3. objective
• To discuss about evaluation and management eclampsia on epilepsy
by Zerihun W. 3
4. Identification
• Name …. T . T
• Age …….. 29
• Sex ……… F
• MRN ……1026864
• DOA …….13/12/13 E.C
• DOD …….01/13/13 E.C
by Zerihun W. 4
5. Referral On 12/12/13
• She refered from K/H/C as a case of epilepsy + Twin pregnancy
• This is 29 yrs. old GII PI(Alive by VD) whose GA was 32W3D from
early ultrasound. She had regular ANC
PE
V/S BP 110/70
Baseline investigation
VDRL
PICT Negative
HBSAg
BG O+ve
Reason for referral
For better management
by Zerihun W. 5
6. Duty R2 EVALUATION @ 12;30 PM 13/12/13
• This is 29 years old GII PI(alive by VD) whose clamed Amenorrhea for the
past 08 month GA form 22w5d ultrasound 32w4d. She had regular ANC
follow up at local HC where routine care given.
• She was referred as a case Twin + epilepsy and linked from regular ANC
with sever record of BP
• She is a know epileptic patient for the last 10 years started after delivery of
first baby. She had repeated attack of abnormal body movement which
involved all extremity with up roving of the eye & drooling of saliva
followed by loss of conscious of unknown duration.
• Before the attack she experience shortness of breath.
by Zerihun W. 6
7. • For this compliant She wanted to holy water for the first 06 years. Then
because of the repeated attack she was visit to HC and start unspecified
medication for about 02 years and discontinued because drug was not
available at HC and unafforded to buy outside.
• The pregnancy was followed at HC since 5 month this pregnancy. Until 8
month she had not attach through out the pregnancy. The first attack in this
px at home involved all extremity followed by loss of conscious, it was 5
day before arrival to our hospital
• Otherwise
She didn’t have fever, pushing down pain, leakage of liquor
She didn’t have known chronic illness in her family as well as herself
such as chronic hypertension, cardiac and family history
Previous pregnancy was uneventful
by Zerihun W. 7
8. P/E
• GA :- well looking
• V/S :- Bp :- 155113 PR:- 88 RR:- 20 T:- ATT
• HEENT :- Pink conjunctiva & NIS
• LG :- No Palpable LN
• CHEST :- Clear & Resonance
• CVS :- S1 & S2 Well heard, No M or G
• ABD :- term size gravid uterus
multiple fetal part palpable
FHR both twin normal
by Zerihun W. 8
9. • GUS :- no vaginal bleeding or leakage of liquor
• MUK :- No Edema
• CNS :- COTPP
9
10. Ass,t
pp
Early preterm px
Twin px (?MCDA)
Known Epilepsy (not on medication)
PE w SF (raised BP)
Plan
Do CBC, ECG, OFT, Bilirubin
Target scan
To consult medical side
Stabilized with mgso4 and start methyldopa 500 mg po TID
Dexamethasone started
Initiate antiepileptic after consultation
Consult R3
by Zerihun W. 10
normal
11. R3 evaluation 13/12/13
• HX and PE revised and the same
• Obstetric ultrasound done by Y3
Twin px
TA EFW 1.7 RBPP
TB EFW 1.5 RBPP
Single placenta
Intertwin membrane 1.8cm
Fetal sex the same
N Doppler
• Plan
Start anticonvulsant after consult medical side
Continues dexa, methyldopa, mgso4
