1. Diagnostic testing:
Deep Vein Thrombosis
Compression Duplex ultrasound is the primary diagnostic test for DVT. If ultrasound confirms the diagnosis of DVT, anticoagulant treatment should be continued. If ultrasound is negative and a high level of clinical suspicion exists, anticoagulant treatment should be discontinued and the ultrasound repeated on days 3 and 7. If repeat testing is negative, no further treatment is required. If repeat testing confirms DVT, anticoagulant treatment should be recommenced and continued. When iliac vein thrombosis is suspected, (back pain and swelling of the entire limb), Doppler ultrasound of the vein, magnetic resonance venography or conventional contrast venography may be considered, and discussed with a radiologist.
Pulmonary Embolism
Perform chest X-ray. This may provide a reason for the chest symptoms. The woman’s legs should be carefully assessed for symptoms and/or signs of DVT. An electrocardiograph should be performed and pulse oximetry is often more useful and safer than arterial blood gases.
If the chest x-ray is normal, PE is suspected, and there are symptoms and/or signs of DVT, leg Doppler scans should be performed. If these show a DVT, anticoagulant treatment should be continued and further radiological investigations are not required.
If the chest x-ray is normal, PE is suspected and there are NO symptoms and/or signs of DVT, a ventilation/perfusion scan (VQ scan) or CT-pulmonary angiography (CT-PA) should be performed. V/Q scanning is first line investigation for suspected PTE in all maternity units within NHS GG&C. If the patient has an abnormal chest X-ray or is unstable, a CT-PA is the investigation of choice.
2. Blood tests: that should be performed prior to starting heparin, include:
- full blood count
- coagulation screen
- U&Es and LFTs
Testing fo r D-dimers and performing a thrombophilia screen in the acute situation, should not be performed.
3. Embolic Stockings:
Organise for fitting of a graduated elastic compression stocking on the affected leg via an orthotics department (or an equivalent locally available service). Accurate fitting and careful instruction in the correct application of the hosiery is essential to avoid discomfort and assist rather than prevent venous return.
4. Start treatment with a LMWH:
Refer to the RCOG guideline, ‘Thromboembolic disease in pregnancy and the puerperium: acute management’ (April 2015).
There is more experience of enoxaparin (Clexane) being used in pregnancy.
(i) Initial dose of enoxaparin (~1mg/kg SC 12 hourly, or 1.5mg/kg SC once daily) is determined as follows:
Early Pregnancy Weight
|
Initial Dose of Enoxaparin
|
|
1mg/kg SC 12 hourly
|
1.5mg/kg SC once daily
|
<50kg
50-69kg
70-89kg
|
40mg twice daily
60mg twice daily
80mg twice daily
|
Use a dose of 1.5 mg/kg, choosing a prefilled syringe dose (syringes available include 60, 80, 100, 120 and 150 mg). If the dose used is +/- 10% of correct dose, check anti-Xa level approximately 4 hours post dose after at least 3 doses have been given
|
90-109kg
|
100mg twice daily
|
110-125kg
|
120mg twice daily
|
› 125kg
|
Discuss with haematologist
|
5. Monitoring LMWH therapy:
Anti-Xa activity - Routine measurement of peak anti-Xa activity for patients on LMWH for treatment of acute VTE in pregnancy or post-partum is not recommended except in women at extremes of body weight (<50kg and >90kg) or with other complicating factors (for example with renal impairment or recurrent VTE) putting them at high risk.
If once daily dosing is commenced, (1.5 mg/kg) and a prefilled syringe with the exact dose is not available, (see above), the anti-Xa level should be checked if the dose is +/- 10% of the calculated dose. Where monitoring of peak anti-Xa activity is indicated, a level of 0.5–1.2 units/ml, approximately 4 hours post- injection, after at least 3 doses have been given, is the aim.
Platelets - Routine platelet count monitoring is not required in obstetric patients who have received only LMWH. If the patient has received heparin (unfrationated or LMWH) in the last 100 days, then the platelet count should be checked after 24 hours of initiating treatment. Further, obstetric patients who are postoperative and receiving unfractionated heparin, should have platelet count monitoring performed every 2-3 days from days 4-14 or until heparin is stopped.
6. LMWH:
Full dose LMWH should be continued throughout pregnancy (enoxaparin 1mg/kg 12 hourly or 1.5mg/kg daily).
Pregnant women who develop heparin-induced thrombocytopenia or have heparin allergy and require continuing anticoagulant therapy should be managed with the heparinoid, danaparoid sodium or fondaparinux, under specialist advice.
7. Labour:
Advise a woman to withhold enoxaparin once she thinks she is in labour - further doses will be prescribed by hospital staff following assessment.
Patients undergoing induction of labour or elective Caesarean section should discontinue their heparin treatment temporarily 24 hours before IOL or section (see section 9). Where delays occur leading to a prolonged period off anticoagulation, discuss management with a consultant obstetrician.
Where the thromboembolism has occurred ≥36+0 weeks gestation or the onset of labour occurs within 4 weeks of the acute episode of thrombosis, the advice of a senior haematologist should be sought – this may involve the use of unfractionated heparin or an IVC filter.
8. Regional anaesthesia:
Regional anaesthesia/analgesia may not be an option for women on anticoagulant therapy and the anaesthetists should be aware of such patients when in labour ward and preferably earlier if delivery has been planned.
