Warning

Audience

  • Highland HSCP only
  • Primary and Secondary Care
  • Adults only

Acute pulmonary embolism (PE) is a common and sometimes fatal disease with a variable clinical presentation. This guideline details the investigation, diagnosis, management and follow up of patients with PE.

Suspected PE: Investigations

Simplified Geneva
Previous DVT/PE 1
HR 75 to 94 1
HR ≥95 2
Surgery or fracture within the last month 1
Haemoptysis 1
Active Cancer 1
Unilateral lower limb pain 1
Pain on deep vein palpation 1
Age ≥65 1

Confirmed PE: Risk stratification

sPESI: Simplified PESI
Age >80 1
Cancer 1
Chronic Heart Failure 1
HR ≥110 1
Systolic BP <100 1
Arterial saturation <90% 1

Thrombolysis for haemodynamically unstable patients

If NO contraindications to thrombolysis, give alteplase:

  • Weight ≥65kg: 100mg over 2 hours, administered as:
    • 10mg IV bolus over 1 to 2 min, THEN
    • 90mg IV infusion over 2 hours
  • Weight <65kg: 1.5mg/kg over 2 hours, administered as:
    • 10mg IV bolus over 1 to 2 min, THEN
    • Remainder of dose as IV infusion over 2 hours

Injectable Medicines Guide access:

Absolute contra-indications to thrombolysis include:

  • Intracranial neoplasm
  • Recent (<2 months) intracranial or spinal surgery or trauma
  • History of a haemorrhagic stroke
  • Active bleeding or bleeding diathesis (eg, severe thrombocytopenia)
  • Treatment with anticoagulant
  • Or non-haemorrhagic stroke, within the previous three months.

Relative contra-indications to thrombolysis include:

  • Severe uncontrolled hypertension (systolic blood pressure >200 mmHg or diastolic blood pressure >110 mmHg)
  • Non-haemorrhagic stroke more than three months prior
  • Surgery within the previous 10 days
  • Pregnancy
  • Haemorrhagic or ischaemic stroke in preceding 6 months

Complete drug information: Actilyse 10 mg powder and solvent for solution for injection and infusion - Summary of Product Characteristics

Anticoagulation for haemodynamically stable patients

Direct oral anticoagulants (DOACs)

First-line option:

Apixaban

  • 10mg twice daily for 7 days, THEN
  • 5mg twice daily for at least 3 months (See: Treatment duration and follow-up)

Detailed drug information: Apixaban 5mg Film-Coated Tablets - Summary of Product Characteristics (SmPC)

Second-line options:

Rivaroxaban

  • 15mg twice daily for 21 days, THEN
  • 20mg once daily for at least 3 month (See: Treatment duration and follow-up)

Detailed drug information: Xarelto 15mg film-coated tablets - Summary of Product Characteristics (SmPC)

Dabigatran and edoxaban.

  • Note: requirement for 5 days of treatment dose low molecular weight heparin before initiating edoxaban for PE.
  • See SPC’s for detailed prescribing information.

Notes: 

  • All patients commenced DOAC should have medications reviewed:
    • Antiplatelets: consider stopping, unless clear indication to continue antiplatelet in combination with DOAC. Consider discussing with Cardiology, where appropriate.
    • NSAID’s: bleeding risk, avoid where possible.
  • Check detailed drug interaction information: Medicines Complete — Stockley's Interactions Checker
  • All patients initiated on DOAC should receive verbal and written information prior to discharge, see: DOAC Counselling Tool (NHS Highland intranet access required)

DOAC contra-indicated or unsuitable at present:

Low Molecular Weight Heparin (LMWH):

Enoxaparin

  • CrCl ≥30mL/min AND low risk of recurrence:
    1.5mg/kg once daily by subcutaneous injection
  • CrCl ≥30mL/min AND additional risk factors (eg, obesity, cancer, recurrent VTE, symptomatic PE):
    1mg/kg twice daily (12 hourly) by subcutaneous injection
  • CrCl <30mL/min:
    1mg/kg once daily by subcutaneous injection

Maximum initiation dose of enoxaparin is 120mg. In patients who weigh >120kg, use 120mg twice daily (provided CrCl >30mL/min), and seek specialist haematology advice +/- monitoring of Xa levels.

Treatment Duration and Follow-Up

Treatment Duration

Provoked PEs (transient/reversible risk factor)

  • Discontinue anticoagulation after 3 months (6 months in active cancer)

Unprovoked or recurrent PEs:

  • Continue anticoagulation for at least 6 months and refer to PE clinic

Follow-up

Patients who should be referred to the PE service for follow-up include:

  • All patients under the age of 50 with PE
  • All unprovoked PE
  • Recurrent PE
  • All intermediate-high and high risk PE, as determined by the Risk Stratification above

Treatment duration >6 months may be appropriate for high risk / recurrent PE patients. Final decision will be made at PE clinic.

Pregnancy

Please contact obstetrics/gynaecology

Editorial Information

Last reviewed: 27/06/2024

Next review date: 30/06/2027

Author(s): Departments of Respiratory & Haematology.

Version: 1.1

Approved By: TAMSG of the ADTC

Reviewer name(s): Dr H Said, Consultant Respiratory Physician.

Document Id: TAM635