Abstract
Background and Objectives: Transcatheter arterial embolization (TAE) is the mainstay of treatment for acute major hemorrhage, even in patients with coagulopathy and spontaneous bleeding. Coagulopathy is associated with worsening bleeding severity and higher mortality and clinical failure rates. Furthermore, some unanswered questions remain, such as the definition of coagulopathy, the indication for TAE or conservative treatment, and the choice of embolic agent. This study aims to assess the efficacy and safety of TAE for spontaneous non-neurovascular acute bleeding in patients with coagulopathy. Materials and Methods: This study is a multicenter analysis of retrospectively collected data of consecutive patients with coagulopathy who had undergone, from January 2018 to May 2023, transcatheter arterial embolization for the management of spontaneous hemorrhages. Results: During the study interval (January 2018–May 2023), 120 patients with coagulopathy underwent TAE for spontaneous non-neurovascular acute bleeding. The abdominal wall was the most common bleeding site (72.5%). The most commonly used embolic agent was polyvinyl alcohol (PVA) particles or microspheres (25.0%), whereas coils and gelatin sponge together accounted for 32.5% of the embolic agents used. Technical success was achieved in all cases, with a 92.5% clinical success rate related to 9 cases of rebleeding. Complications were recorded in 12 (10%) patients. Clinical success was significantly better in the group of patients who underwent correction of the coagulopathy within 24 h of TAE. Conclusions: Transcatheter arterial embolization (TAE) is effective and safe for the management of acute non-neurovascular bleeding in patients with coagulopathy. Correction of coagulopathy should not delay TAE and vice versa, as better clinical outcomes were noted in the subgroup of patients undergoing correction of coagulopathy within 24 h of TAE.
Keywords: coagulopathy, bleeding, TAE, embolization, hemorrhage, embolic agents, endovascular
1. Introduction
Transcatheter arterial embolization (TAE) is the mainstay of treatment for acute major hemorrhage [1,2,3]. A multitude of conditions, including trauma, tumors, iatrogenic injuries, and coagulation disorders, can cause major acute bleeding and may benefit from TAE [4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30].
Despite TAE in patients with coagulation disorders being a well-known area of endovascular therapy, the definition of coagulopathy differs among authors [4,19,31,32]. The Cardiovascular and Interventional Radiological Society of Europe (CIRSE) and the Society of Interventional Radiology (SIR) issued some documents on peri-operative anticoagulation management in patients undergoing interventional radiology procedures [33,34,35]. Interestingly, some authors have defined the condition of coagulopathy by choosing some cut-off values that previous guidelines or investigations have used to recommend the correction of coagulation function in order to safely perform an endovascular procedure [19,32]. However, the coagulopathy condition in patients undergoing TAE is a separate clinical setting and goes beyond the safety issues related to the endovascular treatment in itself and vascular access site management, as it results in a number of well-known consequences: (1) worsening of the severity of bleeding [36,37], (2) predicting mortality [37] and rebleeding [24,38], (3) higher risk of clinical failure after TAE [39], and (4) high clinical failure rates with embolic agents that act by clot formation, such as gelatin sponge and coils [4,32,40,41,42,43,44].
Moreover, the indication for TAE in patients with coagulopathy is another controversial point. Previous reports demonstrated that conservative management could also be effective in patients with coagulopathy and spontaneous hemorrhages [45,46]. Reversal or withdrawal of anticoagulation therapy, correction of acid–base imbalance, volume resuscitation, vasoactive drugs, transfusions, and correction of coagulopathy with fresh frozen plasma and prothrombin complex concentrate are the main conservative interventions described in previous reports [10,32,39,45,46,47]. However, hemodynamic instability, detection of active bleeding on CT-angiography (CTA), and hematoma volume are the main predictors of unsuccessful conservative management; furthermore, failure of conservative management should be previously recognized [10,45,48,49].
Determining the cause of coagulopathy is crucial, given the possibility of initial conservative management. Coagulopathies recognize congenital or acquired causes. Among the acquired causes, some conditions, such as COVID-19-related coagulopathy, thromboprophylaxis with anticoagulants, and trauma-induced coagulopathy, are of particular interest, as they are frequent causes of acute major bleeding requiring TAE [19,50,51,52].
Unfortunately, the existing evidence on the safety and efficacy of TAE in patients with coagulopathy is inconsistent; often limited to small populations, retrospective-based case series [19], or subgroup analyses; and performed in a single-center fashion [31,32,39,44,53,54]. Our study aims to assess the efficacy and safety of TAE for spontaneous non-neurovascular acute bleeds in patients with coagulopathy via a multicenter, retrospective, large cohort evaluation.
2. Materials and Methods
2.1. Study Design
This study is a multicenter (Dulbecco University Hospital, Catanzaro, Italy; Circolo Hospital, Varese, Italy; Maggiore della Carità University Hospital, Novara, Italy; Mater Domini University Hospital, Catanzaro, Italy; Pugliese-Ciaccio Hospital, Catanzaro, Italy; Cardarelli Hospital, Campobasso, Italy; San Timoteo Hospital, Termoli, Italy) analysis of retrospectively collected data of consecutive patients with coagulopathy who underwent, from January 2018 to May 2023, transcatheter arterial embolization for the management of acute bleeding (Figure 1, Figure 2, Figure 3 and Figure 4). Inclusion criteria were (I) TAE performed due to spontaneous non-neurovascular acute bleeding according to the indications provided by the Society of Interventional Radiology (SIR) guidelines for percutaneous transcatheter embolization [3], (II) coagulopathy at the time of embolization, (III) age of at least 18 years, and (IV) evaluation by a multidisciplinary team of surgeons, interventional radiologists and anesthesiologists. The exclusion criteria were (I) pregnant or breastfeeding women; (II) platelet count < 20,000/μL and refusal of transfusion, according to SIR guidelines for low bleeding risk procedures that require arterial access [34]; (III) international normalized ratio (INR) greater than 1.8 for femoral access or greater than 2.2 for radial access, according to SIR guidelines for low bleeding risk procedures that require arterial access [34]; (IV) hypersensitivity to available embolic agents; and (V) bleeding sustained by the internal carotid artery or its branches.
In order to constitute a control group, we retrospectively examined consecutive patients with normal coagulation function who underwent TAE to manage acute non-neurovascular bleeding, starting from January 2018 until equal sample size of the group of patients with coagulopathy was constituted. Ethics committee approval was not required due to the retrospective nature of the study. The study was conducted in accordance with the Helsinki Declaration. All patients signed a written informed consent before receiving the endovascular treatment.
2.2. Treatment
All patients underwent pre-treatment evaluation with CT-angiography (CTA), except in special cases, based on international guidelines or expert opinions (e.g., upper gastrointestinal bleeding refractory to endoscopic treatment [55]). The endovascular procedure was performed in dedicated angiographic suites by an experienced interventional radiologist (at least 5 years of experience). A high-level infection protection protocol was adopted before, during, and after the endovascular procedure for COVID-19 patients, similar to what was suggested by Ierardi et al. [56]. Diagnostic angiography always preceded the super-selective catheterization of the bleeding/pseudoaneurysm-feeding arteries. The choice of embolic agent depended on operator preference. The embolic agent was prepared and injected under fluoroscopic guidance according to the instructions for use. The microcatheter was never reused or washed after the use of a non-adhesive liquid embolic agent (NALEA) or N-butyl cyanoacrylate (NBCA). In the absence of angiographic signs of bleeding, a blind embolization was performed [48]. Assessment of technical success and non-target embolization were performed by postembolization angiography, taking into account the possible collateral circulation based on the anatomical site of the bleeding. When appropriate, the anesthesiologist performed sedation during the embolization to improve patient comfort and provided analgesic therapy after the procedure. All patients underwent clinical evaluation and follow-up imaging before the hospital discharge and 1 month after TAE.
2.3. Outcomes and Definitions
The primary efficacy endpoint was the rate of technical success. The clinical success rate was selected as a secondary efficacy endpoint. The primary safety endpoint was the rate of complications. The non-target embolization rate and the rate of major complications graded according to the 2003 SIR classification [57] were selected as secondary safety endpoints.
Unless otherwise specified, reporting standards of the Society for Interventional Radiology for percutaneous transcatheter embolization were used (e.g., technical success was defined by the exclusion defined by angiographically appreciable bleeding stopping immediately after embolization; the resolution of the signs of bleeding, which made TAE necessary, defined the clinical success) [58]. The coagulopathy was defined as in Loffroy et al. [4]: INR greater than 1.5, partial thromboplastin time longer than 45 s, or platelet count less than 80,000/mm3. Ct-to-groin time, procedure time, and CT-to-embolization time were calculated by taking into account the times indicated in the CT report and the surgical operative log. Complications linked to TAE were graded according to the 2017 SIR classification [59], the 2003 SIR classification [57], and the CIRSE classification [60].
