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ECLAMPSIA
Dr Sneha Ronge
MBBS, MS OBGY (Pune)
ECLAMPSIA
According to ACOG eclampsia is defined
as convulsions occurring in a patient with
preeclampsia.
OR
Preeclampsia complicated with convulsion
and / or coma is called eclampsia. It can also
occur in patients who have preeclampsia
superimposed on essential hypertension or
chronic nephritis
An Eclamptic Fit
⚫It occurs in four stages:
⚫Premonitory stage:
⚫ -The head may be drawn to one side with rolling of
eyes.
⚫ -Twitching of hands and face.
⚫ -Loss of consciousness.
⚫ -Lasts for 30 sec.
⚫Tonic stage:
⚫-Entire body becomes rigid (state of spasm).
⚫-Arms are flexed, hands are clenched,legs are inverted.
⚫Face is distorted,tongue protrudes between the teeth.
An Eclamptic Fit
⚫Breath holding with cyanosis.
⚫Lasts for 30 sec.
⚫Clonic stage:
⚫All the muscles of the body including facial muscles
contract and relax alternatively in rapid succession. Jaws
and eyelids begin to open and close violently. Tonguebite
may occur.
⚫Bloodstained ,frothy secretions come out of mouth and
nose.
⚫Cyanosis gradually passes off, face and eyes are
congested.
⚫Lasts for 1-3 min.
An Eclamptic Fit
⚫Stage of coma:
⚫For short period.
⚫Pulse ,resp rate increases,BP is raised, Temp. may
increase.
⚫On regaining consciousness patient is confused,does not
remember the incidence.
Preeclampsia - Pathophsiology
⚫Neurological:
⚫, visual disturbances, CNS hyperexcitability,
hyperreflexia
⚫Seizures = eclampsia – causes
⚫ Hypertensive encephalopathy
⚫ Loss of cerebral autoregulation
⚫ Vasospasm
⚫ Microinfarctions, punctate hemorrhages
⚫ Thrombosis
⚫ Cerebral edema
ECLAMPSIA
Pathogenesis of eclampsia
- Unknown
- Severe arterial vasospasm
Rupture of the vascular endothelium
Pericapillary hemorrhage
Development foci of abnormal electrical discharge that may
generalized
Convulsions
Period of gestation convulsions occur
In 50% of cases >36 wks of gestation
Antepartum - 46.3%
Intrapartum - 16.4%
Postparum - 37.3%
usually within 48 hrs
of delivery
Sibai BM et al Obstet Gynaecol 1981, 58 : 609.
⚫ Eclampsia
⚫ Epilepsy
⚫ Cerebral malaria in tropics
⚫ Encephalitis
⚫ Meningitis
⚫ Intracranial tumors
⚫ Peripheral cerebral thrombosis
⚫ Poisoning
⚫ Hysteria
Differential Diagnosis
⚫ Injuries
⚫ Pulmonary edema
⚫ Pneumonia
⚫ Acute LVF
⚫ Cerebral hemorrhage
⚫ Renal failure
⚫ Pulmonary embolism
⚫Hyperpyrexia
⚫Hepatic necrosis
⚫DIC
⚫Postpartum shock
⚫Puerperal sepsis
⚫Disturbed vision
⚫Psychosis
Complications of eclampsia
⚫ Cerebral haemorrhage
⚫ Anoxia
⚫ Cardiac failure
⚫ Pulmonary oedema
⚫Aspiration pneumonia
⚫Pulmonary embolism
⚫Postpartum shock
⚫Puerperal sepsis
Causes of maternal / Perinatal mortality
Causes of perinatal mortality :
‱ Prematurity
‱ Intrauterine asphyxia
‱ Effects of drugs used to control convulsion
‱ Trauma during delivery
‱ Perinatal mortality 30 to 50%
‱ Sibai BM et al American Journal of Obstet Gynaecol 1983; 146 :
307.