Follow with preeclampsia chart
Admit to MW(14/12/13)
by Zerihun W. 11
12. • HX and PE revised and the same
She had one episode of abnormal body movement witnessed in EOPD
lasting than 1 mint
• Ass the same
• Plan
Phenytoin load with 1g po the 100 mg po TID
Continues obs follow-up
Consult neurologic side
Consult psychiatric side
by Zerihun W. 12
Medical side evaluation on 13/12/13
13. Psychiatry evaluation 13/12/13
• Hx Revised and the same
She has no loss of interest, or mood change
She had no hx elevated mood, irritability or increase energy
She has no hx of suspiciousness, hearing voice or seeing other can't see
She has no aggressive behavior of disorganized behavior
She has no hx of suicidal attempt pt. self harm
She has no hx of excessive wariness or fear
She has no hx of head injury or family hx of seizures
• Ass the same
• Plan
Need frequent psychiatric screening
No current mental health disorder
Consult medical side and neurology
by Zerihun W. 13
14. R2 evaluation MW
• Hx & Px Revised and the same
• Ass
PP
Early preterm px
Twin px (MCDA)
Known Epilepsy
PE w SF (raised BP)
Selective IUGR of TB
• Target scan
TA 2 kg TB 1.3 kg discrepancy 35 %
MCDA
Doppler N
by Zerihun W. 14
15. • Plan
Update CBC, OFT 2x weekly
Continue Phenytoin 100 mg po TID
Continue methyldopa 500 mg po TID
Dexa,, mgso4 :- completed
Follow with preeclampsia chart
Lung maturity test at 36 week
by Zerihun W. 15
16. R3 decision note 26/12/13 @ 4 pm
• This is 29 yrs. old Gll Pl whose GA 34w5d from 22w6d us kept MW for 02 wk.
with Ass of
PP
Early preterm px
Twin px (MCDA)
Known Epilepsy
PE w SF (raised BP)
Selective IUGR of TB
• She develop one episode of abnormal body movement involving the whole
extremity lasting less than 1 min and loss of consciousness which was
immediately regained. associated with this She has up roving of the eye.
Witnessed by health professional
• Otherwise
She had droving of saliva
She had no headache, blurred vision
She had no nausea epigastric pain vomiting, change in mentation
by Zerihun W. 16
17. P/E
• GA :- ASL RBS 120
• V/S :- Bp :- 13090 PR:- 100 RR:- 20 T:- 36.9 spo2 96 and support w INo2
• HEENT :- Pink conjunctiva & NIS
• LG :- No Palpable LN
• CHEST :- Clear & Resonance
• CVS :- S1 & S2 Well heard, No M or G
• ABD :- term size gravid uterus
multiple fetal part palpable
FHR both twin normal
• GUS :- no vaginal bleeding or leakage of liquor
• MUK :- No Edema
• CNS :- COTPP, GCS 15/15
by Zerihun W. 17
18. • Ass
PP
Early preterm px
Twin px (MCDA)
Known Epilepsy
PE w SF (raised BP)
Selective IUGR of TB
Eclampsia
• Plan
Dexamethasone 6mg IM salvage dose
Load with mgso4
Catheterized
Transfer to LW for Emergency cs
Update CBC, OFT Serum e-
Involve consultant
by Zerihun W. 18
19. 26/12/13
• Emergency caesarean section done with outcome of
TA 1900 gram female alive neonate with APGAR score of 7 & 8
TB 1450 gram female alive neonate with APGAR score of 7 & 8
• IOF
Single placenta with two Dividing mm :- MCDA
by Zerihun W. 19
20. • Post op order
Ampicillin 2g IV QID