2.4. Statistical Analysis
Data were maintained in an Excel spreadsheet (Microsoft Inc., Redmond, WA, USA) and the statistical analyses were performed on an intention-to-treat basis, using SPSS software (SPSS, version 22 for Windows; SPSS Inc., Chicago, IL, USA) and R/R Studio software. The analyses were based on the modified intention-to-treat population, defined as all randomized patients who received at least one embolization treatment [61,62]. The Kolmogorov–Smirnov test and the Shapiro–Wilk test were used to verify the normality assumption of data. Categorical data are presented as frequencies (percentage value). Continuous normally distributed data are presented as means ± standard deviations. Continuous not normally distributed data are presented as medians (first–third quartile) [63,64,65]. The unpaired Student’ t-test was used to assess statistical differences for continuous normally distributed data [66], whereas categorical and continuous not normally distributed data were assessed using the Chi-squared/Fisher’s exact tests and the Mann–Whitney test, respectively [67,68]. A p-value of <0.05 was considered statistically significant for the aforementioned tests.
3. Results
During the study interval (January 2018–May 2023), 120 patients with coagulopathy underwent transcatheter arterial embolization for spontaneous non-neurovascular acute bleeding. An INR > 1.5 was observed in 72 (60.0%) patients, an aPTT > 45 s in 72 (60.0%) patients, and a PLT value below 80,000/mm3 in 66 (55.0%) patients. CT-angiography was performed in 117 (97.5%) cases and bleeding was detected in 111 (92.5%) patients. The mean hematoma volume measured on CT was 238.6 (±263.3) mL. In total, 99 (82.5%) patients were on antiplatelet or anticoagulant therapy. Details are given in Table 1.
Table 1.
Variables | All Patients (n = 120) |
---|---|
Age (years) | 63.6 (±15.9) |
Sex (M/F) | 78 (65.0%)/42 (35%) |
BMI | 26.4 (±3.7) |
eGFR (mL/min) | 68.7 (±24.1) |
CKD Stage | 2 (1–3) |
INR | 1.6 (±0.3) |
aPTT (s) | 46.2 (±5.7) |
PT (s) | 15.8 (±2.6) |
Platelet count (No. ×103/μL) | 206.7 (±163.6) |
Coagulopathy
|
72 (60.0%) 72 (60.0%) 66 (55.0%) |
Hemoglobin (g/dL) | 7.8 (±0.8) |
CT-angiography execution | 117 (97.5%) |
Bleeding on CT-angiography | 111 (92.5%) |
Hematoma volume (mL) | 238.6 (±263.3) |
Antiplatelet therapy
|
18 (15.0%) 12 (10.0%) 5 (5%) |
Anticoagulant therapy | 81 (67.5%) |
Antiplatelet AND anticoagulant therapy | 0 (0%) |
Antiplatelet OR nticoagulant therapy | 99 (82.5%) |
120 transcatheter arterial embolizations were performed. In three cases no bleeding was detected on X-ray angiography (XA); thus blind embolizations were performed (i.e., embolization of lumbar arteries guided by CT findings). The abdominal wall was the most common bleeding site (72.5%). The most commonly used embolic agent was polyvinyl alcohol (PVA) particles or microspheres (25.0%), whereas coils and gelatin sponge together account for 32.5% of the embolic agents used. In 27 (22.5%) cases Onyx or Squid was used. The mean volume of iodinated contrast media used during embolizations was 38.1 (±14) mL. The mean volume-of-contrast-to-creatinine-clearance ratio was 0.73 (±0.7). The most common vascular access site was the common femoral artery (70%). The mean CT-to-groin time, the mean procedure time, the mean CT-to-embolization time, and the mean fluoroscopy time were 52.8 (±58.7) min, 30.7 (±10.5) min, 83.8 (±59.2) min, and 8.3 (±3.4) min, respectively. Radiation exposure expressed by cumulative air kerma and total dose area product was 159.7 (±62) mGy and 25.5 (±9.7) Gy/cm2, respectively.
Procedure data are detailed in Table 2.
Table 2.
Variables | All Patients (n = 120) |
---|---|
Bleeding on XA | 117 (97.5%) |
Blind embolization | 3 (2.5%) |
Site of bleeding
|
3 (2.5%) 12 (10.0%) 87 (72.5%) 12 (10.0%) 6 (5.0%) |
Number of embolized vessels | 1.1 (±0.4) |
Embolic agent
|
12 (10.0%) 27 (22.5%) 30 (25.0%) 24 (20.0%) 27 (22.5%) |
Intraoperative contrast medium (mL) | 38.1 (±14) |
Volume-of-contrast-to-creatinine-clearance ratio | 0.73 (±0.7) |
Vascular access site
|
84 (70.0%) 30 (25.0%) 6 (5%) |
Sheath diameter, 4F/5F/6F/≥7F | 15 (12.5%)/102 (85%)/3 (2.5%)/0 (0%) |
CT-to-groin time (min) | 52.8 (±58.7) |
Procedure time (min) | 30.7 (±10.5) |
CT-to-embolization time (min) | 83.8 (±59.2) |
Fluoroscopy time (min) | 8.3 (±3.4) |
Cumulative air kerma (mGy) | 159.7 (±62) |
Dose area product (DAP) (Gy/cm2) | 25.5 (±9.7) |
Technical success was achieved in all cases, with a 92.5% clinical success rate related to 9 cases of rebleeding. No cases of non-target embolization were observed. Complications were recorded in 12 (10%) patients. Vascular access site complications (VASCs) were recorded in six (5%) cases, related to three pseudoaneurysms and three groin hematomas. Furthermore, three liver abscesses and three psoas abscesses were noted. According to the 2017 SIR classification for complications [59], all complications observed were grade 2 events. The 30 day bleeding-related mortality was 5%, related to 6 cases of hypovolemic shock and multiple organ dysfunction syndrome (MODS); another 6 (5%) patients died within the deadline of the 30 day follow-up from causes not related to the bleeding.
Details are given in Table 3.
Table 3.
Variables | All Patients (n = 120) |
---|---|
Technical success | 120 (100%) |
Clinical success | 111 (92.5%) |
Coagulopathy correction within 24 h of TAE | 57 (47.5%) |
Vascular access site hemostasis
|
63 (52.5%) 57 (47.5%) |
Units of packed red blood cells transfused per patient | 1.4 (±1.2) |
Rebleeding | 9 (7.5%) |
Non-target embolization | 0 (0%) |
Complications | 12 (10%) |
Vascular access-site complications (VASCs) | 6 (5%) |
Complications, according to SIR classifications
|
108 (90%) 12 (10%) 0 (0%) |
Complications, according to CIRSE classification
|
108 (90%) 12 (10%) |
Treatment required for complications
|
108 (90%) 6 (5%) 6 (5%) 0 (0%) |
30 day bleeding-related mortality | 6 (5%) |
No statistically significant differences were observed between Group 1 (patients who did not undergo correction of the coagulopathy within 24 h of the TAE) and Group 2 (patients who underwent correction of the coagulopathy within 24 h of the TAE) in terms of preoperative INR, platelet count, procedure time, technical success, and complications. Statistically significant differences were observed between Group 1 and Group 2 in terms of preoperative hemoglobin, anticoagulant therapy, hematoma volume, CT-to-groin time, fluoroscopy time, clinical success, rebleeding rate, and 30 day bleeding-related mortality.
A comparison of data between Group 1 and Group 2 is reported in Table 4.
Table 4.
Variables | Group 1 (n° = 63) | Group 2 (n° = 57) | p-Value |
---|---|---|---|
Preoperative INR | 1.59 (±0.3) | 1.52 (±0.3) | 0.242 |
Platelet count (No. ×103/μL) | 202.4 (±166) | 211.3 (±162.3) | 0.9263 |
Preoperative hemoglobin (g/dL) | 7.6 (±0.5) | 7.9 (±0.9) | 0.0419 |
Anticoagulant therapy | 27 (42.9%) | 54 (94.7%) | <0.0001 |
Hematoma volume (mL) | 183.4 (±253.7) | 303.5 (±261.9) | <0.0001 |
CT-to-groin time (min) | 41.6 (±46.4) | 64.6 (±67.8) | 0.0107 |
Procedure time (min) | 29.1 (±10.2) | 32.4 (±10.6) | 0.0523 |
Fluoroscopy time (min) | 7.7 (±2.8) | 9 (±3.8) | 0.0135 |
Technical success | 63 (100%) | 57 (100%) | 1 |
Clinical success | 54 (85.7%) | 57 (100%) | 0.0031 |
Rebleeding rate | 9 (14.3%) | 0 (0%) | 0.0031 |
Complications | 9 (14.3%) | 3 (5.3%) | 0.1317 |
30 day bleeding-related mortality | 6 (9.5%) | 0 (0%) | 0.0285 |
No statistically significant differences were observed between patients with coagulopathy undergoing TAE for acute non-neurovascular bleeding and the control group consisting of patients with normal coagulation function in terms of preoperative hemoglobin (p = 0.397), procedure time (p = 0.141), technical success (p = 0.247), clinical success (p = 0.595), rebleeding rate (p = 0.811), complications (p = 0.649), or 30 day bleeding-related mortality (p = 0.758). Preoperative INR (p < 0.001), platelet count (p < 0.001), and age (p = 0.009) were not comparable between the abovementioned groups. Details are reported in Table 5.
