Reducing the Risk: TE during Pregnancy & Puerperium, Flashcards

1
Q

Prepregnancy and antenatal risk assessment
What are the risk factors for venous thromboembolism (VTE) in pregnancy and the puerperium and
what is the magnitude of risk for these factors?

A
- All women documented assessment of risk factors for VTE in 
1 - early pregnancy or 
2 - prepregnancy.
3 - repeated 
A - if admitted for any reason or 
B - develops other intercurrent problems.
C - intrapartum or 
D - immediately postpartum.
  • with four or more current risk factors shown in (other than previous VTE or thrombophilia) for prophylactic LMWH throughout antenatal & 6 wks postnatally but postnatal risk reassessment should be made.
  • with three current risk factors (other than previous VTE or thrombophilia) for prophylactic LMWH from 28 wks & usually require prophylactic LMWH for 6 weeks postnatally but postnatal risk reassessment be made.
  • with two current risk factors shown in (other than previous VTE or thrombophilia) consider prophylactic LMWH for at least 10 days postpartum.
  • admitted to hospital pregnant (including to gynaecology ward with hyperemesis gravidarum or ovarian hyperstimulation syndrome) usually offer thromboprophylaxis
  • unless specific contraindication such as risk of labour or active bleeding.
  • risk of VTE discuss with women & reasons for individual recommendations explained.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

How should women with single previous VTE be managed in pregnancy?

A
  • offer prepregnancy counselling & prospective MX plan for thromboprophylaxis in pregnancy.
  • become pregnant before receiving such counselling refer at earliest opportunity in pregnancy to clinician with expertise in thrombosis in pregnancy.
  • previous VTE (except single previous VTE related to major surgery and no other risk factors) offer thromboprophylaxis with LMWH throughout antenatal period.
  • previous VTE careful history documented. Where objective documentation is not available, the previous diagnosis of VTE can be assumed in cases where the woman gives a good history and received prolonged (greater than 6 weeks) therapeutic anticoagulation.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Heritable thrombophilia

A
  • previous VTE associated with antithrombin deficiency (often be on long-term oral anticoagulation) offer thromboprophylaxis, higher dose LMWH (either 50%, 75% or full treatment dose) antenatally and for 6 weeks postpartum or until returned to oral anticoagulant therapy after delivery.
  • MX undertaken in collaboration with a haematologist with expertise in thrombosis in pregnancy & consideration given to antenatal anti-Xa monitoring & potential for antithrombin replacement at initiation of labour or prior to caesarean section.
  • If anti-Xa levels are measured, test not use exogenous antithrombin should be used and 4-hour peak levels of 0.5–1.0 iu/ml aimed for.
  • Other heritable thrombophilic defect lower risk & can be managed with standard doses of thromboprophylaxis.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Acquired thrombophilia – see also section 4.4

A
  • VTE associated with APS (who will often be on longterm oral anticoagulation) should be offered thromboprophylaxis with higher dose LMWH (either 50%, 75% or full treatment dose) antenatally and for 6 weeks postpartum or until returned to oral anticoagulant therapy after delivery.
  • APS and prior VTE or arterial thromboses should be managed in collaboration with haematologist and/or rheumatologist with expertise in this area.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What extra advice is needed for women with previous recurrent VTE?

A
  • doses advice of LMWH in pregnancy from clinician with expertise in haemostasis and pregnancy.
  • Some with previous recurrent VTE require higher doses of LMWH.
  • on long-term warfarin or other oral anticoagulants counsell risks of these to fetus & advised to stop their oral anticoagulant therapy & change to LMWH as soon as pregnancy is confirmed, ideally within 2 weeks of missed period and before 6th wk.
  • Women not on warfarin or other oral anticoagulants advise start LMWH as soon as positive pregnancy test.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

How should women with previous VTE be stratified to determine management in pregnancy?