Put of MF 500 ml NS/DNS 5%/RL over 24hr
Continue Phenytoin 100mg po TID
Continue Mgso4 maintenance
Keep catheter for at least 12hr
Put on continues VS monitoring
Keep family in her bedside
Watch for vaginal bleeding
Transfer neonates to NICU for evaluation
by Zerihun W. 20
21. NICU evaluation
• Ass
TA :- TA + LBW + AGA + Discordant twin
TA :- TB + LBW + LGA + Discordant twin
• Plan
Send CBC determine BG
Attach baby to the Mather
Start breast feeding
• IVX
B/G B+
HCT TA 41 TB 39%
23% Discordant
by Zerihun W. 21
22. Post op evaluation 27/12/13
• P1 :- 29 yrs. old PII lady on 1st post op day after LUTCS was done for the
indication of Eclampsia + Twin Px with outcome of TA 1900 gram female
alive neonate with APGAR score of 7 & 8 and TB 1450 gram female alive
neonate with APGAR score of 7 & 8. neonate in mother side after
evaluated by pediatric side
• P2 :- Eclampsia
• P3 :- Known epileptic
• S poorly adherent to medication
• Otherwise
She has no headache, blurred vision
She has no abnormal body movement
by Zerihun W. 22
23. P/E
• GA :- well looking
• V/S :- Bp :- 140102 PR:- 80 RR:- 20 T:- 36.1
• HEENT :- Pink conjunctiva & NIS
• LG :- No Palpable LN
• CHEST :- Clear & Resonance
• CVS :- S1 & S2 Well heard, No M or G
• ABD :- 20 wk. sided well contracted uterus
• GUS :- no vaginal bleeding
• MUK :- No Edema
• CNS :- COTPP
by Zerihun W. 23
24. • Ass
smooth post op day
• Plan
Continue phenytoin 100 mg po TID
Nifedipine 10mg po daily
Mgso4 completed
Update CBC, OFT
Follow with PE chart
Advice the mother on drug adherence
Psychiatric side consulted( plan is to link to psychiatric side after discharge
for frequent psychiatric screening)
Folic acid 4 mg po daily
Brain MRI, EEG up on discharge
Next pregnancy follow up should be in hospital and require preconception
care
by Zerihun W. 24
25. INVESTIGATION SUMMERY
by Zerihun W. 25
13/19/13 20/12/13 27/12/13 29/10/20 01/10/20
WBC 4.3X103 4.6X103 6.8X103 7.8X103 6.9X103
HCT 32.8 36 34.6 9.2/25.5 8.5/24.5
PLT 160
u/a -ve
147 179 58 194
OFT Got – 6
Gpt – 13.3
Cr – 0.5
Bun – 15.1
Got – 7.8
Gpt – 13.8
Cr – 0.48
Bun – 18
D bil - <1.16,
T bil - <0.12
Got – 96
Gpt – 84
Cr – 0.58
Bun – 19
D bil – 0.11
T bil - 19
Got – 38
Gpt – 20
Cr – 0.42
Bun – 14
Electrolyte Na+ 138
K+ 4.9
26. U/S SUMMERY
by Zerihun W. 26
13/12/13 15/12/13 18/12/13 22/12/13 25/12/13 26/12/13
TA 1.5kg, SDP
3.8
TB 1.7 kg , SDP
3.8
Mm Thickness
1.8mm
Fetal sex the same
Index
RBPP
N Doppler
?MCDA
TA SDP
3.5CM
TB SDP 4
CM
Thick
dividing mm
Index
RBPP
TA 2kg
TB 1.3 kg
Index
RBPP
N
Doppler
TB
selective
IUGR
MCDA
TA SDP 3
CM
TB SDP
2.1 CM
Index
RBPP
TA SDP 2.7
CM
TB SDP 2.4
CM
Index
RBPP
N doppler
TA SDP 4
CM
TB SDP 3.5
CM
Index
RBPP
N doppler
27. by Zerihun W. 27
Pre OP Follow-up at MW
Post OP Followp-up
28. Summery
• This is 29 yrs. old GII PI lady a known epileptic patient for the last 10 yrs.,
she was took antiepileptic medication for 02 yrs. and discounted 02 yrs.
Back prior to this pregnancy because of finical reason. she had repeated
attack before this pregnancy .
