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DOI: 10.1055/s-0044-1786755
Optimizing Venous Stenting: Consensus Recommendations for Enhanced Management of Lower Extremity Deep Vein Thrombosis
Abstract
Introduction Deep vein thrombosis (DVT) poses a complex challenge and often leads to postthrombotic syndrome (PTS), a debilitating complication. The emergence of venous stents offers a potential preventive avenue against this complication. This study aimed to provide consensus recommendations on the use of venous stent for DVT.
Materials and Methods From June to July 2023, 20 internal medicine, angiology and vascular surgery, and vascular and interventional radiology experts were involved in the Delphi process. Thirty-one recommendations, categorized into three thematic areas, were rigorously evaluated: indications for stent use, stent selection and placement, and monitoring and prevention of complications. Agreement was evaluated using a Likert scale, with consensus defined as agreement by two-thirds of the participants.
Results Consensus was reached for 23 (74.2%) of 31 recommendations. The agreement was centered on considerations, such as stent placement in specific acute DVT scenarios, emphasizing pivotal stent characteristics. However, there were divergences in the recommended stent length to prevent migration and stent characteristics based on iliocaval bifurcation morphology. Notably, there was no consensus on whether patients with DVT caused by a major transient risk factor need more than 3 months of anticoagulation therapy or whether aspirin should be added to anticoagulant treatment after venous stenting.
Conclusions These consensus recommendations offer practical insights into optimizing venous stent use to prevent PTS in DVT patients. Addressing the critical aspects of stent selection, placement, and postprocedural care, these recommendations contribute to clinical decision-making. The identified divergences underscore the importance of consensus and thus indicate the need for further investigation.
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Keywords
deep vein thrombosis - postthrombotic syndrome - endovascular interventions - venous stent - stenting - consensusVenous thrombosis is estimated to affect 1 in 1,000 people annually, with two-thirds presenting with deep vein thrombosis (DVT) and one-third presenting with pulmonary embolism.[1] In addition to diminished quality of life, which can be comparable to that of other chronic diseases in the short term,[2] DVT is associated with important complications, including pulmonary embolism and postthrombotic syndrome (PTS). PTS occurs in 20 to 50% of patients with DVT despite anticoagulant treatment and is severe in 5 to 10% of patients.[3] [4] [5] Moreover, DVT has a high recurrence rate, with a 5-year cumulative incidence of recurrent DVT of 21.5% after the first DVT and 27.9% after the second DVT.[6] It is associated with a 1-year all-cause mortality rate of 4.6 (3.8–5.7) and 8.0 (7.1–9.0) person-years for isolated distal DVT and proximal DVT, respectively.[7]
Strategies for managing DVT, including nonpharmacological and pharmacological strategies, are well delineated in the current clinical practice guidelines.[8] [9] [10] However, there are no well-established effective treatments for PTS. While elastic compression stockings and lifestyle measures such as elevating the legs, losing weight, and exercising may offer some relief, endovascular interventions are selectively employed due to limited available evidence.[11] It is crucial to emphasize that the cornerstone of PTS management lies in prevention.[5] [11]
Technical improvements in endovascular interventions have led to the increasing use of venous stenting for the management of venous obstruction in patients with acute or chronic DVT symptoms. In many cases, venous stenting serves as an adjuvant treatment alongside other endovascular interventions, such as catheter-directed thrombolysis.[12] [13] This intervention has also evolved with increasing clinical experience, improvements in venous imaging, and the approval of dedicated venous stents for iliac vein use by some regulatory authorities.[14] However, evidence supporting this procedure is scarce.[12] [13]
Only a few randomized clinical trials have assessed the efficacy of venous stenting for DVT management.[15] [16] [17] Information on the use of venous stenting and its complications in patients with acute or chronic DVT is largely based on observational studies, primarily consisting of case series and retrospective studies, as shown in recent systematic reviews.[18] [19] [20] [21] [22] [23] [24] [25]
In this context, a panel of experts from the Spanish Society of Internal Medicine, Spanish Society of Vascular and Interventional Radiology, and Spanish Society of Angiology and Vascular Surgery was assembled by the collaborating societies. We aimed to evaluate the available evidence and formulate specific recommendations regarding the indications, placement, follow-up, and prevention of complications associated with the use of venous stents for the management of DVT of the lower extremity.
