Abstract
Early diagnosis and treatment of deep vein thrombosis (DVT) is a main issue in the Emergency setting. With the aim of assisting clinicians in the diagnosis and the subsequent management of DVT in the Emergency Departments, a Nominal Group Technique (NGT) study was conducted. A panel of 5 Italian experts developed 21 consensus statements based on available evidence and their clinical experience. The agreed consensus statements may assist clinicians in applying the results of clinical studies and clinical experience to routine care settings, providing guidance on all aspects of the risk assessment, prophylaxis, early diagnosis and appropriate treatment of DVT in the EDs.
Keywords
Introduction
Venous thromboembolism (VTE), which refers to a diagnosis of deep vein thrombosis (DVT) and/or pulmonary embolism (PE), is a common, often preventable life-threatening complication in the Emergency Department (ED) patients. 1,2 Indeed, early diagnosis and treatment of DVT and PE remains challenging to ED due to the presence of ambiguous clinical signs and symptoms and the potential for a fatal outcome. 3
During the last few years, the therapeutic armamentarium of VTE has been enriched with the introduction of direct oral anticoagulants (DOACs) that are associated with additional benefits in emergency situations where monitoring methods are limited, 4 including a lower risk of major hemorrhage such as intracranial hemorrhage. 5 –7
Because of the above evidence, International guidelines encourage early discharge of low risk PE patients and outpatient management of low risk DVT patients. 8,9
Currently, most cases of VTE are diagnosed in the ED 3 and a significant number of patients (>50%) continue to be managed as in-patients, including those potentially suitable for out of hospital management. 3,10
Although several diagnostic algorithms have been developed, 11,12 there are no clear indications for the diagnosis and the subsequent management of DVT and PE in the ED. Until such indications will be available, a structured consensus technique appears a well-suited method to develop consensus statements, which reflect the collective diagnostic and management patterns of experts with considerable knowledge and experience in the current management of VTE in the Italian EDs.
In this study, a Nominal Group Technique (NGT) 13 aimed to providing advice to ED physicians on all aspects of the risk assessment, prophylaxis, early diagnosis and appropriate treatment of VTE based upon the best available information, including situations where the actual evidences are limited. This is the first of 2 papers on the study, providing indications on diagnosis and management of DVT in the ED. A second paper will present the study’s results on the diagnosis and treatment of PE in the emergency setting.
Methods
Design of the Study
The 3 most common consensus methods used for medical and health services research are the Delphi method, the consensus development conference, and the NGT. 13 –15 The NGT, that was the method selected in the present study, is a structured, facilitated, multistep, group meeting technique used to generate and prioritize responses to specific questions by a group of experts. 16
The NGT meeting usually comprises the following steps:
17
Introduction: the facilitator illustrates the purpose of the meeting and, eventually, summarizes the results of recent research on studied topics. Silent generation: each expert notes individually his “ideas” on the subject. Sharing: each expert shares his notes in turn and the facilitator registers them. Discussion: the facilitator leads the discussion and give the experts an equal opportunity to contribute their personal views during the discussion by presenting their own list of “ideas”. At the end of the discussion, the experts come to a shared list of ideas. Ranking: participants express their level of agreement with respect to the list of ideas. The facilitator consolidates the results and presents them to the group.
In our study, from May 2018 to January 2019, two NGT meetings were conducted in order to reach a consensus statement on early diagnosis and appropriate treatment of DVT and PE in the ED.
Preliminary Phases: Expert Identification and Survey
Experts were purposively selected to participate in the NGT: all experts had at least 15 years’ experience in ED and 2 peer-reviewed publications on Emergency Medicine within the last 10 years. Five experts—that are the authors of this paper—agreed to participate in the study.
Before the NGT process, a survey was carried out in order to investigate pathways to VTE diagnosis in the Italian ED, with a particular focus on the processes, events, and factors influencing treatment pathways and clinical outcomes.
