONCLUSION

TEG can be readily applied in the intraoperative period to individualize transfusion needs in patients with rare inherited coagulopathy.

Key Words: Factor XI deficiency; Thromboelastography; Transfusion; Intraoperative; Coagulopathy; Case report

Core Tip: Factor XI (FXI) deficiency is a rare bleeding disorder of unpredictable severity that correlates poorly with FXI coagulation activity and that poses great challenges for perioperative hemostatic management. Thromboelastography (TEG) is a method for testing blood coagulation using a viscoelastic hemostatic assay of whole blood to assess overall coagulation status; it is readily available and provides real-time monitoring. This case report highlights the importance of using TEG in the intraoperative period to individualize transfusion needs for patients with rare inherited coagulopathy and to minimize transfusion-related risks.

INTRODUCTION

Hemophilia C, or factor XI (FXI) deficiency, is a rare autosomal coagulation disorder[1]. Patients may be asymptomatic until they are hemodynamically challenged following trauma or surgery. In other cases, these coagulopathies are discovered as incidental laboratory findings along with other medical conditions. The unpredictability of bleeding patterns often poses perioperative challenges for clinicians[2]. Thromboelastography (TEG) is a method that is used to monitor and analyze the viscoelastic properties of blood clot formation and lysis. It has the advantages of working with the patient’s whole blood, providing real-time quantitative results on global hemostasis assessments[3]. Its adaptability for point-of-care (POC) testing makes this test particularly useful for intraoperative blood transfusion guidance. Here, we present a case in which the patient was diagnosed with FXI deficiency during a preoperative workup for macrodactyly reconstructive surgery. POC-TEG monitoring was successfully used to help assess the need for intraoperative transfusion.

CASE PRESENTATION

Chief complaints

A 21-year-old man was scheduled to undergo reconstructive surgery for macrodactyly of the left foot under general anesthesia.

History of present illness

The patient presented with significant enlargement of his left foot since birth, complicated by recurrent episodes of paronychia. He was scheduled to have reconstructive surgery at a local hospital. However, the surgery was deferred due to the unexpected perioperative discovery of abnormal coagulation studies.

History of past illness

The patient denied a previous history of easy bleeding or bruising.

Physical examination

There was significant swelling of the patient’s left foot without erythema, rash, or discoloration. The bilateral lower extremity pulses were equal. The patient had a normal gait. Motor and sensations were intact.

Laboratory examinations

Preoperative laboratory workup showed an increased activated plasma thromboplastin time (APTT) of 83.9 s (reference: 23.3-32.5 s), a normal prothrombin time (PT) of 12 s (reference: 10.4-12.6 s), and an internationalized normal ratio (INR) of 1.04 (reference 0.86-1.14). Further workup revealed the patient’s FXI activity to be 3%. The mixing study (Table 1) showed that the patient’s APTT could be corrected by mixing his plasma 1:1 with normal serum to achieve normalization of coagulation function.

Table 1 Mixing study.

APTT (normal)	APTT (normal-2 h)	APTT (patient)	APTT (patient-2 h)	APTT (1:1)	APTT (1:1-2 h)
26.1 s	27.4 s	84.2 s	83.1 s	29.8 s	31.3 s

APTT: Activated partial thromboplastin time. APTT reference 23.3-32.5 s.

FINAL DIAGNOSIS

The diagnosis of FXI deficiency was confirmed by a hematologist.

TREATMENT

Preoperative hematology consultation suggested empirically giving fresh frozen plasma (FFP) as prophylactic FXI replacement at a dose of 15-20 mL/kg body weight (patient weight 60 kg, prophylactic dose 900-1200 mL FFP) before surgery. Subsequent FFP transfusion would be adjusted per surgical need. Oral tranexamic acid was suggested for one week postoperatively.