Table 5.
Variables | Coagulopathy (n° = 120) |
Normal Coagulation Function (n° = 120) |
p-Value |
---|---|---|---|
Age (years) | 63.6 (±15.9) | 55.9 (±20.3) | 0.009 |
Preoperative INR (s) | 1.6 (±0.3) | 1.3 (±0.3) | <0.001 |
Platelet count (No. ×103/μL) | 206.7 (±163.6) | 357.4 (±111) | <0.001 |
Preoperative hemoglobin (g/dL) | 7.8 (±0.8) | 7.7 (±0.8) | 0.397 |
Procedure time (min) | 30.7 (±10.5) | 28.4 (±9) | 0.141 |
Technical success | 120 (100%) | 117 (97.5%) | 0.247 |
Clinical success | 111 (92.5%) | 114 (95%) | 0.595 |
Rebleeding rate | 9 (7.5%) | 10 (8.3%) | 0.811 |
Complications | 12 (10%) | 9 (7.5%) | 0.649 |
30 day bleeding-related mortality | 6 (5%) | 5 (4.2%) | 0.758 |
4. Discussion
In this multicenter retrospective cohort study, acute major non-neurovascular bleeding in patients with coagulopathy was effectively managed by TAE.
Technical success was achieved in all cases, with a clinical success rate of 92.5%; 9 cases of rebleeding were all successfully retreated with TAE. These results are in keeping with previous investigations evaluating TAE in acute bleeding of patients with coagulopathy [19,31,32,39,44,53,54]. Spiliopoulos et al. reported a technical success rate of 100% in their case series of 17 patients with coagulopathy who underwent TAE for acute bleeding [19]. Interestingly, they successfully used gelatin sponge, coils, or a combination of both in eight (47.1%) cases. The only rebleeding event was observed in a patient treated with gelatin sponge alone, thus recording a rebleeding rate of 5.9% [19]. In a recent case series of 35 cirrhotic patients by Patidar et al., 91.4% of patients had coagulopathy, and technical and clinical success was achieved in 100% and 82.8% of patients, respectively [31]. Yonemitsu et al. achieved primary hemostasis in 50 of the 63 bleeding arteries (80%) in patients with a coagulopathic condition. Interestingly, the primary hemostatic rates in the gelatin sponge, coils, and NBCA groups were 67% (18 of 27), 80% (16 of 20), and 100% (16 of 16), respectively. Secondary hemostasis was achieved in 60 of the 63 hemorrhagic arteries (95%) [32]. According to Jae et al., TAE with NBCA was associated with a high clinical success rate (83%) in patients with coagulopathy [69]. Less recent reports have shown lower technical success rates, such as 43% reported by Encarnacion et al. [70] and 46% reported by Schenker et al. [71], demonstrating the gradual improvement of TAE efficacy over time. Hence, we can speculate that, despite the lack of specific guidelines, TAE represents an effective treatment option for acute major hemorrhages in patients with coagulopathy. Finally, our results are in keeping with the control group consisting of patients with normal coagulation function and with outcomes reported in other investigations for acute non-neurovascular bleeding in patients with normal coagulation function [5,6,11,58].
In our study, TAE showed a good safety profile in the treatment of acute non-neurovascular bleeding in patients with coagulopathy. Complication rate and 30 day bleeding-related mortality were 10% and 5%, respectively. Lee et al. demonstrated that coagulopathy is an independent predictor of rebleeding and mortality [38]. Interestingly, Aina et al. pointed out a higher rate of rebleeding in patients with coagulopathy undergoing TAE than in patients with normal coagulation function [72]. Encarnacion et al. and Schenker et al. observed that TAE was 2.9 times and 2.8 times, respectively, more likely to fail in patients with coagulopathy [70,71]. This finding should be put in context with more recent evidence that, with technological advances and better rationale for using embolic agents, has shown a marked improvement in the rebleeding rates. Recently, Spiliopoulos et al. reported no cases of bleeding-related 30 day mortality; in all cases, they used a vascular closure device to achieve vascular access site hemostasis, with no major bleeding-related VASCs or procedure-related complications noted [19]. In their case series on 63 TAEs performed in patients with a coagulopathic condition, Yonemitsu et al. observed a significantly higher rebleeding rate in the gelatin sponge group compared to the coil group (23% vs. 0%; p = 0.048), as well as in the gelatin sponge group compared to the NBCA group (23% vs. 0%; p = 0.048) [32]. In a recent case series of 35 cirrhotic patients by Patidar et al., 91.4% of patients had coagulopathy; the 30-day mortality rate and bleeding-related mortality rate were 48% and 17%, respectively; and the rebleeding rate was 8.6%. The overall complication rate was 8.5%, with no major procedure-related complications noted. Interestingly, NBCA was used as the embolic agent and only the greater number of RBC units transfused before the embolization procedure was significantly associated with clinical failure [31]. Hence, in our investigation, the safety outcomes, including VASCs, are consistent with other studies in the field of endovascular treatments and TAEs [6,15,25,29,73,74,75,76,77,78,79,80] and with the control group consisting of patients with normal coagulation function.
The heterogeneity of data and some unanswered questions on TAE in patients with coagulopathy should be recognized. Firstly, the definition of coagulopathy may vary according to various authors, as well as the inclusion criteria. Loffroy et al. defined the coagulopathy subgroup as patients having a platelet count of less than 80,000/μL, an international normalized ratio (INR) greater than 1.5, or an activated partial thromboplastin time (aPTT) longer than 45 s or [4]. Yonemitsu et al. defined the condition of coagulopathy as platelet count < 50,000/μL and/or INR < 1.5 because these values required correction by infusion of platelets or fresh frozen plasma according to previous indications [32]. According to the guidelines for periprocedural management of coagulation status and hemostasis risk in percutaneous image-guided interventions issued in 2012 by SIR, procedures requiring an introducer sheath up to 7Fr should be performed after optimization of the coagulation status to the following values: platelet count > 50,000/μL, INR < 1.5, and aPTT < 1.5 x laboratory reference values [81]. These guidelines were cited by other authors to justify their definition of coagulopathy. Spiliopoulos et al. define the coagulopathy subgroup as patients presenting with thrombocytopenia (platelet count < 50,000/μL) and/or INR ≥ 2.0, and/or aPTT > 45 s, and/or a known underlying blood-clotting disorder such as factor VIII, von Willebrand disease, or hepatic cirrhosis with abnormal liver function tests [19]. Similar inclusion criteria were used by Hur et al. [39]. In 2019, SIR issued updated Consensus Guidelines for the Periprocedural Management of Thrombotic and Bleeding Risk in Patients Undergoing Percutaneous Image-Guided Interventions, recommending the correction of INR within the range of ≤2.0–3.0 and a platelet count > 20,000/μL to safely perform low bleeding risk procedures including embolotherapy. Interestingly, the low quality of evidence supporting this recommendation should also be noted [34,35]. International Society on Thrombosis and Haemostasis interim guidance on recognition and management of coagulopathy in COVID-19 defined the condition of coagulopathy in COVID-19 patients as prothrombin time (PT) prolongation above laboratory reference values (may vary depending on the reagent used), D-dimer ≥ 1.5 mg/L, fibrinogen < 2 g/L, or platelet count less than 100,000/μL [50]. Recently, CIRSE issued a standard of practice document on peri-operative anticoagulation management during interventional radiology procedures recommending a platelet count > 20,000/μL and an INR < 2.0 to perform low bleeding risk procedures such as embolization [33]. The above guidelines define cut-off values to safely perform the percutaneous treatment and adequately manage the vascular access site. Instead, the definition of coagulopathy in patients undergoing TAE should also be aimed at directing the choice of embolic agent, since some of them act by clot formation. A previous investigation by Loffroy et al. demonstrated that the use of coils as the sole embolic agent and the presence of coagulopathy are independent predictors of early rebleeding; interestingly, higher cut-off values were used to define the coagulopathy status [4]. Therefore, it is our opinion that the heterogeneity in the coagulopathy definition can lead to errors in comparing published data and that it would be desirable to use a common, broader definition of coagulopathy, such as those proposed by Spiliopoulos et al., Loffroy et al., or the International Society on Thrombosis and Haemostasis [4,19,50]. Future perspectives include the development of a predictive model of the clinical efficacy of various embolic agents based on different values of PLT, aPTT, and INR.
