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Hypertension in Pregnancy
This talk
 How to measure BP
 When is a pregnant woman hypertensive
 What is the Differential Diagnosis
 What tests are required and how do you
interpret them
 Tests for proteinuria
 Risk factors for pre-eclampsia
 Pathophysiology of pre eclampsia
 How to manage the hypertensive gravida
 Which is the best drug to lower BP
This talk(2)
 Who should be delivered? How & Where
 Best practice intrapartum care
 Who requires an anticonvulsant?
 What is the best drug for Eclampsia?
 Best practice postpartum care
 Best practice anaesthetic care
 Prognosis after pre-eclampsia
 Can pre-eclampsia be predicted?
 Can pre-eclampsia be prevented?
How to Measure BP in a Pregnant Woman
o Automated machines not recommended
o Unless calibrated against a mercury sphygmomanometer in
the individual patient
 Appropriate sized cuff
 Seated for 2 - 3 minutes with feet supported
 Both arms first visit
 Palpate systolic and go 20 mm higher
 Deflate slowly 2 mm every sec
 Use Korotkoff 5 (or 4 if 5 absent) for diastolic
 Repeated measures may be required
 Ambulatory monitoring useful for White Coat
Hypertension
When is a Pregnant Woman
Hypertensive?
 >140/90 on >one occasion
 (Rise of >30 systolic or >15 diastolic)
 Knowledge of prior BP very important
 Not in itself diagnostic – look for other problems
 Severe hypertension is >169 systolic and
or diastolic >109
 Requires admission and urgent Rx
 However, the diagnosis is more important
than the actual level of BP.
Differential Diagnosis of Hypertension
in Pregnancy
 Gestational Hypertension
 Sustained hypertension after 20w of pregnancy without any
other organ involvement. Returns to normal in 3m
 Preeclampsia
 Sustained hypertension after 20w of pregnancy with
evidence of other organ involvement. Returns to normal in
3m
 Chronic Hypertension
 Hypertensive before 20w. 95% is Essential Hypertension
Includes “White Coat Hypertension”
Systems involved in Preeclampsia
 Renal
 Significant proteinuria (>300 mg in 24 hours or P:C > 0.30)
 S Creat >90
 Oliguria
 Hepatic
 Elevated transaminases (AST or ALT >70)
 Epigastric or RUQ pain
 Haematological
 Thrombocytopenia (<100)
 Haemolysis
 DIC
 CNS
 Eclampsia or stroke
 Hyperreflexia with sustained clonus
 Severe headache or visual disturbance
 Cardiovascular
 Pulmonary oedema
 Placental
 IUGR
 Abruption
Please note
 I have not used the words “Pregnancy induced
Hypertension” or PIH
 No mention is made of oedema
 Proteinuria is the most common manifestation of
“other system involvement” and some method of
assessment is critical to good obstetric care
 Evidence for other organ involvement in Pre
eclampsia is a mix of symptoms, signs and tests
Tests of Proteinuria
 The screening test is by dipstick
 Have a sensitivity >90% using ≥ 1+
 But correlate poorly with high protein loss
 And false negative rates up to 20%
 Will miss >300 mg/24 hours in up to 1:8 patients
 And the test strips spoil quickly in humidity
 Boiling urine is sensitive and quantifiable
 But messy and disliked by midwives
 24 hour collection and quantification by lab
 Is the gold standard
 But labour intensive and slow
 The protein:creatinine ratio on a spot sample is a
good compromise
Proteinuria in Practice
 Significant proteinuria occurs when...