Materials and methods
Development of the Questionnaire and Expert Selection
The project coordinator (J.T.S.) selected a group of six experts (two from each participating society) to assemble a scientific committee. Subsequently, the scientific committee identified and invited from the three participating societies 22 individuals with at least 5 years of experience in assessing the indications and/or managing and placing venous stents to participate in the Delphi consensus.
During a meeting held on April 13, 2023, the Scientific Committee, drawing upon their knowledge, clinical experience, and comprehensive review of the evidence, formulated a document containing 31 recommendations on the use of stents for the management of DVT. These recommendations were grouped into three overarching thematic areas: (1) indications for the use of venous stents, which, in turn, addressed patient profiles for whom the use of a stent is recommended (4 recommendations) and situations where stent usage should be avoided (3 recommendations); (2) stent selection and placement, which explored factors influencing stent selection (10 recommendations), necessary evaluations before stent insertion (1 recommendation), and considerations for stent deployment (3 recommendations); and (3) complication monitoring and prevention, with a focus on strategies to manage the conditions of patients after stent placement (10 recommendations).
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The Delphi method
The Delphi method is a frequently used system for collecting opinions on a specific issue in a structured manner from a group of experts.[26] It is used when evidence on that specific topic is very limited, and it has been applied to different health care contexts, including technology assessment and clinical practice development.[26] The key features of this method are the anonymous nature of the survey and the fact that participants receive feedback on their responses and can adjust their initial responses according to the feedback through an iterative process.[26] [27]
The participants were provided with a Microsoft Forms web link to complete the questionnaire. The participants scored each recommendation using a 9-point Likert scale, with 1 indicating strongly disagree and 9 indicating strongly agree. Additionally, participants had the option of including comments for each recommendation in a free-text field.
Two rounds of the Delphi method were completed. The questionnaire was administered in the first round. Recommendations lacking a consensus were discussed by the scientific committee. Based on this discussion, the recommendations with or without modifications (see below) proceeded to the second round of the Delphi. In the second round, participants received feedback on the overall results of the first round along with information about the individual responses.
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Statistical Analysis
The responses on the Likert scale were categorized into three groups: disagree (scores 1–3), neither agree nor disagree (scores 4–6), and agree (scores 7–9). For each recommendation, the absolute and relative frequencies were calculated for each Likert scale score. The median was also estimated as an indicator of the strength of the agreement, identifying the triad of responses within which the median fell. Consensus was determined to be achieved if two-thirds of the responses (66.6%) were within the triad.
The results are presented in summary tables with information on the round in which consensus was reached, the number of experts who responded to that recommendation in the respective round, the relative frequency of responses across the 9 points of the Likert scale, the proportion of consensuses reached, and the median ([Tables 1] [2] [3]). Recommendations with consensuses are highlighted by shading the triad of responses, in which the consensus is situated in gray.
Note: Values in %C are in bold when there was agreement
Abbreviations: DVT, deep vein thrombosis; % C, proportion of consensus; Agree, agreement; M, median; N, number of respondents.
Note: Values in %C are in bold when there was agreement
Abbreviations: CT, computed tomography; MRI, magnetic resonance imaging; % C, proportion of consensus; Agree, agreement; M, median; N, number of respondents.
Note: Values in %C are in bold when there was agreement
Abbreviations: DVT, deep vein thrombosis; % C, proportion of consensus; M, median; N, number of respondents.
Statistical analyses were performed using the IBM SPSS software package (IBM Corp. Released 2011, IBM SPSS Statistics for Windows, Version 20.0, Armonk, New York: IBM Corp.).