It is noteworthy that 30 day survival after TAE could be predicted by clinical success [82]. Moreover, coagulopathy has been previously reported as a significant negative predictor for recurrent bleeding, in-hospital mortality, and procedure-related complication rates [1,2,24,39,83,84]. Interestingly, a higher risk of rebleeding has been observed in patients with impaired coagulation even after successful TAE [83]. In contrast, other reports have shown similar rates of TAE success and rebleeding between patients with coagulopathy and those without [19]. Additionally, the coronavirus disease 2019 (COVID-19) pandemic has resulted in increased reports on effective conservative management of spontaneous major bleeds in patients with coagulopathy [45,46,85]. Therefore, data on TAE in patients with coagulopathy are controversial, and the management of major acute bleeding in patients with coagulopathy is still debated. Loffroy et al. advocated for TAE for patients with coagulopathy; they argued that endovascular treatment should not be refused and that correction of the coagulopathy should be performed as soon as possible, regardless of TAE [83]. Similarly, if large-volume bleeding causing hemodynamic instability is noted, better clinical outcomes will be expected in case of a shorter time to embolization; waiting for normalization of the coagulation state is not a good option [3]. Hence, TAE should not delay the correction of coagulopathy, and vice versa. Our findings support this speculation, as a reduced rebleeding rate was observed in the subgroup of patients who underwent correction of the coagulopathy within 24 h of TAE. Spiliopoulos et al. speculated that several factors, including local expertise in multidisciplinary bleeding management, correction of coagulopathy, and the timing and technique of TAE, are crucial for improved outcomes. Notably, in their investigation normalization of the coagulation state within 24 h was recorded in 58% of the patients [19].
The choice of the best embolic agent is another key point. Previous reports support the hypothesis that embolization with a gelatin sponge or coils only is less effective in patients with coagulopathy, as their mechanism of action is primarily based on clot formation [4,32,40,41,42,43,44]. However, patients with significantly prolonged INR were successfully treated with coil-only embolization [86], and dense coil packing or a combination of dense coiling with gelatin sponge was suggested for patients with coagulopathy undergoing TAE [19]. Coils could guarantee a proximal embolization with reduced risk of migration compared to NBCA, particles, or NALEAs, but in patients with coagulopathy, the dense coil-packing technique is necessary, although it is less user-friendly for less experienced interventionists. Hence, we believe that an imperfect coil embolization technique could jeopardize the outcomes of TAE, especially if there is no strong experience in the dense coil-packing technique. Conversely, particles and liquid embolics guarantee rapid and effective mechanical embolization, not requiring the activation of coagulation [87,88]. PVA particles and microspheres cause mechanical vascular occlusion by depositing in vessels and causing an inflammatory and then a fibrotic reaction in the vessel wall, and they are available in different size ranges, which determine their ability to penetrate even very small vessels [89,90]. Non-adhesive liquid embolic agent (NALEA) and N-butyl cyanoacrylate (NBCA) have been proposed as the most effective embolic agents in patients with coagulopathy, as they act by polymerization (NBCA) and solidification (Onyx), thus embolizing the target vessel independently from the clot formation [44,74,91]. TAE with NBCA has a favorable cost-effectiveness ratio [92], but its use requires a longer learning curve than coils and is probably less user-friendly than non-adhesive liquid embolic agents (NALEAs) due to the higher risk of insidious adverse events such as the gluing of the microcatheter tip [40].
One could argue extensively over the safety management of the vascular access site in patients with coagulopathy. According to SIR guidelines for low bleeding risk procedures that require arterial access, femoral access requires an INR of 1.8 or less, whereas radial access requires an INR of 2.2 or less [34]. Furthermore, the use of vascular closure devices may facilitate hemostasis of the femoral access site, and deferring the removal of the introducer sheath until correction of the coagulopathy may be an option [19]. In our study, the incidence of bleeding-related VASCs was low and comparable to other reports in the literature on TAE and other endovascular treatments in patients with normal coagulation status [6,15,74,76,93,94].
Therefore, our results together with the review of data in the literature allow us to support some speculations regarding patients with coagulopathy and major acute bleeding, which can be summarized as follows: (1) The different definitions of coagulopathy and the variability of the embolic agents used determine a heterogeneity of data in the literature, thus resulting in controversial and difficult-to-compare outcomes; (2) conservative management may be an option but the main predictors of its failure must be considered, including hemodynamic instability, detection of active bleeding on CTA, and hematoma volume; (3) identifying the causes of coagulopathy is crucial given that the correction of coagulopathy improves outcome; (4) TAE is a safe and effective option; (5) TAE should not delay the correction of coagulopathy, and vice versa; (6) the choice of embolic agents not acting by clot formation might promote the achievement of efficacy rates similar to TAE in patients with normal coagulation function; (7) INR guides the choice of vascular access to safely perform TAE; and (8) coagulopathy does not preclude the safe management of vascular access, thanks also to the use of VCDs and the possibility of postponing the removal of the introducer sheath.
Limitations of the study are the retrospectivity of the analysis, the heterogeneity of the indications, the short-term follow-up, and the scarcity of data in the literature, which are necessary to evaluate the congruence and the consistency of the data presented. Besides, as this is a retrospective study, the sample size calculation could not be performed, and thus, the statistical power of the study may not be optimal.
5. Conclusions
The results of the current investigation demonstrate that transcatheter arterial embolization (TAE) is an effective, safe, and potentially life-saving option for the management of acute non-neurovascular bleeding in patients with coagulopathy. Correction of coagulopathy should not delay TAE, and vice versa, as better clinical outcomes were noted in the subgroup of patients undergoing correction of coagulopathy within 24 h of TAE.
Further studies are warranted to better understand the impact on outcomes of some factors, such as the choice of the best embolic agent, the indications to TAE, and the time to angiography in patients with coagulopathy.
Abbreviations
APTT: activated partial thromboplastin time; CKD: chronic kidney disease; CIRSE: Cardiovascular and Interventional Radiological Society of Europe; COVID-19: coronavirus disease 2019; CTA: CT-angiography; DAP: dose–area product; eGFR: estimated glomerular filtration rate; EVOH: ethylene-vinyl alcohol; INR: international normalized ratio; MODS: multiple organ dysfunction syndrome; NALEA: non-adhesive liquid embolic agent; NBCA: N-butyl cyanoacrylate; PT: prothrombin time; PVA: polyvinyl alcohol; SIR: Society of Interventional Radiology; TAE: transcatheter arterial embolization; VASCs: vascular access site complications; XA: X-ray angiography.
Author Contributions
Conceptualization, R.M. and D.L.; methodology, R.M. and D.L.; software, M.V.; validation, R.M., D.L., F.F., M.V., G.G., A.C., F.P., B.B., R.S. (Raffaele Serra), R.S. (Rita Santoro), D.C., N.I., P.G., B.A., MGJR Research Team, L.B. and M.S.; formal analysis, A.C. and F.P.; investigation, R.S. (Raffaele Serra), D.C. and N.I.; resources, P.G. and B.A.; data curation, D.L.; writing—original draft preparation, R.M., D.L., F.F., M.V., G.G., A.C., F.P., B.B., R.S. (Raffaele Serra), R.S. (Rita Santoro), D.C., N.I., P.G., B.A., MGJR Research Team, L.B. and M.S.; writing—review and editing, L.B. and MGJR Research Team; visualization, R.M., D.L., F.F., M.V., G.G., A.C., F.P., B.B., R.S. (Raffaele Serra), R.S. (Rita Santoro), D.C., N.I., P.G., B.A., MGJR Research Team, L.B. and M.S.; supervision, D.L. All authors have read and agreed to the published version of the manuscript.
Institutional Review Board Statement
Ethical review and approval were waived for this study due to the retrospective nature of the investigation.
Informed Consent Statement
Informed consent was obtained from all patients undergoing endovascular treatment.
Data Availability Statement
The data presented in this study are available on request from the corresponding author. The data are not publicly available due to privacy issues.
Conflicts of Interest
The authors declare no conflict of interest.
Funding Statement
This research received no external funding.
Footnotes
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.