• At GA of 32w3d she was referred as a case of epilepsy from KHC. She was
liked from ANC with sever range BP
• She was admitted PP + Early preterm px + Twin px (MCDA) + Known
Epilepsy + PE w SF (raised BP) + Selective IUGR of TB
• Prior 5 day of referral she has abnormal body movement and 01 episode
witnessed at EOPD, Phenytoin load and on 100 mg po TID
• She stay MW for two weeks. As GA of 34+5 she develop abnormal body
movement of one episode which last less than one minute and considering
eclampsia mgso4 loaded and emergency cs decided with outcome of TA 1.9
kg and TB 1.4 kg
by Zerihun W. 28
31. Eclampsia
• the occurrence of new-onset, generalized, tonic- clonic seizures or coma in
a woman with preeclampsia in the absence of other neurologic condition
• Incidence
GHTN <0.1%
0.6 % PE with out severity feature
2 to 3 PE with severity feature
Developed : 1.5 to 10 cases per 10,000 Deliveries
Developing : 6 to 157 cases per 10,000 Deliveries
by Zerihun W. 31
32. • Risk factor
Nulliparity
Preeclampsia in a previous pregnancy
Age >40 years or <18 years
Family history of preeclampsia
Chronic hypertension
Chronic renal disease
Autoimmune disease (eg, antiphospholipid syndrome, systemic lupus
erythematosus)
Vascular disease
Diabetes mellitus (pregestational and gestational)
Multifetal gestation
Obesity
by Zerihun W. 32
33. Black race
Hydrops fetalis
Woman herself was small for gestational age
Fetal growth restriction, abruptio placentae, or fetal demise in a previous
pregnancy
Prolonged interpregnancy interval if the previous pregnancy was
normotensive; if the previous pregnancy was preeclamptic, a short
interpreg``1nancy interval increases the risk of recurrence
Partner-related factors (new partner, limited sperm exposure
[eg, previous use of barrier contraception])
In vitro fertilization
by Zerihun W. 33
In our case risk Factor for PE
Multiple gestation
Epilepsy
34. • Timing
59 percent -antepartum,
20 percent - intrapartum, and
21 percent -postpartum (90%-with in 1week
by Zerihun W. 34
35. • Supportive of eclampsia
Abnormal body movement typical of eclampsia
PE w SF.
Twin px
• Against eclampsia
She is a know epileptic patient
She had the some attach in this pregnance
Poor adherent to medication
Cerebral symptom absent before and after convulsion
by Zerihun W. 35
In our case
36. Epilepsy
• Seizure is defined as a paroxysmal disorder of the central nervous system
characterized by an abnormal neuronal discharge with or without loss of
consciousness.
• Epilepsy encompasses different syndromes whose cardinal feature is a
predisposition to recurrent unprovoked seizures
Focal Seizures
Generalized Seizures
by Zerihun W. 36
37. • Incidence
Epilepsy affects approximately 1 to 2%
is the most frequent major neurologic complication encountered in
pregnancy.
• Diagnosis
Two unprovoked seizures or
One seizure in a patient with clinical features that make a second seizure
likely
Findings on brain MRI
EEG that are consistent with a diagnosis of
epilepsy
A family history of epilepsy
by Zerihun W. 37
38. • Perinatal morbidity and mortality
increased among women with epilepsy
complications include
preeclampsia,
preterm labor,
bleeding,
placental abruption,
poor fetal growth,
prematurity,
fetal death, and
maternal mortality
by Zerihun W. 38
39. • Risk estimates derived from a population-based cohort study
Maternal death: 80 deaths per 100,000 pregnancies among women with
epilepsy, compared with 6 deaths per 100,000 pregnancies among
women without epilepsy
Cesarean delivery: 41 versus 33 percent
Pregnancy-related hypertension (11 versus 8 percent) and preeclampsia
(7 versus 4 percent)
Antepartum hemorrhage (2.1 versus 1.5 percent)
PPH,(0.7 versus 0.4)
Preterm labor (11 versus 7 percent)
Poor fetal growth (4 versus 2 percent)
Stillbirth (0.8 versus 0.6)
by Zerihun W. 39
In our case
Preeclapmsia
eclampsia
40. • Effect of pregnancy on seizures
For the majority of women with epilepsy (54% to 80%), seizure
frequency will remain similar to their baseline seizure frequency.