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Results
Overall Results
Finally, 20 of the 22 selected experts agreed to participate, with 8 specializing in internal medicine, 8 specializing in angiology and vascular surgery and 4 specializing in vascular and interventional radiology. Ten of the 20 experts that agreed to participate had more than 15 years of experience, 6 had 10 to 15 years of experience and 4 had 5 to 10 years of experience.
The first round of the Delphi method was conducted in June 2023, during which all 20 selected experts provided responses. Overall, a consensus was reached on 19 (61.3%) of the 31 recommendations. Among the 12 recommendations lacking consensus ([Supplementary Table S1], available in the online version only), 2 originated from the section on indications for the use of venous stents (2 of 7), 5 from the stent selection and placement section (5 of 14), and 5 from the monitoring and prevention of complications section (5 of 10). The Scientific Committee convened to scrutinize these items and modified the wording of six of them ([Supplementary Table S1]).
Subsequently, these 12 recommendations were included in the second round of the Delphi in July 2023, with responses from the same 20 selected experts. Among the 12 recommendations evaluated in this round, a consensus was reached on four ([Tables 1] [2] [3]). Overall, a consensus was thus reached for 23 of the 31 recommendations (74.2%) ([Table 4]). The combined results of the two rounds are presented below.
Abbreviations: CT, computed tomography; DVT, deep vein thrombosis; MRI, magnetic resonance imaging.
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Indications for the Use of Venous Stents
After these two rounds, consensus was achieved on six of the seven recommendations in this section ([Table 1]). It was collectively agreed that the use of stents can be considered for patients with acute DVT caused by compression involving at least the iliac vein, and who present with severe symptoms and exhibit a favorable prior functional state. Additionally, a consensus was reached for patients with persistent severe symptoms despite initial anticoagulation treatment following thrombolysis (mechanical or pharmacomechanical) (median: 9). Furthermore, consensus extended to use of stents in individuals with chronic DVT of both compressive (median: 9) and noncompressive causes (median: 8), with iliac involvement and experiencing moderate to severe PTS with significant impact on patients' quality of life. However, there was no consensus regarding the use of stents in patients with acute DVT of noncompressive causes. Although proximity to agreement was observed (median: 8), a predefined level of consensus was not reached, with 65% agreement and three experts disagreeing.
There was a consensus that stent placement should be avoided in patients with acute or chronic DVT exhibiting isolated involvement of the femoral, popliteal, or calf muscle veins (median: 9) or in the presence of an active infectious disease (median: 9). Furthermore, a consensus was reached among experts that stent placement should be avoided in children (median: 8).
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Stent Selection and Placement
Among the 14 recommendations in this section, consensus was reached on 10 ([Table 2]).
Experts considered an intravascular ultrasound (IVUS) study to be very useful in determining the necessary stent characteristics, such as caliber and length, positioning, and intraoperative control of the implant (median: 9). A consensus was established for various stent attributes, including great flexibility, radial strength, and high resistance (median: 9); a diameter at least 20% greater than that of the vein (median: 8); a standard recommended diameter of 14 to 16 mm for the iliac axis (median: 9); and a standard diameter of 12 to 14 mm for the iliofemoral axis (median: 9). Additionally, there was consensus that the stent should allow good visibility to enhance precision during implantation (median: 9) and should facilitate easy and precise release to prevent migration (median: 9). However, there was no consensus on the notion that to prevent migration, an implant should be at least 80 mm long (median: 8). In this regard, 35% of the experts were indifferent, although they leaned toward agreement. There was also no consensus on stent characteristics based on whether the iliocaval bifurcation exhibited a vertical morphology (median: 8) or a more horizontal morphology (median: 7); nevertheless, 65% agreed with both statements.
Experts unanimously agreed that for the evaluation preceding venous stent placement, in addition to Doppler ultrasound, an axial imaging test with contrast agent (such as computed tomography [CT], CT phlebography, magnetic resonance imaging [MRI], or venography) should be recommended for visualizing the iliofemoral venous axis (median: 9).