References
- 1.Valek V., Husty J. Quality improvement guidelines for transcatheter embolization for acute gastrointestinal nonvariceal hemorrhage. Cardiovasc. Interv. Radiol. 2013;36:608–612. doi: 10.1007/s00270-012-0462-5. [DOI] [PubMed] [Google Scholar]
- 2.Angle J.F., Siddiqi N.H., Wallace M.J., Kundu S., Stokes L., Wojak J.C., Cardella J.F. Society of Interventional Radiology Standards of Practice Committee Quality improvement guidelines for percutaneous transcatheter embolization: Society of Interventional Radiology Standards of Practice Committee. J. Vasc. Interv. Radiol. 2010;21:1479–1486. doi: 10.1016/j.jvir.2010.06.014. [DOI] [PubMed] [Google Scholar]
- 3.Chakraverty S., Flood K., Kessel D., McPherson S., Nicholson T., Ray C.E., Robertson I., van Delden O.M. CIRSE guidelines: Quality improvement guidelines for endovascular treatment of traumatic hemorrhage. Cardiovasc. Interv. Radiol. 2012;35:472–482. doi: 10.1007/s00270-012-0339-7. [DOI] [PubMed] [Google Scholar]
- 4.Loffroy R., Guiu B., D’Athis P., Mezzetta L., Gagnaire A., Jouve J.-L., Ortega-Deballon P., Cheynel N., Cercueil J.-P., Krausé D. Arterial embolotherapy for endoscopically unmanageable acute gastroduodenal hemorrhage: Predictors of early rebleeding. Clin. Gastroenterol. Hepatol. 2009;7:515–523. doi: 10.1016/j.cgh.2009.02.003. [DOI] [PubMed] [Google Scholar]
- 5.Loffroy R., Guiu B. Role of transcatheter arterial embolization for massive bleeding from gastroduodenal ulcers. World J. Gastroenterol. 2009;15:5889–5897. doi: 10.3748/wjg.15.5889. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Sapoval M., Vidal V., Déan C., Del Giudice C., Tradi F., Chevallier O., Charles-Nelson A., Pellerin O., Loffroy R. Safety and Efficacy of Peripheral Embolization with EASYX Liquid Embolic Agent: A Multicenter Prospective Study. J. Vasc. Interv. Radiol. 2021;32:1136–1143. doi: 10.1016/j.jvir.2021.05.014. [DOI] [PubMed] [Google Scholar]
- 7.Augustin A.M., Fluck F., Bley T., Kickuth R. Endovascular Therapy of Gastrointestinal Bleeding. Rofo. 2019;191:1073–1082. doi: 10.1055/a-0891-1116. [DOI] [PubMed] [Google Scholar]
- 8.Minici R., Venturini M., Fontana F., Guzzardi G., Pingitore A., Piacentino F., Serra R., Coppola A., Santoro R., Laganà D. Efficacy and Safety of Ethylene-Vinyl Alcohol (EVOH) Copolymer-Based Non-Adhesive Liquid Embolic Agents (NALEAs) in Transcatheter Arterial Embolization (TAE) of Acute Non-Neurovascular Bleeding: A Multicenter Retrospective Cohort Study. Medicina. 2023;59:710. doi: 10.3390/medicina59040710. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Valisena S., Abboud A.-E., Andereggen E., Ansorge A., Gamulin A. Management of high-energy blunt pelvic ring injuries: A retrospective cohort study evaluating an institutional protocol. Injury. 2022;53:4054–4061. doi: 10.1016/j.injury.2022.09.020. [DOI] [PubMed] [Google Scholar]
- 10.Tiralongo F., Seminatore S., Di Pietro S., Distefano G., Galioto F., Vacirca F., Giurazza F., Palmucci S., Venturini M., Scaglione M., et al. Spontaneous Retroperitoneal Hematoma Treated with Percutaneous Transarterial Embolization in COVID-19 Era: Diagnostic Findings and Procedural Outcome. Tomography. 2022;8:1228–1240. doi: 10.3390/tomography8030101. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Lucatelli P., Corona M., Teodoli L., Nardis P., Cannavale A., Rocco B., Trobiani C., Cipollari S., Zilahi de Gyurgyokai S., Bezzi M., et al. Use of Phil Embolic Agent for Bleeding in Non-Neurological Interventions. J. Clin. Med. 2021;10:701. doi: 10.3390/jcm10040701. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Ling G., Zhou J., Ding X., Long Q. Emergency Transcatheter Arterial Embolization for Acute Mediastinal Hemorrhage. Thorac. Cardiovasc. Surg. 2022;70:652–657. doi: 10.1055/s-0041-1735827. [DOI] [PubMed] [Google Scholar]
- 13.Kettenbach J., Ittrich H., Gaubert J.Y., Gebauer B., Vos J.A. CIRSE Standards of Practice on Bronchial Artery Embolisation. Cardiovasc. Interv. Radiol. 2022;45:721–732. doi: 10.1007/s00270-022-03127-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Pecoraro F., Dinoto E., Bracale U.M., Badalamenti G., Farina A., Bajardi G. Symptomatic Deep Femoral Artery Pseudoaneurysm Endovascular Exclusion. Case Report and Literature Review. Ann. Vasc. Surg. 2017;42:303.e5–303.e9. doi: 10.1016/j.avsg.2016.11.026. [DOI] [PubMed] [Google Scholar]
- 15.Kim P.H., Tsauo J., Shin J.H., Yun S.-C. Transcatheter Arterial Embolization of Gastrointestinal Bleeding with N-Butyl Cyanoacrylate: A Systematic Review and Meta-Analysis of Safety and Efficacy. J. Vasc. Interv. Radiol. 2017;28:522–531.e5. doi: 10.1016/j.jvir.2016.12.1220. [DOI] [PubMed] [Google Scholar]
- 16.Pereira J., Phan T. Management of bleeding in patients with advanced cancer. Oncologist. 2004;9:561–570. doi: 10.1634/theoncologist.9-5-561. [DOI] [PubMed] [Google Scholar]
- 17.Johnstone C., Rich S.E. Bleeding in cancer patients and its treatment: A review. Ann. Palliat. Med. 2018;7:265–273. doi: 10.21037/apm.2017.11.01. [DOI] [PubMed] [Google Scholar]
- 18.Bassi N., Caratozzolo E., Bonariol L., Ruffolo C., Bridda A., Padoan L., Antoniutti M., Massani M. Management of ruptured hepatocellular carcinoma: Implications for therapy. World J. Gastroenterol. 2010;16:1221–1225. doi: 10.3748/wjg.v16.i10.1221. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Spiliopoulos S., Katsanos K., Paraskevopoulos I., Mariappan M., Festas G., Kitrou P., Papageorgiou C., Reppas L., Palialexis K., Karnabatidis D., et al. Multicenter retrospective study of transcatheter arterial embolisation for life-threatening haemorrhage in patients with uncorrected bleeding diathesis. CVIR Endovasc. 2020;3:95. doi: 10.1186/s42155-020-00186-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Hiraki S., Sato F., Osugi M., Watanabe Y., Ichinose Y. Transcatheter arterial embolization for acute lower gastrointestinal bleeding using imipenem/cilastatin: A single-center retrospective study. CVIR Endovasc. 2023;6:12. doi: 10.1186/s42155-023-00359-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Becce F., Richarme D., Omoumi P., Djahangiri A., Farron A., Meuli R., Theumann N. Direct MR arthrography of the shoulder under axial traction: Feasibility study to evaluate the superior labrum-biceps tendon complex and articular cartilage. J. Magn. Reson. Imaging. 2013;37:1228–1233. doi: 10.1002/jmri.23824. [DOI] [PubMed] [Google Scholar]
- 22.McGraw J.R., Kiefer R.M., Shah A., Clark T.W.I., Shlansky-Goldberg R.D., Nadolski G.J., Hunt S.J., Gade T.P. Outcomes of Transarterial Embolization for Acute Nonvariceal Upper Gastrointestinal Bleeding: Correlation with Periprocedural Endoscopy. J. Vasc. Interv. Radiol. 2023;34:1062–1069. doi: 10.1016/j.jvir.2023.01.026. [DOI] [PubMed] [Google Scholar]
- 23.Alrashidi I., Kim T.-H., Shin J.H., Alreshidi M., Park M., Jang E.B. Efficacy and safety of transcatheter arterial embolization for active arterial esophageal bleeding: A single-center experience. Diagn. Interv. Radiol. 2021;27:519–523. doi: 10.5152/dir.2021.20253. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Ephraim Joseph K., Devane A.M., Abrams G.A. Patient and endoscopic characteristics and clinical outcomes in subjects with non-variceal GI bleeding referred for transarterial embolization: A single-center experience. Abdom. Radiol. 2022;47:3883–3891. doi: 10.1007/s00261-022-03650-x. [DOI] [PubMed] [Google Scholar]
- 25.Kim Y.S., Kwon J.H., Han K., Kim M.-D., Lee J., Kim G.M., Won J.Y. Superselective transcatheter arterial embolization for acute small bowel bleeding: Clinical outcomes and prognostic factors for ischemic complications. Acta Radiol. 2021;62:574–583. doi: 10.1177/0284185120936258. [DOI] [PubMed] [Google Scholar]