 There is ≥ 2+ on dipstick
 Trace or 1+ should be regarded as equivocal
 The 24 hour urine collection is > 300 mg
 The spot urine protein:creatinine ratio is ≥
30 mg/mmol
 There is > “cloud” on boiled urine
 When significant proteinuria has been
detected there is little point in repeating
the measure
Some rare causes of preeclampsia
before 20w
 Hydatidiform mole
 Fetal triploidy (with or without partial mole)
 Severe renal disease
 Lupus obstetric syndrome
Renal Disease in Pregnancy
 Responsible for about 5% of chronic hypertension
 Causes include:
 chronic or recurrent infection
 glomerulonephritis
 renal artery stenosis
 Must be assessed by creatinine clearance (CC)
which doubles in normal pregnancy
 When CC falls below 50% the prognosis is very
bad
 Monitoring for superimposed pre eclampsia can
be difficult if there is chronic proteinuria
 Donors of a kidney have 2.4-fold increased risk
of PE but usually not severe
Some rare causes of hypertension
 Coarctation of the aorta
 Sometimes the clue is to measure BP in both arms
 There is a systolic murmur that can be heard in the
back
 Phaeochromocytoma
 Paroxysms of symptomatic hypertension
 The clue to diagnosis is to think of it
 Associated with high levels of catecholamines
 Hyperaldosteronism
 Also known as Conn’s disease
 Placental tissue
 In healthy pregnancies cytotrophoblast
infiltrates the decidual portion of the uterine
spiral arteries
 In order to increase maternal blood flow to the
placenta
 In patients destined to develop pre eclampsia
this fails to occur
 This results in placental hypoperfusion
 These changes occur at <16 weeks gestation
but the pre eclampsia may not be manifest until
much later in the pregnancy
Pathophysiology of Pre eclampsia
 Hypoperfusion of the Placenta
 Becomes worse as pregnancy progresses
 The abnormal uterine vasculature is unable to
accommodate the normal rise in blood flow to
the fetus/placenta that occurs with increasing
gestational age.
 Late placental changes consistent with
ischemia include atherosis (lipid-laden cells in
the wall arterioles), fibrinoid necrosis,
thrombosis, sclerotic narrowing of arterioles,
and placental infarction
Pathophysiology of Pre eclampsia
 An ‘immunolgical’ response to pregnancy
---in ‘at risk’ or predisposed women
 A response to a conceptus whose genetic
material is 50% foreign (from the father)
 A failure of ‘Blocking Antibody’
 This disease is still a mystery
Pathophysiology WHY?
 Contracted intravascular volume of mother
 In reality a failure to increase plasma volume
 ↑Sensitivity to pressure agents
 Leaky Capillaries
 Reduced oncotic pressure
 In part due to low serum albumen
 Poor placental reserve
 A fetus at risk of hypoxia and death
Pathophysiology WHAT?
 Hypertension/ Proteinuria/ oedema
 Low platelets Consumption
 Raised urate Cell (DNA) death
 Raised Haematocrit Reduced plasma volume
 Haemolysis
 Abnormal LFT’s
 Abnormal clotting Widespread DIC
Pathophysiology WHAT?
Tests for the Hypertensive Gravida
 Blood tests
 FBC - look at HB, Haematocrit and Platelets
 UEC - look at Creatinine Should be < 0.07 (or 70)
 URATE - equivalent to weeks gestation
 Liver enzymes – AST & ALT should be <70. Ignore ALP
 Urine Tests
 UMCS - exclude UTI and look for casts
 Protein:Creatinine ratio from spot test >30 significant
 24 hr protein excretion >300 mg/day significant
 Assess fetal welfare by CTG & Scan for AFI
and UA Dopplers
Frequency of Testing
Management of Hypertensive
Gravida
 Hospitalise if pre-eclamptic
 Discharge if “just BP”
 Bed rest only when there is proteinuria
 Control BP to protect mother from severe
hypertension
 Role of antihypertensive agents for mild &
moderate chronic hypertension is
controversial
 Delivery will cure pre eclampsia & gestational
hypertension
 Remember thromboprophylaxis
Tests of Fetal Welfare
Which Drug is Best for
Hypertension in Pregnancy?
 The drug that you know best
 Aldomet
 Up to 2250 mg per day
 Labetalol
 Up to 1200 mg/day
 Oxyprenalol
 Up to 480 mg/day
 Nifedipine
 Up to 120 mg/day
 Prazosin
 Up to 15 mg/day
Drugs for Hypertension in
Pregnancy?
 Combination therapy of drugs from
different classes is possible e.g.
 Aldomet + Beta blocker + Prazosin
 Do not use…
 Thiazide diuretics – reduce plasma volume
 Highly selective beta blokers – cause IUGR
 ACE inhibitors – may cause IUFD
 Aim for BP 130 -150 systolic and 80 –
100 diastolic
Which Drug is Best for Acute
Hypertension?