⚫ General management
⚫ To control convulsions using MgSO4
⚫ To control Hypertension
⚫ To avoid Diuretics
⚫ To limit IV fluids unless excessive fluid loss
⚫ To investigate
⚫ To terminate the pregnancy
⚫ Care in puerperium
⚫ Follow up.
Principles of Management of Eclampsia
General management
⚫To place in a railed cot in an isolated place
⚫To maintain airway
⚫To administer oxygen 8-10lit/min
⚫To take detail history from relatives
⚫After proper sedation quick examination
⚫Catheterization and check for proteinuria
⚫œ an hourly Pulse, Temp, RR, BP, uterine contraction,
FHS.
⚫1 hrly urine output
⚫Maintain fluid balance with CVP monitoring
⚫To administer antibiotics
Management of Eclampsia
Specific management
To control seizures and to prevent its recurrence
Magnesium sulfate: the drug of choice
Regimens Loading dose Maintenance dose
Pritchard 4gm IV over 3 to 4 min 5gm buttock 4 hrly
10gm deep IM
Zuspan 4gm IV over 5 to 10 min 1-2gm hrly IV infu
Sibai 6gm IV over 20 min 2gm hrly IV infusion
Sardesai 4 gm IV or IM 2 gm 3 hrly IV or IM
Therapeutic level of MgSO4 – 4 to 7mRQ/litre
Monitor
Presence of patellar reflex (8 to 10mEQ/litre đŸĄȘ diagnose)
Respiratory rate >16 (>12mEQ /litre đŸĄȘ depression)
Urinary output 30ml/hr
Continuation for 24 hrs after the last seizure
M.M. 0.4%
⚫It probably works by neuronal calcium blocking
through the glutamate channel
⚫It will nearly always arrest convulsions
⚫It does not depress the maternal sensorium
⚫The fetus is least affected
⚫It is currently the anticonvulsant of choice in
eclampsia
Magnesium Sulphate
Magnesium Sulphate
Protocol
⚫4 gms IV as 20% soln @ 1 gm/min
⚫10 gms of 50% soln. 5 gms in each buttock
⚫If convulsions persist after 15 min give 2 gms IV
again as 20 % soln
⚫Every 4 hours 5 gms of 50% soln given in
alternate buttock
⚫Discontinued 24 hours after delivery
⚫If Mg levels are monitored it must be between
4 -7 mEq/L
⚫If clinical monitoring only
ïżœ The patellar reflex must be present
ïżœ Respiration not depressed
ïżœ Urine output > 100 mL in the last 4 hours
Magnesium Sulphate
Protocol
Diazepam
⚫ It is a very good agent to terminate a fit (10 mg IV
repeated if necessary)
⚫ It is not a good agent to prevent a fit
⚫ If depresses maternal CNS
⚫ Doses more than 40 mg must not be used in 24 hours
⚫ It accumulates in the fetus and results in problems
after birth
Lytic cocktail regimen
On admission
25mg chlorpromazine +100mg pethidine in 20ml of 5%
solution iv followed by 50mg chlorpromazine + 25 mg
promethazine im.
Later on
Promethazine 25mg and chlorpromazine 50mg given
alternately lM till 24 hr of last fit or
IV 500ml containing 100mg pethidine drip rate adjusted to
20-30 drops/min till 24 hrs of last fit and not to exceed
300 mg /day.
Maternal Mortality (MM): 2.2%
Diazepam regimen
Initial drug of 100mg iv further 40mg in 500ml of Ringer lactate i. v. at 30
drops/min M.M. 5%
Phenytoin therapy
10mg/kg IV followed by 5mg/kg 2 hrs later
Sedatives can be used with above regimen
To control hypertension
Inspite of sedative if BP >160/110mg then
antihypertensive drugs are administered
Hydralazine
- 5mg iv slowly
- rate 10mg every 20 minutes
-Monitoring BP every 5 minutes
- Repeat the dose when diastolic BP >110mmHg
labetalol - 20 mg i.v., repeated every 30 min & can
be doubled maximum upto 80 mg
Nifedepine : 5 to 10 mg every 15 min to
maximum upto 30 mg
Status eclampticus
⚫Phenytoin sodium 0.5gm dissolve in 20mg of
5% dextose iv given slowly
⚫If no response then complete anesthesia,
muscle relaxant, assisted ventilation and C.