- 26.Kuellmer A., Mangold T., Bettinger D., Maruschke L., Wannhoff A., Caca K., Wedi E., Hosseini A.S.A., Kleemann T., Schulz T., et al. Over-the-scope clip versus transcatheter arterial embolization for refractory peptic ulcer bleeding-A propensity score matched analysis. United Eur. Gastroenterol. J. 2021;9:1048–1056. doi: 10.1002/ueg2.12135. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Fontana F., Piacentino F., Ossola C., Coppola A., Curti M., Macchi E., De Marchi G., Floridi C., Ierardi A.M., Carrafiello G., et al. Transcatheter Arterial Embolization in Acute Non-Variceal Gastrointestinal Bleedings: A Ten-Year Single-Center Experience in 91 Patients and Review of the Literature. J. Clin. Med. 2021;10:4979. doi: 10.3390/jcm10214979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Minici R., Siciliano M.A., Ammendola M., Santoro R.C., Barbieri V., Ranieri G., Laganà D. Prognostic Role of Neutrophil-to-Lymphocyte Ratio (NLR), Lymphocyte-to-Monocyte Ratio (LMR), Platelet-to-Lymphocyte Ratio (PLR) and Lymphocyte-to-C Reactive Protein Ratio (LCR) in Patients with Hepatocellular Carcinoma (HCC) undergoing Chemoembolizations (TACE) of the Liver: The Unexplored Corner Linking Tumor Microenvironment, Biomarkers and Interventional Radiology. Cancers. 2022;15:257. doi: 10.3390/cancers15010257. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Kinoshita M., Kondo H., Hitomi S., Hara T., Zako R., Yamamoto M., Hiraoka J., Takaoka Y., Enomoto H., Matsunaga N., et al. Ultraselective transcatheter arterial embolization with small-sized microcoils for acute lower gastrointestinal bleeding. CVIR Endovasc. 2021;4:28. doi: 10.1186/s42155-021-00215-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Ini’ C., Distefano G., Sanfilippo F., Castiglione D.G., Falsaperla D., Giurazza F., Mosconi C., Tiralongo F., Foti P.V., Palmucci S., et al. Embolization for acute nonvariceal bleeding of upper and lower gastrointestinal tract: A systematic review. CVIR Endovasc. 2023;6:18. doi: 10.1186/s42155-023-00360-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Patidar Y., Srinivasan S.V., Singh J., Patel R.K., Chandel K., Mukund A., Sharma M.K., Sarin S.K. Clinical Outcomes of Transcatheter Arterial Embolization Using N-butyl-2-cyanoacrylate (NBCA) in Cirrhotic Patients. J. Clin. Exp. Hepatol. 2022;12:353–361. doi: 10.1016/j.jceh.2021.07.014. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Yonemitsu T., Kawai N., Sato M., Tanihata H., Takasaka I., Nakai M., Minamiguchi H., Sahara S., Iwasaki Y., Shima Y., et al. Evaluation of transcatheter arterial embolization with gelatin sponge particles, microcoils, and n-butyl cyanoacrylate for acute arterial bleeding in a coagulopathic condition. J. Vasc. Interv. Radiol. 2009;20:1176–1187. doi: 10.1016/j.jvir.2009.06.005. [DOI] [PubMed] [Google Scholar]
- 33.Hadi M., Walker C., Desborough M., Basile A., Tsetis D., Hunt B., Müller-Hüllsbeck S., Rand T., van Delden O., Uberoi R. CIRSE Standards of Practice on Peri-operative Anticoagulation Management During Interventional Radiology Procedures. Cardiovasc. Interv. Radiol. 2021;44:523–536. doi: 10.1007/s00270-020-02763-4. [DOI] [PubMed] [Google Scholar]
- 34.Patel I.J., Rahim S., Davidson J.C., Hanks S.E., Tam A.L., Walker T.G., Wilkins L.R., Sarode R., Weinberg I. Society of Interventional Radiology Consensus Guidelines for the Periprocedural Management of Thrombotic and Bleeding Risk in Patients Undergoing Percutaneous Image-Guided Interventions—Part II: Recommendations: Endorsed by the Canadian Association for Interventional Radiology and the Cardiovascular and Interventional Radiological Society of Europe. J. Vasc. Interv. Radiol. 2019;30:1168–1184.e1. doi: 10.1016/j.jvir.2019.04.017. [DOI] [PubMed] [Google Scholar]
- 35.Davidson J.C., Rahim S., Hanks S.E., Patel I.J., Tam A.L., Walker T.G., Weinberg I., Wilkins L.R., Sarode R. Society of Interventional Radiology Consensus Guidelines for the Periprocedural Management of Thrombotic and Bleeding Risk in Patients Undergoing Percutaneous Image-Guided Interventions-Part I: Review of Anticoagulation Agents and Clinical Considerations: Endorsed by the Canadian Association for Interventional Radiology and the Cardiovascular and Interventional Radiological Society of Europe. J. Vasc. Interv. Radiol. 2019;30:1155–1167. doi: 10.1016/j.jvir.2019.04.016. [DOI] [PubMed] [Google Scholar]
- 36.Spiliopoulos S., Festas G., Theodosis A., Palialexis K., Reppas L., Konstantos C., Brountzos E. Incidence and endovascular treatment of severe spontaneous non-cerebral bleeding: A single-institution experience. Eur. Radiol. 2019;29:3296–3307. doi: 10.1007/s00330-018-5869-1. [DOI] [PubMed] [Google Scholar]
- 37.Maegele M. The Diagnosis and Treatment of Acute Traumatic Bleeding and Coagulopathy. Dtsch. Ärzteblatt Int. 2019;116:799–806. doi: 10.3238/arztebl.2019.0799. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Lee S., Kim T., Han S.C., Pak H., Jeon H.H. Transcatheter arterial embolization for gastrointestinal bleeding: Clinical outcomes and prognostic factors predicting mortality. Medicine. 2022;101:e29342. doi: 10.1097/MD.0000000000029342. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Hur S., Jae H.J., Lee M., Kim H.-C., Chung J.W. Safety and Efficacy of Transcatheter Arterial Embolization for Lower Gastrointestinal Bleeding: A Single-center Experience with 112 Patients. J. Vasc. Interv. Radiol. 2014;25:10–19. doi: 10.1016/j.jvir.2013.09.012. [DOI] [PubMed] [Google Scholar]
- 40.Tipaldi M.A., Orgera G., Krokidis M., Rebonato A., Maiettini D., Vagnarelli S., Ambrogi C., Rossi M. Trans Arterial Embolization of Non-variceal Upper Gastrointestinal Bleeding: Is the Use of Ethylene-Vinyl Alcohol Copolymer as Safe as Coils? Cardiovasc. Interv. Radiol. 2018;41:1340–1345. doi: 10.1007/s00270-018-1981-5. [DOI] [PubMed] [Google Scholar]
- 41.Yonemitsu T., Kawai N., Sato M., Sonomura T., Takasaka I., Nakai M., Minamiguchi H., Sahara S., Iwasaki Y., Naka T., et al. Comparison of hemostatic durability between N-butyl cyanoacrylate and gelatin sponge particles in transcatheter arterial embolization for acute arterial hemorrhage in a coagulopathic condition in a swine model. Cardiovasc. Interv. Radiol. 2010;33:1192–1197. doi: 10.1007/s00270-010-9863-5. [DOI] [PubMed] [Google Scholar]
- 42.Huang Y.-S., Chang C.-C., Liou J.-M., Jaw F.-S., Liu K.-L. Transcatheter arterial embolization with N-butyl cyanoacrylate for nonvariceal upper gastrointestinal bleeding in hemodynamically unstable patients: Results and predictors of clinical outcomes. J. Vasc. Interv. Radiol. 2014;25:1850–1857. doi: 10.1016/j.jvir.2014.08.005. [DOI] [PubMed] [Google Scholar]
- 43.Abdulmalak G., Chevallier O., Falvo N., Di Marco L., Bertaut A., Moulin B., Abi-Khalil C., Gehin S., Charles P.-E., Latournerie M., et al. Safety and efficacy of transcatheter embolization with Glubran®2 cyanoacrylate glue for acute arterial bleeding: A single-center experience with 104 patients. Abdom. Radiol. 2018;43:723–733. doi: 10.1007/s00261-017-1267-4. [DOI] [PubMed] [Google Scholar]
- 44.Shi Z.X., Yang J., Liang H.W., Cai Z.H., Bai B. Emergency transcatheter arterial embolization for massive gastrointestinal arterial hemorrhage. Medicine. 2017;96:e9437. doi: 10.1097/MD.0000000000009437. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.Riu P., Albarello F., Di Stefano F., Vergori A., D’Abramo A., Cerini C., Nocioni M., Morucci M., Tetaj N., Cristofaro M., et al. Management of Spontaneous Bleeding in COVID-19 Inpatients: Is Embolization Always Needed? J. Clin. Med. 2021;10:4119. doi: 10.3390/jcm10184119. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46.Trentadue M., Calligaro P., Lazzarini G., Boseggia F.B., Residori E., Hu J., Vanti S., Lillo L., Varischi G., Cerini R. Spontaneous bleeding in COVID-19: A retrospective experience of an Italian COVID-19 hospital. SA J. Radiol. 2022;26:2509. doi: 10.4102/sajr.v26i1.2509. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47.Spiliopoulos S., Inchingolo R., Lucatelli P., Iezzi R., Diamantopoulos A., Posa A., Barry B., Ricci C., Cini M., Konstantos C., et al. Transcatheter Arterial Embolization for Bleeding Peptic Ulcers: A Multicenter Study. Cardiovasc. Interv. Radiol. 2018;41:1333–1339. doi: 10.1007/s00270-018-1966-4. [DOI] [PubMed] [Google Scholar]