 The drug that you know best
 IV Hydralazine 5 – 10 mg every 20-30 min
 or by infusion
 IV Labetalol 20 – 50 mg over 2 min.
 Repeat after 15 – 30 min
 Nifedipine crushed oral 10 mg
 Repeat after 30 min
 IV Diazoxide 15 – 45 mg bolus
 Repeat after 5 min to a maximum of 300 mg
Which Drug is Best for Eclampsia?
 First aid is more important than drugs
 Protect from injury
 Secure an airway
 Administer oxygen
 Then secure IV access
 IV MgSO4 4G over 10 – 15 min
 Then 1 -2 G/hour by infusion
 If seizure recurs then give another 2 – 4 G
bolus
 IV Diazepam only for status eclampticus
 Monitor urine output, respirations, O2
saturation and DTJ’s
Who Needs Fluid Expansion?
 If there is severe proteinuria and oliguria
 Then give 500 – 1000 ml cautiously
 Injudicious use carries a risk of pulmonary oedema and
adult RDS
 Pre load prior to epidural or spinal
 Consult with anaesthetist
 Use colloids rather than crystalloids
 Sometimes required if BP drops suddenly
 Sometimes occurs with Diazoxide/Hydralazine
 CTG monitoring desirable
 Abruption requires prompt resuscitation
 Often requires blood
 Watch urine output and/or JVP
Who Requires Delivery?
 Pre eclampsia >36 completed weeks
 Uncontrollable hypertension
 Deteriorating renal, hepatic or haematologic
state
 For GA >32w and good neonatal facilities
delay only long enough to give steroids
 Eclampsia or imminently eclamptic
 Fetus is compromised
 APH - abruption
Induction of Labour vs Expectant Management for
Gestational Hypertension Koopmans et al Lancet 2009
 The HYPITAT study
 A multicentre RCT of 756 women in Netherlands
 Were 36 – 41 weeks with a diagnosis of mild pre
eclampsia or gestational hypertension
 Of the women randomised to induction of labour
31% had a poor outcome vs 44% for observation
(RR=0.71, CI 0.59-0.86, p<0.001)
 Poor outcomes included eclampsia, HELLP, severe
pre eclampsia and PPH
 No greater risk of Caesarean or neonatal morbidity
 Active management is also more cost effective
How to Deliver
 Deliver vaginally if >37w and Cx is favourable
 or can be ripened
 Caesarean only if the above not met
 Elective CS usually at gestations <35w
 Inappropriate attempts at delivery when it is
not indicated is an invitation to CS (and more
CS)
 Deliver in an environment that can cope with
a severe multisystem disease
 Don’t overlook patient’s and family’s psychological needs
Intrapartum Care
 Assess convulsive risk and consider
prophylactic MgSO4
 Control BP with an epidural or IV Hydralazine
 Careful fluid balance
 Monitor the fetus
 Avoid ergometrine
 SVD is not a sin!
Anaesthetic Implications
 Epidural good for both vaginal & abdominal
delivery
 Spinal + Vasopressin also okay
 Spinal plus epidural for a few cases
 Low dose aspirin okay for epidural
 GA for acute fetal compromise or low
platelets
 <50, and 50 – 75 is a grey zone
 Watch for hypertension during GA intubation
 Use antacid and lateral tilt
 Cautious use of oxytocin boluses
Postpartum Care
 Things may get worse before they get
better
 Oliguria for 24 hours is common
 Seizure risk is greatest for 48 hrs
 Continue MgSO4 infusion for 24 hrs
 Avoid NSAIDs
 Treat any BP >150/100
 Use Nifedipine PRN
 OK to discharge 3d after BP control
 Follow up weekly to 6w then 3m
The Prognosis after Pre eclampsia
 Mild pre eclampsia near term has a low
recurrence risk
 Unless there is a new partner or a long gap to the next
pregnancy
 Severe pre eclampsia prior to 34w has a 50-
66% recurrence risk
 Most recover by 12w but these patients are at
increased lifetime risk of hypertension and
related disease
Can Preeclampsia be predicted
and prevented?
