IMPEDE-VTE

Predicts risk of venous thromboembolism in multiple myeloma

Jennifer Glen

Provided by EVAL Foundation
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In patients with multiple myeloma (MM), venous thromboembolism (VTE) is a common cause of morbidity and mortality. The Myeloma Working Group (IMWG) developed and validated a risk prediction score to quantify risk of VTE in patients with MM starting chemotherapy (Sanfilippo et al., 2019). The IMPEDE-VTE score comprises the following nine variables: Immunomodulatory drugs (IMDs); Body Mass Index (BMI); Pelvic, hip or femur fracture; use of Erythropoiesis-stimulating agents (ESAs); use of Dexamethasone/Doxorubicin; Ethnicity/Race; VTE history; Tunneled line/CVC; and Existing thromboprophylaxis. The IMEPDE-VTE score outperformed the risk stratification in the IMWG/NCCN guidelines. Sanfilippo et al. (2019) suggest, "Risk assessment can help clinicians select thromboprophylaxis in high-risk patients, and avoid anticoagulants in those at low VTE risk. These data suggest that the IMPEDE VTE score could replace the risk stratification within the current guidelines for identification of patients with MM at high risk of VTE."

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Summary

VTE The Myeloma Working Group (IMWG) developed and validated a risk prediction score to quantify risk of venous thromboembolism (VTE) in patients with multiple myeloma (MM) starting chemotherapy (Sanfilippo et al., 2019). 

 

The IMPEDE-VTE score comprises the following nine variables: Immunomodulatory drugs (IMDs); Body Mass Index (BMI); Pelvic, hip or femur fracture; use of Erythropoiesis-stimulating agents (ESAs); use of Dexamethasone/Doxorubicin; Ethnicity/Race; VTE history; Tunneled line/CVC; and Existing thromboprophylaxis. 

 

Scoring and Recommendations

 

The IMPEDE-VTE Score is calculated by the addition of the selected points.

 

 

VariablePoints
Use of Immunomodulatory drugs (IMDs)

No               0

Yes              4

Body Mass Index (BMI) ≥ 25 kg/m²

No               0

Yes              4

Pelvic, hip or femur fracture

No               0

Yes              1

Erythropoiesis-stimulating agents (ESAs)

No               0

Yes              1

Dexamethasone use

No               0

Low dose    2

High dose   4

Doxorubicin use

No               0

Yes              3

Ethnicity/Race is Asian or Pacific Islander

No              -3

Yes              0

History of VTE before multiple myeloma

No               0

Yes              5

Tunneled line or central venous catheter

No               0

Yes              2

Existing thromboprophylaxis: i.e. therapeutic LMWH* or warfarin use

No               0

Yes             -4

Existing thromboprophylaxis: i.e. therapeutic LMWH or aspirin use

No               0

Yes             -3

 

*LMWH: Low molecular weight heparin

 

 

IMPEDE-VTE ScoreResult
≤ 3Low Risk of VTE within 6 months of treatment initiation.
4-7Intermediate Risk of VTE within 6 months of treatment initiation.
≥ 8High Risk of VTE within 6 months of treatment initiation.
≥ 4

Consider VTE prophylaxis in high risk patients

  • The 2022 NCCN Guidelines suggest a cutoff of  ≥ 4 as high risk.
  • The primary and validation research of the IMPEDE-VTE score suggest a cutoff of ≥ 8 as high risk.
  • Follow the standard of care for your practice.

 

 

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All questions & possible results

Section OneTitle not visible
BMI ≥ 25 kg/m²

Select one option:

  • No
  • Yes
  • Help me calculate BMI
Section TwoTitle not visible
BMI ≥ 25 kg/m² (Results from the BMI Calculator)

Select one option:

  • No
  • Yes
Immunomodulatory drug use

Select one option:

  • No
  • Yes
Pelvic, hip or femur fracture

Select one option:

  • No
  • Yes
Erythropoiesis-stimulating agent

Select one option:

  • No
  • Yes
Doxorubicin use

Select one option:

  • No
  • Yes
Dexamethasone use

Select one option:

  • No
  • Low dose
  • High dose
Ethnicity (race) is Asian or Pacific Islander

Select one option:

  • No
  • Yes
History of venous thromboembolism (VTE) before multiple myeloma

Select one option:

  • No
  • Yes
Tunneled line or central venous catheter

Select one option:

  • No
  • Yes
Existing thromboprophylaxis (i.e. therapeutic LMWH or warfarin use)

low molecular weight heparin (LMWH)

Select one option:

  • No
  • Yes
Existing thromboprophylaxis (i.e. therapeutic LMWH or aspirin use)

Select one option:

  • No
  • Yes
Default SectionTitle not visible
Weight

A number between 0 and 800, in kg or lbs.

Height

A number between 0 and 200, in cm or in.

Target BMI

A number between 2 and 60, in kg/m².

Possible results
IMPEDE-VTE Score: Intermediate Risk (4-7 pts)

Intermediate Risk of VTE within 6 months of treatment initiation.

IMPEDE-VTE Score: Low Risk ( ≤ 3 pts)

Low Risk of VTE within 6 months of treatment initiation.

Consider VTE prophylaxis in high risk patients

The 2022 NCCN Guidelines suggest a cutoff of  ≥ 4 as high risk.

 

The primary and validation research of the IMPEDE-VTE score suggest a cutoff of ≥ 8 as high risk.

 

Follow the standard of care for your practice.

IMPEDE-VTE Score: High Risk (8-24 pts)

High Risk of VTE within 6 months of treatment initiation.

Class 1 obesity
Body Surface Area
Class 2 obesity
Target Weight for BMI Target

Target Weight for BMI Target

Underweight
Overweight
Class 3 obesity
Normal Weight
Body Mass Index

BMI may be a simple and cost-effective measure of body fat. BMI evaluates the relationship of body mass to height, but it may not be accurate for everyone. BMI does not differentiate between the ratio of body fat to muscle present in body mass nor factor gender, developmental or ethnic considerations. Examples of BMI Limitations:

  • May be an inappropriate measure for muscular or fit body types. Body fat measurements may be more accurate.
  • Ethnic variations in height and stature.

Literature