- 48.Di Pietro S., Tiralongo F., Desiderio C.M., Vacirca F., Palmucci S., Giurazza F., Venturini M., Basile A. Efficacy of Percutaneous Transarterial Embolization in Patients with Spontaneous Abdominal Wall Hematoma and Comparison between Blind and Targeted Embolization Approaches. J. Clin. Med. 2022;11:1270. doi: 10.3390/jcm11051270. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Dohan A., Darnige L., Sapoval M., Pellerin O. Spontaneous soft tissue hematomas. Diagn. Interv. Imaging. 2015;96:789–796. doi: 10.1016/j.diii.2015.03.014. [DOI] [PubMed] [Google Scholar]
- 50.Thachil J., Tang N., Gando S., Falanga A., Cattaneo M., Levi M., Clark C., Iba T. ISTH interim guidance on recognition and management of coagulopathy in COVID-19. J. Thromb. Haemost. 2020;18:1023–1026. doi: 10.1111/jth.14810. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 51.Hayakawa M. Pathophysiology of trauma-induced coagulopathy: Disseminated intravascular coagulation with the fibrinolytic phenotype. J. Intensive Care. 2017;5:14. doi: 10.1186/s40560-016-0200-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Moore E.E., Moore H.B., Kornblith L.Z., Neal M.D., Hoffman M., Mutch N.J., Schöchl H., Hunt B.J., Sauaia A. Trauma-induced coagulopathy. Nat. Rev. Dis. Primers. 2021;7:30. doi: 10.1038/s41572-021-00264-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 53.Jaffe T.A., Raiff D., Ho L.M., Kim C.Y. Management of Anticoagulant and Antiplatelet Medications in Adults Undergoing Percutaneous Interventions. AJR Am. J. Roentgenol. 2015;205:421–428. doi: 10.2214/AJR.14.13342. [DOI] [PubMed] [Google Scholar]
- 54.Baron T.H., Kamath P.S., McBane R.D. Management of antithrombotic therapy in patients undergoing invasive procedures. N. Engl. J. Med. 2013;368:2113–2124. doi: 10.1056/NEJMra1206531. [DOI] [PubMed] [Google Scholar]
- 55.Loffroy R., Guillen K., Chevallier O. Is CT scan needed before transcatheter arterial embolisation of upper gastrointestinal bleeding following endoscopic resection? Br. J. Radiol. 2022;95:20210573. doi: 10.1259/bjr.20210573. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 56.Ierardi A.M., Wood B.J., Gaudino C., Angileri S.A., Jones E.C., Hausegger K., Carrafiello G. How to Handle a COVID-19 Patient in the Angiographic Suite. Cardiovasc. Interv. Radiol. 2020;43:820. doi: 10.1007/s00270-020-02476-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 57.Sacks D., McClenny T.E., Cardella J.F., Lewis C.A. Society of Interventional Radiology Clinical Practice Guidelines. J. Vasc. Interv. Radiol. 2003;14:S199–S202. doi: 10.1097/01.RVI.0000094584.83406.3e. [DOI] [PubMed] [Google Scholar]
- 58.Dariushnia S.R., Redstone E.A., Heran M.K.S., Cramer H.R., Ganguli S., Gomes A.S., Hogan M.J., Himes E.A., Patel S., Schiro B.J., et al. Society of Interventional Radiology Quality Improvement Standards for Percutaneous Transcatheter Embolization. J. Vasc. Interv. Radiol. 2021;32:476.e1–476.e33. doi: 10.1016/j.jvir.2020.10.022. [DOI] [PubMed] [Google Scholar]
- 59.Khalilzadeh O., Baerlocher M.O., Shyn P.B., Connolly B.L., Devane A.M., Morris C.S., Cohen A.M., Midia M., Thornton R.H., Gross K., et al. Proposal of a New Adverse Event Classification by the Society of Interventional Radiology Standards of Practice Committee. J. Vasc. Interv. Radiol. 2017;28:1432–1437.e3. doi: 10.1016/j.jvir.2017.06.019. [DOI] [PubMed] [Google Scholar]
- 60.Filippiadis D.K., Binkert C., Pellerin O., Hoffmann R.T., Krajina A., Pereira P.L. Cirse Quality Assurance Document and Standards for Classification of Complications: The Cirse Classification System. Cardiovasc. Interv. Radiol. 2017;40:1141–1146. doi: 10.1007/s00270-017-1703-4. [DOI] [PubMed] [Google Scholar]
- 61.Minici R., Ammendola M., Manti F., Siciliano M.A., Minici M., Komaei I., Currò G., Laganà D. Safety and Efficacy of Degradable Starch Microspheres Transcatheter Arterial Chemoembolization (DSM-TACE) in the Downstaging of Intermediate-Stage Hepatocellular Carcinoma (HCC) in Patients With a Child-Pugh Score of 8-9. Front. Pharmacol. 2021;12:634087. doi: 10.3389/fphar.2021.634087. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 62.Minici R., Ammendola M., Manti F., Siciliano M.A., Giglio E., Minici M., Melina M., Currò G., Laganà D. Safety and Efficacy of Degradable Starch Microspheres Transcatheter Arterial Chemoembolization as a Bridging Therapy in Patients with Early Stage Hepatocellular Carcinoma and Child-Pugh Stage B Eligible for Liver Transplant. Front. Pharmacol. 2021;12:634084. doi: 10.3389/fphar.2021.634084. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 63.Minici R., Mercurio M., Iannò B., Galasso O., Gasparini G., Laganà D. Advantages of the Use of Axial Traction Magnetic Resonance Imaging (MRI) of the Shoulder in Patients with Suspected Rota-Tor Cuff Tears: An Exploratory Pilot Study. Healthcare. 2023;11:724. doi: 10.3390/healthcare11050724. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 64.Cernigliaro M., Stanca C., Galbiati A., Spinetta M., Coda C., Negroni D., Laganà D., Minici R., Airoldi C., Carriero A., et al. Innovation in Acute Ischemic Stroke Patients over 80 y/o—A Retrospective Monocentric Study on Mechanical Thrombectomy of Consecutive Patients: Is Age an Adequate Selection Criterion? J. Clin. Med. 2023;12:3688. doi: 10.3390/jcm12113688. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 65.Ammendola M., Filice F., Battaglia C., Romano R., Manti F., Minici R., de’Angelis N., Memeo R., Laganà D., Navarra G., et al. Left hemicolectomy and low anterior resection in colorectal cancer patients: Knight-griffen vs. transanal purse-string suture anastomosis with no-coil placement. Front. Surg. 2023;10:1093347. doi: 10.3389/fsurg.2023.1093347. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 66.Costa D., Ielapi N., Minici R., Peluso A., Bracale U.M., Andreucci M., Serra R. Risk Factors for Bleeding Varicose Veins in Patients with Chronic Venous Disease. Medicina. 2023;59:1034. doi: 10.3390/medicina59061034. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 67.Rossi R., Talarico M., Schepis F., Coppi F., Sgura F.A., Monopoli D.E., Minici R., Boriani G. Effects of sildenafil on right ventricle remodelling in Portopulmonary hypertension. Pulm. Pharmacol. Ther. 2021;70:102071. doi: 10.1016/j.pupt.2021.102071. [DOI] [PubMed] [Google Scholar]
- 68.Rossi R., Talarico M., Pascale A., Pascale V., Minici R., Boriani G. Low Levels of Vitamin D and Silent Myocardial Ischemia in Type 2 Diabetes: Clinical Correlations and Prognostic Significance. Diagnostics. 2022;12:2572. doi: 10.3390/diagnostics12112572. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 69.Jae H.J., Chung J.W., Jung A.Y., Lee W., Park J.H. Transcatheter arterial embolization of nonvariceal upper gastrointestinal bleeding with N-butyl cyanoacrylate. Korean J. Radiol. 2007;8:48–56. doi: 10.3348/kjr.2007.8.1.48. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 70.Encarnacion C.E., Kadir S., Beam C.A., Payne C.S. Gastrointestinal bleeding: Treatment with gastrointestinal arterial embolization. Radiology. 1992;183:505–508. doi: 10.1148/radiology.183.2.1561358. [DOI] [PubMed] [Google Scholar]
- 71.Schenker M.P., Duszak R., Soulen M.C., Smith K.P., Baum R.A., Cope C., Freiman D.B., Roberts D.A., Shlansky-Goldberg R.D. Upper gastrointestinal hemorrhage and transcatheter embolotherapy: Clinical and technical factors impacting success and survival. J. Vasc. Interv. Radiol. 2001;12:1263–1271. doi: 10.1016/S1051-0443(07)61549-8. [DOI] [PubMed] [Google Scholar]