Across several studies, seizure frequency increased in 15.8% to 32% of
women and decreased in 3% to 24%.
Seizure free for 9 months prior to pregnancy is associated with an
84% to 92% chance of remaining seizure free during pregnancy.
increased seizure frequency among sleep deprived, stressed or
noncompliant
Labor and delivery are not usually associated with increased
complications.
increased prevalence of comorbid depression and anxiety
by Zerihun W. 40
In our case
She was not on medication
and she multiple seizure
attach so she will have 54 to
80 % risk of seizure
41. • Effect of pregnancy on AED
Altered protein binding,
Delayed gastric emptying,
Nausea and vomiting,
Changes in plasma volume,
Changes in the volume of distribution, and
Even folic acid supplementation can affect the levels of
anticonvulsant medications.
by Zerihun W. 41
42. • Lamotrigine is the most common AED prescribed in pregnancy.
• Given the interindividual variation in AED metabolism and
susceptibility to changes during pregnancy, checking AED drug levels
monthly is recommended for all AEDs.
by Zerihun W. 42
43. • Supportive epilepsy
She is a know epileptic patient
Multiple attach before
Poorly adherent
• Against of epilepsy
PE w SF
by Zerihun W. 43
In our case
44. Epilepsy or Eclampsia: A Diagnostic Dilemma?
• While eclampsia is the serious complication of the preeclampsia specific
for gestational period and epilepsy is a preexisting pathology of pregnancy.
• Both syndrome are characterized by neuroconvulsive syndrome. On the
other hand, epilepsy can be aggravated by the association of preeclampsia
and eclampsia during the pregnancy, both by increasing the number of
convulsive seizures.
• Seizures are diagnosed for the first time during pregnancy, they should
be evaluated as eclampsia until proved otherwise
by Zerihun W. 44
45. • Clinical symptoms helpful in establishing the diagnosis of eclampsia, at
least one of these symptoms in 59% to 75% of the cases
Excessive weight gain
Persistent occipital or frontal headaches 50% to 75%
Blurred vision 19% to 32%
Photophobia,
Epigastric or right upper quadrant pain 19%
Altered mental status.
• 20% to 40% of eclamptic women do not have any premonitory signs or
symptoms before the onset of convulsions.
by Zerihun W. 45
46. • The initial management active seizure in pregnancy should include
maintenance of the airway, oxygenation, and support of adequate perfusion.
• Seizure mgt:
Convulsive seizures be treated promptly with intravenous
benzodiazepines; Lorazepam(0.1-0.2mg/kg) is considered the drug of
choice.
Intravenous phenytoin is also highly effective and has a longer duration
of action.
Mgso4 should be consider if the seizure recurred despite of conventional
anticonvulsant agent
• Monitoring-
Close monitoring for maternal condition and continuous fetal heart rate
monitoring is recommended in the event of a seizure, as well as for a
period of at least an hour after administration of benzodiazepines
by Zerihun W. 46
Literature review in Magnesium sulfate for non-eclamptic status epilepticus
Seizure reduction/control with IV MgSO4 occurred in 14 of the 28 patients
(50.0%), with 2 (7.1%) and 12 (42.9%) displaying partial and complete
responses respectively. Seizures recurred upon withdrawal of MgSO4 therapy
in 50% of the patients whom had reduction/control
Conclusions
Routine use of IV MgSO4 in non-eclamptic SE/RSE cannot be recommended
at this time. Further prospective study of this drug is required in order to
determine its efficacy as an anti-epileptic in this setting.
47. by Zerihun W. 47
Case Report
A 41-year-old pregnant woman Who is a known epilepsy for 15 years and managed with
antiepileptic and PE. At the 34w GA, she had an episode of seizures
• Intravenous diazepam (10 mg), following which seizures subsided.
