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', 'sub-massive' 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).
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 And | 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 |
is a life threatening condition
|
Intermediate-high Risk |
. |
Intermediate-low Risk |
|
Low Risk |
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):
References:
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