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Protocol for
MANAGEMENT OF
SEVERE
PRE-ECLAMPSIA/
ECLAMPSIA
Green top guideline
2010
Prof. Aboubakr Elnashar
Benha university Hospital, Egypt
ABOUBAKR ELNASHAR
BACKGROUND
Eclampsia (E)
convulsions superimposed on pre-eclampsia.
Preeclampsia (PE)
PIH in association with proteinuria (> 0.3 g/24 h) ±
oedema
Severe PE
Significant proteinuria (1 g/litre) PLUS
DBP ≥ 110 mmHg on 2 occasions OR
SBP ≥ 170 mmHg on 2 occasions OR
DBP ≥ 100 mmHg on 2 occasions & with at least 2 S or
S of imminent E.
HELLP syndrome:
Variant of severe PET (haemolysis, elevated liver
enzymes and low platelet count).ABOUBAKR ELNASHAR
Clinical features of severe PET
in addition to hypertension & proteinuria:
Severe headache
Visual disturbance
Papilloedema
Liver tenderness
Epigastric pain and/or vomiting
Signs of clonus
Platelet count <100 x 106/l
Abnormal liver enzymes
(ALT or AST rising to above 70 iu/l)
HELLP syndrome.
ABOUBAKR ELNASHAR
MANAGEMENT
I. Maternal monitoring
II. Foetal assessment
III.Control BP
IV.Prevention of seizures
V.Control of seizures
VI. Fluid balance
VII.Delivery
VIII. Postparum
ABOUBAKR ELNASHAR
I. Maternal monitoring
1.BP:
/15 m until the woman is stabilised and then /30 m in the
initial phase of assessment.
/4-h if a conservative management plan
2. Input and output chart.
3. Full blood count, liver function and renal function
tests.
Repeated at least daily when the results are normal but
more often if the clinical condition changes
•AST >75 iu/l or ALT >70 iu/l Significant
>150 iu/l: increased maternal morbidity
Uric acid should not be used for clinical decision-making.
Platelet count<100x106: consideration for delivery.
4. Clotting studies
not required if the platelet count >100 x 106/l.ABOUBAKR ELNASHAR
•Diagnosis of HELLP syndrome
1. Haemolysis:
LDH levels, or blood film (fragmented red cells).
2. Platelet count: <100 x 106
ABOUBAKR ELNASHAR
II. Foetal assessment
•In the acute setting:
CTG
•In labour:
continuous electronic fetal monitoring.
ABOUBAKR ELNASHAR
•In Conservative management:
1. US :
F wt
A FI
2. Umbilical artery Doppler
3. CTG
ABOUBAKR ELNASHAR
III. Control BP: Antihypertensive treatment
Indications:
1. SBP> 160 mmHg or
DBP>100 mmHg.
2. SBP <160 plus
severe disease :
heavy proteinuria or
disordered liver or haematological test
ABOUBAKR ELNASHAR
•Drugs:
•Acute , severe:
Nifedipine: oral not sublingually
IR cap:10 mg initial; repeat after 30 m if necessary
IR cap: 10-30 mg tid; not to exceed 120-180 mg/d
ABOUBAKR ELNASHAR
Hydralazine
IV: 5 mg over 5 min, repeat /20 min until
DBP 95 mmHg, No more than 4 doses.
If not give Labetalol or Nifidipine.
Maintenance: 10 mg/h
Add 2ml NS to reconstitute 20 mg
hydralazine.
Withdraw 0.5 ml hydralazine solution
and add 9.5 ml NS to give total 10 ml
solution.
ABOUBAKR ELNASHAR
Labetalol:
IV: 20 mg; subsequent doses of 40, 80,
80 mg IV at 20-min intervals.
Maintenance: 40 mg/h
Oral: 100 mg BID
ABOUBAKR ELNASHAR
Chronic, moderate
Nifedipine
SR tab: 30-60 mg qd; not to exceed 90-120 mg/d
Hydralazine.
Oral: 25 mg tds
•Methyldopa
was the most commonly used therapies in the UK.
safe in long term follow-up of the delivered babies
some studies have suggested some benefits of labetalol.
•Atenolol
increase in IUGR.
•ACE inhibitors and ARBs
contraindicated {unacceptable fetal adverse effects}.
•Diuretics
relatively contraindicated for hypertension
should be reserved for pulmonary oedema.
ABOUBAKR ELNASHAR
IV. Prevention of seizures
Indications:
1. Severe PET:
once a delivery decision has been made and in the
immediate postpartum period.
When conservative management of a woman with
severe hypertension and a premature fetus is made
it would be reasonable not to treat until the decision
to deliver has been made.