Regarding stent placement, a consensus emerged that when the inguinal ligament is crossed, it is recommended that two stents do not overlap at that level and that only a single stent should make contact with it (median: 8). Furthermore, interference at the iliocaval confluence in contralateral iliac flow should be avoided (median: 8). However, there was no consensus on the consideration of endophlebectomy and its association with a temporal arteriovenous fistula if severe involvement of the common femoral vein encompassing the ostia of the deep femoral vein and its branches is present (median: 7). In this particular recommendation, seven respondents positioned themselves at the midpoint of the scale, indicating a neutral stance.
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Monitoring and Prevention of Complications
Among the 10 recommendations in this section, a consensus was reached for 7 ([Table 3]).
Concerning anticoagulation therapy, there was a consensus that it should be started early or immediately after stent implantation (median: 9). The consensus further extended to the preference for initial treatment with low-molecular-weight heparin (median: 8). Prolonged anticoagulation was recommended for at least the first 6 months, especially if the bleeding risk was low or moderate and if the DVT was either idiopathic or provoked by a minor transient risk factor (median: 8). However, there was no consensus on anticoagulation therapy maintenance beyond the first 3 months despite the low to moderate bleeding risk in patients with DVT related to a major transient risk factor (for example, orthopedic surgery) (median: 7; 65% consensus). Additionally, Echo-Doppler imaging was recommended as an “ultra-early” follow-up assessment in the first 2 to 3 days and before discharge (median: 9).
There was no consensus on adding antiplatelet treatment to anticoagulation therapy either during the first month (median: 3.5) or during the first 6- to 12 months (median: 3) after venous stenting. As indicated by the medians, a significant percentage (50–55%) expressed disagreement with these statements. However, there was agreement to recommend antiplatelet treatment in the event of discontinuation of anticoagulant treatment (median: 8).
Close follow-up was advised during the first month after stent insertion, followed by subsequent specialist follow-ups at a frequency established by the center (median: 9). Finally, in the event of in-stent thrombosis, the experts agreed to consider mechanical or pharmacochemical thrombolysis (median: 9).
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Discussion
The aim of this consensus was to provide some recommendations regarding key aspects of venous stent utilization for lower extremity DVT management, and we achieved a 75% consensus rate among experts. Limited evidence on stent usage contributes to the challenge of consensus building, aligning with the scarcity of specific recommendations in clinical practice guidelines, except those from the Society of Interventional Radiology.[14] [28]
In acute DVT with iliac vein compression, severe symptoms, and a preserved functional state, the experts recommended to consider stenting. Similar to the Society of Interventional Radiology guidelines, they suggested stent placement after thrombolysis, emphasizing the need for patient discussion regarding long-term risks.[28] Conversely, some guidelines prioritize anticoagulation therapy over intervention for acute thrombosis.[8]
For chronic DVT with iliac vein involvement and moderate-to-severe PTS, our experts aligned with the European Society of Cardiology recommendations.[29] The consensus rejected stent placement for isolated femoral, popliteal, or calf vein involvement, aligning with the European Society of Vascular Surgery and Society of Interventional Radiology guidelines.[28] [30] The unanimous agreement against stent placement in children mirrored the existing recommendations.[28] The importance of IVUS for stent assessment reached a consensus. Some guidelines recommend the use of IVUS along with venography in most patients to improve vein assessment after thrombus removal, but this recommendation is weak.[28] [31]
The experts reached a consensus on the key characteristics of an ideal stent, including flexibility, radial strength, and high compression resistance. Stent requirements vary based on location, with a special emphasis on compression resistance when crossing the inguinal ligament.[31] [32] The diameter consensus includes a size at least 20% larger than the vein, with standards of 14 to 16 mm for the iliac axis and 12 to 14 mm for the iliofemoral axis. Preventing migration is crucial, with an agreement on easy and precise release; however, no consensus has been reached on a minimum length of 80 mm. Other guidelines only make broad recommendations, such as ensuring that the stent has the optimal diameter and length to facilitate long-lasting patency, prevent pain, and avoid migration.[14] [28] According to recent reviews, an ideal stent should exhibit characteristics such as high radial strength, flexibility, appropriate size, fixation to prevent migration, conformity to the vein, clear visibility, nonthrombogenicity, biostability, resistance to infection, durability, and cost-effectiveness.[32]