 Identifying the patient at risk
 Early pregnancy testing
 Prevention strategies
 Especially the role of low dose aspirin
Risk factors for severe pre eclampsia
 Previous pre eclampsia at <35w
 Renal disease
 Thombophilias
 Autoimmune disease e.g. SLE
 Diabetes
 Multiple pregnancy
 Severe alloimmunisation
 Family history of pre eclampsia
 Obesity
 Increasing maternal age
Patients at risk
Prediction of Pre eclampsia
 Risk factors alone are insensitive and non
specific
 Response to an infusion of angiotensin
 Suitable only in a research setting
 Measure vasoactive proteins in serum
 PAPP-A, Placental growth factor (PlGF)
 Doppler studies at 12 – 14w
 Placental resistance & Uterine artery pulsatility
 Together these last two can identify 90% of
women who will get PE before 34w
 With false positive rate of 10%
The prevention of pre eclampsia
with low dose Aspirin – WHO?
 History of fetal death or severe IUGR
 Patients who previously required delivery
for pre eclampsia prior to 34w
 Conditions with high risk of pre eclampsia
eg Lupus or homozygous for thrombophilia
 These patients also require heparin
 Patients identified by Screening at 12 –
14w (London FMF program)
 Also use Ca supplements of 1.5G daily
The prevention of pre eclampsia
with low dose Aspirin - Results
 Meta analysis suggests that 100 – 150 mg
daily started BEFORE 16 w
 Reduces risk of early onset pre-eclampsia by 50 –
90%
 Less valuable if started after 16w
 You need to treat 4-5 women to prevent one FDIU
or severe IUGR
 RISKS
 Does not increase the risk of APH, PPH or fetal
intracranial haemoorhage
 It is also not teratogenic
Other measures to prevent
preeclampsia
 Anti oxidant supplements (Vitamins C, E)
 Increase the risk of stillbirth and IUGR. Trials stopped
 Folic acid and multivitamins
 Requires more RCTs
 Metformin
 Improves uteroplacental circulation and reduces the rate
of pre eclampsia and pre term birth for PCO patients who
take it in early pregnancy. Needs study in a wider group of
patients
 Abdominal decompression
 Unproven and abandonded
For the NICE Guideline go
to
http://pathways.nice.org.uk/pathways/hyperten
sion-in-pregnancy
Any Questions or
Comments?
Please leave a note on the
Welcome Page to this website

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HypertensionPregnancyPG.ppt

  • 2. This talk  How to measure BP  When is a pregnant woman hypertensive  What is the Differential Diagnosis  What tests are required and how do you interpret them  Tests for proteinuria  Risk factors for pre-eclampsia  Pathophysiology of pre eclampsia  How to manage the hypertensive gravida  Which is the best drug to lower BP
  • 3. This talk(2)  Who should be delivered? How & Where  Best practice intrapartum care  Who requires an anticonvulsant?  What is the best drug for Eclampsia?  Best practice postpartum care  Best practice anaesthetic care  Prognosis after pre-eclampsia  Can pre-eclampsia be predicted?  Can pre-eclampsia be prevented?
  • 4. How to Measure BP in a Pregnant Woman o Automated machines not recommended o Unless calibrated against a mercury sphygmomanometer in the individual patient  Appropriate sized cuff  Seated for 2 - 3 minutes with feet supported  Both arms first visit  Palpate systolic and go 20 mm higher  Deflate slowly 2 mm every sec  Use Korotkoff 5 (or 4 if 5 absent) for diastolic  Repeated measures may be required  Ambulatory monitoring useful for White Coat Hypertension
  • 5. When is a Pregnant Woman Hypertensive?  >140/90 on >one occasion  (Rise of >30 systolic or >15 diastolic)  Knowledge of prior BP very important  Not in itself diagnostic – look for other problems  Severe hypertension is >169 systolic and or diastolic >109  Requires admission and urgent Rx  However, the diagnosis is more important than the actual level of BP.
