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Treatment of pulmonary embolism

Last reviewed dd mmm yyyy. Last edited dd mmm yyyy

Authoring team

NICE suggest (1):

 

The task force for the diagnosis and management of acute pulmonary embolism of the European Society of Cardiology suggest that the severity of PE should be understood according to the PE-related early mortality risk rather than the anatomical burden and the shape and distribution of intrapulmonary emboli (2).

Hence the task force suggests that the currently used terms such as 'massive', 'submassive' and 'non-massive' be replaced with the estimated level of the risk of PE-related early death (during the acute phase in the hospital or within 30 days ) (2).

  • initial risk stratification of suspected or confirmed PE, based on the presence of haemodynamic instability, is recommended to identify patients at high risk of early mortality

  • in patients without haemodynamic instability, further stratification of patients with acute PE into intermediate- and low-risk categories is recommended

  • in patients without haemodynamic instability, use of clinical prediction rules integrating PE severity and comorbidity, preferably the PESI or sPESI (simplified Pulmonary Embolism Severity Index) , should be considered for risk assessment in the acute phase of PE

  • assessment of the RV by imaging methodsc or laboratory biomarkersd should be considered, even in the presence of a low PESI or a negative sPESI

  • in patients without haemodynamic instability, use of validated scores combining clinical, imaging, and laboratory PE-related prognostic factors may be considered to further stratify the severity of the acute PE episode

Definition of haemodynamic instability, which delineates acute high-risk pulmonary embolism (one of the following clinical manifestations at presentation)

Cardiac arrest

Obstructive Shock

Persistent hypotension

Need for cardiopulmonary resuscitation

Systolic BP <90 mmHg or vasopressors required
to achieve a BP >= 90 mmHg despite adequate
filling status

And
End-organ hypoperfusion (altered mental status;
cold, clammy skin; oliguria/anuria; increased
serum lactate)

Systolic BP <90 mmHg or systolic BP drop >=40 mmHg, lasting longer than 15 min and not caused by new-onset arrhythmia, hypovolaemia, or sepsis

European guidance defines PE severity and the risk

High Risk

  • haemodynamic instability plus (a)

  • Clinical parameters of PE severity and/or comorbidity: PESI class III–V or sPESI >= 1 (d) plus

  • RV dysfunction on TTE or CTPA (b) plus

  • Elevated cardiac troponin levels(c)

 

is a life threatening condition

  • requires specific diagnostic and therapaeutic strategies

 

  • short term mortality is >15%

 

 

Intermediate-high Risk


  • NO haemodynamic instability (a) plus

  • Clinical parameters of PE severity and/or comorbidity: PESI class III–V or sPESI >= 1


  • RV dysfunction on TTE or CTPA (b) plus

  • Elevated cardiac troponin levels

.

 

Intermediate-low Risk

  • NO haemodynamic instability (a)

  • Clinical parameters of PE severity and/or comorbidity: PESI class III–V or sPESI >= 1 plus


  • plus one or none of either (c)
    • RV dysfunction on TTE or CTPA (b) OR
    • Elevated cardiac troponin levels

Low Risk

  • NO haemodynamic instability (a) plus

  • NO Clinical parameters of PE severity and/or comorbidity: PESI class III–V or sPESI >= 1


  • NO RV dysfunction on TTE or CTPA (b) plus

  • NO Elevated cardiac troponin level (c)
    • Assessment optional; if assessed, negative

low risk PE - all checked RV dysfunction and myocardial injury markers are found negative, short term PE related mortality is <1%

key:

BP: blood pressure; CTPA: computed tomography pulmonary angiography; H-FABP:heart-type fatty acid-binding protein; NT-proBNP: N-terminal pro B-type natriuretic peptide; PE: pulmonary embolism; PESI: Pulmonary Embolism Severity Index; RV: right ventricular; sPESI: simplified Pulmonary Embolism Severity Index; TTE: transthoracic echocardiogram.

(a) One of the following clinical presentations: cardiac arrest, obstructive shock (systolic BP <90 mmHg or vasopressors required to achieve a BP >= 90 mmHg despite an adequate filling status, in combination with end-organ hypoperfusion), or persistent hypotension (systolic BP <90 mmHg or a systolic BP drop >= 40 mmHg for >15 min, not caused by new-onset arrhythmia, hypovolaemia, or sepsis)

(b) Prognostically relevant imaging (TTE or CTPA) findings in patients with acute PE

(c) Elevation of further laboratory biomarkers, such as NT-proBNP >= 600 ng/L, H-FABP >= 6 ng/mL, or copeptin >= 24 pmol/ L, may provide additional prognostic information. These markers have been validated in cohort studies but they have not yet been used to guide treatment decisions in randomized controlled trials

(d) Haemodynamic instability, combined with PE confirmation on CTPA and/or evidence of RV dysfunction on TTE, is sufficient to classify a patient into the high-risk PE category. In these cases, neither calculation of the PESI nor measurement of troponins or other cardiac biomarkers is necessary.

(e) Signs of RV dysfunction on TTE (or CTPA) or elevated cardiac biomarker levels may be present, despite a calculated PESI of I–II or an sPESI of 0.

Recommendations for High Risk PEs - acute treatment (2):

  • anticoagulation with UFH, including a weight-adjusted bolus injection, be initiated without delay in patients with high-risk PE
  • systemic thrombolytic therapy is recommended for high-risk PE
  • surgical pulmonary embolectomy is recommended for patients with high-risk PE, in whom thrombolysis is contraindicated or has failed
  • percutaneous catheter-directed treatment should be considered for patients with high-risk PE, in whom thrombolysis is contraindicated or has failed
  • norepinephrine and/or dobutamine should be considered in patients with high-risk PE
  • ECMO (extracorporeal membrane oxygenation) may be considered, in combination with surgical embolectomy or catheter-directed treatment, in patients with PE and refractory circulatory collapse or cardiac arrest

Reference:


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