Anticoagulation in pregnancy

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

## Contents

* 1 Overview
* 2 Indications
* 3 Strategies
* 3.1 Mechanical heart valves
* 4 See also
* 5 References

## Overview

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Anticoagulation in pregnancy is an issue that occurs in women who are at risk for clot formation and subsequently become pregnant. While the general consensus among physicians is that the safety of the mother supersedes the safety of the developing fetus, changes in the anticoagulation regimen during pregnancy can be performed to minimize the risks to the developing fetus while maintaining therapeutic levels of anticoagulation in the mother.

The main issue with anticoagulation in pregnancy is that warfarin, the most commonly used anticoagulant in chronic administration, is known to have teratogenic effects on the fetus if administered in early pregnancy.[1][2]

## Indications

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In general, the indications for anticoagulation during pregnancy are the same as the general population. This includes (but is not limited to) a recent history of deep venous thrombosis or pulmonary embolism, a metallic prosthetic heart valve, and atrial fibrillation in the setting of structural heart disease.

In addition to these indications, anticoagulation may be of benefit in individuals with SLE and a history of previous spontaneous abortions,[citation needed] individuals who have a history of deep venous thrombosis (DVT) or pulmonary embolism (PE) associated with a previous pregnancy,[citation needed] and even with individuals with a history of coagulation factor deficiencies and DVT not associated with a previous pregnancy.[3]

In a normal pregnancy, there is progressive increase in plasma thrombin-antithrombin III levels and decrease in protein S levels.[4] This may contribute to the increased incidence of thrombosis in certain individuals during pregnancy.

## Strategies

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There is no consensus opinion on the correct anticoagulation regimen during pregnancy. Treatment is tailored to the particular individual based on their risk of complications. Because of the teratogenic effects associated with warfarin and other vitamin K inhibiting agents during the first trimester of pregnancy,[5] women who are on chronic anticoagulation may be given the option of conversion to either heparin or low molecular weight heparin (LMWH) prior to a planned conception.[6] Delaying the conversion from warfarin to another agent until pregnancy is confirmed is also an acceptable policy.[citation needed]

While unfractionated heparin is typically given in an intravenous formulation, this is inconvenient for the prolonged period of administration required in pregnancy. In these cases, subcutaneous heparin at doses of 10,000 to 20,000 IU every 12 hours may be given, titrating to an aPTT of 1.5 times the control when measured 6 hours after dosing.[citation needed]

Whether warfarin can be re-initiated after the twelfth week of pregnancy is unclear. In a recent retrospective analysis, it was suggested that resumption of warfarin after the first trimester is completed is associated with increased risk of loss of the fetus.[7] However, this analysis included only individuals who were anticoagulated for mechanical heart valves, which generally require high levels of anticoagulation.

### Mechanical heart valves

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The optimal anticoagulation regimen for mechanical heart valves in pregnancy is particularly unclear. It is clear from prior studies that anticoagulation with subcutaneous heparin in this setting is associated with a high incidence of thrombosis of the valve and death.[8][9] Similar issues are likely associated with the use of enoxaparin (a low molecular weight heparin) in these high-risk individuals.[10]

## See also

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* Valvular heart disease and pregnancy

## References

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1. ↑ Sathienkijkanchai A, Wasant P. (2005). "Fetal warfarin syndrome". J Med Assoc Thai. 88 (Suppl 8): S246–50. PMID 16856447.
2. ↑ Schaefer C, Hannemann D, Meister R, Eléfant E, Paulus W, Vial T, Reuvers M, Robert-Gnansia E, Arnon J, De Santis M, Clementi M, Rodriguez-Pinilla E, Dolivo A, Merlob P. (2006). "Vitamin K antagonists and pregnancy outcome. A multi-centre prospective study". Thromb Haemost. 95 (6): 949–57. PMID 16732373.CS1 maint: Multiple names: authors list (link)
3. ↑ Couto E, Nomura ML, Barini R, Pinto e Silva JL. (2005). "Pregnancy-associated venous thromboembolism in combined heterozygous factor V Leiden and prothrombin G20210A mutations". Sao Paulo Med J. 123 (6): 286–8. PMID 16444389.CS1 maint: Multiple names: authors list (link)
4. ↑ de Boer K, ten Cate JW, Sturk A, Borm JJ, Treffers PE. (1989). "Enhanced thrombin generation in normal and hypertensive pregnancy". Am J Obstet Gynecol. 160 (1): 95–100. PMID 2521425.CS1 maint: Multiple names: authors list (link)
5. ↑ Shaul WL, Emery H, Hall JG. (1975). "Chondrodysplasia punctata and maternal warfarin use during pregnancy". Am J Dis Child. 129 (3): 360–2. PMID 1121966.CS1 maint: Multiple names: authors list (link)
6. ↑ James AH, Grotegut CA, Brancazio LR, Brown H. (2007). "Thromboembolism in pregnancy: recurrence and its prevention". Semin Perinatol. 31 (3): 167–75. PMID 17531898.CS1 maint: Multiple names: authors list (link)
7. ↑ Kim BJ, An SJ, Shim SS, Jun JK, Yoon BH, Syn HC, Park JS. (2006). "Pregnancy outcomes in women with mechanical heart valves". J Reprod Med. 51 (8): 649–54. PMID 16967636.CS1 maint: Multiple names: authors list (link)
8. ↑ Iturbe-Alessio I, Fonseca MC, Mutchinik O, Santos MA, Zajarías A, Salazar E. (1986). "Risks of anticoagulant therapy in pregnant women with artificial heart valves". N Engl J Med. 315 (22): 1390–3. PMID 3773964.CS1 maint: Multiple names: authors list (link)
9. ↑ Salazar E, Izaguirre R, Verdejo J, Mutchinick O. (1996). "Failure of adjusted doses of subcutaneous heparin to prevent thromboembolic phenomena in pregnant patients with mechanical cardiac valve prostheses". J Am Coll Cardiol. 27 (7): 1698–703. PMID 8636556.CS1 maint: Multiple names: authors list (link)
10. ↑ Ginsberg JS, Chan WS, Bates SM, Kaatz S. (2003). "Anticoagulation of pregnant women with mechanical heart valves" (PDF). Arch Intern Med. 163 (6): 694–8. PMID 12639202.CS1 maint: Multiple names: authors list (link)

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