Based on the available evidence on the diagnosis and management of VTE, items of a closed-ended questionnaire were defined by research team members (2 psychologists and 1 sociologist with extensive experience in standardized consensus methods). Using a dedicated online platform, a sample of 98 Italian ED physicians were asked to answer individually to the questionnaire. The survey platform was online for 10 weeks. Ultimately, 21 physicians answered to the questionnaire (response rate 21.9%). Results of the survey were analysed by research team members. Descriptive statistical analyses were performed using SPSS ver. 25.
NGT Meetings
The first NGT was held in Rome on the 9 May 2018. Phases and steps of the NGT meetings are showed in Figure 1. At the start of the meeting, an overview of the study was presented, and the aim of the NGT and NGT process were briefly explained to the experts by the facilitator (Step 1: introduction). Then results of the survey were presented, while emphasizing the low response rate, followed by discussion among experts. Then research questions were presented and redefined with the help of the experts: considering the characteristics of the 2 pathological conditions, it was decided to evaluate separately for DVT and PE, the aspects related to the risk assessment, prophylaxis, early diagnosis and appropriate treatment in the ED.

NGT meetings and steps.
In step 2 (silent generation), experts were given 45 minutes to think and generate individually items in response to research questions. Then, each expert was asked to comment individually his statements (Step 3: sharing). During the discussion (Step 4) experts were invited to include comments. At the end of the first NGT meeting, participants generated 24 consensus statements for DVT and 28 for PE. 17
Following the meeting, the research team reviewed all the materials and defined a list of consensus statements topically organized that was circulated among the experts by e-mail. Experts were invited to include comment and indicate statements to be discarded or modified and literature on statements that they considered acceptable.
The second meeting was held in Rome on the 28 January 2019. During the meeting, all statements were discussed in depth taking into account updated evidence on diagnosis and treatment of DVT and PE. Overall, during the final discussion, 33 statements (15 for DVT and 18 for PE) were reformulated or merged; for the remaining ones, only minor linguistic modifications were agreed.
During the final voting phase (Step 5: ranking), experts were invited to rate individually each statement on a 5-point Likert-type scale indicating their level of “agreement” and the “importance” of each statement. At the end of the meeting, results were communicated to the whole group.
The definition of the consensus was determined before the analysis and was set at ≥75% agreement.
Results
The final list included 21 consensus statements for DVT. The statements regarding DVT were grouped into the following 4 categories: 1) From clinical suspicion to diagnosis; 2) Patient management with DVT; 3) Treatment of DVT in the acute phase.
The complete list of statements on DVT that reached the consensus is provided in Tables 1.
Consensus Statements on DVT.
Most statements were revised during the second NGT meeting. Ultimately, all statements included in the final list reached the defined level of consensus as ≥75% of participants, indicated by a score of 4 (agree) or 5 (strongly agree) (Figure S1-online-only supplementary materials).
Discussion
In this study, NGT method was used to build consensus among a panel of 5 experts who had substantial experience in the current management of DVT in the ED.
In this section, we present final consensus statements (Table 1), with supplementary comments that reflect reasoning behind them, based on experts’ discussion, supported by references where appropriate.
Consensus Statements
1. From clinical suspicion to diagnosis
It is desirable that the diagnostic work-up of the DVT should be completed in the ED with a multidisciplinary approach that can be variable depending on levels of care of the ED.
The clinical manifestations of DVT are not specific: the diagnostic process must be guided by the pre-test clinical probability.
The dichotomized Wells score proved to be accurate in stratifying the pre-test probability of DVT in ED, therefore it is necessary to acquire the information to calculate it before any further investigation.
The determination of D-dimer and the use of non-invasive study of the veins of the lower limbs such as CUS (
It is recommended that each laboratory has a specific reference cut-off for d-dimer test and it is necessary an age-correction during the interpretation of this value.
In a patient with Wells pre-test score “unlikely” and negative D-Dimer, the diagnosis of DVT can be reasonably excluded.