Section is done.
Planning the delivery
‱Delivery is the ultimate cure
Vaginal
‱ LSCS is done for obstetric reasons, or
before 32 weeks of gestation.
‱ Anesthesia –
‱ General to be avoided, as it increases blood
pressure during intubation and extubation.
‱ Epidural is better than spinal.
Route of delivery
⚫Probability of achieving vaginal delivery after
induction through an unripe cervix are below
20%
Hall DR et al, BJOG 2000
Haddad B et al, AJOG 2004
⚫Prolonged labor can be detrimental for
mother and fetus
⚫Caesarean delivery is preferable
Sibai BM et al, COG 2005
Post Partum Care
⚫Over 40% of maternal deaths occur postpartum
⚫Post delivery a relative oliguria is not uncommon,
occuring in 30% of patients with severe disease
⚫Continued close monitoring is required in a suitable
environment
⚫Taper antihypertensive agents
⚫Contraception Counseling and Follow up
Long term prognosis.
⚫PE and Eclampsia is a forerunner of later life
cardiovascular risk
⚫It is more in early onset PE.
⚫Does not affect long term renal function.
⚫No long term residual hepatic disease.
⚫Recurrence Risk-20 to 50 %.
⚫HELLP-2 to 6 %.
⚫Hemolysis
Schistocytes in the blood smear
S.Bilirubin > or equal to 1.2 mg%
Absent Plasma hapatoglobin
⚫Elevated Liver Enzymes
SGOT > 72 IU/L
LDH > 600 IU/L
⚫Low Platelet Count
Diagnosis of HELLP Syndrome
HELLP Syndrome
⚫Hemolysis, Elevated Liver Enzymes, Low Platelets
and PIH
⚫Differential Dx:
⚫ Hepatitis, gallbladder dz, acute fatty liver of pregnancy,
thrombocytopenic purpura (TTP)
⚫ Etiology unknown
⚫ 20% present postpartum, the rest preterm
⚫ Peak is 24-48 hrs postpartum
⚫ Initial c/o RUQ pain
⚫ 80% have PIH before dx
HELLP Syndrome
⚫Complications:
⚫ DIC
⚫ Placental abruption
⚫ Need for blood transfusion
⚫ Pleural effusion
⚫ Acute renal failure
⚫ Wound infection
⚫If develops postpartum there is a higher incidence of
pulmonary edema and renal failure
HELLP Syndrome
⚫Time course of thrombocytopenia is v. important
⚫ If stable at 80,000 PLT, then regional is OK
⚫ If dropping fast at 80,000, then regional is dangerous –
epidural hematoma
⚫Treatment - delivery
HELLP Syndrome.
⚫Prompt delivery , if it develops beyond 34 weeks.
⚫Dilemma- Before 34 weeks, administrations of
corticosteroid for 48 hrs for both maternal and fetal
benefits. But the results are variable in different
studies.
Preanesthetic Evaluation
⚫Fluid status
⚫Hemodynamic status
⚫Coagulation status
⚫ Bleeding time
⚫ PLT count
⚫ PT/aPTT
Anesthetic Mgmt
⚫Technique – Epidural vs. Spinal
⚫Treatment of side effects:
⚫ Hypotension
⚫ Difficult airway
⚫ Coagulation
⚫Urgent C/S
⚫Postpartum
⚫ Analgesia
⚫ Fluid balance
⚫ MgSO4
⚫ Hemodynamic control
Thanks for your attention !

