Acute Management of TE during Pregnancy & Puerperium, Flashcards

1
Q

How is acute VTE diagnosed in pregnancy?

A
  • Any with symptoms and/or signs suggestive of VTE objective testing performed expeditiously & treatment with LMWH given.until diagnosis excluded by objective testing, unless treatment is strongly contraindicated.
  • Individual hospitals agreed protocol for objective diagnosis of suspected VTE during pregnancy. This may recommend involvement of obstetricians, radiologists, physicians and haematologists.
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2
Q

What investigations are needed for the diagnosis of an acute DVT?

A
  • Compression duplex ultrasound; where clinical suspicion of DVT.
  • If ultrasound negative & low level of clinical suspicion, anticoagulant treatment can be discontinued.
  • If ultrasound negative & high level of clinical suspicion exists, anticoagulant treatment discontinued but US repeated on days 3 and 7.
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3
Q

What investigations are needed for the diagnosis of an acute pulmonary embolism (PE)?

A
  • presenting with symptoms and signs of acute PE should have ECG & CXR.
  • with suspected PE, also symptoms and signs of DVT, compression duplex US perform. If compression ultrasonography confirms the presence of DVT,
    no further investigation necessary & treatment VTE continue.
  • with suspected PE without symptoms and signs of DVT, V/Q lung scan or CTPA performed.
  • chest X-ray: abnormal & clinical suspicion of PE, CTPA perform, in preference to a V/Q scan.
  • Alternative or repeat testing carried out where V/Q scan or CTPA is normal but clinical suspicion of PE remains. Anticoagulant treatment should be continued until PE is definitively excluded.
  • with suspected PE: advise that, compared with CTPA, V/Q scanning may carry slightly increased risk of childhood cancer but is associated with a lower risk of maternal breast cancer; in both situations, absolute risk is very small.
  • Where feasible, women should be involved in decision to undergo CTPA or V/Q scanning. Ideally, informed consent obtained before tests are undertaken.
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4
Q

Should D-dimer testing be performed prior to objective diagnosis?

A
  • not performed in investigation of acute VTE in pregnancy.
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5
Q

What baseline blood investigations should be performed before initiating anticoagulant therapy?

A
  • Before anticoagulant therapy is commenced, blood should be taken for a full blood count, coagulation screen, urea and electrolytes, and liver function tests.
  • Performing a thrombophilia screen prior to therapy is not recommended.
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6
Q

What is the initial treatment of VTE in pregnancy?

A
  • In clinically suspected DVT or PE, treatment with LMWH commence immediately until diagnosis excluded by objective testing, unless treatment is strongly contraindicated.
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7
Q

What is the therapeutic dose of LMWH in pregnancy?

A
  • doses titrated against booking or early pregnancy weight.
  • insufficient evidence to recommend dose of LMWH once daily or in two divided doses.
  • should be clear local guidelines for dosage of LMWH
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8
Q

Should blood tests be performed to monitor heparin therapy in pregnancy?

A
  • Routine measurement of peak anti-Xa activity for LMWH treatment of acute VTE in pregnancy or postpartum is not recommended except
    1 - extremes of body weight (< 50 kg & 90 kg or more)
    2 - with other complicating factors (for example,
    A - with renal impairment or
    B - recurrent VTE).
  • Routine platelet count monitoring not carried out.
  • Obstetric postoperative and receiving unfractionated heparin platelet count monitoring performed every 2–3 days from days 4 to 14 or until heparin is stopped.
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9
Q

How should massive life-threatening PE in pregnancy and the puerperium be managed?

A
  • Collapsed, shocked. pregnant orpuerperium assess by team of experienced clinicians including on-call consultant obstetrician.
  • managed on an individual basis regarding:
    1 - IV UFH
    2 - thrombolytic therapy or thoracotomy and
    3 - surgical embolectomy.
  • MX involve MDT including senior physicians, obstetricians and radiologists.
  • IV UFH preferred, initial treatment in massive PE with
    cardiovascular compromise.
  • Maternity units develop guidelines for administration of intravenous unfractionated heparin.
  • on-call medical team contacted immediately.
  • urgent portable echocardiogram or CTPA within 1 hour of presentation arranged. If massive PE is confirmed, or in extreme circumstances prior to confirmation, immediate thrombolysis should be considered.
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10
Q

Should graduated elastic compression stockings be employed in the acute management of VTE in pregnancy?