• After 5 hours, the seizure recurred, and an injection of diazepam (10 mg) and a loading
dose of phenytoin were administered intravenously.
• She again had an episode of seizures. Midazolam given & A loading dose of valproate was
administered over 30 minutes, followed by 400 mg 3 times daily.
• Later A diagnosis of eclampsia and epilepsy was made. An injection of Mgso4 &
emergency cesarean delivery and seizure controlled.
Conclusions
• The initial management administration of a parenteral benzodiazepine, followed by
intravenous phenytoin at conventional doses, is a reasonable approach.
• If the is recurrent generalized tonic-clonic seizures with features suggestive of eclampsia
along with a history of epilepsy then eclampsia with epilepsy should Consider and
termination of pregnancy and Mgso4 treatment require.
48. Intrapartum
• Mode of delivery:
most women have a normal vaginal delivery. elective cesarean section
may be justified in selected cases.
• Epidural analgesia:
Although no evidence exists to support or challenge epidural analgesia
in patients with epilepsy, it is typically utilized to decrease stress and
allow the mother to rest during a long labor.
by Zerihun W. 48
49. postpartum
• Dose adjustment
if the antiseizure drug dose has been altered during pregnancy, a return
to prepregnancy levels should be considered during the first few weeks
after delivery.
Advice on the importance of adequate rest, sleep and compliance with
drug therapy.
Precautions need to be taken to protect the infant if the mother has a
seizure.
by Zerihun W. 49
50. • Breast feeding
All of the antiseizure drugs are measurable in breast milk.
The reported percentage of maternal plasma levels in breast milk varies
from 5 to10% with valproate to 90 percent with ethosuximide.
Most experts believe that taking antiseizure drugs does not generally
contraindicate breast feeding, as probable benefits outweigh risks.
by Zerihun W. 50
51. Twin Px Vs Preeclapmsia, IUGR
• DZ twins arise in about 1% to 1.5% of pregnancies, and MZ twins occur in
0.4% of pregnancies
• There are Certain complications anticipated in the management of labor
and delivery of multiple gestations
Except post Term and macrosomia
by Zerihun W. 51
52. • Maternal complications
GHTN and preeclampsia
Rates of gestational hypertension and preeclampsia were twice as
high in twin compared with singleton pregnancies (13 percent in
twins versus 5 to 6 percent in singletons for both disorders).
Early severe preeclampsia and HELLP syndrome tended to occur
more frequently in multiple gestations.
Other
Gestational diabetes –
Acute fatty liver –
APH, PPH
Manual placenta extraction
iron deficiency anemia,
hyperemesis gravidarum
thromboembolism.
by Zerihun W. 52
53. • Fetal complications
All twins
Growth restriction
Congenital anomalies
Preterm delivery
Monochorionic twins
Selective fetal growth restriction
Single fetal demise of one twin
Twin-twin transfusion syndrome (TTTS) –
Twin anemia-polycythemia sequence (TAPS) –
Twin reversed arterial perfusion sequence (TRAP) –
Monoamniotic twins
Intertwin cord entanglement
Conjoined twins
by Zerihun W. 53
In our case
Maternal and fetal complication of twin px
• Preeclapmsia
• Selected IUGR(there was no poly-oligo
sequence, doppler normal & wight
discrepancy 30% and post natal evaluation
wight discrepancy 21.6%, Hct 41 & 39)
54. Time of termination
• ACOG
Twin Px
Complicated
MCDA with isolated fetal growth restriction termination at 32 to
34 wk.
DCDA with isolated fetal growth restriction termination at 36 to
37 wk.
Uncomplicated MCDA twin is between 34 and 37 6/7 wks.
PE W SF with stable maternal and fetal condition termination at 34 wk.
or at diagnosis if diagnosis later after 34 wk. of GA
by Zerihun W. 54
In our case
lung maturity test planed at 36
wk.