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Eclampsia

  • 2. ECLAMPSIA According to ACOG eclampsia is defined as convulsions occurring in a patient with preeclampsia. OR Preeclampsia complicated with convulsion and / or coma is called eclampsia. It can also occur in patients who have preeclampsia superimposed on essential hypertension or chronic nephritis
  • 3. An Eclamptic Fit ⚫It occurs in four stages: ⚫Premonitory stage: ⚫ -The head may be drawn to one side with rolling of eyes. ⚫ -Twitching of hands and face. ⚫ -Loss of consciousness. ⚫ -Lasts for 30 sec. ⚫Tonic stage: ⚫-Entire body becomes rigid (state of spasm). ⚫-Arms are flexed, hands are clenched,legs are inverted. ⚫Face is distorted,tongue protrudes between the teeth.
  • 4. An Eclamptic Fit ⚫Breath holding with cyanosis. ⚫Lasts for 30 sec. ⚫Clonic stage: ⚫All the muscles of the body including facial muscles contract and relax alternatively in rapid succession. Jaws and eyelids begin to open and close violently. Tonguebite may occur. ⚫Bloodstained ,frothy secretions come out of mouth and nose. ⚫Cyanosis gradually passes off, face and eyes are congested. ⚫Lasts for 1-3 min.
  • 5. An Eclamptic Fit ⚫Stage of coma: ⚫For short period. ⚫Pulse ,resp rate increases,BP is raised, Temp. may increase. ⚫On regaining consciousness patient is confused,does not remember the incidence.
  • 6. Preeclampsia - Pathophsiology ⚫Neurological: ⚫, visual disturbances, CNS hyperexcitability, hyperreflexia ⚫Seizures = eclampsia – causes ⚫ Hypertensive encephalopathy ⚫ Loss of cerebral autoregulation ⚫ Vasospasm ⚫ Microinfarctions, punctate hemorrhages ⚫ Thrombosis ⚫ Cerebral edema
  • 7. ECLAMPSIA Pathogenesis of eclampsia - Unknown - Severe arterial vasospasm Rupture of the vascular endothelium Pericapillary hemorrhage Development foci of abnormal electrical discharge that may generalized Convulsions
  • 8. Period of gestation convulsions occur In 50% of cases >36 wks of gestation Antepartum - 46.3% Intrapartum - 16.4% Postparum - 37.3% usually within 48 hrs of delivery Sibai BM et al Obstet Gynaecol 1981, 58 : 609.
  • 9. ⚫ Eclampsia ⚫ Epilepsy ⚫ Cerebral malaria in tropics ⚫ Encephalitis ⚫ Meningitis ⚫ Intracranial tumors ⚫ Peripheral cerebral thrombosis ⚫ Poisoning ⚫ Hysteria Differential Diagnosis
  • 10. ⚫ Injuries ⚫ Pulmonary edema ⚫ Pneumonia ⚫ Acute LVF ⚫ Cerebral hemorrhage ⚫ Renal failure ⚫ Pulmonary embolism ⚫Hyperpyrexia ⚫Hepatic necrosis ⚫DIC ⚫Postpartum shock ⚫Puerperal sepsis ⚫Disturbed vision ⚫Psychosis Complications of eclampsia
  • 11. ⚫ Cerebral haemorrhage ⚫ Anoxia ⚫ Cardiac failure ⚫ Pulmonary oedema ⚫Aspiration pneumonia ⚫Pulmonary embolism ⚫Postpartum shock ⚫Puerperal sepsis Causes of maternal / Perinatal mortality Causes of perinatal mortality : ‱ Prematurity ‱ Intrauterine asphyxia ‱ Effects of drugs used to control convulsion ‱ Trauma during delivery ‱ Perinatal mortality 30 to 50% ‱ Sibai BM et al American Journal of Obstet Gynaecol 1983; 146 : 307.