If Wells score is “unlikely” for DVT and D-Dimer test is positive it is recommended to perform CUS; if CUS is negative it is indicated to perform complete venous ultrasound (US) evaluation (preferably in 48-72 hours); if venous US is negative, the diagnosis is reasonably excluded. If US is not available, it is indicated to perform a second CUS at 5-7 days.
If Wells score is “likely” for DVT it is recommended to perform CUS; if CUS is negative, it is indicated to perform a complete venous US evaluation (preferably in 48-72 hours) to rule out isolated distal DVT, if available, or, if not, repeat CUS at 5-7 days.
If Wells score is “likely” for DVT with a positive CUS evaluation, it is recommended to start anticoagulant therapy.
If the patient has a positive CUS and a positive D-Dimer test the diagnosis of DVT is confirmed regardless of Wells pre-test probability.
In pregnant women with significant edema in one or both the lower limbs or with clinical suspected deep venous thrombosis of other vascular districts, evaluation performing venous Ultrasound (US) is mandatory.
It is not recommended the use of invasive or expensive tests such as phlebography, Computed Tomography (CT) or Magnetic Resonance Imaging (MRI) for the diagnosis of DVT.
In patients with DVT, further investigations are not necessary to exclude Pulmonary Embolism (PE) in absence of specific symptoms.
Supplementary Comments
The CUS, that can be “2-points” (also called “limited”, that investigate popliteal and common femoral veins) or “3-points” (also called “extended”, that investigate popliteal, common femoral and superficial femoral veins). 22,25,26
According to the Panel of experts, the anticoagulant treatment for isolated distal DVT should be considered in patients characterized by a high risk of thrombosis extension. 34 Risk factors for DVT extension are: positive D-dimer test, severe symptoms, extended thrombosis (>5 cm in length, >7 mm in diameter or involving multiple veins), thrombosis localized nearly a proximal circulation vein, absence of removable risk factors, history of previous DVT or active cancer and in-patients status. 35 On the other hand, for patients at high risk for bleeding, monitoring with CUS is more appropriate that starting anticoagulation therapy, even for patients at high risk of DVT extension.
2. Management of DVT
14. The management of DVT should be as outpatients except in presence of one of them:
ongoing bleeding or high bleeding risk (VTE BLEED risk score);
severe renal failure (eVFG < 30 ml/min);
metastatic cancer
Massive DVT, involving iliac femoral vein, caval vein or severely symptomatic patients (phlegmasia dolens);
Inadequate home-care setting.
15. It is recommended that all EDs refer to shared protocols for the out of hospital management and follow-up of patient with an ED diagnosis and initial treatment of DVT.
Supplementary Comments
On the other hand, the proportion of patients with DVT currently managed as outpatients in clinical practice is still very low: in an analysis of RIETE registry was 31-38%. 42
3. DVT treatment in the acute phase
16. Prompt initiation of anticoagulant therapy after a diagnosis of DVT is mandatory.
17. Anticoagulant therapy should begin in the ED right after the diagnosis of DVT, regardless of the patient’s subsequent destination.
18. While awaiting for the result of diagnostic evaluation of patient with likely DVT (according to the dichotomized Wells score), anticoagulant therapy can also be considered after weighing both thrombotic and hemorrhagic risk.
19. The choice of the anticoagulant drug must take into account not only the common criteria of good clinical practice, but also patient renal and hepatic function, comorbidities, compliance, preferences and opportunity of early discharge.
20. DOACs (Direct Oral Anti-Coagulant) represent the better anticoagulant approach especially for patients discharge directly, or after a brief observation, from ED.
21. Vena cava filters placement or endovascular procedures are indicated in patients with DVT and contraindications to anticoagulant therapy, depending on hospital skills and availability.
Supplementary Comments
In case of obesity and renal failure, unfractionated heparin continuous intravenous infusion or subcutaneous injections represents of treatment of choice.