Epidural anaesthesia can be sited only after discussion with a senior anaesthetist, in keeping with local anaesthetic protocols. When a woman presents whilst on a therapeutic regimen of LMWH, regional techniques should not be employed for at least 24 hours after the last dose of LMWH. LMWH should not be given for at least four hours after the epidural catheter has been removed and the cannula should not be removed within 12 hours of the most recent injection.
9. Elective Caesarean section:
Enoxaparin - omit the previous evening’s dose and the morning dose of enoxaparin and give a thromboprophylactic dose (enoxaparin 40mg) 4 hours post caesarean section (or more than 4 hours post removal of epidural catheter). Re-commence full treatment dose LMWH 24 hours following the prophylactic enoxaparin dose.
Because of the increased risk of wound haematoma in patients receiving therapeutic doses of LMWH, consideration should be given to the use of drains (abdominal and rectus sheath) and closing the skin incision with staples or interrupted sutures to allow drainage of any haematoma.
10. Haemorrhage:
Any woman considered to be at high risk of haemorrhage, in whom continued heparin treatment is considered essential, should be managed with IV unfractionated heparin until the risk factors for haemorrhage have resolved eg major ante-partum haemorrhage, coagulopathy, progressive wound haematoma, suspected intra- abdominal bleeding, post partum haemorrhage. Unfractionated heparin has a shorter half life than LMWH and its activity is more completely reversed with protamine sulphate.
11. Administration of intravenous unfractionated heparin:
Note: prolonged use of unfractionated heparin in pregnancy is associated with osteoporosis and fractures.
- loading dose of 80 units/kg, followed by a continuous intravenous infusion of 18 units/kg/hour
- if a patient has received thrombolysis (see below), the loading dose of heparin should be omitted and an infusion started at 18 units/kg/hour
- it is mandatory to measure APTT level 4 - 6 hours after the loading dose, 6 hours after any dose change and then at least daily when in the therapeutic range. The therapeutic target APTT ratio is usually 1.5- 2.5 times the average laboratory control value.
- using this weight-adjusted regimen, the infusion rate should be adjusted according to the APTT ratio as below:
APTT ratio
|
dose change (units/kg/hr)
|
additional action
|
next APTT (hr)
|
< 1.2
|
+ 4
|
Re-bolus 80 u/kg
|
6
|
1.2 - 1.5
|
+ 2
|
Re-bolus 40 u/kg
|
6
|
1.5 - 2.5
|
no change
|
|
24
|
2.5 - 3.0
|
- 2
|
|
6
|
> 3.0
|
- 3
|
stop infusion 1 hr
|
6
|
12. Postnatal anticoagulation:
Anticoagulant therapy should be continued for the duration of the pregnancy and for at least 6 weeks postnatally and until at least 3 months of treatment has been given in total. Women should be offered a choice of LMWH or oral anticoagulant for postnatal therapy after discussion about the need for regular blood tests for monitoring of warfarin, particularly during the first 10 days of treatment.
Postpartum warfarin should be avoided until at least the fifth day and for longer in women at increased risk of postpartum haemorrhage.
Warfarin therapy should be administered at 1800 hours. A loading regimen of 7mg day 1, 7mg day 2 should be commenced. Check INR on morning of day 3 and daily thereafter to determine dose from chart below. LMWH should be continued until the INR is satisfactory (2 - 3) on two successive days. Once the INR has been 2-3 for 2 consecutive days a repeat INR should be performed within one week. The patient must always be referred to an appropriate outpatient monitoring service.
The direct oral anticoagulants (DOACs) can be considered in the post partum period if a woman has decided not to breastfeed. The DOAC of choice in GG&C is apixaban. This should be commenced at a dose of 5mg bd as long as the woman has already received at least 1 week of therapeutic dose LMWH. This should be commenced once the woman is considered to no longer to be at increased bleeding risk. The first dose should be 12 hours (bd LMWH regimen) or 24 hours (od LMWH regimen) after the last dose of LMWH.
Anticoagulant service providers
Within GG&C all community INR monitoring services are provided by the Glasgow and Clyde Anticoagulant Service (GCAS), rather than individual GPs.
The GCAS Anticoagulant Monitoring and Clinic referral form contains all necessary information and other contact details – see StaffNet
Breast feeding is not contra-indicated with either heparin or warfarin.
Suggested protocol for commencing warfarin treatment in the puerperium (RCOG, 2015)
Day of warfarin treatment |
INR |
Warfarin dose (mg) |
First |
|
7.0 |
Second |
|
7.0 |
Third |
<2.0
2.0-2.1
2.2-2.3
2.4-2.5
2.6-2.7
2.8-2.9
3.0-3.1
3.2-3.3
3.4
3.5
|
7.0
5.0
4.5
4.0
3.5
3.0
2.5
2.0
1.5
1.0
|
Fourth |
<1.4
1.4
1.5
1.6-1.7
1.8
1.9
2.0-2.1
2.2-2.3
2.4-2.6
2.7-3.0
3.1-3.5
3.6-4.0
4.1-4.5
>4.5
|
>8.0
8.0
7.5
7.0
6.5
6.0
5.5
5.0
4.5
4.0
3.5
3.0
omit next day's dose then give 2mg
omit two days' doses then give 1mg
|
13. Discharge Planning
Following DVT, a graduated elastic compression stocking should be worn on the affected leg to reduce pain and swelling. This should be appropriately fitted by an orthotics department (or an equivalent locally available service). The role of stockings in the prevention of post-thrombotic syndrome is unclear.
Patients developing VTE in pregnancy should be referred to anticoagulant clinic:
Please refer to current version of “Therapeutics: A Handbook for Prescribers”.