A
  • VTE associated with either antithrombin deficiency or APS or with recurrent VTE (who will often be on long-term oral anticoagulation) offer thromboprophylaxis with higher dose LMWH (either 50%, 75% or full treatment dose) antenatally and for 6 weeks postpartum or until returned to oral anticoagulant therapy after delivery.
  • specialist management by experts in haemostasis and pregnancy.
  • original VTE was unprovoked/idiopathic or related to estrogen (estrogen-containing contraception/pregnancy) or related to a transient risk factor other than major surgery or who have other risk factors should be offered thromboprophylaxis with LMWH throughout the antenatal period.
  • original VTE was provoked by major surgery from which they have recovered and who have no other risk factors, thromboprophylaxis with LMWH can be withheld antenatally until 28 weeks provided no additional risk factors (in which case offer LMWH).
  • They require close surveillance for the development of other risk factors.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Which women with prior VTE require thrombophilia testing?

A
  • Prior to testing for thrombophilia, women should be counselled regarding the implications for themselves and family members of a positive or negative result.
  • results should be interpreted by clinicians with specific expertise in area.
  • family history of VTE and either antithrombin deficiency or if specific thrombophilia has not been detected test for antithrombin deficiency.
  • an unprovoked VTE test for presence of APL antibodies.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

How should women with asymptomatic thrombophilia be treated?

A
  • stratified according to level of risk associated with their thrombophilia & presence or absence of a family history or other risk factors.
  • with asymptomatic antithrombin, protein C or S deficiency or with > one thrombophilic defect (including homozygous factor V Leiden, homozygous prothrombin gene mutation and compound heterozygotes) refer to local expert & antenatal prophylaxis considered. recommend for six weeks’ postnatal prophylaxis even
    in absence of additional risk factors.
  • Heterozygosity for factor V Leiden or prothrombin gene mutation or antiphospholipid antibodies considered as risk factors for thrombosis in asymptomatic women.
  • In presence of three other risk factors such women consider for antenatal thromboprophylaxis,
  • if two other risk factors thromboprophylaxis consider from 28 weeks & if one other risk factor postnatal thromboprophylaxis for 10 days consider.
  • no personal history or risk factors for VTE but who have a family history of an unprovoked or estrogen-provoked VTE in a first-degree relative when aged < 50 years consider for thrombophilia testing. more informative if relative has a known thrombophilia.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

How should women with antiphospholipid antibodies be treated?

A
  • Persistent antiphospholipid antibodies (lupus anticoagulant and/or anticardiolipin and/or β2-glycoprotein 1 antibodies) without previous VTE consider as risk factor for thrombosis such that if she has other risk factors, maybe considered for antenatal or postnatal thromboprophylaxis as above.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

When should thromboprophylaxis be started?

A
  • Antenatal thromboprophylaxis for previous VTE begin as early in pregnancy as practical.
  • without previous VTE & without particular first trimester risk factors or admission to hospital, but with four other risk factors, consider for antenatal prophylaxis throughout pregnancy.
  • without previous VTE & without particular Ist trimester risk factors or admission to hospital, but 3 other risk factors, can start antenatal prophylaxis at 28 wks.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What are the first trimester risk factors for VTE and how should they be managed?

A
  • admitted with hyperemesis consider for thromboprophylaxis with LMWH & discontinue thromboprophylaxis when hyperemesis resolves.
  • with OHSS, consider thromboprophylaxis with LMWH in first trimester.
  • IVF pregnancy and three other risk factors consider for thromboprophylaxis with LMWH starting in first trimester.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

When should thromboprophylaxis be interrupted for delivery?

A
  • receiving antenatal LMWH: advise if any vaginal bleeding or once labour begins, not inject any further LMWH. reassessed on admission to hospital and further doses should be prescribed by medical staff.
  • Regional techniques avoided if possible until at least 12 hours after previous prophylactic dose of LMWH.
  • LMWH not given for 4 hours after spinal anaesthesia or after epidural catheter removed and catheter should not be removed within 12 hours of most recent injection.
  • woman presents while on a therapeutic regimen of LMWH, regional techniques avoided if possible for at least 24 hours after last dose of LMWH.
  • receiving antenatal LMWH having elective CS receive
    thromboprophylactic dose of LMWH on day prior to delivery and, on day of delivery, any morning dose omitted & operation performed that morning.
  • first thromboprophylactic dose of LMWH given ASAP after delivery provided no PPH & regional analgesia not been used.
  • high risk of haemorrhage with risk factors including major APH, coagulopathy, progressive wound haematoma, suspected intra-abdominal bleeding and
    PPH may be managed with anti-embolism stockings (AES), foot impulse devices or intermittent pneumatic compression devices.
  • Unfractionated heparin (UFT) may also be considered.
    If develops haemorrhagic problem while on LMWH treatment should be stopped & expert haematological advice sought.
  • Thromboprophylaxis should be started or reinstituted as soon as immediate risk of haemorrhage reduced
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What are the risk factors for VTE after delivery?