45
As for apixaban, the Caravaggio trial 50 compared daltheparin and apixaban efficacy and safety; the study is ongoing but data derived from ADAM-VTE study (small study comparing apixaban vs daltheparin) suggest a lower major bleeding risk and VTE recurrence in patients treated with apixaban. 51 DOACS must be avoided in patient suffering from severe renal failure, antiphospholipidic syndrome, DVT in atypical districts, and in patients with vena cava filters. 47
Conclusions
The assessment of the pretest probability is necessary in the emergency setting, and it is the base for correct management of DVT. An
DVT risk stratification through a validated and easy to use CPR
An age adjusted d-dimer cut off
Bedside CUS testing performed directly in the ED
Furthermore, when appropriate outpatient management of DVT is considered safe and effective and beneficial to the healthcare system alike. 52 For this purpose, it is necessary to develop out-of-hospital pathways in order to ensure opportunities for follow-up, patient education and communication between primary and secondary care. 53
Dentali et al, 42 examined Italian patient enrolled in RIETE registry with a diagnosis of DVT, showing that 53.7% of patients were treated as outpatients. This rate was higher in other cohorts, reaching out of 80%. 54
A 2018 American College of Emergency Physician (ACEP) clinical policy on DVT states DOACs as a safe, more easily administered, and effective treatment in patients with DVT. 55 DOACs, especially those with single drug approach (i.e. DOACS not requiring bridge therapy using LMWH), allow the patient to be directly discharged from the ED, 56 ensuring an easy out of hospital management. 57 Moreover, apixaban and rivaroxaban offer the added benefit of monotherapy from the beginning of anticoagulation, and are also associated with a lower risk of bleeding compared to the standard LMWH/ VKA combination. 58,59 In the AMPLIFY study—which compares immediate administration of apixaban 10 mg twice a day for 7 days followed by 5 mg twice a day vs enoxaparin followed by warfarin in 5395 patient with acute VTE (of which 3532 had isolated DVT) randomly assigned—no difference emerged in outcomes events (RR: 0.84; 95%CI 0.60-1.18) while major bleeding and major/ CNRM bleeding were lower in apixaban cohort (RR: 0.31: 95%CI 0.17-0.55 and RR: 0.44, 95%CI 0.36-0.55 respectively). 60
The EINSTEIN DVT randomized study compared immediate administration of rivaroxaban 15 mg twice a day for 3 weeks followed by 20 mg once a day vs enoxaparin followed by warfarin in 3449 patient with acute symptomatic DVT; no difference emerged in the outcome events (HR: 0.68; 95%CI 0.44-1.04) and major bleedings (HR: 0.65; 95%CI 0.33-1.30). 61
Furthermore, although the risk of bleeding appears lower, the reversal agents now available (idarucizumab for dabigatran and andexanet alfa for factor Xa inibitors) are a further security in daily practice. 62,63
Strengths and Limitations of the Study
Our study has several strengths. We adopted strict criteria to help ensure that the panel of experts comprised leader experts on the management of VTE in the ED. Furthermore, face-to-face meeting allowed experts to explain and defend ideas, which might improve the quality of the final list of statements. Consensus statements are based on existing evidence and on experts’ experience. However, further research is required to further support some of the issues mentioned in the statements.
Supplemental Material
supplementary_material - Diagnosis and Treatment of Deep Vein Thrombosis in the Emergency Department: Results of an Italian Nominal Group Technique Study
supplementary_material for Diagnosis and Treatment of Deep Vein Thrombosis in the Emergency Department: Results of an Italian Nominal Group Technique Study by Aldo Salvi, Cinzia Nitti, Andrea Fabbri, Paolo Groff, Enrico Giuseppe Ruggiero and Giancarlo Agnelli in Clinical and Applied Thrombosis/Hemostasis
Footnotes
Acknowledgments
Content Ed Net provided organizational and methodological support for the conduction of the study.
Declaration of Conflicting Interests
The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
Funding
The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article. This project was supported by Bristol Meyer Squibb, Italy. Bristol Meyer Squibb had no role in study design, collection of evidence, interpretation of data, writing the manuscript, or decision to publish.
Supplemental Material
Supplemental material for this article is available online.
References
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