  • 6. Differential Diagnosis of Hypertension in Pregnancy  Gestational Hypertension  Sustained hypertension after 20w of pregnancy without any other organ involvement. Returns to normal in 3m  Preeclampsia  Sustained hypertension after 20w of pregnancy with evidence of other organ involvement. Returns to normal in 3m  Chronic Hypertension  Hypertensive before 20w. 95% is Essential Hypertension Includes “White Coat Hypertension”
  • 7. Systems involved in Preeclampsia  Renal  Significant proteinuria (>300 mg in 24 hours or P:C > 0.30)  S Creat >90  Oliguria  Hepatic  Elevated transaminases (AST or ALT >70)  Epigastric or RUQ pain  Haematological  Thrombocytopenia (<100)  Haemolysis  DIC  CNS  Eclampsia or stroke  Hyperreflexia with sustained clonus  Severe headache or visual disturbance  Cardiovascular  Pulmonary oedema  Placental  IUGR  Abruption
  • 8. Please note  I have not used the words “Pregnancy induced Hypertension” or PIH  No mention is made of oedema  Proteinuria is the most common manifestation of “other system involvement” and some method of assessment is critical to good obstetric care  Evidence for other organ involvement in Pre eclampsia is a mix of symptoms, signs and tests
  • 9. Tests of Proteinuria  The screening test is by dipstick  Have a sensitivity >90% using ≥ 1+  But correlate poorly with high protein loss  And false negative rates up to 20%  Will miss >300 mg/24 hours in up to 1:8 patients  And the test strips spoil quickly in humidity  Boiling urine is sensitive and quantifiable  But messy and disliked by midwives  24 hour collection and quantification by lab  Is the gold standard  But labour intensive and slow  The protein:creatinine ratio on a spot sample is a good compromise
  • 10. Proteinuria in Practice  Significant proteinuria occurs when...  There is ≥ 2+ on dipstick  Trace or 1+ should be regarded as equivocal  The 24 hour urine collection is > 300 mg  The spot urine protein:creatinine ratio is ≥ 30 mg/mmol  There is > “cloud” on boiled urine  When significant proteinuria has been detected there is little point in repeating the measure
  • 11. Some rare causes of preeclampsia before 20w  Hydatidiform mole  Fetal triploidy (with or without partial mole)  Severe renal disease  Lupus obstetric syndrome
  • 12. Renal Disease in Pregnancy  Responsible for about 5% of chronic hypertension  Causes include:  chronic or recurrent infection  glomerulonephritis  renal artery stenosis  Must be assessed by creatinine clearance (CC) which doubles in normal pregnancy  When CC falls below 50% the prognosis is very bad  Monitoring for superimposed pre eclampsia can be difficult if there is chronic proteinuria  Donors of a kidney have 2.4-fold increased risk of PE but usually not severe
  • 13. Some rare causes of hypertension  Coarctation of the aorta  Sometimes the clue is to measure BP in both arms  There is a systolic murmur that can be heard in the back  Phaeochromocytoma  Paroxysms of symptomatic hypertension  The clue to diagnosis is to think of it  Associated with high levels of catecholamines  Hyperaldosteronism  Also known as Conn’s disease
  • 14.  Placental tissue  In healthy pregnancies cytotrophoblast infiltrates the decidual portion of the uterine spiral arteries  In order to increase maternal blood flow to the placenta  In patients destined to develop pre eclampsia this fails to occur  This results in placental hypoperfusion  These changes occur at <16 weeks gestation but the pre eclampsia may not be manifest until much later in the pregnancy Pathophysiology of Pre eclampsia
  • 15.  Hypoperfusion of the Placenta  Becomes worse as pregnancy progresses  The abnormal uterine vasculature is unable to accommodate the normal rise in blood flow to the fetus/placenta that occurs with increasing gestational age.  Late placental changes consistent with ischemia include atherosis (lipid-laden cells in the wall arterioles), fibrinoid necrosis, thrombosis, sclerotic narrowing of arterioles, and placental infarction Pathophysiology of Pre eclampsia
  • 16.  An ‘immunolgical’ response to pregnancy ---in ‘at risk’ or predisposed women  A response to a conceptus whose genetic material is 50% foreign (from the father)  A failure of ‘Blocking Antibody’  This disease is still a mystery Pathophysiology WHY?
  • 17.  Contracted intravascular volume of mother  In reality a failure to increase plasma volume  ↑Sensitivity to pressure agents  Leaky Capillaries  Reduced oncotic pressure  In part due to low serum albumen  Poor placental reserve  A fetus at risk of hypoxia and death Pathophysiology WHAT?