55. Contraception
• LARC such as IUCD will not be affected by enzyme inducing drugs
Can be given to all patients
• OCP, implants, vaginal rings are affected by enzyme inducing AED
Better avoided
• Women taking lamotrigine monotherapy and oestrogen-containing
contraceptives should be informed of the potential increase in seizures due
to a fall in the levels of lamotrigine
by Zerihun W. 55
In our case
She was opted for Implanon and
provided
56. COMMENT
• Referral from HC should be earlier and Feedback should be given
• Documentation and follow up suboptimal
• Termination should be individualized
• Multidepartment involvement in management plan appreciable
• Choice of contraceptive
• Choice of anti epileptic
• Discharge plan good
by Zerihun W. 56
58. REFERENCES
• Williams Obstetrics, 25th Edition
• Gabbe Normal and problem pregnancy, 7th edition
• ACOG. May 2016
• Gabbe 7th Edition
• Uptodate 2018
by Zerihun W. 58
The first visit(13/12/13)
Regular ANC Bp 162/109 the linked to EOPD
10 to 15 percent of women in labor with preeclampsia without severe features will develop signs\symptoms of preeclampsia with severe features
By comparison, smoking decreases the risk of preeclampsia, and Asian and Hispanic women have a lower risk of preeclampsia than white women and a much lower risk than black women
Hypertensive encephalopathy, a possible model for eclampsia
The two conditions share many clinical, radiologic, and pathologic features
Two theories have been proposed to explain these cerebral abnormalities:
Vasospasm: cerebral overregulation and
forced dilation: loss of autoregulation
vasospasm of cerebral arteries, under perfusion of the brain, localized ischemia/infarction, and cytotoxic (intracellular) edema
high systemic pressure (ie, hypertensive encephalopathy) results in hyper perfusion, endothelial damage, and vasogenic (extracellular) edema
-Hypertension is considered the hallmark for the diagnosis of eclampsia. The hypertension can be severe (≥160 mm Hg systolic or ≥110 mm Hg diastolic), as in 20% to 54% of cases, or it can be mild (systolic BP between 140 and 160 mm Hg or diastolic BP between 90 and 110 mm Hg), as in 30% to 60% of cases. However, in 16% of cases, hypertension may be absent. In addition, severe hypertension is more common in patients who develop antepartum eclampsia (58%) and in those who develop eclampsia at 32 weeks’ gestation or later (71%). Moreover, hypertension is absent in only 10% of women who develop eclampsia at or before 32 weeks’ gestation.
-The diagnosis of eclampsia is usually associated with proteinuria (at least 1+ on a dipstick). In a series of 399 women with eclampsia, substantial proteinuria (≥3+ on a dipstick) was present in only 48% of the cases, whereas proteinuria was absent in 14% of the cases. Abnormal weight gain in excess of 2 lb/ wk (with or without clinical edema) during the third trimester might be the first sign before the onset of eclampsia. However, edema was absent in 26% of 399 eclamptic women studied.
-Several clinical symptoms are potentially helpful in establishing the diagnosis of eclampsia. These include persistent occipital or frontal headaches, blurred vision, photophobia, epigastric or right upper quadrant pain, and altered mental status. Women had at least one of these symptoms in 59% to 75% of the cases (Table 31-16). Headaches are reported by 50% to 75% of patients, whereas visual changes are reported in 19% to 32% of patients. These symptoms may occur before or after the onset of convulsions.
-Peripartum seizure is a common manifestation of epilepsy and eclampsia. Epilepsy is a chronic neurologic disorder that may complicate pregnancy, The risk of seizures increases at delivery, with 1% to 2% of women with epilepsy having a seizure during labor or in the first 24 hours postpartum.
-On the other hand, eclampsia is a hypertensive disorder of pregnancy associated with edema, proteinuria, and convulsion. Eclampsia has been reported to be associated with various neurologic problems, such as cerebrovascular accidents and blindness.
