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PREVENTION OF VTE IN 
OBSTETRIC POPULATION 
BY Dr Kanddy Loo 
O&G Updates 
1/11/14 
O&G department 
Miri hospital
CASE SCENARIO 
• 40 year-old P6, post emergency caesarean 
section for acute fetal distress D 6 
• Had BMI of 40 
• Presented with acute onset of SOB and chest 
pain 
• Denied calf swelling 
• Otherwise, no known medical illness; 
normotensive antenatally and intrapartumly 
• Examination showed tachycardia and 
tachypnoea; with saturation under room air of 
80%; normotensive 
• Lungs examination was unremarkable
PROBABLE DIAGNOSIS…..
INTRODUCTION 
• Pulmonary embolism remains the leading direct cause of maternal death 
• Most of the patients who died from PE have identifiable risks 
• 70% of women who died from PE in UK between 2003-2005 had identifiable risk 
• Thromboprophylaxis antenatally and postnatally – estimated to reduce risk of 
VTE in obstetric patients by up to 2/3 
• Objective of this lecture 
• Introduction of state VTE prevention programme 
• Risk stratification of patient according to VTE score to identify patients for 
thromboprophylaxis 
• Antenatal VTE occur in the first trimester 
• Therefore assessment and prophylaxis, if indicated should be given as early as 
possible in pregnancy
MATERNAL MORTALITY - UK 
CEMACH 2003-2005 CEMACH 2006-2008
MATERNAL MORTALITY - MALAYSIA
PATHOPHYSIOLOGY 
• Incidence of VTE in pregnancy – 60/100000 
woman-years 
• 12 fold increase compared to non pregnant 
population 
• Virchow’s Triad
SARAWAK VTE PREVENTION PROGRAMME 
• Introduced on 1 July 2013 
• To be implemented over Sarawak state 
• Initially hospital based 
• Expanded to primary health care centre on Mac 2014 
• Obstetric patients are assessed based on modified VTE scoring system 
• Done as early in pregnancy as possible 
• Repeat assessment if there’s emergence of new risk factors/during hospitalisation 
• Start thromboprophylaxis if 
• VTE score 3 or more antenatally and continue postnatally for 6 weeks 
• VTE score 2 or more postnatally – for at least 1 week 
• Patient with additional persistent risk factor (lasting more then 1/52 postnatal) should 
thromboprophylaxis should be extended for up to 6 weeks or longer
VERY HIGH VTE RISK 
• Needs antenatal high-dose thromboprophylaxis (high prophylactic – 12 
hourly or 75% of treatment dose) antenatally and postnatally 6 weeks 
• Very high risk factors 
• Recurrent VTE associated with APS 
• Patient on long term anticoagulation 
• Antithrombin deficiency
HIGH RISK 
• Thromboprophylaxis antenatally and 6 weeks postnatally 
• Risk factors 
• Previous unprovoked, estrogen related (pregnancy/pills induced), recurrent VTE 
• Previous VTE with risk factors (family history of VTE, thrombophyilia or other risk 
factors 
• Asymptomatic thrombophilia (combine defects, homozygous Factor V Leiden) 
• Combination of 3 or more risk factors
INTERMEDIATE RISK 
• Postnatal thromboprophylaxis (duration ranges from 1 – 6 weeks) 
• Single previous VTE associated with temporary risk factor with no other risk 
factors (thromboprophylaxis upto 6 weeks postnatal) 
• Asymptomatic thrombophilia (except antithrombin deficiency, combined 
defects, homozygous FVL) – 1 week prophylaxis or 6 weeks if presence of 
other risk factors 
• Presence of 2 or more risk factors
THROMBOPHILIA SCREENING 
• Only done for those VTE provoked by minor risk factors 
• Antenatal thromboprophylaxis till postnatal 6/52 
• Previous VTE with thromphilia 
• Asymptomatic thrombophilia with other risk factors 
• Asymptomatic thrombophilia 
• Combine defects 
• Homozygous Factor V Leiden 
• Postnatal thrombophylaxis 
• Other asymptomatic thrombophilia without other risk factors
ANTI COAGULANT AGENTS 
• Low molecular weight heparin 
• Agents of choice 
• As effective as and safer then the unfractionated heparin 
• Lower risk of Heparin induced thrombocytopaenia and osteoporosis 
• Risk of bleeding - <2% with prophylactic dose 
• Monitoring of anti-Xa levers is not required if women have normal renal function 
• Unfractionated Heparin 
• Shorter half life 
• More complete reversal of its activity 
• May be used around the time of delivery in women with very high risk of 
thrombosis
• Fondaparinox 
• Licenced for prevention and treatment of VTE outside pregnancy 