ABOUBAKR ELNASHAR
If Mg So is given:
1. It should be continued for 24 h following delivery
or 24 h after the last seizure
2. Regular assessment of:
a. Urine output: <20 ML/H: STOP
b. Deep tendon reflexes: Loss: Stop
c. Respiratory rate:
d. Oxygen saturation
Antidote: Ca gluconate 1 g (10 ml) over 10 m
ABOUBAKR ELNASHAR
V. Control of seizures
I. 1. Do not leave the patient alone. Prevent maternal
injury during the convulsion.
2. Call for help and place a code blue call- Medical
Emergency call.
4. Initiate resuscitation.
5. Turn the patient into left lateral position when able
to do so.
6. Inform the consultant obstetrician and anesthetist
on call.
II. AIRWAY
1. Assess and maintain patency, using oral suction if
necessary.
2. Insert a plastic oral airway if possible
3. administer oxygen therapy via face mask.
ABOUBAKR ELNASHAR
III. BREATHING
1. Assess respiratory rate and ambubag using
facial mask/laryngeal mask or endotracheal tube if
necessary.
IV. CIRCULATION
1. Evaluate Pulse and B P. If absent, initiate CPR.
2. Secure IV access as soon as possible with main
line infusion, with three-way tap attached, of
Hartmann's Solution, administered at a very slow
rate, as fluid intake will be restricted to 1 ml/kg/h
3. Pulse oximetry is helpful.
ABOUBAKR ELNASHAR
2. Mg SO4 is the therapy of choice
Loading dose: 4 g given by infusion
pump over 5–10 min
Maintenance: infusion of 1 g/h for 24 h
after the last seizure.
Prepare loading dose:
Add 4g (8ml) of 50% MgS04 to 12ml of
NS. Administer slowly IV over 10 m.
 Prepare Maintenance dose:
Add 50g (100ml) of 50% MgS04 to
400ml of NS (withdraw 100mls from
500ml bag of NS, prior to adding
MgS04).
Administer IV via volumetric pump at
10ml/h =1g/h.
ABOUBAKR ELNASHAR
3. Once stabilized
plans should be made to deliver the woman but
there is no particular hurry and a delay of several hrs
to make sure the correct care is in hand is
acceptable
The woman’s condition will always take priority
over the fetal condition.
ABOUBAKR ELNASHAR
Recurrent seizures.
1. Increase the rate of infusion of Mg So4 to 1.5 g
or 2.0 g/h
2. Diazepam or thiopentone may be used, but only
as single doses,
3. Intubation
4. Transfer to intensive care facilities with
intermittent positive pressure ventilation
ABOUBAKR ELNASHAR
VI. Fluid balance
1. Total fluids should be limited to 80 ml/h or 1
ml/kg/h
2. The regime of fluid restriction should be
maintained until there is a postpartum diuresis
3. If there is associated maternal hge, fluid balance
is more difficult and fluid restriction is inappropriate.
ABOUBAKR ELNASHAR
VII. Delivery
When:
•> 34W: Once the woman is stable
•<34 w and delivery can be deferred >24 h:
corticosteroids
•Conservative management at very early
gestations(26W) may improve the perinatal outcome
but must be carefully balanced with maternal
wellbeing, only be considered if the mother remains
stable
ABOUBAKR ELNASHAR
How?
Depend on
1.presentation
2.fetal condition
3.likelihood of success of IOL after assessment of
the cervix.
•>34 w with a cephalic presentation:
vaginal delivery should be considered.
Discuss the mode of delivery with the mother.
Vaginal prostaglandins will increase the chance of
success.
Anti-hypertensive tt should be continued throughout
assessment and labour.
•<32 w: CS is more likely as the success of induction
is reduced
ABOUBAKR ELNASHAR
The third stage:
5 u IM Syntocinon or 5 u IV Syntocinon given slowly.
Ergometrine or Syntometrine should not be given for
prevention of hge
ABOUBAKR ELNASHAR
VIII. Postpartum management
1. .
a. Women who develop hypertension or symptoms
of PE postnatally (headaches, visual
disturbances, nausea and vomiting or epigastric
pain): referred for a specialist opinion and
investigation to exclude PE.
b. Women who deliver with severe PET (or E): close
observation postnatally for 4 days or more
c. Careful review to ensure improving clinical signs
is needed before discharge.
ABOUBAKR ELNASHAR
2. Anti-hypertensive
•Continued as dictated by BP.
•BP should not be allowed to exceed 160/110
mmHg
•A reduction in anti-hypertensive therapy should be
made in a stepwise fashion.
•Avoid alpha methyldopa
•In breastfeeding:
labetalol, atenolol, nifedipine and enalapril can be
given
ABOUBAKR ELNASHAR
3. Follow-up and final diagnosis
1. An assessment of BP and proteinuria at the 6 w.
If hypertension or proteinuria persists then further
investigation is recommended.