The experts agreed that an imaging test with contrast agent (CT, CT phlebography, MRI, or venography) should be recommended for evaluation prior to the placement of a venous stent. Some guidelines consider performing CT phlebography, MRI, or venography when Doppler ultrasonography is inconclusive or not feasible.[30] Other authors believe that these tests are useful for determining the extent of the disease and excluding extravascular causes responsible for the obstruction, such as tumors or retroperitoneal fibrosis.[32]
Regarding stent placement, there was consensus that when the inguinal ligament is crossed, it is recommended that two stents do not overlap at that level and that only one stent contacts it. Based on experience with arterial stents, stent placement across joints has traditionally not been advised because of the risk of focal hyperplasia, stent compression or fracture, and long-term patency problems.[32] The results of a recent systematic review on venous stents extending across the inguinal ligament showed mixed results that, according to the authors, do not allow recommendations to be made for or against.[33] The recommendation of this consensus is based on the experience of the scientific committee.
There was also consensus that interference with the iliocaval confluence in the contralateral iliac flow should be avoided. Stent placement through the iliocaval confluence carries the risk of thrombosis or stenosis of the contralateral iliac vein owing to partial or complete obstruction of the contralateral iliac vein.[34] A systematic review revealed that the incidence of this complication could reach 15%.[24] In one of the included studies, 90% of the patients with contralateral thrombosis did not receive anticoagulant treatment at that time.[35] The authors of this review concluded that patients requiring a stent across the iliocaval confluence may benefit from long-term anticoagulant treatment.[24]
There was no consensus regarding the role of endophlebectomy associated with temporary arteriovenous fistula in patients with severe involvement of the common femoral vein, which involves the ostia of the deep femoral vein and its branches. This technique is described as safe and effective in these patients, although there is little evidence on the creation of an arteriovenous fistula.[36] [37]
Although anticoagulation therapy in patients with DVT plays a key role in symptom control and functional recovery, clinical practice guidelines provide few recommendations regarding the management of anticoagulation after stent implantation, and when included, they are very generic.[14] [30] However, the use of anticoagulants in this setting varies widely.[38] [39] [40] It is not surprising, therefore, that several other consensus attempts have been made on this aspect of stent management.[39] The participants in our Delphi process agreed that anticoagulation should be started early or immediately after stent implantation, that anticoagulation should initially be performed with low-molecular-weight heparins, and that anticoagulation should be maintained long term (at least the first 6 months) if the bleeding risk is low or moderate and if the DVT is idiopathic or caused by a minor transient risk factor. According to the guidelines, anticoagulation therapy is recommended for patients with thrombotic lesions but do not specify the duration or type of treatment.[14] According to the European Society for Vascular Surgery, in patients who underwent thrombectomy with or without stent implantation, anticoagulation therapy should last at least as long as it would have lasted if the treatment had been conservative.[30] The Society of Interventional Radiology guidelines states that it should last “at least several months” in most patients with a history of DVT/PTS.[14] The above-mentioned specific consensus on this topic indicates that anticoagulation should last 6 to 12 months after stent placement, and in patients with a history of multiple thromboses, anticoagulation should last throughout life.[39]
There was no consensus on the addition of antiplatelet treatment to anticoagulation therapy during the first month or during the first 6 to 12 months (in contrast, 50% disagreed with these practices), although it is recommended in cases of discontinuation of anticoagulation therapy. Despite low quality of evidence and a weak strength of recommendation, the Society of Interventional Radiology considers it appropriate to add an antiplatelet agent to anticoagulant treatment for several months for the majority of patients with low bleeding risk.[14] However, in the aforementioned consensus on anticoagulation therapy, there was no agreement on the use of antiplatelet treatment, although 55% of participants considered lifelong antiplatelet treatment necessary for patients with compressive lesions of the iliac vein.[39]
In-stent thrombosis is possibly the most important complication of stent placement. A recent review concluded that the quality of anticoagulation therapy is an important factor for its selection but did not make recommendations in this regard.[25] Likewise, we did not find any recommendations for its management in the clinical practice guidelines. The experts who participated in this consensus agreed to consider thrombolysis for patients with in-stent thrombosis.