• Similar efficacy to LMWH 
• Limited experience in pregnancy 
• Although no adverse effects were observed in newborns, it is premature to conclude its safety in pregnancy 
• Reserved for women intolerance to heparin 
• Local setting – used in postnatal thrombophylaxis 
• Warfarin 
• Associated with warfarin embriopathy 
• 5% risk when exposed between 6 – 12 weeks 
• For patient with mechanical heart valve 
• Can be used postnatally – 5 – 7 days post delivery 
• Safe in breastfeeding 
• Other anti coagulant – avoided in pregnancy 
• Graduated elastic compression stocking
CONTRAINDICATION TO THROMBOPROPHYLAXIS 
• Antenatal or postpartum bleeding 
• Massive PPH – risk factor for VTE; therefore risk and benefits of 
thromboprophylaxis should be weighted 
• Increased risk of major haemorrhage 
• Bleeding diathesis, including thrombocytopaenia 
• Platelet less than 75 x 109 
• Acute stroke in last 4 weeks 
• Severe renal disease 
• Severe liver disease 
• Uncontrolled hypertension (SBP>200mmHg; DBP>120mmHg)
ANAESTHESIA 
• Regional techniques should not be used at least 12 hours after previous 
prophylactic dose of LMWH 
• 24 hours after last dose of therapeutic dose 
• 4 hours after last dose of unfractionated heparin 
• LMWH should not be given for 4 hours after regional anaesthesia or after 
removal of epidural catheter 
• Epidural catheter should not be removed within 10 – 12 hours of the last dose
QUIZ – SCENARIO 1 
• 40 year-old; primigravida; subfertility for 20 years 
• BMI 32 
• Currently at 10 weeks…..
• At 12 weeks, she was admitted with hyperemesis gravidarum…. 
• At 30 weeks, she was again admitted and treated as acute appendicitis; 
appendicectomy was done
• At 38 weeks, she has EMLSCS for fetal compromise; complicated with 
massive PPH and had massive transfusion….
QUIZ – SCENARIO 2 
• 30 year-old G2P1 at 8 weeks; came for booking 
• Previous history of postpartum DVT; completed warfarin treatment for 6 
months 
• Currently well, no leg swelling 
• BM1 25
• At 36 weeks, she presented with SROM with TMSL and os was only 1 cm…. 
• Postnatally….
THANK YOU

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Prevention of Venous Thrombo-Embolism

  • 1. PREVENTION OF VTE IN OBSTETRIC POPULATION BY Dr Kanddy Loo O&G Updates 1/11/14 O&G department Miri hospital
  • 2. CASE SCENARIO • 40 year-old P6, post emergency caesarean section for acute fetal distress D 6 • Had BMI of 40 • Presented with acute onset of SOB and chest pain • Denied calf swelling • Otherwise, no known medical illness; normotensive antenatally and intrapartumly • Examination showed tachycardia and tachypnoea; with saturation under room air of 80%; normotensive • Lungs examination was unremarkable
  • 4. INTRODUCTION • Pulmonary embolism remains the leading direct cause of maternal death • Most of the patients who died from PE have identifiable risks • 70% of women who died from PE in UK between 2003-2005 had identifiable risk • Thromboprophylaxis antenatally and postnatally – estimated to reduce risk of VTE in obstetric patients by up to 2/3 • Objective of this lecture • Introduction of state VTE prevention programme • Risk stratification of patient according to VTE score to identify patients for thromboprophylaxis • Antenatal VTE occur in the first trimester • Therefore assessment and prophylaxis, if indicated should be given as early as possible in pregnancy
  • 5. MATERNAL MORTALITY - UK CEMACH 2003-2005 CEMACH 2006-2008
  • 7. PATHOPHYSIOLOGY • Incidence of VTE in pregnancy – 60/100000 woman-years • 12 fold increase compared to non pregnant population • Virchow’s Triad
  • 8.
  • 9. SARAWAK VTE PREVENTION PROGRAMME • Introduced on 1 July 2013 • To be implemented over Sarawak state • Initially hospital based • Expanded to primary health care centre on Mac 2014 • Obstetric patients are assessed based on modified VTE scoring system • Done as early in pregnancy as possible • Repeat assessment if there’s emergence of new risk factors/during hospitalisation • Start thromboprophylaxis if • VTE score 3 or more antenatally and continue postnatally for 6 weeks • VTE score 2 or more postnatally – for at least 1 week • Patient with additional persistent risk factor (lasting more then 1/52 postnatal) should thromboprophylaxis should be extended for up to 6 weeks or longer
  • 10.