A
  • initial management of DVT, leg elevated & graduated elastic compression stocking applied to reduce oedema.
  • Mobilisation with graduated elastic compression stockings should be encouraged.
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11
Q

What is the role of inferior vena cava filters in the management of VTE in pregnancy?

A

Consider: temporary inferior vena cava filter in peripartum period for patients with iliac vein VTE to reduce risk of PE or in patients with proven DVT & who have recurrent PE despite adequate anticoagulation.

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12
Q

What is the maintenance treatment of DVT or PE?

A
  • Treatment with therapeutic doses of subcut. LMWH during remainder of pregnancy & for at least 6 weeks postnatally and until at least 3 months of treatment has
    been given in total.
  • Women taught to self-inject LMWH and arrangements made to allow safe disposal of needles and syringes.
  • Outpatient follow-up should include clinical assessment and advice with monitoring of blood platelets and peak anti-Xa levels if appropriate.
  • who develop heparin-induced thrombocytopenia or heparin allergy and require continuing anticoagulant therapy managed with an alternative anticoagulant
    under specialist advice.
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13
Q

Can vitamin K antagonists be used during pregnancy for the maintenance treatment of VTE?

A
  • Because of adverse effects on fetus, vit. K antagonists, as warfarin, not be used for antenatal VTE treatment.
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14
Q

Is there a role for the new anticoagulants in the treatment of VTE in pregnancy?

A
  • Consideration given to use of newer anticoagulants (fondaparinux, argatroban or r-hirudin) in pregnant women who are unable to tolerate heparin (LMWH or unfractionated heparin) or danaparoid and who require continuing anticoagulant therapy.
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15
Q

Should anticoagulant therapy be altered during labour and delivery?

A
  • VTE at term, consider IV UFH, more easily manipulated
  • woman on LMWH for maintenance therapy advise that once she is in established labour or thinks that she is in labour, she should not inject any further heparin.
  • delivery is planned, either by elective CS or IOL, LMWH maintenance therapy should be discontinued 24 hours prior to planned delivery.
  • Regional anaesthetic or analgesic techniques not be undertaken until at least 24 hours after last dose of therapeutic LMWH.
  • LMWH not be given for 4 hours after use of spinal anaesthesia or after epidural catheter has been removed, and epidural catheter should not be removed within 12 hours of most recent injection.
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16
Q

Are specific surgical measures required for anticoagulated patients undergoing delivery by caesarean
section?

A
  • receiving therapeutic doses of LMWH, wound drains (abdominal and rectus sheath) consider at CS & skin incision closed with interrupted sutures to allow drainage of any haematoma.
17
Q

What anticoagulant therapy should be employed in women at high risk of haemorrhage?

A
  • at high risk of haemorrhage, & continued heparin treatment is considered essential, should be managed with IV UFH, until risk factors for haemorrhage resolved.
18
Q

How should anticoagulation be managed postnatally?

A
  • Therapeutic anticoagulant therapy:continued for duration of pregnancy & for at least 6 weeks postnatally and until at least 3 months of treatment given in total.
  • Before discontinuing treatment continuing risk of thrombosis assessed.
  • offer choice of LMWH or oral anticoagulant for postnatal therapy after discussion about need for regular blood tests for monitoring of warfarin, particularly during first 10 days of treatment.
  • Postpartum warfarin avoided until at least fifth day and for longer in women at increased risk of PPH.
  • advise that neither heparin (unfractionated or LMWH) nor warfarin is contraindicated in breastfeeding.
19
Q

What measures can be employed to prevent the development of post-thrombotic syndrome?

A
  • advise: prolonged use of LMWH (more than 12 weeks) is associated with significantly lower chance of developing post-thrombotic syndrome.
  • Following DVT, graduated elastic compression stockings worn on affected leg to reduce pain and swelling.
  • role of compression stockings in prevention of post-thrombotic syndrome is unclear.