Venous thromboembolism (VTE) refers to the formation of a thrombus within veins. This can occur anywhere in the venous system but the clinically predominant sites are in the vessels of the leg (giving rise to deep vein thrombosis (DVT)) and in the lungs (resulting in a pulmonary embolus (PE)).
The pathophysiology of VTE in pregnancy appears to relate to the increased venous stasis noted during this period but other factors such as alterations in the balance of proteins of the coagulation and fibrinolytic systems have also been implicated.
- VTE affects about 1 in 100,000 women of childbearing age.
- It is up to 10 times more common in pregnant than in non-pregnant women of a similar age.
- It occurs in about 1/1,000 pregnancies in women under the age of 35.
- It occurs in 2.4/1,000 pregnancies in women over the age of 35.
- Inherited thrombophilia is present in 30-50% of women with pregnancy-associated VTE.
- 10-20% of VTEs are PEs which are the main contributors to VTE mortality. They are the leading direct cause of maternal mortality in the UK, being responsible for a third of maternal deaths.[5, 6]
Thrombosis and thromboembolism was the leading cause of maternal deaths between 2010-2012 in the UK, occurring in 1.08 in 100,000 maternities..
- 62% of women with fatal VTEs die in the first trimester although the risk per day is actually greatest in the weeks following delivery.
- 71% of postpartum deaths from VTE occur following vaginal delivery.
- 10% of postpartum deaths from VTE occur following operative (interventional) vaginal delivery.
There are a number of known risk factors, some hereditary and others acquired. and in 80% of patients, at least one risk factor can be identified. Notably, the antenatal period is known to be a weak risk factor and the postpartum period a moderate risk factor.
Often more than one risk factor is present and these should be actively identified when assessing the patient for VTE during and post-pregnancy:
- Factor V Leiden mutation (most common).
- Prothrombin gene G20210A mutation.
- Antithrombin III deficiency.
- Protein C deficiency.
- Protein S deficiency.
- Disorders of plasminogen and plasminogen activation.
- Strong family history.
- Obesity - body mass index (BMI) ≥30 kg/m2.
- Immobilisation (>4 days of bed rest).
- Previous thrombotic event.
- Inflammatory disorders such as inflammatory bowel disease.
- Oestrogen therapy (including contraception and hormone replacement therapy).
- Sepsis, including urinary tract infections.
- Gross varicose veins.
- Antiphospholipid syndrome.
- Nephrotic syndrome.
- Paroxysmal nocturnal haemoglobinuria.
- Cerebrovascular event.
- Polycythaemia vera.
- Sickle cell disease.
- Long-haul travel of ≥4 hours.
Factors specific to pregnancy
- Venous stasis.
- Maternal age of ≥35 years.
- Gestation <36 weeks.
- Instrument-assisted or caesarean delivery.
- Prolonged labour.
Presentation is similar to non-pregnant patients with DVT or PE:
- DVT: leg pain and discomfort (the left is more commonly affected), swelling, tenderness, oedema, increased temperature and a raised white cell count. There may also be abdominal pain. The difficulty is that some of these symptoms may be found in normal pregnancies. The patient may also be asymptomatic with a retrospective diagnosis being made following a PE.
- PE: dyspnoea, pleuritic chest pain, haemoptysis, faintness, collapse. The patient may have focal signs in the chest, tachypnoea, a raised jugular venous pressure (JVP) and there may be ECG changes (S1Q3T3). Arterial blood gases taken with the patient sitting down may show respiratory alkalosis and hypoxaemia. There may also be symptoms or signs of a DVT.
- DVT: swelling and lower leg discomfort are not unusual in a normal pregnancy. Other possibilities include muscle strain, a ruptured Baker's cyst, cellulitis, superficial thrombophlebitis, ruptured plantaris tendon and trauma.
- PE: potentially extensive but specifically rule out chest infection and an intra-abdominal bleed (look for abdominal signs, shoulder tip pain from diaphragmatic irritation and a low JVP).
Investigations and diagnosis
Any woman with symptoms and signs suggestive of VTE should have objective testing performed promptly. Treatment with low molecular weight heparin (LMWH) - see 'Initiating treatment', below - should be started immediately (before diagnosis), unless treatment is strongly contra-indicated. Many hospitals have local policies regarding the management of these patients. This may involve the obstetricians, haematologists, physicians and radiologists.
