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==Anticoagulation==
==Anticoagulation==
* [[Subcutaneous]] or [[Intravenous]] [[LMWH|Low molecular weight heparin]].
**Hemodynamically stable patients.
* [[Thrombolysis]]
**High Risk Hemodynamically stable patients.
**Hemodynamically Unstable patients.
*[[Pulmonary thrombectomy|Percutaneous mechanical thrombectomy]].
**High risk patients with absolute [[Thrombolysis#Contradictions|contraindications]] to Thrombolytics.
**Patients with failed Thrombolysis.
*[[LMWH|Low molecular weight heparin]] is preferred over [[Vitamin K antagonist]].
**[[Cancer]] patients.
**[[Pregnancy|Pregnant]] patients.


==Dosage==
==Dosage==

Revision as of 17:06, 10 May 2012

Pulmonary Embolism Microchapters

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Editor(s)-In-Chief: The APEX Trial Investigators, C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-In-Chief: Cafer Zorkun, M.D., Ph.D. [2]

Overview

In most cases, anticoagulant therapy is the mainstay of treatment. Acutely, supportive treatments, such as oxygen or analgesia, are often required.

Massive PE causing hemodynamic instability (marked decreased oxygen saturation, tachycardia and/or hypotension) is an indication for thrombolysis, the enzymatic destruction of the clot with medication. Some advocate, the usage of thrombolytic, if right ventricular dysfunction is demonstrated on echocardiography.[1]

Anticoagulation

Dosage

The American College of Cardiology (ACC) Foundation and the American Heart Association (AHA) have proposed the following dosage schedule for the use of thrombolytics: [2]

Loading dose:250 000 IU over 30 min. Maintenance dose:100 000 IU/h over 12–24 hr. Accelerated regimen: 1.5 million IU over 2 hr.

Loading dose:4400 IU/kg over 10 min. Maintenance dose:4400 IU/kg/h over 12–24 hr. Accelerated regimen: 3 million IU over 2 hr.

100 mg over 2 hr or 0.6 mg/kg over 15 min (maximum dose 50 mg).

Another validated nomogram has proposed the following dosage[3].

  • Factor Xa Inhibitors
    • Fondaparinux :
      • Patient weighing less than 50 Kg (110 lb) : 5 mg (once daily).
      • Patient weighing 50 Kg (110 lb) to 110 Kg (220 lb): 7.5 mg (once daily).
      • Patient weighing more than 100 Kg (220 lb) : 10 mg (once daily).
  • Unfractionated heparin
    • Loading Dose: 80 IU/Kg or 5000 IU
    • Mantainace Dose: 18 IU/Kg/Hr to achieve a target aPTT 1.5 to 2.5 times the normal value.

ESC Guidelines treatment High-risk pulmonary embolism (DO NOT EDIT)

[5]

“

Class I

1. Anticoagulation with unfractionated heparin should be initiated without delay in patients with high-risk PE. (Level of Evidence: A)

2. Systemic hypotension should be corrected to prevent progression of RV failure and death due to PE. (Level of Evidence: C)

3. Vasopressive drugs are recommended for hypotensive patients with PE. (Level of Evidence: C)

Class IIa

4. Dobutamine and dopamine may be used in patients with PE, low cardiac output and normal blood pressure. (Level of Evidence: B)

Class III

5. Aggressive fluid challenge is not recommended. (Level of Evidence: B)

Class I

6. Oxygen should be administered in patients with hypoxaemia.(Level of Evidence: C)

7. Thrombolytic therapy should be used in patients with high-risk PE presenting with cardiogenic shock and/or persistent arterial hypotension.(Level of Evidence: A)

8. Surgical pulmonary embolectomy is a recommended therapeutic alternative in patients with high-risk PE in whom thrombolysis is absolutely contraindicated or has failed.(Level of Evidence: C)

Class IIb

9.Catheter embolectomy or fragmentation of proximal pulmonary arterial clots may be considered as an alternative to surgical treatment in high-risk patients when thrombolysis is absolutely contraindicated or has failed. (Level of Evidence: C)

”

ESC Guidelines treatment Non-high-risk pulmonary embolism (DO NOT EDIT)

[5]