On the day of surgery, the patient received 400 mL FFP preoperatively. The first set of TEGs (Figure 1A) performed immediately after FFP transfusion showed moderately increased activated clotting time (ACT), R time, K time, max amplitude (MA), and alpha angle. The operation was performed under general anesthesia and lasted approximately 4 h. A tourniquet was applied above the knee to minimize blood loss. Continuous nasal temperature monitoring was used to ensure no intraoperative hypothermia was experienced. The patient received 2000 mL of Ringer’s lactate and 400 mL FFP intraoperatively. Urine output was 1400 mL, and blood loss was estimated to be approximately 300 mL. The second set of TEGs (Figure 1B) performed toward the end of surgery showed improvements in all parameters.

Figure 1 Intraoperative thromboelastography monitoring. A: Thromboelastography (TEG) results after 400 mL prophylactic fresh frozen plasma (FFP) transfusion; B: TEG results after a total of 800 mL FFP infusion: Improvement of all parameters.

OUTCOME AND FOLLOW-UP

The patient had an uneventful postoperative course (Figure 2). Oral tranexamic acid 0.5 g three times per day was prescribed for one week. Surgical site drainage was 45 mL on postoperative day (POD) 1 and then decreased to a minimal level. The drain was removed on POD3. The patient received 400 mL FFP on POD 4 due to concerns of prolonged elevation of APTT levels (46.4 s, reference: 23.3-32.5 s), while the surgical dressing remained dry and clean. He was discharged on POD 8.

Figure 2 Major perioperative events and laboratory test results. POD: Postoperative day; APTT: Activated partial thromboplastin time; FFP: Fresh frozen plasma.

DISCUSSION

Hemophilia C caused by a deficiency of FXI is a rare autosomal inherited coagulopathy. FXI plays an important role not only in initiating clot formation but also in supporting clot consolidation. Conventional coagulation tests such as PT and APTT are less than satisfactory in the assessment of hemophilia C patients’ clinical profiles and bleeding risks. These tests are limited because they are endpoint assays that test only the speed of blood clot formation. However, they cannot reflect the process of further thrombin formation involved in clot consolidation and maintenance. Compared with hemophilia A and B, the clinical profile and bleeding management of hemophilia C is less clearly understood (Table 2). The relationship between bleeding phenotypes and baseline FXI level is poor, making perioperative bleeding risk hard to predict and manage[4].

Table 2 Genetic and clinical features of different types of hemophilia and their management.

	Hemophilia A	Hemophilia B	Hemophilia C
Genetics	X-linked	X-linked	Autosomal
Pathophysiology	FVIII deficiency	FIX deficiency	FXI deficiency
Clinical manifestations	Bleeding of variable severity correlated with factor levels	Bleeding of variable severity correlated with factor levels	Variable
Routine management	Prophylactic factor replacement	Prophylactic factor replacement	None
Perioperative management	Factor replacement, Cryoprecipitate. The goal is to keep the levels of FVIII > 50% for major surgery	Factor replacement, Prothrombin complex concentrate. The goal is to keep the levels of factor IX > 50% for major surgery	Controversial. May include: FFP, antifibrinolytics, TPE, factor replacement. Optimal FXI level unclear

FVIII: Factor VIII; FIX: Factor IX; FFP: Fresh frozen plasma; TPE: Therapeutic plasma exchange.

TEG is a method of testing the efficiency of blood coagulation using a whole blood-based, viscoelastic hemostatic assay. It can provide a continuous assessment of the elastic properties of clot formation and lysis in both graphics and numbers. TEG measurements collected for analysis include reaction (R) time, coagulation (k) time, α angle, and maximum amplitude (MA), which are reflections of clotting factors, circulating inhibitory activity, fibrinogen and platelet levels and function, etc.[5] TEG’s short turnaround time makes it a promising measurement tool for the assessment of global hemostasis in trauma or perioperative settings. It is better than conventional coagulation tests in monitoring coagulation profiles and predicting transfusion requirements[5]. It reduces the total amount of blood products transfused compared with an empiric transfusion policy or a transfusion protocol guided by conventional coagulation tests[6]. Study results from trauma[7], liver transplant[8] and cardiac surgeries[9] have shown that the goal-directed allogeneic transfusion strategy is believed to provide better hemostatic competence. This was possibly due to the more timely administration of blood products such as plasma and platelets, which in turn resulted in less blood loss[3], reduced blood transfusion needs[10], lower costs, and fewer adverse events[11] in the TEG-guided transfusion group than in the conventional transfusion group. One study also suggested that TEG-guided transfusion could substantially affect patient outcomes, including length of hospital stay, odds of reoperation, and short-term mortality[9]. For inherited coagulopathies such as hemophilia A and B, a combination of standard coagulation laboratory tests and TEG tests results in a better understanding of hemostasis in an individual patient, giving insights into their long-term hemostatic management[12], as well as providing vital insights in more pressing situations such as traumas or surgeries. In later cases, studies from hemophilia A and B patients suggested that TEG could be successfully used in perioperative settings to evaluate the efficacy of various hemostatic agents, such as factor VIII concentrate, cryoprecipitate, and prothrombin complex concentrates[3]. TEG has the potential to assess the role FXI plays in global hemostasis. However, its application in perioperative transfusion management for hemophilia C patients has not been extensively studied.