  • 11. VERY HIGH VTE RISK • Needs antenatal high-dose thromboprophylaxis (high prophylactic – 12 hourly or 75% of treatment dose) antenatally and postnatally 6 weeks • Very high risk factors • Recurrent VTE associated with APS • Patient on long term anticoagulation • Antithrombin deficiency
  • 12. HIGH RISK • Thromboprophylaxis antenatally and 6 weeks postnatally • Risk factors • Previous unprovoked, estrogen related (pregnancy/pills induced), recurrent VTE • Previous VTE with risk factors (family history of VTE, thrombophyilia or other risk factors • Asymptomatic thrombophilia (combine defects, homozygous Factor V Leiden) • Combination of 3 or more risk factors
  • 13. INTERMEDIATE RISK • Postnatal thromboprophylaxis (duration ranges from 1 – 6 weeks) • Single previous VTE associated with temporary risk factor with no other risk factors (thromboprophylaxis upto 6 weeks postnatal) • Asymptomatic thrombophilia (except antithrombin deficiency, combined defects, homozygous FVL) – 1 week prophylaxis or 6 weeks if presence of other risk factors • Presence of 2 or more risk factors
  • 14. THROMBOPHILIA SCREENING • Only done for those VTE provoked by minor risk factors • Antenatal thromboprophylaxis till postnatal 6/52 • Previous VTE with thromphilia • Asymptomatic thrombophilia with other risk factors • Asymptomatic thrombophilia • Combine defects • Homozygous Factor V Leiden • Postnatal thrombophylaxis • Other asymptomatic thrombophilia without other risk factors
  • 15. ANTI COAGULANT AGENTS • Low molecular weight heparin • Agents of choice • As effective as and safer then the unfractionated heparin • Lower risk of Heparin induced thrombocytopaenia and osteoporosis • Risk of bleeding - <2% with prophylactic dose • Monitoring of anti-Xa levers is not required if women have normal renal function • Unfractionated Heparin • Shorter half life • More complete reversal of its activity • May be used around the time of delivery in women with very high risk of thrombosis
  • 16. • Fondaparinox • Licenced for prevention and treatment of VTE outside pregnancy • Similar efficacy to LMWH • Limited experience in pregnancy • Although no adverse effects were observed in newborns, it is premature to conclude its safety in pregnancy • Reserved for women intolerance to heparin • Local setting – used in postnatal thrombophylaxis • Warfarin • Associated with warfarin embriopathy • 5% risk when exposed between 6 – 12 weeks • For patient with mechanical heart valve • Can be used postnatally – 5 – 7 days post delivery • Safe in breastfeeding • Other anti coagulant – avoided in pregnancy • Graduated elastic compression stocking
  • 17.
  • 18. CONTRAINDICATION TO THROMBOPROPHYLAXIS • Antenatal or postpartum bleeding • Massive PPH – risk factor for VTE; therefore risk and benefits of thromboprophylaxis should be weighted • Increased risk of major haemorrhage • Bleeding diathesis, including thrombocytopaenia • Platelet less than 75 x 109 • Acute stroke in last 4 weeks • Severe renal disease • Severe liver disease • Uncontrolled hypertension (SBP>200mmHg; DBP>120mmHg)
  • 19. ANAESTHESIA • Regional techniques should not be used at least 12 hours after previous prophylactic dose of LMWH • 24 hours after last dose of therapeutic dose • 4 hours after last dose of unfractionated heparin • LMWH should not be given for 4 hours after regional anaesthesia or after removal of epidural catheter • Epidural catheter should not be removed within 10 – 12 hours of the last dose
  • 20. QUIZ – SCENARIO 1 • 40 year-old; primigravida; subfertility for 20 years • BMI 32 • Currently at 10 weeks…..
  • 21. • At 12 weeks, she was admitted with hyperemesis gravidarum…. • At 30 weeks, she was again admitted and treated as acute appendicitis; appendicectomy was done
  • 22. • At 38 weeks, she has EMLSCS for fetal compromise; complicated with massive PPH and had massive transfusion….
  • 23. QUIZ – SCENARIO 2 • 30 year-old G2P1 at 8 weeks; came for booking • Previous history of postpartum DVT; completed warfarin treatment for 6 months • Currently well, no leg swelling • BM1 25
  • 24. • At 36 weeks, she presented with SROM with TMSL and os was only 1 cm…. • Postnatally….