Case Report

Anticoagulation for the Pregnant Patient with a Mechanical Heart Valve, No Perfect Therapy: Review of Guidelines for Anticoagulation in the Pregnant Patient

Table 1

ACC/AHA anticoagulation guidelines for pregnant patients with mechanical heart valves.

Class IClass IIaClass IIbClass III

A therapeutic INR of 2-3 (INR of 2.5–3.5 for mitral valves) for all patients prescribed a VKAContinue VKA during first trimester in pregnant patients if dose to achieve therapeutic INR is 5 mg per day or less with full discloser of risksIf daily warfarin dose less than or equal to 5 mg a day to achieve therapeutic INR, adjusted LMWH at least two times a day with target anti-Xa level of 0.8 IU/ml to 1.2 IU/ml 4 to 6 hours after administration may be used during first trimester of pregnancyLMWH should not be administered unless anti-Xa levels are monitored 4 to 6 hours after administration.

In pregnant patients, warfarin may be used to achieve therapeutic INR in second and third trimestersLMWH at least two times a day with target anti-Xa level of 0.8 IU/ml to 1.2 IU/ml 4 to 6 hours after administration during first trimester if daily warfarin dose greater than 5 mg per day for therapeutic INRDose adjusted continuous intravenous UFH with aPTT at least 2 times greater than control for pregnant patients with warfarin dose less than or equal to 5 mg a day for therapeutic INR during the first trimester

Discontinue VKA and initiate IV UFH with activated partial thromboplastin time (aPTT) greater than two times the control before planned vaginal deliveryAdjusted continuous intravenous UFH with aPTT at least 2 times greater than control for pregnant patient if daily warfarin dose greater than 5 mg a day for therapeutic INR

Add low-dose aspirin (75 mg to 100 mg) during second and third trimesters

Class I: treatment should be performed or administered. Class IIa: it is reasonable to perform procedure or administer treatment. Additional studies with focused objectives needed. Class IIb: procedure or treatment may be considered. Additional studies with broad objectives needed. Class III: procedure or treatment should not be performed or administered since it is not helpful and may be harmful.