Normally, FXI-deficient patients will require careful, individualized and multidisciplinary preprocedural planning. Such planning starts with a meticulous assessment of the patient’s bleeding history and bleeding pattern. This is followed by thorough laboratory tests, including basic coagulation function tests, such as PT, APTT, and FXI levels, and mixing studies. Moreover, the nature of the scheduled procedure must also be taken into consideration. Operations on sites with higher fibrinolytic activities, such as the pharynx and urinary tracts, put patients at higher risk for bleeding[13]. The use of antifibrinolytic medication may help improve overall hemostasis[14]. For major procedures in individuals with severe FXI deficiency or with a significant bleeding phenotype, prophylactic replenishment using FXI concentrates or FFP is recommended in the preoperative period[1]. FXI concentrate has been associated with a higher thrombotic risk than FFP[15]. Some practitioners have suggested a “wait and watch” attitude with factor replacement, giving FXI concentrate only when excessive bleeding occurs. Prophylactic FFP replacement is the most commonly used option in our institute. However, this comes with the risk of volume overload. Because FXI levels do not correlate well with bleeding phenotypes, replacement therapy remains somewhat empirical. Therapeutic plasma exchange (TPE) may lower the risk of circulatory volume overload[16]. However, this is a complicated procedure with other transfusion-related adverse effects, and the added costs cannot be overlooked.

The patient we present here had no history of spontaneous bleeding and had no surgical history. This made the perioperative bleeding risk hard to predict and the prophylactic transfusion management strategy hard to plan. The consulting hematologists suggested a FFP loading dose of 15-20 mL/kg body weight to bring the FXI level within a satisfactory range (FXI: C, 30%–45%), which inevitably resulted in the need for a large volume of FFP. It is in this kind of situation that TEG monitoring is especially useful. TEG-guided prophylactic FFP replacement may allow for a more parsimonious use of replacement therapy in patients with severe FXI deficiency undergoing surgery. It can reduce the risks of volume overload, transfusion-related acute lung injury, transmission of infectious diseases, thrombosis, allergic reactions, and the development of inhibitors to FXI[13].Empirically, our patient was to receive a loading dose of 900-1200 mL FFP according to preoperative hematology consultation. In practice, however, based on the results from the intraoperative TEG monitoring, our patient received 800 mL FFP in total before and during the whole procedure with minimal blood loss and uneventful postoperative recovery. This experience is limited to a single case report. However, we believe that with improved TEG technology and accessibility, anesthesiologists and other medical practitioners will be able to provide transfusion therapy tailored to the need of each patient with FXI deficiency.

CONCLUSION

FXI deficiency is an underrecognized disorder with a wide range of clinical presentations and a poor correlation with coagulation studies. It poses great challenges for perioperative management. FXI concentrates, FFP, TPE and antifibrinolytic therapies are the mainstream treatments for FXI patients with surgical needs. POC-TEG could be readily applied in the perioperative period to individualize transfusion requirements on a case-by-case basis, providing guidance regarding the appropriate amount of blood products to be administered and thus minimizing transfusion needs and the associated risks. Further large-scale studies are needed to assess the potential for using TEG for perioperative transfusion guidance in the treatment of FXI patients.