2. Preconceptional counselling
ABOUBAKR ELNASHAR
ABOUBAKR ELNASHAR

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Protocol for MANAGEMENT OF SEVERE PRE-ECLAMPSIA/ ECLAMPSIA Green top guideline 2010

  • 1. Protocol for MANAGEMENT OF SEVERE PRE-ECLAMPSIA/ ECLAMPSIA Green top guideline 2010 Prof. Aboubakr Elnashar Benha university Hospital, Egypt ABOUBAKR ELNASHAR
  • 2. BACKGROUND Eclampsia (E) convulsions superimposed on pre-eclampsia. Preeclampsia (PE) PIH in association with proteinuria (> 0.3 g/24 h) ± oedema Severe PE Significant proteinuria (1 g/litre) PLUS DBP ≥ 110 mmHg on 2 occasions OR SBP ≥ 170 mmHg on 2 occasions OR DBP ≥ 100 mmHg on 2 occasions & with at least 2 S or S of imminent E. HELLP syndrome: Variant of severe PET (haemolysis, elevated liver enzymes and low platelet count).ABOUBAKR ELNASHAR
  • 3. Clinical features of severe PET in addition to hypertension & proteinuria: Severe headache Visual disturbance Papilloedema Liver tenderness Epigastric pain and/or vomiting Signs of clonus Platelet count <100 x 106/l Abnormal liver enzymes (ALT or AST rising to above 70 iu/l) HELLP syndrome. ABOUBAKR ELNASHAR
  • 4. MANAGEMENT I. Maternal monitoring II. Foetal assessment III.Control BP IV.Prevention of seizures V.Control of seizures VI. Fluid balance VII.Delivery VIII. Postparum ABOUBAKR ELNASHAR
  • 5. I. Maternal monitoring 1.BP: /15 m until the woman is stabilised and then /30 m in the initial phase of assessment. /4-h if a conservative management plan 2. Input and output chart. 3. Full blood count, liver function and renal function tests. Repeated at least daily when the results are normal but more often if the clinical condition changes •AST >75 iu/l or ALT >70 iu/l Significant >150 iu/l: increased maternal morbidity Uric acid should not be used for clinical decision-making. Platelet count<100x106: consideration for delivery. 4. Clotting studies not required if the platelet count >100 x 106/l.ABOUBAKR ELNASHAR
  • 6. •Diagnosis of HELLP syndrome 1. Haemolysis: LDH levels, or blood film (fragmented red cells). 2. Platelet count: <100 x 106 ABOUBAKR ELNASHAR
  • 7. II. Foetal assessment •In the acute setting: CTG •In labour: continuous electronic fetal monitoring. ABOUBAKR ELNASHAR
  • 8. •In Conservative management: 1. US : F wt A FI 2. Umbilical artery Doppler 3. CTG ABOUBAKR ELNASHAR
  • 9. III. Control BP: Antihypertensive treatment Indications: 1. SBP> 160 mmHg or DBP>100 mmHg. 2. SBP <160 plus severe disease : heavy proteinuria or disordered liver or haematological test ABOUBAKR ELNASHAR
  • 10. •Drugs: •Acute , severe: Nifedipine: oral not sublingually IR cap:10 mg initial; repeat after 30 m if necessary IR cap: 10-30 mg tid; not to exceed 120-180 mg/d ABOUBAKR ELNASHAR
  • 11. Hydralazine IV: 5 mg over 5 min, repeat /20 min until DBP 95 mmHg, No more than 4 doses. If not give Labetalol or Nifidipine. Maintenance: 10 mg/h Add 2ml NS to reconstitute 20 mg hydralazine. Withdraw 0.5 ml hydralazine solution and add 9.5 ml NS to give total 10 ml solution. ABOUBAKR ELNASHAR
  • 12. Labetalol: IV: 20 mg; subsequent doses of 40, 80, 80 mg IV at 20-min intervals. Maintenance: 40 mg/h Oral: 100 mg BID ABOUBAKR ELNASHAR
  • 13. Chronic, moderate Nifedipine SR tab: 30-60 mg qd; not to exceed 90-120 mg/d Hydralazine. Oral: 25 mg tds •Methyldopa was the most commonly used therapies in the UK. safe in long term follow-up of the delivered babies some studies have suggested some benefits of labetalol. •Atenolol increase in IUGR. •ACE inhibitors and ARBs contraindicated {unacceptable fetal adverse effects}. •Diuretics relatively contraindicated for hypertension should be reserved for pulmonary oedema. ABOUBAKR ELNASHAR
  • 14. IV. Prevention of seizures Indications: 1. Severe PET: once a delivery decision has been made and in the immediate postpartum period. When conservative management of a woman with severe hypertension and a premature fetus is made it would be reasonable not to treat until the decision to deliver has been made. ABOUBAKR ELNASHAR
  • 15. If Mg So is given: 1. It should be continued for 24 h following delivery or 24 h after the last seizure 2. Regular assessment of: a. Urine output: <20 ML/H: STOP b. Deep tendon reflexes: Loss: Stop c. Respiratory rate: d. Oxygen saturation Antidote: Ca gluconate 1 g (10 ml) over 10 m ABOUBAKR ELNASHAR