If there is a clinical suspicion of a DVT, arrange an urgent compression duplex ultrasound scan. If this is negative and your suspicion is low, discontinue treatment. If it is negative but your suspicion is high, repeat the scan (or order an alternative imaging modality) one week later, whilst keeping the patient anticoagulated. If this is negative, discontinue anticoagulation.
NB: if you suspect an iliac vein thrombosis (back pain and swelling of the entire limb), magnetic resonance venography or conventional contrast venography may be considered.
If there is a clinical suspicion of a PE, organise a CXR and if this is normal, arrange compression duplex Doppler. The CXR may identify other pulmonary disease, such as pneumonia, pneumothorax or lobar collapse. If these are negative, the patient needs to have a ventilation-perfusion (V/Q) lung scan or a computed tomography pulmonary angiogram (CTPA) - discuss with the radiologist. If these are normal but the clinical suspicion remains high, continue anticoagulation and repeat the tests a week later.
NB: ideally, informed consent should be obtained before these tests are undertaken, as there are risks associated with these investigations (V/Q scanning carries a slightly increased risk of childhood cancer compared with CTPA - 1/280,000 versus less than 1/1,000,000 - but carries a lower risk of maternal breast cancer).
D-dimer is an unreliable test to carry out in these patients. In pregnancy, it can be elevated because of the physiological changes in the coagulation system and levels become 'abnormal' at term and in the postnatal period in most healthy pregnant women. However, do take blood to check the FBC, coagulation screen, U&Es and LFTs before anticoagulant therapy is commenced. There is controversy surrounding the performance of a thrombophilia screen: it will not affect the immediate management of the patient and results are distorted by the pregnant state and by the presence of a thrombus. However, it can provide information that can influence the duration and intensity of anticoagulation. This is therefore best left to be discussed with everybody involved once the acute situation has been dealt with.
- Collapsed, shocked patients need to be managed by an experienced multidisciplinary team involving senior obstetricians, physicians and radiologists.
- An urgent portable echocardiogram or CTPA within one hour of presentation should be arranged.
- If massive PTE is confirmed or, in extreme circumstances prior to confirmation, immediate thrombolysis should be considered.
- Intravenous unfractionated heparin is the preferred treatment.
- In a woman with a past history of VTE or with a known inherited thrombophilia, it is best to refer her prior to a planned pregnancy for optimum prophylaxis throughout the pregnancy. Refer all women who are on warfarin, as this will have to be stopped or replaced by heparin before the seventh week of conception, depending on her risk of VTE.
- Medical anticoagulation is the treatment of choice for acute VTE. Subsequently, surgical interventions may be considered: patients suffering from recurrent PEs despite adequate anticoagulation (or where there is an absolute contra-indication to anticoagulation) may benefit from placement of a temporary caval filter and, in those cases where there is limb or life-threatening embolus, a surgical embolectomy or thrombus fragmentation may be attempted.
- Anticoagulation is by far the most common treatment option. Heparin is the most frequently used drug, being non-toxic to the fetus (it does not cross the placental barrier). However, its main disadvantages are that it has to be parentally administered and, in the long-term, may give rise to heparin-induced osteoporosis and thrombocytopenia. In some patients, it can also provoke a painful, localised allergic reaction on administration. Warfarin is the other treatment option in the postnatal patient but it must be avoided antenatally, as it is teratogenic and can also cause placental abruption and fetal/neonatal haemorrhage.
- In clinically suspected DVT or PE, treatment with unfractionated heparin or LMWH should be given until the diagnosis is excluded by objective testing, unless treatment is strongly contra-indicated.
There are several different types of heparin to choose from:
- LMWH: this is the drug of choice. It has been shown to be more effective than unfractionated heparin with lower mortality and fewer haemorrhagic complications in the initial treatment of DVT in non-pregnant subjects. LMWHs are as effective as unfractionated heparin for treatment of PE. The exact dose will depend on the manufacturer's recommendations but this is based on the patient's early pregnancy weight and should be administered subcutaneously twice daily. There should be clear local guidelines for the dosage of LMWH to be used.
- Intravenous unfractionated heparin: this is an extensively used drug in the acute management of VTE, particularly massive PE with cardiovascular compromise. It is initiated with a loading dose of 5,000 international units (IU) followed by a continuous infusion of 1,000-2,000 IU/hour depending on activated partial thromboplastin time (aPTT) measurements (daily - at least), the first of which is taken six hours after the loading dose. Thus, there is the benefit of accurate drug administration but it has been demonstrated that there are a number of difficulties with accurate aPTT measurement (when the sample is taken and in the laboratory), particularly late in pregnancy when interpretation of the results can be problematic. Prolonged use in pregnancy may give rise to the problems described above.