  • 12. ⚫ General management ⚫ To control convulsions using MgSO4 ⚫ To control Hypertension ⚫ To avoid Diuretics ⚫ To limit IV fluids unless excessive fluid loss ⚫ To investigate ⚫ To terminate the pregnancy ⚫ Care in puerperium ⚫ Follow up. Principles of Management of Eclampsia
  • 13. General management ⚫To place in a railed cot in an isolated place ⚫To maintain airway ⚫To administer oxygen 8-10lit/min ⚫To take detail history from relatives ⚫After proper sedation quick examination ⚫Catheterization and check for proteinuria âš«Âœ an hourly Pulse, Temp, RR, BP, uterine contraction, FHS. ⚫1 hrly urine output ⚫Maintain fluid balance with CVP monitoring ⚫To administer antibiotics Management of Eclampsia
  • 14. Specific management To control seizures and to prevent its recurrence Magnesium sulfate: the drug of choice Regimens Loading dose Maintenance dose Pritchard 4gm IV over 3 to 4 min 5gm buttock 4 hrly 10gm deep IM Zuspan 4gm IV over 5 to 10 min 1-2gm hrly IV infu Sibai 6gm IV over 20 min 2gm hrly IV infusion Sardesai 4 gm IV or IM 2 gm 3 hrly IV or IM Therapeutic level of MgSO4 – 4 to 7mRQ/litre Monitor Presence of patellar reflex (8 to 10mEQ/litre đŸĄȘ diagnose) Respiratory rate >16 (>12mEQ /litre đŸĄȘ depression) Urinary output 30ml/hr Continuation for 24 hrs after the last seizure M.M. 0.4%
  • 15. ⚫It probably works by neuronal calcium blocking through the glutamate channel ⚫It will nearly always arrest convulsions ⚫It does not depress the maternal sensorium ⚫The fetus is least affected ⚫It is currently the anticonvulsant of choice in eclampsia Magnesium Sulphate
  • 16. Magnesium Sulphate Protocol ⚫4 gms IV as 20% soln @ 1 gm/min ⚫10 gms of 50% soln. 5 gms in each buttock ⚫If convulsions persist after 15 min give 2 gms IV again as 20 % soln ⚫Every 4 hours 5 gms of 50% soln given in alternate buttock ⚫Discontinued 24 hours after delivery
  • 17. ⚫If Mg levels are monitored it must be between 4 -7 mEq/L ⚫If clinical monitoring only ïżœ The patellar reflex must be present ïżœ Respiration not depressed ïżœ Urine output > 100 mL in the last 4 hours Magnesium Sulphate Protocol
  • 18. Diazepam ⚫ It is a very good agent to terminate a fit (10 mg IV repeated if necessary) ⚫ It is not a good agent to prevent a fit ⚫ If depresses maternal CNS ⚫ Doses more than 40 mg must not be used in 24 hours ⚫ It accumulates in the fetus and results in problems after birth
  • 19. Lytic cocktail regimen On admission 25mg chlorpromazine +100mg pethidine in 20ml of 5% solution iv followed by 50mg chlorpromazine + 25 mg promethazine im. Later on Promethazine 25mg and chlorpromazine 50mg given alternately lM till 24 hr of last fit or IV 500ml containing 100mg pethidine drip rate adjusted to 20-30 drops/min till 24 hrs of last fit and not to exceed 300 mg /day. Maternal Mortality (MM): 2.2%
  • 20. Diazepam regimen Initial drug of 100mg iv further 40mg in 500ml of Ringer lactate i. v. at 30 drops/min M.M. 5% Phenytoin therapy 10mg/kg IV followed by 5mg/kg 2 hrs later Sedatives can be used with above regimen
  • 21. To control hypertension Inspite of sedative if BP >160/110mg then antihypertensive drugs are administered Hydralazine - 5mg iv slowly - rate 10mg every 20 minutes -Monitoring BP every 5 minutes - Repeat the dose when diastolic BP >110mmHg labetalol - 20 mg i.v., repeated every 30 min & can be doubled maximum upto 80 mg Nifedepine : 5 to 10 mg every 15 min to maximum upto 30 mg
  • 22. Status eclampticus ⚫Phenytoin sodium 0.5gm dissolve in 20mg of 5% dextose iv given slowly ⚫If no response then complete anesthesia, muscle relaxant, assisted ventilation and C. Section is done.