A
- class 3 obesity (BMI > or = 40 kg/m2 ) consider for
prophylactic LMWH in doses appropriate for their weight for 10 days after delivery. 
  • with two or more persisting risk factors should be considered for LMWH in prophylactic doses appropriate for their weight for 10 days after delivery.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Which women with previous VTE need postpartum thromboprophylaxis?

A
  • previous history of confirmed VTE offer thromboprophylaxis with LMWH or warfarin for at least 6 wks postpartum regardless of mode of delivery.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Asymptomatic thrombophilia

Which women with thrombophilia without previous VTE need postpartum thromboprophylaxis?

A
  • thrombophilia without previous VTE stratified according to both level of risk associated with their thrombophilia & presence or absence of family history or other risk factors.
  • family history of VTE and an identified thrombophilia consider for 6 wks’ postnatal thromboprophylaxis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is the magnitude of risk of VTE after caesarean section?

A
  • had CS consider thromboprophylaxis with LMWH for 10 days after delivery apart from elective CS, consider for thromboprophylaxis with LMWH for 10 days after delivery if they have any additional risk factors.
17
Q

For how long should thromboprophylaxis be continued after delivery?

A
  • Risk assessment performed: at least once following delivery and before discharge and arrangements for LMWH prescription and administration (usually by woman herself) in community where necessary.
  • Thromboprophylaxis for 6 weeks in high-risk women and for 10 days in intermediate-risk women
  • additional persistent (lasting > 10 days postpartum) risk factors, as prolonged admission, wound infection or surgery in puerperium, thromboprophylaxis extended for up to 6 weeks or until additional risk factor/s is/are no longer present.
18
Q

Low-molecular-weight heparin (LMWH)

A
  • agents of choice for antenatal & postnatal thromboprophylaxis.
  • Doses of LMWH are based on weight. (booking or most recent weight).
  • only necessary to monitor platelet count if had prior exposure to UFH.
  • Monitoring of anti-Xa levels not required when LMWH is used for thromboprophylaxis.
  • Doses of LMWH should be reduced in women with renal impairment.
  • LMWH is safe in breastfeeding.
19
Q

Unfractionated heparin

A
  • In women at very high risk of thrombosis, UFH may be used peripartum in preference to LMWH where there is an increased risk of haemorrhage or where regional anaesthetic techniques may be required.
  • If UFH is used after CS (or other surgery), platelet count should be monitored every 2–3 days from days 4–14 or until heparin is stopped.
20
Q

Danaparoid (da nap’ a roid.)

anticoagulant and antithrombic effects involves a complex interaction between 2 components, factor IIa and in particular, factor Xa.

A
  • Potential use in conjunction with consultant haematologist with expertise in haemostasis and pregnancy.
21
Q

Fondaparinux (FON-da-PAR-in-ux)

Selective factor Xa inhibitor

The antithrombotic activity of fondaparinux is the result of ATIII-mediated selective inhibition of Factor Xa. By selectively binding to ATIII, Fondaparinux potentiates (about 300 times) the neutralization of Factor Xa by ATIII.

A
  • reserved for intolerant of heparin compounds.

- use in pregnancy in conjunction with consultant haematologist with expertise in haemostasis and pregnancy.

22
Q

Low-dose aspirin

A
  • not recommended for thromboprophylaxis in obstetric patients.
23
Q

Warfarin

A
  • use in pregnancy is restricted to few situations where heparin is considered unsuitable, e.g. some women with mechanical heart valves.
  • receiving long-term anticoagulation with warfarin can be converted from LMWH to warfarin postpartum when the risk of haemorrhage is reduced, usually 5–7 days after delivery.
  • Warfarin is safe in breastfeeding.
24
Q

Dextran

A

Dextran should be avoided antenatally and intrapartum because of the risk of anaphylactoid reaction.