- Subcutaneous unfractionated heparin: this has been shown to be as effective as the intravenous form. It is administered as a 5,000 IU bolus and subsequent 15,000-20,000 IU doses at 12-hourly intervals. The aPTT needs to be checked and is best done midway between the 12-hourly doses, once every 24 hours. A target of 1.5-2.5 times the control should be aimed for.
Additionally, the leg should be elevated and a graduated elastic compression stocking applied to reduce oedema. Mobilisation with graduated elastic compression stockings should be encouraged.
Heparins are the maintenance treatment of choice. Dose-adjusted subcutaneous, unfractionated heparin or subcutaneous LMWH are effective alternatives to oral anticoagulants in maintenance treatment of VTE.
- Subcutaneous LMWH appears to have advantages over aPTT-monitored unfractionated heparin in the maintenance treatment of VTE in pregnancy. The simplified therapeutic regimen for LMWH tends to be more convenient for patients, minimising blood tests (routine platelet counts are not required and levels of anti-Xa will only need to be monitored where there are extremes of weight: <50 kg or >90 kg) and allowing outpatient treatment. Women should be taught to self-inject and can then be managed as outpatients until delivery.
- If unfractionated heparin is used, monitor the platelet count at least every other day for the first 14 days or until treatment is stopped (whichever comes first).
Seek specialist advice if the patient develops heparin-induced thrombocytopenia or a heparin allergy and requires continuing anticoagulant therapy. She should be managed with the heparinoid, danaparoid sodium or fondaparinux, under specialist supervision.
When the patient thinks she is going into labour, she should stop injecting and get in touch with the delivery ward staff who will manage the anticoagulation throughout labour and immediately post-delivery. Alternatively, planned elective induction of labour or caesarean section at least 12 hours after prophylactic-dose LMWH or 24 hours after therapeutic-dose LMWH can be considered. As these patients are at high risk of haemorrhage, they will be managed with intravenous unfractionated heparin throughout this time. Regional anaesthetic or analgesic techniques should not be undertaken until at least 24 hours after the last dose of therapeutic LMWH.
Depending on the patient's individual circumstances, she may be managed with ongoing heparin treatment or warfarin postpartum. If she opts for warfarin, this needs to be avoided until at least day three postpartum with an INR check at day two of warfarin treatment: aim for an INR between 2 and 3. Continue heparin treatment until there have been two successive readings of an INR >2. Although these drugs are detectable in breast milk, all are safe for use during breast-feeding because warfarin metabolites are inactive and heparin is not absorbed through the gastrointestinal tract.
Postnatal review for women who develop VTE during pregnancy or the puerperium should, whenever possible, be at an obstetric medicine clinic or a joint obstetric haematology clinic.
In theory, therapy should be continued for six months as would be the case for non-pregnant patients. However, the postpartum state is a period of physiological fluctuation of coagulation factors. Therefore, current advice is to continue therapy for at least 6-12 weeks postpartum or until at least three months of therapy have been completed. At that point, the patient should be assessed for the presence of ongoing risk factors for a VTE prior to making the decision to stop anticoagulation therapy.
Thrombophilia and placental vascular complications
- Fetal loss: although the figures are likely to be small (there are not many studies), there is thought to be a doubling of risk of fetal loss in women with genetic thrombophilia.
- Intrauterine growth restriction: a specific association between this and thrombophilia has not been identified but chronic abruption and extensive placental infraction have been noted to occur more frequently in these patients.
- HELLP syndrome: Haemolysis, Elevated Liver enzymes, Low Platelet count - this may be associated with certain forms of thrombophilia.
Up to 60% of patients who have experienced a DVT go on to have post-thrombotic syndrome up to 12 months following the acute event. This arises from damage to the lumen of the vein following the presence of a thrombus. Subsequently, patients manifest symptoms and signs akin to those of varicose veins: aching, swollen legs, pruritus, dermatitis and hyperpigmentation of the affected area. Ulceration and cellulitis may complicate the picture. Compression stockings worn on the affected leg for at least two years have been recommended after the acute event to reduce the risk of developing post-thrombotic syndrome.However, a recent large randomised trial found no evidence to support this.PE is the other complication of DVTs and is discussed above.
Prolonged unfractionated heparin use during pregnancy may result in osteoporosis and fractures.
See also the separate article on the Prevention of Venous Thromboembolism.