  • 18.  Hypertension/ Proteinuria/ oedema  Low platelets Consumption  Raised urate Cell (DNA) death  Raised Haematocrit Reduced plasma volume  Haemolysis  Abnormal LFT’s  Abnormal clotting Widespread DIC Pathophysiology WHAT?
  • 19. Tests for the Hypertensive Gravida  Blood tests  FBC - look at HB, Haematocrit and Platelets  UEC - look at Creatinine Should be < 0.07 (or 70)  URATE - equivalent to weeks gestation  Liver enzymes – AST & ALT should be <70. Ignore ALP  Urine Tests  UMCS - exclude UTI and look for casts  Protein:Creatinine ratio from spot test >30 significant  24 hr protein excretion >300 mg/day significant  Assess fetal welfare by CTG & Scan for AFI and UA Dopplers
  • 21. Management of Hypertensive Gravida  Hospitalise if pre-eclamptic  Discharge if “just BP”  Bed rest only when there is proteinuria  Control BP to protect mother from severe hypertension  Role of antihypertensive agents for mild & moderate chronic hypertension is controversial  Delivery will cure pre eclampsia & gestational hypertension  Remember thromboprophylaxis
  • 22. Tests of Fetal Welfare
  • 23. Which Drug is Best for Hypertension in Pregnancy?  The drug that you know best  Aldomet  Up to 2250 mg per day  Labetalol  Up to 1200 mg/day  Oxyprenalol  Up to 480 mg/day  Nifedipine  Up to 120 mg/day  Prazosin  Up to 15 mg/day
  • 24. Drugs for Hypertension in Pregnancy?  Combination therapy of drugs from different classes is possible e.g.  Aldomet + Beta blocker + Prazosin  Do not use…  Thiazide diuretics – reduce plasma volume  Highly selective beta blokers – cause IUGR  ACE inhibitors – may cause IUFD  Aim for BP 130 -150 systolic and 80 – 100 diastolic
  • 25. Which Drug is Best for Acute Hypertension?  The drug that you know best  IV Hydralazine 5 – 10 mg every 20-30 min  or by infusion  IV Labetalol 20 – 50 mg over 2 min.  Repeat after 15 – 30 min  Nifedipine crushed oral 10 mg  Repeat after 30 min  IV Diazoxide 15 – 45 mg bolus  Repeat after 5 min to a maximum of 300 mg
  • 26. Which Drug is Best for Eclampsia?  First aid is more important than drugs  Protect from injury  Secure an airway  Administer oxygen  Then secure IV access  IV MgSO4 4G over 10 – 15 min  Then 1 -2 G/hour by infusion  If seizure recurs then give another 2 – 4 G bolus  IV Diazepam only for status eclampticus  Monitor urine output, respirations, O2 saturation and DTJ’s
  • 27. Who Needs Fluid Expansion?  If there is severe proteinuria and oliguria  Then give 500 – 1000 ml cautiously  Injudicious use carries a risk of pulmonary oedema and adult RDS  Pre load prior to epidural or spinal  Consult with anaesthetist  Use colloids rather than crystalloids  Sometimes required if BP drops suddenly  Sometimes occurs with Diazoxide/Hydralazine  CTG monitoring desirable  Abruption requires prompt resuscitation  Often requires blood  Watch urine output and/or JVP
  • 28. Who Requires Delivery?  Pre eclampsia >36 completed weeks  Uncontrollable hypertension  Deteriorating renal, hepatic or haematologic state  For GA >32w and good neonatal facilities delay only long enough to give steroids  Eclampsia or imminently eclamptic  Fetus is compromised  APH - abruption
  • 29. Induction of Labour vs Expectant Management for Gestational Hypertension Koopmans et al Lancet 2009  The HYPITAT study  A multicentre RCT of 756 women in Netherlands  Were 36 – 41 weeks with a diagnosis of mild pre eclampsia or gestational hypertension  Of the women randomised to induction of labour 31% had a poor outcome vs 44% for observation (RR=0.71, CI 0.59-0.86, p<0.001)  Poor outcomes included eclampsia, HELLP, severe pre eclampsia and PPH  No greater risk of Caesarean or neonatal morbidity  Active management is also more cost effective
  • 30. How to Deliver  Deliver vaginally if >37w and Cx is favourable  or can be ripened  Caesarean only if the above not met  Elective CS usually at gestations <35w  Inappropriate attempts at delivery when it is not indicated is an invitation to CS (and more CS)  Deliver in an environment that can cope with a severe multisystem disease  Don’t overlook patient’s and family’s psychological needs
  • 31. Intrapartum Care  Assess convulsive risk and consider prophylactic MgSO4  Control BP with an epidural or IV Hydralazine  Careful fluid balance  Monitor the fetus  Avoid ergometrine  SVD is not a sin!
