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ACEP Revises Venous Thromboembolism Clinical Policy

By Stephen J. Wolf, MD, FACEP | on July 17, 2018 | 2 Comments
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ACEP Now: Vol 37 – No 07 – July 2018

ILLUSTRATION: shutterstock.com

In February 2018, the ACEP Board of Directors approved a revised clinical policy on the evaluation and management of adult patients presenting with suspected acute venous thromboembolic disease.1 The policy is available at www.acep.org/patient-care/clinical-policies.

Venous thromboembolism (VTE), including both deep venous thrombosis (DVT) and pulmonary embolism (PE), is a major public health problem. Undiagnosed, untreated patients are believed to be at substantial risk for progressive disease and sudden death typically because of worsening right-sided heart strain and ultimately cardiovascular collapse. Treated patients are at risk for chronic sequelae (ie, vein scarring, leg swelling, and pulmonary hypertension) and adverse events from ongoing anticoagulation (ie, hemorrhage and other medication adverse effects).

One significant challenge for health care providers evaluating patients for VTE lies in the variability of signs and symptoms of the disease that are related to clot burden, location, and the individual patient’s cardiopulmonary reserve. Without perfect, cost-effective tests for the diagnosis of VTE, providers have come to rely on Bayesian decision making to guide their workup, using pretest probability to interpret diagnostic evaluations and generate posttest probability of disease. Doing this allows providers to maximize diagnostic accuracy while minimizing over-testing and patient harm from the risks associated with unnecessary evaluation and treatment.

Table 1. Translation of Classes of Evidence to Recommendation Levels

Table 1. Translation of Classes of Evidence to Recommendation Levels

Efforts to refine this Bayesian approach in emergency medicine have been ongoing. Original studies to determine pretest probability and the accuracy of various screening tests have been validated, and the limits of their efficacy are being explored. Additionally, substantial efforts are being made to advance the treatment of VTE by balancing outcomes, anticoagulation risks to patients, and patient preferences. Non–vitamin K antagonist oral anticoagulants (NOACs) are particularly appealing for long-term anticoagulation because of their simple oral dosing regimens with no need for routine laboratory monitoring.

This most recent revision investigates five areas of interest or controversy in the evaluation and management of VTE. The first two critical questions address the role of unique clinical prediction rules and age-adjusted D-dimer testing in the diagnosis of PE, and the remaining three questions focus on optimal treatment and disposition for individuals receiving a diagnosis of venous thromboembolic disease.

For each critical question, a structured literature review was performed, evidence was systematically graded (see Table 1), and evidence-based recommendations are presented.

Critical Questions

Question 1. In adult patients with suspected acute PE, can a clinical prediction rule be used to identify a group of patients at very low risk for the diagnosis of PE for whom no additional diagnostic workup is required?

Patient Management Recommendations

  • Level A: None specified.
  • Level B: For patients who are at low risk for acute PE, use the Pulmonary Embolism Rule-out Criteria (PERC) to exclude the diagnosis without further diagnostic testing.
  • Level C: None specified.

Question 2. In adult patients with low to intermediate pretest probability for acute PE, does a negative age-adjusted D-dimer result identify a group of patients at very low risk for the diagnosis of PE for whom no additional diagnostic workup is required?

Patient Management Recommendations

  • Level A recommendations: None specified.
  • Level B recommendations: In patients older than 50 years deemed to be at low or intermediate risk for acute PE, clinicians may use a negative age-adjusted D-dimer result to exclude the diagnosis of PE. For highly sensitive D-dimer assays using fibrin equivalent units (FEUs), use a cutoff of age × 10 µg/L; for highly sensitive D-dimer assays using D-dimer units (DDUs), use a cutoff of age × 5 µg/L.
  • Level C recommendations: None specified.

Question 3. In adult patients with subsegmental PE, is it safe to withhold anticoagulation?

Patient Management Recommendations

  • Level A recommendations: None specified.
  • Level B recommendations: None specified.
  • Level C recommendations: Given the lack of evidence, anticoagulation treatment decisions for patients with subsegmental PE without associated DVT should be guided by individual patient risk profiles and preferences (consensus recommendation).

Question 4. In adult patients diagnosed with acute PE, is initiation of anticoagulation and discharge from the emergency department safe?

Patient Management Recommendations

  • Level A recommendations: None specified.
  • Level B recommendations: None specified.
  • Level C recommendations: Selected patients with acute PE who are at low risk for adverse outcomes as determined by Pulmonary Embolism Severity Index (PESI), simplified PESI (sPESI), or the Hestia criteria may be safely discharged from the emergency department on anticoagulation, with close outpatient follow-up.

Question 5. In adult patients diagnosed with acute lower-extremity DVT who are discharged from the emergency department, is treatment with a NOAC safe and effective compared with treatment with low-molecular-weight heparin (LMWH) and a vitamin K antagonist (VKA)?

Patient Management Recommendations

  • Level A recommendations: None specified.
  • Level B recommendations: In selected patients diagnosed with acute DVT, a NOAC may be used as a safe and effective treatment alternative to LMWH/VKA.
  • Level C recommendations: Selected patients with acute DVT may be safely treated with a NOAC and directly discharged from the emergency department.

In summary, the evaluation and management of patients with suspected VTE in the emergency department is rapidly evolving and increasingly nuanced. Newer clinical algorithms using PERC and age-adjusted D-dimer may improve the efficiency and effectiveness of evaluations. Similarly, advances in the understanding of whom to treat, in which setting and with what optimal therapy can improve patient-centered outcomes.


Dr. Wolf is co-chair of the ACEP Clinical Policies Committee, director of service for emergency medicine at Denver Health Medical Center, and vice chair within the department of emergency medicine at the University of Colorado School of Medicine in Aurora.

Reference

  1. Wolf SJ, Hahn SA, Nentwich LM, et al. Clinical policy: critical issues in the evaluation and management of adult patients presenting to the emergency department with suspected acute venous thromboembolic disease. Ann Emerg Med. 2018;71(5):e59-e109.

Pages: 1 2 3 | Multi-Page

Topics: ACEPAmerican College of Emergency PhysiciansClinical GuidelineGuidelinesVenous Thromboembolism

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2 Responses to “ACEP Revises Venous Thromboembolism Clinical Policy”

  1. August 4, 2019

    Erik Auf der Heide, MD, FACEP Reply

    This policy needs to define:
    1) all acronyms
    2) low, intermediate, and high risk

    • August 6, 2019

      Dawn Antoline-Wang Reply

      Please visit https://www.acep.org/patient-care/clinical-policies/ to download the full policy.

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