The experts of this consensus agreed that before discharge, it was advisable to perform Doppler ultrasound in the first 2 to 3 days and to closely monitor the patient during the first month. According to the guidelines, close clinical follow-up is recommended after stent placement to ensure compliance with anticoagulation therapy, monitor bleeding and symptom response, determine the need for reintervention to restore patency if the patient has a recurrence of symptoms, and monitor the appearance of late complications.[14] However, they did not provide specific recommendations. Other experts recommend performing Doppler ultrasound in the first 24 hours after the procedure, at 2 weeks, 6 weeks, 3 months, 6 months, and 12 months after the procedure and then annually thereafter for management.[32] Finally, we believe that venous stents should be implanted only in centers able to immediately respond to emergency situations (e.g., migration, perforation, acute hemorrhage, acute thrombosis).
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Conclusion
These consensus recommendations offer practical insights into optimizing venous stent use to prevent PTS in DVT patients. Addressing the critical aspects of stent selection, placement, and postprocedural care, these findings contribute to informed clinical decision-making. The identified areas of divergence underscore the nature of the consensus and require further investigation.
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Conflict of Interest
P.D.-R. has received honoraria from ROVI, Bayer, Techdow, Menarini, Leo Pharma, Pfizer, Bristol-Myers, Sanofi, and Daiichi-Sankyo. Additionally, he has been involved in advisory roles for Techdow, Leo Pharma, and Pfizer. The remaining authors have no conflicts of interest.
Acknowledgements
We thank Clover SGM (Madrid, España) for the coordination of the project and the editorial assistance; their participation was funded by Becton Dickinson.
Working Group for the Consensus on Venous Stenting (in Alphabetical Order)
Borja Castejón Navarro (Complejo hospitalario Ruber Juan Bravo, Madrid, Spain); Eduardo Crespo Vallejo (Fundación Jiménez Díaz, Madrid, Spain); Eva Criado Paredes (Corporació Sanitària Parc Taulí, Barcelona, Spain); Juan Fontcuberta García (Hospital de La Zarzuela, Hospital de la Moraleja, Madrid, Spain); Francisco Galeano Valle (Hospital Universitario Gregorio Marañón, Madrid, Spain); Íñigo Insausti Gorbea (Clínica Universitaria de Navarra, Pamplona, Spain); Luis Izquierdo Lamoca (Hospital Universitario HM Puerta del Sur, Madrid, Spain); Juan José López Núñez (Hospital Universitari Germans Trias i Pujol. Badalona, Barcelona, Spain); Alicia Lorenzo Hernández (Hospital Universitario La Paz, Madrid, Spain); Ana Maestre Peiró (Hospital Universitario de Vinalopó, Elche Alicante); Oscar Merino Mairal (Clínica Rotger Quironsalud, Palma, Spain); Manuel Jesús Núñez Fernández (Complejo Hospitalario Universitario de Pontevedra, Pontevedra, Spain; Sonia del Pilar Otalora Valderrama (Hospital Clínico Universitario Virgen de la Arrixaca, Murcia, Spain); Maria Luisa Robles Martín (Hospital Quirónsalud, Málaga, Spain); Ruben Rodríguez Carvajal (Hospital Quirónsalud Campo de Gibraltar, Cádiz, Spain).
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