  • 32. Anaesthetic Implications  Epidural good for both vaginal & abdominal delivery  Spinal + Vasopressin also okay  Spinal plus epidural for a few cases  Low dose aspirin okay for epidural  GA for acute fetal compromise or low platelets  <50, and 50 – 75 is a grey zone  Watch for hypertension during GA intubation  Use antacid and lateral tilt  Cautious use of oxytocin boluses
  • 33. Postpartum Care  Things may get worse before they get better  Oliguria for 24 hours is common  Seizure risk is greatest for 48 hrs  Continue MgSO4 infusion for 24 hrs  Avoid NSAIDs  Treat any BP >150/100  Use Nifedipine PRN  OK to discharge 3d after BP control  Follow up weekly to 6w then 3m
  • 34. The Prognosis after Pre eclampsia  Mild pre eclampsia near term has a low recurrence risk  Unless there is a new partner or a long gap to the next pregnancy  Severe pre eclampsia prior to 34w has a 50- 66% recurrence risk  Most recover by 12w but these patients are at increased lifetime risk of hypertension and related disease
  • 35. Can Preeclampsia be predicted and prevented?  Identifying the patient at risk  Early pregnancy testing  Prevention strategies  Especially the role of low dose aspirin
  • 36. Risk factors for severe pre eclampsia  Previous pre eclampsia at <35w  Renal disease  Thombophilias  Autoimmune disease e.g. SLE  Diabetes  Multiple pregnancy  Severe alloimmunisation  Family history of pre eclampsia  Obesity  Increasing maternal age
  • 38. Prediction of Pre eclampsia  Risk factors alone are insensitive and non specific  Response to an infusion of angiotensin  Suitable only in a research setting  Measure vasoactive proteins in serum  PAPP-A, Placental growth factor (PlGF)  Doppler studies at 12 – 14w  Placental resistance & Uterine artery pulsatility  Together these last two can identify 90% of women who will get PE before 34w  With false positive rate of 10%
  • 39. The prevention of pre eclampsia with low dose Aspirin – WHO?  History of fetal death or severe IUGR  Patients who previously required delivery for pre eclampsia prior to 34w  Conditions with high risk of pre eclampsia eg Lupus or homozygous for thrombophilia  These patients also require heparin  Patients identified by Screening at 12 – 14w (London FMF program)  Also use Ca supplements of 1.5G daily
  • 40. The prevention of pre eclampsia with low dose Aspirin - Results  Meta analysis suggests that 100 – 150 mg daily started BEFORE 16 w  Reduces risk of early onset pre-eclampsia by 50 – 90%  Less valuable if started after 16w  You need to treat 4-5 women to prevent one FDIU or severe IUGR  RISKS  Does not increase the risk of APH, PPH or fetal intracranial haemoorhage  It is also not teratogenic
  • 41. Other measures to prevent preeclampsia  Anti oxidant supplements (Vitamins C, E)  Increase the risk of stillbirth and IUGR. Trials stopped  Folic acid and multivitamins  Requires more RCTs  Metformin  Improves uteroplacental circulation and reduces the rate of pre eclampsia and pre term birth for PCO patients who take it in early pregnancy. Needs study in a wider group of patients  Abdominal decompression  Unproven and abandonded
  • 42. For the NICE Guideline go to http://pathways.nice.org.uk/pathways/hyperten sion-in-pregnancy
  • 43. Any Questions or Comments? Please leave a note on the Welcome Page to this website