-Uncontrolled seizures during pregnancy are dangerous to both the mother and fetus. Tonic-clonic seizures can cause physical injury and abruptio placentae in the mother and hypoxia, acidosis, intracranial hemorrhage, and death in the fetus.4 The pregnant patient may aspirate, causing aspiration pneumonitis during seizure episodes. Fetal bradycardias have been reported during and after maternal convulsions.
-The initial management of patients presenting with active seizure in pregnancy should include maintenance of the airway, oxygenation, and support of adequate perfusion.
Immediate attention must also be applied to the fetus, particularly if it has reached a viable gestational age. While an ongoing evaluation is in progress to investigate the organic causes, administration of a parenteral benzodiazepine, followed by intravenous phenytoin at conventional doses, is a reasonable approach. A computed tomographic (CT) scan of the brain is required to differentiate the central organic cause of seizures from that of eclampsia, but concern for safety of the mother and her
fetus because of radiation exposure remains.5 Our patient had recurrent generalized tonic-clonic seizures with features suggestive of eclampsia along with
a history of epilepsy. We were in a dilemma regarding the pharmacotherapeutic management of seizures in this scenario.
-Our patient responded to conventional antiepileptic agents, but there was recurrence of seizures, which later subsided only after the initiation of magnesium therapy. This implies the generally accepted dictum that if the seizures occur in pregnancy, they should be evaluated as eclampsia until proved otherwise and should be treated as such until the attending physician can perform a proper evaluation. Emergency cesarean delivery is required if there are recurrent generalized seizures, to avoid any maternal and fetal morbidity. Thus, evaluation of the cause of seizures remains a limitation in an emergency scenario.
Women had at least one of these symptoms in 59% to 75% of the cases
anti-epileptic properties from N-methyl D-aspartate (NMDA) receptor inhibition. To date, a few animal models support this concept [3–6]. Clinically, MgSO4 has seen much attention within the obstetrics literature as an effective prophylactic and therapeutic agent for pre-eclampsia and eclampsia, respectively [7]. Furthermore, the lack of significant side effects is appealing due to concerns about fetal toxicity. The efficacy of MgSO4 as an AED in the setting of eclampsia is well documented since the early 1900s, with the mechanism of action attributed to both NMDA receptor antagonism and cerebral vasodilation. In addition, systematic reviews have demonstrated the superiority of MgSO4 over diazepam, phenytoin and lytic cocktails in the setting of eclampsia [8–10]. During status epilepticus (SE) and refractory status epilepticus (RSE) the NMDA receptor plays a key role in pharmaco-resistance and epileptigenicity. As seizures remain uncontrolled, there is an up-regulation of the NMDA receptor, leading to a glutamate mediated excitotoxicity and seizure potentiation [11,12]. This has lead to the interest in NMDA receptor antagonists as AED in the setting of SE/RSE. Ketamine is an example of one such drug which has displayed some efficacy in this setting [13]. The use of MgSO4 in the setting of non-eclamptic SE/RSE has been mentioned in protocols and reviews of therapies [14–16]. To date however there are only a small number of cases describing the use of IV MgSO4 for non-eclamptic SE/RSE [17–37]. Our goal was to perform a systematic review of the literature on the use of IV MgSO4, a NMDA receptor antagonist, for non-eclamptic SE/RSE.
women with frequent seizures during the third trimester or a history of status epilepticus during severe stress.
1. Lamotrigine clearance decreases quickly in the first week postpartum, and dose adjustments should be made sooner. In one case series, postpartum taper schedules of lamotrigine appeared to reduce the likelihood of maternal lamotrigine toxicity. The dose was incrementally reduced at postpartum days 3, 7, and 10, with return to preconception dose or preconception dose plus 50 mg to help counteract the effects of sleep deprivation.