  • 23. Planning the delivery ‱Delivery is the ultimate cure Vaginal ‱ LSCS is done for obstetric reasons, or before 32 weeks of gestation. ‱ Anesthesia – ‱ General to be avoided, as it increases blood pressure during intubation and extubation. ‱ Epidural is better than spinal.
  • 24. Route of delivery ⚫Probability of achieving vaginal delivery after induction through an unripe cervix are below 20% Hall DR et al, BJOG 2000 Haddad B et al, AJOG 2004 ⚫Prolonged labor can be detrimental for mother and fetus ⚫Caesarean delivery is preferable Sibai BM et al, COG 2005
  • 25. Post Partum Care ⚫Over 40% of maternal deaths occur postpartum ⚫Post delivery a relative oliguria is not uncommon, occuring in 30% of patients with severe disease ⚫Continued close monitoring is required in a suitable environment ⚫Taper antihypertensive agents ⚫Contraception Counseling and Follow up
  • 26. Long term prognosis. ⚫PE and Eclampsia is a forerunner of later life cardiovascular risk ⚫It is more in early onset PE. ⚫Does not affect long term renal function. ⚫No long term residual hepatic disease. ⚫Recurrence Risk-20 to 50 %. ⚫HELLP-2 to 6 %.
  • 27. ⚫Hemolysis Schistocytes in the blood smear S.Bilirubin > or equal to 1.2 mg% Absent Plasma hapatoglobin ⚫Elevated Liver Enzymes SGOT > 72 IU/L LDH > 600 IU/L ⚫Low Platelet Count Diagnosis of HELLP Syndrome
  • 28. HELLP Syndrome ⚫Hemolysis, Elevated Liver Enzymes, Low Platelets and PIH ⚫Differential Dx: ⚫ Hepatitis, gallbladder dz, acute fatty liver of pregnancy, thrombocytopenic purpura (TTP) ⚫ Etiology unknown ⚫ 20% present postpartum, the rest preterm ⚫ Peak is 24-48 hrs postpartum ⚫ Initial c/o RUQ pain ⚫ 80% have PIH before dx
  • 29. HELLP Syndrome ⚫Complications: ⚫ DIC ⚫ Placental abruption ⚫ Need for blood transfusion ⚫ Pleural effusion ⚫ Acute renal failure ⚫ Wound infection ⚫If develops postpartum there is a higher incidence of pulmonary edema and renal failure
  • 30. HELLP Syndrome ⚫Time course of thrombocytopenia is v. important ⚫ If stable at 80,000 PLT, then regional is OK ⚫ If dropping fast at 80,000, then regional is dangerous – epidural hematoma ⚫Treatment - delivery
  • 31. HELLP Syndrome. ⚫Prompt delivery , if it develops beyond 34 weeks. ⚫Dilemma- Before 34 weeks, administrations of corticosteroid for 48 hrs for both maternal and fetal benefits. But the results are variable in different studies.
  • 32. Preanesthetic Evaluation ⚫Fluid status ⚫Hemodynamic status ⚫Coagulation status ⚫ Bleeding time ⚫ PLT count ⚫ PT/aPTT
  • 33. Anesthetic Mgmt ⚫Technique – Epidural vs. Spinal ⚫Treatment of side effects: ⚫ Hypotension ⚫ Difficult airway ⚫ Coagulation ⚫Urgent C/S ⚫Postpartum ⚫ Analgesia ⚫ Fluid balance ⚫ MgSO4 ⚫ Hemodynamic control
  • 34. Thanks for your attention !