Guidance from the Royal College of Obstetricians and Gynaecologists suggests:
- Regardless of their VTE risk, dehydration and immobilisation of the patient should be avoided throughout pregnancy.
- Women at high risk of VTE in pregnancy should be offered pre-pregnancy counselling and a prospective management plan for thromboprophylaxis in pregnancy. Those who become pregnant before receiving such counselling should be referred to a nominated expert early in pregnancy.
- All women with previous VTE should receive postpartum prophylaxis, as this is the time of highest risk.
- In addition, women whose original VTE was unprovoked, idiopathic or related to oestrogen, or who have other risk factors, a family history of VTE in a first-degree relative or a documented thrombophilia require LMWH antenatally and for six weeks postpartum.
- Women with recurrent VTE may already be on warfarin. They should be advised to stop warfarin and change to LMWH as soon as pregnancy is confirmed, ideally within two weeks of the missed period and before the sixth week of pregnancy. Women not on warfarin should be advised to start LMWH as soon as they have a positive pregnancy test.
- Women with asymptomatic inherited or acquired thrombophilia only, may be managed with close surveillance antenatally and be considered for LMWH for at least seven days postpartum. Exceptions are women with antithrombin deficiency, those with more than one thrombophilic defect (including homozygosity for factor V Leiden) or those with additional risk factors where antenatal prophylaxis should be considered.
Women taking LMWH should be advised that, if they bleed vaginally or contractions begin, they should not inject any further doses. They should be assessed in hospital and further doses be prescribed by medical staff.
- All women with obesity (BMI greater than 40 kg/m2) should be considered for prophylactic LMWH for seven days after delivery. Other postnatal risks include prolonged labour, immobility, infection, haemorrhage and blood transfusion.
- All women who have had an emergency Caesarean section should be considered for LMWH for seven days after delivery. All women who have had an elective caesarean section who have one or more additional risk factors should be considered for LMWH for seven days after delivery.
In addition, properly applied graduated compression stockings are recommended for women travelling long-distance for more than four hours, women who are still outpatients but have prior VTE (usually combined with LMWH), women who are hospitalised and have a contra-indication to LMWH and those who are hospitalised post-caesarean section (combined with LMWH) and considered to be at particularly high risk of VTE.
Further reading and references
; Royal College of Obstetricians and Gynaecologists (April 2015)
; Royal College of Obstericians and Gynaecologists (2015)
; Impact of risk factors on the timing of first postpartum venous thromboembolism: a population-based cohort study from England. Blood. 2014 Oct 30124(18):2872-80. doi: 10.1182/blood-2014-05-572834. Epub 2014 Aug 25.
; Risk of first venous thromboembolism in pregnant women in hospital: population based cohort study from England. BMJ. 2013 Nov 7347:f6099. doi: 10.1136/bmj.f6099.
; Venous thromboembolism in pregnancy. Arterioscler Thromb Vasc Biol. 2009 Mar29(3):326-31. doi: 10.1161/ATVBAHA.109.184127.
; Inherited thrombophilia and pregnancy associated venous thromboembolism. BMJ. 2007 Jun 23334(7607):1318-21.
; Royal College of Obstetricians and Gynaecologists (November 2009)
; Maternal mortality and thromboembolic risk in pregnancy, 2009
; NICE CKS, June 2012 (UK access only )
; MBRRACE-UK, Dec 2014
; Mortality from venous thromboembolism in young Swedish women and its relation to pregnancy and use of oral contraceptives--an approach to specifying rates. Eur J Epidemiol. 200520(6):509-16.
Virkus R et al; Risk Factors for Venous Thromboembolism in 1.3 Million Pregnancies: A Nationwide Prospective Cohort, PLOS One, 2014.
; Royal College of Obstetricians and Gynaecologists (2007)
; Management dilemmas in acute pulmonary embolism. Thorax. 2014 Feb69(2):174-80. doi: 10.1136/thoraxjnl-2013-204667. Epub 2013 Dec 16.
; NICE Evidence Services (UK access only)
; Compression stockings to prevent post-thrombotic syndrome: a randomised placebo-controlled trial. Lancet. 2014 Mar 8383(9920):880-8. doi: 10.1016/S0140-6736(13)61902-9. Epub 2013 Dec 6.
Hi all, I am a newbie here. I am 37 and 11 weeks pregnant with my second baby. I was 28 at the time of first delivery and haven't done any genetic testing at that time. But I know the risk factors...Zaynah
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