Low molecular weight heparin: Difference between revisions
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==Background== | ==Background== | ||
*Class of [[anticoagulant]] medications. | |||
*Defined as heparin salts having an average molecular weight of less than 8000 Dalton | |||
*LMWHs inhibit the coagulation process through binding to antithrombin which in turn inhibits activated factor X.<ref>Garcia DA, Baglin TP, Weitz JI, et al. (2012). "Parenteral anticoagulants: Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines"</ref> | |||
*LMWH therapy is monitored by the anti-factor Xa assay (measures anti-factor Xa activity). | |||
**Cannot be acceptably measured using the partial thromboplastin time (PTT) or activated clotting time (ACT) tests. | |||
== | ==Types== | ||
{| class="wikitable" | |||
|- | |||
! LMWH !! Average molecular weight !! Ratio anti-Xa/anti-IIa activity | |||
|- | |||
| [[Bemiparin]] || 3600 || 8.0 | |||
|- | |||
| [[Nadroparin]] || 4300 || 3.3 | |||
|- | |||
| [[Reviparin]] || 4400 || 4.2 | |||
|- | |||
| [[Enoxaparin]] (Lovenox) || 4500 || 3.9 | |||
|- | |||
| [[Parnaparin]] || 5000 || 2.3 | |||
|- | |||
| [[Certoparin]] || 5400 || 2.4 | |||
|- | |||
| [[Dalteparin]] || 5000 || 2.5 | |||
|- | |||
| [[Tinzaparin]] || 6500 || 1.6 | |||
|- | |||
|} | |||
== | ==Clinical Differences from [[Unfractionated heparin]]== | ||
*Less frequent subcutaneous dosing | |||
*Once or twice daily subcutaneous injection for treatment of venous thromboembolism and in unstable angina instead of intravenous infusion of high dose heparin. | |||
*No need for monitoring of the aPTT coagulation parameter as required for high dose heparin.<ref>http://chestjournal.chestpubs.org/content/119/1_suppl/64S.full</ref> | |||
*Possibly a smaller risk of bleeding | |||
*Smaller risk of osteoporosis in long-term use. | |||
*Smaller risk of [[Heparin-Induced Thrombocytopenia (HIT)|heparin-induced thrombocytopenia]], a potential side effect of [[Unfractionated heparin|heparin]]. | |||
*The anticoagulant effects of heparin are typically reversible with [[Protamine sulfate|protamine sulfate]], while protamine's effect on LMWH is limited. | |||
== | ==Indications== | ||
*[[Deep venous thrombosis]] | |||
*[[Pulmonary embolism]] | |||
*[[Non ST-Elevation Myocardial Infarction (NSTEMI)]] | |||
*[[ST-segment elevation myocardial infarction (STEMI)]] | |||
*[[Stroke (main)]] | |||
==See Also== | ==See Also== | ||
*[[ | *[[Coagulopathy (main)]] | ||
*[[Unfractionated heparin]] | |||
== | ==References== | ||
<references/> | |||
[[Category: | [[Category:Pharmacology]] | ||
[[Category:Heme/Onc]] | [[Category:Heme/Onc]] |
Latest revision as of 17:28, 19 September 2019
Background
- Class of anticoagulant medications.
- Defined as heparin salts having an average molecular weight of less than 8000 Dalton
- LMWHs inhibit the coagulation process through binding to antithrombin which in turn inhibits activated factor X.[1]
- LMWH therapy is monitored by the anti-factor Xa assay (measures anti-factor Xa activity).
- Cannot be acceptably measured using the partial thromboplastin time (PTT) or activated clotting time (ACT) tests.
Types
LMWH | Average molecular weight | Ratio anti-Xa/anti-IIa activity |
---|---|---|
Bemiparin | 3600 | 8.0 |
Nadroparin | 4300 | 3.3 |
Reviparin | 4400 | 4.2 |
Enoxaparin (Lovenox) | 4500 | 3.9 |
Parnaparin | 5000 | 2.3 |
Certoparin | 5400 | 2.4 |
Dalteparin | 5000 | 2.5 |
Tinzaparin | 6500 | 1.6 |
Clinical Differences from Unfractionated heparin
- Less frequent subcutaneous dosing
- Once or twice daily subcutaneous injection for treatment of venous thromboembolism and in unstable angina instead of intravenous infusion of high dose heparin.
- No need for monitoring of the aPTT coagulation parameter as required for high dose heparin.[2]
- Possibly a smaller risk of bleeding
- Smaller risk of osteoporosis in long-term use.
- Smaller risk of heparin-induced thrombocytopenia, a potential side effect of heparin.
- The anticoagulant effects of heparin are typically reversible with protamine sulfate, while protamine's effect on LMWH is limited.
Indications
- Deep venous thrombosis
- Pulmonary embolism
- Non ST-Elevation Myocardial Infarction (NSTEMI)
- ST-segment elevation myocardial infarction (STEMI)
- Stroke (main)
See Also
References
- ↑ Garcia DA, Baglin TP, Weitz JI, et al. (2012). "Parenteral anticoagulants: Antithrombotic Therapy and Prevention of Thrombosis, 9th ed: American College of Chest Physicians Evidence-Based Clinical Practice Guidelines"
- ↑ http://chestjournal.chestpubs.org/content/119/1_suppl/64S.full