“

Class I

1. Anticoagulation should be initiated without delay in patients with high or intermediate clinical probability of PE while diagnostic workup is still ongoing. (Level of Evidence: C)

2. Use of LMWH or fondaparinux is the recommended form of initial treatment for most patients with non-high-risk PE. (Level of Evidence: A)

3. In patients at high risk of bleeding and in those with severe renal dysfunction, unfractionated heparin with an aPTT target range of 1.5–2.5 times normal is a recommended form of initial treatment. (Level of Evidence: C)

4. Initial treatment with unfractionated heparin, LMWH or fondaparinux should be continued for at least 5 days and (Level of Evidence: A) may be replaced by vitamin K antagonists only after achieving target INR levels for at least 2 consecutive days (Level of Evidence: C)

Class IIb

5. Routine use of thrombolysis in non–high-risk PE patients is not recommended, but it may be considered in selected patients with intermediate-risk PE (Level of Evidence: B)

Class III

6. Thrombolytic therapy should be not used in patients with low-risk PE (Level of Evidence: B)

”

ESC Guidelines Recommendations Long-term treatment (DO NOT EDIT)

[5]

“

Class I

1. For patients with PE secondary to a transient (reversible) risk factor, treatment with a VKA is recommended for 3 months.(Level of Evidence: A)

2. For patients with unprovoked PE, treatment with a VKA is recommended for at least 3 months. (Level of Evidence: A)

3. For patients with a second episode of unprovoked PE, long-term treatment is recommended. (Level of Evidence: A)

4. In patients who receive long-term anticoagulant treatment, the risk/benefit ratio of continuing such treatment should be reassessed at regular intervals. (Level of Evidence: C)

5. In patients with PE, the dose of VKA should be adjusted to maintain a target INR of 2.5 (range 2.0–3.0) regardless of treatment duration. (Level of Evidence: A)

Class IIb

6. Patients with a first episode of unprovoked PE and low risk of bleeding, and in whom stable anticoagulation can be achieved, may be considered for long-term oral anticoagulation. (Level of Evidence: B)

Class IIa

7. For patients with PE and cancer, LMWH should be considered for the first 3–6 months (Level of Evidence: B) after this period, anticoagulant therapy with VKA or LMWH should be continued indefinitely or until the cancer is considered cured. (Class I,Level of Evidence: C)

”

Guidelines Resources

  • Guidelines on the diagnosis and management of acute pulmonary embolism[5].

References

  1. ↑ Goldhaber SZ. Pulmonary embolism. Lancet 2004;363:1295-305. PMID 15094276.
  2. ↑ Jaff MR, McMurtry MS, Archer SL, Cushman M, Goldenberg N, Goldhaber SZ; et al. (2011). "Management of massive and submassive pulmonary embolism, iliofemoral deep vein thrombosis, and chronic thromboembolic pulmonary hypertension: a scientific statement from the American Heart Association". Circulation. 123 (16): 1788–830. doi:10.1161/CIR.0b013e318214914f. PMID 21422387.
  3. ↑ Raschke RA, Gollihare B, Peirce JC (1996). "The effectiveness of implementing the weight-based heparin nomogram as a practice guideline". Arch Intern Med. 156 (15): 1645–9. PMID 8694662.
  4. ↑ Fengler BT, Brady WJ (2009). "Fibrinolytic therapy in pulmonary embolism: an evidence-based treatment algorithm". Am J Emerg Med. 27 (1): 84–95. doi:10.1016/j.ajem.2007.10.021. PMID 19041539.
  5. ↑ 5.0 5.1 5.2 5.3 Torbicki A, Perrier A, Konstantinides S, Agnelli G, Galiè N, Pruszczyk P, Bengel F, Brady AJ, Ferreira D, Janssens U, Klepetko W, Mayer E, Remy-Jardin M, Bassand JP (2008). "Guidelines on the diagnosis and management of acute pulmonary embolism: the Task Force for the Diagnosis and Management of Acute Pulmonary Embolism of the European Society of Cardiology (ESC)". Eur. Heart J. 29 (18): 2276–315. doi:10.1093/eurheartj/ehn310. PMID 18757870. Retrieved 2011-12-07. Unknown parameter |month= ignored (help)

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