- 72.Aina R., Oliva V.L., Therasse E., Perreault P., Bui B.T., Dufresne M.P., Soulez G. Arterial embolotherapy for upper gastrointestinal hemorrhage: Outcome assessment. J. Vasc. Interv. Radiol. 2001;12:195–200. doi: 10.1016/S1051-0443(07)61825-9. [DOI] [PubMed] [Google Scholar]
- 73.Minici R., Ammendola M., Talarico M., Luposella M., Minici M., Ciranni S., Guzzardi G., Laganà D. Endovascular recanalization of chronic total occlusions of the native superficial femoral artery after failed femoropopliteal bypass in patients with critical limb ischemia. CVIR Endovasc. 2021;4:68. doi: 10.1186/s42155-021-00256-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 74.Né R., Chevallier O., Falvo N., Facy O., Berthod P.-E., Galland C., Gehin S., Midulla M., Loffroy R. Embolization with ethylene vinyl alcohol copolymer (Onyx®) for peripheral hemostatic and non-hemostatic applications: A feasibility and safety study. Quant. Imaging Med. Surg. 2018;8:280–290. doi: 10.21037/qims.2018.04.03. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 75.Minici R., Paone S., Talarico M., Zappia L., Abdalla K., Petullà M., Laganà D. Percutaneous treatment of vascular access-site complications: A ten years’ experience in two centres. CVIR Endovasc. 2020;3:29. doi: 10.1186/s42155-020-00120-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 76.Minici R., Guzzardi G., Venturini M., Fontana F., Coppola A., Spinetta M., Piacentino F., Pingitore A., Serra R., Costa D., et al. Transcatheter Arterial Embolization (TAE) of Cancer-Related Bleeding. Medicina. 2023;59:1323. doi: 10.3390/medicina59071323. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 77.Sun C.J., Wang C.E., Wang Y.H., Xie L.L., Liu T.H., Ren W.C. Transcatheter arterial embolization of acute gastrointestinal tumor hemorrhage with Onyx. Indian J. Cancer. 2015;51((Suppl. 2)):e56–e59. doi: 10.4103/0019-509X.151988. [DOI] [PubMed] [Google Scholar]
- 78.Minici R., Serra R., Ierardi A.M., Petullà M., Bracale U.M., Carrafiello G., Laganà D. Thoracic endovascular repair for blunt traumatic thoracic aortic injury: Long-term results. Vascular. 2022;0:17085381221127740. doi: 10.1177/17085381221127740. [DOI] [PubMed] [Google Scholar]
- 79.Minici R., Serra R., Giurdanella M., Talarico M., Siciliano M.A., Carrafiello G., Laganà D. Efficacy and Safety of Distal Radial Access for Transcatheter Arterial Chemoembolization (TACE) of the Liver. J. Pers. Med. 2023;13:640. doi: 10.3390/jpm13040640. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 80.Bracale U.M., Peluso A., Panagrosso M., Cecere F., Del Guercio L., Minici R., Giannotta N., Ielapi N., Licastro N., Serraino G.F., et al. Ankle-Brachial Index evaluation in totally percutaneous approach vs. femoral artery cutdown for endovascular aortic repair of abdominal aortic aneurysms. Chirurgia. 2022;35:349–354. doi: 10.23736/S0394-9508.22.05381-5. [DOI] [Google Scholar]
- 81.Patel I.J., Davidson J.C., Nikolic B., Salazar G.M., Schwartzberg M.S., Walker T.G., Saad W.A. Standards of Practice Committee, with Cardiovascular and Interventional Radiological Society of Europe (CIRSE) Endorsement Consensus guidelines for periprocedural management of coagulation status and hemostasis risk in percutaneous image-guided interventions. J. Vasc. Interv. Radiol. 2012;23:727–736. doi: 10.1016/j.jvir.2012.02.012. [DOI] [PubMed] [Google Scholar]
- 82.Park S., Shin J.H., Gwon D.-I., Kim H.J., Sung K.-B., Yoon H.-K., Ko G.-Y., Ko H.K. Transcatheter Arterial Embolization for Gastrointestinal Bleeding Associated with Gastric Carcinoma: Prognostic Factors Predicting Successful Hemostasis and Survival. J. Vasc. Interv. Radiol. 2017;28:1012–1021. doi: 10.1016/j.jvir.2017.03.017. [DOI] [PubMed] [Google Scholar]
- 83.Loffroy R., Rao P., Ota S., De Lin M., Kwak B.-K., Geschwind J.-F. Embolization of acute nonvariceal upper gastrointestinal hemorrhage resistant to endoscopic treatment: Results and predictors of recurrent bleeding. Cardiovasc. Interv. Radiol. 2010;33:1088–1100. doi: 10.1007/s00270-010-9829-7. [DOI] [PubMed] [Google Scholar]
- 84.Lopera J.E. Embolization in trauma: Principles and techniques. Semin. Interv. Radiol. 2010;27:14–28. doi: 10.1055/s-0030-1247885. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 85.Minici R., Fontana F., Venturini M., Guzzardi G., Siciliano A., Piacentino F., Serra R., Coppola A., Guerriero P., Apollonio B., et al. Transcatheter Arterial Embolization (TAE) in the Management of Bleeding in the COVID-19 Patient. Medicina. 2023;59:1062. doi: 10.3390/medicina59061062. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 86.Ramaswamy R.S., Choi H.W., Mouser H.C., Narsinh K.H., McCammack K.C., Treesit T., Kinney T.B. Role of interventional radiology in the management of acute gastrointestinal bleeding. World J. Radiol. 2014;6:82–92. doi: 10.4329/wjr.v6.i4.82. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 87.López-Martínez L., Molina-Nuevo J.D., Pedrosa-Jiménez M.J., Juliá-Mollá E. Spontaneous Haematomas in Anticoagulated Covid-19 Patients: Diagnosis and Treatment by Embolization. Cardiovasc. Interv. Radiol. 2022;45:1001–1006. doi: 10.1007/s00270-021-03049-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 88.Piacentino F., Fontana F., Curti M., Macchi E., Coppola A., Ossola C., Giorgianni A., Marra P., Mosconi C., Ierardi A.M., et al. Non-Adhesive Liquid Embolic Agents in Extra-Cranial District: State of the Art and Review of the Literature. J. Clin. Med. 2021;10:4841. doi: 10.3390/jcm10214841. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 89.Vaidya S., Tozer K.R., Chen J. An overview of embolic agents. Semin. Interv. Radiol. 2008;25:204–215. doi: 10.1055/s-0028-1085930. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 90.Spies J.B., Cornell C., Worthington-Kirsch R., Lipman J.C., Benenati J.F. Long-term outcome from uterine fibroid embolization with tris-acryl gelatin microspheres: Results of a multicenter study. J. Vasc. Interv. Radiol. 2007;18:203–207. doi: 10.1016/j.jvir.2006.12.006. [DOI] [PubMed] [Google Scholar]
- 91.Toyoda H., Nakano S., Kumada T., Takeda I., Sugiyama K., Osada T., Kiriyama S. Estimation of usefulness of N-butyl-2-cyanoacrylate-lipiodol mixture in transcatheter arterial embolization for urgent control of life-threatening massive bleeding from gastric or duodenal ulcer. J. Gastroenterol. Hepatol. 1996;11:252–258. doi: 10.1111/j.1440-1746.1996.tb00071.x. [DOI] [PubMed] [Google Scholar]
- 92.Loffroy R., Guillen K., Chevallier O. Is Ethylene-Vinyl Alcohol Copolymer Really as Cost-Effective as N-Butyl Cyanoacrylate Glue for Transcatheter Arterial Embolization of Gastrointestinal Bleeding in the United States and Outside? Value Health. 2022;25:318–319. doi: 10.1016/j.jval.2021.05.015. [DOI] [PubMed] [Google Scholar]
- 93.Minici R., Serra R., Maglia C., Guzzardi G., Spinetta M., Fontana F., Venturini M., Laganà D. Efficacy and Safety of Axiostat® Hemostatic Dressing in Aiding Manual Compression Closure of the Femoral Arterial Access Site in Patients Undergoing Endovascular Treatments: A Preliminary Clinical Experience in Two Centers. J. Pers. Med. 2023;13:812. doi: 10.3390/jpm13050812. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 94.Minici R., Serra R., De Rosi N., Ciranni S., Talarico M., Petullà M., Guzzardi G., Fontana F., Laganà D. Endovascular treatment of femoro-popliteal occlusions with retrograde tibial access after failure of the antegrade approach. Catheter. Cardiovasc. Interv. 2023;101:1108–1119. doi: 10.1002/ccd.30654. [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The data presented in this study are available on request from the corresponding author. The data are not publicly available due to privacy issues.