  • 16. V. Control of seizures I. 1. Do not leave the patient alone. Prevent maternal injury during the convulsion. 2. Call for help and place a code blue call- Medical Emergency call. 4. Initiate resuscitation. 5. Turn the patient into left lateral position when able to do so. 6. Inform the consultant obstetrician and anesthetist on call. II. AIRWAY 1. Assess and maintain patency, using oral suction if necessary. 2. Insert a plastic oral airway if possible 3. administer oxygen therapy via face mask. ABOUBAKR ELNASHAR
  • 17. III. BREATHING 1. Assess respiratory rate and ambubag using facial mask/laryngeal mask or endotracheal tube if necessary. IV. CIRCULATION 1. Evaluate Pulse and B P. If absent, initiate CPR. 2. Secure IV access as soon as possible with main line infusion, with three-way tap attached, of Hartmann's Solution, administered at a very slow rate, as fluid intake will be restricted to 1 ml/kg/h 3. Pulse oximetry is helpful. ABOUBAKR ELNASHAR
  • 18. 2. Mg SO4 is the therapy of choice Loading dose: 4 g given by infusion pump over 5–10 min Maintenance: infusion of 1 g/h for 24 h after the last seizure. Prepare loading dose: Add 4g (8ml) of 50% MgS04 to 12ml of NS. Administer slowly IV over 10 m.  Prepare Maintenance dose: Add 50g (100ml) of 50% MgS04 to 400ml of NS (withdraw 100mls from 500ml bag of NS, prior to adding MgS04). Administer IV via volumetric pump at 10ml/h =1g/h. ABOUBAKR ELNASHAR
  • 19. 3. Once stabilized plans should be made to deliver the woman but there is no particular hurry and a delay of several hrs to make sure the correct care is in hand is acceptable The woman’s condition will always take priority over the fetal condition. ABOUBAKR ELNASHAR
  • 20. Recurrent seizures. 1. Increase the rate of infusion of Mg So4 to 1.5 g or 2.0 g/h 2. Diazepam or thiopentone may be used, but only as single doses, 3. Intubation 4. Transfer to intensive care facilities with intermittent positive pressure ventilation ABOUBAKR ELNASHAR
  • 21. VI. Fluid balance 1. Total fluids should be limited to 80 ml/h or 1 ml/kg/h 2. The regime of fluid restriction should be maintained until there is a postpartum diuresis 3. If there is associated maternal hge, fluid balance is more difficult and fluid restriction is inappropriate. ABOUBAKR ELNASHAR
  • 22. VII. Delivery When: •> 34W: Once the woman is stable •<34 w and delivery can be deferred >24 h: corticosteroids •Conservative management at very early gestations(26W) may improve the perinatal outcome but must be carefully balanced with maternal wellbeing, only be considered if the mother remains stable ABOUBAKR ELNASHAR
  • 23. How? Depend on 1.presentation 2.fetal condition 3.likelihood of success of IOL after assessment of the cervix. •>34 w with a cephalic presentation: vaginal delivery should be considered. Discuss the mode of delivery with the mother. Vaginal prostaglandins will increase the chance of success. Anti-hypertensive tt should be continued throughout assessment and labour. •<32 w: CS is more likely as the success of induction is reduced ABOUBAKR ELNASHAR
  • 24. The third stage: 5 u IM Syntocinon or 5 u IV Syntocinon given slowly. Ergometrine or Syntometrine should not be given for prevention of hge ABOUBAKR ELNASHAR
  • 25. VIII. Postpartum management 1. . a. Women who develop hypertension or symptoms of PE postnatally (headaches, visual disturbances, nausea and vomiting or epigastric pain): referred for a specialist opinion and investigation to exclude PE. b. Women who deliver with severe PET (or E): close observation postnatally for 4 days or more c. Careful review to ensure improving clinical signs is needed before discharge. ABOUBAKR ELNASHAR
  • 26. 2. Anti-hypertensive •Continued as dictated by BP. •BP should not be allowed to exceed 160/110 mmHg •A reduction in anti-hypertensive therapy should be made in a stepwise fashion. •Avoid alpha methyldopa •In breastfeeding: labetalol, atenolol, nifedipine and enalapril can be given ABOUBAKR ELNASHAR
  • 27. 3. Follow-up and final diagnosis 1. An assessment of BP and proteinuria at the 6 w. If hypertension or proteinuria persists then further investigation is recommended. 2. Preconceptional counselling ABOUBAKR ELNASHAR